Friday, November 17, 2017

Youtube daily report Nov 17 2017

ANNOUNCER: THE FOLLOWING PROGRAM IS PAID FOR BY

THE FRIENDS AND PARTNERS OF JOYCE MEYER MINISTRIES.

[MUSIC]

JOYCE: I WANNA PRAY SOMETHIN' OVER YOU TODAY, AND I JUST WANT

YOU TO RECEIVE IT.

THIS IS SOMETHIN', I THINK, THAT WE COULD AND SHOULD DO ON

A REGULAR BASIS.

AND I LIKE TO PRAY THIS OVER PEOPLE WHEN THEY'RE IN A SERVICE

LIKE THIS, EPHESIANS 3:16.

PAUL PRAYED THIS FOR THE CHURCH AT EPHESUS, SO RECEIVE THIS.

I PRAY THAT: "GOD WOULD GRANT YOU OUT OF THE RICH TREASURY OF

HIS GLORY TO BE STRENGTHENED AND REINFORCED WITH MIGHTY POWER

IN THE INNER MAN.

I PRAY THAT THE HOLY SPIRIT WOULD [INDWELL YOUR INNERMOST

BEING AND YOUR PERSONALITY]," AND THAT YOU WOULD BE STRONG IN

THE LORD AND ABLE TO FACE ANYTHING YOU HAVE TO FACE

AND STILL BE VICTORIOUS, IN JESUS' NAME.

HOW DO WE STAY STRONG IN THE SPIRIT?

WELL, FIRST OF ALL, THE WORD OF GOD IS THE FOOD YOU

NEED FOR YOUR SPIRIT.

JUST LIKE I'M THIRSTY SO I HAD A DRINK OF WATER,

WELL, YOU KNOW WHAT?

JESUS SAID, "I'M THE LIVING DRINK.

IF YOU DRINK OF ME, YOU'LL NEVER THIRST."

HE'S SAID, "I'M YOUR LIVING FOOD.

IF YOU TAKE ME AS YOUR FOOD, YOU'LL NEVER HUNGER."

ALWAYS RESPECT THE WORD OF GOD, AND WHEN YOU HEAR THE WORD OF

GOD, THE WORDS GOIN' FORTH OUT OF MY MOUTH RIGHT NOW,

THEY'RE NOT JUST WORDS.

THEY'RE GOD'S WORDS.

AND SO, THAT MEANS THERE'S POWER.

THE BIBLE SAYS, "THERE'S INHERENT POWER IN

THE WORD OF GOD."

SO, JUST LIKE WHEN YOU EAT FOOD AND YOU CHEW IT AND YOU SWALLOW

IT, THE NUTRITION IS RELEASED, IF YOU REALLY LISTEN, YOU DON'T

JUST PUT YOUR TIME IN IN CHURCH TO THINK THAT YOU'VE MADE GOD

HAPPY BECAUSE YOU SHOWED UP FOR 45 MINUTES, BUT YOU COME WITH

AN ATTITUDE OF, "YOUR WORD IS POWERFUL.

YOUR PRESENCE IS POWERFUL.

THIS IS HELPING ME.

THIS IS STRENGTHENING ME, THIS IS HEALING ME.

THIS IS MAKING A DIFFERENCE IN MY LIFE."

SEE, EVERYTHING THAT YOU GET IN A CHURCH SERVICE IS NOT UP

TO THE PREACHER.

A LOT OF IT IS UP TO THE ATTITUDE THAT YOU COME IN WITH.

[AUDIENCE APPLAUDING]

JOYCE: YOU NEED TO COME HUNGRY.

YOU NEED TO COME EXCITED.

YOU NEED TO COME AND REALIZE WHAT A PRECIOUS TREASURE IT IS

TO SIT AROUND OTHER BELIEVERS THAT HAVE AN ANOINTING ON THEIR

LIFE AND TO HEAR THE WORD OF GOD.

COME ON, LET'S THANK GOD FOR WHAT HE'S DONE IN OUR LIFE.

[AUDIENCE CHEERING]

JOYCE: THIS IS A GOOD PLACE TO BE.

SO, THE WORD STRENGTHENS US IN SPIRIT, GOD'S PRESENCE.

YOU KNOW SOMETHIN' THAT YOU COULD DO?

I DO THIS FROM TIME TO TIME.

HOW MANY OF YOU CAN KINDA TELL WHEN YOU'RE STARTIN' TO RUN

ON EMPTY?

I MEAN, YOUR SYSTEM IS JUST KINDA LIKE, YOU'RE RUNNIN'

ON EMPTY.

WELL, YOU KNOW WHAT?

INSTEAD OF JUST CONTINUING TO PUSH YOURSELF AND GETTIN CRANKY

AND GROUCHY, AND BLAMIN' EVERYBODY AROUND YOU,

AND, YOU KNOW, IT CAN JUST GO FROM BAD TO WORSE.

YOU KNOW THAT, DON'T YOU?

IT CAN JUST, IF IT'S ALREADY BAD, IT'S GONNA GET WORSE IF YOU

DON'T DO SOMETHIN' ABOUT IT.

WELL, I DON'T CARE IF YOU JUST HAVE TO GO LOCK YOURSELF IN

THE BATHROOM, JUST GO AND SIT SOMEWHERE OR STAND SOMEWHERE.

EVEN JUST TAKE 3 MINUTES AND JUST...

[EXHALING]

"GOD, I NEED YOU.

STRENGTHEN ME, LORD.

HELP ME JUST CALM DOWN.

WHEW, MMM, WHEW, OKAY, FEELIN' BETTER NOW."

COME ON, DO YOU UNDERSTAND THAT?

[AUDIENCE APPLAUDING]

JOYCE: I MEAN, THAT'S JUST GOOD PRACTICAL ADVICE.

JUST GET SOMEWHERE BY YOURSELF, ZIP YOUR LIP.

YOU KNOW, WHEN YOU'RE FRUSTRATED, THE MORE YOU TALK,

THE WORSE IT'S GONNA GET.

JUST GET SOMEWHERE FOR A MINUTE, GET QUIET, CALM DOWN, COLLECT

YOURSELF, GET YOURSELF TOGETHER.

AS WE TELL OTHER PEOPLE, "YOU JUST NEED TO GO SOMEWHERE

AND GET YOURSELF TOGETHER."

[AUDIENCE LAUGHING]

JOYCE: GOD'S PRESENCE, PRAYER, BUT I WANNA TALK TO YOU

SPECIFICALLY ABOUT, YES, WE NEED TO PRAY ABOUT EVERYTHING AND

DON'T DO ANYTHING UNTIL YOU AT LEAST MENTION IT TO GOD FIRST,

BUT REPENTANCE.

YOU KNOW, ONE OF THE THINGS THAT KEEPS US WEAK IN SPIRIT IS

HIDDEN SIN, STUFF THAT WE KNOW IS THERE AND GOD KNOWS IS THERE,

BUT WE'RE JUST NOT TALKIN' ABOUT IT.

WE'RE JUST NOT DEALIN' WITH IT.

DAVID PRAYED THAT GOD WOULD CLEAR HIM FROM HIDDEN AND

UNCONSCIOUS FAULTS, THINGS THAT WERE THERE THAT HE HAD MANAGED

TO IGNORE LONG ENOUGH THAT ALTHOUGH HE WAS STILL FEELING

THE WEIGHT OF THEM--DO YOU KNOW THAT WE CAN COMPROMISE TO THE

POINT WHERE WE HAVE MAJOR SIN IN OUR LIFE AND WE DON'T EVEN

REALLY KNOW WHAT IT IS THAT'S BOTHERING US ANYMORE?

AND, YOU KNOW, SOMETIMES, IF YOU'RE JUST NOT FEELIN' RIGHT IN

YOUR LIFE, YOU JUST, "SOMETHIN'S WRONG, I'VE GOT A HEAVINESS.

I DON'T KNOW.

THERE'S NO JOY."

WHY DON'T YOU JUST GO AND GET BY YOURSELF SOMEWHERE AND JUST ASK

GOD A QUESTION THAT HE'S JUST WAITING TO ANSWER?

AND HERE'S THE QUESTION: "GOD, WHAT IS REALLY WRONG

IN MY LIFE?" COME ON, NOT LIKE, HE MAY NOT

TELL YOU, "IT'S YOUR CIRCUMSTANCES."

SEE, WE ALWAYS THINK EVERY TIME WE'RE UNHAPPY,

IT'S OUR CIRCUMSTANCES.

BUT A LOT OF TIMES, IT'S OUR ATTITUDE, OR IT'S SOMETHING

GOING ON IN US, OR SOMETHING THAT WE NEED TO TAKE CARE OF

THAT WE'VE NOT TAKEN CARE OF.

I RECALL A TIME WHEN I WASN'T SLEEPIN' GOOD.

THERE WAS ONE NIGHT I WASN'T SLEEPIN' GOOD.

I TOSSED AND TURNED AND I'D SLEEP FOR A FEW MINUTES AND I'D

WAKE UP, AND IT GOT TO BE ABOUT 5 O'CLOCK IN THE MORNING, AND I

REALLY WISH THAT I WOULD HAVE ASKED GOD SOONER SO I COULD HAVE

GOTTEN SOME SLEEP.

BUT I WAITED TILL 5, AND I FINALLY JUST SAID,

"GOD, WHAT IS WRONG?" COME ON, THAT'S A GOOD QUESTION

TO ASK GOD.

[AUDIENCE APPLAUDING]

JOYCE: WHAT IS WRONG?

AND IMMEDIATELY, HE SHOWED ME SOMETHING THAT I HAD DONE

THE DAY BEFORE.

I HAD HURT SOMEBODY'S FEELINGS AND JUST GLOSSED OVER IT.

DIDN'T DO WHAT I SHOULD HAVE DONE.

DIDN'T TAKE CARE OF IT.

DIDN'T ASK GOD TO FORGIVE ME.

DIDN'T ASK THEM TO FORGIVE ME.

AND I REPENTED IMMEDIATELY, MADE A COMMITMENT TO MAKE THINGS

RIGHT WITH THEM THE NEXT DAY, AND IT WAS ALMOST TIME TO GET UP

ANYWAY, BUT I DID GET ABOUT 30 MINUTES' SLEEP.

COME ON, "GOD WHAT IS WRONG?" [AUDIENCE APPLAUDING]

JOYCE: COME ON, THIS IS GOOD ADVICE, "WHAT'S WRONG?

WHAT'S GOIN' ON?" WE RUN SO FAST IN LIFE THAT MANY

TIMES, WE'RE JUST DRAGGIN' ALL THESE PROBLEMS ALONG WITH US

AND WE DON'T EVEN TAKE THE TIME TO STOP AND ASK GOD WHAT'S

REALLY GOIN' ON.

HOW ABOUT GUILT?

DON'T BE CARRYIN' A BUNCH OF GUILT AROUND WITH YOU.

MAN, THAT WEAKENS US.

OOH, IT'S HARD TO STAY STRONG IN GOD IF YOU'VE GOT A GUILTY

CONSCIENCE AND A BUNCH OF STUFF THAT'S BUGGIN' YOU INSIDE.

HOW 'BOUT KNOWIN' WHO YOU ARE IN CHRIST?

BOY, I TELL YOU, THE DEVIL GETS AFRAID OF YOU WHEN YOU KNOW

WHO YOU ARE IN CHRIST.

PETER TALKED ABOUT IT THIS MORNING.

THAT WAS GREAT WHAT HE SHARED.

WHO ARE YOU?

DO YOU KNOW WHO YOU ARE?

IF YOU KNOW WHO YOU ARE, AND THE DEVIL KNOWS

YOU KNOW WHO YOU ARE, THEN HE'S GONNA BE RUNNIN'

FROM YOU INSTEAD OF YOU RUNNIN' FROM HIM.

BUT YOU KNOW WHAT?

KNOWING, MAINTAINING A RIGHTEOUSNESS CONSCIOUSNESS IN

YOUR LIFE, IT TAKES HUGGIN' UP CLOSE TO GOD AND STAYIN' IN THE

WORD BECAUSE IF THERE'S ANYTHING THE ENEMY WANTS TO DO TO YOU,

HE WANTS TO MAKE YOU FEEL GUILTY AND CONDEMNED AND LIKE YOU'RE

NO GOOD.

YOU GUYS OUT THERE?

[AUDIENCE APPLAUDING]

JOYCE: AM I RIGHT?

HOW MANY OF YOU HAVE TO FIGHT THAT BATTLE?

IT'S LIKE, "WELL, YOU DIDN'T THIS, AND YOU DIDN'T THAT,

AND YOU'RE NOT, AND YOU'RE NOT."

DO YOU EVER GET TIRED OF THE DEVIL TELLIN' YOU WHAT

YOU'RE NOT?

THEN GET IN THE WORD AND LET GOD TELL YOU WHO YOU ARE.

[AUDIENCE APPLAUDING]

JOYCE: AND THEN ANOTHER THING THAT REALLY WEAKENS PEOPLE IS

ANGER, WOW.

FIGHT FOR YOURSELF AND REFUSE TO LET ANGER STEAL THE SPIRITUAL

STRENGTH THAT YOU NEED TO DEAL WITH THINGS IN YOUR LIFE.

I'M TELLIN' YOU, STAYIN' ANGRY AT PEOPLE WILL JUST ZAP IT

RIGHT OUT OF YOU.

AND THEN ONE LAST THING I'LL SAY ABOUT THIS SECTION IS LET'S ALL

WORK TOGETHER AND JUST SEE HOW MANY ISSUES WE CAN HAVE IN OUR

LIFE AND STILL HOLD OUR PEACE WHILE WE GOT 'EM.

THAT'S A NEW GOAL.

I TOLD DAVE TODAY, I SAID, "OKAY, I'VE GOT A NEW GOAL."

I REALLY LOVE PEACE, AND I DO PRETTY GOOD MOST OF THE TIME,

BUT LATELY, I'VE JUST LET A FEW STUPID THINGS AGGRAVATE ME.

ANYBODY EVER DO THAT?

YOU JUST LET SOME REALLY DUMB STUFF JUST GET YOU ALL RATTLED,

AND IT'S NOT ANYTHING THAT'S GONNA BE EARTH SHAKING.

DOESN'T REALLY MATTER THAT MUCH.

AND I HAD ABOUT THREE OR FOUR OF THOSE THINGS LAST WEEK.

IT WAS JUST, LIKE, SILLY STUFF, AND I JUST LET IT--AND YOU KNOW

WHAT I'VE DISCOVERED?

ONCE YOU GET REALLY UPSET, YOU'RE NOT GONNA GET OVER IT

IN 5 SECONDS.

WHEN YOU GET REALLY UPSET, AT LEAST, WHEN I DO, IT TAKES

A TOLL ON ME, AND SOMETIMES IT TAKES A WHILE FOR ME TO

CALM DOWN.

SO, IT'S JUST A LOT LESS EFFORT TO JUST NOT GET UPSET.

COME ON, I'M TELLIN' YOU SOMETHIN' VALUABLE.

IT TAKES A LOT LESS EFFORT TO JUST NOT GET UPSET

THAN IT DOES TO GET UPSET, ACT BAD, HAVE TO REPENT.

THE DEVIL CONDEMNS YOU, YOU KNOW, ALL THAT STUFF.

AND YOU GOTTA GO APOLOGIZE TO FIVE OR SIX PEOPLE.

[AUDIENCE LAUGHING]

JOYCE: IT'S LIKE, "NO, I DON'T WANNA DO THAT ANYMORE."

MY NEW GOAL IS, "JUST DO YOUR BEST, DEVIL, BUT I'M HOLDIN'

MY PEACE."

[AUDIENCE APPLAUDING]

JOYCE: ALL RIGHT, I PROBABLY GOT TOO MUCH MESSAGE AND NOT

ENOUGH TIME.

BUT ALL RIGHT, NOW, YOU KNOW WHAT TIME THAT WE REALLY NEED

TO BE STRONG?

IS WHEN PEOPLE COME AGAINST US.

OR WHEN THEY DISAPPOINT US.

WHAT ABOUT WHEN PEOPLE REALLY, REALLY, REALLY DISAPPOINT YOU?

OKAY, LISTEN TO THIS, 2 TIMOTHY 4:16,

PAUL SAID: "AT MY FIRST TRIAL NOBODY ACTED IN MY DEFENSE,

NOBODY TOOK MY PART, AND NOBODY STOOD WITH ME,

BUT ALL," UNDERLINE "ALL," "FORSOOK ME."

WHAT KIND OF SPIRITUAL STRENGTH DID THIS MAN HAVE?

LOOK AT THE NEXT STATEMENT: "MAY IT NOT BE CHARGED AGAINST THEM!"

YOU KNOW WHAT?

HE WAS A SMART MAN.

HE KNEW THAT IF HE DIDN'T FORGIVE THEM, IF HE LET THAT

ANGER STAY IN HIM, IF HE STAYED MAD AT THEM, THAT HE WAS NOT

GONNA BE ABLE TO GO THROUGH WHAT HE WAS FACIN' RIGHT NOW.

SO EVEN THOUGH NOT ONE OF THEM STOOD WITH HIM, THE FIRST THING

HE SAID IS, "I PRAY THAT IT WON'T BE CHARGED AGAINST THEM."

AND LOOK AT THE NEXT THING THAT HAPPENS:

"BUT THE LORD STOOD BY ME-- [AUDIENCE CHEERING]

JOYCE: "AND THE LORD STRENGTHENED ME, SO THAT THROUGH

ME THE [GOSPEL] MESSAGE MIGHT BE FULLY PREACHED."

"NOBODY STOOD WITH ME.

EVERYBODY CAME AGAINST ME.

I QUICKLY FORGAVE THEM, AND GOD WAS WITH ME,

AND HE STRENGTHENED ME.

AND I STILL CAME OUT VICTORIOUS ON THE OTHER SIDE."

[AUDIENCE CHEERING]

JOYCE: DO ANY OF YOU HAVE ANYBODY IN YOUR LIFE RIGHT NOW

THAT'S COMIN' AGAINST YOU?

HOW 'BOUT ANYBODY, YOU GOT SOMEBODY IN YOUR LIFE THAT, BOY,

YOU'VE BEEN THERE FOR THEM, AND NOW THERE'S A SITUATION AND THEY

JUST DIDN'T HAVE TIME FOR YOU, THEY DIDN'T STAND BY YOU?

YOU KNOW WHAT?

DON'T EVEN WASTE YOUR TIME LETTING IT DRAIN YOU OF

THE ENERGY THAT YOU NEED TO LIVE YOUR LIFE.

FORGIVE THEM--WELL, YOU DIDN'T TAKE THAT TOO WELL.

[AUDIENCE LAUGHING]

[AUDIENCE APPLAUDING]

JOYCE: DON'T WASTE YOUR TIME LETTIN' THEM STEAL YOUR ENERGY.

QUICKLY FORGIVE 'EM, AND THEN YOU KNOW WHAT'LL HAPPEN?

GOD WILL BE MORE TO YOU IN 1 SECOND THAN ALL OF THEM

COULD HAVE BEEN IN A LIFETIME.

[AUDIENCE CHEERING]

JOYCE: THINK STRONG, BE STRONG.

"AS A MAN THINKS IN HIS HEART, SO IS HE."

WHERE YOUR MIND GOES, YOUR ACTIONS WILL FOLLOW.

THINK STRONG, THINK, "I CAN DO IT."

THINK, "THIS IS NOT TOO MUCH FOR ME.

I CAN DO WHAT I NEED TO DO.

I'M NOT GONNA BE AFRAID OF THAT."

MY MOTHER--YOU KNOW, MY DAD SEXUALLY ABUSED ME FOR

A LOT OF YEARS.

MY MOTHER KNEW ABOUT IT, DIDN'T DO ANYTHING ABOUT IT.

AND I STILL MARVEL ABOUT THAT.

IT MAY SOUND RIDICULOUS, BUT I CAN ALMOST UNDERSTAND

WHAT HE DID MORE THAN I CAN WHAT SHE DID.

LIKE, I CAN'T GET A MOTHER KNOWING THAT AND DOIN' NOTHIN'.

BUT I DON'T SAY THAT AS A BITTERNESS STATEMENT, OR--I

MEAN, BOTTOM LINE IS, IS SHE DID IT 'CAUSE SHE WAS WEAK.

SHE JUST WAS WEAK.

SHE WAS NOT--SHE DIDN'T CONFRONT THINGS IN LIFE.

SHE DIDN'T STAND UP TO THINGS.

SHE LET MY DAD ABUSE HER AND BEAT ON HER, AND HE'D COME IN

DRUNK AND PUSH HER AROUND, AND SHE JUST PUT UP WITH IT.

AND 30 YEARS AFTER ALL THIS HAPPENED AND I WAS ALREADY GROWN

AND IN MINISTRY, THIS IS WHAT MY MOTHER SAID TO ME.

SHE SAID, "I'M SORRY FOR WHAT I LET YOUR FATHER DO TO YOU."

NOW, LISTEN, 'CAUSE THIS WAS EYE OPENING TO ME.

SHE SAID, "I DIDN'T LEAVE HIM, BECAUSE I DIDN'T THINK THAT

I COULD SUPPORT YOU AND YOUR BROTHER, AND I DIDN'T THINK THAT

I COULD FACE THE SCANDAL."

SHE DIDN'T THINK SHE COULD, SO SHE DIDN'T, COME ON.

CAN I TELL YA SOMETHIN'?

IF YOU DON'T THINK YOU CAN, YOU'RE DEFEATED BEFORE YOU EVER

GET STARTED.

[AUDIENCE CHEERING]

JOYCE: AND I'LL BE HONEST WITH YA, IF YOU DIDN'T COME TO

HEAR ANYTHING BUT THAT, THAT ONE THING CAN BE LIFE CHANGING

FOR YOU.

[AUDIENCE APPLAUDING]

JOYCE: YOU HAVE NO IDEA HOW MANY TIMES IN 1 WEEK THE ENEMY

WILL WHISPER TO ME, "YOU CAN'T."

AND I HAVE TO QUICKLY SAY, "I CAN AND I WILL.

NOT ON MY OWN, BUT IN CHRIST, I CAN AND I WILL.

I CAN DO ALL THINGS THROUGH CHRIST WHO IS--"

COME ONE, DON'T BE WEAK WILLED.

DON'T BE WEAK MINDED.

DON'T BE WEAK IN SPIRIT.

[AUDIENCE CHEERING]

JOYCE: IT JUST MAKES ME JUST WANNA SCREAM WHEN I THINK ABOUT

WHAT MY MOTHER PUT UP WITH, AND SHE BELIEVED IN JESUS.

I MEAN, SHE COULD'VE--MY GOSH, IF SHE WOULD'VE JUST STOOD UP

TO HIM.

NOT ONLY WOULD IT HAVE HELPED ME, IT WOULD HAVE HELPED MY

BROTHER, IT WOULD HAVE HELPED HER, BUT ACTUALLY, IT WOULD HAVE

ENDED UP HELPIN' MY DAD.

SEE, SOMETIMES WHEN YOU DON'T STAND UP TO PEOPLE THAT ARE

ABUSING YOU OR MISTREATING YOU, YOU'RE NOT HELPING THEM.

YOU'RE JUST INVITING THEM TO KEEP DOIN' THE SAME THING.

[AUDIENCE APPLAUDING]

JOYCE: THINK STRONG.

"I CAN."

YOU KNOW, THERE'D BE NO POINT IN ME STANDING HERE TODAY TRYIN' TO

TELL YOU WHAT IT TOOK FOR ME TO GET FROM WHERE I WAS TO WHERE

I AM, YOU KNOW?

BUT YOU COULDN'T UNDERSTAND IT IF I TRIED TO TAKE 100 YEARS TO

TELL YOU.

BUT WHEN I STARTED DOIN' WHAT I'M DOIN', WOMEN DIDN'T DO THIS.

[AUDIENCE APPLAUDING]

JOYCE: AND I DON'T MEAN THIS IN ANY KIND OF A WRONG OR

A PRIDEFUL WAY, BUT I THINK GOD HAS USED ME AND THE--GOD'S GIVEN

ME A GIFT OF DETERMINATION.

I MEAN, I WOULDN'T HAVE MADE IT THROUGH WHAT I WENT THROUGH

AS A CHILD IF I WOULDN'T HAVE HAD THAT.

AND SO, I GIVE HIM THE CREDIT FOR IT.

BUT IF I WOULDN'T HAVE HAD THAT, I MEAN, I WOULD HAVE BEEN

DEFEATED BEFORE I EVER GOT STARTED.

AND I THINK THAT GOD HAS ALLOWED ME TO KINDA PAVE THE WAY FOR

A LOT OF OTHER WOMEN NOW THAT CAN COME BEHIND.

[AUDIENCE CHEERING]

JOYCE: AND THINGS ARE EASY FOR THEM BECAUSE SOMEBODY

WENT AHEAD.

AND YOU KNOW WHAT?

NOW, LISTEN TO ME, EVERY TIME THAT YOU FIGHT FOR A VICTORY

IN YOUR LIFE, YOU'RE NOT JUST WINNING A BATTLE FOR YOU.

YOU'RE WINNING A BATTLE FOR OTHER PEOPLE THAT ARE GONNA

COME BEHIND.

[AUDIENCE CHEERING]

JOYCE: YOU KNOW, I JUST FEEL IT STRONG IN MY SPIRIT TODAY,

THAT THIS IS JUST A WORD FROM GOD FOR SOME OF YOU.

IT'S JUST, LIKE, GET OVER THINKIN' YOU'RE GONNA GIVE UP.

YOU ARE NOT GONNA GIVE UP.

GOD IS ON YOUR SIDE.

YOU'RE GONNA GO THROUGH, BE ALL GOD WANTS YOU TO BE, HAVE ALL

THAT GOD WANTS YOU TO HAVE, AND DO ALL THAT GOD WANTS YOU TO DO.

AMEN?

[AUDIENCE CHEERING]

JOYCE: AND WE'RE NOT GONNA LIVE ON EMERGENCIES.

WE'RE GONNA DO WHAT WE NEED TO DO EVERY DAY OF OUR LIFE.

I'M GONNA STUDY THE WORD AND I'M GONNA STUDY IT AGAIN

AND AGAIN AND AGAIN AND AGAIN AND AGAIN AND AGAIN.

AND I'M GONNA CONFESS THE WORD AGAIN AND AGAIN AND AGAIN

AND AGAIN.

AND I'M GONNA SPEND TIME WITH GOD EVERY MORNING,

EVERY MORNING, EVERY MORNING, EVERY MORNING, EVERY MORNING.

AND I'M NOT GONNA QUIT.

I'M NOT GONNA SHUT UP.

AND I'M NOT GONNA GIVE UP.

[AUDIENCE CHEERING]

JOYCE: AMEN, LET ME END WITH ONE LITTLE STORY HERE.

I CAN'T BELIEVE THE TIME IS OVER, BUT IT IS.

LET ME JUST END WITH ONE LITTLE QUICK STORY.

THIS AMAZES ME.

JEREMIAH WAS A GREAT PROPHET, AND HE HAD A SECRETARY,

BARUCH, WHO RECORDED ALL OF HIS PROPHECIES.

AND, YOU KNOW, THEY DIDN'T HAVE A NICE LITTLE BALLPOINT PEN THAT

THEY COULD JUST FLICK THE END, AND A NICE LITTLE PAD OF PAPER.

I MEAN, RECORDING ANYTHING WAS A MONUMENTAL JOB.

THEY HAD TO GET THE INK.

THEY HAD TO GET THE QUILL.

THEY HAD TO GET THE PARCHMENT.

IT JUST TOOK A LONG, LONG, LONG, LONG TIME.

AND THERE'S ACTUALLY AN ACCOUNT IN THE BIBLE OF WHERE JEREMIAH

HAD GOTTEN THIS PROPHECY FROM GOD, AND IT WAS READ TO THE KING

AND THE KING DIDN'T LIKE IT.

AND SO, HE RIPPED IT UP, JUST RIPPED UP JEREMIAH'S PROPHECIES.

AND THIS IS, LIKE, IN JEREMIAH 36.

CAN YOU IMAGINE HOW HE FELT WHEN ALL OF HIS WORK WAS JUST

RIPPED UP?

I KNOW ONE TIME, BEFORE I LEARNED THE WISDOM OF NEVER

LEAVING ANYTHING ON A COMPUTER WITHOUT SAVING IT ON

ANOTHER FILE--

[AUDIENCE LAUGHING]

JOYCE: I LOST 1/2 OF A BOOK THAT I HAD WRITTEN AND NEVER

COULD GET IT BACK.

I WON'T GO INTO THE LONG AND THE SHORT OF IT.

I WAS SO JUST, LIKE, SICK, JUST ABSOLUTELY SICK.

I MEAN, MY GOSH, IT'D TAKE SO LONG TO WRITE THAT MUCH, JUST--

BECAUSE I DIDN'T DO MY MAINTENANCE.

[LAUGHING]

COME ON, ARE YOU THERE?

[AUDIENCE APPLAUDING]

JOYCE: I DIDN'T WANNA TAKE THE TIME TO GO GET THE LITTLE

THING, TO STICK IT IN THE SIDE OF THE COMPUTER TO, YOU KNOW?

AND I PAID THE PRICE.

WELL, I DON'T DO THAT ANYMORE.

YOU KNOW WHAT?

I HAD TO DO IT AGAIN.

[AUDIENCE APPLAUDING]

JOYCE: I HAD TO DO IT AGAIN.

SO, THIS AMAZES ME.

CAN YOU IMAGINE HOW JEREMIAH MUST HAVE FELT WHEN HE LEARNED

THAT ALL OF HIS HARD WORK HAD BEEN BURNED UP?

THIS KING, I GUESS, WAS SITTIN' BY THE FIRE HAVIN' A NICE LITTLE

COMFY EVENING, AND HE JUST RIPPED UP ALL--THREW 'EM IN

THE FIRE PIECE BY PIECE.

THIS IS WHAT GOD TOLD JEREMIAH: "TAKE ANOTHER SCROLL AND WRITE

ON IT ALL THE FORMER WORDS THAT WERE ON THE FIRST SCROLL."

AND GOD BASICALLY SAID TO JEREMIAH WHAT I'M SAYIN' TO YOU

TODAY: "I DON'T CARE HOW MANY TIMES YOU'VE DONE IT, OR HOW

OFTEN YOU THINK IT HASN'T WORKED, OR WHAT THE DEVIL'S

TAKEN AWAY FROM YOU.

HERE'S THE ANSWER TO ALL YOUR PROBLEMS: DO IT AGAIN."

[AUDIENCE CHEERING]

JOYCE: "I'M GONNA DO IT AGAIN, DEVIL, AND AGAIN

AND AGAIN AND AGAIN AND AGAIN AND AGAIN AND AGAIN AND AGAIN.

AND YOU ARE NOT GONNA DEFEAT ME," AMEN?

JOYCE: PHILIPPIANS 4:13 REMINDS US THAT: "WE CAN DO ALL

THINGS THROUGH CHRIST WHO IS OUR STRENGTH."

NO MATTER WHAT COMES AGAINST US, WE DON'T HAVE TO GIVE UP.

WE CAN PRESS INTO GOD AND WE WILL MAKE IT THROUGH.

TODAY, WE'RE OFFERING 4 HOURS OF TEACHING ON

"PURSUING WHAT MATTERS MOST."

AND THERE ARE SO MANY THINGS THAT WE CAN GIVE OUR TIME TO IN

THE WORLD TODAY, AND THE NUMBER OF OPTIONS IS INCREASING,

SOMETIMES I FEEL LIKE DAILY.

SO IT'S VERY IMPORTANT FOR US TO OCCASIONALLY JUST DRAW BACK FOR

A LITTLE BIT AND TAKE A LITTLE INVENTORY OF WHAT WE'RE DOING

WITH OUR TIME.

AND MAKE SURE THAT WE'RE PUTTING IT INTO THINGS THAT WE'RE GONNA

BE SATISFIED WITH LATER ON.

I THINK YOU'RE REALLY GONNA ENJOY THIS TEACHING.

SO GET THOSE TEACHINGS TODAY, AND I BELIEVE THAT THEY WILL BE

A REAL BLESSING TO YOU.

MAKE A CHOICE TODAY TO PURSUE WHAT MATTERS MOST.

ANNOUNCER: WE ALL HAVE PURSUITS IN LIFE, WHETHER IT MAY

BE SUCCESS, BETTER PAY, A BETTER JOB, ANYTHING.

AND WHILE IT'S NOT WRONG TO DESIRE THESE THINGS,

WE SHOULDN'T LET THEM BE THE FIRST PRIORITY.

SO, LEARN TO PUT GOD FIRST ON THE LIST, NO MATTER WHAT THE

CIRCUMSTANCES, AND DISCOVER THE SECRET TO TRUE JOY AND PEACE.

ORDER JOYCE'S TEACHING SERIES, "PURSUING WHAT MATTERS MOST."

AS WE LEARN TO KEEP HIM FIRST, EVERYTHING ELSE IN LIFE

WILL WORK OUT.

AND WHEN YOU CALL TO ORDER, YOU'LL ALSO RECEIVE THIS

"HAND OF HOPE" NOTEPAD AND PEN SET.

THIS FOUR-TEACHING CD SERIES, NOTEPAD, AND PEN CAN ALL BE

YOURS TODAY FOR A GIFT OF...OR MORE.

CONTACT US NOW...

OR VISIT US AT JOYCEMEYER.ORG.

GINGER: YEAH, EVERYWHERE WE GO, ALL OVER THE WORLD, WE CAN'T

HELP BUT JUST FALL IN LOVE WITH THE CHILDREN.

LIKE, 4-YEAR-OLD IMINATI HERE.

BUT HERE IN THE EASTERN CAPE OF SOUTH AFRICA, MY HEART HAS ALSO

BEEN REALLY PULLED TOWARD THE MOTHERS AND THE GRANDMOTHERS.

THEY ARE WORKING HARD TO PROVIDE FOR THEIR CHILDREN, AND THEY

NEED OUR HELP.

SO, THESE CLASSROOMS OF HOPE THAT WE PROVIDE ARE HELPING

THE ENTIRE FAMILY, AND WE CAN'T DO IT WITHOUT YOU.

SO, KNOW THAT YOUR SPECIAL GIFT TODAY WILL MAKE A HUGE

DIFFERENCE IN NOT ONLY HERE, BUT OTHER AREAS, SUCH AS ASIA,

THE INNER CITIES IN THE UNITED STATES.

BUT WE NEED YOU TO HELP US.

PICK UP THE PHONE, GO TO THE WEBSITE, JOYCEMEYER.ORG,

AND LET US KNOW THAT YOU'RE STANDING WITH US.

ANNOUNCER: FOR YOUR DONATION TODAY OF ANY AMOUNT, WE'D LIKE

TO SAY, "THANK YOU," WITH THE BOOKS OF PSALMS

AND PROVERBS FROM THE NEW "BATTLEFIELD OF THE MIND

STUDY BIBLE."

CONTACT US RIGHT NOW...

OR GO TO JOYCEMEYER.ORG.

DR. BUDI: STARTED WHEN I APPLIED FOR MEDICAL SCHOOL,

YOU KNOW, I WAS HAVING SUCH A DIFFICULTY, AND I

PROMISED GOD THAT IF I MADE IT, I WOULD GIVE MY PROFESSION TO

HIS SERVICE, TO HIS KINGDOM.

AND I GUESS HE REMEMBERED.

[LAUGHING]

YOU KNOW, HOPEFULLY THAT WE COULD TALK TO THEIR

FAITH ALSO, AND BRING THEM CLOSER TO THE FATHER.

AND IT IS A WONDERFUL THING.

[MUSIC]

JOYCE: I JUST SENSED GOD SPEAKIN' IN MY HEART OR PUTTING

A DESIRE IN MY HEART, YOU KNOW, TO TEACH THE WORD.

AND I FELT THAT THIS DREAM CAME TO ME THAT I WAS GONNA GO ALL

OVER THE WORLD AND TEACH THE WORD.

WHICH, OF COURSE, WAS, IN THE NATURAL, TOTALLY RIDICULOUS.

AND SO MANY TIMES, WHEN GOD DOES SPEAK SOMETHING TO US OR HE

CALLS US TO DO SOMETHING, TO THE NATURAL MIND, IT IS RIDICULOUS.

BUT TRULY, WITH GOD, ALL THINGS ARE POSSIBLE.

AND I'VE ACTUALLY BEEN MEDITATING EVEN THIS WEEK ON

EPHESIANS 3:20, THAT SAYS THAT: "GOD CAN DO EXCEEDINGLY

ABUNDANTLY ABOVE AND BEYOND ALL THAT WE COULD EVER DARE TO HOPE,

ASK, OR THINK THROUGH HIS POWER THAT WORKS IN US."

AND SO, GOD DOES GREAT THINGS, BUT HE DOES THEM THROUGH PEOPLE.

[MUSIC]

[MUSIC]

ANNOUNCER: GET YOUR FREE SUBSCRIPTION TO

"ENJOYING EVERYDAY LIFE" MAGAZINE TODAY

AT JOYCEMEYER.ORG.

ANNOUNCER: YOU MEAN MORE TO US AT JOYCE MEYER MINISTRIES

THAN YOU MAY EVER KNOW.

WE APPRECIATE YOU, AND WE THANK OUR FRIENDS AND PARTNERS FOR

MAKING THIS WORLDWIDE MINISTRY POSSIBLE.

TOGETHER, WE'RE FEEDING THE HUNGRY, CLOTHING THE POOR,

AND PRESENTING THE GOSPEL TO THE NATIONS.

PLEASE CONTACT US OR VISIT JOYCEMEYER.ORG TODAY TO SHARE

YOUR PRAYER REQUESTS, FIND OUT MORE ABOUT OUR RESOURCES,

SEE JOYCE'S CONFERENCE SCHEDULE, AND TO JOIN US IN PARTNERSHIP

AS WE SHARE THE LOVE OF CHRIST AROUND THE GLOBE.

CC BY ABERDEEN CAPTIONING 1-800-688-6621 WWW.ABERCAP.COM

ANNOUNCER: THE PRECEDING WAS PAID FOR BY

THE FRIENDS AND PARTNERS OF JOYCE MEYER MINISTRIES.

For more infomation >> Staying Strong - Part 2 - Enjoying Everyday Life - Duration: 28:33.

-------------------------------------------

CBS 11 News - Duration: 2:38.

For more infomation >> CBS 11 News - Duration: 2:38.

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Lib Tech T-Rice HP C2 157W 2018 Product Video at Blue Tomato - Duration: 2:18.

Hello my name is Didi. I represent Mervin Manufacturing here in Austria. Among others with the brand LibTech.

Mervin is the most environmentally friendly snowboard factory or snowboard brand in the world.

And today I introduce to you the pro model by Travis Rice, the T-Rice Horsepower.

You know Travis Rice. By now you can already call him a legend. With films like "The Art of Flight" and "The Fourth Phase".

An absolute insane rider. He has several pro models with us.

This one is the T-Rice Horsepower. Horsepower means we have built in three different types of wood.

In addition, we use a basalt fiber. It is an environmentally friendly material, volcanic rock. Volcanic material. Biodegradable. Environmentally friendly.

Bio Bean Topsheet. Sintered Base.

Looking at the shape, it is a hybrid. C2 means Rocker between the binding and then Camber in the front and in the back.

In the versions up to 1.61,5 cm length we have a Blunted Nose and Tail.

Which means weight reduction, rather park-heavy. Of course, slopes as well, but leaning more towards park riding. Reduces spin weight.

Which gives you a better feeling when jumping or on rails etc.

In addition we have Magne-Traction, the patent of Mervin.

A wavy edge provides more contact surface, more aggressiveness. More grip on hard, icy slopes. Of course in the park too.

The Magne-Traction is just as normal for grinding as any other board. Nowadays, most shops have modern machines,

so that's no problem at all. Or just do it by hand.

This board by Travis Rice is just awesome.

If you want to ride like him – buy this boad. It's rad!

It's not for beginners because it's a bit harder but for advanced and good riders. You will love it. Check it out.

For more infomation >> Lib Tech T-Rice HP C2 157W 2018 Product Video at Blue Tomato - Duration: 2:18.

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Life Below the Ocean Surface | StarTalk - Duration: 2:35.

So you know that's a fish.

Oh, that's cool.

He's cute, or she.

You can't even tell.

But what is that fish thinking?

Is it like-- is it nostalgia?

Is it rage?

Maybe I'm just projecting.

But you can't really tell what it's thinking.

It's a mystery.

It's an enigma.

But watch this.

Eyebrows.

Now, you see it.

Now, this fish has an emotional life.

You can really empathize with.

So you want fish to have eyebrows.

That's the secret.

Yes.

So is that so hard?

Is it so wrong?

Can you do that please?

I'll work on it.

Thank you.

That'll be your next big genetic project.

It's just for their advantage.

I mean, look at that.

Well, Sylvia Earle loves every fish in the sea, no matter

what, with or without eyebrows.

And I asked her about her love of the ocean.

Just tell me, speak the love.

And let's see what she says.

When I think of people who love the ocean, many of them

just like sailing the ocean.

Yeah, or surfing.

Surfing, right.

So the ocean to them is a surface.

I know.

And to you, it's a three dimensional--

The ocean

Is the wet part.

The wet part.

Really?

It's not the top.

What is the top?

It is the bottom.

Boat people, the ocean is a surface.

Right?

No, it's the juicy part in the middle.

It's this part.

And it's alive.

That's the thing.

If people think of the ocean, they think rocks and water

and, you know, a place to sail or swim or to dump things

or to take things out of the ocean.

But no.

The ocean is a living system.

So Laurie, first, remind us what it means for the ocean

to be a living system.

Because to most people, it's just water.

And it contains living things.

But to think of it as a living system, take us there.

So in the same way that a forest with birds and trees

and bugs that are all interacting is a living system,

the ocean's the same way.

It's not only full of life, but it's all interacting

together in in connected way that kind

of keeps it all functioning.

Isn't it just big fish eat little fish?

That's part of it.

But there's a whole complex food web

there that most people just don't see

and take into consideration.

For more infomation >> Life Below the Ocean Surface | StarTalk - Duration: 2:35.

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ランボルギーニ、ブガッティ、ポルシェなどスーパーカーを擁するドバイ警察情報 - Duration: 9:25.

For more infomation >> ランボルギーニ、ブガッティ、ポルシェなどスーパーカーを擁するドバイ警察情報 - Duration: 9:25.

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Funny BEDTIME STORIES [Nighttime 🌒 SHADOW PLAY FUN] | Roman and Auroras Childhood Adventures - Duration: 4:27.

- [Woman] I'm sleepwalking.

- [Man] Dance for me in your sleep.

- [Woman] Okay.

(jaunty piano music)

(Roman laughs)

- [Man] That's music for sleepwalkers.

- [Boy] Join us for Roman's and Aurora's

- [Boy and Girl] Childhood Adventures!

- We are ready for the nighttime shadows, right kids?

- Noooo!

(jaunty piano music)

- [Man] Hey, you, listen to my music.

(saxophone plays)

- [Woman] I'm sleepwalking.

- [Man] Dance for me in your sleep.

- [Woman] Okay.

(saxophone plays)

(Roman laughs)

- [Man] That's music for sleepwalkers.

Hey, you, get out of here and stop

making my wife dance in her sleep.

- [Woman] Hi, honey.

- [Man] Why are you walking around sleeping again?

(Roman laughs)

- [Woman] I like to do that because

then I get ice cream in the night.

- [Man] Oh, well, get me some too, please.

- [Woman] Okay.

(canned laughter)

(doorbell rings)

- [Woman] Hello, who's there?

- [Man] I've come to clean your chimney.

- [Woman] Oh, I wasn't expecting you at this time.

- [Man] Oh, yeah, I'm a little early, but it's okay.

- [Woman] Okay, come in.

- [Man] I'll just go over here outside

in the chimney and, HAHA, I fooled you!

(woman gasps)

Now I'm going to climb up and steal your chimney.

- [Woman] Oh no, oh no!

I need to call the police.

(sirens)

- [Man] Wait, you!

What do you think you're doing?

Stealing my chimney!

All right, I guess I'll just ...

I'm sorry about that.

Now get out of here!

(canned laughter)

I am the best flying saxophonist in the air.

(airplane engine)

Nobody can fly like me.

- [Woman] Hi, Mister Saxophonist.

Do you wanna join the party?

We definitely need somebody to play.

- [Man] I am the party, I'm partying on the plane.

- [Woman] You are the party, that's

why I want you to join my party.

Oh, are you okay?

- [Man] Yes, I'm okay, I'm all right.

- [Woman] Please, come for us,

please, and I'll put my disguise.

(saxophone plays)

- [Man] All right, party time, party time.

Party time, party time ...

party time, party time ...

(man sings)

In the party.

- [Woman] Good night.

(airplane engine)

- [Man] The end.

(applause)

- A round of applause!

Thanks for watching Roman

and Aurora's Childhood Adventures!

Bye!

Don't forget to subscribe, bye, bye.

(Roman mumbles to himself)

I'm sneaking.

Nobody will know if you're my horn, my horn.

Nobody will ever hear my horn, my horn.

(children laugh)

(jaunty piano music ends with a flourish)

For more infomation >> Funny BEDTIME STORIES [Nighttime 🌒 SHADOW PLAY FUN] | Roman and Auroras Childhood Adventures - Duration: 4:27.

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Olaf's Frozen Adventure

For more infomation >> Olaf's Frozen Adventure

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Flowee - ITC - Michael Winkelman - Šamanismus a jeho význam pro moderního člověka - Duration: 3:25.

For more infomation >> Flowee - ITC - Michael Winkelman - Šamanismus a jeho význam pro moderního člověka - Duration: 3:25.

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Daniel Caesar - Best Part (feat. H.E.R.) | Cover by Sidney Frenz - Duration: 1:34.

(Calm intro music)

(beat kicks in)

It's the sunrise

And those brown eyes

You're the one that I desire

When we wake up

And then we make love

It makes me feel so nice

You're my water when I'm stuck in the desert

You're the Tylenol I take when my head hurts

You're the sunshine on my life

I just wanna see how

Beautiful you are

You know that I see it

I know you're a star

Where you go I follow

No matter how far

If life is a movie

Then you're the best part

Oh

You're the best part

Oh

Best part

For more infomation >> Daniel Caesar - Best Part (feat. H.E.R.) | Cover by Sidney Frenz - Duration: 1:34.

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Place BAKING SODA IN YOUR VA.GI.NA and look what Happens!! - Duration: 3:55.

Place BAKING SODA IN YOUR VA.GI.NA and look what Happens!!

For more infomation >> Place BAKING SODA IN YOUR VA.GI.NA and look what Happens!! - Duration: 3:55.

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周杰伦把她写进歌里,林俊杰现场表白,蔡依林:傻子也能看出来 - Duration: 2:56.

For more infomation >> 周杰伦把她写进歌里,林俊杰现场表白,蔡依林:傻子也能看出来 - Duration: 2:56.

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UPDATE UPDATE - MY NEW SETUP - TELE CAUSE & THE SHIMAI 💅💼🎧🎼🎮🎬👾🕹📲💻🎙📽 - Duration: 4:29.

UPDATE STATION - MY NEW SETUP - TELE Slack & THE SHIMAI 💅💼🎧🎼🎮🎬👾🕹📲💻🎙📽

In this video we are going to update our location

creating a setup that we can lend to different features

In fact, this station will be mainly dedicated:

- gaming - the editing

- sound system - TV station

- nail art station - make up station

- location reviews - workstation

- location study - and many other uses

Also this is a low budget post but nevertheless it is almost perfect

In fact we can say that this is my first official station

and not to have experienced the result does not It is not bad

Also I wanted to thank the following companies for providing me with the material for

the cable management.

https://www.amazon.it/s?marketplaceID=APJ6JRA9NG5V4&me=A3GW4TB7XV6RM5&merchant=A3GW4TB7XV6RM5&redirect=true https://www.amazon.it/s?marketplaceID=APJ6JRA9NG5V4&me=A1XJNKT45LJAHC&merchant=A1XJNKT45LJAHC&redirect=true

I recommend them both products as you see Also from the video are excellent

and the vendors are friendly and helpful products used for the cable managemet:

- https://www.amazon.it/gp/product/B075KBCTG9/ref=oh_aui_detailpage_o00_s00?ie=UTF8&psc=1 - https://www.amazon.it/gp/product/B07414BM71/ref=oh_aui_detailpage_o00_s00?ie=UTF8&psc=1

- https://www.amazon.it/gp/product/B075KBCTG9/ref=oh_aui_detailpage_o00_s00?ie=UTF8&psc=1 _____________________ IMPORTANT______________________________

you are a company or an individual? this is the my business email:

francescocastresebosco@gmail.com but if you're one youtuber I want to advise

my network where you can probably get to join.

I leave the link below: http://www.among-us.it

Also would you like to buy games bargain prices?

I have the solution for you. istantgaming here is the link:

https://www.instant-gaming.com/it/?igr=youtubekidfamily If you prefer the physical copy to you

found on this site with your purchases will support not only

but the channel will contribute to the organization new contest and give away

http://www.howtoshop.it/shop If you do not find what you are looking to baste

contact me on facebook and add Article interested

very quickly. Also you find me on the best social and

blog of my network youtubekidfamily network

http://www.among-us.it/blog shop store: http://www.howtoshop.it/shop

_________________cosa use for youtube___________________________ https://www.amazon.it/hz/wishlist/ls/1XFRKE1O38KO?&sort=default

______________________I MY SOCIAL______________________________ I find on the best social and Blog

my network "Youtubekidfamily network":

http://www.among-us.it/blog PROFILE FB: https://www.facebook.com/telecazzeggioyt

FB PAGE: https://www.facebook.com/telecazzeggio/ FAN CLUB FB: https://www.facebook.com/I3nullafacentifanclub/

CHANNEL TELEGRAM: https://t.me/TelecazzeggioOfficialTubo TELEGRAM GROUP: https://t.me/joinchat/CTWXpEKqS7INSDHjsVdjpA

WEB SITE: https: //telecazzeggio.jimdo.com/ TWITTER: https://twitter.com/Telecazzeggio

Instagram: https://www.instagram.com/telecazzeggio_official/?hl=it SEVER MISMATCH: https://discord.gg/ffxxS5

THE CHANNEL SHIMAI: https://www.youtube.com/channel/UCX71Dgl6GJiEP04U0BQnZPQ mail: francescocastresebosco@gmail.com

For more infomation >> UPDATE UPDATE - MY NEW SETUP - TELE CAUSE & THE SHIMAI 💅💼🎧🎼🎮🎬👾🕹📲💻🎙📽 - Duration: 4:29.

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Elle a perdu 15 kilos en 6 semaines en faisant ceci chaque soir avant d'aller au lit - Duration: 8:36.

For more infomation >> Elle a perdu 15 kilos en 6 semaines en faisant ceci chaque soir avant d'aller au lit - Duration: 8:36.

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'혼자남'은 '집밥' 좋아한다는 김구라 말에 김숙이 날린 한 마디 - Duration: 3:13.

For more infomation >> '혼자남'은 '집밥' 좋아한다는 김구라 말에 김숙이 날린 한 마디 - Duration: 3:13.

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¿Cuántos años tienes? Vive este instante - Duration: 3:34.

For more infomation >> ¿Cuántos años tienes? Vive este instante - Duration: 3:34.

-------------------------------------------

#85 analyse photo - Duration: 7:42.

For more infomation >> #85 analyse photo - Duration: 7:42.

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Simplify Your Grocery Shoppi...

For more infomation >> Simplify Your Grocery Shoppi...

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Consen­te­ment sexuel à 13 ans : Nagui « supplie » la ministre d'in­ter­ve­nir pour - Duration: 3:24.

For more infomation >> Consen­te­ment sexuel à 13 ans : Nagui « supplie » la ministre d'in­ter­ve­nir pour - Duration: 3:24.

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Pour investir en éducation, pas besoin d'être au pays des licornes ! - Duration: 4:06.

For more infomation >> Pour investir en éducation, pas besoin d'être au pays des licornes ! - Duration: 4:06.

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CHUYỆN THẦM KÍN - 10 BÍ MẬT CHUYỆN NỮ GIỚI TH.Ủ D.ÂM KHIẾN CÁNH ĐÀN ÔNG PHÁT HOẢNG - Duration: 14:54.

For more infomation >> CHUYỆN THẦM KÍN - 10 BÍ MẬT CHUYỆN NỮ GIỚI TH.Ủ D.ÂM KHIẾN CÁNH ĐÀN ÔNG PHÁT HOẢNG - Duration: 14:54.

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ข้าว41 combine harvester รถเกี่ยวข้าวจ้าวช้าง 23 12HT 6m61T มีคลิปรถไถรถแม็คโคร ดำรงค์รถเกี่ยว - Duration: 2:03.

For more infomation >> ข้าว41 combine harvester รถเกี่ยวข้าวจ้าวช้าง 23 12HT 6m61T มีคลิปรถไถรถแม็คโคร ดำรงค์รถเกี่ยว - Duration: 2:03.

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Johnny Hallyday hospitalisé d'urgence, il serait très inquiet - Duration: 2:50.

For more infomation >> Johnny Hallyday hospitalisé d'urgence, il serait très inquiet - Duration: 2:50.

-------------------------------------------

Tanki Online V-LOG: Episode 153 - Duration: 5:45.

WARNING: This video may potentially trigger seizures for people with photosensitive epilepsy. Viewer discretion is advised.

In today's V-LOG

we'll be telling you at what stage of development the HTML5 version of Tanki Online is,

talking about the final stage of Clan Championship X

and telling you about the Battle of Social Networks - VK vs OK.

Hello Tankers!

Earlier this week we announced Tankiball -

a new community event organized by the Event Helpers!

The goal is simple: gather friends,

register as a team and make sure you bring enough Vikings and Hammers with you

- you'll need to shoot a special tank playing the role of the ball.

Registrations are already open, so hurry up and submit your application!

The work on the HTML5 version of Tanki is our top priority right now.

Here's the current progress:

Testing of the new version of "Tanki Online" started earlier this year in August.

Back then we let 5% of the new players through the new version of Tanki.

Our goals were: to find and fix the critical issues

and compare the results with the Flash version for new players.

In the end we faced performance issues.

More powerful PCs could play the new version without any problems.

But less powerful laptops with integrated video cards had a tough time.

Initially, HTML5 version performed much slower compared to Flash.

Next, we started to optimize things.

Performance on less powerful machines was slightly improved.

And then a little bit more, and a bit more.

This way using special testing laptops with old hardware

we managed to raise FPS up to 20 frames per second,

even though at the beginning nothing worked at all.

One more big accomplishment - the interface.

To launch the new version as soon as possible, we used emulation of the old interface,

which isn't the fastest solution for the browser.

Now the interface is being properly redone from the ground up.

The hardest part of it, of course, is the Garage.

It contains the maximum number of the technical features -

like turning your tank, drag and scroll interface

and several menus with upgrades, equipment and gifts.

For the best performance it's important for us to make the game stable,

and, of course, to fix small and annoying bugs.

Let's recap:

HTML5 version is a bit behind Flash compared to its performance,

and has a few negligible problems.

And now let's answer the question "When is the release?":

A full and immediate switch to HTML5 probably won't happen.

We will move players to the new version over time.

And regarding when - as soon as the new version is on the same level of performance as Flash.

The deciding stage of Clan Championship X is about to begin.

On Tuesday, November 14th, 4 finalists of the tournament were decided.

In honor of their victory, 4 special paints can now be purchased in the Garage.

Buy one of the paints to support your team -

this will give them +3 to team power.

And if you correctly guess the winner, you will get 5 Gold Boxes and 1 day of Premium!

Don't miss your chance of buying fan paints -

after the morning restart on November 19th

all the 4 paints will become unavailable for purchase

and the first match starts the same day.

As a reminder, fan paints will remain in your Garage only if you bought one.

Watch the finals - it's gonna to be brutal!

The next part is even better.

The battle between two popular social networks "OK vs VK" is raging on,

and it's a mashup of the fan paints and crazy weekend events.

Upon buying one of the paints you choose a side -

for vKontakte or for Odnoklassniki.

Next, the race is going on two fronts:

On one hand, every player is interested in making the most kills during the battle.

The more kills you make, the bigger the prize.

On the other hand, it's good to keep checking your K/D.

A higher average K/D of your team means better chances

for you to get double rewards in the personal race.

Top 10 players from each side will get additional prizes,

including the animated paint "Flow".

And the best part of this madness is that the kills and the K/D counter

work in both standard and non-PRO battles, if you have one of the paints equipped.

So don't forget to do that!

Video of the week.

In the last V-LOG you sent us a bunch of very cool

and absolutely not staged capture the flag videos.

Let's watch the winner of the week:

Next time make a video, again - not staged, with a killstreak

- a series of kills without a single destruction of your own tank.

Make sure you're wearing either the OK or the VK paint.

Good luck!

That's it for today, tankers!

Watch the V-LOGs!

Christmas is getting closer, and with it a lot of cool info.

Next week there won't be a new V-LOG, but we'll have a special Tankiball stream,

check it out on the official TO channel!

Last time Magnum blew itself up on the Rio map in Space mode.

You had to guess which mark it would reach by flying up from the explosion.

The right answer is - 7!

As always, we've randomly chosen 10 lucky tankers among the right answers.

Welcome the winners and here's the new question.

Who will survive?

For more infomation >> Tanki Online V-LOG: Episode 153 - Duration: 5:45.

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#85 analyse photo - Duration: 7:42.

For more infomation >> #85 analyse photo - Duration: 7:42.

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Japanese Trying Russian Food PART2 - Duration: 12:41.

For more infomation >> Japanese Trying Russian Food PART2 - Duration: 12:41.

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1er parrure de pierre suspendue - Duration: 4:43.

For more infomation >> 1er parrure de pierre suspendue - Duration: 4:43.

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Does A2 Milk Carry Less Autism Risk? - Duration: 7:48.

For more infomation >> Does A2 Milk Carry Less Autism Risk? - Duration: 7:48.

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The castle haunted by horses - Duration: 5:14.

For more infomation >> The castle haunted by horses - Duration: 5:14.

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Johnny Hallyday hospitalisé d'urgence, il serait très inquiet - Duration: 2:54.

For more infomation >> Johnny Hallyday hospitalisé d'urgence, il serait très inquiet - Duration: 2:54.

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Entrepreneur(e) : Boostez votre efficacité professionnelle ! - Duration: 1:29.

For more infomation >> Entrepreneur(e) : Boostez votre efficacité professionnelle ! - Duration: 1:29.

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Wake Up - Graham Kendrick (with lyrics) - Duration: 4:03.

For more infomation >> Wake Up - Graham Kendrick (with lyrics) - Duration: 4:03.

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HOW THE FDA RESPONDS WHEN ASKED TO PROVE THAT IT'S SAFE TO INJECT MERCURY THIMEROSAL INTO BABIES - Duration: 46:35.

HOW THE FDA RESPONDS WHEN ASKED TO PROVE THAT IT�S SAFE TO INJECT MERCURY (THIMEROSAL)

INTO BABIES

BY ROBERT F. KENNEDY JR.

Background: Peter Patriarca, an FDA employee, admitted back in 1999, in a confidential e-mail

obtained through FOIA, that, �� the greatest point of vulnerability on this issue is that

the systematic review of thimerosal in vaccines by the FDA could have been done years ago

and on an ongoing basis as the childhood immunization schedule became more complex.

The calculations done by FDA are not complex.

I�m not sure if there will be an easy way out of the potential perception that the FDA,

CDC and immunization policy bodies may have been �asleep at the switch� re: thimerosal

until now�.

Since 1999, an entire generation of children both in the US and internationally has continued

to be exposed to thimerosal � and it is time for this to stop.

Nobody should be exposed to a known neurotoxin.

The Ongoing Saga: On March 30, 2017, Robert F. Kennedy, Jr., and the World Mercury Project

(WMP) team met with the Director of the FDA�s Center for Biologics Evaluation and Research

(CBER) Dr. Peter Marks, M.D., Ph.D. and his colleagues to discuss the agency�s ongoing

refusal to ban thimerosal, a mercury-based preservative, from vaccines in the United

States.

CBER is the division of the FDA responsible for approving and monitoring the safety of

all biological products, including vaccines, allergenic products, blood and blood products,

and cellular, tissue, and gene therapies.

At the meeting, we presented a large amount of research showing the toxicity of thimerosal

in humans, animals and cellular models, including at levels similar to those resulting from

vaccine exposures.

We expressed our alarm regarding the total lack of adequate safety testing of thimerosal

prior to licensure, especially given its current use in vaccines approved for infants and pregnant

women and its worldwide use in millions of vaccines given to children, particularly in

developing countries.

Dr. Marks promised to look over the studies and seriously consider our concerns.

After many months of back and forth emails, Dr. Marks sent a letter to us on July 11th

that didn�t even look like he was in the same meeting.

World Mercury Project was dismayed by CBER�s apparent unwillingness to seriously review

the large archive of published science suggesting that using thimerosal is poisoning a generation

of American children.

From his follow-up response, it is clear that none of the information WMP provided was seriously

read or even minimally digested.

He made it clear in his letter that CBER does not intend to give any serious consideration

to the abundant and mushrooming evidence of thimerosal�s profound toxicity.

His letter was simply an exercise in blindly promoting an incredible vaccine industry orthodoxy

that is unsupportable by empirical evidence.

Below is my letter back to Dr. Marks.

We are awaiting his response.

Re: Response to your letter regarding the use of mercury in prescription drugs and vaccines.

Dear Dr. Marks,

On March 30th, Robert F. Kennedy Jr. and members of the World Mercury Project met with you

and your colleagues at the FDA to discuss our concerns regarding the continued use of

the mercury-based preservative, thimerosal, in prescription drugs and influenza vaccines

administered to pregnant women, infants and children.

During the meeting and in written letters following the meeting, we voiced concerns

regarding:

Lack of adequate safety studies prior to marketing thimerosal as a vaccine preservative.

Thimerosal�s toxicity and ineffectiveness as a preservative.

Mercury exposure from thimerosal-containing vaccine administration resulting in mercury

levels known to cause adverse outcomes.

Exposure to vaccine-level thimerosal resulting in harmful depositions of inorganic mercury

in the brain.

The California Environmental Protection Agency�s listing of all mercury-containing products

as reproductive and developmental toxicants under their Proposition 65 law.

Thimerosal was removed from all over-the-counter products when the FDA issued final rules in

the Federal Register in 1998 acknowledging that thimerosal is not generally recognized

as being safe or effective (GRASE).

Why is this same product allowed in prescription drugs and vaccines?

At the end of our meeting, you reassured us that you would take our concerns seriously

and would �follow the science� wherever it might lead you.

For several months after our meeting, I contacted the FDA public liaison Ms. McNeill inquiring

when we might expect to hear back from you regarding our concerns.

Ms. McNeill told me that we had provided the agency with extensive information and that

it was taking additional time to review the material.

I was hopeful that FDA might finally, therefore, implement the 2001 recommendation of the Institute

of Medicine that pregnant women, infants and children not be exposed to thimerosal-containing

vaccines.

On July 11th, we received your written response to our concerns.

I was dismayed by your agency�s apparent unwillingness to seriously review the large

archive of published science suggesting that using thimerosal is poisoning a generation

of American children.

From your follow-up written response, it is clear that none of the information we provided

was seriously read or even minimally digested.

You make it clear in your letter that you do not intend to give any serious consideration

to the abundant and mushrooming evidence of thimerosal�s profound toxicity.

Your letter is simply an exercise in blindly promoting an incredible vaccine industry orthodoxy

that is unsupportable by empirical evidence.

You cite in your written response FDA�s mushy biologics regulations which define safety

as �the relative freedom from harmful effect to persons affected, directly or indirectly,

by a product when prudently administered, taking into consideration the character of

the product in relation to the condition of the recipient at the time.� 21CFR 600.39(p).

You report that in applying this elastic regulatory standard, �FDA must weigh the risk of a

vaccine or any drug against its benefits when determining whether a product is safe.

If the benefits of the vaccine or other pharmaceutical product outweigh the risks of its side effects,

then the FDA finds the product to be safe.� You further acknowledge that �the determination

of a products safety is a relative rather than absolute measurement�,entirely subject

to FDA�s �discretion and expertise.� Even operating under these malleable standards,

FDA should consider that vaccines are products given to healthy individuals, and their risks

should be measured by an extremely high bar since they are not treating a disease.

Furthermore, FDA has no capacity to evaluate risks of thimerosal since, by FDA�s own

admission to Congress, there has never been a long-term safety study performed on thimerosal

in any human population including infants and pregnant women.

Vaccines containing thimerosal in the U.S. are predominantly influenza vaccines.

Furthermore, thimerosal is still widely used in vaccines given to tens of millions of children

in the developing world and, since U.S. policy influences worldwide policy, FDA bears responsibility

for these policies.

In the U.S., thimerosal-containing vaccines are administered to healthy six-month old

infants, young children and pregnant women despite never having been safety tested in

those populations.

According to their product inserts, influenza vaccines have been associated with an increased

incidence of seizures and Guillain-Barre Syndrome.

Recent studies have linked influenza vaccines to miscarriage, autism and, possibly, birth

defects.

A significant percentage of influenza vaccines still contain thimerosal and studies should

be done to see if thimerosal played a role in these outcomes.

There has been limited testing of influenza vaccines in animal models, however, there

have not been any adequate and well-controlled studies in pregnant women.

Because animal studies are not always predictive of human response, the package inserts for

flu vaccines reiterate that flu vaccines �should be given to a pregnant woman only if clearly

needed�.

In addition, there are numerous VAERS reports of injuries from thimerosal-containing vaccines.

Therefore, it is imperative that vaccines administered to sensitive populations (pregnant

women, infants and children) be held to the highest standards of safety.

I think parents and the American public would be appalled to learn that vaccine safety determinations

are �relative� and are within an FDA employee�s �discretion and expertise.� That discretion

and expertise should actually require a factual basis, not just opinion.

Needless to say, these decisions should be guided by the precautionary principle.

I have organized the remainder of my response into addressing the erroneous claims made

in your letter.

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Your Claim: The agency evaluates whether a preservative contained in a product is at

such levels that when used at the recommended dose is not toxic to the recipient and that

the �FDA � has repeatedly found that the vaccines currently being marketed that contain

thimerosal are safe��

WMP Response: Please show us the data used to evaluate thimerosal safety in infants and

pregnant women.

We do not believe they exist.

In an email discussion regarding the use of thimerosal-containing influenza vaccines administered

to pregnant women, infants and children, in 1999, Dr. William Egan, acting Director of

the Center for Drugs and Biologics (CDER), recommended that the statement, �The chronic,

daily ingestion reported (in several studies-primarily Seychelles study) greatly exceeds the amount

of mercury that a pregnant woman would receive from a single annual dose of thimerosal-containing

influenza vaccine� �might well be deleted.� Egan went on to justify his recommendation

by saying that the statement ��in some ways is misleading.

I am not sure that I would want to argue, for example, that one could take the allowed

amount of mercury for a year and administer it as a bolus injection with the same outcome

as having it spaced out evenly over the year: the issue then becomes one of how much of

a bolus can one give at one time without harmful effect and this data does not exist (or at

least I�m not aware of them).�

Dr. Egan was right then and he is right today; such safety data do not exist.

In fact, many toxicologists believe that large bolus dose exposures such as those resulting

from thimerosal-containing vaccines are more harmful in comparison to small daily dose

exposures that the body is much more capable of excreting without overburdening detoxification

pathways in the body.

This concern is supported by research that found a mercury dose given acutely may produce

toxic effects, whereas the same dose distributed over a period of time may give no evidence

of poisoning.

(Koos and Longo,1976).

Your Claim: �Thimerosal has a long record of safe and effective use in preventing bacterial

and fungal contamination of vaccines with no ill effects other than occasional hypersensitivity

and minor local reactions at the site of injection.�.

WMP Response: There is ample evidence provided in multiple studies by federal agencies and

independent scientists that spans the last 90 years which documents that thimerosal is

neither an effective nor a safe vaccine preservative.

In a study published in the Journal of the American Medical Association in 1948 titled

�The bacteriostatic and bactericidal actions of some mercurial compounds on hemolytic streptococci,�

the authors vigorously argued that thimerosal was ineffective as a �disinfectant, germicide

and antiseptic.� In the review of the literature in this paper, the authors cited eight studies

from 1928, 1935, 1937, 1938, and 1944 all of which drew similar conclusions.

In 1975, the FDA convened a panel of experts to evaluate mercury-containing over-the-counter

(OTC) products.

The panel issued its reports in 1980 and in 1982.

The FDA issued a report of the panel�s findings in the Federal Register where they concluded

that �some mercury-containing preparations are not effective and others are not safe

and effective for OTC topical antimicrobial use�.

With respect to thimerosal in particular, that panel found evidence from 1950 which

concluded that �thimerosal was no better than water in protecting mice from potential

fatal streptococcal infections.� Additionally, citing a 1935 study, the panel reported that

thimerosal was �35.3 times more toxic for embryonic chick heart tissue than for Staphylococcus

aureus.� Most of the literature reviewed addressed mercury�s lack of antibacterial

properties.

One review published in 1971 titled, �Three thousand years of mercury.

A plea for abandonment of a dangerous, unproven therapy,� addressed mercury�s lack of

effectiveness against fungal contamination as well.

The FDA-appointed expert panel concluded that �thimerosal was not safe for OTC topical

use because of its potential for cell damage if applied to broken skin and its allergy

potential.

It is not effective as a topical antimicrobial because its bacteriostatic action can be reversed.�

However, it wasn�t until 1998 that the FDA issued its final report banning the use of

thimerosal in topical OTC products because it was not �safe and effective.�

There are also several more recent published reports of thimerosal�s failure as a preservative.

Clusters of disease from Group A streptococcus infections were traced back to multi-dose

vials of diphtheria toxoid, pertussis, and tetanus toxoid (DPT) vaccine which were contaminated

after being opened.

Additionally, in 2004, a Chiron plant that manufactured Fluvirin was forced to close

because its vaccine was contaminated with Serratia marcescens.

This vaccine used thimerosal as a preservative.

In this case and in the many others cited, thimerosal failed to prevent bacterial growth.

In response to the reports from the FDA expert panel who reviewed the use of thimerosal in

over-the-counter products in the 1980�s, the FDA published in the April 22, 1998 Federal

Register Status of Certain Additional Over-the-Counter Drug Category II and III Active Ingredients.

(April 22, 1998);63(77):19799-19802.

21 CFR Part 310 [Docket No. 75N-183F, 75N-183D, and 80N-0280 concluding that the use of thimerosal

in over the counter products is not �generally recognized as safe or effective� (GRASE).

In the final rulemaking, the FDA states that �safety and effectiveness have not been

established for the ingredients (mercury-based preservatives) included in this current final

rule and manufacturers have not submitted the necessary data in response to earlier

opportunities.

The agency�s experience has been that under these circumstances companies have not submitted

data in response to yet another opportunity.

Consumers will benefit from the early removal from the marketplace of products containing

ingredients for which safety and effectiveness has not been established.�

The World Mercury Project would like to know how is it possible that one division of the

FDA recognizes that there is absolutely no safety or effectiveness data available for

the use of mercury in over the counter products and essentially bans its use, while your FDA

division of blood and biologics continues to recklessly allow its widespread use in

over 100 prescription products including vaccines?

Your claim: �Under the FDA Modernization Act (FDAMA) of 1997, the FDA conducted a comprehensive

review of the use of thimerosal in childhood vaccines.

Conducted in 1999, this review found no evidence of harm from the use of thimerosal as a vaccine

preservative, other than local hypersensitivity reactions (Ball et al. 2001).�

WMP Response: It�s disturbing that according to internal emails obtained by FOIA, Dr. Ball

never conducted an extensive review of reports of harm.

On November 23, 1998, Dr. Leslie Ball of the FDA asked internal reviewers to perform a

Medwatch query on thimerosal.

Medwatch is the FDA�s database for reporting adverse drug events.

On January 7, 1999, Dr. Ball was informed by Fredrick Varricchio of FDA that there were

7000 reports containing the word thimerosal on FDA�s Medwatch.

He stated, �I have some results for you.

Problem is that there are 7000 reports that mention thimerosal.

What to do now.

Obviously looking at all 7,000 is a brute force approach.� Dr. Ball responded by saying,

�perhaps you can get records on a subset of 50 or so we can look at them and get a

general feel for what�s been reported before we go any further.� In a subsequent email

on January 19th, Mr. Varricchio noted that the �plan is to get whatever is on the summary

for every 100th report.� This means that only 70 adverse events out of 7000 reported

to the FDA were actually reviewed by Dr. Ball and her team.

This email calls into question the findings reported by Dr. Ball and also suggests that

an extensive investigation has never been conducted by the FDA with regard to adverse

events associated with the use of thimerosal.

Would you allow any other medical product to be widely used based on review of one percent

of the information available?

I am also, Sir, frankly shocked at your unwillingness to acknowledge the robust body of literature

that has been published the last 18 years since concerns regarding thimerosal first

surfaced within the FDA in 1999.

There are literally hundreds of peer-reviewed, published studies that document the toxicity

of thimerosal.

Many of these investigated levels of mercury known to occur from vaccine exposure in cell

and animal models.

In 2013, Jose G. Dorea published a meta-analysis of thimerosal research related to vaccine

exposure.

Dorea searched major databases for human and experimental studies that addressed issues

related to early life exposure to TCVs.

The author concluded that: � a) mercury load in fetuses, neonates, and infants resulting

from TCVs remains in blood of neonates and infants at sufficient concentration and for

enough time to penetrate the brain and to exert a neurologic impact and a probable influence

on neurodevelopment of susceptible infants; b) etHg metabolism related to neurodevelopmental

delays has been demonstrated experimentally and observed in population studies; c) unlike

chronic Hg exposure during pregnancy, neurodevelopmental effects caused by acute (repeated/cumulative)

early life exposure to TCV-etHg remain unrecognized; and d) the uncertainty surrounding low-dose

toxicity of etHg is challenging but recent evidence indicates that avoiding cumulative

insults by alkyl-mercury forms (which include Thimerosal) is warranted.� Dorea emphasized

the importance of �a) maintaining trust in vaccines while reinforcing current public

health policies to abate mercury exposure in infancy; b) supporting WHO policies that

recommend vaccination to prevent and control existing and impending infectious diseases;

and c) not confusing the �need� to use a specific �product� (TCV) by accepting

as �innocuous� (or without consequences) the presence of a proven �toxic alkyl-mercury�

(etHg) at levels that have not been proven to be toxicologically safe.�

For your convenience, I have included a sampling of 35 abstracts that represent the more current

state of the science regarding thimerosal that has emerged since 1999 as an appendix.

Even if Dr. Ball�s review had been adequate at that time, surely 18 years of further research

should prompt an updated evaluation by the FDA.

Your Claim: A 2014 modeling study by your own Centers for Biologics Evaluation and Research

employee, Dr. Robert Mitkus, showed that �peak body burdens of mercury following episodic

exposures to thimerosal in this worst case did not exceed the corresponding safe body

burden of mercury from MeHg at any time�.

WMP Response: The Mitkus study reported that the body burden of mercury in infants, over

the first 4.5 years of life following yearly exposures to thimerosal from annual flu vaccines,

was two orders of magnitude lower than that estimated for exposures to the lowest regulatory

threshold for MeHg over the same time period.

The author relies completely on these findings to conclude that their pharmacokinetic analysis

supports the safety of thimerosal when used as a preservative at current levels in certain

multi-dose infant vaccines in the United States.

Mitkus fails to acknowledge the past levels of exposure that infants received from vaccines

starting in the late 1980s and extending well into 2000, that were 187.5 mcg etHg the first

year of life versus 12.5 mcg etHg from flu vaccines annually.

He also makes the assumption that there are no other mercury exposures outside of thimerosal,

which is not supported by either established science or common sense.

The model developed by Mitkus relied solely on blood levels and did not take into consideration

the accumulation of mercury in the brain tissue.

Data from the Burbacherstudy that assessed exposures from both methyl and ethyl mercury

in infant non-human primates, based on vaccine level exposures, found that although there

was little accumulation of Hg in the blood with repeated vaccinations, accumulation of

Hg in the brain of infants did occur.

In fact, there was a much higher proportion of inorganic Hg in the brain of thimerosal

monkeys than in the brains of MeHg monkeys (up to 71% vs. 10%).

Absolute inorganic Hg concentrations in the brains of the thimerosal-exposed monkeys were

approximately twice that of the MeHg monkeys.

Burbacher concluded that �the safety of thimerosal drawn from blood Hg clearance data

in human infants receiving vaccines may not be valid, given the significantly slower half-life

of Hg in the brain as observed in the infant macaques.� But that is exactly what Mitkus

does in his model and reports in his study.

Mitkus also makes the statement that thimerosal is more quickly and extensively metabolized

to inorganic mercury in the brain than is MeHg and that process of dealkylation �may

be� a detoxification step.

According to Burbacher, who is the author of the studies relied on by Mitkus in the

development of his model, the statement that dealkylation may be a detoxification process

is purely speculative and has not been established.

Mitkus is referring to previous reports that have indicated that dealkylation of Hg is

a detoxification process that helps to protect the central nervous system (Magos 2003; Magos

et al. 1985).

These reports are largely based on histology and histochemistry studies of adult rodents

exposed to Hg for a short period of time.

The results of these studies indicated that damage to the cerebellum was observed only

in MeHg-treated animals that had much lower levels of inorganic Hg in the brain than animals

comparably treated with ethylmercury.

Moreover, the results did not indicate the presence of inorganic Hg deposits in the area

where the cerebellar damage was localized (granular layer).

In contrast, previous studies of adult M. fascicularis monkeys exposed chronically to

MeHg have indicated that demethylation of Hg occurs in the brain over a long period

of time after MeHg exposure and that this is not a detoxification process (Charleston

et al. 1994, 1995, 1996; Vahter et al. 1994, 1995).

Results from these studies indicated higher inorganic Hg concentrations in the brain 6

months after MeHg exposure had ended, whereas organic Hg had cleared from the brain.

The estimated half-life of organic Hg in the brain of these adult monkeys was consistent

across various brain regions at approximately 37 days (similar to the brain half-life in

the Burbacher study).

Stereologic and autometallographic studies on the brains of these adult monkeys indicated

that the persistence of inorganic Hg in the brain was associated with a significant increase

in the number of microglia in the brain.

(Charleston et al. 1994, 1995,1996).

The microgliosis and neuroinflamation documented in the brains of the adult monkeys in association

with deposits of inorganic mercury are two hallmark findings in brain tissue of both

children and adults with autism.

Neuropathological studies of brain tissues from cerebellum, midfrontal, and cingulate

gyrus obtained at autopsy from 11 patients with autism demonstrated the presence of an

active neuroinflammatory processes in the cerebral cortex, white matter and, most notably,

the cerebellum.

In a subsequent study, microglia appeared markedly activated in five of 13 cases with

autism, including two of three under age six, and marginally activated in an additional

four of 13 cases.

The authors concluded that microglial activation �represents a neuropathological alteration

in a sizeable fraction of cases with autism.

Given its early presence, microglial activation may play a central role in the pathogenesis

of autism in a substantial proportion of patients.�

In responding to the Mitkus study, I also need to refer back to previous meetings with

FDA CBER employees.

When FDA assigned its pediatrician, Dr. Leslie Ball, to oversee the review, analysis and

public reporting of thimerosal, Dr. Ball had little knowledge of toxicology or thimerosal.

In 1999, Dr. Ball and her colleagues conducted an analysis that was prompted by the Food

and Drug Modernization Act of 1997 which required FDA to compile a list of drugs and food that

contain �intentionally� introduced mercury compounds and provide a qualitative and quantitative

analysis of the exposure levels.

They reported that the limits of exposure to mercury for an infant in the first year

of life should be between 200-230 mcg total.

Infants are exposed to approximately 80 to 100 mcg of organic mercury from environmental

sources alone.

Therefore, additional exposures from thimerosal-containing vaccines should be below 120 to 130 mcg the

first year of life according to the FDA�s own findings.

At the time this analysis was done, American children were routinely receiving 187.5 mcg

of organic mercury during the first year of life from vaccines.

This means American children were being exposed to cumulative levels of organic mercury in

excess of federal safety guidelines.

The FDA consulted with an expert in the field of toxicology, Dr. Barry Rumack, MD, to better

understand the potential impact of these exposure levels.

Dr. Rumack had a private consulting practice where he offered �toxicologic and pharmacologic

evaluation of drugs, biological and potentially toxic or hazardous agents for government and

industry�.

After creating several scenarios based on infants� ages and weights, Dr. Rumack modeled

both blood and body burden levels.

The models predicted sharp peaks of mercury concentrations in both blood and tissue, in

a stair step sequence following each of the new thimerosal-containing vaccines given during

the first six months of life.

Based on these models, Rumack predicted exposure to thimerosal-containing vaccines was dosing

American children with mercury levels far exceeding all three federal safety guidelines

established by EPA, FDA and ATSDR.

There was no point in time from birth to approximately 16-18 months of age that infants were below

the EPA guidelines for allowable mercury exposure.

In fact, according to the models, blood and body burden levels of mercury peaked at six

months of age at a shockingly high level of 120 ng/liter.

To put this in perspective, the CDC classifies mercury poisoning as blood levels of mercury

greater than 10 ng/liter.

What is even more concerning is that the models developed by Dr. Rumack did not take into

account background exposures from environmental and dietary sources of mercury.

In reporting the mercury exposure levels that result from thimerosal containing vaccines,

the FDA chose not to report the findings from Rumack and Ball.

Instead, they averaged the exposures over the first six months of life, even though

the exposures only occurred at birth, two, four, and six months of age or during four

days out of 180 days.

In doing so, the agency could report that the exposures were below FDA and ATSDR guidelines

in an effort to minimize concern.

In discussing this with independent toxicologists, I have been told that averaging exposures

is not appropriate due to the fact that large bolus dose exposures are known to be more

injurious than small daily dose exposures.

If the FDA had reported the exposure levels from a daily dose perspective, it would reveal

that infants were being exposed to mercury far in excess of ALL federal safety guidelines:

FDA, ATSDR and EPA.

For example, my son at two months of age weighed 5 kg and received 62.5mcg Et Hg from his vaccines.

According to the EPA methyl mercury guidelines of .1 mcg per kg per day, his maximum exposure

level for that one day was 0.5 mcg of mercury.

He received 125 times his daily allowable exposure level or 125 days of his daily allowable

exposure.

An analogy would be that it would be allowable to give my infant son a � tsp of Tylenol

four times a day (320 mg), but if I gave him a 30-day dose of Tylenol (9,600 mg) on one

day, it would be lethal.

When I personally asked Dr. Ball why she reported the mercury exposure levels in this deceptive

fashion, she responded, �That is what I was told to do.�

In a subsequent email to her superiors at FDA on July 6th, 1999 (six months after she

had started her review of thimerosal), marked as being highly important and confidential

and obtained through a Freedom of Information Act request, Dr. Ball asked Norman Baylor,

PH D, Director of the Office of Vaccines Research Review, �Has the application of these calculations

as exposure guidelines received the sign off by toxicologists?

In prior discussions, the toxicologists seemed reluctant to state any Hg (mercury) level

was �safe�.� Although there was no response back from Dr. Baylor in the FOIA documents

we received, it is obvious that the answer was no.

By 2000, there was already a mountain of evidence that thimerosal was unsafe and ineffective.

For example, in 1987 the Commission of the European Communities initiated a research

project on 10 known or suspected spindle poisons including thimerosal.

In 1993, as described in Mutation Research, 287 (1993) 17-22 thimerosal was identified

as a strong inhibitor of microtubular assembly, a process which is essential for proper neuronal

development.

In 2000, Stajich et al. measured blood Hg levels in newborns administered the Hepatitis

B vaccine, containing 12.5 mcg ethyl mercury, and found elevated post-immunization concentrations

relative to pre-immunization levels in all neonates studied.

Levels of blood mercury after exposure in low birth weight infants were 7.36 mcg/L (� 4.99).

One infant was found to have mercury levels of 23.6 mcg/L after exposure, which supports

the inter-individual variability of mercury intoxication.

The study subjects had measurable blood Hg concentrations prior to immunization, indicating

that risk assessment must include background mercury levels from other sources.

I also find it disturbing that safety assessments you reference take the position that thimerosal

is a necessary ingredient for influenza vaccines.

This, of course, is not true.

Influenza manufacturers presently make approximately two-thirds of the U.S. influenza vaccine supply

without the use of thimerosal by placing the vaccine in a single dose vial or syringe,

which completely eliminates the need for a preservative.

Your Claim: The scientific evidence collected over the past 15 years does not show any evidence

of harm, including serious neurodevelopmental disorders from the use of thimerosal in vaccines.

The Institute of Medicine report from 2004 concluded that the evidence favors rejection

of a link between thimerosal and autism based on several epidemiological studies.

WMP Response: A causal relationship between autism and vaccinations cannot be proven or

rejected based on evidence from population-based epidemiologic studies � period.

Epidemiological studies, by definition, are not designed to prove causality; they can

provide only statistical associations.

Therefore, the committee�s conclusion that the �body of epidemiologic evidence favors

rejection of a causal relationship�� has no scientific meaning.

Further, in the IOM report the committee admitted that population-based studies would not be

able to detect subpopulations that could be genetically more vulnerable to mercury at

lower doses than typical.

On page 139, the report states that �This hypothesis cannot be excluded by epidemiological

data from large population groups that do not show an association between a vaccine

and an adverse outcome.

Depending upon the frequency of the genetic defect, a rare event caused by genetic susceptibility

could be missed even in large study samples.�

What you also failed to acknowledge is that several of the same epidemiological studies

reviewed by the IOM in 2004 documented an association between thimerosal-containing

vaccine exposures during infancy and the subsequent development of motor and phonic tics.

Tics are a family of neurological disorders that are also associated with a diagnosis

of autism.

A significant association between Hg exposure from thimerosal-containing childhood vaccines

and a diagnosis of tic disorder (TD) has now been found in six epidemiological studies

(Verstraeten et al. 2003, Andrews et al. 2004, Thompson et al. 2007, Young et al, 2008, Barile

et al. 2012, Geier et al. 2015).

The Thompson study states that, �The replication of the findings regarding tics suggests the

potential need for further studies.� Tozzi et al. 2009, also found trends towards increased

motor and phonic tics with increased thimerosal exposure but these did not reach statistical

significance, possibly because of the lack of a non-exposed control group.

These studies employed various epidemiological methods such as case�control or cohort designs,

and were conducted on cohorts of children from several different countries.

In addition, several of these studies observed significant dose-dependent relationships between

Hg exposure from thimerosal in vaccines and the risk of diagnosed TD.

A study by Young et al. found a dose-dependent relationship between increasing Hg exposure

from thimerosal in vaccines given between birth and seven months and also between birth

and 13 months of age and the risk of a diagnosed TD.

Researchers observed that, for a 100 �g Hg difference in exposure between birth and

seven months of age, the risk for diagnosed TD was significantly increased (3.39-fold).

For the same 100 �g Hg difference in exposure between birth and 13 months of age, the risk

for diagnosed tics was also found to be significantly increased (4.11-fold).

Autism etiology and severity have also been associated with mercury levels.

In June of this year, the international journal Science of the Total Environment published

a compelling study from the Republic of Korea.

The study identifies a strong relationship between prenatal and early childhood exposure

to mercury and autistic behaviors in five-year-olds.

The MOCEH study examines environmental exposures during pregnancy and childhood and their effects

on children�s growth and development.

A unique feature is that it includes five different blood samples: maternal blood from

early and late pregnancy; cord blood; and samples from children at two and three years

of age.

In addition, the study asks mothers to complete three follow-up surveys and�when their child

reaches age five�the 65-item Social Responsiveness Scale (SRS), which assesses autistic behaviors.

The investigators report a significant linear relationship between mercury exposure and

autistic behaviors (as indicated by a scaled score called an SRS T-score).

Strikingly, they find that with a doubling of blood mercury levels at four time points

(late pregnancy, cord blood, and at two and three years of age), SRS T-scores are significantly

higher.

They also looked specifically at SRS T-scores greater than or equal to 60.

Sixty and above is the accepted threshold for detecting �mild to moderate� deficits

of social behavior related to autism; scores of 76 or more are in the �severe� range.

In these analyses, the same linear relationship holds for late pregnancy and birth (i.e.,

cord blood).

With a doubling of blood mercury levels at these two time points, there is a 31% and

28% increase, respectively, in the risk of an SRS T-score of 60 or more.

Finally, the researchers identify a stronger association between late-pregnancy mercury

exposure and autistic behaviors in five-year-old boys versus five-year-old girls, perhaps due

to mercury�s endocrine-disrupting properties.

Your Claim: Schechter and Grether, 2008, showed that California�s rates of autism continued

to rise while thimerosal was being phased out from three of the early childhood vaccines.

WMP Response: This study has significant limitations in addressing what was really going on in

the time period from 1999 to 2003.

Schechter and Grether estimated exposure for each birth cohort but made no attempt to look

at the actual thimerosal exposures of individual children relative to their diagnosis.

In fact, looking at the data for the CDDS for the years immediately following their

study, there was a notable flattening of the autism prevalence growth curve in the 2004-2006

birth cohorts, suggesting a possible effect of thimerosal phase-out.

At the same time, however, any downward effect on autism rates would have been blunted by

three national autism awareness campaigns, by Autism Speaks, the CDC and the AAP , starting

early in 2005 and continuing into 2006 which raised public awareness dramatically.

While thimerosal was being phased out of the Hepatitis B, Hib and DTaP vaccines over those

four years, thimerosal exposure through influenza vaccines was increasing.

In 2004, the CDC started recommending flu shots for pregnant women in any trimester.

In 2004, over 90% of the supply of influenza vaccines contained thimerosal.

Studies of methyl mercury show that mercury is typically 1.7 times higher in cord blood

than in maternal blood and there are no studies investigating the pharmacokinetics of ethylmercury

in pregnancy.

Concurrently, in January 2003, the CDC recommended flu shots with thimerosal for all children

starting at six months of age.

The idea that children were no longer being exposed to thimerosal was and is a fallacy.

Beyond California, in the spring of 2016, the CDC�s ADDM network finally reported

the autism prevalence of children born in 2004.

For the first time that data did not show an increase in autism prevalence compared

to the 2002 birth year cohort.

They both had a one in 68 prevalence.

This suggests that the removal of thimerosal from the three pediatric vaccines may have

flattened autism rates prior to the widespread uptake of the flu vaccine and increased awareness.

That same paper, based on children born in 2004, reported a prevalence of Autism Spectrum

Disorders with IQ<70 of 4.0 per 1000.

This was a 15% drop from the previous report based on children born in 2002, when the prevalence

of ASDs with IQ<70 was 4.7 per 1000.

Note that this had nothing to do with percentages of the ASD population or additional higher-functioning

children being diagnosed � this meant that there were actually fewer severely affected

children on a population basis.

Finally, your focus on autism ignores the evidence of thimerosal�s associations with

a range of other disorders including ADHD, speech disorders, seizure disorders, autoimmunity

and eczema and the broader associations of mercury with auditory and speech impairment,

nephrotoxicity and somatosensory disorders.

According to the CDC, one in six American children of the thimerosal generation now

suffers from a neurodevelopmental disorder.

An HHS funded study found that 54% of children have a chronic disease.

What evidence have you, if any, that thimerosal is not a major culprit in the epidemics that

have devastated this generation?

�None� is the answer!

Dr. Marks, I perceive you to be a smart man and sincere in your desire to protect children

from harm.

Do you, as an individual, not as the Director of CBER, really believe that the continued

use of thimerosal in products given to pregnant women, infants and children, when it is completely

unnecessary, is appropriate?

I�m appealing to you as the mother of a young man who will never be able to take advantage

of his full potential because he was harmed by thimerosal and other sources of mercury.

It is my life�s mission, much like the mother who started MADD, to protect all children

from this completely unnecessary exposure to mercury.

I ask that you please again take our concerns to heart and help support our efforts instead

of regurgitating the inaccurate and indefensible positions of your agency.

For more infomation >> HOW THE FDA RESPONDS WHEN ASKED TO PROVE THAT IT'S SAFE TO INJECT MERCURY THIMEROSAL INTO BABIES - Duration: 46:35.

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A Fazenda 9 Marcelo Ié Ié é o nono eliminado de "A Fazenda 9" - Duration: 2:31.

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படவாய்ப்பு கிடைக்காததால் பைத்தியம் ஆகி அநாதையாக சுற்றி திரியும் பாய்ஸ் பட மணிகண்டன் | Kollywood News - Duration: 1:29.

For more infomation >> படவாய்ப்பு கிடைக்காததால் பைத்தியம் ஆகி அநாதையாக சுற்றி திரியும் பாய்ஸ் பட மணிகண்டன் | Kollywood News - Duration: 1:29.

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Elle a perdu 15 kilos en 6 semaines en faisant ceci chaque soir avant d'aller au lit - Duration: 8:36.

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Featuring Musician Megan Ni...

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Lib Tech T-Rice HP C2 157W 2018 Product Video at Blue Tomato - Duration: 2:18.

Hello my name is Didi. I represent Mervin Manufacturing here in Austria. Among others with the brand LibTech.

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This one is the T-Rice Horsepower. Horsepower means we have built in three different types of wood.

In addition, we use a basalt fiber. It is an environmentally friendly material, volcanic rock. Volcanic material. Biodegradable. Environmentally friendly.

Bio Bean Topsheet. Sintered Base.

Looking at the shape, it is a hybrid. C2 means Rocker between the binding and then Camber in the front and in the back.

In the versions up to 1.61,5 cm length we have a Blunted Nose and Tail.

Which means weight reduction, rather park-heavy. Of course, slopes as well, but leaning more towards park riding. Reduces spin weight.

Which gives you a better feeling when jumping or on rails etc.

In addition we have Magne-Traction, the patent of Mervin.

A wavy edge provides more contact surface, more aggressiveness. More grip on hard, icy slopes. Of course in the park too.

The Magne-Traction is just as normal for grinding as any other board. Nowadays, most shops have modern machines,

so that's no problem at all. Or just do it by hand.

This board by Travis Rice is just awesome.

If you want to ride like him – buy this boad. It's rad!

It's not for beginners because it's a bit harder but for advanced and good riders. You will love it. Check it out.

For more infomation >> Lib Tech T-Rice HP C2 157W 2018 Product Video at Blue Tomato - Duration: 2:18.

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HOW THE FDA RESPONDS WHEN ASKED TO PROVE THAT IT'S SAFE TO INJECT MERCURY THIMEROSAL INTO BABIES - Duration: 46:35.

HOW THE FDA RESPONDS WHEN ASKED TO PROVE THAT IT�S SAFE TO INJECT MERCURY (THIMEROSAL)

INTO BABIES

BY ROBERT F. KENNEDY JR.

Background: Peter Patriarca, an FDA employee, admitted back in 1999, in a confidential e-mail

obtained through FOIA, that, �� the greatest point of vulnerability on this issue is that

the systematic review of thimerosal in vaccines by the FDA could have been done years ago

and on an ongoing basis as the childhood immunization schedule became more complex.

The calculations done by FDA are not complex.

I�m not sure if there will be an easy way out of the potential perception that the FDA,

CDC and immunization policy bodies may have been �asleep at the switch� re: thimerosal

until now�.

Since 1999, an entire generation of children both in the US and internationally has continued

to be exposed to thimerosal � and it is time for this to stop.

Nobody should be exposed to a known neurotoxin.

The Ongoing Saga: On March 30, 2017, Robert F. Kennedy, Jr., and the World Mercury Project

(WMP) team met with the Director of the FDA�s Center for Biologics Evaluation and Research

(CBER) Dr. Peter Marks, M.D., Ph.D. and his colleagues to discuss the agency�s ongoing

refusal to ban thimerosal, a mercury-based preservative, from vaccines in the United

States.

CBER is the division of the FDA responsible for approving and monitoring the safety of

all biological products, including vaccines, allergenic products, blood and blood products,

and cellular, tissue, and gene therapies.

At the meeting, we presented a large amount of research showing the toxicity of thimerosal

in humans, animals and cellular models, including at levels similar to those resulting from

vaccine exposures.

We expressed our alarm regarding the total lack of adequate safety testing of thimerosal

prior to licensure, especially given its current use in vaccines approved for infants and pregnant

women and its worldwide use in millions of vaccines given to children, particularly in

developing countries.

Dr. Marks promised to look over the studies and seriously consider our concerns.

After many months of back and forth emails, Dr. Marks sent a letter to us on July 11th

that didn�t even look like he was in the same meeting.

World Mercury Project was dismayed by CBER�s apparent unwillingness to seriously review

the large archive of published science suggesting that using thimerosal is poisoning a generation

of American children.

From his follow-up response, it is clear that none of the information WMP provided was seriously

read or even minimally digested.

He made it clear in his letter that CBER does not intend to give any serious consideration

to the abundant and mushrooming evidence of thimerosal�s profound toxicity.

His letter was simply an exercise in blindly promoting an incredible vaccine industry orthodoxy

that is unsupportable by empirical evidence.

Below is my letter back to Dr. Marks.

We are awaiting his response.

Re: Response to your letter regarding the use of mercury in prescription drugs and vaccines.

Dear Dr. Marks,

On March 30th, Robert F. Kennedy Jr. and members of the World Mercury Project met with you

and your colleagues at the FDA to discuss our concerns regarding the continued use of

the mercury-based preservative, thimerosal, in prescription drugs and influenza vaccines

administered to pregnant women, infants and children.

During the meeting and in written letters following the meeting, we voiced concerns

regarding:

Lack of adequate safety studies prior to marketing thimerosal as a vaccine preservative.

Thimerosal�s toxicity and ineffectiveness as a preservative.

Mercury exposure from thimerosal-containing vaccine administration resulting in mercury

levels known to cause adverse outcomes.

Exposure to vaccine-level thimerosal resulting in harmful depositions of inorganic mercury

in the brain.

The California Environmental Protection Agency�s listing of all mercury-containing products

as reproductive and developmental toxicants under their Proposition 65 law.

Thimerosal was removed from all over-the-counter products when the FDA issued final rules in

the Federal Register in 1998 acknowledging that thimerosal is not generally recognized

as being safe or effective (GRASE).

Why is this same product allowed in prescription drugs and vaccines?

At the end of our meeting, you reassured us that you would take our concerns seriously

and would �follow the science� wherever it might lead you.

For several months after our meeting, I contacted the FDA public liaison Ms. McNeill inquiring

when we might expect to hear back from you regarding our concerns.

Ms. McNeill told me that we had provided the agency with extensive information and that

it was taking additional time to review the material.

I was hopeful that FDA might finally, therefore, implement the 2001 recommendation of the Institute

of Medicine that pregnant women, infants and children not be exposed to thimerosal-containing

vaccines.

On July 11th, we received your written response to our concerns.

I was dismayed by your agency�s apparent unwillingness to seriously review the large

archive of published science suggesting that using thimerosal is poisoning a generation

of American children.

From your follow-up written response, it is clear that none of the information we provided

was seriously read or even minimally digested.

You make it clear in your letter that you do not intend to give any serious consideration

to the abundant and mushrooming evidence of thimerosal�s profound toxicity.

Your letter is simply an exercise in blindly promoting an incredible vaccine industry orthodoxy

that is unsupportable by empirical evidence.

You cite in your written response FDA�s mushy biologics regulations which define safety

as �the relative freedom from harmful effect to persons affected, directly or indirectly,

by a product when prudently administered, taking into consideration the character of

the product in relation to the condition of the recipient at the time.� 21CFR 600.39(p).

You report that in applying this elastic regulatory standard, �FDA must weigh the risk of a

vaccine or any drug against its benefits when determining whether a product is safe.

If the benefits of the vaccine or other pharmaceutical product outweigh the risks of its side effects,

then the FDA finds the product to be safe.� You further acknowledge that �the determination

of a products safety is a relative rather than absolute measurement�,entirely subject

to FDA�s �discretion and expertise.� Even operating under these malleable standards,

FDA should consider that vaccines are products given to healthy individuals, and their risks

should be measured by an extremely high bar since they are not treating a disease.

Furthermore, FDA has no capacity to evaluate risks of thimerosal since, by FDA�s own

admission to Congress, there has never been a long-term safety study performed on thimerosal

in any human population including infants and pregnant women.

Vaccines containing thimerosal in the U.S. are predominantly influenza vaccines.

Furthermore, thimerosal is still widely used in vaccines given to tens of millions of children

in the developing world and, since U.S. policy influences worldwide policy, FDA bears responsibility

for these policies.

In the U.S., thimerosal-containing vaccines are administered to healthy six-month old

infants, young children and pregnant women despite never having been safety tested in

those populations.

According to their product inserts, influenza vaccines have been associated with an increased

incidence of seizures and Guillain-Barre Syndrome.

Recent studies have linked influenza vaccines to miscarriage, autism and, possibly, birth

defects.

A significant percentage of influenza vaccines still contain thimerosal and studies should

be done to see if thimerosal played a role in these outcomes.

There has been limited testing of influenza vaccines in animal models, however, there

have not been any adequate and well-controlled studies in pregnant women.

Because animal studies are not always predictive of human response, the package inserts for

flu vaccines reiterate that flu vaccines �should be given to a pregnant woman only if clearly

needed�.

In addition, there are numerous VAERS reports of injuries from thimerosal-containing vaccines.

Therefore, it is imperative that vaccines administered to sensitive populations (pregnant

women, infants and children) be held to the highest standards of safety.

I think parents and the American public would be appalled to learn that vaccine safety determinations

are �relative� and are within an FDA employee�s �discretion and expertise.� That discretion

and expertise should actually require a factual basis, not just opinion.

Needless to say, these decisions should be guided by the precautionary principle.

I have organized the remainder of my response into addressing the erroneous claims made

in your letter.

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Your Claim: The agency evaluates whether a preservative contained in a product is at

such levels that when used at the recommended dose is not toxic to the recipient and that

the �FDA � has repeatedly found that the vaccines currently being marketed that contain

thimerosal are safe��

WMP Response: Please show us the data used to evaluate thimerosal safety in infants and

pregnant women.

We do not believe they exist.

In an email discussion regarding the use of thimerosal-containing influenza vaccines administered

to pregnant women, infants and children, in 1999, Dr. William Egan, acting Director of

the Center for Drugs and Biologics (CDER), recommended that the statement, �The chronic,

daily ingestion reported (in several studies-primarily Seychelles study) greatly exceeds the amount

of mercury that a pregnant woman would receive from a single annual dose of thimerosal-containing

influenza vaccine� �might well be deleted.� Egan went on to justify his recommendation

by saying that the statement ��in some ways is misleading.

I am not sure that I would want to argue, for example, that one could take the allowed

amount of mercury for a year and administer it as a bolus injection with the same outcome

as having it spaced out evenly over the year: the issue then becomes one of how much of

a bolus can one give at one time without harmful effect and this data does not exist (or at

least I�m not aware of them).�

Dr. Egan was right then and he is right today; such safety data do not exist.

In fact, many toxicologists believe that large bolus dose exposures such as those resulting

from thimerosal-containing vaccines are more harmful in comparison to small daily dose

exposures that the body is much more capable of excreting without overburdening detoxification

pathways in the body.

This concern is supported by research that found a mercury dose given acutely may produce

toxic effects, whereas the same dose distributed over a period of time may give no evidence

of poisoning.

(Koos and Longo,1976).

Your Claim: �Thimerosal has a long record of safe and effective use in preventing bacterial

and fungal contamination of vaccines with no ill effects other than occasional hypersensitivity

and minor local reactions at the site of injection.�.

WMP Response: There is ample evidence provided in multiple studies by federal agencies and

independent scientists that spans the last 90 years which documents that thimerosal is

neither an effective nor a safe vaccine preservative.

In a study published in the Journal of the American Medical Association in 1948 titled

�The bacteriostatic and bactericidal actions of some mercurial compounds on hemolytic streptococci,�

the authors vigorously argued that thimerosal was ineffective as a �disinfectant, germicide

and antiseptic.� In the review of the literature in this paper, the authors cited eight studies

from 1928, 1935, 1937, 1938, and 1944 all of which drew similar conclusions.

In 1975, the FDA convened a panel of experts to evaluate mercury-containing over-the-counter

(OTC) products.

The panel issued its reports in 1980 and in 1982.

The FDA issued a report of the panel�s findings in the Federal Register where they concluded

that �some mercury-containing preparations are not effective and others are not safe

and effective for OTC topical antimicrobial use�.

With respect to thimerosal in particular, that panel found evidence from 1950 which

concluded that �thimerosal was no better than water in protecting mice from potential

fatal streptococcal infections.� Additionally, citing a 1935 study, the panel reported that

thimerosal was �35.3 times more toxic for embryonic chick heart tissue than for Staphylococcus

aureus.� Most of the literature reviewed addressed mercury�s lack of antibacterial

properties.

One review published in 1971 titled, �Three thousand years of mercury.

A plea for abandonment of a dangerous, unproven therapy,� addressed mercury�s lack of

effectiveness against fungal contamination as well.

The FDA-appointed expert panel concluded that �thimerosal was not safe for OTC topical

use because of its potential for cell damage if applied to broken skin and its allergy

potential.

It is not effective as a topical antimicrobial because its bacteriostatic action can be reversed.�

However, it wasn�t until 1998 that the FDA issued its final report banning the use of

thimerosal in topical OTC products because it was not �safe and effective.�

There are also several more recent published reports of thimerosal�s failure as a preservative.

Clusters of disease from Group A streptococcus infections were traced back to multi-dose

vials of diphtheria toxoid, pertussis, and tetanus toxoid (DPT) vaccine which were contaminated

after being opened.

Additionally, in 2004, a Chiron plant that manufactured Fluvirin was forced to close

because its vaccine was contaminated with Serratia marcescens.

This vaccine used thimerosal as a preservative.

In this case and in the many others cited, thimerosal failed to prevent bacterial growth.

In response to the reports from the FDA expert panel who reviewed the use of thimerosal in

over-the-counter products in the 1980�s, the FDA published in the April 22, 1998 Federal

Register Status of Certain Additional Over-the-Counter Drug Category II and III Active Ingredients.

(April 22, 1998);63(77):19799-19802.

21 CFR Part 310 [Docket No. 75N-183F, 75N-183D, and 80N-0280 concluding that the use of thimerosal

in over the counter products is not �generally recognized as safe or effective� (GRASE).

In the final rulemaking, the FDA states that �safety and effectiveness have not been

established for the ingredients (mercury-based preservatives) included in this current final

rule and manufacturers have not submitted the necessary data in response to earlier

opportunities.

The agency�s experience has been that under these circumstances companies have not submitted

data in response to yet another opportunity.

Consumers will benefit from the early removal from the marketplace of products containing

ingredients for which safety and effectiveness has not been established.�

The World Mercury Project would like to know how is it possible that one division of the

FDA recognizes that there is absolutely no safety or effectiveness data available for

the use of mercury in over the counter products and essentially bans its use, while your FDA

division of blood and biologics continues to recklessly allow its widespread use in

over 100 prescription products including vaccines?

Your claim: �Under the FDA Modernization Act (FDAMA) of 1997, the FDA conducted a comprehensive

review of the use of thimerosal in childhood vaccines.

Conducted in 1999, this review found no evidence of harm from the use of thimerosal as a vaccine

preservative, other than local hypersensitivity reactions (Ball et al. 2001).�

WMP Response: It�s disturbing that according to internal emails obtained by FOIA, Dr. Ball

never conducted an extensive review of reports of harm.

On November 23, 1998, Dr. Leslie Ball of the FDA asked internal reviewers to perform a

Medwatch query on thimerosal.

Medwatch is the FDA�s database for reporting adverse drug events.

On January 7, 1999, Dr. Ball was informed by Fredrick Varricchio of FDA that there were

7000 reports containing the word thimerosal on FDA�s Medwatch.

He stated, �I have some results for you.

Problem is that there are 7000 reports that mention thimerosal.

What to do now.

Obviously looking at all 7,000 is a brute force approach.� Dr. Ball responded by saying,

�perhaps you can get records on a subset of 50 or so we can look at them and get a

general feel for what�s been reported before we go any further.� In a subsequent email

on January 19th, Mr. Varricchio noted that the �plan is to get whatever is on the summary

for every 100th report.� This means that only 70 adverse events out of 7000 reported

to the FDA were actually reviewed by Dr. Ball and her team.

This email calls into question the findings reported by Dr. Ball and also suggests that

an extensive investigation has never been conducted by the FDA with regard to adverse

events associated with the use of thimerosal.

Would you allow any other medical product to be widely used based on review of one percent

of the information available?

I am also, Sir, frankly shocked at your unwillingness to acknowledge the robust body of literature

that has been published the last 18 years since concerns regarding thimerosal first

surfaced within the FDA in 1999.

There are literally hundreds of peer-reviewed, published studies that document the toxicity

of thimerosal.

Many of these investigated levels of mercury known to occur from vaccine exposure in cell

and animal models.

In 2013, Jose G. Dorea published a meta-analysis of thimerosal research related to vaccine

exposure.

Dorea searched major databases for human and experimental studies that addressed issues

related to early life exposure to TCVs.

The author concluded that: � a) mercury load in fetuses, neonates, and infants resulting

from TCVs remains in blood of neonates and infants at sufficient concentration and for

enough time to penetrate the brain and to exert a neurologic impact and a probable influence

on neurodevelopment of susceptible infants; b) etHg metabolism related to neurodevelopmental

delays has been demonstrated experimentally and observed in population studies; c) unlike

chronic Hg exposure during pregnancy, neurodevelopmental effects caused by acute (repeated/cumulative)

early life exposure to TCV-etHg remain unrecognized; and d) the uncertainty surrounding low-dose

toxicity of etHg is challenging but recent evidence indicates that avoiding cumulative

insults by alkyl-mercury forms (which include Thimerosal) is warranted.� Dorea emphasized

the importance of �a) maintaining trust in vaccines while reinforcing current public

health policies to abate mercury exposure in infancy; b) supporting WHO policies that

recommend vaccination to prevent and control existing and impending infectious diseases;

and c) not confusing the �need� to use a specific �product� (TCV) by accepting

as �innocuous� (or without consequences) the presence of a proven �toxic alkyl-mercury�

(etHg) at levels that have not been proven to be toxicologically safe.�

For your convenience, I have included a sampling of 35 abstracts that represent the more current

state of the science regarding thimerosal that has emerged since 1999 as an appendix.

Even if Dr. Ball�s review had been adequate at that time, surely 18 years of further research

should prompt an updated evaluation by the FDA.

Your Claim: A 2014 modeling study by your own Centers for Biologics Evaluation and Research

employee, Dr. Robert Mitkus, showed that �peak body burdens of mercury following episodic

exposures to thimerosal in this worst case did not exceed the corresponding safe body

burden of mercury from MeHg at any time�.

WMP Response: The Mitkus study reported that the body burden of mercury in infants, over

the first 4.5 years of life following yearly exposures to thimerosal from annual flu vaccines,

was two orders of magnitude lower than that estimated for exposures to the lowest regulatory

threshold for MeHg over the same time period.

The author relies completely on these findings to conclude that their pharmacokinetic analysis

supports the safety of thimerosal when used as a preservative at current levels in certain

multi-dose infant vaccines in the United States.

Mitkus fails to acknowledge the past levels of exposure that infants received from vaccines

starting in the late 1980s and extending well into 2000, that were 187.5 mcg etHg the first

year of life versus 12.5 mcg etHg from flu vaccines annually.

He also makes the assumption that there are no other mercury exposures outside of thimerosal,

which is not supported by either established science or common sense.

The model developed by Mitkus relied solely on blood levels and did not take into consideration

the accumulation of mercury in the brain tissue.

Data from the Burbacherstudy that assessed exposures from both methyl and ethyl mercury

in infant non-human primates, based on vaccine level exposures, found that although there

was little accumulation of Hg in the blood with repeated vaccinations, accumulation of

Hg in the brain of infants did occur.

In fact, there was a much higher proportion of inorganic Hg in the brain of thimerosal

monkeys than in the brains of MeHg monkeys (up to 71% vs. 10%).

Absolute inorganic Hg concentrations in the brains of the thimerosal-exposed monkeys were

approximately twice that of the MeHg monkeys.

Burbacher concluded that �the safety of thimerosal drawn from blood Hg clearance data

in human infants receiving vaccines may not be valid, given the significantly slower half-life

of Hg in the brain as observed in the infant macaques.� But that is exactly what Mitkus

does in his model and reports in his study.

Mitkus also makes the statement that thimerosal is more quickly and extensively metabolized

to inorganic mercury in the brain than is MeHg and that process of dealkylation �may

be� a detoxification step.

According to Burbacher, who is the author of the studies relied on by Mitkus in the

development of his model, the statement that dealkylation may be a detoxification process

is purely speculative and has not been established.

Mitkus is referring to previous reports that have indicated that dealkylation of Hg is

a detoxification process that helps to protect the central nervous system (Magos 2003; Magos

et al. 1985).

These reports are largely based on histology and histochemistry studies of adult rodents

exposed to Hg for a short period of time.

The results of these studies indicated that damage to the cerebellum was observed only

in MeHg-treated animals that had much lower levels of inorganic Hg in the brain than animals

comparably treated with ethylmercury.

Moreover, the results did not indicate the presence of inorganic Hg deposits in the area

where the cerebellar damage was localized (granular layer).

In contrast, previous studies of adult M. fascicularis monkeys exposed chronically to

MeHg have indicated that demethylation of Hg occurs in the brain over a long period

of time after MeHg exposure and that this is not a detoxification process (Charleston

et al. 1994, 1995, 1996; Vahter et al. 1994, 1995).

Results from these studies indicated higher inorganic Hg concentrations in the brain 6

months after MeHg exposure had ended, whereas organic Hg had cleared from the brain.

The estimated half-life of organic Hg in the brain of these adult monkeys was consistent

across various brain regions at approximately 37 days (similar to the brain half-life in

the Burbacher study).

Stereologic and autometallographic studies on the brains of these adult monkeys indicated

that the persistence of inorganic Hg in the brain was associated with a significant increase

in the number of microglia in the brain.

(Charleston et al. 1994, 1995,1996).

The microgliosis and neuroinflamation documented in the brains of the adult monkeys in association

with deposits of inorganic mercury are two hallmark findings in brain tissue of both

children and adults with autism.

Neuropathological studies of brain tissues from cerebellum, midfrontal, and cingulate

gyrus obtained at autopsy from 11 patients with autism demonstrated the presence of an

active neuroinflammatory processes in the cerebral cortex, white matter and, most notably,

the cerebellum.

In a subsequent study, microglia appeared markedly activated in five of 13 cases with

autism, including two of three under age six, and marginally activated in an additional

four of 13 cases.

The authors concluded that microglial activation �represents a neuropathological alteration

in a sizeable fraction of cases with autism.

Given its early presence, microglial activation may play a central role in the pathogenesis

of autism in a substantial proportion of patients.�

In responding to the Mitkus study, I also need to refer back to previous meetings with

FDA CBER employees.

When FDA assigned its pediatrician, Dr. Leslie Ball, to oversee the review, analysis and

public reporting of thimerosal, Dr. Ball had little knowledge of toxicology or thimerosal.

In 1999, Dr. Ball and her colleagues conducted an analysis that was prompted by the Food

and Drug Modernization Act of 1997 which required FDA to compile a list of drugs and food that

contain �intentionally� introduced mercury compounds and provide a qualitative and quantitative

analysis of the exposure levels.

They reported that the limits of exposure to mercury for an infant in the first year

of life should be between 200-230 mcg total.

Infants are exposed to approximately 80 to 100 mcg of organic mercury from environmental

sources alone.

Therefore, additional exposures from thimerosal-containing vaccines should be below 120 to 130 mcg the

first year of life according to the FDA�s own findings.

At the time this analysis was done, American children were routinely receiving 187.5 mcg

of organic mercury during the first year of life from vaccines.

This means American children were being exposed to cumulative levels of organic mercury in

excess of federal safety guidelines.

The FDA consulted with an expert in the field of toxicology, Dr. Barry Rumack, MD, to better

understand the potential impact of these exposure levels.

Dr. Rumack had a private consulting practice where he offered �toxicologic and pharmacologic

evaluation of drugs, biological and potentially toxic or hazardous agents for government and

industry�.

After creating several scenarios based on infants� ages and weights, Dr. Rumack modeled

both blood and body burden levels.

The models predicted sharp peaks of mercury concentrations in both blood and tissue, in

a stair step sequence following each of the new thimerosal-containing vaccines given during

the first six months of life.

Based on these models, Rumack predicted exposure to thimerosal-containing vaccines was dosing

American children with mercury levels far exceeding all three federal safety guidelines

established by EPA, FDA and ATSDR.

There was no point in time from birth to approximately 16-18 months of age that infants were below

the EPA guidelines for allowable mercury exposure.

In fact, according to the models, blood and body burden levels of mercury peaked at six

months of age at a shockingly high level of 120 ng/liter.

To put this in perspective, the CDC classifies mercury poisoning as blood levels of mercury

greater than 10 ng/liter.

What is even more concerning is that the models developed by Dr. Rumack did not take into

account background exposures from environmental and dietary sources of mercury.

In reporting the mercury exposure levels that result from thimerosal containing vaccines,

the FDA chose not to report the findings from Rumack and Ball.

Instead, they averaged the exposures over the first six months of life, even though

the exposures only occurred at birth, two, four, and six months of age or during four

days out of 180 days.

In doing so, the agency could report that the exposures were below FDA and ATSDR guidelines

in an effort to minimize concern.

In discussing this with independent toxicologists, I have been told that averaging exposures

is not appropriate due to the fact that large bolus dose exposures are known to be more

injurious than small daily dose exposures.

If the FDA had reported the exposure levels from a daily dose perspective, it would reveal

that infants were being exposed to mercury far in excess of ALL federal safety guidelines:

FDA, ATSDR and EPA.

For example, my son at two months of age weighed 5 kg and received 62.5mcg Et Hg from his vaccines.

According to the EPA methyl mercury guidelines of .1 mcg per kg per day, his maximum exposure

level for that one day was 0.5 mcg of mercury.

He received 125 times his daily allowable exposure level or 125 days of his daily allowable

exposure.

An analogy would be that it would be allowable to give my infant son a � tsp of Tylenol

four times a day (320 mg), but if I gave him a 30-day dose of Tylenol (9,600 mg) on one

day, it would be lethal.

When I personally asked Dr. Ball why she reported the mercury exposure levels in this deceptive

fashion, she responded, �That is what I was told to do.�

In a subsequent email to her superiors at FDA on July 6th, 1999 (six months after she

had started her review of thimerosal), marked as being highly important and confidential

and obtained through a Freedom of Information Act request, Dr. Ball asked Norman Baylor,

PH D, Director of the Office of Vaccines Research Review, �Has the application of these calculations

as exposure guidelines received the sign off by toxicologists?

In prior discussions, the toxicologists seemed reluctant to state any Hg (mercury) level

was �safe�.� Although there was no response back from Dr. Baylor in the FOIA documents

we received, it is obvious that the answer was no.

By 2000, there was already a mountain of evidence that thimerosal was unsafe and ineffective.

For example, in 1987 the Commission of the European Communities initiated a research

project on 10 known or suspected spindle poisons including thimerosal.

In 1993, as described in Mutation Research, 287 (1993) 17-22 thimerosal was identified

as a strong inhibitor of microtubular assembly, a process which is essential for proper neuronal

development.

In 2000, Stajich et al. measured blood Hg levels in newborns administered the Hepatitis

B vaccine, containing 12.5 mcg ethyl mercury, and found elevated post-immunization concentrations

relative to pre-immunization levels in all neonates studied.

Levels of blood mercury after exposure in low birth weight infants were 7.36 mcg/L (� 4.99).

One infant was found to have mercury levels of 23.6 mcg/L after exposure, which supports

the inter-individual variability of mercury intoxication.

The study subjects had measurable blood Hg concentrations prior to immunization, indicating

that risk assessment must include background mercury levels from other sources.

I also find it disturbing that safety assessments you reference take the position that thimerosal

is a necessary ingredient for influenza vaccines.

This, of course, is not true.

Influenza manufacturers presently make approximately two-thirds of the U.S. influenza vaccine supply

without the use of thimerosal by placing the vaccine in a single dose vial or syringe,

which completely eliminates the need for a preservative.

Your Claim: The scientific evidence collected over the past 15 years does not show any evidence

of harm, including serious neurodevelopmental disorders from the use of thimerosal in vaccines.

The Institute of Medicine report from 2004 concluded that the evidence favors rejection

of a link between thimerosal and autism based on several epidemiological studies.

WMP Response: A causal relationship between autism and vaccinations cannot be proven or

rejected based on evidence from population-based epidemiologic studies � period.

Epidemiological studies, by definition, are not designed to prove causality; they can

provide only statistical associations.

Therefore, the committee�s conclusion that the �body of epidemiologic evidence favors

rejection of a causal relationship�� has no scientific meaning.

Further, in the IOM report the committee admitted that population-based studies would not be

able to detect subpopulations that could be genetically more vulnerable to mercury at

lower doses than typical.

On page 139, the report states that �This hypothesis cannot be excluded by epidemiological

data from large population groups that do not show an association between a vaccine

and an adverse outcome.

Depending upon the frequency of the genetic defect, a rare event caused by genetic susceptibility

could be missed even in large study samples.�

What you also failed to acknowledge is that several of the same epidemiological studies

reviewed by the IOM in 2004 documented an association between thimerosal-containing

vaccine exposures during infancy and the subsequent development of motor and phonic tics.

Tics are a family of neurological disorders that are also associated with a diagnosis

of autism.

A significant association between Hg exposure from thimerosal-containing childhood vaccines

and a diagnosis of tic disorder (TD) has now been found in six epidemiological studies

(Verstraeten et al. 2003, Andrews et al. 2004, Thompson et al. 2007, Young et al, 2008, Barile

et al. 2012, Geier et al. 2015).

The Thompson study states that, �The replication of the findings regarding tics suggests the

potential need for further studies.� Tozzi et al. 2009, also found trends towards increased

motor and phonic tics with increased thimerosal exposure but these did not reach statistical

significance, possibly because of the lack of a non-exposed control group.

These studies employed various epidemiological methods such as case�control or cohort designs,

and were conducted on cohorts of children from several different countries.

In addition, several of these studies observed significant dose-dependent relationships between

Hg exposure from thimerosal in vaccines and the risk of diagnosed TD.

A study by Young et al. found a dose-dependent relationship between increasing Hg exposure

from thimerosal in vaccines given between birth and seven months and also between birth

and 13 months of age and the risk of a diagnosed TD.

Researchers observed that, for a 100 �g Hg difference in exposure between birth and

seven months of age, the risk for diagnosed TD was significantly increased (3.39-fold).

For the same 100 �g Hg difference in exposure between birth and 13 months of age, the risk

for diagnosed tics was also found to be significantly increased (4.11-fold).

Autism etiology and severity have also been associated with mercury levels.

In June of this year, the international journal Science of the Total Environment published

a compelling study from the Republic of Korea.

The study identifies a strong relationship between prenatal and early childhood exposure

to mercury and autistic behaviors in five-year-olds.

The MOCEH study examines environmental exposures during pregnancy and childhood and their effects

on children�s growth and development.

A unique feature is that it includes five different blood samples: maternal blood from

early and late pregnancy; cord blood; and samples from children at two and three years

of age.

In addition, the study asks mothers to complete three follow-up surveys and�when their child

reaches age five�the 65-item Social Responsiveness Scale (SRS), which assesses autistic behaviors.

The investigators report a significant linear relationship between mercury exposure and

autistic behaviors (as indicated by a scaled score called an SRS T-score).

Strikingly, they find that with a doubling of blood mercury levels at four time points

(late pregnancy, cord blood, and at two and three years of age), SRS T-scores are significantly

higher.

They also looked specifically at SRS T-scores greater than or equal to 60.

Sixty and above is the accepted threshold for detecting �mild to moderate� deficits

of social behavior related to autism; scores of 76 or more are in the �severe� range.

In these analyses, the same linear relationship holds for late pregnancy and birth (i.e.,

cord blood).

With a doubling of blood mercury levels at these two time points, there is a 31% and

28% increase, respectively, in the risk of an SRS T-score of 60 or more.

Finally, the researchers identify a stronger association between late-pregnancy mercury

exposure and autistic behaviors in five-year-old boys versus five-year-old girls, perhaps due

to mercury�s endocrine-disrupting properties.

Your Claim: Schechter and Grether, 2008, showed that California�s rates of autism continued

to rise while thimerosal was being phased out from three of the early childhood vaccines.

WMP Response: This study has significant limitations in addressing what was really going on in

the time period from 1999 to 2003.

Schechter and Grether estimated exposure for each birth cohort but made no attempt to look

at the actual thimerosal exposures of individual children relative to their diagnosis.

In fact, looking at the data for the CDDS for the years immediately following their

study, there was a notable flattening of the autism prevalence growth curve in the 2004-2006

birth cohorts, suggesting a possible effect of thimerosal phase-out.

At the same time, however, any downward effect on autism rates would have been blunted by

three national autism awareness campaigns, by Autism Speaks, the CDC and the AAP , starting

early in 2005 and continuing into 2006 which raised public awareness dramatically.

While thimerosal was being phased out of the Hepatitis B, Hib and DTaP vaccines over those

four years, thimerosal exposure through influenza vaccines was increasing.

In 2004, the CDC started recommending flu shots for pregnant women in any trimester.

In 2004, over 90% of the supply of influenza vaccines contained thimerosal.

Studies of methyl mercury show that mercury is typically 1.7 times higher in cord blood

than in maternal blood and there are no studies investigating the pharmacokinetics of ethylmercury

in pregnancy.

Concurrently, in January 2003, the CDC recommended flu shots with thimerosal for all children

starting at six months of age.

The idea that children were no longer being exposed to thimerosal was and is a fallacy.

Beyond California, in the spring of 2016, the CDC�s ADDM network finally reported

the autism prevalence of children born in 2004.

For the first time that data did not show an increase in autism prevalence compared

to the 2002 birth year cohort.

They both had a one in 68 prevalence.

This suggests that the removal of thimerosal from the three pediatric vaccines may have

flattened autism rates prior to the widespread uptake of the flu vaccine and increased awareness.

That same paper, based on children born in 2004, reported a prevalence of Autism Spectrum

Disorders with IQ<70 of 4.0 per 1000.

This was a 15% drop from the previous report based on children born in 2002, when the prevalence

of ASDs with IQ<70 was 4.7 per 1000.

Note that this had nothing to do with percentages of the ASD population or additional higher-functioning

children being diagnosed � this meant that there were actually fewer severely affected

children on a population basis.

Finally, your focus on autism ignores the evidence of thimerosal�s associations with

a range of other disorders including ADHD, speech disorders, seizure disorders, autoimmunity

and eczema and the broader associations of mercury with auditory and speech impairment,

nephrotoxicity and somatosensory disorders.

According to the CDC, one in six American children of the thimerosal generation now

suffers from a neurodevelopmental disorder.

An HHS funded study found that 54% of children have a chronic disease.

What evidence have you, if any, that thimerosal is not a major culprit in the epidemics that

have devastated this generation?

�None� is the answer!

Dr. Marks, I perceive you to be a smart man and sincere in your desire to protect children

from harm.

Do you, as an individual, not as the Director of CBER, really believe that the continued

use of thimerosal in products given to pregnant women, infants and children, when it is completely

unnecessary, is appropriate?

I�m appealing to you as the mother of a young man who will never be able to take advantage

of his full potential because he was harmed by thimerosal and other sources of mercury.

It is my life�s mission, much like the mother who started MADD, to protect all children

from this completely unnecessary exposure to mercury.

I ask that you please again take our concerns to heart and help support our efforts instead

of regurgitating the inaccurate and indefensible positions of your agency.

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