Me And My Ms

I HAVE HAD MS NOW FOR OVER 10YRS AND WHEN I WAS DIAGNOISED I TOO THOUGHT IT WAS A DEATH SENTENCE AND FOR A WHILE I WAS DEPRESSED THINKING MY LIFE HAD ENDED I  CRYED ALL THE TIME I KEPT THE DIAGNOES TO MY SELF AS WELL AS THE PAIN IT WAS CAUSING. FIRST SIGNS TRIPPING ALL THE TIME AND FALLING I THOUGH I WAS JUST BEING CLUMSY THEN CAME THE  PAIN AND THE MEMEORY LOST WHICH WAS NOT GOOD CAUSE I WORKED IN THE HOSPITAL ER WAS IN SO MUCH PAIN  ONE NIGHT I ENDED UP IN THE ER OF MY OWN JOB AND I WAS ADMITTERD THE NEXT DAY SEVERAL ATTENDING SAW ME AND KEW WHAT I HAD THEY ALL SAID MS BUT THE ME SPECIALIST SAID I DID NOT HAVE IT I DID NOT FALL IN AVERAGE  SO I HAD A SPINAL TaP FOR A TROTTERS REST WHICH WOULD SAY IF I HAD IT OR NOT AND I WAS SENT HOME WELL AFTER A FEW DAYS I ENDED UP BACK IN THE ER IN SERVERE PAIN AND THE NEUROLOGIST CAME IN AND SAID MY RESULTS WERE BACK AND I FOR SURE HAD  MS AND THE FELT I HAD IT FOR A WHILE SO I BECAME DPRESSED AND I MEAN BAD , THE CRYING AND ALL AND THE QUESTION WHY ME WHY DO  I HAVE IT AND NO ONE ELSE IN MY FAMILY I FELT LIKE I WAS THE ONLY PERSON IN THE WORLD WITH IT. I REMEMBER SOME CELEBRITIES HAVING IT AND OTHER PEOPLE I THOUGHT MS ALWAYS MET THAT AT SOME POINT I WOULD END UP IN A WHEEL CHAIR DOOM FOR LIFE. SINCE I WAS IN MY EARLY 40'S  AND I WAS DATING I WAS SCARED TO LET ANYONE KNOW FOR I DID NOT KNOW HOW THEY WOULD TREAT ME OR HOW MY JOB WOULD REACT WELL SOME WAS GOOD AND POSTIVE AND SOME WAS BAD  JOB WAS BAD EVRYONE ELSE WAS PREETY GOOD. MY FAMILY WAS VERY SUPPORTIVE BUT I TOO STARTED TO READ EVERYTHING ABOUT MS AND HAVE A BETTER UNDERSTANDING OF IT OT THE MOSTER AS THEY CALL IT I LEARNED HOW TO CONTROL IT AND NOT IT CONTROL ME I STILL GET TREMORS, VISION PROBLESM CAN'T WALK. OR THINK AT TIMES NUMBNESS TOO BUT I TAKE IT IN STRIDE I 'VE LEARNED TO TELL PEOPLE I HAVE IT AND NOT BE ASHAME ABOUT IT I HAVE A2 SOUTH RUSSIAN SHEEP DOGS RARE DOGS THERE ARE ONLY 127 IN THE US OTHER WISE THEY ARE ONLY IN RUSSIA ONE WEIGHS 115 AND THE OTHER WEIGHT 100

 SO YOU CAN MAKE IT I DID

mya720148 mya720148
46-50, F
3 Responses Feb 26, 2010

thank you for your brave heartfelt story.

Hey, do you have silver fillings? Mine caused 70 symptoms of MS: from ataxia, numbness of my toes, "a burning brain," loss of peripheral vision, memory loss, chronic fatigue, and a host of other symptoms. <br />
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This is because silver fillings are 50-70% mercury, which is released into the body as ethylmercury vapor. Anywhere from 3-29 micrograms of mercury are released by these fillings every day. The symptoms of MS and mercury poisoning are effectively the same. I got them removed and most of my symptoms are gone, I just have to spend a few years getting rid of the residual mercury from my tissues. Believe me or not, I honestly don't care. It's not going to be the case for everyone. I just know it worked for me. <br />
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Also if you've been exposed to a lot of thimerosal from vaccines, this could have triggered it. Also the government is now admitting that Hepatitis B vaccines can trigger demyelinating diseases. Check out the FDA's website if you want to confirm there is mercury in vaccines. No level is safe, considering it's more toxic than lead and arsenic. It is the most toxic non-radioactive substance known to man. I'm just trying to help.

THANK YOU FOR SHARING! TAKE CARE!!!