toribird97
08-15-2006, 12:44 PM
does anyone know if there is a research center that specializes in polymyositis??
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JoJoJim
08-16-2006, 02:51 AM
Dear Tori,
I personally do not know of any type of research center devoted JUST to Polymyositis. I am aware of the Myositis Organization---they can point you in the right direction. The MDA is also pretty knowledgeable in Polymyositis. For me, it was a relief to FINALLY have just one doctor KNOW what I was dealing with.
Peace Always,
the DragonLady
I personally do not know of any type of research center devoted JUST to Polymyositis. I am aware of the Myositis Organization---they can point you in the right direction. The MDA is also pretty knowledgeable in Polymyositis. For me, it was a relief to FINALLY have just one doctor KNOW what I was dealing with.
Peace Always,
the DragonLady
toribird97
08-16-2006, 05:53 PM
THANK YOU FOR THE INFO I HAVE TO SAY THIS IS SO FRUSTRATING TO DEAL WITH-- ITS ACTUALLY MY MOM WHO HAS THIS CONDITION.
I HAVE BEEN LOOKING INTO POLYMYOSITIS ON THE COMPUTER & I READ THAT SOMEONE STARTED TAKING ZITHROMAX (ANTIBIOTIC) ALONG WITH METHOTREXATE- BUT STARTED FEELING SO MUCH BETTER WITH THE ZITHROMAX- HE IS ON VERY LOW DOSE OF METHOTREXATE HAS ANYONE ELSE HEARD OF THIS??? :confused:
I HAVE BEEN LOOKING INTO POLYMYOSITIS ON THE COMPUTER & I READ THAT SOMEONE STARTED TAKING ZITHROMAX (ANTIBIOTIC) ALONG WITH METHOTREXATE- BUT STARTED FEELING SO MUCH BETTER WITH THE ZITHROMAX- HE IS ON VERY LOW DOSE OF METHOTREXATE HAS ANYONE ELSE HEARD OF THIS??? :confused:

