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Re: seen the rheumatologist

From: mdustin (anonymous@obgyn.net)
Fri Nov 30 06:46:49 2007


Niki,

I also am still having issues post Lupron. I am in the process of trying to find a rhueumatologist. Did you have any of the issues that you have now before Lupron? I did not. But I am also aware that there are not "many" doctors out there that will admit, even the possability that anything is an actual side effect from Lupron itself. I was curious how you went about talking to and finding your rheumatologist? My widespread pain and spasming has only become more and more intense and constant this week and I have come to a T. I am sure that the best option for me would be to see a rheumatologist, right? My other doctors have completely shrugged off my issues after a simple blood test came back fine...CBC. And that was that. I don't understand what is going on with me and what to really do about it. (I also now have vison problems that is keeping me from even being able to drive.)

Any advice is greatly appreciated. Thanks.

~Maggie

At Thu, 29 Nov 2007, niki wrote: >
>Hi all. I am still having issues post lupron. So i followed up with
>the rheumatologist. Im being tested for several autoimmune disorders.
>His thoughts are lupus or fibromyalgia with reumatoid arthritis closesly
>following. I have several of the tender points for the fibro as well as
>numerous other symptoms. He told me that lupus and fibro have alot of
>the same common symptoms. He had me do bloodwork, gave me a
>corticosteroid shot and started me on lyrica. He said with me having
>endo, and another autoimmune disorder (hashimotos thyroiditis) that my
>risk triples for having more than one autoimmune. He said he should
>have the lab results by monday. Im worried though it will be a relief
>to finally have a answer. If it is lupus the idea of us conceiving
>would put my health in risk. So we may have to rethink some things. Ill
>keep you posted. I just want this widespread pain to leave as well as
>the tingling/numbness in my feet and fingers.






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