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Re: Wigs

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Ruth, I know it would feel better in Florida, but my head would looks like a tan bowling ball...Good grief charley brown//Connieolehomepla wrote: Hi Connie....I think wigs would be tooo hot for me!! Especially in the midwest in the summer. Come to think of it bald might not be bad at least for the summer ;)Ruth Has anyone experience hair loss

with Remicade? I am thinking it is from the increased Methotrexate (up to .09CC from .05cc) over the last 3 weeks since Methotrexate is a chemo med. So now must I choose between feeling better and being bald? > Oh well...I can get ready to leave the house faster..and no need to worry about answering the door with morning hair > TTFN> Ruth > > > ~~~~ *** ~~~ *** ~~~ *** ~~~~> The Neurosarcoidosis Community> > NS CHAT:- Has been cancelled for now.> > Message Archives:-> http://groups.yahoo.com/group/Neurosarcoidosis/messages> > Members Database:-> Listings of locations, phone numbers, and instant messengers.> http://groups.yahoo.com/group/Neurosarcoidosis/database > >

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