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scleroderma

Jan Ellis

Message 2 of 4 Previous Next



I just found out I have limited scleroderma. I have had Raynauds for approximately 10 years and finally went to the doctor. So far, the only thing affected are my hands and feet. Thanks for the tip on the hand warmers. At this point, I guess Raynauds is the least of my worries. I don't know what to expect from Limited Scleroderma.

 
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