is it okay to workout? would it make the disease better or worse?
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Hello everyoneI have just been diagnosed with MCTD. It's disconcerting that I have had the symptoms for over 7 years with no treatment. My question is does anyone else experience heat sensitivity on top of cold sensitivity. I struggle with both.
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I previously wrote: I’m going to start Plaquenil and was wondering whether injections or pills work better. UGH...my brain is NOT what it used to be! I meant to say “I’m going to start Metheltrexate and was wondering if injections are better than pills.” Thanks!
has anyone worked with a functional medicine Dr? I am followed by a rheum but am thinking of augmenting with a functional medicine doc if worthwhile. It is very expensive so would love to hear anyone's opinion/experience on this matter. Thanks!