Do any of you get Botox injections and have you noticed any effects on your MCTD?
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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!
Hi all. Glad to have found this forum, alternating between trying to pretend I don't have MCTD and bawling my eyes out about it. I am newly diagnosed, waiting on an appointment with a rheumatologist. I'm 42 years old, no previous health problems whatsoever. Healthy. No medicaions, active, work full time as a nurse and always on the go. I went on vacation and did a pretty vigorous bike ride. Next...
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Hi Guys,Hope you're coping as well as possible! I was wondering if anyone else has had pins&needles/tingling in their hands and feet? I've had it really bad for 6 months now, i got checked yesterday for "peripheral neuropathy" but it all came through clear, so i'm no closer to an answer. I also get very cold hands and feet. Any treatment advice?