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Does anyone else have MCTD with systemic sceladerma? Anyone else?
Autoimmune Diseases | Last Active: Oct 19, 2025 | Replies (13)Comment receiving replies
@grandmal65 Hi and thanks for reply how do you know you’re systemic sceladerma is in overdrive? And may I ask what are your CK levels. And is the stomach the only troublesome area? Thanks again I’ll be wiring n reply
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@sonnyforee10 I'm unfamiliar with MCTD. My lupus does flare up off and on. My systemic scleraderma is bad. I have very cold hands and feet. I have to wear socks all day and night. Gloves I do occasionally just because I am busy during the day. Lots of doctor appointments. Currently doing physical therapy for my spine. The whole spine. Getting ready for a 2nd neck surgery. Nerves are moderately being pinched in C6 and C7. Had previous surgery last year at C4-C5. Wish me luck!