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CIDP related to Covid?

Autoimmune Diseases | Last Active: Jun 9 1:57pm | Replies (14)
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@arlenelmh

I was diagnosed with limited systemic scleroderma following Covid where I had similar symptoms (Covid toes and finger issues), not CIDP. My husband got transverse myelitis from Covid and needed multiple courses of plasmapheresis to halt it from reaching his diaphragm. His feet are still numb 2 years later. I wonder if he should be tested for that.

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Replies to "I was diagnosed with limited systemic scleroderma following Covid where I had similar symptoms (Covid toes..."
bearmom | @bearmom | Jun 7 8:26pm

Transverse myelitis is also part of my diagnosis since I have a signal change in my thoracic cord, bladder symptoms, weakness and at one point was paralyzed from the neck down, on a ventilator (because it was affecting my diaphragm) and a feeding tube. My feet are still very numb as well 3 years later. Has his doctor ever mentioned IVIG?

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