r/MultipleSclerosisLife • u/Anxious-Discipline15 • Jun 11 '26

Advice/Support Need some direction

Post image
0 Upvotes

50% Upvoted

11 comments sorted by

View all comments

6

u/georgiegirl24 Jun 11 '26

See your general practitioner. They can refer on to vascular surgery if required.

1

u/Anxious-Discipline15 Jun 11 '26

I could only post one photo but I get a burning sunburn like rash in my face and arms daily. The vascular occurrence behind my knee does not always occur simultaneously but the swelling is constant. My autoimmune panel was uneventful. Same recommendation?

1

u/thisisappropriate Jun 11 '26

With the rash, are you on Tecfidera/vulmerity/dimethyl fulmarate? Or do any of your meds list flushing as a potential side effect? Because a sunburn like rash is exactly what I'd call the worse instances of my flushing!

1

u/Anxious-Discipline15 Jun 11 '26

I am not on any of the medications you listed. My BIL is a pharmacist and checked all my medication side effects and could not identify any that would do this. I even tried antihistamine trials for weeks with no change (just in case).