Possible Skin GVHD?
I have been suffering with itchy skin for about 2 months now. It started underneath my armpits and my doctor said it was ezcema. I never felt like my skin was dry though. Just slightly pink and itchy.
Now it is all over my stomach in patches, again the skin isn’t dry it just looks like patches of slightly raised pink blotches.
Please could anybody share how skin gvhd looked like for them in the early stages / how they manage flare ups?
I have been really lucky having absolutely no issues since transplant and I’m just starting to come off my Tacrolimus (had bad side effects from ciclosplorin)
I really really really don’t fancy having to take steroids again and really want to catch it early if possible
I will speak to my nurse on Monday but I think I will just be really paranoid until then!
Any help would be amazing and I hope everyone is okay