Fumaderm side effects - my worst case senario

[OneBigItch]

Hi everyone, long time no speak. I thought I'd give you all an update on where I am with everything. 

Following on from my last posts - after being told I had trace amounts of blood in my urine and having 're tests and an ultrasound, they didn't find a cause so left me. Thankfully my psoriasis was completely clear so the decision was made to stay off fumaderm and see what happens. 

Well I managed to stay clear for almost a full year, but now I've got patches on my legs again and it's starting to appear on my arms and head. I've seen the doc and they are happy for me to start Skilarence when I feel l need to.

I'm not sure if I'm ready to go on to it just yet, however I'm going to Florida next May so feel pressure to have decent legs a least, plus I don't know what I'll be like on it. 

As you may remember my experience with Fumaderm was amazing! It was a wonder drug and I managed 100% clearance on just 4 initial tablets a day! I am clearly very sensitive to DMF, hopefully Skilarence will be just the same.

I'll keep you updated when I finally start treatment. 

Apologies for the long post.