Starting Skilarence.

[MrGnomusy]

I've been lurking around on this forum for about 2 years and thought it'd now be a good time to come out of the closet. I thought about starting posting last Oktober when I went over from yearly UV-B light therapy to Metotrexat (due to the fact that I've hit the lifetime limit of UV exposure apparently) but I held off. I've had severe Gutate Psoriasis since 2002 when I was 19 until now (34). Light therapy was a life saver for me until the spring of 2016 when it was determined that I had to give it up. Got really depressed that summer and with a big flare up to boot. Got on Methotrexate in September and it worked (decently) until my liver values shot up over 3.2. What values they measure exactly I don't really know. But I had to give it up. Just as well cuz ever since I started I've been feeling weaker week by week. (20mg a week) with a 5mg folic acid tablet the day after. This spring I also started taking the biosimilar Benepali, but I feel it's done nothing for me.  
I've been checking in on this forum often and have been keeping tabs on what you guys have been talking about, and from what I've gathered (fumaric acid esters) seems to be really good for a lot of you. I really wanted to start with Fumaderm (I've heard good things about it), but my dermatologist said that since Skilarence is on the Swedish market and it's the same activ substance ie. The same thing It's not possible to get it imported anymore.
I've only seen discussions about Skilarence on here, and no accounts to my knowledge of any one here being on it, so I thought I'd share my upcoming experience with it with all of you. So if everything goes according to plan I'll start taking it next week. Cheers!