Introduction by Trampledrosie

[Trampledrosie]

Since Fred pointed you to the thread on Acitretin I should add that shortly after I was first diagnosed I was prescribed Acitretin.  It was scary reading how I couldn't give blood for something like 3 years and that it could harm a fetus so not to take if planning to get pregnant.  I wasn't planning on that but I thought how bad is this to take if it could harm a fetus and stay in my system so long that they don't want my blood???    But the light therapy and topical wasn't working and the doctor at that time told me oral meds were the next step.  Basically it went, topical, light therapy, oral then biologics I think.  So I took it.  And I have to say it helped A LOT!  But I was a bit concerned on taking it.  When I was "better" I stopped.

But I do have to say that it helped me. 

Sadly I've had some flares since then and I didn't want to go back to Acitretin due to just not understanding what it may do over time.

Thanks Kat for sharing that. When I had cancer they couldn’t get blood or do IVs for my treatments because of my genetic tiny veins so I have a port in my chest. I kept it in so I can continue IV lidocaine for my neuropathy caused by chemo. The only nurses allowed to draw blood through my port are those at the cancer clinic. Now that I have finished treatment they can’t do bloodwork for me anymore. I only have one arm to use for blood, I’ve, etc because of lymphedema in one arm. The blood tests are going to be a big roadblock for some treatments so we’ll see what the derm recommends.