Sun-26-05-2024, 13:42 PM
(Sat-25-05-2024, 19:27 PM)Trampledrosie Wrote:(Fri-24-05-2024, 18:08 PM)D Foster Wrote: Welcome Trampledrosie. , I have been rather up to my neck in it recently so I haven't been on a lot.Thanks Dave! It really is incredible what Fred has done and what a warm welcome I have received from you all Wish I could find some folks with palmoplantar pustular psoriasis as there isn’t a ton of info out there in the world. Makes sense since it only represents about 1% of all people with psoriasis. Looking forward to diving in to all this info and talking to all of you lovely people!
This is the best site that you will come across on the subject with lots of information on P and PsA in fact I don't think that you will be able to find anywhere with more information than this. The people on here are first class and , like me, you will get to call them real friends , Fred has collected together in one place some of the most genuine people I have come across. Looking forward to hearing from you ,take care Dave.
I have used methotrexate for quite a number of years both oral and injection , it was ok up to a point.
I have been on Stelara for well over 10 years now for both the P and PsA , a lot of people , like Fred, it stopped working after a few years but it's still going strong for me.