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
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.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!
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.