Hi all. I've just been diagnosed with PSA, and found it to be a huge relief- I have been in pain for a long time, but never found an answer. Finally I have.
Anyway, I've been out on sulfasalazine and understand the need for regular bloods. I've been given this record book, but how does it work? Do they keep the record book until they have the results and then write in it?
I have shared care when it comes to my PsA , my rheumy sorts my humira but my docs surgery do my bloods.. When I ring to order my script at the hospital they check my blood results first and if they're not right it goes straight to my rheumy for him to make a decision !