I have just got a new script for Sulphasalazine and hoping it helps.
Unfortunately the Remicade infusions alone are not working optimally. So we are trying adding Sulpha with the Remicade.
On Remicade I am having breakthrough Crohns flares and it’s not controlling my RA either.
Hoping it doesn’t give too many side effects.
I’m bracing myself and hoping for the best.
Anyone take Sulpha? What is your experience?
How long before seeing results from Entyvio?
Lactoferrin and ferritin (with a bit of calprotectin thrown in for good measure...)
Is this a sign I'm getting better
