Thanks for being interested in discerning my statement. Maybe there was an assumption of the reason I was on Sulfasalazine. But I do not have Ulcerative Colitis; I had undiagnosed autoimmune Celiac Sprue until 2016. Only in recent years have I begun having increased widespread pain, fatigue, bilateral and polyarticular arthritis that was unremitting since 2023. (It is not uncommon for those who are diagnosed with one autoimmune disease to have others.) Joint pain, and paresthesia is common from having a late diagnosis of Celiac Disease.

Luckily, I am being treated so far with Sulfasalazine that has reduced much the inflammation and swelling in my hands, feet and knees, although not completely removing all the pain. There is a likely chance I have SERONEGATIVE RA. The rheumatologist has explained to me that my being on the Disease Modifying Anti Rheumatic Drug (DMARD) Sulfasalazine will likely mask those blood lab markers, and they will not show in blood lab while I am on the med.

Treating the inflammation and progression of the disease and inflammation more important, than letting it damage my joints and tendons. Persons 75 years ago did not get that same treatment. Bloodwork and physical exams continue every 3-6 months. I am at risk for other conditions from Celiac disease despite being gluten-free, such as anemia from low vitamin B and Iron. I am fortunate as well to have started weekly 50,000 IU Vit D Rx when diagnosed with Celiac Disease because it caused me to have low vit d levels, and supplementation weekly give me normal levels.

Good luck on your journey too, I hope for better treatment and results for you!