Hello everyone,
I see a lot of introductions here, but I put mine in the section for introducing yourself and since I went off on a tangent about my medication history... I won't do that to you here.
I just wanted to thank everyone for sharing, it's great to see that others have the same thoughts or reactions to medication.
I did see where a couple people asked about test for psoriatic arthritis and someone was even confused about the blood test that were done - it is my understanding that the blood test, in addition to the regular things, also measures your "sed" level and then they look at you and your families for psoriasis. Also since it doesn't happen in a parallel way, ie: both thumbs like rheumatoid but travels here and there, causes "sausage" fingers and affects your connective tissue and joints - they can get a pretty good diagnosis. Not sure that is all correct but it's how I understood it to be.
Thank you all again. Hi Ews and welcome to the forum. I know in my instance that the labs are worthless. I'm in clinical remission for RA and labs are all negative. RA is soooo much better but PsA is flaring and my labs are normal. It takes multiple visits over a period of time for a RD to diagnose PsA, especially if there is no skin involvement.
"We have found that there are certain genetic markers present on the membranes of white blood cells, also serve as indicators of progression, and these may be more important than the clinical features, which may change with time. These markers are known as HLA antigens. Many people may recognize this term in conjunction with organ transplantation. Although HLA antigens were initially identified in the context of transplantation, it soon became clear that they were important in the immune response, the ability of our bodies to fight off infections. Certain of these markers are more likely to occur among patients with Psoriasis and Psoriatic Arthritis than in the general population, and thus are thought to play a role in the development of the disease".