Its so frustrating waiting for answers and having sooooo many tests. I start to question how much they really know about RA and other issues that are similar in nature. I'm fearful, scared, tired and just want some answers. I am so glad to have this group and everyone to share my concerns. I'm trying to remain positive, but at times I feel defeated. I will keep pushing. Brian, I hope you are doing well. You are a very inspiring individual and I hope I can get to that place one day. Be well and stay well and continue to be a positive energy in this group.

My low white blood count is due to having Evans Syndrome

Hi Patti,

I'm sorry you're having to deal with all these tests trying to figure out where you stand. Some medications will lower your white blood cells. Are you on any medications for RA? I was first diagnosed with lupus, but that was wrong. I went for another opinion because of the amount of joint pain I had. It's good to get second, third and more opinions if necessary. Just something you may want to consider. I have found teaching medical centers to be my best option. Hope you feel better soon.

Thank you so much. The prayers are greatly appreciated. Have a wonderful day.

I Have both and Lupus seems to be more relevant. lupus seems to be getting worse I am also on HCQ and Azathioprine I have a cream for the rashes vaginal cream for UTI’S and every other month I swear I have an UTI and test is negative
My eyes well I need glasses for the glare so I dont get migraines and my fingers well seem to be getting deformed from RA I am not complaining just stating what is going on with my body and some days are great and I have to stay positive or I would be depressed and I dont want that for me
I will be praying for you as I do for all in this group