Hello from Colorado
Hello everyone. Just looking for some support and guidance as I'm freaking out a little. I don't know anyone that has lupus. I actually have not yet been diagnosed, my first rhumatologist appt is on Friday and I feel like it will never come. I am so nervous and afraid to be diagnosed. I was pretty convinced I had RA. A few months ago I started having severe joint pain, muscle pain, fatigue, rashes,numbness and tingling, frequent urination. So I finally went to the family dr. She said either lupus or RA and decided to do blood tests. Didn't even look me over or do a UA. I got a call the next week from the nurse said all my results were negative and I have depression. I was very angry because I have had depression before and did not feel at all depressed. The next day nurse called to say more results came in and my I'm not sure what its called inflammation in my body came back a little high, on the day of the blood draw I wasn't having severe pain just a little. She said she didn't know why because I was neg for lupus and RA and that I could come back in for more tests. I told her I wanted a referal. At this point my pain was getting severe so I called the specialist and they scheduled me 2 weeks out. Now my pain is mild except the stiffness. But last night I started doing research on RA and Lupus and realized the problem with my face for the last 2 months has not been dryness or allergies but a butterfly rash. And for the last two months I have been getting mouth ulcers. So I'm fairly sure its not RA but now I'm freaked out. Are there other causes of these symtoms, friday is so far away. Now I'm worried about kidney biopsys and ect. I should have never looked it up, one site said 80% of people live 10 years. Sorry I'm ranting, just scared.