Today I went to the neuro thinking we were just gonna over the RA and Lyme again and see what other options there were. But today they sat me down and said I have lupus. This was a bittersweet diagnosis. I now know why I can barely move some days but the severity of the condition is devastating I thought this pain was going to just be something very treatable but I now find that I will learn to live with it that life will be different now and some of the pain may subside if i do not have an active
Click HERE to see how I have UNdiagnosed my Lupus!! No Lupus and Immortality? Awesome!
Ever since I was diagnosed with Lupus 2 years ago, I have had people who are newly diagnosed (or suspecting that their symptoms are Lupus without confirmation yet) ask me how to deal with having the disease. Instead of rewriting it all here, I am directing you to today's post on my blog titled, "So You Have Lupus. What Are You Going To Do About It?" Click HERE if you are interested in reading it. Warning...I tend to be blunt when I communicate. =)
I'm Ali and I'm new to We Have Lupus. I wanted to say hello to everyone. I've been dealing with the lupus pretty much on my own, and I would like to become more involved with others who know what it's like to deal with this ... have a few laughs ... lend support ... seek support ...
Warmest wishes to you all!
Can Lupus be a blessing? I think sometimes it can. Click HERE to see how.