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| Beverly from California |
I was terrified. The only other person I'd ever heard of having lupus was my cousin, who died from complications of this disease less than a year after her symptoms showed up.
However, I'm thrilled to say, 5 years later, I'm doing very well. I was blessed with an amazing rheumatologist and support system. I believe lupus can be a very isolating disease. It's hard to explain to someone who does not have it, what it's like on those really bad days. My countertop looks like a small pharmacy. The list of drugs I have to take just to feel *okay* is overwhelming.
I have participated in WALK FOR LUPUS NOW® for four years. One of the amazing things about the walk is that it reminds you that you are not alone. There is a whole community of people who understand how you feel and what you’re going through.
We need more resources. We need more research. We NEED a CURE.
So I walk. I walk for research. I walk for support. I walk for my daughters. I walk in my memory of my cousin. I walk for the hope of some day finding a cure, so that I may once again, be LUPUS FREE.
Please join me and sign up today for a WALK FOR LUPUS NOW® event in your community. Together, we CAN FIGHT this terrible and life-altering disease.

Our 2011 Fall Walks have begun! Join the Lupus Foundation of America (LFA) Walk for Lupus Now® and help bring us one step closer to finding a cure. Walk to make a difference in the lives of people affected by lupus and raise urgently needed funds for research, education, and support services. Walks held during August and September are listed below.
(Washington, DC) – Join the Lupus Foundation of America (LFA) and the 2011 










