I am joining thousands of people across the country for the Walk to End Lupus Now®. I hope that you will join me either by lacing up your sneakers or by donating to my fundraising page. I was diagnosed with Discord Lupus in May of 2019 I didn’t  want to reveal my diagnosis at that time it has taken me a while to accept the fact that I have  Lupus ,when I first found out I was really sick and I could see my sickness didn’t know what was wrong I loss 30 pounds in one month my diagnosis was found in my scalp I also loss all my hair I am now able to talk about it I take my medication and I try to keep my diet at a minimum and so far I am doing great with the love and support of family and friends thank you guys for always being there for me.

You can make a difference by donating to help me reach my personal fundraising goal and support the Foundation's efforts to improve the quality of life for all people affected by lupus! A generous contribution of $25 or $55 can make a definite impact. What’s more, if your employer offers a Matching Gift Program to employees, you may be able to double your contribution with just a little bit of paperwork. Trust me, it’s worth the effort! Every single dollar counts.

Did you know?

Lupus is a mysterious and misunderstood autoimmune disease. It strikes without warning, affects each person differently, and has no known causes or cure.

Lupus symptoms can be severe and highly unpredictable and can damage any organ or tissue, from the skin or joints to the heart or kidneys.

While lupus can strike anyone at any time, 90% of people living with lupus are women. Women of color are at especially high risk.

Lupus is hard to diagnose, but the Lupus Foundation of America is working to make life easier and more comfortable for the estimated 1.5 million people living with lupus in the United States.  Together, we can solve the cruel mystery of lupus. Thank you for your generosity!