Welcome to our fundraising team page.
Hello my name is Tina. In 2010 I was diagnosed with Systemic Lupus. For anyone that doesn't know this is an autoimmune illness meaning instead of my body fighting the bad to keep me healthy it fights against it's self and the good. Anyone with lupus goes through so many daily trials. Many of us go through life with a smile on our face trying to hide the hurt we feel from our illness. Lupus can and does affect everone who has it differently no flare is ever the same. Meaning each time it rares it's ugly head it's always something different. I have headaches that have caused me to lose the hearing and vision in one side of my head, i've had multiple mini strokes, the joint and muscle pain, the red skin blotches and that's just to name a few. This illness can go as far as to also attack your organs and even further as to kill those who aren't so lucky. I am asking all my friends and family to please help raise awareness and contribute so that they can continue research not only for the ones that lost the lupus battle but so that us that fight everyday can hopefully be so to overcome it. Thank all of you for taking the time to read this and for your donations. Anyone who wants to join my team please feel free I would love to have you on my side.
Imagine a day when doctors can say, "There is a cure for lupus". Until that day though, there is work to be done. That's why we are taking action in the fight against lupus. Join us as we participate in the Lupus Foundation of America's Walk to End Lupus Now® to raise critical funds for the estimated 1.5 million people living with lupus in the United States.
Will you join our team and help us reach our fundraising goal? You’ll be supporting the Foundation's efforts to improve the quality of life for all people affected by lupus. You can also support by making a secure contribution on our walk page. Every single dollar counts!
Did you know?
Together, we can solve the cruel mystery of lupus. Join our team today and support our efforts!