We are raising funds for Lyme disease sufferers who can't afford better testing and treatment. Donations will go to the Lymetap, a financing program, and other programs which support Lyme sufferers in need
My Personal experience with Lyme Disease
I have personal experience with late-stage chronic Lyme disease and understand how difficult it can make normal day to day tasks. For years I suffered, searching for the best tests, treatments, doctors, and diets that would help me. I tried everything, spent thousands of dollars, and even tried a few dangerous experimental treatments, some of which only worsened my symptoms. It's been an exhausting journey, but eventually through trial and error I've acquired invaluable knowledge and made friends with the best doctors who would help me attain a better quality of life.
Why I Started this Charity
The quality of life for chronic, post-treatment and late-stage Lyme disease patients is among the lowest in contrast to most other infectious diseases, something I can attest to with my history with the disease. I started this foundation to help those who have suffered as I have from the nerve pain, heart problems, anxiety attacks, memory loss, depression, and a myriad of other symptoms accompanied by the illness. The foundation throws events to collect donations to help people get tested, afford treatments, and provide a source of education here at our website for those who need it. In addition, we work with the best doctors to help us review our content and even help provide free advice to those who reach out.
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