I was diagnosed with LAM (Lymphangioleiomyomatosis) about 3 years ago. I was told at that time that I would never again live without being on an oxygen tank. By American medicine standards, I was given no hope of my condition improving and was told that this disease will shorten my life considerably.

Finally, for the first time in 3 years, I was given hope. There is a treatment in Mexico that has great promise in not only improving my condition but likely giving me back a life not tied to an oxygen tank. The biggest issue is being in Mexico, I can't use any kind of insurance to pay for the treatment. I am simply asking for help to cover the costs to give me the chance to live.