IMAGINE… living with constant crawling, itching and biting sensations. Having skin lesions, some small and superficial, others deep non-healing wounds, which break out all over your body and extrude strange, unidentifiable fibers. Experiencing such cognitive and neurological decline that you are no longer able to work. Watching your children suffer from a disease that is not recognizedand has no known cure. Going to your doctor for help and being told that your symptoms are purely psychosomatic. Feeling so physically ill, and feeling so completely alone and abandoned by medicine… This is the reality for thousands of Morgellons disease sufferers.

I am fundraising to:

- raise awareness of Morgellons Disease

- lobby for its official recognition as a rare disease

- provide a global support group for Morgellons sufferers & their families