Hiking for those who can't- Sue Hikes the AT 2024

In 2022, Cory became one of the millions of people disabled by ME/CFS- a condition with no cure and very little research funding.

ME (myalgic encephalomyelitis) is a neuroimmune condition which impacts every system of the body. 75% of ME patients are unable to work, 25% are entirely bed bound. With no treatment options and few symptom management options, only 5% of people recover or experience complete symptom remission.

Sue's 2023 Appalachian Trail adventure (and her months of training hikes) are dedicated to Cory and the millions of ME/CFS patients around the world.

The Solve ME/CFS Initiative (Solve M.E.) is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for ME/CFS, Long Covid and other post-infection diseases. Their work with the scientific, medical, and pharmaceutical communities, advocacy with government agencies, and alliances with patient groups around the world is laying the foundation for breakthroughs that can improve the lives of millions.

Thank you for helping us support Solve ME's mission to make ME/CFS, Long Covid and other post-infection diseases widely understood, diagnosable, and treatable.