Physically disabling, and emotionally distressing, ME/CFS turns formerly vital, productive people into prisoners of their own bodies and homes. Yet, our government spends more money on hayfever, so patients live without treatments or hope.
We need your help to support crucial private funding for the Solve ME/CFS Initiative. They have fought for patient rights and provided seed grants to researchers for 27 years.
Now is the time to help them do more. Please lend your support. Your donation will go directly to the Solve ME/CFS Initiative, and is tax deductible.