Move in any way they can to raise awareness and funds for the ME Association.

Every step, stretch, pedal, roll of wheels, or meet-up represents movement that people with ME/CFS are often denied. I’m going to move see how far I can move this month. I currently have ME/CFS and it has robbed me of a completely normal life and often have setbacks which dramatically affect my life

Wear blue too to raise awareness.

Why this matters

ME/CFS isn’t “just tiredness.” It’s a complex neurological illness where even small exertion can cause severe and long-lasting crashes. Rest doesn’t restore energy - it’s survival.

When you #moveforme, you:

Raise awareness of an invisible illness

Help fund research, advocacy, and patient support

Remind people with ME/CFS that they are seen and not forgotten

people move for me helps me feel less invisible. It reminds me (and others living with ME/CFS) that our lives, no matter how small, still matter, even when our bodies won’t cooperate.

Thank you for Moving For ME.

Please join Catherine and Move for ME this May!

I have ME myself and want to help people like me who have this disease