I read the tragic news of Beth Mazur's passing this morning. We didn't know each other per se--we'd followed each other on Twitter for years--but her death hits hard. As co-founder of M.E. Action, she did so much to help persons with Myalgic Encephalomyelitis, it's unspeakably awful that it killed her.

If you have the strength, contact your Congressional representatives and explain to them why M.E. needs vastly more federal research dollars.

More on Beth Mazur's passing here:

Sad News From Our Community — Content Warning

Good night, all. Hope you're doing as well as possible.

Day 8 of 365

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #pwme #cfsisamisnomer #ChronicIllness #bethmazur