ME/CFS doesn’t stop at one person. While the person living with it carries the heaviest burden, like the debilitating symptoms, the losses, the daily fight, this disease reaches into every corner of a family’s life. Our new three-part video series, ME/CFS and the Family, brings those voices forward: the parents and siblings navigating their own reality alongside someone they love.

You’ll hear honest accounts of what life actually looks like when a devastating illness goes without adequate research, without FDA-approved treatments, without trained clinicians, and without public understanding. That absence of support prolongs suffering in ways that are entirely preventable, and it’s exactly what #NotJustFatigue exists to change.​​​​​​​​​​​​​​​​

All three videos in the series are linked below in order: