ME/CFS is often misunderstood and misrepresented. It’s time for you to speak out, share your truth – and support other people with ME/CFS.
This is a safe space and anything you say will be 100% anonymous. So, take a deep breath and share your story.
Years of managing your fatigue? Or still on a journey to diagnosis? Everyone’s welcome here.
Please help others – and yourself – by sharing your story.
Need some inspiration? Tell us how you’re doing, how you manage your ME/CFS, any advice you have, or just get something off your chest. Telling your ME/CFS story should be as much for you as other people. So feel free to write anything at all.