We can imagine that you would like to hear the experience of other patients and how they felt when they were diagnosed with ME/CFS or other PAIS such as post-COVID. Or from caregivers and what it means for them to care for frineds or family members with ME/CFS (or post-COVID).
But also stories from patients and healthy controls who participated in the NMCB study and how that felt for them.
That is why we have collected some stories and will try to add new stories every now and then. They can be found under the following buttons: