Are there any resources for spouses/partners/families of people with EDS to help them better understand what EDS is and how it affects a person’s abilities and mental and physical health. Really struggling with a partner who truly believes I do not want to get better and that I use EDS and POTS and MCAS and seizure disorder to get out of having to do things around the house or do things with friends and family. It’s heartbreaking.

Posted by Deleted (8a7365ce) at 2022-10-04 14:56:34 UTC