Just realised today is ten-year anniversary of me and my son getting our hEDS diagnosis. My daughter got an unofficial “she clearly has it” but she was only four and he didn’t see kids that young. Though he did write a letter to the school anyway calling her his “patient” so I’ll include her too! Just wanted to say I’ve gotten more (EDS specific) help and support in my first week here than I got anywhere else in last ten years!!! Thank you @Jeannie Di Bon for creating this app. Worth every penny. Need to remember to leave review in AppStore so more people can find their way here.
Posted by Deleted (5e0240cb) at 2023-07-17 08:29:58 UTC