Update on Hypermobile type of Ehlers-Danlos Syndromes (EDS).

[@maryr7593]

The EDS/HSD Society (in US) has a world wide registry of everyone diagnosed (and not yet diagnosed). They encourage everyone to signup in the registry as this helps with writing grants for funding, AI statistical searches as well as gives researchers a group of people who match their criteria for their research.

[@Truerealism747]

No mention of autism the course