Podiatrist, Julie, was able diagnose her whole family after coming to one of our talks. Read more
We support hypermobile people and the professionals who work with them. There’s room for every bendy body under our umbrella
Our Facebook groups for members, application instructions, how to become a member and find your local group.
#SelfCareSunday #CraftHour - A regular online slot on social media, open to everyone, where we chat about both self-care and crafts. Read more
*Postponed due to the pandemic. New Dates will be advertised when known* A masterclass that covers hypermobility and the relationship with fibromyalgia and medically unexplained symptoms, with a focus on condition management. Read more
A weekly live online relaxation session for HMSA members, led by Hypno/Psychotherapist Kim Clayden Read more
Our regular Friday night kids and teens post, and the pink CV19 elephant in the room... Read more
More #2020Hindsight! ‘Advice for life’ with hEDS to my younger self' now I’m nearly 50. (in the style of Baz Luhrmann ‘Sunscreen’) Read more
Zoe's story, she's one of our most truly rare EDS members, at the time of writing EDS Arthrochalasia cases numbered around 40, globally. Read more