Latest News

Tackling Misinformation about Ehlers-Danlos Syndrome, Hypermobility Spectrum Disorders and Postural Tachycardia Syndrome – A shared statement from The Ehlers-Danlos Support UK, PoTS UK and The Hypermobility Syndromes Association (HMSA)

Launch of new hypermobility Quick Reference Guide

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Local Group news

Q&A with Jo Southall, live this evening.

An introduction for new members (or a refresher for forgetful ones) to the weekly #MellowMonday Relaxation sessions.

"The HMSA was the first charity I came across that provided vital information" -said Zoe Walker, most recent addition to the Board.

Announcement from Local Groups Coordinator

Our favourite day of the year

Working with a new Trustee Board and a new CEO

Would you like to take a refreshing and challenging role in forming the future of a vital health charity in a rapidly evolving third sector environment?

The School Toolkit for EDS & JHS has launched this morning, aimed at improving awareness and understanding among teachers in mainstream primary and secondary schools

It is with great sadness that we hear of the passing of Professor Howard Bird, who has done so much for the hypermobile community.

The HMSA has been awarded 3 grants to support our online work.

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"New study confirms systemic nature of hypermobility syndromes, that late diagnosis is common and associated with negative health outcomes."

Joint HMSA and EDS UK Response to the BSPAR Guidance for Management of Symptomatic Hypermobility in Children and Young People

Living Well With Series, 2023