Hypermobility Syndromes Association

Featured Articles:

Our New Helpline number is 03330 116 388

Want to write and submit an article for the HMSA Journal? Click on this link.

Donate Join

Latest News

Formal Statement from both the HMSA and EDS UK
August 19, 2016
Fundraising Team roles.
August 10, 2016
UPDATE: Bristol Symposium postponement.
July 27, 2016
High Profile Therapists Speak at Major International Conference
July 10, 2016
Bristol symposium!
June 30, 2016

Welcome to the HMSA website

The Information Standard

The HMSA is Information Standard certified. This demonstrates our commitment to providing trustworthy advice. Read our disclaimer and more about our work towards the Standard HERE.

Our Volunteer Programme

The HMSA gives a huge thank you to the Big Lottery Fund for supporting our Volunteer Programme. The Grant means we can continue to provide training for our volunteer staff and strengthen our network throughout the UK.

Our Family Programme

The HMSA is grateful to Jeans for Genes in sponsoring our Family Programme. Jeans for Genes raises money for Genetic Disorders UK and aims to change the world for children with genetic disorders. Click here: www.jeansforgenesday.org

The HMSA provides information on the Heritable Disorders of Connective Tissue (the ‘Hypermobility Syndromes’) through its website, publications, forums, local groups, advice line, and education programmes.

Disclaimer: The information provided by the HMSA should not take the place of advice and guidance from your own health-care providers. Material in this site is provided for educational and informational purposes only. Be sure to check with your doctor before making any changes in your treatment plan. Articles were last reviewed by our Medical Advisors as being correct and up to date on 5th June 2004.

Please be aware that information posted on the discussion boards is the opinion of the authors and has not necessarily been approved or endorsed by the medical advisors.