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

The HMSA is 25!
June 16, 2017
HMSA 25th Anniversary Family fun day picnic!
June 7, 2017
Exciting News! HMSA and EDS UK Residential Conference
May 12, 2017
Growing up a Bendy #MarfanMonday
May 8, 2017
vEDS Awareness

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.