Skip over main navigation
  • Sign up
  • Log in
  • Basket: (0 items)
Hypermobility Syndromes Association (HMSA)
  • Search
  • Facebook
  • Twitter
  • YouTube
Shop Donate
Menu
  • Who we are
    • About the HMSA
    • Our Board of Trustees
  • What we do
    • Support and Advice
    • Information (and the Information Standard)
    • Education
    • Research
    • Awareness
  • Hypermobility
    • What are hypermobility syndromes?
    • Types of HMS
      • Hypermobility Spectrum Disorder
      • Ehlers Danlos Syndromes
      • Marfan Syndrome
      • Osteogenesis Imperfecta
      • Stickler syndrome
      • Pseudoxanthoma Elasticum
    • Living with an HMS
    • Hypermobility FAQs
    • Kids Zone
    • Videos
  • Professionals
    • The Kent Model
    • Hypermobility Disorders – An Update for Clinicians
    • Professional Membership
  • Membership
    • Standard Membership
    • Family Membership
    • Professional Membership
    • Our Local Groups
    • Log in
  • Get help
    • Helpline
    • Other sources of help
  • Get involved
    • Donate
    • Businesses which support the HMSA
    • Our Fundraisers
    • Fundraise
      • Ways to fundraise
      • Set up a fundraising page
      • Fundraising events
      • Create a fundraising event
    • Volunteer
      • Volunteer Vacancies
      • Apply to volunteer
    • Submit a blog post
  • Latest
    • News
    • Blogs
    • Events
  • Admin
    • Log in
  • Basket: (0 items)
  • What we do

What we do

The HMSA is the only charity offering both practical support and Information Standards accredited health and care information to people who have a hypermobility syndrome, or who are involved in the care of someone with any of the hypermobility syndromes; including Hypermobility Spectrum Disorders (such as Joint Hypermobility syndrome), Ehlers-Danlos syndrome (all sub-types), Marfan syndrome, Sticklers and Osteogenesis Imperfecta.

The Information Standard is a certification programme for organisations producing evidence-based health and care information for the public. Any organisation achieving the Information Standard has undergone rigorous assessment to check that the information they produce is clear, accurate, balanced, evidence-based, relevant and up-to-date.

This certification gives medical professionals confidence in the reliability of information from our website and publications, helping people with a hypermobility syndrome get the treatment they need.

Run by people affected by a hypermobility syndrome, for people with a hypermobility syndrome, a number of the HMSA’s staff and volunteers are also medical professionals in their own right, which enables the charity to offer advice and support to relevant professionals (including social workers, GPs, consultants, physiotherapists, Occupational therapists, psychologists and teachers). The Hypermobility Syndromes Association (HMSA) is therefore one of the few charities, offering support both to people with a medical condition and the professionals treating and supporting them.

Support and advice for people affected by hypermobility

The HMSA is a dynamic charity providing a network of support groups throughout the UK. All our Group Leaders are trained and have clear DBSs (previously called a Criminal Records Bureau check). The HMSA is proud that our groups are recommended by many hospitals and individual professionals because of our positive ethos and the dedication and professionalism of our Group Leaders.

  • IS accredited website. ( dedicated professional members area under development)
  • Free Helpline for support and advice, 5 days a week with additional answerphone service
  • Local support groups, run by trained volunteers*
  • Locally run Facebook groups* – secure places to ask questions and gain valuable peer support, moderated by trained volunteers.
  • Residential conferences and HMSA Hypermobility Masterclass events, offering a chance to socialise with others who understand life with a hypermobility syndrome and improve understanding of hypermobility syndromes and their management**
  • 1:1 advice from trained staff.*
  • Advocacy is offered on a case by case basis. (This is not a guaranteed service as it depends on staff time and also proof of diagnosis via a medical letter.)*

 Education

  • We provide education to schools, sporting establishments and medical professions including consultants, GP's, physiotherapists, occupational therapists, podiatrists, dieticians and psychologists, who wish to advance their knowledge and understanding of the hypermobility syndromes in all their forms.
  • Patient focussed residential conferences and HMSA Hypermobility Masterclass events, which can include lectures on various aspects of hypermobility and it’s management, group physiotherapy and hydrotherapy sessions.**
  • Printed information – leaflets, booklets and posters – all of which meet the stringent standards set by the IS. (some of these booklets are included with membership packs)
  • Monthly e-newsletter*
  • Bi-annual Journals - in each issue we have articles written by our Medical Advisors and other members of the association, keeping our members informed of current progress in the world of hypermobility syndromes.* †

Focussed support for children and young people

  • Tailored information for children and their parents to help families who often just don’t know where to turn.
  • Specialist family programmes, where families can learn together how best to manage the many symptoms relating to hypermobility, gain confidence and ask any questions they may have.
  • Specific ‘Kids and teens’ area of the website – with information at a level which children can easily understand, and schools can also find useful.
  • ‘Youth Journalist’ role – where each year a teenager is selected to write for the HMSA Journal and website, building their confidence and communication skills.
  • Sections of the HMSA Journal specifically aimed at children and teenagers
  • HMSA Hypermobility Masterclasses and residential conferences have separate programs for children - encouraging good management and helping them address any concerns they have about their condition **
  • Educational Support Facebook group (run by nurses, OTs, teachers, physios etc) for parents to get advice on accessing the support available to their child.*
  • 1:1 sessions with trained staff.*

Support and advice for professionals working with people affected by hypermobility

  • Work closely with hypermobility related specialist service providers to improve their service provision, including running patient focus groups.
  • Run training courses and seminars on hypermobility syndromes and their recognition and treatment for medical professionals.
  • Access to advice from qualified medical, health and social care professionals who work for, or with, the HMSA. †
  • A copy of the twice-yearly HMSA Journal in the spring and autumn. (Professionals can contribute to the Journal by submitting articles, case studies and research opportunities.) †
  • Quarterly professional-only e-newsletter. (Professionals can submit information for the HMSA to share amongst other professionals, such as study days, conferences or research studies.) †
  • Assistance with recruitment for research projects, access to non-identifying patient data, dissemination and the option of the HMSA being the ‘patient partner’. †

Raising awareness

  • Stands at various events, both local and national, across the country, and at relevant medical conferences, such as the British School of Rheumatology conference
  • Social media and website advertising campaigns
  • Posters and awareness leaflets for GP surgeries, hospitals etc.
  • News stories and press releases.

Research

Research into all aspects of hypermobility is key to gaining a better understanding of the needs of those with an hms and ensuring treatment provision. The HMSA contributes to research by providing assistance with recruitment for research projects, access to non-identifying patient data, dissemination and the option of the HMSA being the ‘patient partner’. †

 

 *denotes a members only benefits

**priority given to members

† denotes professional membership benefits

Published: 25th July, 2019

Updated: 28th July, 2019

Author: Hannah Ensor

Related topics:
  • What we do
Share this page
  • Email
  • Facebook
  • Twitter

Latest

  • Working Is Not Your Worth

    Working Is Not Your Worth

    HMSA Volunteer Sophie Harvey reminds us all that we are so much more than what we do for a living.

  • Professor Howard Bird

    Professor Howard Bird

    The HMSA sadly note the passing of our former board member, medical advisor, contributor, colleague and friend, Professor Howard Bird.

  • Rachel King (Trustee)

    Rachel King (Trustee)

  • Communicating about hidden disabilities and symptoms (Webinar) April 2021

    Communicating about hidden disabilities and symptoms (Webinar) April 2021

    A 1 hour webinar on "Communicating about hidden disabilities and symptoms" with Hannah Ensor, exploring effective ways to improve communication with, and help gain understanding from, family and loved ones (who we may all be spending a LOT more time with for the immediate future!)

Related

  • The HMSA is to become a Charitable Incorporated Organisation

  • Information (and the Information Standard)

    We provide quality health and social care information to patients, medical staff, educators and employers, we're proud of our IS accreditation.

  • Where we work

    We're a UK based charity, but membership and all our online members' groups are open to people across the world. While we can't provide Local Groups for our members in Canada, Australia, The Netherlands and the US we do offer international shipping.

Most read

  • Response to BSR statement March 4th 2020

    Response to BSR statement March 4th 2020

    We are aware of the BSR statement and have prepared a response detailing our position on the subject.

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

    This long awaited and eagerly anticipated paper has been published today on BMJ Open. Authors of this study are Joanne C Demmler, Mark D Atkinson, Emma J Reinhold, Ernest Choy, Ronan A Lyons, Sinead T Brophy.

  • What are hypermobility syndromes?

    Hypermobility syndromes is an umbrella term for a number of complex heritable disorders of the connective tissue (HDCTs) which feature among a diverse constellation of symptoms, some hypermobility in some or all of the musculoskeletal system.

  • HMSAware - Marfan syndrome, EDS is not the only 'fruit' of the hypermobility family tree

    HMSAware - Marfan syndrome, EDS is not the only 'fruit' of the hypermobility family tree

    There's more to connective tissue disorders than EDS - Marfan patients often feel aggrieved that they (and others) are left out of the hypermobility conversation which is largely dominated by Ehlers-Danlos syndrome. #HMSAware

  • Hypermobility Syndromes Association COVID19 collated resources, regularly updated.

    Hypermobility Syndromes Association COVID19 collated resources, regularly updated.

    Reliable and credible information on Coronavirus for people with hypermobility related health issues, a collation of solid advice from International, European and UK organisations dealing with associated conditions.

  • Dental health

    Dental health

    How hypermobility syndromes can affect the teeth and mouth, and how to maximise dental health.

  • HMSAware - HMSAnonQ, FAQ and the big question...

    During the 2018 HMSAware campaign we took questions from the public and formulated them into an FAQ, with an Anonymous Question on the Wednesday evening, taking a look at that perennial question of whether or not hypermobility related health problems are rare. It is reproduced below, with an update taking into account more recent UK based research.

  • HSD: Symptoms

    HSD: Symptoms

    A short overview of common symptoms of hypermobility spectrum disorder

  • Skin in EDS and HSD

    Skin in EDS and HSD

    How the skin can be affected in the Ehlers-Danlos syndromes and hypermobility spectrum disorders

  • Hormones and Hypermobility

    Hormones and Hypermobility

    How various hormones interact with hypermobility, including why symptoms may worsen around menstruation and things to consider regarding hormonal contraceptives.

Tag cloud

2017conference child EDS EDSPage hEDS HMS HSD hypermobile ehlers danlos hypermobility hypermobility spectrum disorder Kent Model kid Marfan marfan syndrome MarfanPage Membership

Sign up for our newsletter

Please enter your first name
Please enter your last name
Please enter your email address Please enter a valid email address (e.g. [email protected])


This is a general update enews - not the members-only enews which is a member benefit.

For more information on how your data is stored and used, please see our Privacy Policy.

Find us

Registered Office (Postal Address)
49 Greek Street
Soho
London
W1D 4EG

Contact us
+44 (0)33 3011 6388 (Helpline)
[email protected]

Links

  • Sitemap
  • Accessibility
  • Terms & Conditions
  • Privacy Policy

Follow us

  • Facebook
  • Twitter
  • Youtube

Registered as Charity number 1186735