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    Achalasia Action Meetings

    Talking to others with achalasia is a good way of getting ideas that might help with particular problems.

    Achalasia Action holds regular support meetings, mostly online so that everybody can have access to them. After COVID we aim to re-start some meetings in person.

    To see summaries of specialist-led meetings, click on 'See All Meetings' in the box to the right, and then visit 'Specialist-led Meetings'

    Upcoming Meetings

    Sunday 3rd March 2024, 3pm

    Achalasia Action Writing Group

    Sunday 10th March 2024, 2pm

    Achalasia Action London Online Meetup

    See all Meetings
  • About Us

    About Us

    How We Can Help

    Our main aim is to provide help and support within a friendly and well informed community to those with Achalasia and oesophageal motility and peristalsis problems.

    Contact

    Contact us for all patient and general enquiries.

    Achalasia Resources

    Downloadable information leaflets, reports and policies

    Trustees

    Achalasia Action benefits from the huge range of knowledge and experience brought by our trustees.

    News & Blog

    See all the recent updates from across the UK, and the latest news and blog articles about Achalasia.
  • Information & Support

    Information & Support

    FAQs

    Get answers to frequently asked questions about support and treatment of Achalasia.

    Meeting Forums

    Regular meetings across the UK providing key influence and support to Achalasia Action.
  • Research

    Research

    Research News

    See all latest Achalasia research news and articles.

    For Researchers

    Documentation, archives and links to key information for researchers of Achalasia.

    Get Involved With Research

    See how you can get involved with research.
  • Medical Professionals

    Medical Professionals

    Assessing motility
    problems

    Achalasia in the GP surgery

    Resources

    Resources for medical professionals.

    For Your Patients

    Information to help medical professionals introduce and guide patients on Achalasia.

    Events

    Take part in upcoming events on Achalasia.
  • Get Involved

    Get Involved

    Donate

    We rely on the support and generosity from donors to promote, support, raise public awareness and providing research into Achalasia. The sky remains the limit for what we might do.

    Meetings

    Join our regular online and venue-based meetings across the UK.

    Fundraising

    There are lots of ways you can help raise funds and awareness for Achalasia Action and by doing so you are giving more and more people living with the condition better access to vital research, information and treatment.

    Volunteer

    Volunteer for Achalasia Action and help us make a difference.
Donate

"Talking with others with achalasia has helped me adjust to living with this painful condition"

How we can help

Get help and support within a friendly well-informed community

Our ultimate directive is to provide help and support within a friendly and well informed community to those with Achalasia and oesophageal motility and peristalsis problems.
We provide the means for people with achalasia to communicate with each other, to learn more about their condition and to support each other. We aim to advance education about achalasia, to support people with achalasia and their friends and families, and to encourage and support relevant research.

If you need help...

Our telephone helpline is 0300 772 7795
If we do not reply straight away we will ring you back if you leave a message for us.

Or email us
For patient support: info@achalasia-action.org
For fundraising, questions about our charity and anything else: admin@achalasia-action.org

Our aims include

  • To preserve and protect the health of people with achalasia, including their friends and families
  • To advance education about achalasia and associated conditions
  • To encourage and support research into achalasia

Need help? Call the helpline on 0300 772 7795 or email admin@achalasia-action.org

Need help?
Call the helpline on 0300 772 7795
or email
admin@achalasia-action.org

Achalasia Action helping patients, families and professionals

Awareness

Creating awareness of the disease for patients, families and professionals

Support

Providing support and guidance for patients affected by achalasia

Information

Essential content and research to help diagnosis and living with achalasia

Network

A well-informed community prividing help and support when needed

Lobbying

Uniting voices within our sector for a common cause
Achalasia is a long-term condition that cannot be cured at present, but there are treatments that can improve the symptoms.
See treatment options

"Treatment for Achalasia is wide and increasingly varied, and experiences often differ patient to patient and care centre to care centre"

See how Achalasia can be treated

Treatment options

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Donate to Achalasia Action

Your donation will be put to good use in promoting the well being of achalasia patients, providing support and education, raising public awareness and providing research into the condition. The sky remains the limit for what we might do.
Donate Today
  • © Achalasia Action Charity 2024. Charity No:1187367
  • Privacy
  • © Achalasia Action Charity 2024
  • Charity No:1187367
  • Privacy
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