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'
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.
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.
Events
Join us at upcoming events 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.
"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.
