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.
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.
If you would like to help with an extension to Melika Kalantari’s research in Mapping the Experiences of People with Achalasia by developing a co-designed workbook to help people with living with achalasia, please contact Melika
