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    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'

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    Sunday 3rd March 2024, 3pm

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    Sunday 10th March 2024, 2pm

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    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.

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OPERA

31/07/2022
|
Achalasia Action

The OPERA study commenced in 2022 and aims to review cases of children with achalasia.  

It is being undertaken by the Paediatric Surgery Trainee Research Network – www.pstrnuk.org  including Jonny Nevill, Academic Clinical Fellow, Paediatric Surgery, University of Southampton

Research progress will be updated here

Multicentre retrospective study investigating the management and outcomes of paediatric achalasia

​Achalasia is a rare disease in children. There is no consensus on management and a paucity of evidence regarding current outcomes.​

Methodology: 

Retrospective multicentre study investigating current investigations and management strategies, and documentations of outcomes.

Share this research article

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Medical Treatment of Spasms

Achalasia Action are keen to support a project looking at how we can treat spasms/ chest pains as this has been one of the most recurrent themes raised

MORE

I-PASS study

This study (International – Patient reported outcome of Achalasia Symptom Score) is being run by Professor Giovanni Zaninotto from Imperial College and Assistant Professor Sheraz Markar.

MORE

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