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The Coalition of Ankylosing Spondylitis Patients (CASP) is an organisation founded by people with AS to co-ordinate campaigning activities on behalf of AS patients and carers throughout the UK

CASP aims to:

Raise the profile of AS nationally and campaign for greater awareness of the disease in both public and political domains

Direct patients and carers to useful information resources about AS, its symptoms, associated health conditions and treatments

Campaign for fair treatment access for AS patients through each stage of the disease from diagnosis to medication and support services

Facilitate contact between individual patients and people and organisations that can help them access the best treatment and support available

CASP is not a membership organisation! It is an alliance of people who share a collective aspiration for a better deal for AS patients throughout the UK. If you, or a loved one are struggling to get access to the treatment or support services that all people with AS deserve, get in touch with your regional co-ordinator who can give you the tools to contact the relevant body.

For information about our first campaign in Westminster and the devolved administrations this summer please follow the link at the top of the page.
Thank you for visiting our website and supporting CASP in improving the lives of AS patients throughout the UK.
Yours faithfully, Gillian Eames, CASP Chairman

theCASP

The Coalition of Ankylosing Spondylitis Patients (CASP) is an organisation founded by people with AS to co-ordinate campaigning activities on behalf of AS patients and carers throughout the UK

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