M.E. advocacy service

Action For M.E. has opened an advocacy service for people affected by Chronic Fatigue Syndrome (CFS) or M.E.
Lady with a kind face

Action For M.E. has a dedicated team for anyone living with or supporting someone with M.E. They can offer understanding, empathy, source practical assistance and provide an advocacy service for people affected by Chronic Fatigue Syndrome (CFS) or M.E.

The issues they offer support with could include Housing, Health and social care (issues with GP, including complaints in relation to social care services), Employment, Relationships/Family, Discrimination, or Access to education.

The service may be of benefit for anyone who has a diagnosis of CFS/M.E. and:

  • wishes their voice to be heard on issues that are important to them

  • needs to defend and safeguard their rights

  • wants their views and wishes genuinely considered when decisions are being made about their lives

  • does not have anyone appropriate who can support them with this.

The service is mostly telephone, email, or video conference-based in terms of the direct support provided. There is also support for people with M.E. to develop self-advocacy skills.

contact advocacy@actionforme.org.uk to self-refer

call 0117 927 9551 (10am to 5pm Monday to Friday)