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Be a part of our Act4ME Network and join other people with M.E./CFS, friends and family, in fighting for an end to the ignorance, injustice and neglect as well as call for increases of investment from Government. 

How does this work?

We will contact you once a month with a suggested action you can take. This may include:

  • responding to a survey which will inform our work
  • contacting your elected representative 
  • attending a virtual rally or event
  • lobbying an individual or organisation on social media

We recognise that M.E. symptoms may mean not everyone can be involved but we will try and be as inclusive as possible and we are happy to work with family/friends on behalf of others, if that's helpful.. At first we will be running the network primarily online however we are aiming to open it up to those who may find it difficult to access a computer in the near future. We will also look to do specific actions for people who live in Scotland, Wales or Northern Ireland, as well as to highlight regional issues in England. 

We believe that by working together our voice will be stronger and we can push for real change to benefit people with M.E./CFS.

The information you provide will be held by Action for M.E. and used only for the purposes of the Act4ME Network. You can request for your information to be deleted at any point. To do this, you can e-mail or click 'unsubscribe' on any of the e-mails you receive as part of the Act4ME Network.

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* 1. Would you like to join the Act4ME Campaign Network? If you opt in we will use the details you provide below to contact you (monthly) in relation to the Act4ME Network.

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* 2. Where do you live?

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