You can find out more about our Christmas Angels project on our website 👇
www.actionforme.org.uk/christmas-an...

We ask that all cards arrive at our office by Monday 8 December to allow us time to process and send them on.
This project is open to anyone with ME of any age. If you’re aged 18 and under, you need to be a member of our free Young People’s Community to take part.

Our Christmas Angels project, now in it’s 15th year, enables people with ME to send Christmas cards to each other – all via the Action for ME office!

To take part, complete our online form 👇

forms.gle/VQ51jyCiKGYN...

You can also find information about the conference here 👇

aliancamillionsmissing.org/2-conferenci...

#MECFS #pwME #MyagicE #MyalgicEncephalomyelitis #LongCovid #Research

We will be sharing a recording of Sian's presentation afterwards on our YouTube channel.

Register now to attend online, for one or both days 👇

aliancamillionsmissing.org/2-conferencia/

Sian, an Action for ME staff member who is also a member of the PPI steering group for DecodeME and PPI Coordinator for the PRIME project, will be presenting about DecodeME PPI as part of the 'Patient Advocacy Panel’ session!

The conference aims to raise awareness and understanding among healthcare professionals, researchers, policy makers, patients and advocates about ME/CFS, long Covid and other post-viral illnesses.

📆 When? 12-13 November 2025

📍 Where? Online

3/3
We are incredibly grateful to our judging panel of people with ME and medical professionals, who are now carefully assessing all the entries.

We will announce the winner in the first week of December!

2/3
"Thank you for the opportunity to take part in such an important and timely competition. I am grateful for the chance to deepen my understanding of ME/CFS and contribute to a more compassionate and evidence-informed future for patients."

@longcovidkids.bsky.social @longcovidsupport.bsky.social

Ask your MP to attend using the form on the Overlapping Illness Alliance website, linked below.

You can read more about the Overlapping Illness Alliance here 👇

www.overlappingillnessalliance.org.uk

This founding group will turn collaboration into action, creating one voice for the progress our communities need.

The Overlapping Illness Alliance are hosting a drop-in session at the House of Parliament on Tuesday, 25 November to inform MPs about these illnesses, and what they can do to support.

If you would like to send or receive a card from another person with ME this Christmas, or know someone severely affected who would appreciate a card, complete the form below 👇

forms.gle/VQ51jyCiKGYN...

You can read more about this project on our website:

www.actionforme.org.uk/christmas-an...

“I loved it last year! Receiving a card was so lovely and brightened my Christmas!”

Our Christmas Angels project is open to anyone with ME of any age. If you’re aged 18 and under, you need to be a part of our free Young People’s Community to take part.

You can read more about the guidelines, including about some of the people working on them, on our website 👇

www.actionforme.org.uk/the-british-...

More on DecodeME and our partnership with the University of Edinburgh 👇

www.actionforme.org.uk/research-cam...

#MyalgicE #MyalgicEncephalomyelitis #MEAwareness