European ME Coalition (EMEC)
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emec.bsky.social
European ME Coalition (EMEC)
@emec.bsky.social
Advocacy organization for ME/CFS patients and their carers in Europe
Here's an overview of the program and speakers. MEP Laura BALLARIN, a member of the Panel for the Future of Science and Technology (STOA), just made the introduction.

Prof. Evelina TACCONELLI's talk just started.
September 30, 2025 at 12:18 PM
1) A first draft for the Horizon Europe work program 2026-2027 has been published by the European Commission.

While it no longer includes the previous call on high-burden under-researched conditions, there’s now a new call on ‘post-infection long-term conditions’
September 26, 2025 at 9:09 AM
🇪🇪 Does anyone know any ME/CFS patient organisations from Estonia?

If you are an ME/CFS patient in Estonia, could you perhaps reach out to us at europeanmecoalition@outlook.com?

Many thanks in advance!
September 9, 2025 at 8:56 AM
2) For the #HorizonEurope call Tackling high-burden for patients and under-researched medical conditions (HORIZON-HLTH-2025-01-DISEASE-07) the Commission has created a new selection procedure (explained in the screenshot below).

ec.europa.eu/info/funding...
June 18, 2025 at 11:56 AM
1) Important news: there is now a much greater chance than ever before for #MECFS scientists to obtain funding from #HorizonEurope.
June 18, 2025 at 11:56 AM
#BlueSunday2025 at the EMEC headquarters 💙
Coffee or lemonade with cookies and a game of Rummikub to celebrate this special day. Our dog mascot Shifra got some biscuits too.

We donated to the @irishmecfsassoc.bsky.social in honor of our friend @tomkindlon.bsky.social

#TeaPartyForME #MECFS
May 18, 2025 at 12:06 PM
3) The scope of the call are illnesses with a high disease burden that remain under-researched. The description is still quite broad (we argued that it should be more specific). Nonetheless ME/CFS is mentioned as the first example.
April 28, 2025 at 2:10 PM
1) Good news: the European call on high-burden, under-researched conditions will likely be renewed in the 2025 work program of Horizon Europe.

#MECFS is prominently mentioned as an example.
April 28, 2025 at 2:10 PM
3) The commission has now replied, but their answer is rather disappointing and non-specific.

You can read the reply here:
www.europarl.europa.eu/doceo/docume...
January 27, 2025 at 2:23 PM
1) Member of the European Parliament Pascal Arimont (EPP) submitted a written question on ME/CFS in november last year.
January 27, 2025 at 2:23 PM
4) A scoping study was commissioned to define what high-burden, under-researched conditions are. EMEC, the World ME Alliance, and other charities provided input to this study.

The final list looks like this
January 11, 2025 at 10:27 AM
1) It’s been a long time since you heard from us, but we can finally give an update of what we have been doing behind the scenes.

#MECFS #LongCovid
January 11, 2025 at 10:27 AM
1) Happy holidays to everyone affected by ME/CFS.
December 17, 2024 at 10:42 AM
Many thanks to the ME/CFS Research Foundation for organizing this challenge and funding scientific research on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
#MECFS #LongCovid
December 14, 2024 at 11:08 AM
We are supporting the #LemonChallengeMECFS 🍋 The lemon acts as a symbol for the bitterness of the disease but also for the hope of healing.

We challenge:

MEP Pascal Arimont
Prof. Jos Bosch
Mr. Anil Van Der Zee

More info:
mecfs-research.org/en/lemonchal...
December 14, 2024 at 11:08 AM
Member of the European Parliament Pascal Arimont has submitted a written question asking the new European Commission how it will stimulate ME/CFS research.

We are very grateful for MEP Arimont’s strong and continued support for ME/CFS patients.
November 13, 2024 at 3:01 PM
It has been a while since we gave an update about our work. Our efforts have mostly taken place behind the scenes this past year. This doesn’t mean nothing has happened!
December 22, 2023 at 5:52 AM