European ME Alliance
@europeanmealliance.bsky.social
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The European ME Alliance (EMEA) is a grouping of European organisations founded in 2008 by national patient organisations and charities across Europe, and dedicated to supporting patients suffering from Myalgic Encephalomyelitis (ME), also known as ME/CFS
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europeanmealliance.bsky.social
As UN prepares its Political Declaration for 4th High-Level Meeting on NCDs has requested the inclusion of Myalgic Encephalomyelitis #mecfs in its implementation and for it to be recognised in global health strategies

europeanmealliance.org/news-Q32025-... #UNHLM4 #DisabilityRights
A poster regarding dtatistics relating to myalgic encephalomyelitis (ME) and the upcoming United Nations implementation of the Political Declaration of UNHL4
europeanmealliance.bsky.social
Switzerland is putting in place one of Europe’s first national strategies specifically dedicated to improving care and research for ME/CFS and Long Covid
www.europeanmealliance.org/news-Q32025-...
#mecfs #Longcovid #EuropeanMEalliance
Banner with Swiss flag and red background
Reposted by European ME Alliance
europeanmealliance.bsky.social
#WorldPatientSafetyDay
EMEA highlights the need to see, hear, protect even the most invisible children-those with a disease still too often ignored - Myalgic Encephalomyelitis #mecfs
www.europeanmealliance.org/news-Q32025-...
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europeanmealliance.bsky.social
On #WorldPatientSafetyDay EMEA calls for children’s safety and care
Every child deserves to be believed and supported - Patient safety from the start
www.europeanmealliance.org/news-Q32025-...

#ChildHealth #SafetyFirst #mecfs
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europeanmealliance.bsky.social
This is a patient safety issue. Children with ME need to be believed, supported, & given care adapted to their needs to help avoid more severe disability levels
www.europeanmealliance.org/news-Q32025-...
#WorldPatientSafetyDay
#ChildHealth #SafetyFirst #mecfs
europeanmealliance.bsky.social
Children with Myalgic Encephalomyelitis (ME, sometimes referred to as #mecfs) are too often overlooked. Missed school, lost friendships, & families doubted are real risks
www.europeanmealliance.org/news-Q32025-...

#ChildHealth #SafetyFirst #WorldPatientSafetyDay
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europeanmealliance.bsky.social
#WorldPatientSafetyDay
EMEA highlights the need to see, hear, protect even the most invisible children-those with a disease still too often ignored - Myalgic Encephalomyelitis #mecfs
www.europeanmealliance.org/news-Q32025-...
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europeanmealliance.bsky.social
ME must be explicitly included in UN & WHO global NCD strategies
Recognition is first step toward accountability & action
European ME Alliance is pressing for change-because people with #MECFS should not wait any longer
www.europeanmealliance.org/news-Q32025-...
#UNHLM4 #DisabilityRights #EUHealth
europeanmealliance.bsky.social
ME affects an estimated 240 million people worldwide
In Europe, the average wait for diagnosis is 7 years
-Delays and disbelief worsen disability.
-This is not just a health issue—it is a human rights issue
www.europeanmealliance.org/news-Q32025-...
#MECFS #UNHLM4 #DisabilityRights
europeanmealliance.bsky.social
As UN prepares Political Declaration for #UNHLM4 on NCDs, we urge Member States to:
- Recognise #mecfs as a disabling NCD
- Fund strategy of biomedical research & safe care
- Ensure disability & social protections
- Train clinicians/expand telemedicine
#DisabilityRights
www.europeanmealliance.org
europeanmealliance.bsky.social
People with #mecfs are among most vulnerable
Too often misdiagnosed, disbelieved, denied support
Many are house- or bedbound, unable to care for themselves or defend their rights
Yet ME is absent from global health policy
www.europeanmealliance.org/news-Q32025-...
#MECFS #UNHLM4 #DisabilityRights
www.europeanmealliance.org
europeanmealliance.bsky.social
As UN prepares its Political Declaration for 4th High-Level Meeting on NCDs, Myalgic Encephalomyelitis (ME) remains invisible
@Euromeall challenges this neglect - calling for ME to be recognised in global health strategies
www.europeanmealliance.org/news-Q32025-...
#MECFS #UNHLM4 #DisabilityRights
EMEA fact poster
Reposted by European ME Alliance
youngemerg.bsky.social
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#youngEMERG consists of early career researchers from the UK, Austria, Norway, Spain and Germany 🌍 We are passionate about making a difference in the #MECFS community by working collaboratively to drive the ME/CFS research further and support young researchers in the field 🔬
Reposted by European ME Alliance
youngemerg.bsky.social
👋 Meet young EMERG and get to know us!

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#youngEMERG is part of European ME Research Group (EMERG), a network of researchers from across Europe focused on advancing knowledge and understanding in #MECFS.

youngemerg.com/aboutus.shtml
youngemerg.com
europeanmealliance.bsky.social
#WorldSuicidePreventionDay
Changing the Narrative on Suicide
Healthcare professionals play key role in suicide prevention for people with #MECFS
Yet risk signs are missed
Recognition, referral, stigma reduction can save lives
www.europeanmealliance.org/news-Q32025-...
#EUHealth 3/3
europeanmealliance.bsky.social
One of the top 3 causes of death in people with #MECFS :-https://www.tandfonline.com/doi/full/10.1080/21641846.2025.2543201?src=
Recognition & evidence-based care are urgent public health priorities
www.europeanmealliance.org/news-Q32025-...
#WorldSuicidePreventionDay #EUHealth 2/3
www.europeanmealliance.org
europeanmealliance.bsky.social
Sensitive topic
#WorldSuicidePreventionDay
#MECFS - a serious neuro-immune disease.
69% cannot work, 25% are house- or bed-bound.
Stigma, lack of treatments, isolation, societal neglect drive suicide risk well above population norms
www.europeanmealliance.org/news-Q32025-...
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europeanmealliance.bsky.social
ME is a too often ignored humanitarian crisis in many European countries
Today is #WorldHumanitarianDay – EMEA has called for EU to:
-Use proven EU mechanisms
-Fund & formalise existing efforts
-Treat ME/CFS as a legitimate public health challenge

www.europeanmealliance.org/documents/eu...
#mecfs
European flags on a blue background for EMEA's call for action from EU
europeanmealliance.bsky.social
Switzerland Advances National Strategy
on ME and Long Covid

www.europeanmealliance.org/news-Q32025-...
#mecfs #Longcovid
Swiss flag
Reposted by European ME Alliance
myedf.bsky.social
Urban mobility and development should be sustainable and inclusive!

That's what our project #Act4Dys is about!

We work to improve awareness, accessibility and sustainability, while empowering youth engagement and education.

More info in our newsletter: act4dys.eu
Act4Dys: The EU initiative addressing urban mobility challenges.

- eLearning platform to explore inclusive mobility and climate action
 - Training package for youth trainers to support disability-inclusive
urban development 
- ePortfolio of good practices in urban mobility and development

Sign up to the newsletter to not miss project updates

Project co-funded by the European Union
Project partners: 
- CARDET (Centre for Advancement of Research and Development in Educational Technology)
- Proportional Message
- Innovation Training Center (ITC)
- European Disability Forum (EDF)
- Spectrum Research Centre (SRC)
europeanmealliance.bsky.social
EMEA Press Release

Severe ME - European ME Alliance's practical and achievable proposal for taking action for this Human and Economic Crisis that Europe Can No Longer Ignore

www.europeanmealliance.org/documents/eu...
#mecfs #SevereME #research
europeanmealliance.bsky.social
EMEA's proposals the EU can take now-with existing tools:
✔️ Fund EU-level ME impact study
✔️ Coordinate research via @euromeresearch & @YoungEmerg
✔️ Provide open-access training for clinicians
✔️ Include ME in disability policy frameworks
www.europeanmealliance.org/news-Q32025-...
#SevereMEDay
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EMEA logo of European countries and highlighting EMEA's action plan
europeanmealliance.bsky.social
❗Patients too often told it is “all in their head”
#MECFS-a serious neurological disease (WHO ICD-11: 8E49)
Average diagnosis - 𝟲.𝟴 𝘆𝗲𝗮𝗿𝘀
Harmful therapies, lack of training, and no care pathways leave patients isolated, healthcare systems overwhelmed
#SevereMEDay
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A man and woman affected byt he consequences of myalgic encephalomyelitis
europeanmealliance.bsky.social
💜 Over 2 million Europeans live with ME
🛌 25% are house-or bedbound, often for decades
📉 Billions are lost in disability claims, productivity, and delayed care

This is more than a health crisis — it is also an economic crisis hiding in plain sight
#MECFS #SevereMEDay
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Facts about the effects of myalgic encephalomyelitis on citizens and on economies
europeanmealliance.bsky.social
August 8th- a moment to spotlight a disease that devastates lives and drains economies

𝗠𝘆𝗮𝗹𝗴𝗶𝗰 𝗘𝗻𝗰𝗲𝗽𝗵𝗮𝗹𝗼𝗺𝘆𝗲𝗹𝗶𝘁𝗶𝘀 (ME, also known as #MECFS) affects 2 million+ in Europe

EMEA has practical, achievable proposals the EU can adopt now:
#SevereMEDay
Read on
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A  woman affected by the consequences of myalgic encephalomyelitis - ignoring ME/CFS leads to severe disability