ME is a global health crisis – up to 30 million people are living with this disease worldwide, and when we take into account the effect on families, carers and friends too, the impact of this disease cannot be overstated. But there is much to be learnt from this disease…
April 01, 2022 Responding to the lifting of the Covid restrictions today (1 April), Action for M.E.’s Ruth Richardson, Director of Business Support and Development said:“For many people with M.E.… This post appeared first on Action for M.E. Read more >>
As we extend our reach across the globe, we are pleased to have one of the foremost ME organisation in Northern Ireland joining us. Hope 4 ME & Fibro Northern Ireland have an impressive track record in their country over the past decade, and we look forward to seeing how…
Member Hope 4 ME & Fibromyalgia Northern Ireland is a registered charity run by patients and volunteers. Founded in 2011, they have grown from strength to strength, achieving charitable status in 2014, and honoured with receiving the Queen’s Award for Voluntary Services in 2020; becoming a foremost charitable organisation working…
Op 24 april staat 12ME op LetsLousArt in Gent, een creatieve markt van 11u tot 17u30, waar we creaties zullen verkopen van patiënten met ME/CVS en hun naasten We zijn nog op zoek naar enkele enthousiastelingen om ons te helpen: Iemand met een auto die de spullen in… On April…
Support Research, Support Patients A recent survey from our friends at Research!America found that over 80% of Americans believe our government should fund “basic scientific research that advances the frontiers... This post appeared first on Solve ME/CFS Initiative. Read More
Were you one of the many who attended the Learn about M.E. Social Care webinar on M.E./CFS & Long Covid? If you were unable to attend, you will be pleased to know that we have shared… This post appeared first on Action for M.E. Read more >>
Our Alliance is growing, and we a thrilled to announce that the CFS/ME Associazione Italiana is joining our ranks. This small organisation works incredibly hard to ensure that people with ME in Italy have access to the information and resources they need to get the healthcare they deserve. The organisation…
Member The CFS/ME Associazione Italiana is a small organisation working to ensure people with ME in Italy have access to information about their disease from across the world. The organisation focuses on raising awareness, translating information and resources into Italian, and providing people with ME with information about their rights…
In honor of Women’s History Month, #MEAction asked our community to share which woman or women have inspired them in their advocacy work. The responses are heartfelt, moving, and inspiring. We hope you enjoy reading them! "This Women's History Month, I like many others, will be thinking about the contribution…