THE MYALGIC ENCEPHALOPATHY ASSOCIATION LIMITED

The ME Association - The ME Association

We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RPs do not necessarily mean endorsement. We help to make the UK a better place for people with ME/CFS, PVFS, and Long Covid. To provide information and support for people with ME/CFS/PVFS
801279
IČO
1989
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MK18 4DF
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meassociation.org.uk
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MEAssociation
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meassociation
Facebook (33870)
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🌟 Thank you for all the hard work you're doing to raise awareness and support for those affected by ME/CFS and Long Covid! It's vital that we come together to help each other and advocate for better understanding and treatment. 💚
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🙏 Grateful for the ME Association’s tireless efforts to shine a light on the struggles faced by so many. Let's keep pushing for research, support, and hope for everyone dealing with these challenging conditions! 💪✨
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Poslední diskuze

1. What strategies can we implement to raise awareness about the underdiagnosis of ME/CFS and its connection to Long Covid among healthcare professionals?
Odpovědí: 3, Naposledy před 1 den detail
2. How can the ME Association better support the mental health needs of individuals living with ME/CFS and Long Covid in the UK?
Odpovědí: 3, Naposledy před 1 den detail

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MK18 4DF
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O společnosti

- G99, E90, H30, H90 -

educating informing influencing supporting funding research Were here for you The ME Associationhas been providing expert help since 1980. We understand the challenges faced by people with MECFS and Long Covid and believe that nobody should struggle alone. Health Crisis We estimate that at least 250000 people in the UK have MECFS. In addition a significant but unknown number of people diagnosed with some form of Long Covid also meet diagnostic criteria for MECFS.

Nemoci, poruchy a lékařské disciplíny jinde neuvedené. Ošetřovatelské služby obecné (zahrnuje Candy Stripers) Výzkum rakoviny Výzkum specializované medicíny
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