There may not be any effective treatments or cures for Myalgic Encephalomyelitis also sometimes known as Chronic Fatigue Syndrome (M.E/C.F.S.), but people living with M.E/C.F.S find themselves on hospital estates for a variety of reasons including appointments for tests for M.E/C.F.S-related symptoms, tests/treatments for other illnesses, or in their role as a parent/guardian/partner of a …
Our vision is to improve the quality of life of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients. How do we do this? The experience of having the disease is bad enough but patients also have to deal with poor ‘treatment’ and support from those who have a duty of care over them. We are improving the quality …
Blog from our Founder and Managing Director Sally Callow for International Women’s Day 2021. Sally, Wow, you have just graduated as a mature student, you did it! Well done you! Today is your 30th birthday, you do not know this yet but in just 9 weeks’ time, your life will be changed forever. All your …
I am baffled. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (M.E./C.F.S) is not a new condition. The illness itself, under various names, has been around for at least 150 years (Florence Nightingale herself is said to have had an M.E-like illness and was bedbound for part of her life) and was classified as neurological by the World Health …
Firstly we, Stripy Lightbulb CIC, think #Valuable500 has amazing potential for increasing inclusivity and diversity in the workplace. We hope it lives up to their Twitter bio which states – #Valuable500 exists to release the social & economic potential of 1.3 billion people. What is #Valuable? It launched 24 January 2019. https://businessdisabilityforum.org.uk/media-centre/news/the-valuable-500-launches-at-the-world-economic-forum-annual-summit What concerns Stripy Lightbulb CIC …