As a social enterprise based in England, we work for the benefit of the M.E./C.F.S. community in all nations of the UK and internationally. We don’t allow our work to be restricted by geographical borders or political boundaries. Our work …
New Year Message from Stripy Lightbulb CIC’s Founder and Managing Director, Sally Callow. Hi All, Firstly, Happy New Year! Secondly, I am hoping that 2024 is a year of positive change for the M.E./C.F.S. community, Stripy Lightbulb CIC may be …
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 …
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 …
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 …
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 …
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 …
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