Sally Callow reports on the DecodeME study using DNA to try to find out more about M.E/CFS. Sally suffers from M.E herself, is participating in the study, and is also the founder of Stripy Lightbulb [… read more ]
Local resident and founder of Stripy Lightbulb CIC, Sally Callow, shares her experience of ‘long Covid’ as someone living with M.E and explains growing concerns that for many, Covid-19 may trigger M.E. As a M.E [… read more ]
Local parent, researcher and writer, Maddie Wallace, continues her daily diary describing the experience first, of self-isolating, and now of being in lockdown with her children in Southsea. We’re at Day 66, and Maddie decides to [… read more ]
Sally Callow, Portsmouth resident, M.E patient and M.E patient advocate reports on the growing concerns about the implications of Covid-19 as a potential cause of M.E, as expressed by the ME Association and others. Sally [… read more ]
Local resident and Founder of Startup Disruptors, Becky Lodge, writes about her experience of Covid-19 – unconfirmed, as she was not tested, despite the severity and longevity of her illness. I have wanted to write [… read more ]
An estimated 250,000 people in the UK suffer from Myalgic Encephalomyelitis (M.E.), with roughly a quarter of these patients house- or bed-bound. But research into the condition is significantly underfunded as less than 1% of [… read more ]
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