Originally posted on A Prescription for M.E.:
On Friday I watched the award-winning documentary Unrest at Sheffield Doc Fest. The film includes clips from the video journal of director and US M.E. advocate Jennifer Brea since she became ill with M.E. in 2013, along with interviews with some of the other 17 million people worldwide…
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Disability, Lifestyle, And Random Thoughts
Celebrate a day in the life of #MedComms on 10 June 2020
This is the research blog of Dr Sally Pezaro. Sally is 'The Academic Midwife' working to secure excellence in teaching and maternity services. Specialist interests include maternity services, workforce and midwifery research.
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Living with Fibromyalgia
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Fibromyalgia and Depression. Fighting the stigma attached to yet another illness not widely understood. We search for answers from the experts who are just searching for the answers themselves. We must take our lives back into our own hands!.... One step at a time... One day at a time!.... Because if you don't who will??
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IT'S TO CAUSE AWARENESS ABOUT PEOPLE LIVING WITH EPILEPSY
Newly disabled, welcome to my frank, honest & often bizarre thoughts about this 'new life', my new world & anything else else that pricks my attention.....
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