By Matthew: Today would be the 20th anniversary of the start of Lynn Gilderdale's illness.
She is no longer with us but many others are still suffering, both from the effects of the illness and the cruelty and disbelief of others.
We should fight for ME to be recognised by the medical and social service establishments, so that nobody else suffers the same way again.
One Last Goodbye @ amazon.co.uk
2 comments:
It's tragic that if Lynn hadn't committed suicide she could possibly be taking Rituximab right now and, if she was a responder, becoming the public face/voice of ME/CFS patients around the world.
And now this
http://www.dailymail.co.uk/health/article-2061267/Schoolgirl-left-waking-coma-sleeps-23-hours-day-severe-reaction-cervical-cancer-jab.html
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