Finger on the Trigger's: This is an honest appraisal of over 50 years of experiences and memories whilst dealing with MS, not just myself and my mother but also the entire dealings I have had with the world of neuroscience and neurology. I try to highlight the areas of the varying conditions and how little progress has been made. I want to make it a reality check for everyone who is unlucky enough to be diagnosed with the illnesses, and what they can expect in terms of support, plus the areas of pointless interaction with the medical establishment. Especially those "potential" life changing pharmaceutical treatments that have little or negative benefits. It's a book to make you focus on living and working through your bucket lists ?
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