Motor neurone disease took my partner at 51 but a poster campaign means people across the country can learn from our experience
On 26 August 2009, life for my partner, Steve, and me changed forever when he was diagnosed with motor neurone disease (MND). It began with difficulties moving a finger in his right hand, then muscles twitching in his neck. Neurological tests followed, then a diagnosis. MND progresses rapidly and Steve died just two years and seven months later, aged 51.
Related: My husband is disabled. One day I stood up and made MPs listen to our story
Continue reading...from Voluntary Sector Network | The Guardian http://ift.tt/2as9dgu
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