In one of the most touching stories we've ever printed, @jodydv78 tells all of his brave battle with MND. Via https://t.co/KTWRgsA0xw pic.twitter.com/rpn8C46APg— Gay Times Magazine (@GayTimesMag) September 23, 2016
This blog follows my life since being diagnosed with terminal Motor Neurone Disease / ALS on 2nd July 2014 at the age of 36. A music addict, travel & photography enthusiast & gay, when diagnosed I was enjoying life in Sydney Australia. I returned to the UK in June 2015 to be closer to family, have access to further healthcare & support to help me battle this brutal disease. Expect posts about the condition, its progression and any issues as they arise.
What is MND/ALS?
What is MND/ALS?
MND/ALS is characterised by progressive degeneration of the motor nerve cells in the brain and spinal cord. The motor cells (neurones) control the muscles that enable us to move around, speak, breathe, and swallow. With no nerves to activate them, muscles gradually weaken and waste. Symptoms may include muscle weakness and paralysis, as well as impaired speaking, swallowing, and breathing. In most cases, it does not affect intellect, memory or the senses. Progress is relentless and generally rapid, with a life expectancy of between 2 and 5 years from the onset of symptoms. There is no known cause and there is no known cure. See links on the right for further information.
Showing posts with label 2016. Show all posts
Showing posts with label 2016. Show all posts
Friday, 30 September 2016
Gay Times
Very proud to be raising awareness on Motor Neurone Disease specifically in the gay community, which I believe may be a first, by sharing my story over a 4 page article in Gay Times. Thank you to MND Association and Gay Times Magazine for making this all possible. Available digitally and in the shops now.
Friday, 1 January 2016
Happy New Year 2016
London Welcomes 2016Watch: London welcomes 2016 with an 11-minute fireworks display and a rendition of Auld Lang Syne #HappyNewYear
Posted by Sky News on Thursday, 31 December 2015
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