My Dad died this morning, 6 months after diagnosis with this shitty disease. He never came to terms with the MND and the rapid decline, a year ago he was fine, still riding his bike and today he is gone.
The MND wouldn't even allow him to rest after he had died, the twitching just carried on. I'm bitter that him and Mum never got the proper support they were promised, his so called specialist nurse saw him once after his diagnosis, they were left to get on with it.
Am thankful in the end he died at home, peacefully in his sleep, with us all and that he no longer has to struggle. He was the best Dad, I'm going to miss him so much.
The MND wouldn't even allow him to rest after he had died, the twitching just carried on. I'm bitter that him and Mum never got the proper support they were promised, his so called specialist nurse saw him once after his diagnosis, they were left to get on with it.
Am thankful in the end he died at home, peacefully in his sleep, with us all and that he no longer has to struggle. He was the best Dad, I'm going to miss him so much.
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