Just read about this website - please do have a look, and donate if you can.
www.gordonsfightback.com
This blog has been set up to give readers an opportunity to understand what it is like being diagnosed and living with MND from my own personal experience. To read the whole story, you need to go to the 'Blog Archive' below right, start with 'What is MND? and why a Blog?' and read forward to the present day. Pass on the link to anyone you think may be interested. If you want to email me or leave a comment, please do so. Also, add your email address to the email updates box below to keep updated.
A photo of me at home
Tuesday, 24 March 2015
Sunday, 8 March 2015
A Program on Channel 5
Just a heads up to those readers who may be interested.
There is a documentary on Channel 5 (UK TV Channel) on Wednesday 11 March at 7pm. It is about a man with Motor neurone (not Gordon) revealing the effects of the condition on his life. I do not know how good the program is, but thought I would let this blog readers know.
If you cannot catch it live, it may be on Demand 5, the web replay service.
There is a documentary on Channel 5 (UK TV Channel) on Wednesday 11 March at 7pm. It is about a man with Motor neurone (not Gordon) revealing the effects of the condition on his life. I do not know how good the program is, but thought I would let this blog readers know.
If you cannot catch it live, it may be on Demand 5, the web replay service.
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