Starting a blog is never easy. I have decided to write it for a number of reasons: my father died from pneumonia on the 16 May 2013 having suffered from Progressive Supranuclear Palsy (PSP) for around four years. Before he died I decided that I wanted to raise awareness of the disease and tell his story so that I could help other people to recognise the symptoms that their relatives or loved ones may be suffering from.
Living with Progressive Supranuclear Palsy (PSP): The carers - good and bad...
Living with Progressive Supranuclear Palsy (PSP): The carers - good and bad...: My Dad only had live in carers for the last 10 months of his life. Until then, my Mum mainly coped on her own relying on minimal help from v...
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