What Were You Doing Last Easter?

Four months have passed since the diagnosis. This is the impact it has.

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Fear is Psychological

[N.B. This post is about caring for someone with a PEG. For a perspective on living with¬†motor neurone disease and a feeding tube, please click here.] Three weeks ago, Mum finally¬†had her PEG fitted. Right from the start of this journey, we knew she needed the PEG. By the time we received her diagnosis, her... Continue Reading →

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