Mum and I attended the MNDA's 2017 Parliamentary Reception, where she met Charlotte Hawkins!
It's hard to imagine half a year has passed, and harder to think about just how drastically our lives have changed.
Mum's new electric wheelchair has given her a new independence she thoroughly enjoys.
Please invite your MP to the Parliamentary Reception, to raise awareness of what they can do to support people with MND and their carers.
Congratulations to Mum and Tim, who married on Saturday 26th August 2017.
The surreal moment you walk into a corner shop and your bride-to-be Mum is smiling at you from the cover of a newspaper...
Four months have passed since the diagnosis. This is the impact it has.
A thank you to the specialist teams who help us refocus on the positive side of life.
When you wait for a bus and four hit you at once.
[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 Fear is Psychological