Ian and Rachael Flatt: Our journey with MND

We spoke to Ian and Rachael Flatt about their family's experience with MND.
56-year-old Ian was diagnosed with MND in early 2019 and receives care and treatment at the current Motor Neurone Disease Centre at Leeds Teaching Hospitals NHS Trust.
Rachael and Ian speak about the impact MND has had on their lives, why we need a new centre in Leeds and the difference this would make to families like theirs.
On May 4th, Ian is climbing Snowdon in his tangerine dream machine to raise funds for our Rob Burrow Centre for MND appeal and the MND Association.
You can find out more and donate to Ian's fundraiser here donate.giveasy...

[@kevinandgillian1]

I work for the charity on behalf of SEC Fundraising and it's an incredible journey, you get to hear lots of stories about people's experiences in hospital and how our charity has helped them. I will try my upmost to keep the vital funding coming in to help get the centre built for MND patients like Ian and his family

[@metalmitch]

I live in Australia and I have just been diagnosed with motor neurone disease, I know that there is no cure for it and I know that I am going to die possibly in the next 2 years. But I would like to talk to anyone who has mnd ,for there prospective, so if anyone knows of any online forums could you please leave the details here. Thank you 😊

[@janheard3826]

Hi sorry you have this illness. If you google MND forum or ALS forum there are several available.

[@wendyqallab6906]

Lovely family.

[@VirginNenang]

One of MND po

[@nickywilks7928]

What a gorgeos brave man with a gorgeous brave family.