My real voice vs my cloned voice

Has Spring finally arrived?

Day 16 100 miles in March for @m@MND Association

Thanks to MND getting dressed looks a bit different these days.

Friday 13th hundred miles in March update

Day 12 of 100 Miles in March for the @MND Association

 Day 11 - 100 miles in March for @m@MND Associationpdate

Today’s walk was built around the school run, which helped me get half a mile in.

I’ve been gently reminded I’m no longer 20 anymore plus I have a little old thing called MND🤦🏻‍♂️

Day 5 - Didn’t go to plan thanks to MND 🥱

Day 4 – I had to really force myself out the door today, but I’m glad I did. 2.63 miles banked.

Day 3 - legs like lead but 2.5 miles added to the total today 🦾

Day 2 walking 100 miles in March for the @m@MND Association

Donate here 👇 https://socialsync.app/fundraiser/cr-o6vrqoyro3qqv?currentTab=feed

My wife is no longer just my wife thanks to MND/ALS😢

Did I ‘milk’ it? 🥛

MND’ing my weight ⚖️

You’ve got to Shein it to believe it.

Don’t ‘mnd’ me I’m just sitting here.

MND has been chipping away at me recently 🤬

These are rather annoying and a reminder of what is to come 🤬

As a family we hope we never have to use this but so glad we have a Life Vac

I now have a man cupboard thanks to MND.

How I’m trying to combat tiredness with MND.

How MND effects my sleep currently!

My latest piece of equipment really blows 💨

One of the ways I’m trying to overcome and manage fatigue with MND this year. 💪

There’s still some nice people out there. Thank you to the stranger that helps me open this gate.

My trick to staying hydrated 💦

How do I feed myself when I can’t use my hands living with motor neurone disease?

My hands free bathroom upgrade 🚿 Aqualisa Q Digital Display Smart Shower.@Aqualisa Showers

How I use my MND hands to help tidy up!

Come walk with me. Oh and Happy New Year.🥳

ALS forced me to do this.#ad #ALS #RareDisease #ALSNewsToday #bionewsrare

A MASSIVE THANK YOU TO THE NEW CHANNEL MEMBERS 🙏🏻🥰

No arm in trying 🤣 Merry Christmas

A for effort ⛳️

What the start of MND muscle weakness looks like for me 😢

Channeling my inner superhero… but instead of super soldier serum, it’s just good ol’ B12! 💪✨

Adapting to keep some independence with ALS is key.

My young carer to the rescue.

POV - Getting out the door now takes a lot more effort these days.

Motor neurone disease continues to make the simplest of things harder and more frustrating. 😖

How I measure my independence living with Motor Neurone Disease 💪🏻

Disabled parking spots are so important especially when they are full.

MND/ALS progression update hand edition

Something I’ve not yet had trouble doing is putting on weight with MND. More to love I say 🤣

POV - Get ready with me.