Mother of 3 World just tipped upside down with a diagnoses of MND/ALS 💔
United Kingdom
Joined February 2009
- Tweets3.7K
- Following884
- Followers966
- Likes3.6K
Debbie Whitehouse retweeted
🚨 | Yasmin is the new favourite to win Big Brother 2026, according to the current betting odds.
This is Yasmin’s first time as the favourite to win.
#BBUK
Debbie Whitehouse retweeted
We're helping improve access to tofersen for people living with SOD1-MND in Scotland. Too many are being prevented from accessing this treatment, and that must change.
We’re partnering with @mndassoc to support people who are having to travel out their area to receive tofersen.
😢
An actor with motor neurone disease who won one of the UK's biggest drama awards for a "legendary" performance as Richard III in a wheelchair has died aged 35. bbc.in/3OtZlsS
Debbie Whitehouse retweeted
The Spring sunshine is here. ☀️
For people living with motor neurone disease, getting out into the garden, enjoying the sunshine, and keeping up with hobbies can sometimes take a little extra support.
That’s where our versatile Wellbeing Support Fund can make a real difference. It, for example, can help you continue the activities you love — like gardening — or help with the cost of support to maintain your outdoor space.
Find out more: mndassoc.org/supportfunds
Debbie Whitehouse retweeted
We're so sorry to hear this sad news - our sympathies are with Geoff's family and everyone @LeedsRhinos who has worked so closely with the Burrow family over so many years.
It is with deep sadness that the club has learnt of the passing of Geoff Burrow, the father of Rob Burrow. Our deepest condolences go to Geoff's wife Irene and the whole Burrow family at this time. May he rest in peace
therhinos.co.uk/article/2311…
💔💔💔
It is with deep sadness that the club has learnt of the passing of Geoff Burrow, the father of Rob Burrow. Our deepest condolences go to Geoff's wife Irene and the whole Burrow family at this time. May he rest in peace
therhinos.co.uk/article/2311…
My amazing son Jacob and his wonderful partner are running the half marathon in this year’s Rob Burrow Leeds Marathon to raise money for a charity very close to my heart: the Mel Evans MBE Foundation, which funds vital research to find a cure for MND click.contact.justgiving.com…
Debbie Whitehouse retweeted
We're giving you the chance to win a VIP Experience for 2 at @FTLoveOfAnime!
1X photograph for 2 people, with every guest at the show
2X Weekend Diamond Entry to the event
To enter...
Follow @FTLoveOfAnime
Like & RT this post
Tag who you're going with!
Comp closes 27/03
Debbie Whitehouse retweeted
A message from Jayne, known to many of us.
"Please ignore direct messages from @jaynes__world as her account has been compromised!"
This is one of the bullies that has been saying that I am faking my symptoms for financial gain and yet he is sharing “ selfies “ of his peg. It’s a stock photo from Google 😂 he has blocked me, but please be aware of his lies! 🤢 Geoff Binh
Debbie Whitehouse retweeted
This morning, as both MP for Liverpool West Derby and Chair of the All-Party Parliamentary Group on MND, I sent a letter to the Walton Centre NHS Trust, requesting its provision of tofersen - a drug which would be life-changing for people with SOD1 MND (about 2% of the MND population).
I am pleased so many of my fellow parliamentarians, both in Westminster and the Senedd, have co-signed this letter to the Walton Centre, to encourage its speciality Liverpool MND Care Centre to provide tofersen to any people in its catchment area who may need it.
Tofersen is available free on the NHS. The drug is there - let’s make sure everyone can access it.
2/2 after posting this on their group this morning!
1 I’ve never had a podcast
2 I’ve never said my legs don’t work
3 I never asked either of you to join the group
4 the picture you used was two years ago
5 you have never “ called me out” 😂
Over two years ago, I was asked by James Smith to be a moderator on a support group for people with MND called “MND and beyond” I left the group in June 2024 after being bullied out by Simon Chippendale and Binh Binh (Geoff) but it seems like they are still obsessed with me 1/2
Debbie Whitehouse retweeted
This is us, the MND Association. Renewed, united and driven every day to make change happen.
Every day we support people affected by motor neurone disease, campaign for better care and fund ground-breaking research.
Because with MND, every day matters.
Debbie Whitehouse retweeted
Woman, 19, refused access to motor neurone drug hampshirechronicle.co.uk/new…
