98% of the junior doctor who voted have voted for strike action.
We are right behind them. Please RT if you are too and help show them they are not alone.
#JuniorDoctors
@JaneCanDoSE4@BrocJackTheatre I'm so sorry we had to move away so no longer have the delights of the Jack Studio Theatre on our doorstep but I do encourage friends still in the area to support them. And I'm not so far away that I can't visit occasionally!
Good morning everyone yesterday I had a very active day I managed to do 25 leg squats! I have got to get this body looking good ready for my James Bond Audition!! 🤣🤣
@mndassoc
We’re sorry but this is absolutely amazing…
180 pupils from @NunthorpePri Primary School in Middlesbrough, lined the streets to support Kev Sinfield and the #Ultra7in7 team. What a boost!
A very special moment 💙 https://t.co/pW92Aj9ndU
Woolger said: “It would be easy for people to try and get photos of aspects of homelessness or what they’ve been exposed to in London from their own experiences. But this project is about being more positive than that” 📸Aija Kalnina
The 2023 calendar will launch this week with @CafeArtuk holding a pop-up exhibition in London to show off the photos for the first time 📸Alan Miller
https://t.co/anzLc4Msog
One of the six to have died on 20/06/22 was my husband Andy Cawdell. He resisted the inevitable as long as he could but eventually could not avoid it. RIP my love.💓
Thanks to the bravery of people like @EdSlater and others who share their MND diagnosis, the awareness of the disease is increased.
Make sure at least one more person knows about the impact of motor neurone disease by sharing our key facts.
Our vision is a 🌍 free from #MND!
We're saddened to hear our trustee Andy Cawdell has died.
Elected in 2019, Andy was an invaluable member of the board, bringing his professional skill and his own experiences of living with MND to the role.
Our thoughts are with Andy's wife Jeanie, daughter, family and friends.
@mndassoc Andy was amazing! He endured much and hoped above hope that a cure would come in time for him. That was not to be but I hope for a time when no-one will suffer again with this wretched disease. RIP my love.
A STATEMENT by @United2EndMND, who are hopeful talks today with @GovUK will open up a way to release the £50m promised!
"Having raised the hopes of people suffering with #MND, it would be an act of remarkable cruelty to dash those hopes at this stage..."
https://t.co/3XVy1mzPIb