MND Association
@mndassoc • 46,420 subscribers
Every day we support people affected by motor neurone disease. Because with MND, every day matters.
Shorts
Videos
What a way to end the day! 👑🧡 Their Royal Highnesses, The Prince and Princess of Wales, joined us at Wakefield Trinity for a very special event ahead of cheering on our patron, Sir Kevin Sinfield, and his incredible team as they completed Day 3 of their final 7 in 7 Challenge. The Prince and Princess met members of the MND community, Association fundraisers and volunteers, hearing their stories, experiences and what this challenge means to our community. Then, it was out onto the pitch to welcome Sir Kev and his team as they crossed the finish line on another incredible day. 🧡 Three down, four to go. Let’s keep going! 💪 #7in7 #7in7GrandFinale The Prince and Princess of Wales
MND Association19,404 görüntüleme • 3 gün önce
💙🧡 So incredibley deserved. Congratulations Rob Burrow CBE, Lindsey and Kev! #PrideOfBritain
MND Association1,204,960 görüntüleme • 3 yıl önce
Join MND Association patron, Eddie Redmayne, as he chats with Lesley Connor, one of our remarkable volunteers. Eddie discovers Lesley's 20-year journey, some of her invaluable roles, and the impact she's made on those affected with #MND. Watch below 💙 #GlobalMNDAwarenessDay
MND Association193,765 görüntüleme • 3 yıl önce
Turning the Tide A documentary highlighting pioneering MND research by a team at @UCL funded by the MND Association, @LifeArc1 and My Name'5 Doddie Foundation Foundation. Jo and Lucy, living with #MND, share an honest insight into how the disease has impacted their lives. 🔬 #TurningTheTide
MND Association44,857 görüntüleme • 2 yıl önce
One week to go... Kevin Sinfield's 7 in 7 Challenge 👏 Kev and his team will be running home for Christmas - seven ultra marathons, in seven regions, in seven consecutive days starting Sunday 1 December. Click below to find out more and see Kev's route! #7in7
MND Association29,847 görüntüleme • 1 yıl önce
Kyle, 14, is believed to be the youngest person living with MND in the UK. He and his family have been living in hospital for almost nine months as their home is not adaptable, and no other housing is available. Here, the family and the MND Association’s Jen Mills speak to BBC Wales about their situation. #MND
MND Association15,717 görüntüleme • 1 yıl önce
Thank you for your support in 2023 💙 We simply couldn't do what we do, without 𝐲𝐨𝐮.
MND Association22,127 görüntüleme • 2 yıl önce