Scott from Shefffield braving the shave in aid of muscular dystrophy charity
Scott from Shefffield braving the shave in aid of muscular dystrophy charity
Jun 12, 2020
thestar.co.uk
Muscular Dystrophy Walk Fundraiser
Muscular Dystrophy Walk Fundraiser
Aug 21, 2012
patch.com
Marilyn Monroe’s Heart of Gold: 1955 Muscular Dystrophy Charity in New York #reels #reelsfb #reelsvideo #trendingreel #viralnow #marilynmonroe #fblifestyle | Founding Lens
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Marilyn Monroe’s Heart of Gold: 1955 Muscular Dystrophy Charity in New York #reels #reelsfb #reelsvideo #trendingreel #viralnow #marilynmonroe #fblifestyle | Founding Lens
678 views7 months ago
FacebookFounding Lens
Going the extra mile: Woman with muscular dystrophy completes 12 half-marathons to raise funds
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Going the extra mile: Woman with muscular dystrophy completes 12 half-marathons to raise funds
Oct 8, 2024
Fox NewsMelissa Rudy
Nashville first responders honor 9/11 with charity hockey game for muscular dystrophy
1:53
Nashville first responders honor 9/11 with charity hockey game for muscular dystrophy
8 months ago
MSNNewsChannel 5 WTVF Nashville,TN
Raising money for muscular dystrophy
4:23
Raising money for muscular dystrophy
Jul 14, 2017
Global News
Gillingham family fundraise to fight Muscular Dystrophy with Christmas-themed fun
2:25
Gillingham family fundraise to fight Muscular Dystrophy with Christmas-themed fun
5 months ago
kentonline.co.uk
0:20
🚨One donation. Twice the impact. 🚨 This week, your generosity goes twice as far. Every pound you donate will be doubled by our donors and trusts. Help us fund research into more treatments for muscle wasting conditions. Together we can change the future of muscle wasting conditions. Double your impact and make a difference today: https://loom.ly/3b4wqR4 | Muscular Dystrophy UK
3.5K views5 months ago
FacebookMuscular Dystrophy UK
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Let’s come together once again to support Muscular Dystrophy UK !🤍 On October 25, Honest Gaming and friends go live for an action-packed charity stream. Get your KV-5 or FCM 50 t ready and join the bash. Make every ram-kill count! | World of Tanks
12.8K views7 months ago
FacebookWorld of Tanks
1:31
Today marks the beginning of a new chapter. We’re launching our bold ambitious ten-year strategy to transform the lives of people living with muscle wasting conditions. Over the next decade, we’ll be focusing all our energy and efforts on four strategic goals: 🧡 Transforming diagnosis – speeding up and improving the accuracy of diagnosis. 👥 No one faces their journey alone – ensuring support from day one 🧬 New treatments, universal support – accelerating the development of new treatments and
4.6K views8 months ago
FacebookMuscular Dystrophy UK
1:01
We’re celebrating 75 years of progress! 🎉 The Muscular Dystrophy Association has been at the forefront of breakthroughs in research, care, and advocacy for neuromuscular diseases since 1950. 💙💛 Watch our new PSA, Legacy. Impact. Momentum. – and see how YOU have been part of this incredible journey. Together, we can create a future without neuromuscular disease. Visit MDA75.org to learn more. https://www.mda.org/press-releases/2025/mda-launches-75th-anniversary-campaign-and-premieres-new-psa-t
1.5K viewsJan 28, 2025
FacebookMuscular Dystrophy Association
3:14
Nominations for our annual President’s Awards are now open. Help us to celebrate the strength and diversity of the incredible muscle wasting and weakening community - from research, support and campaigning to volunteering and fundraising. Gabby Logan, our charity President, invites you to nominate the people who give their all to make a difference for those living with a muscle wasting and weakening condition. Find more information on our website: https://www.musculardystrophyuk.org/our-presiden
629 viewsApr 12, 2024
FacebookMuscular Dystrophy UK
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Today, on World Health Day, the Muscular Dystrophy Association reaffirms our commitment to ensuring that every person we serve who lives with a neuromuscular disease—has equitable access to healthcare. We believe that access to lifesaving treatments, specialized care, and groundbreaking research is not a privilege but a right. Together, we are driving real change, but there is more work to be done. Join us in making a difference: MDA.org/Advocacy | Muscular Dystrophy Association
4.6K viewsApr 7, 2025
FacebookMuscular Dystrophy Association
1:05
I am proud to team up with the Muscular Dystrophy Association, a nonprofit organization that’s been supporting families living with neuromuscular diseases for 75 years by advancing research, improving care, and ensuring no one faces the journey alone. If you’ve ever wondered how to show up for our community: Start here. Start small. Start by signing. It takes less than 1 minute. Muscular Dystrophy Association has a generous donor who is turning signatures into support for families in need. Every
8K views11 months ago
FacebookJessie Owen
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Mansfield Doctor Discusses Life With Muscular Dystrophy, Passion for MDA “Muscle Walk”
Sep 24, 2015
nbcdfw.com
1:17
🌍 On this #InternationalDayOfCharity, we're inspired by individuals like Lily, whose passion and purpose are transforming the world for people with neuromuscular diseases. Diagnosed with Charcot-Marie-Tooth (CMT) disease, Lily has turned her personal journey into a powerful force for change. She found a sense of belonging and discovered her advocacy voice at MDA Summer Camp, and she has carried that passion all the way to the halls of Congress in Washington, DC, where she works to ensure the vo
1.9K views8 months ago
FacebookMuscular Dystrophy Association
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On my way to #londoncity for an awesome charity event in honour of those who lost their lives in the Twin Tower disaster in the USA, with Muscular Dystrophy UK at the #BGCCharityDay More coverage to follow tomorrow with hopefully the odd celebrity selfie, whilst I try my best to raise as much money as I can for #MDUK #juniorambassador #charityevent #Fundraising travelling on the SWR | Carmela MBE Stands Up To Muscular Dystrophy
1.6K views8 months ago
FacebookCarmela MBE Stands Up To Muscular Dystrophy
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Today 11-year-old Carmela Chillery-Watson kicked off her incredible charity walking challenge at Southampton Children’s Hospital 🌟 Carmela, who has congenital muscular dystrophy, is using all 657 affected muscles to take 6,570 steps in each of the hospitals where she has received care 💜 Her goal? To help create 657 dream experiences for others living with neuromuscular conditions, raising money for The Muscle Help Foundation. This morning staff lined to the corridors of G level to support Carm
8.8K views6 months ago
FacebookSouthampton Children’s Hospital
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From Sister to Mom: A 40-Year Journey with Muscular Dystrophy #musculardystrophy
310 views2 weeks ago
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