Raising money for muscular dystrophy
4:23
Global News
Raising money for muscular dystrophy
Richard Collins and Elijah Roy talk about the Mission Firefighter Truck Pull this weekend to raise funds for a worthy cause
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5.7K views · 97 reactions |  Your donation has double the power this week! Every pound you donate will be doubled by our donors and trusts. Over 110,000 people in the UK struggle with muscle wasting conditions. It can be exhausting and lonely. Help us give life-changing support, treatment advances, and help to those who need it most. Double your impact and make a difference today: https://loom.ly/yCGAwVE #GivingTuesday | Muscular Dystrophy UK | Facebook
0:19
5.7K views · 97 reactions |  Your donation has double the power this week! Every pound you donate will be doubled by our donors and trusts. Over 110,000 people in the UK struggle with muscle wasting conditions. It can be exhausting and lonely. Help us give life-changing support, treatment advances, and help to those who need it most. Double your impact and make a difference today: https://loom.ly/yCGAwVE #GivingTuesday | Muscular Dystrophy UK | Facebook
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We are so grateful to Ethan LyBrand, who lives with Duchenne muscular dystrophy, for serving in his role as MDA National Ambassador for the last three years. Ethan has brought so much joy as he raised awareness and funds for MDA to empower all families living with neuromuscular disease. Let’s take a look back at some of the laughs he gave us along the way in his series “Joke of the Day for MDA”! Thank you, Ethan! | Muscular Dystrophy Association
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We are so grateful to Ethan LyBrand, who lives with Duchenne muscular dystrophy, for serving in his role as MDA National Ambassador for the last three years. Ethan has brought so much joy as he raised awareness and funds for MDA to empower all families living with neuromuscular disease. Let’s take a look back at some of the laughs he gave us along the way in his series “Joke of the Day for MDA”! Thank you, Ethan! | Muscular Dystrophy Association
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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
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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
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5.7K views · 97 reactions |  Your donation has double the power this week! Every pound you donate will be doubled by our donors and trusts. Over 110,000 people in the UK struggle with muscle wasting conditions. It can be exhausting and lonely. Help us give life-changing support, treatment advances, and help to those who need it most. Double your impact and make a difference today: https://loom.ly/yCGAwVE #GivingTuesday | Muscular Dystrophy UK | Facebook
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5.7K views · 97 reactions |  Your donation has double the power thi…
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FacebookMuscular Dystrophy UK
We are so grateful to Ethan LyBrand, who lives with Duchenne muscular dystrophy, for serving in his role as MDA National Ambassador for the last three years. Ethan has brought so much joy as he raised awareness and funds for MDA to empower all families living with neuromuscular disease. Let’s take a look back at some of the laughs he gave us along the way in his series “Joke of the Day for MDA”! Thank you, Ethan! | Muscular Dystrophy Association
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We are so grateful to Ethan LyBrand, who lives with Duchenn…
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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
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Community rallies around Michael to support muscular dystrophy campaign. $3 million so far.
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🌍 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
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