Weekly Spotlight - 31.10.24

Genetic breakthroughs in muscular dystrophy; community support initiatives; inspiring advocacy for disability awareness

In the News

Finnish Founder Variant Found in Estonian Family's Muscular Dystrophy Case

An Estonian family was found to have the Finnish founder variant (FINmaj) causing muscular dystrophies. This discovery marks the first detection outside Finland, raising questions about its origin. The study highlights the importance of genetic research in understanding and managing these conditions, offering hope for affected families.

MDA's Holiday Campaign Supports Families with Neuromuscular Diseases

The Muscular Dystrophy Association's Holiday Retail Campaign runs nationwide from November to January, aiming to raise £750,000. Retail partners like GPM Investments and Circle K encourage donations at checkout. Funds support research and care for neuromuscular diseases, fostering hope and independence for affected families.

Rhys Hoskins Wins Two Prestigious Players Choice Awards for 2024

Rhys Hoskins, a Muscular Dystrophy Association advocate, received two 2024 Players Choice Awards for his philanthropy and community service. His dedication to MDA, alongside his wife Jayme, has significantly impacted families with neuromuscular diseases, raising funds and awareness. Their efforts inspire hope and support within the community.

Victoria Nedza Inspires Change for Disability Awareness and Inclusion

Victoria Nedza, diagnosed with Limb-Girdle Muscular Dystrophy, advocates for disability awareness. She speaks at schools and Capitol Hill, promoting inclusion and empathy. As a representative for The Speak Foundation, she inspires others. A robotic arm from Widener University students aids her independence, highlighting community support and innovation.

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Health Spotlight’s LGMD2L is a Contentive publication in the Healthcare division