Our Public Engagement Activities
Giving back to the rare disease community
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Giving back to the rare disease community 〰️
The SMA Trust Mud Run: A great way to get muddy and raise money!
MDUK 10K Town and Gown: A great way to get fit and raise money!
The SMA Trust Ride the Scorpion: A great way to get fit and raise money (with the Talbot and Turner lab members)!
Annual Cure SMA Family and Research Conference: Losing again at the annual wheelchair race and promoting SMA awareness at Disney (with the Claus, Wirth, Murray, Kothary and Rage lab members)!
Soapbox Science: A great way to promote women scientists and our research on muscle in health and disease.
Bake Sale: a great way to raise funds for charities such as Muscular Dystrophy UK and SMA UK.
Keswick to Barrow walk: a challenging way to raise funds for SMA UK
SMA Europe & Rolling Journalists Interview: https://www.linkedin.com/posts/321rolling-smaeurope-spinalmuscularatrophy-ugcPost-7493955633365417984-CNDJ/?utm_source=share&utm_medium=member_desktop&rcm=ACoAAF6P6HAB4cGrUZOk6DejjtA-4SsKXHxlZGE
Origins Health Insights & Bedrock Healthcare Communications Rare Disease Day 2021 awareness video: https://bedrock-health.com/rdd/
Neural Central Peek Behind The Paper Interview: https://www.neuro-central.com/2019/08/20/peek-behind-paper-melissa-bowerman-spinal-muscular-atrophy-need-continued-funding/
SMA Support UK SMA scientist Q&A: http://www.smasupportuk.org.uk/melissa-bowerman