The Duchenne Research Fund
Non-profit Organizations • 
United Kingdom • 1-10 Employees
Company overview
| Headquarters | United Kingdom |
| Phone number | +441119068 |
| Website | |
| NAICS | 813 |
| SIC | 873 |
| Founded | 2007 |
| Employees | 1-10 |
| Socials |
Key Contact at The Duchenne Research Fund
Sheli Rodney
Director of Operations
About The Duchenne Research Fund
The Duchenne Research Fund, previously the GM Trust, was established in May 2007 to identify and fund research into finding a cure for the devastating disease that is Duchenne Muscular Dystrophy (DMD). DMD is a progressive and fatal muscle-wasting disease that currently boasts a 100% fatality rate. It almost exclusively affects boys, causing them to be wheelchair bound by their teens and fighting for their lives in their early twenties. One in every 3,500 baby boys are born with DMD worldwide. In the UK, 100 boys a year are born with DMD and 2 boys die each week of the disease, making it one of the World’s biggest genetic killers. We are committed to looking at any possible route for such a cure and will not stop looking until a cure is found. We will facilitate and fund new research into minority strains of DMD and focus on the exceptions of the condition with the belief that this will hold the key to the cure. The Duchenne Research Fund will continue to raise the funds needed to facilitate this process.
The Duchenne Research Fund revenue & valuation
| Annual revenue | $434,543 |
| Revenue per employee | $109,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Non-profit Organizations industry and current estimated revenues | $1,400,000 |
| Total funding | No funding |
Employees by Management Level
Total employees: 1-10
Seniority
Employees
Funding Data
The Duchenne Research Fund has never raised funding before.
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