11. Duchenne UK Family Funds
We know that the people who are most passionate about raising money to find treatments and a cure for Duchenne Muscular Dystrophy are those who live with it every day. That's why we at Duchenne UK ...
12 Syys 20199min
9. Growing Up With DMD - Saul Catlin
Our host Clare Runacres speaks to Saul Catlin about growing up with DMD. Saul is an 18 year old man living with DMD. He is studying games design at university. If you have any questions or would lik...
31 Heinä 201914min
8. The DMD Hub - Alex Johnson, Emily Crossley, Prof Volker Straub and Emma Helsop
Our host Clare Runacres speaks about the DMD Hub with Prof Volker Straub - Professor of Medicine and Professor of Neuromuscular Genetics at Newcastle University, Emma Heslop - DMD Hub manager and Duch...
8 Heinä 201912min
7. What Is Duchenne - Dr David Bull
Our host Clare Runacres speaks with Duchenne UK's Director of Research, Dr David Bull, about Duchenne muscular dystrophy. If you have any questions please email support@duchenneuk.org.
24 Kesä 201926min
6. SPECIAL EPISODE - Testosterone as a treatment for DMD with Prof Volker Straub
In this podcast we speak with Prof Volker Straub about Testosterone, which is sometimes given to patients with Duchenne Muscular Dystrophy (DMD) who take steroids. Steroids are part of the recognise...
1 Huhti 201912min
5. Decoding Duchenne - Clinical trials with Dr David Bull
In this episode Dr David Bull gives a breakdown about how clinical trials work. This was recorded at our Patient Information Day in September 2018. We host free patient information days twice a year. ...
7 Tammi 201917min
4. Decoding Duchenne - Advice From Parents
In this weeks episode of Duchenne UK's DECODING DUCHENNE podcast series, our host Clare Runacres interviews Lisa Kuhwald and Alex Johnson, whose son's both have Duchenne, about the time of diagnosis. ...
21 Joulu 201825min
