Bertie’s Buccaneers is a fundraising community and in particular a Family Fund for Muscular Dystrophy UK. Family Funds like ours together raise vital funds for groundbreaking research into Bertie’s condition. We are currently awaiting the final report on Prof. Muntoni’s recent project. Prof. Muntoni is now one of Bertie’s consultants at Great Ormond Street. Ullrich […]
Facilitating clinical trials for collagen VI-related conditions Here is just one of the vital projects into Bertie’s condition. It is being undertaken by Prof. Volker Straub at Newcastle (who diagnosed Bertie in 2014). This research is funded by the Family Funds for Muscular Dystrophy UK (MDUK). We are very proud to be making a difference. […]
We are often asked to explain Bertie’s condition. This is tough because it is complicated. However, as it is Rare Disease Day, here goes: One of Bertie’s genes is faulty, specifically a collagen VI gene. In his case he didn’t inherit a faulty gene, although you can. It just went askew and created an error […]