Freddie is a happy, gorgeous, determined little boy. Two years ago he was diagnosed with Creatine Transporter Deficiency (CTD). He was born with a mutation in his gene which is responsible for moving creatine around the body. Creatine is essential to sustain the high levels of energy needed for muscle and brain development. 

There is currently no treatment options for CTD but Freddie  continues to fight to achieve and lives life to the full. However his condition severely impacts his quality of life and ours as a family.

The ACD is doing incredibly vital work that is getting us closer to finding a cure or a real treatment every day. There are a number of ongoing initiatives that have a real chance of finding a cure and bringing it to market. All we can currently do is help raise a little money to fund some of this groundbreaking research in the hope that one day Freddie can benefit.

For Freddie your contribution will make an impact whether you donate a little or a lot. 

Thank you for all your support.

Annabelle, James and family x 

I've included below a video with some more information 

https://www.youtube.com/watch?v=1VbJUHWhOqs

Challenges

On Sunday 2nd August we are doing a Walk for Strength for Freddie and the ACD. Our family and friends have registered to walk and we will all be walking to celebrate Freddie and raise awareness