We are glad you have found us!

Perhaps you have DM yourself, or are a parent of a child with Congenital Myotonic Dystrophy. You may be a grandparent, a relative or friend. Maybe you are a professional, researching the condition, or perhaps you are still unsure whether you or your child or loved one has Myotonic Dystrophy - everyone is welcome!

Please take time to have a good look at our site, and if you have any questions, ideas, information, or just want to say hello - please do feel free to email us!



Cure DM Residential at Calvert Trust.

Introduction video:

After watching the video, please click the following image to check out the

 PDF Booklet 

for more details and information:



Would you like to join us?

Register your interest HERE!




Miles Cubs!

Cure DM are delighted to announce our new campaign.

Miles is our much loved Mascot for our families and children living with DM, and in the past we have sent him to families in need of support or having a celebration. He is getting a bit old now, and wants to have a bit of a rest so will reside with the CURE DM team.

CLICK HERE to find out how you could have your own cub!

We will be sending cubs out to the children in our community. This campaign is funded by our amazing supporters, we cannot do this without the ongoing fundraising and support we are receiving.

THANK YOU to everyone who is helping make this possible. 


Donate/Fundraise for Cure DM

Raising Awareness / Provide Support / Fund Research


Cure DM is a registered charity, where all funds are used to provide family help and support to those living with the condition NOW. We arrange get togethers and enable families to connect, as well as funding/facilitating research. 

We would love your support in any way at all, please contact us to find out how we can help you, to help us, to help others!

email: curedm@outlook.com