As I approach my 65th birthday in December, I am choosing to celebrate in a meaningful way by shining a light on a rare condition that has unexpectedly touched our family. Earlier this year, we received the news that my son has been diagnosed with Myotonic Dystrophy Type 1 (DM1) - a rare genetic condition that affects muscles and other vital systems of the body, including the heart and lungs, and is characterized by progressive muscle weakness and wasting.

Not long after this diagnosis, we discovered that my husband also has the condition. It has been a lot to come to terms with, as we had never heard of this condition before. If it hadn't been for a friend who identified the symptoms & immediately encouraged us to seek help, we may never have known about it. I am incredibly grateful to our friend & our GP who was wonderfully proactive in referring him to a neurologist who confirmed the diagnosis after tests.

At present, there is no cure and no specific treatment for Myotonic Dystrophy. This is why research is so vital. The dedicated team at Glasgow University is carrying out groundbreaking work on new ways to manage and eventually treat this condition. I am reaching out to family, friends, and anyone who can help by making a donation to support this important research. No matter the size of your contribution, it will help fund hope for better care and a brighter future for those affected by this condition.

Our target amount is £1,000