26 June 2024
Patient Thomas Hobbs, who has lived with myotonic dystrophy, an incurable muscle-wasting disease, for over 10 years attended the day and said:
"I found the Myotonic Dystrophy Patient Information Day very informative. The first talk on research was very encouraging with tests going on and research providing positive results. It was good to find out about the patient registry and I will be signing on to it. It was fantastic to have so many professionals together on the day to give so much valuable advice. These events give patients and carers the opportunity to meet up and talk to others in the same situation and this is greatly appreciated."
Myotonic dystrophy is the commonest form of muscular dystrophy affecting multiple organs other than skeletal muscles, such as the heart muscle, muscles important for breathing, eyes, bowels, and pancreas and even the brain and skin. Impact on cognition can lead to poor concentration, memory, and ability to motivate self.
Myotonia (the inability to relax muscles at will) is another key feature of the condition; this can be demonstrated in the hands by the inability to let grip go following a handshake.
There are two types of myotonic dystrophy. Type 1 tends to be more severe and is more common than type 2. Type 2 is usually diagnosed in adulthood whilst type 1 can be present and diagnosed from birth through to late adulthood.
Here’s a few facts about our services and the specialist care and support we provide to patients from across the region and beyond, including South Yorkshire, North Derbyshire and North Lincolnshire as one of 24 MDUK Centre of Excellences in the UK:
ENDS