Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (2024)

25 April 2024

Over the past two months we’ve held information days in Scotland, England and Wales. We look back at the great feedback and talks from our three most recent events.

Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (1)

Over the past two months, following the success of our October 2023 Northern Ireland Information Day, we’ve held information days in Scotland, England and Wales. We look back at the great feedback and talks from our three most recent events.

Our information days have brought together people living with a muscle wasting condition, their families and carers, neuromuscular specialists, physiotherapist and many more. We’ve been blown away by the response and attendance at these events. As well as presentations from specialists in the neuromuscular field and updates from our own staff about the services we provide and the research we fund, people from the community have shared their own valuable lived experience, including tips and advice for others.

England Information Day

Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (2)

We held our on Saturday 9 March in Birmingham. People from all over England came to participate in an interactive day full of presentations, talks, and discussions.

The participants heard from a range of speakers including Dr John Ashworth and Dr Yvette Easthope-Mowatt on the emotional impact of living with a neuromuscular condition; Heather McMurchie and Jo Reffin on physiotherapy management; Angela Reddy, Critical Care Lead Dietician, on nutrition in adult muscular dystrophies; and Jane ‘O’ Connor, Neuromuscular Care Advisor for Transition, on understanding transition. 

Several people from our online therapeutic support sessions also attended, including the group facilitator and counsellor, Louise Halling, and they were able to meet in person for the first time, holding a breakout session together.

“The information day was a great chance to meet people face to face, people I had met on a screen. It was also a chance for those who took part in the therapeutic support groups to meet each other in person which has strengthened their bonds and friendship. All of this leads to a greater sense of support and camaraderie and above all, helps people (including me) to feel less isolated and alone.”

Louise Halling

Professional counsellor and psychotherapist (facilitates our virtual therapuetic support sessions)

Our Care, Campaigns and Support team were available all day to talk to people about our work and the services we provide, while ensuring attendees found the day positive and helpful.

“It was a great opportunity to meet up with my mentor who has the same strain of muscular dystrophy as myself. It was really nice to be able to meet face to face and chat about our life experience living with this condition. The conference itself gave my wife and I a greater insight into how the muscular dystrophy community works and the help and advice it can provide.”

Alan

England Information Day attendee

Scottish Conference

Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (3)

Our Scottish Conference took place on Saturday 23 March in Stirling. This was the first time it had been held in Scotland since 2018 and the community were happy to come together in person once again. There were talks from specialists, including Marina Di Marco, Consultant Neuromuscular Physiotherapist, on adult physiotherapy, exercise and fatigue management; Dr Lisa McCann, Senior Lecturer in Digital Health and Care, on attending university and higher education; and a panel discussion on inclusive education in primary and secondary school with Paul Nugent, headteacher, Gerry McMenemy, parent, and Martin Donald, teacher.

Attendees also got to hear from Sanjeev Mann, who lives with duch*enne muscular dystrophy, about his impressive music career and how his music supports his mental wellbeing.

“Sanjeev brought the Scottish conference to a close with a really powerful presentation showing that anything is possible in a world with a complete under-representation of disabled artists.”

Jackie Munro

Head of Regional Support, Outreach and Information (Muscular Dystrophy UK)

The team received lots of positive feedback about the success of the day:

“I attended MDUK’s Scottish conference today. The sessions were all so informative and valuable. For me, nothing is ever quite as valuable as connecting with others and feeling less alone as we navigate this journey.”

Anonymous

Scottish conference attendee

Wales Information Day

Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (4)

Our final information day was held on Thursday 18 April in Wales with people in the community, neuromuscular experts, and staff coming together. The day included talks from Rhiannon Edwards, Rare Diseases Implementation Group, Public Health Wales, on the Wales Rare Diseases Action Plan; Neuromuscular Specialist Physiotherapists Heledd Tomos and Hayley Davis on physiotherapy, exercise and fatigue management; Neuromuscular Care Advisor, Fiona Davies and Neuromuscular Clinical Nurse Specialist Clare Fletcher on information and support in the community. We also heard from voices in the community, Hasminder Alukah and John Foxwell.

One of the highlights from the day was John Foxwell’s talk about living with Pompe disease, his diagnosis, and what he’s done to raise awareness of the condition. Attendee Stuart said:

“Some of the sessions have been absolutely excellent. The last two were my favourites, on Pompe disease and physio.”

Stuart

Wales information day attendee

Everyone who attended said the day was informative, fun and eye-opening:

“The Information Day is so important because it’s a way for people with all types of muscular dystrophy to come together, share different experiences and feel less alone in their lives. It’s just been great to communicate with people who can relate to me and can understand what I’m going through. And also gather some new advice and information from specialists and people living in the muscular dystrophy community. I can’t wait until the next event.”

Cerys

Wales information day attendee

Upcoming Events

We have many opportunities throughout this year to connect with others in the community.

Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (5)

Information Days

Throughout the year we holdin-personInformation Days across theUK,whereyou can meet other people, get expertinformationand advice, and find out more about the services and support that we offer.

Read more

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Muscle Groups

Local Muscle Groups are our network of support groups across the UK. They’re a great opportunity to share experiences and meet other people affected by muscle wasting and weakening conditions in your area.

Read More

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More support groups

We know that talking to people with similar experiences is powerful. Our support groups are safe and welcoming places to talk to others affected by muscle wasting and weakening conditions, share experiences and meet people who understand whatyou’regoing through. Whetheryou’relooking to find support in-person, or online,we’vegot a support group for you.

Read more

Coming together as a community: celebrating our recent Information Days - Muscular Dystrophy UK (2024)

FAQs

How does muscular dystrophy affect day to day life? ›

Walking and climbing stairs may become difficult and some people may be unable to hop or stand on their heels. Onset of distal MD is typically between the ages of 40 and 60. Although distal MD is primarily an autosomal dominant disorder, autosomal recessive forms have been reported in young adults.

What does muscular dystrophy in the UK do? ›

The charity for muscle wasting conditions

With endless medical appointments, physiotherapy, treatments and respiratory support. That's why, for over 60 years, we've been building our community.

When is muscular dystrophy awareness month in the UK? ›

September is Muscular Dystrophy Month and as part the effort to raise awareness of this condition, we will be discussing what muscular dystrophy is, how it affects our bodies, and how cord blood stem cells could help sufferers.

What is the life expectancy for muscular dystrophy? ›

The life expectancy for muscular dystrophy varies significantly depending on the type. For example, people with duch*enne muscular dystrophy (DMD) often die from the condition by the age of 25. But other forms of muscular dystrophy, such as oculopharyngeal muscular dystrophy, don't typically affect life expectancy.

What foods should you avoid with muscular dystrophy? ›

We want to limit butter and other full- fat dairy products, fatty meats, fried foods, and packaged foods containing trans fat (partially hydrogenated or hydrogenated oils).

Will muscular dystrophy be cured? ›

Although there's no cure for any form of muscular dystrophy, treatment for some forms of the disease can help extend the time a person with the disease can remain mobile and help with heart and lung muscle strength. Trials of new therapies are ongoing.

Is muscular dystrophy a mental illness? ›

Muscular dystrophy is a progressive disease of muscle weakness, muscle atrophy and cardiac dysfunction. Patients afflicted with muscular dystrophy exhibit autonomic dysfunction along with cognitive impairment, severe depression, sadness, and anxiety.

Is muscular dystrophy painful? ›

In fact, preliminary results of our recent survey of people with MD show that 249 out of 321 people (78%) reported at least some daily pain. Of these individuals, 25% rated their average pain as being “severe,” or greater than five points on a scale of one (no pain) to ten (most severe pain).

Is muscular dystrophy inherited? ›

Most cases of MD are caused by gene mutations (changes in the DNA sequence) that affect muscle proteins. The mutations are usually inherited, but in some cases they occur spontaneously. These spontaneous mutations can then be inherited by an affected person's offspring.

Can babies have muscular dystrophy? ›

Myotonic Dystrophy: Myotonic dystrophy is the most common muscular dystrophy in adults but can also affect newborns and children. Newborns with myotonic dystrophy have low muscle tone and weakness at birth and typically need support for breathing and feeding.

Does muscular dystrophy affect the brain? ›

In addition, some patients with DMD have mild intellectual delay and heart problems (cardiomyopathy) due to lack of the dystrophin protein in the brain and in the heart muscle.

How does muscular dystrophy affect quality of life? ›

duch*enne muscular dystrophy (DMD) is a progressive, severe genetic disease. Most patients with DMD lose the ability to walk by their early teenage years and rarely survive beyond their 20s. Due to the physical symptoms of DMD, patients experience reduced quality of life (QoL) that hinders their abilities to work.

What lifestyle changes for muscular dystrophy? ›

Dietary and lifestyle changes cannot directly impact muscular degradation. However, many people with muscular dystrophy have limited mobility, which makes proper nutrition essential. A high-fiber, high-protein, low-calorie diet with proper fluid intake is recommended for many patients with muscular dystrophy.

How does muscular dystrophy affect social life? ›

Cognitive deficits (language problems, mental retardation, ADHD, etc.) causing social difficulties. Psychosocial factors such as anxiety or depression. The physical limitations and fatigue caused by duch*enne making it difficult for the child to keep up with others during play activities, sports, or games.

How does muscular dystrophy affect behavior? ›

However, young boys with DMD may have more difficulty with impulsivity and emotional control than other children their age. They are also more likely to be rigid and inflexible in their thinking, which can result in noncompliance or arguing. They may have difficulty making transitions.

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