Medical Independent: New molecular technology required for SCID and SMA screening – HSE
The introduction of new molecular technology to the National Newborn Bloodspot Screening Laboratory (NNBSL) is required to implement screening for severe combined immunodeficiency (SCID) and spinal muscular atrophy (SMA), according to the HSE. The Executive indicated this was an additional requirement to the “substantial” body of work required to introduce any new condition to the programme.
Help Us Understand Pain in Children and Young Adults With Physical Disabilities
By sharing your experiences, you will help improve understanding, shape future research, and contribute to better supports aimed at reducing pain for children and young people with physical disabilities.
Translarna™ (ataluren) Market Authorisation Not Renewed by European Commission.
The European Commission (EC) has announced that it will not renew the market authorisation of Translarna™ (ataluren) for treating nonsense mutation Duchenne muscular dystrophy. After re-examining the data, the EMA’s human medicines committee (CHMP) concluded that the effectiveness of Translarna could not be confirmed.
Collaboration with Brona Mulligan – Exploring Health-Related Quality of Life of Adults living with Neuromuscular Conditions
MDI had the pleasure of collaborating with Brona Mulligan, who was completing her Master’s in Health Psychology at the University of Galway. A dedicated group of PPI contributors - individuals with lived experience of neuromuscular conditions - worked closely with Brona to help shape her research question and played an integral role throughout the research process.
Call of interest: Global DMD Adult Group
In the coming months, the group hopes to expand these discussions, focusing on issues like navigating life’s milestones differently, especially as adults with DMD and BMD face unique challenges in adulthood. In collaboration with the World Duchenne Organization, the group intends to explore themes such as independence, relationships, and navigating life transitions.
New Resource Available: Becker Muscular Dystrophy Guide for Families Now in English!
This guide offers an accessible yet comprehensive overview of BMD, providing essential information on the condition’s many aspects. Available in digital format, it’s a valuable resource for patients and families seeking clarity and guidance.
EMA Recommend Against Renewing Translarna for DMD
The Committee for Medicinal Products for Human Use (CHMP), part of the European Medicines Agency, has again advised against renewing approval for Translarna (ataluren), a drug used to treat Duchenne muscular dystrophy (DMD) caused by a nonsense mutation in the dystrophin gene.
Inclusion of children and young people in clinical trials across Europe
The aim of this group is to facilitate the inclusion of children and young people in clinical trials across Europe avoiding any language barriers. The group recently identified that some patients could not take part in a clinical trial because they do not speak the official language of the country where the trial is performed.
MDI is a proud member of Health Research Charities Ireland and supports the HRCI manifesto
HRCI members demand a strong, forward-thinking Programme for Government which includes a genuine commitment to improving health outcomes and reducing the burden of illness. Investing in health research (including life sciences, clinical research and all forms of R&D in health) is a commitment to the well-being of the population, the advancement of medicine and care, and the overall prosperity of our society.
September 30th is Limb Girdle Muscular Dystrophy Awareness Day!
Limb Girdle Muscular Dystrophy Awareness Day is an annual collaborative effort to globally raise awareness of individuals living with limb girdle muscular dystrophy (LGMD).
Brain Involvement in Dystrophinopathies (BIND) Project
The BIND project is the first large-scale effort to better understand brain involvement in Duchenne and Becker Muscular Dystrophy (DMD and BMD). Funded by the EU, it brings together 19 partners from Europe and Japan. While muscle weakness has been the primary focus in recent decades, brain involvement has received less attention.
September 25th is World Ataxia Awareness Day
International Ataxia Awareness Day (IAAD) is on September 25th of each year. It is a coordinated effort from individuals and Ataxia organizations around the world to help shed light on this rare disease. NAF is committed to leading the way on this outreach effort – but we need your help! We encourage individuals and disease organizations to join us by planning events and/or awareness campaigns for IAAD.
Today is World Myositis Day!
Myositis is an inflammatory autoimmune condition that can cause muscles to become weak and painful. Idiopathic inflammatory myopathies are an umbrella term for the different types of myositis. These autoimmune conditions mean the body attacks its own muscles, connective tissue, blood vessels, skin, lungs, and other organs. This often occurs together with other symptoms, such as muscle swelling, pain, fatigue, difficulty moving limbs or lifting arms, increased falls, trouble swallowing, and others.
This Week is World Mitochondrial Awareness Week!
World Mitochondrial Disease Week raises awareness about mitochondrial diseases (mito). It aims to improve the lives of people affected by mito and to increase awareness among doctors and the general public.
Today Is International Myotonic Dystrophy Awareness Day!
The colour green has been chosen to represent International Myotonic Dystrophy Awareness Day which takes place on 15 September and many buildings throughout the world will be lit up green on the day! As MDI’s News Update focused on Myotonic dystrophy last January, we are happy to provide an update on research developments since then.
Thank you to everyone who has participated in our research collaboration studies!
Thank you to everyone who has participated in our research collaboration studies this year. ‘Supporting Transitions to Adulthood Resources (STAR) Project’ and ‘The Lived Experience of Health-Related Quality of Life for Adults with Muscular Dystrophy’ have closed. We will publish reports on our website once the results have been analysed.
7 September is World Duchenne Awareness Day
On 7 September the World Duchenne Organisation will launch a documentary that portrays the lives of people living with Duchenne muscular dystrophy across the globe, it will share their journeys, challenges and successes, and captures the resilience and determination of the Duchenne community. People are encouraged to share it with their wider communities.
MDI is a partner in Rare Diseases Irelands campaign ‘Get Rare Aware’.
This campaign is calling on the Government to urgently double the number of conditions screened for in Ireland’s newborn bloodspot screening (NBS) programme also known as the ‘heel prick test’ to the European average of 18.
CHMP Issues Negative Opinion on Translarna™ Following European Commission Request for Review
EMA’s human medicines committee (CHMP) has recommended non-renewal of the conditional marketing authorisation of Translarna™ (ataluren) for the treatment of nonsense mutation Duchenne muscular dystrophy in Europe. This opinion follows the return of the previously issued negative opinion by the European Commission for re-review. Click here to read PTC Therapetics press release.
New Study on Biomarkers for Charcot-Marie-Tooth Type 1
This study is a continuation of prior research that has shown promising results in understanding CMT1A more deeply. Participation requires a single visit to Tallaght University Hospital for a standard blood draw and clinical assessment, which is conducted in one day to minimise inconvenience to participants. Full details about this study are available here.