Canadian Fire Fighters, donors, like-minded partners and the neuromuscular community are driving real progress in research – breaking barriers by building hope

FOR IMMEDIATE RELEASE – Muscular Dystrophy Canada is thrilled to advance neuromuscular research by awarding $900,000 to the recipients of the 2025 annual Neuromuscular Research Grants competition. Through this year’s competition we are excited to be supporting clinical and translational research projects focused on managing symptoms, healthcare assessments, understanding diagnosis and disease progression, enhancing care, discovering new treatments, therapies and moving research towards the development of cures. While this year’s competition supports research across a range of neuromuscular disorders, we are especially proud to fund two projects focused on Friedreich ataxia (FA) – made possible through a dedicated joint sub-call in partnership with Ataxia Canada.

“These grants are a vital step in breaking down barriers for the Canadian neuromuscular community. Through them, we can expand research infrastructure by funding research across a broad set of neuromuscular disorders, while also helping to fill current gaps in the funding landscape and honouring our commitment to improve the lives of individuals affected by neuromuscular disorders,” said Stacey Lintern, CEO, Muscular Dystrophy Canada. “A special thank you to the clinicians and researchers on our Scientific Review Panel, and our Lived Experience Readers who volunteered their time and expertise in selecting this year’s recipients and ensuring a rigorous, high integrity selection process.”

Neuromuscular research grants are made possible each year thanks to the generosity of our supporters who work tirelessly to support the neuromuscular community. Generous donors, passionate fundraisers, like-minded partners, and dedicated Fire Fighters across the country make it possible for Muscular Dystrophy Canada to fund these projects, ensuring that Canada is prepared to provide access to new life-changing treatments, while also filling the immediate need for advanced treatment and care options. Muscular Dystrophy Canada is committed to working alongside our donors and partners to keep neuromuscular research moving forward—especially in rare conditions like FA, where joint funding leverages shared resources and significantly amplifies impact. By funding ground-breaking research for all neuromuscular disorders, we can continue to leverage the momentum and progress that has been made to date, and fuel future discoveries.

The projects submitted this year for consideration were of remarkable quality, and we thank each and every team for their commitment in doing this important work. Together, we’re shaping a future where every Canadian diagnosed with a neuromuscular disorder can access the care and research they need. From the entire neuromuscular community, congratulations to all recipients!

2025 CLINICAL AND TRANSLATIONAL SCIENCE RESEARCH GRANT RECIPIENTS:

Dr Carolina Barnett-Tapia MD PhD
Multimodal remote screening for bulbar dysfunction in myasthenia gravis – University Health Network Toronto General Hospital

Dr Cynthia Gagnon PhD
Selecting a patient-reported outcome to enhance dysphagia assessment in myotonic dystrophy type 1 and Friedreich ataxia – Université de Sherbrooke

Dr Jodi Warman-Chardon MD PhD FRCPC (Neurology)
Biomarker discovery in inclusion body myositis – Ottawa Hospital Research Institute

Dr Melissa Fiscaletti MD FRCP(C) MSc
Harnessing polygenic risk scores to transform osteoporosis screening in Duchenne muscular dystrophy – Centre hospitalier universitaire Sainte-Justine

Dr Vincent Picher-Martel MD
Development of antisense oligonucleotide therapy for oculopharyngeal muscular dystrophy using advanced 3D tissue modeling – Centre de recherche du CHU de Québec-Université Laval

Dr Marie-Claude Sincennes PhD
Analysis of tissue organization and cell type-specific defects in oculopharyngeal muscular dystrophy – National Institute of Scientific Research

Dr Mark Currie PhD
Developing a reporter system for rapid screening of drugs to treat Emery-Dreifus muscular dystrophy – University of Toronto

Dr Yan Burelle PhD
Targeting mitochondrial quality control to promote muscle regeneration in Duchenne muscular dystrophy – University of Ottawa

Dr Toshifumi Yokota PhD FCAHS
Development of an enhanced antisense therapy using lipid nanoparticles for Friedreich ataxia and spinobulbar muscular atrophy – University of Alberta

Learn more about Muscular Dystrophy Canada’s research investments and the incredible projects that will improve our understanding and drive the development of new treatments and cures for neuromuscular disorders by visiting muscle.ca.

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ABOUT MUSCULAR DYSTROPHY CANADA

Muscular Dystrophy Canada’s mission is to enhance the lives of those affected by neuromuscular disorders by continually working to provide ongoing support and resources while relentlessly searching for a cure through well-funded research. To learn more about Muscular Dystrophy Canada, please visit muscle.ca or call our toll-free number at 1-800-567-2873.

MEDIA CONTACT

Homira Osman
Vice President, Research and Public Policy
Homira.Osman@muscle.ca
437-912-9037

$360,000 in fellowships awarded to advance neuromuscular research and healthcare

FOR IMMEDIATE RELEASE January 19, 2023

Muscular Dystrophy Canada (MDC) together with the Neuromuscular Disease Network for Canada (NMD4C) are excited to announce the recipients of a funding competition, which awarded national post-doctoral fellowships in neuromuscular research and clinical fellowships in neuromuscular medicine and electromyography.
This competition saw many incredible applicants and involved a thorough and extensive review by leading Canadian neuromuscular researchers and clinicians to ensure the most promising and top-ranked researchers, and leaders in neuromuscular care, received funding.

“This initiative helps train and educate the next generation of neuromuscular researchers and clinicians. The post-doctoral fellowships help strengthen neuromuscular research capacity, and the clinical fellowships will strengthen the specialist care available to the neuromuscular community,” said Stacey Lintern, CEO, Muscular Dystrophy Canada. “For our clients, that means we are investing in the sustainability of neuromuscular research, which brings us one step closer to finding cures, and in skilled clinicians that will provide clinical care to individuals affected by neuromuscular disorders and help raise standards of care.”

Learn more “$360,000 in fellowships awarded to advance neuromuscular research and healthcare”

International research competition results in funding for innovative Collagen 6- related dystrophy research projects

Muscular Dystrophy Canada (MDC) is pleased to announce two Collagen 6- related dystrophy (Col6-RD) research projects will be funded thanks to generous donors, and a partnership with Cure CMD (Congenital Muscular Dystrophy).

Collagen 6- related dystrophies (Col6-RD) are genetic types of muscular dystrophies that include Bethlem myopathy, Ullrich congenital muscular dystrophy and intermediate forms (Limb-girdle muscular dystrophy R22/D2). They are characterized by muscle weakness that can begin in infancy and can affect mobility, breathing, eating and activities of daily living.

Currently there is no cure for Col6-RD and knowledge on how the disorder develops is limited. Research is the essential next step towards therapy development.

Learn more “International research competition results in funding for innovative Collagen 6- related dystrophy research projects”

Announcing Muscular Dystrophy Canada’s 2022 Research Grant Competition winners!

We are pleased to share that we are funding nine new clinical and translational science research projects focusing on spinal muscular atrophy, Duchenne and Becker muscular dystrophies, immune mediated neuropathies, congenital myasthenic syndromes, immune-mediated neuromuscular junction disorders, myotonic dystrophy, occulopharyngeal muscular dystrophy, spinal bulbar muscular atrophy (Kennedy disease), and other related neuromuscular disorders.

Thank you to our donors who helped make this possible and to our Research Grant Review Panels of researchers, clinicians and community members with lived experience who volunteered their time to carefully review and help narrow down applications to our final projects.

“Through these exciting projects, these talented and dedicated Canadian researchers will develop new methods for disease diagnosis, uncover novel insight into disease pathogenesis, and develop new treatments options, amongst other meritorious projects,” says Dr. Robin Parks, Chair of the Medical and Scientific Advisory Committee for Muscular Dystrophy Canada (MDC) and Chair of the Translational Science Review Panel. “Through their support of MDC, donors, patients and their families are helping fund outstanding research projects that will move neuromuscular research forward and ultimately improve care and quality of life for those affected by neuromuscular disorders – which aligns with MDC’s mission.”

“We are extremely pleased with breadth of proposals received to our call for clinical and translational science research proposals we received this year. This is a hopeful sign of the continued momentum and progress in neuromuscular research. The nine selected recipients show exemplary innovation, dedication and promise of potential impact for a wide range of neuromuscular disorders,” says Stacey Lintern, CEO of Muscular Dystrophy Canada. “Because of our incredible community, we are able to fill a critical gap in research funding. We know how much change is possible from Canadian researchers and we are continually working with our supporters to ensure we invest in meaningful ways.”

Thank you to the Canadian neuromuscular research community for putting forward impactful applications.

2022-2023 WINNERS:

  • Dr. Thomas Durcan, MD, The Royal Institution for the Advancement of Learning/McGill University
    Building a screenable human 3D neuromuscular junction model for neuromuscular disorders
  • Dr. Christopher Perry, MD, York University
    Mitochondrial-targeted therapies to improve Duchenne muscular dystrophy outcomes
  • Dr. Craig Campbell, MD, London Health Sciences Centre Research Inc. (Lawson Health Research Institute)
    Genome-wide DNA methylation profile in Duchenne Muscular Dystrophy
  • Dr. Michael Berger, MD, University of British Columbia
    Measuring balance in chronic inflammatory demyelinating polyneuropathy
  • Dr. Bernard Jasmin, MD, University of Ottawa
    Endurance training as a novel therapeutic strategy for Myotonic Dystrophy type 1
  • Dr. Jodi Warman-Chardon, MD, Ottawa Hospital Research Institute
    QP-OPMD: Quantitative MRI Imaging to Assess Progression in Oculopharyngeal Muscular Dystrophy
  • Dr. Kerri Schellenberg, MD, The University of Saskatchewan
    Exploring the impact of Spinal Bulbar Muscular Atrophy on persons self-identifying as Indigenous
  • Dr. Reshma Amin, MD, The Hospital for Sick Children Dr. Aaron Izenberg, MD, Sunnybrook Health Sciences Centre
    The Transition of TEENagers with Spinal Muscular Atrophy to a Multi-Disciplinary Adult Program
  • Dr. Maryam Oskoui, MD, The Research Institute of the McGill University Health Centre
    Motor network connectivity in spinal muscular atrophy: new pathways for intervention

WATCH THE ANNOUNCEMENT

MDC funds seven new projects to propel research forward during challenging times

Toronto, Ontario – Muscular Dystrophy Canada (MDC) is proud to announce an investment of $400,000 to fund seven new research projects in 2021 through the MDC Neuromuscular Disorder (NMD) Research Grant Competition, a dedicated Canadian source of funding for neuromuscular research. MDC will also invest in an international, collaborative, $1.15 million, research project through the European Joint Programme on Rare Diseases (EJP RD).

“Despite an unprecedented time, during which many like-minded organizations and agencies are not in a position to offer research funds in Canada, MDC is able to demonstrate its ongoing commitment to discovering cures,” stated Stacey Lintern, CEO, Muscular Dystrophy Canada. She added, “while others redirected their research funds towards the coronavirus, and this was much-needed, MDC recognized the need to maintain momentum, and ensure the incredible advances currently taking place in research are accelerated.”

In addition to the seven new projects being funded, MDC will continue its support of 12 active research studies from the previous year.

“MDC grant recipients are selected by medical and scientific professionals, as well as Canadians with lived experience. Research proposals are judged based on scientific merit, and the potential to translate findings into initiatives that will positively impact the NMD community,” said Dr. Daria Wojtal, Director of Research, Muscular Dystrophy Canada.

MDC relies on the generosity of donors to fund life-changing research.

Dr. Rashmi Kothary, Deputy Scientific Director and Senior Scientist at the Ottawa Hospital Research Institute and 2019-2020 MDC research grant recipient, said “to the families and donors, I would have to say a huge thank you. From my first day as a researcher, getting my first grant from MDC, you were there. Thank you for sticking by the research community for many, many years. Hopefully we can pay back the trust that you put in us.”

MDC is honoured to fund the exceptional and bright researchers, clinicians and academics who will lead these seven new projects taking place in hospitals and universities across Canada, and around the world.

The 2020-2021 research grant recipients are:

  • Dr. Alex Parker
    A Pharmacogenetic Pipeline for Charcot-Marie-Tooth Disease
  • Dr. Colin Crist
    Promoting Muscle Repair by Pharmacological Inhibition of eIF2a Dephosphorylation
  • Dr. Mohamed Chahine
    Human iPSC-derived Neurons as a Model of Congenital Myotonic Dystrophy Type 1
  • Dr. Nadine Wiper-Bergeron
    Improving Myoblast Transplantation Outcomes via Pharmacological Reprogramming
  • Dr. Nicolas Dumont
    Targeting Defective Stem Cells in a Preclinical Model of Myotonic Dystrophy Type 1
  • Dr. Rima Al-Awar (EJPRD/CIHR Co-funded)
    Safety and Efficacy of a Possible Epigenetic Therapy for Facioscapulohumeral Muscular Dystrophy
  • Dr. Toshifumi Yokota
    Enhancing the Efficacy of Antisense Oligonucleotide Therapy for Facioscapulohumeral Muscular Dystrophy

“Congratulations to the 2020-2021 grant recipients. MDC is committed to supporting opportunities that fulfill our commitment to invest in research that leads to information on diagnosis, treatment and health management of neuromuscular disorders; and, we’re confident that the research funded this year will bring us closer to cures for all children, youth, adults and families affected by neuromuscular disorders,” added Lintern.

DISCOVER THE PROJECTS WE SUPPORT

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ABOUT MUSCULAR DYSTROPHY CANADA

Muscular Dystrophy Canada’s mission is to enhance the lives of those impacted with neuromuscular disorders by continually working to provide ongoing support and resources while relentlessly searching for a cure through well-funded research. To learn more about Muscular Dystrophy Canada, please explore our website or call our toll-free number at 1-800-567-2873

MEDIA CONTACT

Heather Rice
Muscular Dystrophy Canada
heather.rice@muscle.ca
902-440-3714