Written by Daniel Charouf, Medical Fellow in Neurogenetics at the McGill University Health Centre
As a pediatric neurologist trained in Lebanon, my journey into neurogenetics has been shaped by both challenge and opportunity. Moving to Montreal, Canada, to pursue a fellowship in pediatric neurogenetics has been a transformative experience, both professionally and personally.
Montreal is a uniquely cosmopolitan city, home to individuals from diverse ethnic, cultural, and genetic backgrounds. This diversity is reflected in the clinical cases we encounter at the McGill University Health Centre (MUHC), one of the largest referral centers in the region of rare diseases. The volume, complexity, and rarity of cases seen here have significantly enriched my clinical and research training.
Another important difference has been the availability of research opportunities. During my medical training in Lebanon, opportunities to participate in clinical research trials, particularly in neurology and rare diseases, were relatively limited compared with those available in Canada. Clinical trials were influenced by a variety of factors, including available infrastructure and the challenges of attracting industry-sponsored studies in a region facing economic and political uncertainties. Consequently, patients seeking access to experimental therapies or participation in specialized research studies often pursued these opportunities abroad.
In Canada, the landscape is markedly different. I am currently involved in more than six clinical trials, many of which are directly related to neurogenetic conditions. The accessibility of resources, structured research networks, and availability of investigational therapies have not only enhanced my academic growth but have also allowed me to contribute meaningfully to advancing patient care.
Photo : Daniel Charouf
Joining the RARE.QC network has been one of the most rewarding aspects of my experience here. I had the privilege of participating in their first scientific research day as an evaluator, an opportunity that allowed me to engage with passionate clinicians and researchers dedicated to rare diseases. Being part of this network has gone beyond academic enrichment; it has had a profound personal impact.
Witnessing the strength of collaboration among physicians and their shared commitment to improving patient outcomes has been truly inspiring. Hearing directly from patients and their families made an even deeper impression, as their stories and experiences highlighted the real impact of coordinated care and research. These moments have reshaped how I see my role, not only as a physician but also as a trainee working toward a larger purpose.
RARE.QC has opened doors for meaningful collaboration in ways I had not experienced before, bringing together clinicians and aspiring physicians to work collectively toward advancing research in rare diseases. Being part of this network has shown me, firsthand, the value of building strong connections and learning from one another. It has reinforced my belief that collaboration is not just beneficial, but essential in driving innovation in diagnosis, treatment, and ultimately improving patient care.
To learn more about Dr Charouf’s work or to get in touch, please contact him at daniel.charouf@outlook.com
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