CGEM works with families to develop tailored treatments for each patient. We are pleased to share our success stories that shine a spotlight on how innovative treatments are leading to best practices in genomic medicine.
Our Patient Success Stories
The Gift of Seeing Colour: For those of you who are parents, think back to that emotional day in the hospital when your child was born. Now imagine that prior to delivery, your doctor tells you there’s a 50-50 chance that your child could have FEVR, a gene mutation that causes blindness...
The Gift of Mowing the Lawn:
Growing up, most of us dream of owning a home. But for people like Ryan, who was born with Fabry disease, the burden of upkeep often makes home ownership unattainable...
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Patients participating in CGEM studies are by referral only. If you are a patient who is interested in genomic medicine, please speak to your doctor who will connect with one of our referring clinicians.