Why it matters
CASK gene disorders are rare, complex, and life-changing. Families need clear information, community support, and a stronger research pathway.
About the mission
Built for families, research, and hope.
Project CASK Canada's mission is to drive the scientific breakthroughs needed to treat and cure CASK gene disorders.
What is CASK?
A rare genetic disorder that affects brain development.
CASK-related disorders are rare genetic conditions caused by pathogenic changes in the CASK gene, which is located on the X chromosome. The CASK gene provides instructions for making a protein that is important for brain development and neuron function.
The CASK-related disorder spectrum can include microcephaly with pontine and cerebellar hypoplasia (MICPCH) and X-linked intellectual disability with or without nystagmus. The effects can vary widely from person to person.
Families may face complex medical, developmental, and support needs. Project CASK Canada focuses on awareness, family connection, and research support so families are not navigating that path alone.
What we do
We raise awareness, support medical research, advocate for families, and create meaningful opportunities for people to contribute.
Where support goes
Current donations help establish early initiatives, outreach, and research-focused programs. Project CASK Canada is currently operating as a non-profit organization while working towards charitable status.
Guiding values
Hope with practical action.
- Family-first: communicate with clarity, warmth, and respect.
- Research-focused: keep attention on treatment progress and credible science.
- Community-driven: make it easy for supporters to help and share the mission.