Together, we raise awareness, demystify and share about #cavernousmalformation! Join in our events, contribute to our mission, wear your CM gear, and share CM information widely! Events | Cavernous Malformation Canada #raredisease
We celebrate physicians that make an impact to patients with #cavernousmalformation. Even in times of change, they provide high levels of care. From primary care to specialists involved in the care our our community, thank you! #cavernoma#NationalPhysiciansDay
Taylor bravely voices her unique experience of being diagnosed with a sporadic #cavernousmalformation as she awaited the birth of her first child. To read her inspiring story of hope, faith and remembering to see the good tr.ee/199cFy9jqh#patientvoice#cavernoma
Simona's story is courageously told by her husband "It is my hope that by sharing Simona's story I can spread awareness about cavernous malformation and rare disease" To learn more Simona's Story | Cavernous Malformation Canada
#RareDiseaseDay#cavernousmalformation
Kailley courageously shares her story of #spinalCM. As we lead up to #rarediseaseday, we think of patients that have a rare disease experience, like Kailley does. You are not alone. Kailley's Story | Cavernous Malformation Canada
#cavernousmalformation#cavernoma
Join us for an educational event featuring expert speakers, and meaningful moments of connection with others impacted by #cavernousmalformation. Register at 2026 Conference | Cavernous Malformation Canada cavernousmalformation.ca
Open to patients and family members of patients 18 years of age or older. Your peer support facilitator takes the discussion into relevant topics as you share, listen or feel a bit less alone in your journey. Register at events.teams.microsoft.com/.…... #cavernousmalformation