CANADIAN CHIARI ASSOCIATION
TV Show Host, mom; former @townofajax Mayoral Candidate & @lakeridgehealth Trustee. By #carionfennfoundation The Carion Fenn Foundation is a Registered Charity established to provide support, education and resources to the public and individuals impacted by Syringomyelia, Chiari Malformation, Mental Health, Chronic Diseases and Rare Diseases.
The Canadian Chiari Association (CCA) is a nonprofit charitable organization based in Canada, dedicated to raising awareness, providing support, and improving the quality of life for individuals affected by Chiari malformations. Established with the mission to serve those living with this neurological condition, the CCA works to connect patients, caregivers, and healthcare providers through education and advocacy efforts.
Mission and Activities
The primary focus of the Canadian Chiari Association is to enhance public and medical community awareness about Chiari malformations, a disorder involving structural defects in the cerebellum at the base of the skull. Through its initiatives, the CCA provides resources and support networks for individuals diagnosed with Chiari malformations, helping them navigate medical, social, and emotional challenges associated with the condition. The organization also promotes research and collaboration among clinicians and scientists to advance understanding and treatment of Chiari malformations.
Organizational Structure
The CCA operates as a registered charitable organization under business registration number 836112433RR0001. It functions as a community-benefit organization with a focus on core health care and treatment support related to Chiari malformations. Its nonprofit status enables it to mobilize resources, host awareness campaigns, and facilitate patient and family engagement on a national scale.
Impact
By fostering a supportive community and disseminating information, the Canadian Chiari Association plays a critical role in addressing the needs of Chiari malformation sufferers in Canada. The organization empowers patients through education and advocacy, while also encouraging participation in clinical research that seeks to improve diagnostic and therapeutic options.
Related Research
The Canadian Chiari Association supports and encourages involvement in research studies such as those investigating the hereditary basis of Chiari type I malformation and associated conditions like syringomyelia. Such research aims to uncover genetic factors contributing to the condition and ultimately improve patient care.
This summary reflects the Canadian Chiari Association's dedication to supporting individuals affected by Chiari malformations in Canada through awareness, education, community support, and advocacy for research advancement.
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