Founder & CEO


Jenni is Founder & CEO for Canadian CdLS Foundation

Representing

Description of role

Jenni is the founder and CEO, with over 20 years of healthcare experience in the clinical, education, leadership and governance roles in acute care, public health and education sectors. She is also the mother of a child with CdLS. Through this experience she has realized the challenges of those with rare diseases in Canada in terms of access to healthcare and education and the demands placed on those who care, educate and support individuals with CdLS

About the website contents

All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at: 

Send a email: info@cdlsWorld.org