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CCHA 2011 Annual Report
CCHA 2011 Annual Report


Sponsors:
CCHA for life sponsors



There are more than 180,000 Canadian children and adults with congenital heart defects who need your help.

CCHA For life - Forum The Canadian Congenital Heart Alliance (CCHA) is a volunteer-run registered charitable organization made up of patients with a congenital heart defect, their friends, families, and the medical community. With your support, we aim to improve the quality of care for these patients, many of whom require lifelong expert care.

If you’re a Canadian adult with CHD and haven’t participated in our two surveys here are the links. Thank you!   Survey #1 http://survey.constantcontact.com/survey/a07e5mlleusgyx5ezxn/start ©Survey #2 http://survey.constantcontact.com/survey/a07e5ssippqh0s4ru69/start

This is such a great newsletter that I want to make sure everyone has a chance to read it. You can also read previous issues by going to www.heartbeats.ca and clicking on the “Newsletters menu.   Keeping the Beat – Spring …[more]

Walk, Run, Cycle or Sponsor Team CCHA on Sunday May 27, 2012 and help us reach our fundraising goal of $6,500. On Sunday May 27, 2012 team CCHA will walk/run/cycle in the Cardiac Health Foundation of Canada’s “WALK OF LIFE”. …[more]

The Children’s Hospital of Eastern Ontario and The Hospital for Sick Children are working together on a project to encourage children with heart problems to be healthy and active in their community.   They would love to speak with parents, …[more]

Living with Truncus Arteriosus Tuesday, April 17, 2012, 7-8 pm EDT Register for the webinar here. Are you an adult living with truncus arteriosus (TA) or the family member of someone with TA? If so, you won’t want to miss …[more]

Born with a Broken Heart
Please watch our film!

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Reasons for joining CCHA

To help support people with congenital heart defects (CHD)

To stay up-to-date with CHD news, clinical trials, fundraisers, etc.

To advocate for improved care for people with CHD

To be part of a growing community of CHD patients and their friends, families and the medical community

CCHA has a new bilingual brochure!
CCHA brochure

Sign petition to support CHD genetic research and funding!
CCHA brochure