We e-mail out monthly e-news to all of our members. It is full of stories and photos of children with Congenital Heart Defects. Contains information, resources and local activities.

You can visit our website and read stories, order our products, view our e-news archive page, view our CHD facts page and resource page. It is a great referral source and full of helpful information.

We offer support and hope through our network of families.

We can facilitate you in finding another family of a child born with the same or similar congenital heart defect. You can share stories, experiences and draw support from other families that have gone through a similar situation.

If you are not in direct need of support at this time, you can help us by offering your support to other parents in need. Just by sharing your stories and experiences with new members you can help relieve some of the stress new families are experiencing upon receiving their child’s diagnosis.

We have an annual get-together with our members during the month of February to recognize CHD Awareness Day, February 14th. It gives our members a chance to meet other local families and children affected by a congenital heart defect.

You will receive a list of resources in your membership packet. It is full of helpful information about our local hospitals, therapy services, phone numbers and CHD facts. You will also receive helpful tips and ideas given by families whose children have gone through open-heart surgery.

Once we receive your completed membership form you will be invited to join our online support group. This is a fantastic way to contact other families, post questions to the group, receive support, helpful tips and information from other parents going through similar situations.