Friday, June 15, 2007

It's time for Heart Walk 2007!

In less than a month, we will be commemorating the one year anniversary of Nova's death, and so it's time to kick off our efforts for this year's Walk.

Once again, we're working with the American Heart Association to raise funds and Awareness in the battle against Congenital Heart Defects. If you're receiving this email from me, most likely, you know our story, and how we've lost 2 of our children in 5 years to the effects of Congenital Heart Defects.

Nearly 40,000 babies have been born with CHD since you last heard from me about last year's Heart Walk, and nearly 4000 have died as a result. We want to honor Alexis' and Nova's memories by doing our part in helping future parents avoid experiencing the devastating loss of a child.

Please help us battle the #1 birth defect, and the leading cause of defect-related infant death by making a donation of $25, $50 or more.

Thank you so much for your support!

Erin and Scott
(in loving memory of Alexis and Nova LeClair)

Follow This Link to visit my personal web page and help me in my efforts to support American Heart Association - Charlotte, NC

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posted by Erin @ 1:19 AM   3 comments

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Donovan "Nova" LeClair

Monroe, North Carolina
Nova was our second child to be born with congenital heart defects. We lost our daughter at 12 days after open heart surgery in 2001. Nova was born 12/2/05, with Pulmonary Atresia with VSD. He lived 6 weeks after surgery, and passed away on April 6th, 2006. This blog is his story, and the on-going story of how our family is dealing with the loss of our beautiful boy.
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