Hello from Nolan Nation!
I'm mom to Heart Hero Nolan, our brave, inquisitive and super silly almost 4 year old. Before we learned of his complex CHD during our 20 week anatomy scan, the term "CHD" wasn't even remotely on my radar. Now, it is so much a part of us as a family that it's hard to fathom not knowing. I'm happy to share that Nolan is doing great. He had his 3rd surgery, the Fontan, a year ago.
We are the lucky ones. The ones who were fortunate enough to bring their newborn baby home. The ones who got to celebrate first birthdays, first steps and first words. The ones who walked out of the hospital, with their child, only a couple short weeks after a life-changing surgery. Sadly, so many other families can't say the same. There is still much work to be done - awareness to be raised, new medical discoveries to be had and most importantly, lives to be saved and made better. We can't do this without money to fund crucial medical research.
This is why we walk. This is why I'm asking you to join us and if you can, make a donation to help further the efforts of two extremely important agencies within our CHD community.
Thank you for visiting my Congenital Heart Walk fundraising page. Please consider making a tax deductible contribution to support my fundraising efforts on behalf of The Children’s Heart Foundation and the Adult Congenital Heart Association. All funds raised benefit CHD research and programs. I appreciate your support!
Big heartfelt hugs,
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