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Welcome to Melissa's Page

Melissa Lee

Melissa Lee

Hello Friends and Family!

I cannot thank you enough for taking this important step in helping us raise awareness and funds to fight CHD! As you know, Elliot is the light of my life and such a strong little fighter, as most heart kids have to be. No one should ever have to go through this and our journey is never something that I never would have chosen, but I am continuously seeking out the good in it. I believe that it's made me a stronger, more patient parent who cherishes every moment as a gift that was at risk of never becoming a reality. It also encourages me to strive harder to make sure that Elliot has the same rich opportunities and life experiences as every other child, part of the reason that she's learning Mandarin and is a world traveler at age 4!

This heart journey has also connected me with so many strong parents and families in the CHD community that I would not have met otherwise, but with whom I inherently share many things - including a passion to make things better for our heart babies. It's really the latter that has inspired me to commit to the CHD Heart Walk each year. I am honored and excited to take it to another level as the CHD Heart Walk Chair for Boston for the second year in a row!

Let's rally to support Elliot and all of our heart warriors with an amazing turnout to the CHD Heart Walk on April 20! I hope that you will join us in person, and/or through your kind and generous donation - thank you in advance!

ELLIOT'S STORY

February 10, 2014 is a day that I can never forget. I was 21 weeks along and went in for a mid-term check-up. Everything had been fine to date, and we had no reason to believe that this appointment would be any different. We were looking forward to finding out if we needed to start buying pink frilly frocks or tiny blue bow ties. Disappointment cannot even begin to describe the unexpected news that came along with finding out that we were having a little girl. Our little miss had only half of a heart. Initially, the doctors said that the defect was so severe that they didn't recommend continuing with the pregnancy. I crumbled. From then on, every tiny kick and flutter brought a painful reminder that my daughter may not be able to survive life outside her cozy home in my belly. I went from floating in the clouds with excitement to a very dark place in a matter of minutes.

The next several weeks were a blur - filled with prayers, tears, online research, phone calls and doctors appointments. I couldn't understand why this was happening. You only hear about these things occasionally - and they only happen to other people, right?!

With each appointment and meeting, our new support team of doctors, nurses and social workers at Boston Children's brought hope and truth. Once we had gathered all of the information that we could, I decided that we were going to continue on our journey. My new mission became clear: To remain positive, hopeful and do everything within my power to bring a healthy little girl into the world -- and keep her that way!

She came out kicking and screaming on June 24, 2014 at 10:02AM -- the single happiest...and scariest...minute of my entire life. I was fortunate enough to cuddle with her for 5 minutes before she was whisked away to Boston Children's where she was admitted to cardiac ICU. Someone had literally taken away a precious piece of me -- and there was nothing that I could do about it. Admittedly, I was very jealous hearing babies crying in the other rooms around me -- while I had to be delivered in a wheel chair to visit mine in a different hospital.

We had three precious days with her before her first open heart surgery. Even though we didn't know her well, we knew that she was a fighter. She recovered in record time and was home in 13 days. When I say "record", I'm not just being a proud mommy. The average hospital stay for a Stage 1 Norwood operation is 6-8 weeks. Elliot Grace was a superstar!

In the months that followed, she continued to thrive and gain weight - by far the biggest challenge for heart babies who expend most of their energy making their heart keep up with their body. Often times, they have little energy to eat. Our Elli Belly, on the other hand, never fell below the 25% percentile and developed the chubbiest, most kissable cheeks you've ever seen! As planned, she had her second open heart surgery (Stage 2 Glen) on December 11, 2014 -- and amazed us again with a six day recovery before returning home just before Christmas. She had her final scheduled surgery -- the Fontan -- on April 7, 2017. In true Elliot fashion, she rocked it and was out in ten days! Although we feel incredibly blessed that she has fared so well during this harrowing journey, we also recognize that many other children and families aren't as fortunate. We fight the good fight against CHD - not only for Elliot's future, but for all of those who have come before and who will come after her. They each deserve a fighting chance that is not possible without continued advancements in research. They deserve to live long and healthy lives. They deserve to not only have a childhood, but also an adulthood with families and dreams of their own.

There is no cure for CHD.
Elliot is, by far, the most amazing little human that I have ever known and despite all that she has been through, she continues to defy the odds and makes me smile a million times a day - even when I'm just thinking about her. She has the best laugh, most adorable smile, and is shaping into a gorgeous little lady with a lot of sweet and a little bit of sass!

On April 20th, we walk in honor of Elliot Grace -- and so many other children and adults like her. We walk for people - like you and me - who were born with special hearts through no fault of thier own. They had no choice but we do have a choice. By walking and donating to the Children's Heart Foundation - we can do our small part to fund research and programming, and to raise awareness about CHD for Elliot and millions of others! We can give them a present and a future.

Thank you for your support and we hope to see you in Boston Common on April 20th!

Very fondly,

Melissa



FOOD FOR THOUGHT:

- CHDs (congenital heart defects) are the most common birth defects.
- CHDs occur in almost 1% of births - that's 1 in 100 children.
- An approximate 100-200 deaths are due to unrecognized heart disease in newborns each year. These numbers exclude those dying before diagnosis.
- Nearly 40,000 infants in the U.S. are born each year with CHDs.
- CHDs are as common as autism and about twenty-five times more common than cystic fibrosis.

p.s. I have to tell you that all donations are tax deductible in support of The Children's Heart Foundation. Please check to see if your employer will match your donation so we can DOUBLE our impact!

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$10,245
raised of $12,000 goal
 

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