Hope for Hearts

Hope for Hearts Hope for Hearts is dedicated to raising awareness
and providing support for children and families affected by congenital heart defects.

TODAY IS THE LAST DAY!This is your LAST chance to become a monthly donor and receive a FREE Hope for Hearts t-shirt!Sign...
08/31/2026

TODAY IS THE LAST DAY!

This is your LAST chance to become a monthly donor and receive a FREE Hope for Hearts t-shirt!

Sign up as a monthly donor TODAY, August 31, and we’ll send you a FREE Hope for Hearts t-shirt as our thank-you!

Your monthly support helps us continue providing assistance and hope to families impacted by congenital heart defects and pediatric transplants. Every monthly gift, no matter the amount, helps us be there for families when they need it most.

🩵 Become a monthly donor
👕 Receive a FREE Hope for Hearts t-shirt
❤️ Help heart families all year long

The campaign ends TONIGHT, don’t miss your chance!

Thank you for helping us continue Hannah’s legacy and reminding heart families that they are never alone.

Sign up at our website: www.hopeforheartssd.org

🩵 Hannah’s Gift of Hope: Atticus🩵Atticus’s story is one of incredible strength, patience, and hope. For nearly his entir...
08/30/2026

🩵 Hannah’s Gift of Hope: Atticus🩵

Atticus’s story is one of incredible strength, patience, and hope. For nearly his entire first year of life, Atticus and his family have called the hospital home while waiting for the gift that would ultimately save his life.

Atticus is 11 months old, and his family has spent over 380 days by his side in the hospital. Throughout this journey, his parents and extended family have remained actively involved in his care, advocating for him, attending to his needs, and making sure he is surrounded by love and support every step of the way.

For nearly 10 months, Atticus was supported by a Berlin Heart as he waited for a donor heart. His family endured day after day of uncertainty, always holding onto hope that the phone call they were waiting for would finally come.

And then it did. After waiting approximately 380 days, Atticus finally received his hero heart. His transplant, however, has not been an easy road. Atticus did not do well immediately following his transplant and needed to be placed on ECMO. He has faced challenges during his recovery, but through it all, his parents have remained strong and hopeful for their little boy.

Atticus is a happy baby who has captured the hearts of everyone on his hospital unit. He is a little warrior, surrounded by a family who continues to encourage him and advocate for him every single day.

His parents shared: “It’s been a really long journey so far, we have been impatient for 380 days. Atticus was on a Berlin heart for 10 months and a few weeks ago. He finally received his hero heart. He didn’t do well straight after transplant and was placed on ECMO. We will never take this gift for granted”

Despite the challenges, Atticus’s family continues to hold onto hope and remain encouraged each day. They know that his recovery may take time, but they are thankful for every step forward and every moment they get to spend with their little warrior.

A heart transplant is more than a surgery. It is a gift of life made possible by another family’s decision to give through organ donation. Atticus’s family knows just how precious that gift is, and they will carry that gratitude with them for the rest of their lives.

Because of your generosity, Hope for Hearts was able to provide financial support to Atticus’s family during this incredibly long hospital journey. While we cannot take away the uncertainty or challenges they have faced, we can help ease some of the financial burden and allow them to focus on what matters most, being there for Atticus.

Please join us in sending love, strength, and hope to Atticus and his family as he continues his recovery.

Keep fighting, sweet Atticus. So many people are cheering you on.🩵

💙 Hope for Hearts Support Group💙Join us Wednesday, August 26th at 4:30 PM CSTfor our Hope for Hearts Support Group.Wheth...
08/26/2026

💙 Hope for Hearts Support Group💙

Join us Wednesday, August 26th at 4:30 PM CSTfor our Hope for Hearts Support Group.

Whether you’re a parent navigating a CHD diagnosis, a heart warrior, a caregiver, or simply looking for people who understand, you are welcome here.

Come as you are, share as much or as little as you’d like, and connect with others who truly get it.

We’d love to have you join us!

Hope for Hearts Support Group
Wednesday, Aug 26 · 4:30–5:30 PM
Google Meet joining info
Video call link: https://meet.google.com/vbn-hwii-rky
Or dial: +1 475-221-6312 PIN: 143594044
More phone numbers: https://tel.meet/vbn-hwii-rky?pin=4854426422025

Two years ago today, we lost Hannah, and many lives were forever changed. Today, her absence is still deeply felt, but s...
08/21/2026

Two years ago today, we lost Hannah, and many lives were forever changed. Today, her absence is still deeply felt, but so is the love she left behind. She is the reason this mission exists, the reason we keep showing up, and the reason we will never stop making a difference. Everything we do carries a piece of Hannah with it. Forever loved. Forever missed. Forever our why.

🩵 Hannah's Gift of Hope: Mabel 🩵 Mabel’s story is one of incredible strength, resilience, and unwavering hope as she wai...
08/19/2026

🩵 Hannah's Gift of Hope: Mabel 🩵

Mabel’s story is one of incredible strength, resilience, and unwavering hope as she waits for the gift of a new heart.

Mabel, her parents’ first child, was diagnosed after birth with Hypoplastic Left Heart Syndrome (HLHS) and a congenital diaphragmatic hernia. From the moment she entered the world, her fight began. Her parents have spent their journey navigating parenthood within ICU walls, moving cities to be closer to specialized care, learning to care for their daughter alongside her medical team, holding her through procedures, and advocating for her every step of the way.

Since February 18, Mabel has been waiting for a heart transplant. She is currently supported by a ventricular assist device, lovingly referred to by her family as her “external heart,” specifically a Berlin Heart, which is helping keep her strong while she waits for her donor heart.

Despite everything Mabel has endured, her medical team describes her as a tiny but incredibly strong warrior. Her family is deeply involved in her care, attending rounds each day so they can stay informed and make sure they understand every update. Their dedication to Mabel is evident in every decision they make and every moment they spend by her side.

Mabel’s mom has also found a beautiful way to bring comfort to other families during their own hospital journeys. She hand-knits patients’ names to hang above their hospital doors, helping children and families feel seen and special during some of their hardest days. Even while facing an unimaginable wait for her own daughter, she continues to spread kindness to those around her.

Behind Mabel’s strength is a family carrying an enormous emotional and financial burden. Their lives have been centered around getting Mabel the specialized care she needs, while everyday expenses never stopped. Relocating to be near her care, ongoing medical expenses, food, travel, and the necessities of simply caring for themselves while remaining by Mabel’s side have created significant financial stress.

“We are so incredibly grateful to Hope for Hearts for helping us relieve some of that financial stress through donating to our family. Our lives halted, but bills did not. Moving our lives to be near her specialized care, never-ending medical bills, and the necessities of eating and still taking care of ourselves through it all add up, and never stop.” -Mabel's Family

Mabel’s family is now waiting for the phone call that could change everything, the call that a donor heart has become available and that their daughter will finally have the opportunity to live beyond the hospital walls.

“We are so grateful for you making donations to families like ours possible. I’d love to encourage you to google our daughter’s name, Mabel Rose Correal, and read her story. My mission as her mom is to spread awareness of CHD, the most common birth defect affecting 1 in 100 babies every year, and to spread awareness on organ donation. Without organ donation, our daughter won’t have the chance at living outside of these four walls. In our waiting, we are so thankful for the kindest of strangers. You among them. Thank you.” -Mabel's Family

Thank you for helping provide hope, comfort, and financial relief to Mabel and her family. Because of your generosity, they can carry a little less of the financial burden while continuing to focus on what matters most, being present for Mabel, advocating for her, and waiting together for the heart that will give this tiny warrior the chance to come home.

🩵 Our Parent Support Group is TOMORROW!🩵Whether you’re newly navigating a congenital heart defect diagnosis, living year...
08/11/2026

🩵 Our Parent Support Group is TOMORROW!🩵

Whether you’re newly navigating a congenital heart defect diagnosis, living years into your heart warrior’s journey, waiting for a transplant, or simply looking for people who get it, you’re invited.

Join Hope for Hearts and other CHD parents for a safe, supportive space to share, listen, connect, and remind each other that you are not alone.

✨ No judgment.
✨ No expectations.
✨ Just parents supporting parents.

Come as you are. You don’t have to have the right words, and you don’t have to share if you don’t want to. Sometimes, simply being surrounded by people who understand is enough.

We’d love to have you join us!

Wednesday, August 12 · 12:00 – 1:00pm
Time zone: America/Chicago
Google Meet joining info
Video call link: https://buff.ly/4BJ3gR5
Or dial: (US) +1 321-465-4949 PIN: 875 777 375 #
More phone numbers: https://buff.ly/7AlEWzI

A Heartfelt Thank You to Our 2026 Sponsors!Every family we serve, every financial grant we provide, and every moment of ...
08/05/2026

A Heartfelt Thank You to Our 2026 Sponsors!

Every family we serve, every financial grant we provide, and every moment of hope we help create is made possible because of generous supporters like you.

To our amazing 2026 sponsors, THANK YOU, for believing in the mission of Hope for Hearts and standing beside families impacted by congenital heart defects and transplants. Your generosity is creating real, lasting change in the lives of heart warriors and their loved ones.

We are incredibly grateful for your partnership and the difference you're making in our community and beyond.

✨ Want to make an impact, too? We're always looking for businesses, organizations, and individuals who want to partner with us as sponsors. Whether you're interested in supporting an event, funding a program, or making a year-round difference, we'd love to connect with you.

Together, we can ensure more heart families receive the hope, support, and resources they deserve.

Message us or visit our website to learn more about becoming a Hope for Hearts sponsor.

Thank you to everyone who helps us keep hope beating.

🩵 Join Team Hannah for the Heart Walk!🩵We invite you to join us as we walk together in honor of heart warriors everywher...
08/03/2026

🩵 Join Team Hannah for the Heart Walk!🩵

We invite you to join us as we walk together in honor of heart warriors everywhere at the Children’s Heart Foundation Heart Walk!

This walk is about so much more than taking steps. It is a day to celebrate the strength of children living with congenital heart defects, honor the lives of those we carry in our hearts, and stand beside the families who continue to navigate their heart journeys.

By joining Team Hannah, you are helping support the mission of the Children’s Heart Foundation and Hope for Hearts, bringing awareness, advancing research, and providing hope and support to families impacted by congenital heart disease.

Whether you are walking in memory, in honor, or simply in support of heart families, we would love to have you join our team. Every step represents hope, love, and a commitment to creating a brighter future for heart warriors.

Join Team Hannah today!
Click the link below, send us a message, or comment below and we’ll help get you connected. https://buff.ly/p2C38iV

📍 Sunday, September 13th | Watertown, SD**
⏰ Check-In: 2:00 PM
🩵 Opening Ceremony: 2:30 PM
🚶 Walk Kick-Off: 3:00 PM

Together, we can walk for heart warriors everywhere.

A few years ago, Natalie, Nick and I  met while her son was waiting for his heart transplant and Hannah, was waiting for...
08/02/2026

A few years ago, Natalie, Nick and I met while her son was waiting for his heart transplant and Hannah, was waiting for hers. We celebrated victories together, carried one another through heartbreak, and somehow became family.

This weekend, we had the honor of standing next to her on her wedding day. Without telling Nick or I, Natalie and Nathan, and their wedding party donated an entire cooler full of incredible auction items. During their wedding reception, they auctioned it off, with 100% of the proceeds benefiting Hope for Hearts.

We had absolutely no idea. We were completely speechless.

Because of their generosity, and the generosity of every guest who participated, the auction raised an incredible $3,000 for Hope for Hearts.

This is so much more than a donation. It's a reminder that Hannah's life continues to bring people together, inspire kindness, and create hope for families walking the congenital heart disease journey.

To the newlyweds and your amazing wedding party, thank you for choosing to share your joy with heart families. On one of the biggest days of your lives, you chose to make a difference in the lives of others, and that is something we will never forget.

Congratulations, and thank you for helping us continue to bring hope to heart families. 🩵

✨ A New Chapter Begins Today ✨We have an exciting announcement to share!Beginning today, Hope for Hearts is expanding ou...
08/01/2026

✨ A New Chapter Begins Today ✨

We have an exciting announcement to share!

Beginning today, Hope for Hearts is expanding our mission to support adults living with congenital heart disease (CHD) through Hannah’s Gift of Hope.

Congenital heart disease is the most common birth defect, but it isn’t something people outgrow. CHD is lifelong. As children become adults, they continue to face surgeries, procedures, hospitalizations, lifelong medical care, and unique challenges that deserve support and understanding.

For the last year and a half, Hope for Hearts has been honored to walk alongside children and families navigating congenital heart disease. Now, we’re proud to extend that same compassion, encouragement, and hope to adults in the CHD community.

Hannah’s Gift of Hope was created to remind every person living with congenital heart disease that they are seen, valued, and never alone. Through this expansion, we hope to provide meaningful support, build community, and continue advocating for those whose heart journey lasts a lifetime.

This is just the beginning, and we can’t wait to share what’s ahead.

Because hope doesn’t have an age limit. ❤️

CHDAwareness

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Po Box 32
Dell Rapids, SD
57022

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