Lauren Elise Memorial Foundation

Lauren Elise Memorial Foundation Lauren Elise Memorial Foundation in loving memory of Lauren Elise Hilsheimer to fight against the #1

Founded in loving memory of our beautiful daughter, the Lauren Elise Memorial Foundation's mission is to support awareness, research, diagnosis, and treatment of Congenital Heart Defects (CHD) in children, and to provide for the care and well being of children affected with CHD, and their families. We want to thank you personally for visiting our page. Lauren's legacy will live forever in

the lives of all of those whom she touched in her three-plus years on this Earth. We are dedicated to enhancing her legacy by sharing her amazing story of love and courage, and by stepping up to help lead the fight against CHD, the world's most common, and deadliest form of birth-defect. Our Foundation takes seriously the responsibility to identify organizations who are effectively raising awareness, as well as those who are funding and performing vital research to advance technologies and methodologies related to early diagnosis and treatment. Furthermore, we aim to support facilities providing critical care and treatment to CHD kids and their families.

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/14/2025

🩷Congenital Heart Defect Awareness Week🩷
Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Lauren Elise Hilsheimer
6.3.08🩷7.22.11

Tricuspid Atresia, Dextrocardioversion, Atrial Septal Defect, Ventricular Septal Defect, Malposition of Aorta, and Hypoplastic Right Ventricle

"Lauren's life was a gift. She was a beautiful, vibrant little girl - full of life, love, and hope! There is not a day of her 3 years with us we take for granted and not a day in her absence has been lived without missing her.
She lives in our hearts forever.
Lauren's legacy lives on through her many examples of courage, strength, love, bravery, faith, and hope. Her legacy also lives on through the works of this Foundation, for which she is not only the namesake, but the inspiration."
-Mark & Kirsten Hilsheimer

www.ilovelauren.org/donate

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/13/2025

🩷Congenital Heart Defect Awareness Week🩷
Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Cameron Parks Singleton
Tricupsid Atresia and Unbalanced AV Canal
2.6.2020 💙5.6.2020

"Cam underwent open heart surgery of PA banding and atrial septectomy at 1 month of age. Despite difficulties with feeds requiring continues NJ tube feeding and a number of tests, Cam was the smiliest and sweetest baby. On May 6, 2020 He unexpectedly experienced cardiac arrest.
As Cam's parents, we want to honor and remember him by raising awareness and giving support to families and children with CHD. Cam completely changed us in the best way possible and we are forever thankful for the gift he is to our family."
~Krista Singelton, Cam's mom

www.ilovelauren.org/donate

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/12/2025

🩷Congenital Heart Defect Awareness Week🩷
Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Lia Kate Stone
Tricuspid Atresia, Transposition of the Great Vessels, Coarcation of Aorta,
Full Norwood Repair
16 years old
"Lia is 16 years old and a Jr. in High School. She serves as an athletic trainer and is WAY TOO social! We are feeling super grateful today and every day for our girl. "
~Lisa, Lia's mom

🩷Lia and Lauren were destined to be friends...we met them following Lauren's 2nd open heart. We treasure this photo of the girls together. Thank you Lisa for sharing this photo of our Heart Girls together.🩷

www.ilovelauren.org/donate

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/11/2025

🩷Congenital Heart Defect Awareness Week🩷
Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Raylen Tye Wyckoff
3-3-15💙8-17-19
Undiagnosed Hypoplastic Left Heart Syndrome with Mitral & Aortic Stenosis

"Raylen left an imprint on everyone's heart that he ever met. He was full of like, he as fearless, he was so special to so many people. Raylen loved the US Navy Blue Angels and anything to do with aviation. He loved chasing butterflies and he could never be pushed high enough or fast enough on his swing set. He was 100% boy and if there was a mud puddle you could guarantee that he would be in it. Hanging out with his daddy and little brother were the highlight of his day and there isn't a day the we don't wish for more time with him.

Raylen was a strong little boy who fought his whole life and is so terribly missed. But, we know that he is no longer struggling to breathe, that he can run like a four year should, and he will never have to be stuck by a needle or cut open again.
He was one of the greatest blessings our family could have asked for. We can't wait until we will all be reunited again."
Megan Wyckoff - Raylen's mom

www.ilovelauren.org/donate

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/10/2025

🩷Congenital Heart Defect Awareness Week🩷
Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Dawsey Hutch Worthington
2.5 months old

Double Inlet Left Ventricle
Pulmonary Stenosis
Large VSD
Transposition of the Great Arteries

Dawsey spent 24 days in the NICU following PDA Stent placement. He is home with his parents now and will undergo open heart surgery in the spring of 2025.

www.ilovelauren.org/donate

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/09/2025

🩷Congenital Heart Defect Awareness Week🩷
Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Evan Bradley
1.24.11💙 4.30.11
Pulmonary Atresia & Tetralogy of Fallot
"Evan was a fighter. Our precious little boy blessed our lives for 96 amazing days on this earth."
-Alissa & Travis Bradley

www.ilovelauren.org/donate

🩷Congenital Heart Defect Awareness Week🩷Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($...
02/08/2025

🩷Congenital Heart Defect Awareness Week🩷

Honor a 💓Heart Warrior💓 by giving a single $7️⃣ donation OR gift $7️⃣ per day ($4️⃣9️⃣) during CHD Week. Every dollar counts!

Gracie Ledbetter
10 Years Old
Partial Atrial Septal Defect repaired

"We couldn't be more thankful for our beautiful heart warrior! Gracie is silly observant strong (willed!), forgiving, loving, smart, and helpful.
Keep shining your light ... we all need to see it!"
~Sarah, Grace's mom

www.ilovelauren.org/donate

CHD Awareness Week is right around the corner! Mark and I have been researching some exciting new projects to fund - mor...
02/05/2025

CHD Awareness Week is right around the corner! Mark and I have been researching some exciting new projects to fund - more to come!
We would love to have your support February 8-14 as we Honor 7 AMAZING Heart Warriors.

www.ilovelauren.org/donate

Happy 13th Birthday Lauren!
06/03/2021

Happy 13th Birthday Lauren!

02/15/2021

💗💗💗And the winner is .........

Thank you to all who donated during our CHD Heart Week Campaign! We raised an additional $1300 to add to the fight against CHD!

💗💗💗💗💗💗💗💗💗💗💗💗💗💗7 Days 💗 7 Warriors 💗$7💗💗💗💗💗💗💗💗💗💗💗💗💗Help us make a difference!Honor a Heart Warrior by making a of a singl...
02/14/2021

💗💗💗💗💗💗💗💗💗💗💗💗💗
💗7 Days 💗 7 Warriors 💗$7
💗💗💗💗💗💗💗💗💗💗💗💗💗
Help us make a difference!
Honor a Heart Warrior by making a of a single {$7} gift OR $7 for 7 days {$49}. Every dollar counts. Thank you for your support!

Lauren Elise
6.3.08 💗 7.22.11
Tricuspid Atresia, Dextrocardioversion, Atrial Septal Defect, Ventricular Septal Defect, Malposition of Aorta, and Hypoplastic Right Ventricle

"Lauren's life was a gift. She was a beautiful, vibrant little girl - full of life, love, and hope! There is not a day of her 3 years with us we take for granted and not a day in her absence has been lived without missing her.
She lives in our hearts forever.

Lauren's legacy lives on through her many examples of courage, strength, love, bravery, faith, and hope. Her legacy also lives on through the works of this Foundation, for which she is not only the namesake, but the inspiration."

www.ilovelauren.org/donate

Address

Jenks, OK
74037

Telephone

+611663183

Website

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