Blanket Hugs CHD Program

A year ago, Blanket Hugs launched a new program specifically for kids with Congenital Heart Defects and heart disease. We had met numerous families and saw the need the kids and parents could use. From there Heart Packs were born.

We create huge packages filled with toys and awareness items not only for the kid with CHD but for the whole family.

We recently launched a new program that provides information for newly diagnosed families and families who travel for care.


1. You must be 18 yrs or younger (NO EXCEPTIONS)

2. You must live in the USA.

3. This program is ONLY for kids with CHD

4. A parent needs to fill out the application.

5. Please conatct us to be placed on a waiting list.




Click on photo for link to purchase!

In honor of


Adalynn Grace Rogers was born on Janurary 11, 2016 with a Congenital Heart Defect (CHD) called, Hypoplastic Left Heart Syndrome (HLHS). Addy was living with half a heart. Addy had her first open heart surgery shortly after. Five months later another one followed. Addy was followed very carefully by her team but was a normal toddler full of life and spunk, other then getting fed through her tummy. November came and Addy declined fast, she was diagnosed to be in heart failure and a heart transplant was needed. Addy lived in the hospital since that day, undergoing many procedures to save her life until a heart came. However that heart never came and Addy suffered severe brain damage from lack of oxygen on Jan. 23rd. Her family made the rough decision to take her off life support and Addy passed on Jan. 26th. She left behind her amazing parents, two older brothers and a new baby brother. Addy meant a lot to the BH family. We promised we would share her story forever and the importance of organ donation. We hope you will do the same too. #foreveraddystrong


EST. 2015

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