This page is dedicated to all of the kids (and adults!) who are living with half a heart. Even though Jackson's fight on earth is over, the hope is that the treatments for HLHS will continue to improve, and with that, the chance for long-term survival. As little as 25 years ago, HLHS was 100% fatal. Some still don't make it, but there are so many that are continuing to live and will do so hopefully for a long time. There is no life expectancy for a child born with HLHS, because no one knows yet! These kids are proof that there is Hope for Children with HLHS!
(Note: Some CarePages and CaringBridge sites will require login)
If you would like to have your child's web page (carepage, journal, myspace, etc.) added to this list, send an email to Jessica@jacksonsheart.com with his/her name, DOB, and link, and a sentence intro if you want.
~Andrew |
CHD Fighters
