335heart.org
335 Heart Foundation - 335 Heart Foundation - A Charitable Non-Profit serving families afflicted by Congenital Heart Defects335 Heart Foundation
http://www.335heart.org/
335 Heart Foundation
http://www.335heart.org/
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335 Heart Foundation - 335 Heart Foundation - A Charitable Non-Profit serving families afflicted by Congenital Heart Defects | 335heart.org Reviews
https://335heart.org
335 Heart Foundation
335heart.org
How to Help | 335 Heart Foundation
http://335heart.org/donate
Share Your CHD Story. Where will my donation money go? Awareness initiatives in the form off printed materials and items to educate the general public about CHD. Advocacy programs – both public policy as well as parent/child. Family grants and Charitable Giving. Support funeral costs for children who lose their battle with CHD. State / Province / Region. Postal / Zip Code. Don’t want to donate online? Mooresville, NC 28115. Are you looking to donate items instead of money? To let us know what your talent...
About Us | 335 Heart Foundation
http://335heart.org/about-us
Share Your CHD Story. Morgan Avery Smith received her open heart surgery repair by Sanger Cardiology at Levines Children’s Hospital at 4 days old. The 335 Heart Foundation, Inc. was founded by the Smith Family (Jeff and Kristina) of Mooresville, North Carolina. Their daughter, Morgan Avery, was born with a congenital heart defect, Truncus Arteriosis, on July 12, 2014. She received open heart surgery to correct the structure of her heart on July 16th 2014 at Levines Children’s Hospital. WHAT DOES 335 MEAN?
Congenital Heart Legislative Conference 2015
http://335heart.org/congenital-heart-legislative-conference-2015
Share Your CHD Story. Congenital Heart Legislative Conference 2015. On: February 28, 2015. National Heart Blood and Lung Institute. From Left: Anmarie Wyrick and Deborah Gilchrest with Camp LUCK, Congresswoman Alma Adams (D-NC), Kristina Smith with 335 Heart Foundation, Chris Perez and Valerie King with Mended Little Hearts. This year, the three big asking points that were lobbied for:. 1 ) Increase Congenital Heart Futures Act funding for CDC surveillance program from $4 million to $10 million in 2016.
Congenital Heart Defect Awareness Week
http://335heart.org/events/congenital-heart-awareness-week
Share Your CHD Story. Congenital Heart Defect Awareness Week. Congenital Heart Defect Awareness Week. 7 February, 2015 at. February 7 – 14 is Congenital Heart Defect Awareness Week! We at 335HF are super excited because it is also our official launch week! We have some neat things planned to help bring awareness to CHD, so keep your eyes peeled on Facebook at Twitter to see what is going on. Our number 1 goal this week is to enlighten as many people as possible about CHD! Larr; Previous Event. Centers fo...
Board of Directors | 335 Heart Foundation
http://335heart.org/board-of-directors
Share Your CHD Story. Jeff Smith – Co-Founder, Director and President. Jeff is the father to four beautiful children, Gavin, Taylor, Brooklyn and Morgan (angel heart baby). Jeff is a real estate broker in the state of North Carolina, is an amateur photographer and loves to hunt, fish and ride dirt bikes. Kristina Smith – Co-Founder, Director, Treasurer and Secretary. Kathy Peterson – Director. Diagnosed with a serious atrial septal defect at birth, Kathy’s condition was corrected 30 years later tha...
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Addler Family in NC: CHD Week - Day Eight - Tribute to my Warrior
http://addler99.blogspot.com/2015/02/chd-week-day-eight-tribute-to-my-warrior.html
Saturday, February 14, 2015. CHD Week - Day Eight - Tribute to my Warrior. Since becoming a Heart Warrior Madelynn has been on a magazine cover. She was even one of the featured children on the inside of the magazine. She became the poster child for the second quarter for Dairy Queen's involvement with the Children's Miracle Network last year all over the US. She is helping spread awareness with the 335 Heart Foundation. It became a game that she would run away and Daddy would chase her (2010). But we ar...
Addler Family in NC: February 2015
http://addler99.blogspot.com/2015_02_01_archive.html
Saturday, February 28, 2015. 7 days a week, 365 days a year. Today ends Heart Month! For families with children fighting heart defects the journey never ends. There is no remission, there is NO CURE. We are reminded 365 days a year and not 28. We find the strength to surrender our warriors to a surgeon knowing no matter what the result our lives will never be the same after. Would I choose this life? Do I regret it? Because of Madelynn's CHD, I have learned to pray more, accept whatever decision the Lord...
Resources — Camp LUCK
http://www.campluck.com/resources
Youth Board of Directors. More Than A Camp. Hug N Heal Pillows. Youth Board of Directors. More Than A Camp. Hug N Heal Pillows. Below are some links that our families have found helpful. A children’s hospital that combines the medical expertise the community already relies on with a spectacular new state-of-the-art facility designed to care for the physical and emotional needs of children and their families. Sanger Heart and Vascular Institute. Novant Health Heart and Vascular Institute. Founded in 1996,...
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335 Glencairn Avenue - Home
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335 Heart Foundation - 335 Heart Foundation - A Charitable Non-Profit serving families afflicted by Congenital Heart Defects
Share Your CHD Story. Critical CHD babies typically. Require surgery within the. First year to survive. 18 billion per year in CHD related healthcare costs. HOW CAN YOU HELP? Do you know that congenital heart defects (CHD) kills more children each year than all children’s cancers combined? Although it is relatively common for babies to be born with a heart defect, funding for research, support programs and advocacy is unacceptably low. You can help by raising awareness! SHARE YOUR CHD STORY. North Caroli...
335 Hillcrest Avenue - Home
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