Join me, & Team Braxtonn in supporting congenital heart defect research!
Hello, so our journey started when i was pregnant with my son, Braxtonn...Not knowing anything about CHD or how itll effect my life or my childs, or in general...till i was 26 weeks pregnant with my son, Braxtonn...I went to ALL the appointments while i was pregnant to get better prepared on his defect. Braxtonn had a heart defect called "Transposition of the Great Arteries - TGA.
and hit with every unexpected turn after his birth was the most devastating thing any mom or parent would have to ever endure. After a 50/50 chance and beating all the odds my son is now thriving at 6 1/2 months old. The happiest little man considering what hes been through. I can go on and on about my little man, but one thing is for sure he is a strong little man and a strong heart warrior. and my heart is with every parent who has gone, or is going through this with their loved ones. If i can help make a difference while supporting my son, Ill be honored.
Raising funds for congenital heart defect (CHD) research is not only critically important to all babies born with, and children and adults living with CHDs, it is also personally meaningful to me.
By donating to help me reach my fundraising goal, you’re helping to fund the most promising research into CHDs - America’s most common birth defect.
Together we can make a life-saving difference! Thank you in advance for your support.
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