Join me in supporting congenital heart defect research!
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.
Because our son was born with a CHD, and we didn’t find out until after birth. He was first diagnosed with a VSD- An on Feb 12th, 2018, he was diagnosed at 2 month corrected with PVS- Pulmonary Vein Stenosis.
Kaspian was then directly admitted to CHOA for specialized testing and we were given the option to fight for him or let go.
Younger the babies are when diagnosed and multiple veins effected are considered pro-prognosis markers.
That didn’t stop Kaspian 2- Open Heart Surgeries, Heart Caths Roughly every 3-4 months for the last 4years. 60 Heart Procdures. Two chemo trials and he will still here fighting!
That is why this why CHD Awareness and Funding is so important and near and dear to our hearts
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.
If you think this page contains objectionable content, please inform the system administrator.