
Happy Valentine's Day to everyone! We received an early Valentine present (and birthday present for me--it is tomorrow) on February 11th: James Benedict Haberman was born at 2:03 pm on Wednesday. They decided to perform the c-section early as my blood pressure rose and I had protein in my urine (gross, I know). Also, James' fluid level had been cut in half. We were sent to the hospital on Tuesday and James arrived the next day. We were nervous because he was only 36 weeks, 4 days gestation, but he came out crying and breathing without the help of oxygen. We also found out that James had TWO (yes, two) knots in his cord, which Dr. Tinker told us is very rare. James was baptized by the sweetest deacon right after birth and was transported to LeBonheur shortly after that. James is now resting comfortably at LeBonheur, awaiting surgery. Please visit www.caringbridge.org/visit/jameshaberman to read more about our newest miracle!
Today is a bitter sweet Valentine's Day. We have welcomed a true miracle, yet we are missing another one. Today is National Congenital Heart Defect Awareness Day. This time last year, we never would have guessed what an impact CHDs would have on our lives. CHDs are horrible, but with enough funding and support, one day they can hopefully be erased. That is the problem: there is not near enough funding for research, yet so many children are affected by CHDs. It is our hope that one day CHDs will no longer exist. Here is some helpful information on congenital heart defects (from http://www.itsmyheart.org/):
* Congenital Heart Defects are the #1 birth defect. Source: March of Dimes
* Congenital Heart Defects are the #1 cause of birth defect related deaths. Source: March of Dimes
* About 1 out of every 100 babies are born each year with some type of Congenital Heart Defect. (approx. 40,000/year) Source: Children’s Heart Foundation
* The American Heart Association directs only $0.30 of every dollar donated toward research. The remainder goes toward administration, education and fundraising efforts. Of the $0.30 that goes toward research only $0.01 goes toward pediatric cardiology for CHD. Source: Children’s Heart Foundation
* This year approximately 4,000 babies will not live to see their first birthday because of Congenital Heart Defects. Source: Children’s Heart Foundation
* The cost for inpatient surgery to repair Congenital Heart Defects exceeds $2.2 billion a year. Source: Children’s Heart Foundation
* Of every dollar the government spends on medical funding only a fraction of a penny is directed toward Congenital Heart Defect research. Source: Children’s Heart Foundation
* Though research is ongoing, at least 35 defects have now been identified.
* 4-8% born with CHD have Hypoplastic Left Heart Syndrome
* 4-10% born with CHD have Atrioventricular Septal Defects
* 8-11% born with CHD have Coarctation of the Aorta
* 9-14% born with CHD have Tetralogy of Fallot
* 10-11% born with CHD have Transposition of the Great Arteries
* 14-16% born with CHD have Ventricular Septal Defects
* Although some babies will be diagnosed during gestation or at birth, sometimes the diagnosis is not made until days, weeks, months, or even years after. In some cases, CHD is not detected until adolescence or adulthood. Source: March of Dimes
* It is a proven fact that the earlier CHD is detected and treated, it is more likely the affected child will survive and have less long term health complications. Source: March of Dimes
* Congenital Heart Defects are the #1 cause of birth defect related deaths. Source: March of Dimes
* About 1 out of every 100 babies are born each year with some type of Congenital Heart Defect. (approx. 40,000/year) Source: Children’s Heart Foundation
* The American Heart Association directs only $0.30 of every dollar donated toward research. The remainder goes toward administration, education and fundraising efforts. Of the $0.30 that goes toward research only $0.01 goes toward pediatric cardiology for CHD. Source: Children’s Heart Foundation
* This year approximately 4,000 babies will not live to see their first birthday because of Congenital Heart Defects. Source: Children’s Heart Foundation
* The cost for inpatient surgery to repair Congenital Heart Defects exceeds $2.2 billion a year. Source: Children’s Heart Foundation
* Of every dollar the government spends on medical funding only a fraction of a penny is directed toward Congenital Heart Defect research. Source: Children’s Heart Foundation
* Though research is ongoing, at least 35 defects have now been identified.
* 4-8% born with CHD have Hypoplastic Left Heart Syndrome
* 4-10% born with CHD have Atrioventricular Septal Defects
* 8-11% born with CHD have Coarctation of the Aorta
* 9-14% born with CHD have Tetralogy of Fallot
* 10-11% born with CHD have Transposition of the Great Arteries
* 14-16% born with CHD have Ventricular Septal Defects
* Although some babies will be diagnosed during gestation or at birth, sometimes the diagnosis is not made until days, weeks, months, or even years after. In some cases, CHD is not detected until adolescence or adulthood. Source: March of Dimes
* It is a proven fact that the earlier CHD is detected and treated, it is more likely the affected child will survive and have less long term health complications. Source: March of Dimes
These are some scary statistics. Please join us in prayer that research for CHDs will receive the funding that is desperately needs. There is an HLHS baby in the NICU with James right now and it breaks our hearts to think about what that sweet baby and his/her parents are going through right now. Please pray for this sweet baby as well as all of the other sweet babies fighting right now. Thank you for continuing to check in on us and for showing your support for our family. We are so thankful for you all and for our angel Luke. God bless you all!!!!
