The post Congenital heart defects: What every mom and mom-to-be should know appeared first on All4Baby.
]]>If you were to ask expectant mothers what a CHD is, not many would know the answer and this is because you only really become affected by these defects if you are lucky enough to have them identified early on.
CHD deaths can be avoided through education and knowledge. If moms are armed with the information they need to protect their babies from CHD related issues, death could potentially be avoided. All moms need to do is ask.
“Hudson was born on January 14th, 2013. Two days later, the hospital appointed paediatrician identified what he thought to be a heart murmur and immediately called the resident cardiologist to check it out. It turned out, Hudson had a congenital heart defect (CHD) called Truncus Arteriosus.
He underwent surgery at six weeks of age and everything looked so positive that we’d all but stopped worrying about his heart; so it was completely unexpected when he passed away in the early hours of the morning of May 17th.
In a sad way, we were lucky. Hudson’s CHD was identified early on and we could do everything possible to try and save him. While we weren’t successful and are struggling through the grief of losing our child, we believe that Hudson’s story can help to make a difference in saving the lives of future CHD kids”, says Hudson’s mom, Andrea Slater.
There aren’t many OB Gyns who routinely perform the necessary scans for CHDs during pregnancy. Most scan routinely for Down’s Syndrome and various other genetic disorders, but the dangers that face unborn children go further than just these.
If heart related disorders are identified, expectant mothers can, for instance, opt for caesarean sections rather than natural birth, thereby relieving the stress on the infant’s heart and body.
Pulse Ox is a simple screening test that measures how much oxygen is in a baby’s blood. When performed after the baby is 24 hours old (or before discharge), the test can help identify babies who may have serious heart problems before they go home.
Join pages like The Hudson Initiative on Facebook, where we bring focus to CHDs, what’s being done about them in South Africa, what mothers can do to protect their kids going forward and raise funds to help raise awareness around CHDs. Talk to us, we can help you save a heart.
About the Author: Andrea Slater is mother to a CHD angel and all she wants is to help other tiny people get a fighting chance in this life. Readers are welcome to visit her blog for more on Hudson’s journey.
The post Congenital heart defects: What every mom and mom-to-be should know appeared first on All4Baby.
]]>The post Babies shouldn’t die of a broken heart, says Hudson Initiative appeared first on All4Baby.
]]>Around 1 in every 100 babies is born with a heart defect, and in South Africa, many of those go undetected. It’s estimated that at least one in every five babies who dies of Sudden Infant Death Syndrome (SIDS) was an undetected CHD sufferer – but it doesn’t have to be that way.
Cardiac surgeon Professor Robin Kinsley says advances in paediatric cardiology and cardiac surgery have made it possible for survival into adulthood for the majority of babies born with congenitally malformed hearts, but this is not the case on the African continent.
“Here, this is a dream as roughly 280 000 neonates born every year on the continent are left untreated, demonstrating the natural history of the congenitally malformed heart by default,” he says. “This is due in point to lack of finances, lack of locally developed personnel and proper understanding of the problem.”
The statistics get scarier when you hear that globally, twice as many children die from congenital heart defects each year than from all forms of childhood cancer combined, yet funding for pediatric cancer research is five times higher than funding for CHD.
The Hudson Initiative faces a long, arduous road – one that is starting with awareness, will encompass a growth in research funding and the collection of funds to help families who cannot afford the surgeries needed to help their babies, and will end in the creation of Hudson’s Law.
To explain the end goal, detecting CHDs is as simple as administering a test, called Pulse Oximetry, which measures how much oxygen is in a baby’s blood, after the baby is 24 hours old. This dramatically increases their chances of survival, says Andrea Slater, the driving force behind The Hudson Initiative.
“This is the most important part of our focus: We’re going to make sure that screening for heart defects become as normal a scan as the Downs Syndrome check at 20 weeks. We’re going to make sure that Pulse Oximetry tests are performed on all newborn babies before they are sent home. And we’re going to make sure that the terms CHD and congenital heart defect is no longer foreign or misunderstood,” says Slater.
“If mothers are armed with the information they need to protect their babies from CHD-related issues, these deaths could potentially be avoided. CHDs are scary but they’re not the end. CHD babies live. They thrive. Post-surgery, hope is very much alive.”
Ultimately, the Initiative will realise the introduction of Hudson’s Law, which will see Pulse Oximetry testing becoming compulsory. In the meantime, the initiative is raising money to fund CHD awareness campaigns and pay for Pulse Oximetry testing in infants. The long-term goal is to pay for surgeries needed by babies whose families who cannot afford them.
Interested parties can sign a petition and spread the word by visiting www.hudsoninitiative.org. They can also be part of the social media campaign using the #JustAsk hashtag, which prompts expectant mothers to do three things:
“Our journey with Hudson was a very real, very painful, very testing and an extraordinarily fulfilling one. We like to think he chose us because he knew we would do something to address the concerning statistics around the sheer number of babies who are sent home with undiagnosed CHDs. We’re going to change things on behalf of the boy who changed our world.”
About the Author: Andrea Slater is mother to a CHD angel and all she wants is to help other tiny people get a fighting chance in this life. Readers are welcome to visit her blog for more on Hudson’s journey. For more information visit www.hudsoninitiative.org
The post Babies shouldn’t die of a broken heart, says Hudson Initiative appeared first on All4Baby.
]]>