Hello visitors!
Welcome to the ALL NEW!! website, i am a mum on a mission fighting for more awareness of Hypoplastic left heart syndrome and other heart defects in which my son and many more children are born with everyday. He is one of the survivors here are some quick facts..
Hypoplastic Left Heart Syndrome (HLHS) is a Congenital Heart Disease (or Congenital Heart Defect as it is known in America) it is the number one killer in babies and children, it is more fatal than cancer. As there is still .......no national awareness in the UK, the majority of people do not seem to know a lot about Congenital Heart Disease (CHD).
Everyone is welcome here, people from all around the world, people who are not even affected by CHD please do read through and educate yourselves on CHD's.
We have live blog's, RSS feeds facebook and twitter share links, and a membership forum page for all discussions. Please join our community and together we can work hard to bring more awareness and to educate those who do not know about real broken hearts.
This website is built that in the hope we can all be.....heart aware and let’s spread the word!! "One heart one mind countless voices".
DISCLAIMER: We are not medical personnel and do not intend to take away from your physician’s advice. Individual evaluation by an experienced paediatric or adult congenital cardiologist and cardiac surgeon is needed to determine proper diagnosis and the best course of treatment. We are only here to help raise awareness, educate and inform through personal life experiences. We do not hold any responsibility for any actions taken by reading this website.
Hypoplastic Left Heart Syndrome (HLHS) is a Congenital Heart Disease (or Congenital Heart Defect as it is known in America) it is the number one killer in babies and children, it is more fatal than cancer. As there is still .......no national awareness in the UK, the majority of people do not seem to know a lot about Congenital Heart Disease (CHD).
Everyone is welcome here, people from all around the world, people who are not even affected by CHD please do read through and educate yourselves on CHD's.
We have live blog's, RSS feeds facebook and twitter share links, and a membership forum page for all discussions. Please join our community and together we can work hard to bring more awareness and to educate those who do not know about real broken hearts.
This website is built that in the hope we can all be.....heart aware and let’s spread the word!! "One heart one mind countless voices".
DISCLAIMER: We are not medical personnel and do not intend to take away from your physician’s advice. Individual evaluation by an experienced paediatric or adult congenital cardiologist and cardiac surgeon is needed to determine proper diagnosis and the best course of treatment. We are only here to help raise awareness, educate and inform through personal life experiences. We do not hold any responsibility for any actions taken by reading this website.
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