“Hi, my name is Harry Austin and I’m writing this, with the hope that it will give some hope and comfort, however big or small, to children with congenital heart problems.”
I was born with a coarctation of the aorta and a bicuspid valve in August 1999 and in the October of 1999, I underwent surgery to have my coarctation repaired.
Due to the amazing work of all the surgeons, doctors and staff at the LGI, and the love support and strength of my amazing family, the surgert was very successful.
Thankfully, this meant I haven’t had to have any more heart surgery.
I am currently a very active and fit 22 year old man who lives a very full life.
I am about to start my master’s degree, in political theory, in September this year, having graduated with a degree in politics in 2021.
Harry with his mum at the LGI after open heart surgery at 2 months old.
I hope sharing my story and experience of the Leeds Congenital Heart Unit and how me and muy family were supported by Children’s Heart Surgery Fund helps serve as an example to children who are experiencing things similar to what I have.
I would like to say that even though they might be going through one of the cruellest and unbearable experiences imaginable, no matter what you can overcome it and live a full, happy and rewarding life. Just like I did and am.
Thank you to CHSF for allowing me to share my story, and thank you to all the doctors, surgeons, and staff at the LGI that saved my life 22 years ago – and continue to save countless others.
All your work doesn’t go unnoticed, and you and your work is extremely appreciated. Myself and my family will be forever grateful. Thank you. 🙏 ❤️
On #WarriorWednesday, we celebrate the amazing heart heroes we support in our region.
We tell their stories to raise vital awareness of congenital heart disease and recognise the care of the Leeds Congenital Heart Unit.
If you would like to make a regular or one-off donation to help fund CHSF’s life-saving work, you can do so here. Thank you.
More from the blog…
Jacob
Born at home in Kippax Leeds, Jacob's heart defect was detected in his first week of life after being admitted to Leeds Children's Hospital when he wasn't feeding well...Jacob's mum, Iona, said: "Jacob was born at home; everything was amazing and there was no sign...
Daisy
Daisy's mum, Lucinda, said: "Our experience with congenital heart disease began at our 20 week scan. Having previously had a history of problems, we were told that baby would be checked very carefully. Upon her silence we immediately knew the sonographer had found...
Rebecca
Although Rebecca was born with the heart murmur, it wasn't until she was pregnant with her second child that her heart problems became more apparent...Rebecca said: "From birth I have had a heart condition. I was born with a heart murmur and was under the care of...