“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.
![CHSF Warrior Wednesday LOGO [png]](https://chsf.org.uk/wp-content/uploads/2021/02/CHSF-Warrior-Wednesday-LOGO-png.png)
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…
Elijah
"HAPPY HEART MONTH HEART WARRIORS! "This month we stand united with our heart community. We share our stories in hope that someone going through the same gets some kind of reassurance they’re not alone. "This month we remember the highs and lows of being a heart...
Freddie
Last year, Freddie was the first child in the UK to undergo the innovative Yasui repair instead of the Fontan. Freddie was born with Hypoplastic Left Heart Syndrome and a large VSD and since 2016 had already overcome multiple heart surgeries. Mum Casey shares...
Sally
Sally's heart defect wasn't identified until after she was born and had open heart surgery at 18 days to correct her CHD. Doctors at the Leeds Congenital Heart Unit stated that without this operation, Sally wouldn't live past 6 months old. Now 21, Sally has already...