My Long QT story – by Jodie Pearson, age 36 I was diagnosed with Long QT1 in 2010 when I was 27 years old. A
I would like to share our story to help raise awareness of fatal Genetic Heart Conditions. In March 2016, our daughter – Hollie Cannon, then
It’s been 18 years since I was diagnosed with long QT syndrome and had my very first permanent pacemaker implanted; and 25 years since my
George Ashby has made an inspiring video about his experience after being diagnosed with a heart condition. George’s mother, Amelia Ashby found that George has
My journey with congenital heart disease began on 19th March 2018 when I was 18 years old. I was at work and had just gone
Since having my little boy 3 years ago this month I haven’t really felt well and have been suffering palpitations, dizzy spells and feeling breathless.
Earlier this year I decided to do a bit of a fundraiser, cheap but wanted it to be something a bit different. I chose these
