My story so far – Left Ventricular Non-Compaction Cardiomyopathy
Hello. My name is Phoebe and I’m 22 years old. When I was three years old, I was admitted to Great Ormond Street Hospital to
Hello. My name is Phoebe and I’m 22 years old. When I was three years old, I was admitted to Great Ormond Street Hospital to
Being in lockdown, being in isolation it’s made me re-experience a life I had before and compare the feelings I have now, to that I
Monday 16th March I celebrated my 12th re-birthday, re-birthday is a term that all cardiac arrest survivors use to celebrate surviving a cardiac arrest. I
A digital copy of the myheart Newsletter 2018 is now available to read here on Issuu. Catch up on the latest news and updates, research
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.
Be part of the CRY Great Cake Bake during CRY’s raising awareness week in 2018 (17th – 25th November). Register online and receive your free
#TEDICATED – CHAPTER 3 – CARDIAC ABLATION AND THE ROAD TO RECOVERY It has been some 8 months since my diagnosis of Wolff-Parkinson-White Syndrome. (see
June will mark 4 years since I first discovered something wasn’t right. I was playing pool at the time in a competition match for prize
12 years ago, last year, last week or even yesterday; it doesn’t matter how long ago it was when they died of an undiagnosed genetic
Hi there, I’m Laura from Belfast and I’m 31. I’ve been having palpitations I think since I was about 18. They went undiagnosed for a
Hi Everyone, It has taken me a long time to find somewhere to share stories, thoughts and experiences with others in a similar position. And