We are delighted that Chapman Robinson & Moore Accountants Oxford have chosen to support Tiny Tickers throughout the year. In the last few months of …read more
CRM Oxford announces new ‘heartfelt’ charity partnership
Nominate Tiny Tickers And Help Us Do More For Tiny Hearts This October.
We are taking part in a charity nomination poll throughout October at My Favourite Voucher Codes and we have a chance of winning 20% of …read more
Charity partnership set to increase early congenital heart disease detection
Children’s Heart Surgery Fund (CHSF) have awarded a grant of over £17k to Tiny Tickers to fund vital cardiac sonography training across the Yorkshire region. …read more
Tiny Tickers commissioned to start training in NHS Scotland health boards.
We are delighted to announce the start of our fetal cardiac training program in Scotland. This will focus on implementing the 3vt (3 vessel trachea) …read more
Have YOUR say on the future of Congenital Heart Disease research.
A national study has been launched to identify and prioritise the areas of future research in congenital heart disease that are most important to patients, their families, and healthcare professionals.
New pulse oximeters for birthing units at Shropshire’s hospitals
The Trust that runs Shropshire’s two acute hospitals has received new pulse oximetry machines to improve the detection and early care of babies with serious …read more
Tiny Tickers launches new condition specific webinars for health professionals
By Tiny Tickers’ Head of Training, Anne Rhodes As Head of Training for Tiny Tickers, my focus is mainly on delivering training to sonographers and …read more
#RightNow: Tiny Tickers backs call to give charities the support they need to deliver their vital work.
On the 17th February 2021, hundreds of charities, including Tiny Tickers, will take to social media to back the Right Now Campaign and call on …read more
Right Now: Congenital heart disease has not stopped because of the pandemic
By Tiny Tickers CEO, Jon Arnold On the 17th February 2021, hundreds of charities, including Tiny Tickers, are backing the Right Now #nevermoreneeded Campaign and …read more
Fundraising from your sofa…
Here Katie, our Head of Fundraising and Comms, talks about some other ideas if your fundraising plans have been postponed or cancelled. All of these can be done from home, and from the comfort of your sofa!
Tiny Tickers response to BBC News investigation into private baby scans
Tiny Tickers is concerned by the findings of the BBC News investigation into private baby scans. We have long backed calls for sonography to be …read more
Support & Advice for Cardiac Nurse Specialists
By Tiny Tickers Head of Training, Anne Rhodes. One group of health professionals that are quietly, and constantly on the frontline of CHD treatment, care …read more
Our Pulse Oximetry Project is up and running again…
We’re delighted that we have been able to start placing pulse oximetry machines in maternity wards across the UK once again. These monitors, which can …read more
Helping sonographers communicate unexpected baby scan news to expectant parents
Tiny Tickers is delighted to have played a part in creating new guidelines for sonographers that will help thousands of expectant parents affected by pregnancy …read more
Harrison’s Story
Harrison tragically passed away from an undetected heart defect when he was 32 days old. His mum, Katie, shares their story:
SVT and Aortic Stenosis: Arthur’s Story
After ten magical days at home, Arthur suddenly went into heart failure. He was diagnosed with SVT and aortic stenosis. This is his story, told …read more
The Hebridean Way is “mostly flat”
According to Google, the Hebridean Way is “mostly flat.” This team of fundraisers does not agree. Tiny Tickers supporter, Mick Bailey, recounts his experience of …read more
VSD (Ventricular Septal Defect): George’s Story
George’s VSD (hole in the heart) was detected soon after he was born, but his journey to having it corrected was a long and difficult …read more
Patent Ductus Arteriosus (PDA) and Aortic Stenosis: Emilia’s Story
Emilia was critically ill when she was diagnosed with patent ductus arteriosus (PDA) and aortic stenosis. This is her story, told by her mum, Lucy:
The journey of a heart parent
The journey of a heart parent – by Emma Louise Hart You got to take your baby home;We took ours to another hospital.You got to …read more
