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Tiny Tickers
เข้าร่วมเมื่อ 7 ส.ค. 2012
We're the national UK charity working to improve early detection and treatment of babies with serious heart conditions: www.tinytickers.org
Tiny Tickers Family Support Webinars - Supporting Everyday Life: Starting Nursery or School
This is the latest webinar in a new series offering practical tips and support to families of babies with congenital heart disease (CHD). This free session will provide you advice about your child with CHD beginning nursery or school - a topic that is commonly discussed on our Facebook group for parents and carers. Speakers will include a cardiac nurse specialist; a clinical psychologist; and Tiny Tickers staff and volunteers who have personal experience of this topic as parents of children with CHD.
Our family support webinar series is funded by Global Make Some Noise.
Our family support webinar series is funded by Global Make Some Noise.
มุมมอง: 44
วีดีโอ
Tiny Tickers Family Support Webinars - Supporting Everyday Life: Travel and Holidays
มุมมอง 62หลายเดือนก่อน
This is our second webinar in a new series offering practical tips and support to families of babies with congenital heart disease (CHD). Heart parents often ask questions about travel and holidays in our Tiny Tickers Parent Support Group. In this webinar, we aim to answer the most common questions and provide more general advice. Speakers include Tiny Tickers staff members, who are also heart ...
Tiny Tickers Family Support Webinars - Looking After Your Mental Health: A Toolkit
มุมมอง 1082 หลายเดือนก่อน
This is the first webinar in a new series from UK charity Tiny Tickers offering practical tips and support to families of babies with congenital heart disease. The webinar includes a toolkit for looking after your mental health - a vitally important topic for parents and carers of children with CHD. Speakers include professional mental health workers; peer support experts; and parents with live...
Amy's Story
มุมมอง 1523 หลายเดือนก่อน
22-year old Amy was born with the serious heart condition hypoplastic left heart syndrome (HLHS). Her parents were told to prepare for the worst and she wasn't expected to survive. Amy has defied all expectations. Doctors told her that she'd need a heart transplant in her early twenties, but this will now be delayed until her forties. Working as a personal trainer, she went from being "ill and ...
Join us on a fetal cardiac study day
มุมมอง 1024 หลายเดือนก่อน
Join our Project Support Officer, Abby, at our fetal cardiac study day for sonographers, which we held in collaboration with the North West CHD network, Alder Hey Children's Hospital Trust and Liverpool Women's Hospital. The event, held in April 2024, was sponsored by GE Healthcare.
An Ode to Heart Week Fundraisers
มุมมอง 1276 หลายเดือนก่อน
Tiny Tickers Heart Week 2024 has been a huge success and we couldn't have done it without our fantastic fundraisers! Here's a poem we wrote for them, read by our Head of Fundraising and Partnerships, Kym Kitching and featuring photos of our Heart Week heroes.
Lullaby by Katie Burke for Tiny Tickers Heart Week 2024
มุมมอง 1886 หลายเดือนก่อน
Tiny Tickers supporter, Katie Burke, wrote and performed this beautiful song for Tiny Tickers Heart Week 2024. If it has moved you, please donate to her page, to make a difference for babies born with congenital heart defects and their families. Donate here: www.justgiving.com/page/musicalstorybox #tinytickersheartweek #heartweek #chd #chdawareness #congenitalheartdefects #heart #hearts #heartb...
Tiny Tickers
มุมมอง 2789 หลายเดือนก่อน
Tiny Tickers is working hard to help give babies with serious heart conditions a better start. We want babies with congenital heart disease (CHD) to get the treatment they need as early as possible. We want them to get the right care at the right time to give them the best chance of survival and a good quality of life. And we want their families to receive the support they need.
Tetralogy of Fallot: Rafe's Story. Part 3: Surgery and Beyond
มุมมอง 1.5K2 ปีที่แล้ว
In the third part of their story, Catherine talks about Rafe's surgery, recovery and the future.
Tetralogy of Fallot: Rafe's Story. Part 2: Birth and Before Surgery
มุมมอง 2.2K2 ปีที่แล้ว
In the second of a three part series, Catherine talks about events that occurred after her son, Rafe, was born with congenital heart disease (CHD). He was diagnosed with Tetralogy of Fallot (TOF) at her 20-week scan and not expected to need surgery until six-months-old. In part one, Catherine shared her experiences of the diagnosis and in part three she talks about Rafe's surgery and life after...
Tetralogy of Fallot: Rafe's Story. Part 1: Diagnosis
มุมมอง 2.3K2 ปีที่แล้ว
In the first in a three-part series, Catherine shares her experiences of finding out her second son, Rafe, has congenital heart disease (CHD) when he was diagnosed with Tetralogy of Fallot (TOF) at her 20-week scan. Part two covers Rafe's birth and first few weeks and in part three Catherine talks about Rafe's surgery and life after surgery.
Test For Tommy
มุมมอง 2K2 ปีที่แล้ว
Every newborn baby deserves the test that could help save their life. However, at present, pulse oximetry testing is not a compulsory part of newborn checks. In this video you can watch a midwife carry out a pulse oximetry test on a newborn baby and find out why, through our Test for Tommy campaign, we aim to place pulse oximetry machines at maternity units throughout the UK. Please support us....
Zoe's Story
มุมมอง 3303 ปีที่แล้ว
Tiny Tickers CEO and heart dad, Jon Arnold, shares his daughter Zoe's story and discusses why the early detection of her heart condition by a sonographer was a crucial part of her journey from survival to thriving.
Helping sonographers communicate unexpected news - BBC Breakfast news report
มุมมอง 4254 ปีที่แล้ว
Helping sonographers communicate unexpected news - BBC Breakfast news report
A coronavirus update from Jon, our chief executive
มุมมอง 824 ปีที่แล้ว
A coronavirus update from Jon, our chief executive
Tiny Tickers - A Better Start For Tiny Hearts
มุมมอง 8255 ปีที่แล้ว
Tiny Tickers - A Better Start For Tiny Hearts
Test For Tommy: What is a pulse oximetry test?
มุมมอง 18K5 ปีที่แล้ว
Test For Tommy: What is a pulse oximetry test?
Test for Tommy - Help Every Tiny Ticker
มุมมอง 3335 ปีที่แล้ว
Test for Tommy - Help Every Tiny Ticker
Family Experiences: Dealing with Bereavement
มุมมอง 1.1K5 ปีที่แล้ว
Family Experiences: Dealing with Bereavement
Thank you for sharing your story! It helps a lot ❤
Your mobile no pl
Wow! Very informative!!
Watching this helps but still scary af my son has tof found in utero where I knew most of the possibilities. Today at 9 days old is his first surgery I’m scared of the worst but hoping for the best.
Wonderful video, thank you!
I am 24 weeks along and my baby has been diagnosed with TOF. Do all TOF babies have chromosomal abnormalities?
Jazdya Herarndz
Jazdya Herarndz
Jazdya Herarndz
Jazdya Herarndz
Jazdya Herarndz
Jazdya Herarndz
So what is cure for this?
I also faced 2 time this problem with my baby
🦌🐺🦌😥🤐🥜🦄🐶hjef😎😘😘😥😏🤔😗🤔🤩🥰😁🤣😘🤗😂😁🤣😃😍😍😘😄😍😉😉😊😍😄😄😄😍😎😐😐🤨🤨😐😐😐😑😶🙂🙂☺️☺️☺️☺️🙂🙂🙂🙂😘🤗🤗☺️🙂😑😑😑☺️🙂☺️🙂🙂😶😶😶😶😶😶😶😶😯😯😯😯🤗🤗🤗🤗🙄🙄😪🙄🙄🙄🙄🙄🙄🙄🙄🙄🙄🙄😪😪😪😪🥞🥞🍄🥔🥔🥔🥕😙😚😚😙😚😚😐😐😐😚😚😚😐😐😚😚😚☺️😚😐😚☺️☺️😑😑☺️😑😶😑☺️😮😮😑☺️😑😑🤐😜🤐😶😶😑😑😑😪😪🙄😘🍆🤩🐎🐷🐈
My mother always told how it was painful not knowing if I was going to survive. I had like 4 defects. I'm 44 and had another surgery at 39. Still here.
سبحان اللہ ۔ الحمد اللہ ۔ اللہُ اکبر
سبحان اللہ ۔ الحمد اللہ ۔ اللہُ اکبر
Thank you very much
Really good video
Thank you for sharing these stories and raise awareness ;(