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Paula Dawson
Приєднався 19 лис 2008
Відео
Becoming a Goalie @ On Ice Goaltending School
Переглядів 2338 років тому
Just over a year ago Nolan decided he wanted to become a goalie. Thank you @onice.goaltending for an amazing first year! Here's a video of Nolan's journey from June 2015 - June 2016. He has worked so hard and we are so proud of him. Thank you Matt, Mike, Justin, Steve, Ryan, Michael & Jamie. He really enjoys his time with all of you!
Becoming A Goalie
Переглядів 1029 років тому
At 8 years old after his fourth season playing hockey he has decided he wanted to be a Goalie. Good luck buddy and have fun! I'll be hiding in the stands with my hands over my eyes ;)
On Ice Goaltending School-Lesson #8 The stick save
Переглядів 729 років тому
Nolan (8) has decided he wants to be a goalie. This is him working on the stick save
Jack's first day at Pre-school (Sept 1, 2015)
Переглядів 4029 років тому
Jack @ 3.2 years on his first day of pre-school. My baby boy is all grown up :)
Fun at SkyZone - Mississauga Ontario
Переглядів 6349 років тому
SkyZone trampoline park Mississauga, Ontario
Happy 5th Birthday Evan!
Переглядів 23510 років тому
This video is dedicated to our sweet little Evan. You are one amazing little boy and you have overcome so many obstacles and continue to prove to us that there's nothing you can't do. We are so proud of you and the little boy you have become. Love Mommy & Daddy xo
YMCA Dance-a-thon for Strong Kids Campaign
Переглядів 93011 років тому
YMCA Dance-a-thon for Strong Kids Campaign
How is he today?
Thank you for posting this. Our granddaughter, now 4 months old, born with TGA, surgery when she was 36 hours old, is doing incredibly well. Jack is now ten, have there been any complications, any concerns we should have moving forward. Thank you again for posting this.
My son D-TGA .His age 62 days. next week open heart surgery,national heart foundation Dhaka, Bangladesh.
How's your baby now ..? Everything is ok
God bless your Baby
How is he doing now? Does he have any problems? My baby also diagnosed with tga ivs. Did your baby have tga ivs or some hole in his heart?
Hello dear I am 3 month 5 days pregnant my baby also diagnosed with tga I am confused what to do I am totally nervous and crying all the time my previous baby girl was preterm and 1.2 kg only but she is feet and fine now I can not think what to do pls suggest me and also give advise that your baby is now fit and another surgery is required or not after birth
I can relate to this my baby was diagnosed at my 20week scan with tga I was terrified as he were my 1st poorly baby outta him being my 7th, my labour ran smoothly obviously tests and regular scans, he were brought 5 days early but apart from 1 mishap with my baby everything went smoothly for him, it is scary I won't lie looking at all tubes in your baby seeing all drains after the operation scared me but once I knew what they were fir I were fine, my baby is now 5month old this month he as check ups every 3 month but is doing fantastically in himself, he as however got a heart murmur which iv been told not to worry about coz they go in their own time , but honestly it is a scary experience but your baby will come out like its never been through awt , good luck x
did u breastfeeding him
Just found out my unborn grandson hasTGA I am so upset what advice can u give me to support my son and daughter in law
May I ask how’s your little man is doing now? I wish him health, happiness and love in his life
I had my baby (Eli) in July he has TGA and coarctation of the aorta, I watched your video of courageous Jack many times before I had Eli, it gave me and still giving me so much strength and hope My baby has the surgery at the children’s hospital of Pittsburgh he had to have a catheter two months after the main surgery. He is doing fine now and I’m grateful for every moment I spend with him I’m always scared for him though especially through this pandemic I just wanted to let you know how much I appreciate you as a parent, and how much I respect and appreciate your little warrior I can’t thank you enough for sharing your experience it has been a wonderful source of hope
❤
My friend,s son also born with that. I was asking some questions to you. 1. Age differents between jack,s mom and dad? 2.blood group of jack,s mom and dad? Please send answer to me soon. Please please
Hi… I had a baby TGA+ Vsd+pulmonarystenosis ..age difference Btwn my hubby and me is 13 yrs .. blood is mine Oneg and husband AB positive
Watching with smiles and tears I have a poem for my son TGA 1999
Mam how is your son now? What is the age difference between you and your husband?
My Grandson is 1 month old and his TGA was just found. He has had 1 surgery on Thursday and is awaiting the second in about 2 weeks. Thanks so much for this video. It has brought me great hope. Our faith is strong and we know he will come home to us soon. 💕 THANK YOU!
What is the age difference between TGA baby,s mom and dad?
simpu s 20 & 20
@@rhimax814 I am Also same age. My son also born in TGA . So which parents are got a marriage in same age, one year, two year and three year old difference that babies are getting faced so much problem. Please get marriage with 7 years different.
simpu s I don’t understand your comment, sorry.
I'm watching this in 2020 in the midst of a pandemic and I am having a boy in July with TGA as well at SickKids in Toronto. I am so glad I was able to find this video of little Jack.. it's great to get a glimpse of what's ahead. He is a beautiful boy and it warmed my heart to see his little smile.. can't wait to meet our little heart warrior
Marija Burcar All the best to your and your little warrior! I’m glad this video has helped you and has brought some sort of comfort to you during this time. I remember that feeling all too well like it was yesterday. You and your little boy are stronger then you know. I’ll be thinking of you both and sending healing heart hugs. An update on Jack - he is turning 8 in June! He plays hockey, baseball and basketball and nothing gets in his way :) Heart Warriors are AMAZING! ❤️💙
Daile Torres so sorry you are having to go through this. We are there with you and will be praying for your baby’s recovery. Our grandson just had 1 of the 2 surgeries he will need.
Same here. 5 months pregnant and doctor told me she suspect TGA on baby girl. I am devastated i have been crying all day... i dont know what to do. I need emotional support. Shirleyveronica05@yahoo.com...
Shirley Ramos so sorry to hear. Stay positive. I’m new to the TGA world but I wish there was more support available.
@Daile Torres i have the appointment tomorrow at 11 am with the specialist... i am devastated crying not eating i dont want to loose my baby girl. I am dying alive
I was there when I was very young.
One of the best shows I've ever seen. Perfect venue, aswell.
My little chloe was diagnosed today with TGA! She has 25 weeks, the doctors said that her surgery will happen after she born!!! I am so scared but this video and this comments are making me few much better!!! God Bless you little jack!!!
What is the age difference between TGA baby,s mom and dad?
simpu s im 32, my wife is 35 and my daughter now is almost 4! She never been so perfect! :)
@@viniciusscarsetto1147 thank you .l asking this question Many TGA parents. They are all said 2 years old different. Yes. Parents Age different must be causing this problem. Please share and finding this matters
simpu s where you from?!
@@viniciusscarsetto1147 in India sir
:))
So Jack was born with TGA AND Coarctation of the Aorta? Were they both known at birth? I am a nursing student getting ready to graduate and Jacks history fascinates me! What a tiny miracle he is! Would you mind helping me understand his particular condition?
Hi Donna. So after his arterial switch operation while he was in the CCU the nurse noticed his feet were ice cold and his pulse in his femoral and feet arteries were very weak. They could barely feel them at all. They ordered a bedside Echo and sure enough there was the coarctation of the aorta :( At that point his chest had already been closed and they told me that this happened as the ductus closed. He was discharged 8 days after his switch but was closely monitored twice a week and then it was time to open him up as they were worried about heart failure as his left ventricle was working so hard. His blood pressure was pretty high as well. I remember they were going to see if they could try to avoid another open heart surgery and go through his side but for whatever reason (can't remember) they couldn't. I remember his surgeon telling us that he hadn't seen a TGA baby with CoA in fourteen years or so. He also showed us a pic of the narrowed piece they cut out. It was a pinhole
Now he's battling pulmonary stenosis in his branches....which is pretty common after the switch. He had a cath balloon dilation when he was 17 months old but it wasn't successful. Since then he's been watched every 6 months and at one point the narrowing wasn't getting any worse but about 6 months ago they were getting tighter. He just had an echo and lung perfusion test a few weeks ago and they are still pretty tight but the blood flow in his lungs is the same as it was when he was 17 months. So now we are waiting again. All this up and down is killing me. Open up little arteries!! I remember them telling me if a second attempt at the balloon dilation doesn't work then he may need another open heart. He's 3 1/2 now and you'd never know. His breathing gets a little heavy at times, but he's so active so it's hard to keep track.
+Paula White I am in awe of your strength and courage! He is truly a tiny miracle!
+Paula White I would LOVE to see a picture of him...what a story! I am fascinated!
+Donna Ruby I tried to post a pic link to the comments but it's not working.
God bless little jack, I was born with TGA, im turning 40 this year,, jack has a bright future ahead. God bless him and his family.
***** Thank you both for sharing : ) It gives me a great sense of relief knowing there are adult survivors out there that are healthy and strong. He's 2 1/2 now and full of so much energy but I'm still a nervous wreck at times. He will possibly need some more surgeries in the future but for now we are waiting to see how his heart/arteries grow. Thank you for your comments, makes me breath a little easier :)
Paula White thank you for sharing this, my fiance is 26 weeks along and we just found out our little man has TGA and will have to have surgery after birth. your story made me cry but also gave me a little hope.
Hi Brent, I shared his story to give others hope. I remember the long drive home in a daze staring at a piece of paper with the letters TGA written on it. The first thing I did was a youtube search looking for some hope and success stories. It's been quite a journey as he's had other CHD's but there's no stopping this little man. He will be three in June :) Good luck to you all and sending lots of strength to your little heart warrior.
Hello again. I recently joined a Facebook group dedicated to people with TGA. Until then I'd never even spoke to somebody else with my condition. It's very helpful and it's also for families of TGA too.
+del80y yes it has definitely helped me meeting other families and talking to other CHD survivors. I still can't believe we lived this, and I have a hard time looking back at pics and videos. It all seems like a dream. He's possibly facing more surgery soon if his pulmonary arteries don't open up but they've been watching closely after the first attempt when he was 17 months didn't work. He's 3 1/2 now and one wildly energetic boy always trying to keep up with his brothers. Who knows what the future holds, but my mind is at ease knowing there are many survivors out there! Thank you for reaching out!!
I am 51 and had the TPGA and the Mustard heart operation in 1963, mustard in 1967. i have been fine ever since. My father said 5 out of 7 died at that time. we have come along way. i'm sure they will be healthy but may have depression it's such a dramatic thing in our lives. love Susan
What a beautiful baby and family!! This video made me cry and remember all the memories of our journey. I have a 11 year old boy who was born with TGA. He is growing and doing well. May your family be blessed!!
loved watching jack's story. My little boy is also a TGA baby. you can see his story here Kevin's Story,Transposition of the Great Arteries.
My daughter is going to be 21 years old in Oct. She was born with TGA: Transposition of the greater arteries, ASD: Atrial septic defect, Pulmonary stenosis, CHD/Scoliosis & Dysphagia Lusoria. Had 3 open hearts and 5 heart caths & 4 spine surgeries She has had to jump threw many hoops & by looking at her you would never know, but she a true miracle. God Bless your miracle child.
From which you perform her surgery i m worried about my son he is also tga,vsd and severe PS
@@littlechamps2181 Sir, what is the age difference between you and your,s wife?
omg this is hilarious im crying :D
This Is funny
Молодец парень,желаю ему успехов в хоккее
Look'in good. He'll be flying around the ice in no time!
Cool Allen Bester!
@theopenempty It was totally hilarious. All the kids just wanted to grab it and take off! Maybe rugby would be a better sport at this age!
illegal hand balls! I would complain if I was an opposing parent!
Cute... Makes me want Candy!
LORI!!!!I didnt recognize you at first!!! You guys really dance!!!Dirty!!!! LMAO I wish I could dance like that!!! I cant dance to save my life!!! Good luck, much love from Portugal my friend! PS edub is sooo cute,its ur nephew right?Really cute!Congrats!
Thanks for all the positive comments! We had so much fun and literally whipped it together.
Awesome dancing!
This is awesome!!! Love it!