3:00pm
Abi's heart is beating now!! The double switch is complete. She's lost a lot of blood, as expected, so she's on continuous transfusion. She's still on the bypass though. More updates in 1 hour. So far the surgery is going according to the plan....
J.
Abigail
![Abigail](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgWOf3o0bBDymwrBMMmguW5f3Xf0mSRRYavcuMo3m3iQ_lWz8WJ9tJMi3QlmAbWUvZR8gkf4kuqp-4MWEi1HZuEYhdYbruj-QzRaTzUng7EGLZ-melHL6i1LlaydyTotSDelxCNvjvdr7VI/s1600-r/Abi_Newborn018.jpg)
Wednesday, December 9, 2009
Update on surgery
12:45pm
Update from a minute ago: first part of the switch is complete; one of the clamps is removed; starting to warm up the room (its 60F now); Jackie - the nurse came to tell us that dr Kirshbom - the surgeon, is an excellent specialist and God is using his hands, and the OR is filled with angels. This was a confirmation of God speaking through others earlier:
Krista G. (12-08-09): "it will be a super natural-natural thing. The surgeon will be a puppet if you will and the HS will be guiding his hands and giving him strength to do the task speaking in to his ear what move to make next. The surgeon will say in the end that is the easiest/complex surgery I have ever done."
Karl C. (12-09-09 12:18pm): While I was praying this morning, I saw Jesus came into the OR and touched Abi on her head, and he then walked around and touch all the surgeons and nurses.
We feel at peace right now...
J.
Update from a minute ago: first part of the switch is complete; one of the clamps is removed; starting to warm up the room (its 60F now); Jackie - the nurse came to tell us that dr Kirshbom - the surgeon, is an excellent specialist and God is using his hands, and the OR is filled with angels. This was a confirmation of God speaking through others earlier:
Krista G. (12-08-09): "it will be a super natural-natural thing. The surgeon will be a puppet if you will and the HS will be guiding his hands and giving him strength to do the task speaking in to his ear what move to make next. The surgeon will say in the end that is the easiest/complex surgery I have ever done."
Karl C. (12-09-09 12:18pm): While I was praying this morning, I saw Jesus came into the OR and touched Abi on her head, and he then walked around and touch all the surgeons and nurses.
We feel at peace right now...
J.
Surgery-the lesson of waiting
11:11am
Abi slept all day yesterday after being sudated and woke up 3 times at night to eat. We could tell she wasn't very
comfortable, so I'm thankful she was asleep for the most part. We are up since 4:40 am. We couldn't give her anything to drink after 5, so it made especially difficult to keep her comfortable. Finnally, she calmed down watching Mickey Mouse- I am actually thankful for TV today. It bought us ans mainly Abi extra 40 min of peace and quiet. She actually smiled to us for the first time after 24h. So precious!
at 7:15am she was given meds to make her sleepy. I held her for an hour
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEj0bmpSeC4GGkZZteEzPTbIyAvoikAidR82m9JKePUC7Vqb7aXsT67wG2GH3DPgxO2Spo8XKaPH5VLyMzAjq8r5hGsU8S_gTBqYFNyTW54ounmAhBKhzYaoye8dSa2ZaULafBkc6kp4RLQL/s288/iphone_photo.jpg)
until we were asked to walk to the OR area, where she was taken by the team of anastesiologists. She opened her eyes and looked with half curious and half frightened eyes as we kisses her goodbye and passed her to the nurse...."you take my mourning and turn it into laughing?"- not necessarily there yet... One of the hardest things to do; place your precious baby into strangers' arms trying to trust they will take good care of her...
So hard ........
We are sitting in the waiting area for updates every 1 hour.
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjuUp2Fn7fwUuiGNdIATRH68DNXfyjpZV7I5cuWQimyohVb7Nad_AFlxFMyyFSe8u-v5TVlVY7b29UCD3aSYKwmscUt-EkoKeBdxvXdssASb9nuj1YPeAJAZdk29fx0PHNOam-N2bobZ6BY/s288/iphone_photo.jpg)
Here's what we have received so far:
9:42 am - after anastesia, the surgery started
11:00 am - Abi's on heart-lung machine; closing VSD.
J.
Abi slept all day yesterday after being sudated and woke up 3 times at night to eat. We could tell she wasn't very
comfortable, so I'm thankful she was asleep for the most part. We are up since 4:40 am. We couldn't give her anything to drink after 5, so it made especially difficult to keep her comfortable. Finnally, she calmed down watching Mickey Mouse- I am actually thankful for TV today. It bought us ans mainly Abi extra 40 min of peace and quiet. She actually smiled to us for the first time after 24h. So precious!
at 7:15am she was given meds to make her sleepy. I held her for an hour
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEj0bmpSeC4GGkZZteEzPTbIyAvoikAidR82m9JKePUC7Vqb7aXsT67wG2GH3DPgxO2Spo8XKaPH5VLyMzAjq8r5hGsU8S_gTBqYFNyTW54ounmAhBKhzYaoye8dSa2ZaULafBkc6kp4RLQL/s288/iphone_photo.jpg)
until we were asked to walk to the OR area, where she was taken by the team of anastesiologists. She opened her eyes and looked with half curious and half frightened eyes as we kisses her goodbye and passed her to the nurse...."you take my mourning and turn it into laughing?"- not necessarily there yet... One of the hardest things to do; place your precious baby into strangers' arms trying to trust they will take good care of her...
So hard ........
We are sitting in the waiting area for updates every 1 hour.
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjuUp2Fn7fwUuiGNdIATRH68DNXfyjpZV7I5cuWQimyohVb7Nad_AFlxFMyyFSe8u-v5TVlVY7b29UCD3aSYKwmscUt-EkoKeBdxvXdssASb9nuj1YPeAJAZdk29fx0PHNOam-N2bobZ6BY/s288/iphone_photo.jpg)
Here's what we have received so far:
9:42 am - after anastesia, the surgery started
11:00 am - Abi's on heart-lung machine; closing VSD.
J.
Tuesday, December 8, 2009
Double switch it is...
7:10pm
It's been a long day filled with doctors, nurses and the army of other people who have continuously been invading Abi's room asking the same questions.
Since Abi returned from the cath, she has been sleeping for the most part of the day. She didn't eat until 4pm- for 13h. Once she started she drank 5oz of cherry flavored pedialite she'd never had before.
Anyway, we spoke with her surgeon and he chose to go with the double switch TOMORROW! Not longer than yesterday he wasn't really keen on doing this now because she is so small! Her systemic valve though leaks a lot so there is no point in waiting longer. We haven't signed up for that- that's for sure. The surgery will last about 8-9 hours and starts at 7.30. Along with the double switch they will be closing her vsd. It's going to be an even longer day. Probably the most terrifying, nerve wracking and .... The worst day of our lives. Our precious little girl will undergo a huge open heart surgery. Just this morning she was all smiles, cuddly and joyful and no one could tell her condition is so bad.
She will probably stay in icu for a good week, then a week or two in the perdiatrics... No, that's definitely not what we came here for... I'm hoping and praying for the best... Home for Christmas? Let's take one day at the time.
J.
It's been a long day filled with doctors, nurses and the army of other people who have continuously been invading Abi's room asking the same questions.
Since Abi returned from the cath, she has been sleeping for the most part of the day. She didn't eat until 4pm- for 13h. Once she started she drank 5oz of cherry flavored pedialite she'd never had before.
Anyway, we spoke with her surgeon and he chose to go with the double switch TOMORROW! Not longer than yesterday he wasn't really keen on doing this now because she is so small! Her systemic valve though leaks a lot so there is no point in waiting longer. We haven't signed up for that- that's for sure. The surgery will last about 8-9 hours and starts at 7.30. Along with the double switch they will be closing her vsd. It's going to be an even longer day. Probably the most terrifying, nerve wracking and .... The worst day of our lives. Our precious little girl will undergo a huge open heart surgery. Just this morning she was all smiles, cuddly and joyful and no one could tell her condition is so bad.
She will probably stay in icu for a good week, then a week or two in the perdiatrics... No, that's definitely not what we came here for... I'm hoping and praying for the best... Home for Christmas? Let's take one day at the time.
J.
Change of plans
11:01am
So here we are, waiting for Abi to come out from the cath procedure. She was taken there
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEi3v3I58z-3mZaaOkllyta-fMp4D5-gDHKUCPMo07W9cRhEceC2a9tXg7vwlKZAroHJudyIlo79E5XkJYZjLEUxbJP-4_-yBvtAXPdXx1M1EnNudID1n9sTUJLJEze5LRUAdRqSOeWTf92D/s288/iphone_photo.jpg)
at 9:30am and we just got an update on her. Fortunately, she's sleeping all the time and she just got some more sudation, so she will not be scared. The reason for cancelling the surgery at the last minute and going with the cath was that her saturation is in the 70-80% instead of 90s and the echo showed no overcirculation in the lungs. They are trying to find out what to do next. There are a few options: 1. Replacing the severely leaking valve only or with closing VSD (right now its 7mm). 2. Doing a double switch now. 3. No surgery for now. The answer to that we'll know maybe today. They mentioned a heart transplant but this option would buy her no more than 20 years (statistically) of life with 2 heart transplants and then it would be "the end of the road" as the doc said this morning.
Apart from that, Abi is doing exceptionally well, she is so easygoing and patient. Sometimes I think she understands more than we think.
She's handling this much better that mom and dad...
Jo
So here we are, waiting for Abi to come out from the cath procedure. She was taken there
![](https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEi3v3I58z-3mZaaOkllyta-fMp4D5-gDHKUCPMo07W9cRhEceC2a9tXg7vwlKZAroHJudyIlo79E5XkJYZjLEUxbJP-4_-yBvtAXPdXx1M1EnNudID1n9sTUJLJEze5LRUAdRqSOeWTf92D/s288/iphone_photo.jpg)
at 9:30am and we just got an update on her. Fortunately, she's sleeping all the time and she just got some more sudation, so she will not be scared. The reason for cancelling the surgery at the last minute and going with the cath was that her saturation is in the 70-80% instead of 90s and the echo showed no overcirculation in the lungs. They are trying to find out what to do next. There are a few options: 1. Replacing the severely leaking valve only or with closing VSD (right now its 7mm). 2. Doing a double switch now. 3. No surgery for now. The answer to that we'll know maybe today. They mentioned a heart transplant but this option would buy her no more than 20 years (statistically) of life with 2 heart transplants and then it would be "the end of the road" as the doc said this morning.
Apart from that, Abi is doing exceptionally well, she is so easygoing and patient. Sometimes I think she understands more than we think.
She's handling this much better that mom and dad...
Jo
Monday, December 7, 2009
No surgery in the morning
Late update
We got to the hospital at 9am. We met many people; cardiologists, phisicians, Cardiothoracic surgeons, anasthesiologists and some others. After answering many many questions, having Abi go through heart echo, chest x-Ray and blood work, we were out of the hospital after 7 hours. Abi did great though they wanted to get good pictures with the echo and they sedated her. This caused her blood saturation drop really bad and they had to give her some oxygen. After all of this when we got home they called us saying they didn't like some of the tests results and they don't want to do the surgery in the morning. They want to do a cath, a line driven up one of the veins to her heart to measure everything from the inside. Once they have more info they will discuss what they are doing next.
We don't know what they will do nor what the next step will be. We
have to be in the hospital at 7am and don't know what next. We will keep you updated.
Artie
- Posted using BlogPress from my iPhone
We got to the hospital at 9am. We met many people; cardiologists, phisicians, Cardiothoracic surgeons, anasthesiologists and some others. After answering many many questions, having Abi go through heart echo, chest x-Ray and blood work, we were out of the hospital after 7 hours. Abi did great though they wanted to get good pictures with the echo and they sedated her. This caused her blood saturation drop really bad and they had to give her some oxygen. After all of this when we got home they called us saying they didn't like some of the tests results and they don't want to do the surgery in the morning. They want to do a cath, a line driven up one of the veins to her heart to measure everything from the inside. Once they have more info they will discuss what they are doing next.
We don't know what they will do nor what the next step will be. We
have to be in the hospital at 7am and don't know what next. We will keep you updated.
Artie
- Posted using BlogPress from my iPhone
We're here...
Finally, granda at home safe and sound and we after 5h trip filled with 4 stops and some adventures-emergency stop to buy a paci we forgot to take for Abi,we reached Atlanta at 10pm. Abi did great during the trip and at night, though found herself most comfortable in my arms, for the first time refusing to sleep in her bed.
Now,we're heading to the hospital for the preop and to meet all the docs , and find out what the plan 4 2morrow is.
We'll post more as we know more....
Thank you for caring 4 Abi ...
Jo.
- Posted using BlogPress from my iPhone
Now,we're heading to the hospital for the preop and to meet all the docs , and find out what the plan 4 2morrow is.
We'll post more as we know more....
Thank you for caring 4 Abi ...
Jo.
- Posted using BlogPress from my iPhone
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About Abi's Blog
HELLO!!
This blog is created not only to keep our family and friends updated on Abi's condition, events, surgeries and everyday life... but also to provide legit and educated information about Congenital Heart Defects that touch 1 in 100 babies.
Welcome to Abi's blog with hopes you will find it useful, interesting, touching and even entertaining...
Here are some facts about our sweet baby girl:
Abi was born on July 24th, 2009 with several heart defects that were detected prenatally at 18 weeks: Congenitally Corrected Transposition of the Great Arteries (Congenitally Corrected Transposition of the Great Vessels) (CCTGA = LTGA = L-TGA), Ebstein's Malformation (Ebstein's Anomaly) (malformed tricuspid valve), Pulmonary Stenosis and VSD.
Her first surgery - PA band - was scheduled for December 8th, 2009, however unexpectedly was changed to an Open Heart Surgery (OHS) called Double Switch performed on December 9th, 2009, originally planned for much later...
This blog is created not only to keep our family and friends updated on Abi's condition, events, surgeries and everyday life... but also to provide legit and educated information about Congenital Heart Defects that touch 1 in 100 babies.
Welcome to Abi's blog with hopes you will find it useful, interesting, touching and even entertaining...
Here are some facts about our sweet baby girl:
Abi was born on July 24th, 2009 with several heart defects that were detected prenatally at 18 weeks: Congenitally Corrected Transposition of the Great Arteries (Congenitally Corrected Transposition of the Great Vessels) (CCTGA = LTGA = L-TGA), Ebstein's Malformation (Ebstein's Anomaly) (malformed tricuspid valve), Pulmonary Stenosis and VSD.
Her first surgery - PA band - was scheduled for December 8th, 2009, however unexpectedly was changed to an Open Heart Surgery (OHS) called Double Switch performed on December 9th, 2009, originally planned for much later...
Second OHS was scheduled for March 3rd, 2010 to correct the baffle created during the 1st surgery.
Thank you for your support and prayers.
Art & Joanna (Asia) & Abi.
Thank you for your support and prayers.
Art & Joanna (Asia) & Abi.
You can CONTACT US at: blog@Care4Abi. com
“You never know how strong you are until being strong is the only choice you have!"
Thank you for your generous heart to help cover for Abi's medical expenses...
Early and Intermediate Outcome After Anatomic Repair of CCTGA
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It's time for the big one. Congenitally Corrected Transposition of the Great Arteries (ccTGA, LTGA). In normal, healthy heart there are...
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CHD Abbreviations:
ASD - Atrial Septal Defect;
DILV - Double Inlet Left Ventricle;
HLHS - Hypoplastic Left Heart Syndrome;
HRV - Hypoplastic Right Ventricle;
LTGA - Levo-Transposition of Great Arteries;
PA - Pulmonary Atresia;
PDA - Patent Ductus Arteriosus;
PS - Pulmonary Stenosis;
TOF - Tetralogy of Fallot
VSD - Ventricular Septal Defect
DILV - Double Inlet Left Ventricle;
HLHS - Hypoplastic Left Heart Syndrome;
HRV - Hypoplastic Right Ventricle;
LTGA - Levo-Transposition of Great Arteries;
PA - Pulmonary Atresia;
PDA - Patent Ductus Arteriosus;
PS - Pulmonary Stenosis;
TOF - Tetralogy of Fallot
VSD - Ventricular Septal Defect