There are days when Abi is a picky eater and since she has a CHD (Congenital Heart Defect) we had to watch her eating habits closely and keep record of every milliliter of milk she had since day 1. I think this has stuck with us, or at least with me and sometimes, I must admit, I am stressing too much about her eating, or rather not eating.
During one of the last cardiologist appointments we talked to Dr. Greene and he said something very important, especially for me. He basically said that if children are offered food and have some choice they won't starve themselves and if Abi was not interested in eating at times, not to stress about it and let her be.
It helped a lot at the time, but couple months later I'm back to stressing about it again, so I started reading a little bit on the subject and thought I would share some of what I read here, with others who may be like me ;-).
Melanie Shay, a registered dietitian, in her article on BabyCenter.com, says that it's common for 2 year olds to seem like they don't eat, but as long as they grow normally, they most probably are fine and we should not force them to eat or eat more.
Here is the best part. Per Melanie Shay, a recent study of children and their eating habits, from the American Dietetic Association showed that when children are presented with variety of foods, almost all of them will eat enough to meet their nutritional needs. How awesome is that?!
Since I am the one usually making deals with Abi just to make her eat a bit more, after reading the entire article and couple others, and looking at the Food Pyramid for Young Children I decided I will give Abi a break. If she doesn't want to eat enough, and by enough I mean according to my standards and expectations, I won't bother her and will let her be. We'll see how this works out for all of us. Her weight gain and my nervous system ;-)
Below I put the screenshots (with the links) of the Food Pyramid for Young Children and couple other links you may find interesting interesting:
Nutrition Guidance for Healthy Children Aged 2 to 11 Years
Kids Eat Right
Art
Abigail
Wednesday, August 10, 2011
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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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Alright, time for another post. For today I picked another of Abigail's heart's complexities, namely Pulmonary Stenosis (PS). There ...
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We found out today about the upcoming surgery in Atlanta.. It's scheduled on December 8th. We're leaving on Sunday, December 6th, ...
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Transposition of the Great Arteries (TGA) In Transpotition of the Great Arteries both, Aorta and Pulmonary Artery are transposed (inverted) ...
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
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