Saturday, January 22, 2011
Friday, January 21, 2011
Happy 1st Birthday
Happy 1st Birthday to my little miracle baby Jayden Chase Taylor.
Dear JaydenOne year ago you where borning and they thought you had a heart murmur so when you was 8hrs old you was transported to WVU childrens hospital and they told us you had one of the worst kind of heart defect there is. They told us we had two choice to let you die in 24hrs or to do the series of three open heart surgeries and we pick the series of heart surgerys. One year ago you was the light of our life and still are we hold you love you and cuddle you which you like. You have show us so many things to life and we are glad that you have. Jayden you are my little miracle baby and will always be. We love you so much and glad you are here with today.
You fight for you life and you still are people dont know much about you and when they ask mommy tells them and if they dont know what Hypoplastic Left Heart Syndrome is we tell them but most of them look at us like we are stupid. We have made to 1 year and many more to come. Just keep up the go work and hopefully when you grow up you will tell you story about living with half heart.
On April 8, 2010 it was the night you had your Glenn we thought that we was going to lose you. Your oxygen sats drop to 6 and your left lung collasped. But you show they doctors nurse and staff at WVU childrens hospital that you was letting go and that you was going to fight for everything you have and you did that is why you are here with you today. We just like to think WVU Childrens Hospital doctors, nurse, and staff for keeping you here with us and especially your surgeon Dr. Gustafons for everything he has done and is still doing for you.
Jayden you had a nice birthday with all of your family and friends so couldnt show up cause they where sick but mommy told them not to come cause she didnt want you sick.
HAPPY 1ST BIRTHDAY MOMMY, DADDY, KATILYNN AND KALEB LOVES YOU
Monday, January 3, 2011
2011
Jayden will be a year in two weeks doesnt ever seem like. On Jan 21,2010 is when Jayden was borning and that is when we found out he had Hypoplastic Left Heart Syndrome and that he would have to have a series of three open heart surgery. Jayden is such a miracle baby to are family and he show us not to take life for granted and that god is good for what he does. We would just like to thank everyone for the support, prays, and thought when we was going through this hard time. It was hard know that my baby was healthy the whole time and me asking they doctor over and over why I was passing out. Founding out 8 hours after he was borning that he had HLHS. We couldnt ask for a better baby then Jayden is we love him so much and glad he is here with us today. Katilynn and Kaleb both love there little brother and want let nothing happen to him and they want let no one to touch him.He weighs 21 pounds and 7.3 ounces and is 28 inches long. So by far he is doing great keep him at home from everyone and if they are sick or feel sick they cant come to my house I want to keep him from getting sick as much as I can. He got his bottom teeth in around christmas time and Katilynn lost her to front teeth on christmas. We had a great christmas Jayden like his toys but he didnt want the paper on them. Jayden is taking solid foods but liquid he still gags and crys. Birth to Three is sending a nurse to help with that. So far 2011 has start out a good year for us. Jayden is very mobile he rolls all over the floor and he like to be on his tummy more. He just like everything Kaleb does is funny.
My goal for 2011 is to keep doing want I am doing with Jayden and to keep him as safe as possible from getting sick. Jayden goes and see the ENT Jan 24, 2011 I am hoping everything goes well there and He goes back in March to see the cardiologist and they maybe do a heart cath on him then to see when he is ready for his FONTAN maybe in sept or oct. He can say momm when he get mad or upset cause he knows mommy with came and get him. Jayden likes to play peck boo and his new thing is when u tell him something he will shack his head NO.
Hope everyone 2011 is great
My goal for 2011 is to keep doing want I am doing with Jayden and to keep him as safe as possible from getting sick. Jayden goes and see the ENT Jan 24, 2011 I am hoping everything goes well there and He goes back in March to see the cardiologist and they maybe do a heart cath on him then to see when he is ready for his FONTAN maybe in sept or oct. He can say momm when he get mad or upset cause he knows mommy with came and get him. Jayden likes to play peck boo and his new thing is when u tell him something he will shack his head NO.
Hope everyone 2011 is great
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