Pray needed

This little girl need alot of pray. Her name is Riley Phares. She will be going to have heart surgery. Riley has a large hole in the the top chamber on the right side of her heart and the right side of the heart is bigger then the left side. If u could please pray for this little girl and her family.

Good Day

Jayden is doing good he is starting to eat by mouth more and he has learned to army crawl. He has also learned to pull his self up but cant stand there by his self. He loves to be outside and talks to the dog thinking they can talk back to him but it is so cute. Jayden likes to pick on his brother and he thinks it is funny and he thinks everything Kaleb does is funny to him. He goes to the cardilogist on March 28 to see how well he is doing and then they will schedule him for a heart cath to see when his fontan will be. Hopefully not soon cause I dont want to hand my baby over now I want to spend all the time I can with him. He is very much so a mommys boy and I like it. I cant wait for spring to come so Jayden and the other to can go outside more they are very much so tried of being in the house. But they have been sick to Jayden has double ear infection , Kaleb has ear infection and Katilynn did have that virus. Jayden weighes 20 pounds and 10 ounces and is 28 inches long he isnt a baby no more where has the time went. I cant believe that he is already 13 months old it just seemed like yesterday I had him. We have a OT nurse starting tomorrow to work with Jayden on feeding and to working on his mobile skills. So hopefully he likes her and doesnt cry on her cause if he dont like you he want go to you and he will cry when you talk to him. Which is a good thing because i dont want him to go to strange or let them talk to him.

JAYDENS 1ST BIRTHDAY

Jayden and Kaylee(Jaydens Cousin)

He like to put his hands in the cake but he didnt like the icing on his hands

Happy 1st Birthday

Happy 1st Birthday to my little miracle baby Jayden Chase Taylor.

Dear Jayden

One 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

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

PRAYING FOR BAYLEIGH

Pray

This post is going to be about a little girl that need EXTRA prays for her and her family her name is Bayleigh. She will be going for her fontan but this will be her 4th open heart surgery and it will be her second one this year so she needs lots of pray. Bayleigh will have her fontan on the thursday the 16th.

This is Bayleigh please pray for her

Jayden

He is doing good and he will be going to morgantown on the 15th for a check up with the surgey to see how thing are going. Jayden is pulling hisself up to sitting and can sit all by hisself. He is very mobile he rolls all over the floor to where ever he wants to go.

Eating

We are still working with Jayden to get him to eat by mouth so far it is going great. He likes mac and cheese , grees beans and banna and yogurt.

We took the kids to see santa and Jayden didnt know what to think of him. He cried when we sit him on his lap but if he was sitting in the floor beside him he was ok. I did get a picture with him on his lap without him crying.

PRAYING FOR BAYLEIGH AND HER FAMILY HOPEFULLY A LAST RECOVER SO SHE CAN BE HOME FOR CHRISTMAS

Sorry it has took me a long to put a blog on here but between moving and getting everything put in the right place have not had no time. Well Jayden like the new home and so does the other two kids. Jayden goes to morgantown and see DR. Gustafson on the dec 15 and he is just going to check his scar and make sure he is doing ok. I took the kids this pasted saturday and let them see santa. Jayden is starting to eat back mouth he likes mac and cheese, bannas and green beans right now but we are trying him with different stuff everyday. He has learned to sit up by hisself and is in a big boy car seat and he loves it cause he can see different stuff. Now that he knows how to sit up he does want to be laid down at all but when he is sleeping. We put are christmas tree up and he roll his way over to it and was playing with the ornaments.