Well kayden is climbing the stairs at Nana's house his mommy isn't to happy about this. It is so cute to see him doing it though! the little stinker can get all the way to the top!! he likes to hold your fingers and walk he is doing so well! He has to go back to Cincinnati October 1 to get his last Echo!! He is weighing in at almost 18 pounds and wanting to eat all big people foods!! His favorite baby food is Prunes!!! I figure he will out grow that!!! He calls me Cookie!! which is way to cute and loves his Mommy to death!! My daughter was to have her second child the end of August but the Doctor changed it to September 10 She is more then ready poor thing! I cant wait to See my Granddaughter and watch her mommy hold her as soon as she is born ! it will be good since she didn't get to hold Kayden for a couple of weeks due to his cdh! Any ways i have been following all the cdh babies and it has been a sad month! I pray for all of the cdh babies family's ! Please keep baby carter in your prayers he is in Cincinnati Children's hospital and just had Heart surgery he is four months old and Kicking cdh butt!! he has been threw so much he and his family need are prayers! you can see his updates on carepages just type in cdh and you should get a list of babies .
Saturday, August 8, 2009
Well its been awhile but My Daughter will have a little girl on August 28. Haylee Nicole Beechler. it is so nice not to have to worry about the stuff we had to with Kayden. It breaks my heart to read about babies that half to struggle just to breath my heart goes out to baby Jacksons family as they have lost there little guy. I cant even think of how they must feel. Kayden is the world to me and i dont think i could have delt with that and he is my Grandson. I wish that no one would have to have Cdh or any other defect! but everyone has a place in heaven and we will see them again. with no tubes or sickness. Kayden is doing well he is 17 pounds and almost walking. he is not leting cdh slow him down! we are so blessed that he is doing so well I thank god for that every day sometimes twice .We will be praying for Carter that his G-tube surgery will be a breeze. and have no more reflux. and for all of the cdh babies that need are prayers. I also want to send a hug and prayers to another Carter in Ohio we follow him everyday and hope he can help his docters find out how to treat him and be on his way home. The picture on the top just reminds me of how much parents have to deal with i have so much respect for you all as i know i could not be as strong as you are!until next time god bless you all.