Entry Title: Trach sometime soon...

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Mrs. Bonecrusher's Comment:

Not one second goes by when I am not thinking of you three. I am sorry that it's come to this for you but since it's the only way to have a healthy, growing Jasper I can embrace it. I love you all.

Posted on January 30, 2009 at 8:10 am

Cousin Ann Marie's Comment:

We are thinking of you guys. Trust that you are in the best hands, and that they will do what is best for Jasper. Hope everything goes well. Give him lots of hugs and kisses! Keep us posted. We love you little Jasper!

Posted on January 30, 2009 at 8:54 am

Shannon Lowry's Comment:

Becca- You don't know me, but I found your blog on one of the heart boards. My son Owen has Tetralogy of Fallot with absent pulmonary valve. I am posting because he has some of Jasper's issues as well. While we managed to get out of the hospital without a trach (it was a possibility because of airway compression) he has a feeding tube and also has craniosynostosis. He was in the hospital altogether for about 3 months, but been home now for over a month (he had his surgery in October at 6 wks old). He turns 5 months next week and things are going a little smoother now. I just wanted to let you know that it does get easier and if you ever want to chat, you can email me at scraig5@hotmail.com. We will be thinking of you guys!

Posted on January 30, 2009 at 9:03 am

Renny Karsten (HRHS)'s Comment:

Thinking of you and your precious beautiful boy. Praying for a sucessful surgery. Our heart kids are made of tough stuff ! Big hugs Renny and Chloe

Posted on February 1, 2009 at 11:09 pm

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