Tuesday, December 1, 2009
Sunday, October 18, 2009
Nothing Short of a Miracle
Saturday, September 12, 2009
Jameson's "little mommy"
Wednesday, September 9, 2009
First Grader!
Sunday, August 30, 2009
DEU!!!!
Monday, August 24, 2009
Our Summer in a Nutshell
We got the courage to start going down the BIG slides!
We decided we really like dolls, but this is Emma's. No we didn't get him his very own, although his Mar Mar was super tempted. Jameson was pointing to baby Jameson's nose...we also learned where the mouth, eyes and ears are.
Friday, June 26, 2009
Beautiful Dolls
And she even got a trophy! If you could have seen the look in Emma's eyes when she received it...that was the highlight of her day!
And of course it wouldn't be complete without flowers for our dancer!
Sunday, April 26, 2009
Video of Jameson Walking
I think I counted 17 steps...he's making tremendous progress. He knows that as soon as he sees the skittles, it's time to walk!!!
Cardiology Appointment
Now we are going to start going every 6 months. I told Dr. Laird that next appt we would possibly be addressing the "dreaded" third surgery, BUT, she pretty much confirmed that unless Jameson shows us otherwise, that we will wait until he is 4 for that one...what a relief!!! So that's a major praise in my book!!! Thank you for your continued prayers! As Mi Mi stated, more time to pray for Jameson's complete healing! Amen to that one!
Thursday, April 16, 2009
Big News
As you all know Jameson started physical therapy last week...he has been doing so well since the first day (prayers answered). I started working out about 3 weeks ago, once I felt comfortable that RSV and Flu season was waining. The sweetest lady from the childcare has worked with kiddos and walking before, so she will take Jameson and work with him while I work out. Today BEFORE working out, she showed me how he will take steps with her hovering over him with her hands right beside him. He doesn't hold on, he just likes the security of knowing she is there. Of course I was so excited and had the BEST workout today, 968 calories burned, but who's counting...ha (just had to throw that in). AFTER working out, and before J saw I was there, she showed me the progress he made during my workout....12+ steps, no help, no nothing, just walking toward her...and I even lost count cause I was jumping up and down and had tears flowing from my eyes, so really he may have taken more. Of course he sees me, and down he goes to his little bottom and scoots right up to me and holds his hands up...if that isn't seeing God work, then I don't know what is. Thank you Lord, and thank you to those who have been prayer warriors for Jameson.
Sunday, April 12, 2009
Happy Easter!!!
Monday, April 6, 2009
Starting Therapy
Two more prayer requests--Jameson has a runny nose and cough and it is making him miserable, so please pray for that to clear up. AND...there has been an outbreak of scabies at Emma's school and at the gym childcare where Jameson goes while I work out...I am FREAKING out because anyone who knows me knows I really HATE bugs...so please pray that neither one of my children contract these yucky bugs!!!
Thursday, April 2, 2009
Bathtime
Thursday, March 26, 2009
An Emma Funny
Tuesday, March 17, 2009
Washington DC
Wednesday, February 25, 2009
Pray for these Families
The May family received news Monday that there is nothing further the doctors, nurses, etc, can do to keep Caleb alive. He is living on machines and medicines, he is in kidney failure, and has extensive brain damage. Ironically, his heart is doing well after having the Norwood procedure. I am uncertain of what has been done this far, but I know that his parents will be or already have made a decision unimaginable to all of us. It would be so kind of you to leave an encouraging word on his site. www.caringbridge.org/visit/calebmay
Also, I am in shock because I just read Baby Maverick's blog and he died yesterday (Tuesday) morning. If you go to http://babymaverick.blogspot.com/ you can read about him and maybe leave an encouraging word for his family.
I realize this is so much to handle, but please pray for these families. Now that our family is a part of the CHD Community, it's not just about Jameson, but so many other little lives too. There are so many blessings involved and so many tears, I just never realized it would be this many tears.
Friday, February 13, 2009
HLHS Story (An Answered Prayer)
"Hi Kellie, Yes, my son was born with a heart defect. He has Hypoplastic Left Heart. He’ll turn 19 this May, and is in his second semester at University of Arizona. He’s studying Pre-Med. If you looked at him he looks totally normal. He visits his cardiologist yearly which creates a little problem. He still sees his Ped Cardiologist. The normal adult Cardiologist is not familiar with his condition. He’s had 5 surgeries. The last one was when he was 5 years old. He’s a straight A student, and on a full academic scholarship to UoA. He was not allowed to play competitive sport, so he was very active in Boy Scouts. He earned his Eagle, and loves to backpack. He’s even been down in the Grand Canyon a couple of times which blows his doctors minds. It sounds like your son is doing very well.
If you ever run into anyone with our sons conditions don’t hesitate to give them my contact information. It’s really scary, and we would have loved to have had someone to talk with back then."
Wow! HUH? What a Mighty God we serve, when He listens someone like me and answers my PRAYERS!!!! and promises me in Jeremiah 29:11 that He has plans for Jameson, to give him hope and a future!!!
Have a Blessed DAY!!!
Thursday, February 12, 2009
7 Websites about CHD
Vote Here: www.colgate.com/ShowTheLove
About HLHS: http://hlhsinfo.homestead.com/
http://www.childrens.com/HealthLibrary/HealthLibContent.cfm?pageid=P01798 This is has a great picture of the heart.
Other sites:tchin.org
http://www.savinglittlehearts.com/
http://learnaboutchd.blogspot.com/ Love this one!
http://heartnhands.org/ Our support group