Nov 2009
We need to make a mental note for years to come that Octobers will be busy medical months. Just straight up busy. I think next year we need to plan and utilize September better too. Our little man has had so many doctors appointments this last month I honestly lost count. He’s had chest xrays, blood work (4 vials! Such a champ!), flu shot, 2 year old shots, H1N1 shot, 3 hour annual appointment at Phoenix Children’s Hospital (which, that’s like a whole other post, but I’m choosing to forget this whole experience, ha!), pediatrician appointments, and something else I’m forgetting…anyways, despite all that Asher still smiles. God has truly built him for Cystic Fibrosis. He is already such an example to us, I can’t imagine the impact he’ll make on our lives when he can actually talk :).
Not only has God built Asher for this journey, but you and J too. You are such a blessing to all around you.
Wow, what a hard month on all of you. Asher is so brave! I pray that November is better!
Gotta love that smile…what a brave little boy. You’re always in our prayers. We love you, Asher.
It has been a long month for you. I am glad that God got you through it.
I also love the tree.
You’ve got that right Grandma O,His smile warms your heart!
Asher sure is a champ! He faces so many challenges with courage & a smile. . . definitely following his dad & mom’s footsteps!
I just keep coming back to this picture-I love it. His smile makes me so happy. And , I just noticed his initials carved into the tree-precious!
What a perfect picture! God is Good, Rachel! PS…sorry I haven’t gotten back to you! We are expecting about 450 people and will be rolling in about $2200 in tix sales for CF. We will also raise money by selling pucks for “Chuck a Puck.” I’ll keep you posted. Thank you so much for your prayers. Like I said earlier…this is for Asher too!!!!