Thanks for posting this. You look great, of course. I'll be in SL this week. Are you busy? I'd love to see all of you, and buy a t-shirt or 5. Give me a call if you've got time.
I am getting sooooo excited to see you, Elliot, and the rest of your fam. I loved the T.V. clip. I am trying to think of the right words to say and all that comes to mind is, "Wow". I am deeply touched.
It has been such a long time! I stumbled across your blog and I was so saddened to hear about your cute little Elliot.
I don't know what it is like to live with Cystic Fibrosis but my little girl, Eliza, has a progressive and terminal disease called Metachromatic Leukodystrophy (MLD). I know how awful it is to receive any sort of diagnosis.
However, I am sure that you have learned so much from it...I know we have. Even though it is so difficult, it is amazing to live with such choice children.
Channel 4 did a little story on Eliza as well. Visit www.elizaswish.org if you want to see it.
Take care and know that I am thinking about you and praying for your family.
Wow, Alta, you are so strong. I am touched at all you have had to go through and your sweet little Elliot. I hope things are going better, keep pushing for such an important cause! It was good to see you visited our blog, too!
wow, i feel like the worst friend in the universe. I didn't even know your baby had CF. It feels like last week when I ran into you at the zoo and we were pregnant. i bet you are learning so much. i saw your blog from kristine's - hope you don't feel like i'm stalking...you can check out our blog at: matthewandjodi.blogspot.com congrats on elliot gaining weight and doing well. hope you're doing well too!
8 comments:
HOORAY!! THE WALK WAS SO MUCH FUN ON SATURDAY! WAY TO GO!
What awesome coverage. There is so much hope. Wish I could have been there, I hope it was a great turn out. Can't wait to hear more about it.
Thanks for posting this. You look great, of course. I'll be in SL this week. Are you busy? I'd love to see all of you, and buy a t-shirt or 5. Give me a call if you've got time.
Hey Mcdonoughs I would love to play this week. Give me a call when you get into town.
I am getting sooooo excited to see you, Elliot, and the rest of your fam. I loved the T.V. clip. I am trying to think of the right words to say and all that comes to mind is, "Wow". I am deeply touched.
Alta-
It has been such a long time! I stumbled across your blog and I was so saddened to hear about your cute little Elliot.
I don't know what it is like to live with Cystic Fibrosis but my little girl, Eliza, has a progressive and terminal disease called Metachromatic Leukodystrophy (MLD). I know how awful it is to receive any sort of diagnosis.
However, I am sure that you have learned so much from it...I know we have. Even though it is so difficult, it is amazing to live with such choice children.
Channel 4 did a little story on Eliza as well. Visit www.elizaswish.org if you want to see it.
Take care and know that I am thinking about you and praying for your family.
Nikki (Norman) Williams
Wow, Alta, you are so strong. I am touched at all you have had to go through and your sweet little Elliot. I hope things are going better, keep pushing for such an important cause! It was good to see you visited our blog, too!
wow, i feel like the worst friend in the universe. I didn't even know your baby had CF. It feels like last week when I ran into you at the zoo and we were pregnant. i bet you are learning so much. i saw your blog from kristine's - hope you don't feel like i'm stalking...you can check out our blog at: matthewandjodi.blogspot.com
congrats on elliot gaining weight and doing well. hope you're doing well too!
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