See my Great Strides Website to join my team and walk with us, and/or donate to finding a cure for CF. Any donation is appreciated :). Great Strides happens all over the United States so if you can't walk with us, consider joining another team or creating your own team- go to www.cff.org/Great_Strides for more information.
Go Team Emily!
~Em
2 comments:
HI!
Every so often, I google Cystic fibrosis + Emily. This time, I found you.
My 3 year old has CF. She is named Emily Jayne.
I just wanted to take a moment to thank you for your blog. I will be back to read through more fully...but for now I wanted you to know that you've made a difference to a CF mom.
Here (hopefully) is a link to my onetruemedia video for my Em this year... Emily's Dream . If the link doesn't work, please e-mail me at tdraxler@yahoo.com if you'd like to see it.
We'll be walking in 2 Great Strides events this year, in Wisconsin.
Thanks again for the hope.
Tami
Hey Emily,
Sorry we didn't make it to the BBQ today. We went to Disneyland earlier and Kylie was having a meltdown...it was just too busy of a weekend for her. But know that our thoughts adn prayers were with you and I hope you raise a ton of money...actually, I know you will!
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