.... to this amazing little man...
Please join Kyle's team. walk with us; donate as we walk; walk with us & have others sponsor you as you walk - You can do all three or any combination! To be involved click above on the March of Dimes link and it will take you to my personal March of Dimes page where you can:
1. click on DONATE NOW which is sponsoring me as I walk! - don't forget to leave a message on my page when you do!
OR
2. WALK WITH ME which is joining Team Kyle and walking with us on April 25th! If you choose this option March of Dimes will have you set up your own fund raising paige. You will be linked to TEAM KYLE and will be able to get others to sponsor you as you walk. Don't be intimidated by this - it is all for a great cause and raising even $10 is a huge step toward the future of children born too early!
You can also click the TEAM KYLE link at the top of this post or HERE to visit the Team Kyle page - you can donate or sign up from here too. You can also view the Team Kyle roster and our total donations! I will be in contact with everyone on TEAM KYLE to let you know details soon!
THE WALK is 5 miles - however if you want to be a part of TEAM KYLE and don't feel like you can make the 5 miles - don't worry you can come and see us off and welcome us back and hang out under the family teams tent! You can also walk as far as you can and stop at a check point and one of the volunteers will give you a ride back to the finish area! also - wheel chairs are welcome!
There will be lots going this day - food, fun for the kids - it is really a whole day family event! So come and have fun!
More than anything - for my own heart - to stand shoulder to shoulder and walk the March of Dimes walk with those that walked Kyle's journey with me - I can not imagine any picture more beautiful. Please come join us!
3 comments:
Sounds great! I'm putting it on my calendar!
Kyle is so precious and what a miracle. I started reading your blog about the time Kyle was born. What a story.........He is such a cutie - I wish I still lived in Texas so I could meet him in person!
Hi Kelly~ It's Jaime Dadd from the other night at the NICU. Thank you so much for coming and talking & then for talking to me more on the way out..I really appreciate it. It's so amazing to see Kyle in person..what a miracle he is! I wanted to ask you a question about ROP...did Kyle have this and did you have to do an intervention for it? I wasn't too worried about it b/c Peyton hasn't been on high 02 settings, but they found something today that is concerning called "Plus Disease"...sounds like it's correctable with laser, so I'm thankful but scared about the laser at the same time. Just thought I'd see what insight you had...they seem so vague about the eyes and it's so hard to understand if it's serious or not! Thanks so much, Jaime
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