Texas piano tail gate

Thank you KC for the bump....sorry I missed this the first time around. During our HS season, I don't get on the board much.

Donated today, and what a beautiful little girl. Melted our hearts. Being from Iowa, the family "walk" is almost the same time as our State Track Meet in Des Moines. We are really going to try to WALK AND HELP RAISE MONEY.

 
I can't afford tickets to the texass game. I can't afford tickets to the Piano Tail Gate. But you know what? My wife and I will be there. Being the parents of a child w/ CF leaves me with little choice, if there even is one. The Cystic Fibrosis Foundation is one of the national leaders in converting fundraiser monies to research dollars as 92% of money raised is committed directly to research. And We are SOOO F'n close to finding the cure. So Close...YOU can make a difference. The science is there, but the money is not. We hope to see you all there.
She's beautiful! I hope they make tons of money for this cause. :)

 
Your generosity is heartwarming. Things aren't exactly going great for us right now in this tough economy but we will make it there on our own dime. If you feel like there is something you would like to do for the CF foundation and can't make it there, my family and I would very much appreciate it if you would make a donation directly to the foundation. Wherever you are in the country you should be able to get ahold of someone @ www.cff.org/great_strides/teresamack

Thank you for your compliments on our little girl. We like her a little bit
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Done. I urge all others to donate as well.
I can't give much but you got $25 out of me. Good luck my friend!

And done here as well. Always here to help a fellow Husker fan. If you can help, this is a good cause. I mean just look at that little angel. Any little bit helps of course.
Skers, thank you brotha. Even 5 dollars helps of course so every little bit helps. Cacti and I just want to see that 3000 dollar goal reached for this little lady. Hope you got a chance to watch the video at the bottom of the site.
Indeed. I'll have to watch the video when I get home, because I can't view it at work.
Hey all, this is Mrs.DSMHusker1
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Hopefully I'm doing this post right!!!! I just want to tell you guys that I am beyond moved by your generousity. It is truly unbelievable. EVERY little cent makes such a huge difference. Please know that it is all so greatly appreciated! There will come a point in our lifetime that CF will stand for CURE FOUND and you will know that you had a part in that. THANK YOU!!!!
You are so welcome! Anything for our little kiddos! She is just gorgeous!

 
Bah KC, clean out some of those PM's, it wouldn't let me send you a message about what we needed to do to help.
Your generosity is heartwarming. Things aren't exactly going great for us right now in this tough economy but we will make it there on our own dime. If you feel like there is something you would like to do for the CF foundation and can't make it there, my family and I would very much appreciate it if you would make a donation directly to the foundation. Wherever you are in the country you should be able to get ahold of someone @ www.cff.org/great_strides/teresamack

Thank you for your compliments on our little girl. We like her a little bit
smile.gif
Donation done! I pray that you guys reach your goal! :)

 
Bump.

If you guys can, please donate to this cause. On occasion, wish I could do it more than I can, I still visit this site to help out one of our own, and many others with CF.

Thanks guys.

 
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