Just a reminder that tonight (August 28) is the night Tricia and I will be participating in the "Celebrity Scoop" at Rita's in Southern Shores from 7 to 10pm!
Tricia and I have been invited to scoop some Water Ice and serve up some Frozen Custard in a fun and creative way to support the Cystic Fibrosis Foundation! Rita's will is donating 15% of their sales during those three hours to the CFF!
So, come hang out with us, enjoy some frozen happiness, and help us make CF stand for Cure Found!
Nate
Friday, August 28, 2009
Wednesday, August 26, 2009
Go Tropical!
Eat at Tropical Smoothie tonight (only at MP 10 in Nags Head and MP 1 in Southern Shores)...they'll donate 15% of every penny they make between 5 and 9pm to the Cystic Fibrosis Foundation!
(and, contrary to what the flyer says, you DON'T need to bring the flyer with you!)
Nate
(and, contrary to what the flyer says, you DON'T need to bring the flyer with you!)
Nate
Thursday, August 20, 2009
Kisses, Touchdowns, Peek-a-boo and More!
Gwyneth has been learning so much recently. Here is a video that highlights a few of the new things she's doing. In fact, today was the first day she gave me a kiss! What a blessing!!!
Nate
Celebrity Scoop!
No, I'm not talking about the latest news on Brangelina or the most recent gossip about MJ...I'm talking about a "Celebrity Scoop" at my favorite place for frozen treat's, Rita's!
Tricia and I have been invited to scoop some Water Ice and serve up some Frozen Custard in a fun and creative way to support the Cystic Fibrosis Foundation! Next Friday, August 28, from 7 to 10pm at the Rita's in Southern Shores, we'll be in Rita's uniforms for you! Rita's will donate 15% of their sales during those three hours to the CFF!
So, come on out, meet some "celebrities" (haha...), enjoy some frozen happiness, and help us make CF stand for Cure Found!
Nate
Tricia and I have been invited to scoop some Water Ice and serve up some Frozen Custard in a fun and creative way to support the Cystic Fibrosis Foundation! Next Friday, August 28, from 7 to 10pm at the Rita's in Southern Shores, we'll be in Rita's uniforms for you! Rita's will donate 15% of their sales during those three hours to the CFF!
So, come on out, meet some "celebrities" (haha...), enjoy some frozen happiness, and help us make CF stand for Cure Found!
Nate
Wednesday, August 19, 2009
Meet Levi
I got a call a few weeks ago from a family vacationing on the Outer Banks...they wanted to know if they could meet me while they were here...their one-year old son has Cystic Fibrosis, and they've been following our blog since learning of his diagnosis several months ago.
I'm always up for meeting other CFers and their families, especially if I can help give young parents and children hope for the future. Of course, meeting Levi was just as much a blessing for me. Levi is at about the same place developmentally as Gwyneth (I think they even look very much alike), and he did nothing but smile during the time I spent with him and his parents. He even game me a kiss on the cheek goodbye!
Levi's parents asked me if it were true that all CFers tend to be as happy as Levi...of course! As I have mentioned before, there is something very special about CFers...especially the younger patients. I have never met a CFer who didn't have an overly-abundant love for life and for others...it's as if God gives each of them an extra capacity to experience joy to balance out the difficulty of living with CF. Levi is obviosuly no exception!
It's 2009, and Levi's future with CF is much brighter than his predecesors because of the efforts of the Cystic Fibrosis Foundation and the donations of thousands of people just like you and me. And even though there are promises that we are getting closer, there is still no cure for CF. It is for Levi and the thousands of other CFers that Tricia and I continue to be so passionate about raising money and awareness. One of our dreams is to help find a cure in Tricia's lifetime.
My personal goal this year is to raise $10,000 for our Great Strides Walk for Cystic Fibrosis. I would be forever grateful if you would consider donating to help me reach my goal by visiting my donation page Here. Every penny goes directly to the CFF and their search for a cure, and even $1 can make an incredible difference!
Thank you!
Nate
I'm always up for meeting other CFers and their families, especially if I can help give young parents and children hope for the future. Of course, meeting Levi was just as much a blessing for me. Levi is at about the same place developmentally as Gwyneth (I think they even look very much alike), and he did nothing but smile during the time I spent with him and his parents. He even game me a kiss on the cheek goodbye!
Levi's parents asked me if it were true that all CFers tend to be as happy as Levi...of course! As I have mentioned before, there is something very special about CFers...especially the younger patients. I have never met a CFer who didn't have an overly-abundant love for life and for others...it's as if God gives each of them an extra capacity to experience joy to balance out the difficulty of living with CF. Levi is obviosuly no exception!
It's 2009, and Levi's future with CF is much brighter than his predecesors because of the efforts of the Cystic Fibrosis Foundation and the donations of thousands of people just like you and me. And even though there are promises that we are getting closer, there is still no cure for CF. It is for Levi and the thousands of other CFers that Tricia and I continue to be so passionate about raising money and awareness. One of our dreams is to help find a cure in Tricia's lifetime.
My personal goal this year is to raise $10,000 for our Great Strides Walk for Cystic Fibrosis. I would be forever grateful if you would consider donating to help me reach my goal by visiting my donation page Here. Every penny goes directly to the CFF and their search for a cure, and even $1 can make an incredible difference!
Thank you!
Nate
Eat More Applebee's
Today and tomorrow (Wed. and Thu.), the local Applebee's (at the Outer Banks Mall in Nags Head) is helping to make a difference in the lives of thousands of CF patients! Print off the flyer below and present it to your waitress, or mention that you are "Dining to Donate to Cystic Fibrosis", and Applebee's will donate 15% of your bill to the Cystic Fibrosis Foundation!!!
BTW, did you know that Applebee's Real Heroes winner this year is a CF friend of mine named Emily Schaller? Check it out!
Nate
BTW, did you know that Applebee's Real Heroes winner this year is a CF friend of mine named Emily Schaller? Check it out!Nate
Tuesday, August 18, 2009
Baby Steps
Gwyneth is discovering the fun of playgrounds...steps, slides, more steps. Actually, going down the slides freak her out, so we'll just stick to climbing steps for now...
Nate
Nate
Monday, August 17, 2009
Register Today!
Our Great Strides Walk (Outer Banks) is coming up in less than a month (September 12)! If you're planning on coming, but haven't registered yet online, please do so! And, if you don't have a team, consider joining Team Pattysue!
Nate
Saturday, August 15, 2009
Pancake Dinner Tonight!
Come hang out with us tonight and support the Cystic Fibrosis Foundation! Tricia, Gwyneth and I will be there to serve you the best pancakes on the beach...eat in or take out!
And, if your interested in helping to serve up some pancakes, shoot me an email!
Nate