CF, Invisalign, and DH!

The Great Strides walk for CF on Saturday was so much fun!! Our team almost reached our goal of $10,000 and as a whole Houston raised about $775,000!!!! Way to go Houston!! It felt so great to be apart of something so amazing!! Friday night our team had pizza and beer over at Cara's dads house and it was a lot of fun! Her dad said a thank you speech to all of us for helping Cara and the rest of the CF people by raising money and of course many of us were in tears! He talked about how when she was diagnosed at 1 they told him she probably wouldn't live to be 5. Then when she was about 5 they said, "Guess what, people are raising money for research and we're coming a long way, she might live to be 15!". When she was 10 they were informed that the actual gene for CF had been found so that left even more hope! Now Cara is 27 and it's all because of research that has been funded by people like you and me that help out. I'm so thankful!

Unfortunately I forgot my camera so I didn't get to take any pictures! =( I know Cara and tons of other people took some though so please send them my way and I'll post some soon! I really enjoyed seeing everyone and meeting all the other people that I had only met through blogland, it was so nice to meet yall!! Cara Corps also won the t-shirt contest thanks to Cara and all her hard work. I think she made about 20 shirts! Our team did awesome and I can't wait until next year. I was soooo close to my $1000 goal but I really am pleased with how much I raised, it was the most I've ever raised and I know next year I'll reach $1000!! Thanks so much to all of you that supported me and this cause! It means more to me than you know!!

In other news I got Invisalign last Thursday and I am so excited!! My teeth have been moving closer and closer together over the years so we finally got them some help! I can't wait to have completely straight teeth! I put the first set of trays in on Thursday and they were so tight and really hard to take on and off. My teeth have already moved enough that I can just snap the trays right back into place after I take them out...so exciting!!!! I wear the trays for 2 weeks at a time and every 6 weeks I go back to the doctor to get 3 more sets of trays. I highly recommend it to anyone who is thinking about it. I love it so far but I know I'm not much of a recommendation considering it's only been 6 days! =) Kyle has been making fun of the way I talk with them on but I'm getting used to it so I don't have as much of a lisp anymore!

Lastly I must say that I loved the Desperate Housewives finale!! I just watched it today and thought it was fantastic! I'm not so sure I like what's going on with Bree but I just love what happened to Lynette and the whole MJ, Susan, and Mike scenario was fabulous, didn't you think!?!? I was in tears at the end and now I can't wait until next season. I really hope that was Susan at the wedding!!! Ahhh, I just loved it!

Last Call

Hello friends, family, and strangers! Well, tomorrow is the big day!!

What day is that you ask??

The Cystic Fibrosis Great Strides Walk, duh!! =) My team is really rockin' at raising money and we've almost reached our $10,000 goal! I am very close to my $1000 goal and I would LOVE if you could help me out by donating at least $5!! Every dollar counts so anything you can contribute is very much appreciated!!

New to my blog and you don't know what I'm talking about??

Click on this old post, or this old post to get updated!!

Click here to donate!!!!! Click here to donate!!!!!

Hallelujah!!!

Praise God!!! My friend Cara just posted the BEST blog EVER!! After 7.5 months her husband has just returned home safely from his deployment. He is not only her hero but my hero and so many other peoples hero too! I am so thankful for every single person that fights for our country and I hope they know how much we appreciate them! Thank you Patrick and thank you to all the other Americans who have served this country! We love you and support you all!! God Bless America and may God protect our soldiers!!!

WELCOME HOME P!!!!!!!!!!!!!!!!!!

Check out Caras blog HERE!

You Know You Want To...

Many of you know about my friend, Cara, who has Cystic Fibrosis but let me tell you a little more! First of all if you were to meet her you would never know she was living with a disease! She is always smiling, laughing (I can actually hear her laugh in my head when I see a picture of her giggling!) and lives her life to the fullest! Cara and I met in 6th grade when we started Jr. High and became great friends. Most of my favorite memories consist of slumber parties, swimming in her pool, good ole' Jr. High dance parties, and I do recall a spaghetti fight or two! Now my times with Cara are mostly spent online since we live in different states but we do get to have the occasional dinner out or a bowling extravaganza when she is in town! We also get together for the annual Great Strides walk which I'm really looking forward to! Not only do we get to walk, talk, catch up, and act silly but we also raise money for Cara and the thousands of other CFers so that we can find a cure!! It feels really good and I know you want that warm, fuzzy feeling too! =)

The average CFer lives to be 37 and Cara is 27. Can you imagine? That is just unacceptable! They really are making advancements everyday to get close to finding a cure and the future for CFers is looking up! The walk is in May and that is really sneaking up on me! I need to get busy if I want to reach my goal! Please donate as little or much as you can to help find a cure!

You can CLICK HERE to make your donation.

What a difference it would make if everyone that read this just donated $5!! Thanks again, I appreciate it more than you know!! Help CF stand for Cure Found!!!!!

Here's the new 2009 video for Cara and our team...Watch it! =)