Skip to main content

It's Official & our Vacation

The Dells & Our CF Walk:


I'm sooo proud to announce that Princeton, Illinois (my hometown) will be added to the list of OFFICIAL Great Strides Walks for the Cystic Fibrosis Foundation! Make sure to mark your calendars for June 27, 2014!!!!!

(for those who don't know, I decided to start this walk last year & thanks to my community it was a huge success! Read about it here!

Pic: Me giving a speech last year, wearing my Team CF2 shirt

Here's the info I have so far:
   Zearing Park, Euclid St. check in 9-10am,
  10am the Walk.
   Lunch & dessert is provided to those who registered online!
  There will be lots of Raffles ($1 per ticket), Dj/Music, games, face painting!

Make sure not to miss out on the fun! I will let everyone know when the online registration is ready!

This year since we are our own walk site, we can now sign up numerous teams! This year (2014) our Team CF2 has raised over $14,000 for CF research! The Princeton Walk alone raised over $13,300! So next year lets make our goal $20,000!

Consider starting your own team with your co-workers, family, or friends. Or you are more than welcome to be on my team (CF2). Anyone without a team is welcome to join mine. But I'd love to see multiple teams. Team Leaders can earn prizes too! So gather your family & friends to join your team and have a fun-filled day supporting a great cause!

AND FAMILY, FRIENDS, & COMMUNITY please give yourself a big round of applause, because WE DID IT!!!!!!!!!

And now more has happened...

In the past week I have lost 2 friends from Cystic Fibrosis. One was my best friend and you can read all about her struggle & journey Right Here! She fought long and hard to get new lungs, but sadly she lost her battle last week. Laura was my bestie for a long time, we have known each other since childhood. And the second was an online friend with CF I met a little over a year ago, Alyssa. I've been in touch with about 5 CFers via Facebook on a regular basis. It was so tough to see them struggle. Also this week I dropped before 100 lbs for the first time in over a year.

It's so disappointing to drop in weight, but I just have to wait for the surgery to fix my stomach tube hole. Scroll down to the next blog entry to read about my Stomach Tube Hole problems.

But the sun in all this rainstorm is that my best friend Amanda got married! They decided to get married in the Wisconsin Dells!

Pic: Amanda (Bride) with me & her cutie niece (flower girl)

Which was soo much fun! Andrew works so hard (40 hours a week) plus school on top of that. And with the week I had been having this mini-weekend getaway was perfect!  We got there Saturday around lunch time and the Wedding was that night, then we drove home around 6pm the next day! My last vacation I took was with my uncles to Niagra Falls in 2012 ( Read about it Here). Then Las Vegas with (the Bride, Amanda) which is where she first started dating Jake in 2011. Andrew said he couldn't remember his last vacation, but it would probably be the trips he took in High school to Disney. And since he had never experienced the Dells (the non-waterpark way). I wanted to him to experience it all.  So I planned out 3 meals at the best restuarants, an Orginial Ducks (boat) tour, Mini Golfs, Shopping, Visiting Popcorn and Candy shops, and more!

Here are some of the pics from the weekend!


 Breakfast at Paul Bunyan's Cook Shanty


Everything was soo pretty!

Andrew & our veiw from the Duck (on the water)
 

 One of the scenic Mini-Golfs
(Incase you didn't know Mini Golf is one of our favorite activities)

And one of our desserts!
(Apple Pie Cake studded with Cranberries)


The week has been hard with all of its Up & Downs. And I'm glad to have that mini-weekend getawat! Then when I heard about Princeton being an official GREAT STRIDES WALK Site. I couldn't believe it. Laura would have loved that and would have been sooo proud of me! I plan on donating all the money that (individually collect for donation) in "Memory of Laura Blanchard"

In the next two weeks I'll be focusing on getting the healthiest possible before my surgery! Read about it below in the next post!

 














Comments

Popular posts from this blog

Updates!

 Hey everyone! Sorry it’s been a while. Covid struggles have been all around and we have been focusing our on our kiddo and current life situations (jobs, home, everything really). We have been posting regularly on the Facebook page (www.facebook.com/CherizCFPage). We will keep you updated on there for now,  because we are doing some big changes to our current blog! Stay tuned!  In meantime, message our FB page if you need anything. Keep safe and stay happy.  We will be back. Promise! 

CF isn't all tears and saddness. Get a Full Picture.

  CF and Laughing Cystic Fibrosis can bring sad times and times of tears (like losing a close friend with CF, etc) BUT, it can bring so much joy and love. I've noticed most people love to talk about the people they meet while traveling. This is usually, because they have learned something from the person. Or the person is considered unique to them. I can do the same thanks to my Cystic Fibrosis. I may not have traveled much in my life thus far, but I have learned mountains of lessons from my CF. [Picture right:  Me ready for surgery in 2nd grade!] Forgive my shoutouts (but I must recognize a few amazing people) I have met some of the most amazing doctors: Chatrath, Dr. B Nurses: Sara & Marie (from Clinic), Lizzard, Melody (best IV stick ever), Deb, and Kris (you know a nurse is amazing if you love her after putting tubes down your nose!) Respitory Therapists: Jeannette, Lanell, and Don (you da Man) And Cookie Marrow (Musical Therapist- She would sing to me a...

Video Blog: Life in the hospital (as a child)

The daily life in the hospital! Most people cringe at the idea of a hospital. However, when I was little I never minded going into the hospital. I usually would have at least one other friend with Cystic Fibrosis to hang out with there (before we knew about the "CF Bugs"). I didn't love being sick, but I loved my CF friends that I would hang out with. Also the hospital, nurses, and my parent's tried to make it a "normal" environment. I got up and put on cute clothes, "walked to school", flirted with a couple CF boys, did homework, came "home" (back to my room), my friends would ask my parent if I could go play with them. We'd hang out in the play room or go on a walk with one of my parents! My dad loved taking me on walks and I LOVED going on our walks! Here is a video blog of the route we took and bit of information on what is was like growing up (for a chunks at a time) in the hospital! (it is posted via youtube, let is dow...