Skip to main content

My CF CHALLENGE

CF CHALLENGE!

I have signed up for 3 Greatstrides Walks this year!! I usually bring a couple friends to two of the walks. But, one is very local this year!

There is a walk only 15 mins away (next closest is an hour), so this is very exciting!

I'm really trying to keep on top of doing all my meds. These past few days I have missed some, but overall still doing well.

HOWEVER, I wanted to add some motivation I couldn't resist! Fundraising for the CF Foundation, for researching for a cure, etc.

SO, I proposed this challenge:

For every $100 my team or I raise for my walks (any of them) I will do a full weeks worth of meds! (this includes at least 2 cans of feeding a night and all 10 nebulizers everyday!)

(and if we had coporate or large sponsors/donations those count too)

Last year my team raised $1,200 at one walk and $75 at my smaller one. If we only raised that much this year I would have to do all my meds for roughly 3 months!

We started fundraising and registering for the Walk (June 1, 2013) last week! We have raised $300 so far! :-) I hope that my health will motivate my team to fundraise as much as their contributions will motivate me to be healthy!

PLUS at the end of the year maybe we can see a difference in my Clinic/ Tests Results!!!!!!

To donate or register with my team for our Hollowayville Walk (our main one this year) click HERE!

I also started a Facebook Event: click HERE to read the info!

And of course, a pciture of my team from last year's Peoria Walk! Thanks everyone for donating, helping, and walking- It really means a lot! :-)

Labels:

Comments

Post a Comment

Popular posts from this blog

How Fostering and CF impact my work

I haven't been on my blog much.... I think that is because most of my blogging is currently been done on Health Union's Cystic-Fibrosis.com (here is link to all my posts on their site: https://cystic-fibrosis.com/members/cherizkunkel/ ). I decided last fall to step away from real estate after 3 years in the business. It was tough to say good-bye, especially since I had tripled my volume and business in the last year. However, I didn't have time to add any new clients; I kept saying, maybe next week, next month I can fit more work into my schedule. The truth is fostering takes a lot of time. We have between 5-8 monthly visits at the agency, 1 court ate a month, 2 home visits from the caseworker a month, plus e have 2-3 doctors/specialist appointments for our current kiddo. We have lots of paperwork we fill out, gas mile logs, receipts to add, and more! Our kiddo also participates in gymnastics and dance two nights a week. We go to a fosterparent support group with our kid ...
2 comments
Read more

Oh the Joys of a Colonoscopy!

Colonoscopy, Fun: As you may remember from reading my October Posts (  Oct Post #1   &  2nd Oct Post ) that I was admitted a second time that month for Gastrointestinal issues. I was having stomach cramps and what was believed to be Antibiotic Associated Diarrhea. However, CT scan revealed my colon and intestines were inflammed.  After having a rough 2 months of GI issues, and cuting out most food (diary, meat, grease, carbonated beverages, and sugar). I finally am getting a Colonoscopy to see what in the world is going on! I'm been taking Probiotics, was on meds for both C. diff and AAD. I even added driking Kefir to add to the probiotics and good bacteria.  Only now am I seeing any changes, less stomach aches, etc. I add a 1/2 cup pf the Kefir to my smoothie, its not bad -yum! I really reccommend it and Probiotics (so talk to your doctor about it), it could really help you out! Read about Colonoscopies here! So I'm glad to be g...
4 comments
Read more

Um..Need to clear my head.

I was having a good day, it was one of my babysitting girl's bdays! We went for ice cream, I hung out with a friend and watched "Game of Thrones". I really liked it and I'm hoping to watch more this wknd. Then I logged onto Facebook to see that my best friend Laura (with CF) is down in lung function, on oxygen at night and her doctor is putting her on the Transplant list. I have lots of thoughts going through my head the MAIN one is "Please let her get a Tx soon, heal well and fast, and live her full life, they way she deserves to! PLEASE, PLEASE, PLEASE!" I can't imagine how she must feel, I know I'm sad knowing she is at point she needs one, but HAPPY she will get on the list! Happy, Sad, Scared, Excited. How do I feel..? The worst part is knowing that she is pain. I just want to take all that away, give her some good n plentys (one of our fave candy), kiss her on the forehead, tell her I love her, and that before she knows it she will have...
2 comments
Read more