Skip to main content

Devoured Bdubs, effective meds, & pics!

Craft Show & Some Bdubs!

 Yesterday, was my mom's craft show. She has such cute crocheted products (Hats, Scarves, Earwarmers, Beards, Toys, Purses, etc) that I was soo excited to see how she would do selling her stuff. It was in Naperville, IL. Andrew and I met mom and dad there. It was a great day. Andrew wore one of the crocheted beards mom was selling and walked around in it. AND a couple people came by and said "Oh, this is where the beards are, I saw somebody wearing one earlier" (people love them, they sell quick too for $5).  He's such a good sport!

(Here is what mom's cubicle/booth looked like.) The stacking bins really help organize stuff by size!


Overall, it was a great show and so much fun! (Below is a close up of mom's Hat Bins!) Love her hats!!!  





 However, my stomach hurt really bad for a chunk of the morning (thanks to Colon issues: read my last post about my Colon issues here!)



We spent the day helping mom at her booth and she did great! She sold a lot of stuff, and made more than enough money for the booth deposit, gas (drive to/from show), food we bought, and the other products she bought (like the beautiful wreath she got). A couple of my friends who live in Naperville stopped by to visit too! Andrew, my friend Ryan, and I got to visit my friends' Rebekah n Michael's new home they bought this year! Then Andrew and I hung out with Ryan and went shopping. And of course we went to bdubs (Buffalo Wild Wings) for dinner! I got my favorite "The Ultimate Nachos" I devoured them! I seriously scarfed them down!

(Here I am at Bdubs, after I finished off my nachos, about to lick it clean...LOL kidding...)

We got home just in time for me to do my daily diary (an electronic diary I have to do as part of the Clinical trial). I'm sooo glad I started doing the clinical trial, since I started I have been 100% compliant (research is important to me)!! I've been really paying attention to my breathing while  doing my treatmens!  

 Making sure I breathing through my mouth and not my nose, breathing deeply and thinking about my breathing, and not blocking off the mouthpiece with my tongue. Those are all bad habbits I need to break to do really effective treatments! And since I've started the Clinical Trial I've been paying close attention to my therapies, and I have noticed A DIFFERENCE! I'm having way more productive coughs and less wheezing! Can't wait to see what a difference it will make over the course of the 7 months Clinical Trial! Hopefully, I stay healthy, don't get released from the study  and it goes smoothly! At least smoother than my Evaluation for the Trial ( read about the Mess of an Evaluation here in this past blog!

If my breathing keeps getting better, and I keep walking/ eventually start jogging again, then I will definetly be joining my friend Stacey, for a 5K in the early spring! Also, I'm hoping to do 2 5ks next year, along with the Chicago CF Climb! I couldn't do the climb this year, but Andrew did it ( look at pics and read about it here in the past blog! I'm so proud of Andrew!!!)


So here is to looking forward to a more compliant year with meds and more exercise and lots of positive benefits! :-)

More updates on school tuition reimbursement and Laura's waiting for lungs coming in a few days!






Labels:

Comments

  1. JohnNovember 24, 2013 at 10:40 PM

    AWESOME compliance you know how much that means to me. Did you get a chance to read my blog about effective airway treatments? Keep up the compliance cyster:)

    http://livingmydreamswithcf.blogspot.com/2013/10/effective-airway-treatment-clamp-motto.html

    ReplyDelete
    Replies
    1. CherizNovember 25, 2013 at 10:43 AM

      Thanks! I'm glad you posted the link to the Effective Treatment Blog. It is really important for all CFers to think about their nebs! And hopefully I can keep the compliance up :-)

      Delete

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

What Else Should I Do?

Need Some Feedback.       May has almost come to an end. I love May, nice weather, summer starts, AND its Cystic Fibrosis Awareness Month! A lot of the CF walks are in may and its a great time to raise funds and awareness for CF! However, I'm also excited that it will be June soon! June 28th is the Princeton Cystic Fibrosis Walk. I've helped organize other events in the past. Whether for school or other non-profits I've volunteered at, but this CF Walk is a little different. It is the first time, I've put together a City event. Or put together an event that is so near and dear to my heart. I'm so thankful that I had so many people sign up so quickly. Pretty much everyone family member I have on my mom's side signed up the first day. And I've have had some family and friends help me (giving me ideas, helping me recruit, etc). But, Its the first time I didn't have a committee or team behind me to help execute the ideas and actually plan the event. I lo...
2 comments
Read more