Awesome Chipmunk Choir

Doctors Appointment..

It's so soon...my Clinic ( or Doc appt, Since Dr. B hates the term "clinic", ever since he quit the clinic and started a Private Practice)...

He wanted me to gain weight & improve on lung function...easy...ha ha.

He broke it down into do all nebs, the VEST (which is what I tend to skip), and start jogging or biking etc...

I have been doing very good with my morning med routine, but night routines..I skip a few, not gonna lie. However, that is why I have been blogging more and on FB more... I can type and read a computer screen while doing my nebs and vest..

Why do I skip my vest? Its hilarious, it makes no sense to skip it. You see incase you don't know
what I'm talking bout.... (This black vest inflates and shakes me)

Yep, it shakes me. So I know lots of CFers who sing while doing their vest, it makes our voices sound high pitched and weird...
(I'm not one of them....*whistles & tries to look innocent)

Seriously I shuold post one on youtube...lol. Here is one I found..
She reminds me of myself at that age!
http://www.youtube.com/watch?v=qqKo9rZEC3w

(I'm a bit of a movie nut, so forgive me) BUT you know in My Best Friend's Wedding... the day of the Wedding in the background of the one scenes, there's a shot of 3 guys singing harmony after sucking in some balloons' helium.... ---> kinda sounds like that...

So have you heard of "The Virtual Choir" that Eric Whitacre formed?
http://ericwhitacre.com/blog/the-virtual-choir-how-we-did-it

I think he should have a choir with all people (CFers, Asthmatics, etc) who use the vest, to perform! Ha ha ha. It would sound hilarious. And yes, you can do harmony while shaking in the vest. It has been done before...

Meds done, I'm going to bed!

Comments

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 ...

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...

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...

Cheriz: My life with Cystic Fibrosis

Search This Blog