Skip to main content

The Final Stretch

The Final Stretch

I have my "Clinic" (quarterly CF Doctor's visit) in 9 days!!! I found my Doctor last year and this April was my first complete year with him! [check out my charts of health on my "Clinics" page to see the upward trend in health starting!] He really wants me to do well and his positive attitude towards CF has really  inspired me to try really hard to do the best I can! I've always strived for what I wanted (theatre, career goals, etc), but when it came to my health (I did what was needed)... This meant doing the "majority" of my meds, but putting lots of needed stuff on hold.

Examples: I would get home from play practice, not make my stomach feeding or not do my night nebs, because I was too tired. AND Weekend trips, whether with a youth group or friends, I wouldn't pack my meds. This continued through my college years.

That has all changed now. I refuse to let other things get in they way. When I'd skip one night, I couldn't see a big difference the next day and so I convince myself one more night....and it spirals out of control, until I'm sick and its too hard/ hurts to do meds.

So, I can say since having Dr. B, I have honestly put my health first. I want to be the healthiest I can be! I want to have a career that I can work hard at and kids I can be healthy for. I want to run after them, play baseball with them, etc. And lung functin takes time to bring up, so I made the decision last year to try really hard, no EXCUSES and to see what I can do!


And I find additional motivators along the way, running the 5K with my Uncle Dan in the Fall, even writing this blog helps hold me accountable.

BUT my main one is the Amazing Race(my favorite TV program). Now, I know, I will almost 100% likely get tossed from the pile right away, due to medical problems. The only medical problem they really had on the show was Asthma... So CF, would look risky to them.

But I love the show, I love the idea of traveling, and I'm a goal/ challenge motivated person, so it fits perfect. Dr. B said I had to get my weight up, my FEV1% up, and be able to jog a couple miles... and I have 9 days to prove to him I did it and can do it! I know the reality of my situation and the chances to get on the show are slim. But if I can get Dr. B to consent to it, that means he thinks I could do it and THAT ITSELF is pretty much a win worth more than any money.  

And now, to convince my sister to audition with me....and kick CF's booty at Clinic!

Comments

Popular posts from this blog

Cystic Fibrosis Clinic Results. Not what I wanted, but...

My Results: I went down in lung function 2% points and lost  a couple more lbs. So I'm at 102. I was really disappointed with myself. I know that I have been doing  my meds and I have been doing my stomach feeding most nights too.  I have been making the right decisions and all my friends have been very supportive. I bring my nebulizers over to their houses to do them if we are hanging out, etc. It just wasn't enough this clinic. I really thought there would be a slight increase. However, I haven't been jogging since it is cold outside. And I know waitressing has been making it hard to gain weight. Plus, its winter. It is always harder for me to stay healthy in the winter. Dr. B was still pleased. He said "I should give myself a break, I have been doing everything he asked, I ran a 5K, and I'm still doing well." And that is true 2% increase isn't a huge decrease, only if I continue to decrease then there is a problem. Dr. B told me that I need to focus...

First blog: Hello

My first Blog: A little About Me I'm not sure why I have decided to start a blog, however, here I am.  I have honestly thought about writing about my life for years, but have always chickened out. I have finally decided to share the experiences life has thrown at me. The biggest reason I have been asked to blog by people is because of everything I have dealt with medically. I have Cystic Fibrosis and a few other medical problems...This is probably the best reason why I should blog. I can relate to others who are dealing with medical problems, however,my CF is also why I did not want to write this blog. CF can be embarssing and annoying sometimes... but it  has helped define who I have become to be as a person. Therefore, (yes, even though I want it cured) I don't hate having CF. Let me start off with some basic info and statements. I'm 26 yrs old and have dealt with CF all my life. In this blog you will hear recent stories (good, bad, embarassing); a...

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 ...