Skip to main content

Jobs and Cystic Fibrosis

Jobs and Cystic Fibrosis

Many Cfers and doctors have different opinions on jobs that a CFer can or can't do. Well... shouldn't do. I hate the idea of being limited in jobs, or at all. I know when I was working in DayCare all last year, my doctor wasn't too thrilled. Apparently, I can't work around cleaning products, chemicals, outdoors, in schools, in daycares,  or do heavy lifting, etc. The not working outdoors, teaching, or working in labs with chemicals, kind of killed the idea of Geology. I have over 40 hours of credit in Geology and won't use it for a career, just a hobby. Sad.

Hmmm..so after listening to jobs my doctors have told me to avoid I come up with...desk job. UGH. no offense to those who do work at a a desk job. If you enjoy it then that is great. But, I have way to much energy to sit at a desk all day. I want to be up and about,working with people. I've been thinking about jobs a lot lately, Grad School Programs, etc.

I'm still applying to Grad School Programs (4 different places). And 1 is online/long distance learning, as a back up (incase who knows what...). After going away to College, to leaving it in an amubulance, to starting college over again at a community college, getting healthy enough to try a 4 yr University again, I have learned CF is always going to "spice it up" so I had better be prepared.

I will be in my hometown for at least the next year. In the August 2013, I hope to start a Masters in Public Administration (City Management and Non-Profit Management). Until then I need to have a job or two to pay the bills and save money.

I babysat all last year, and I love the 4 kids I watched, but I need a job that pays more with less hours. So today I put in a few more applications and hope to hear something in the next week or so. And all of the jobs I applied for fit the criteria. I'm happy with them, the family will be okay with them, and Dr. B will be happy with them. Success! Now, to wait...

Comments

Popular posts from this blog

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...

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 ...