Skip to main content

"Mixed Up " Monday. Randomness.


"Mixed Up" Monday

Yesterday, was a day full of random stuff. Random GOOD stuff, but still. I had no car, as it is still dead in my Garage (but it's getting looked at tonight). I spent the morning hanging out with my lil cousin, then had lunch with my friend, Sarah. I finished the outline for my headboard, so it could be cut out. I then just have to paint it and attach it (a project I started over a month ago..lol). I did my meds and went to Tech rehearsal. I'm doing spotlight for Mulan Jr. Which I have never done before. I have worked with running the lightboard once, when I was in high school. But first time ever doing spotlight.

Earlier in the day, after I styled my hair for the day, I realized how boring it was to do my hair. Don't get me wrong, I LOVE my short hair. Short hair looks better on me, but as you may know I never get the same hair style or cut twice. I get bored and like changing it up. With it being short, I can't braid it or anything. I never want to permanently dye my hair, then I couldn't change it. However, I had some washable dye in my cloest and I decided to throw some blue in my bangs.

Of course, Wednesday, I'm going job hunting. Therefore, all the blue will disappear on Tuesday night and reappear Thursday.

As far as job hunting, not sure where all to go, but I know I need a job! Summer almost over, so I will be done watching all the kids. Keeping fingers crosses for something. Besides babysitting, job hunting, and doing Tech, I'm going to start jogging again!

I'm hoping my medical problems will not come back. I found another 5K to do! It is at the beginning of September! Very excited to try again! Fingers crossed this one works out!
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

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...
3 comments
Read more

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...
2 comments
Read more