Skip to main content

Less is More


And I'm not talking about the new hit show "Tidying up with Marie Kondo," although I DO love to purge items and be minimalist as possible. I'm talking about juggling life. Having a career, being a foster mom, with a chronic illness like cystic fibrosis can make it feel like I'm juggling 10 items at a time. I think I'm finally getting an idea of what I need to do!





I sleep 9:00 pm-6:30 am (yes, full 9.5 hours) and I need them. I do nebulizer treatments, pills, and clean medical equipment for 4 hours a day. Between getting the kiddo(s) off/on bus at 8am and noon, making meals, cleaning, errands. It doesn't leave a lot of time for: career, family, volunteering, and other aspects like appointments (both medical and fostering). I'm not complaining. I'm SUPER lucky to have a family and career. Plus, I'm fairly healthy and stable despite my cystic fibrosis.





I have been doing awesome at managing all my meds. SUPER THANKFUL for that! Especially considering I added 2 weeks of Home IV antibiotics on top of my normal 7-10 nebulizer treatments a day (those IVs ended a couple days ago and follow up is March 3rd- stay tuned...). I know my medications have to be a priority. Not only for me, but for me be the healthiest possible for my family.










I try to plan ahead and work smarter, not harder (I think that's from Dave Ramsey) - I listen to his podcast quite often. I just have to get creative sometimes... like recently I did my treatments during my 30 minutes lunch in a 7 hour long real estate seminar. I try to mulit-task as much as I can. I do puzzles with our kiddo(s) or do online real estate work during my treatment times at home too.










Sometimes I need a personal time-out.





Just time to stop and enjoy a mug of decaf black licorice flavor hot tea (No?? maybe coffee in your case ;-P). I want to enjoy every minute. As a foster parent we never know when our time with the children in our home will come to an end. I want to make the most of every minute and soak it all up <3





I have been using my google calendar in my phone more religiously. And trying to not spend time on "how to plan my time effectively," because next thing I know my planner will look beautiful, but I have no time left to be actually PRODUCTIVE. ( Note: I do use a planner for breaking down big campaigns, projects, deadlines, etc. But I minimize time spent writing in the planner. )M





More doing and less planning.





I think only am I starting to learn what it means to spend my time more wisely and soak up every precious moment. My personal time-outs help. I can see a difference in my days, enjoying more and worrying less. Not surviving, but actually living.





What are some ways you manage time effectively? Do you have a personal time-out or quiet time to refocus? I'd love to hear about them? How do you deal with daily life struggles?


Comments

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 ...

Updates!

 Hey everyone! Sorry it’s been a while. Covid struggles have been all around and we have been focusing our on our kiddo and current life situations (jobs, home, everything really). We have been posting regularly on the Facebook page (www.facebook.com/CherizCFPage). We will keep you updated on there for now,  because we are doing some big changes to our current blog! Stay tuned!  In meantime, message our FB page if you need anything. Keep safe and stay happy.  We will be back. Promise! 

My Body Can't Keep Up

I turned 34 in April this year! I love celebrating my birthday each year and seeing more wrinkles and gray hair appear. I LOVE that I am building this beautiful life with my family. I just wish my body could keep up... Being born with cystic fibrosis meant some challenges throughout my life. I never knew when CF would throw me a curve ball. I missed a lot of holidays in the hospital growing up and sometimes my body tells me to stop. The last few months have been more rough for my CF-related Arthritis. And today isn't any different, despite it being Father's Day! Dad & Andrew I had wonderful plans to go home to see my Dad today, then come back home in time to make some dinner for my family when Andrew gets off work around 5 or 6pm tonight. I had a lot of great plans to celebrate my husband and Dad for Father's Day- They deserve it. But, I woke up with frozen/stiff joints and spots all over. I can barely move, let alone walk or drive today. So all those plans went out the...