Skip to main content

Hello June: Chaos & Happiness

It is June already.... Wow, has time been flying by! May was Cystic Fibrosis Month and I spent a lot of the month preparing for the Princeton Cystic Fibrosis Walk (June 10th). If you want to join us or donate, just click here!



 I also attended the Bloomington Great Strides Walk in May! Andrew (my husband) was the guest speaker  (watch video at link) at the walk. I'm so proud of him, he has really stepped up in the last year and has been getting a lot more involved with the CF Foundation!

In the last month I have gotten even more involved as well. I decided to join the CF Foundation Champions committee. We discuss ways to improve daily care and improvements that will help the CF population today. I was also invited to apply for a position on the 2017-2019 (2 year term)  CF Foundation's National CF Adult Advisory Council. The council is made up of 12 individuals that are selected across the United States that are leaders in the CF community. The AAC is responsible for offering a voice for those in the community, providing insight on current information, helping to run/maintain online CF webinars (like BreatheCon), and reviewing the CF impact grants, etc.

I have been very involved in the local CF Community by serving as a volunteer coordinator of most of the Peoria Chapter's events (4 walks, 1 golf outing, 1 gala, etc). The Suzanna Lee Golf Outing is THIS monday (5 days before the Princeton Walk), so it will be a very busy week for the Peoria CF Chapter! I started becoming more involved nationally through my blogging. I have guest-blogged for the National CF Foundation's website 3 times so far...this led me to other national avenues & roles.

I really do think my CF Volunteering comes before all my other volunteer work (and even my job, but not clients I currently have). And of course, my family comes before anything else. I focus on clients, but between clients I do not advertise and take mini-breaks from work to focus on health & CF volunteering.

The last month has been busy, but I have enjoyed every bit! I have added those 2 new CF Foundation roles, co-hosted/coordinated a Peoria Women's Council of Realtors event (I'm on the WCR board),  finished fostercare classes, started a new clinical trial,  AND have a done major renovations to our home (pictures coming soon)!

 I'm sorry dear family & friends I have been distance and haven't had much time for anything lately. BUT I finally feel everything is falling into place. My Real Estate work has picked up a lot since it is beginning of summer, I getting a decent schedule in place, and I cannot wait to finalize the FosterCare paperwork! 2 more inspections and then we will be ready to accept children.

Thank you everyone who has supported us in our decision to grow as a family AND everyone who has helped make the Princeton Walk happen!!! I can't wait to see what the month of JUNE brings us!!!!



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 ...

Laura/Lara- two amazing gals

Laura and Lara Today, was a pretty normal day. Work, Meds, Jog, Blog. Instead of jogging, we walked 2.5 miles. (which I recorded in my spreadsheet and I will be doing data analysis later using all the variables I can come up with...) But here is the more EXCITING part of my day: I was asked a week ago to be a guestblogger for  Lara's Blog . She is climbing  Mt. Kilimanjaro to raise awareness & funds for CF in memory of her best friend Emma! I hope everyone goes to her blog and wishes her good luck! She posted my introduction and guestblog today!!! So check it out  Right HERE! Lara, Thank you for your hard work and dedication to helping find a cure for CF! AND then there is Laura ( a different Laura), she is my best friend. Laura has CF too (we met when we were really young)!!! I know she has been going through a tough time. But she is the one who got me invovled in CF awareness! My first CF fundriaser was in 2008 at a CF Walk that Laura to...

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...