Skip to main content

CF Doesn' t Own Me & Celebrating!

CF: A part of me:

Some Celebrations are this weekend:
First of all, Happy Birthday to my Dad!  I think my Dad is absolutely Amazing!!! Please take a minute to read all about why he is a phenominal father in this past father's day blog post! Also you can read about a funny story with a simple example for how dad is always there to save the day in this lil past post here!


So besides my Dad's Bday being today, Andew and I put up Christmas/Had a Holiday Dinner yesterday! We put up the Christmas Tree, some decorations, listened to Christmas Music and did some baking!  Here are some of our Christmas/Holiday Pictures!

       Our Tree

-------------------------------------------
Media Center



--------------------------------------
Above the Couch



-------------------------------------------
Our Hallway Closet Doors :-) Haha!




We used a Clean/New Stomach Syringe for the Turkey! Seriously, supplies double as so much! What other supplies do you use for other things? We used to squirt colored water out of the syringes to color the snow too!


I'm still working on a fun dinning room table set and coffee table centerpiece!
 
To see last years Christmas Photos: click here
 
Okay, now back the part in the title "CF Doesn't Own Me", this is why I feel it is important to state that:

I've notcied in the last couple of weeks, that I post a lot of CF related posts on my Facebook. Which is okay, since CF is such a huge part of my life. BUT, I try not to post more than once a day. But sometimes there are some really cool news about Clinical Trials, or CF Walks, or even related to my personal health. But I don't always post about it, in fear I will be posting too much. Or not everyone I'm FB friends with wants to read about CF all the time. Plus, I blog usually 2-3 a week, so that is quite a few posts too! I had a group on Facebook where people could find tips on fundraising for walks and photos from the walks, and get new info! But it isn't a page, therefore I can't post in it (and have it go on regular newsfeed and it won't generate an audience. The whole point of starting a page would be to share about the Princeton Walk, other CF Walks I'm doing, and how family, friends, and the community can get involved. Pages are easier to work with, in that anyone can share them, invite others to them, and keep updated! So I've decided to make a page. Feel free to join the page to stay updated! If you are already in the group, feel free to stay in it or leave. I will be posting everything on the page now, and less often in the group. 

Click here to join/ "like" it!
https://www.facebook.com/CherizCFPage?ref=hl#!/CherizCFPage


Updates: Updates on Laura: She got a blood transfusion, and was released to go home on meds & oxygen. So she is still figuring out what to do and how to fight (read about Her fight here!) ,  I'm still waiting to see if I get the tuition back from school, and my Colonscopy is scheduled for Dec 13th. So waiting... I'll keep you all up to date! Oh, and I updated the "MY CF HISTORY page on my blog Read The Updated Page here!

Comments

Popular posts from this blog

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! 

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 ...

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...