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

5K. I could cry. Beyond Annoyed.

My 5K I paid my registartion fee weeks ago, have been training and I'm ready for the 5K. However, I didn't get to run my 5K today. Why? Because Cystic Fibrosis decided to one up me. I got my spots back friday, and they just got worse and worse. They look like this: They take over my feet, and sometimes my calves. I posted about this a few weeks ago. I had them during the last few performances of Hairspray. I call it the "Mummy disease" because when it happens my joints freeze up and I can't move. So the morning of my 5K I wake up and they are on my thighs...     and on my arms. This is the worst they have been in years. I took pictures to show Dr. B at my clinic on the 11th.  I'm just really bummed and upset about my weekend! I was supposed to run my first 5K!!!!! I then had a bags tournament in Peoria for the Dream Factory, and was then going to head to Champaign for Sat night- Monday! My friend Alex, reserved me a ticket for Ren...

My Dad Deserves More Than 1 Day!

Happy Fathers' Day to ALL the Fathers out there! I wanted to post a list to why I'm sooo thankful for my dad (its faster, bit more fun, and I gotta get ready for my Dad's Cookout still)!!! Top 15 (10 isn't enough..lol) reasons Dad should get more than a day of celebration: 15. He loves meeting people, making friends, and is quite social. 14. When something goes wrong, he is the person that can say the right thing to make me smile :-) 13. Is always honest. 12. Few yrs ago, he gave me HIS car, (so i could get back and forth to work/play practices) He rode his bike to work and back (he enjoys it too tho) 11. Best Sense of Humor! 10. He never complains, ever! 9. Growing up my Dad worked 6am-3pm at one job and 4:30-10pm at another. 8. Dad still managed to go to 99.9% of my performances 7. He is the least judgemental person ever, he talks to & helps everyone! 6. He is a pro at making doctors, insurance companies, & hospitals do ...

Society's view on my size

"You are so lucky you are so skinny" "Must be nice to eat anything you want" "Wish I could keep my weight down like you" "You're so tiny and childlike" "You could be in high school still" "Wow you're thirty, you look 16" or hearing these replies: When I say I need to gain weight , "huh, Give you some of mine" Always hearing I'm "cute or adorable," never hearing I'm "beautiful or sexy". All these things can really hurt my feelings. But let me explain further where this post is coming from. Today a friend shared on Facebook about how some posts are body shaming & lots of people don't realize it.  I hear lots of people say things like " I'm not afraid to eat a hamburger. A man likes some curves." Or I hear remarks how all people who are size 0-2 are unrealistic and anorexic, etc. I understand a lot of times people may mean to help boost...