Skip to main content

Ugh, the good, bad, and ugly.

Good and Bad.

I love doing Hairspray and because of the Casts openess and acceptance of me doing neb treatments in front of them, I 've been staying way healthier than I usually do during plays. So no clue why this happens to me once in a while, but I kinda noticed how my legs were sore all day yesterday. Then as the night progressed I was even more sore. I kept thinking, oh its just from all the dancing. So between, being sore and finding out my good friend, Laura (with CF) is back in the hospital, I wasn't as cheery as normal. BUT, the Cast of Hairspray always knows how to put a smile on my face and I still had a FANTASTIC time last night.

Sore from dancing, I wish.

Nope. I woke up this morning barely able to move. I feel like a Mummy when this happens to me!! I also tend to get a fever and pink spots and swelling in my legs (as it gets worse). This happens to me once in a while. I will be so sore that moving makes me cringe or cry. When I was 12 I remember my dad carrying me everywhere.  Right now, its not too bad and I hope it stays that way all through my peformance tonight.

I want to blog about all the aspects my CF affects my life. And unfortunately, this is one of them.

In college, I had some awesome roommates that would help me out (Stacey, THANK YOU)! The last time I had a flare up was last fall and I realized how fortunate I was to have roommates and family always living with me up until this point. Last time, I didn't even want to get up to make my meds/ do my meds.

This time I have to do everything to keep my health at its top. I always give 100% during a performance and I can't do it that if I'm not keeping up with Meds.

What makes this happen to me?
Doctors aren't really sure, they think it has something to do with the liver not properly working and an excess of bacteria building up and crystalizing in the joints. The fever shows I have a bacteria my body's fighting and this is how my body reponds. I usually just wait it out.

If the spots show up later, I will take pictures for Dr. B, cuz he wants to see them (ha, and I can't go all the way to Chicago today).

We'll see what happens. I'm hoping that it just goes away, or postpones itself a few days. Sometimes it only lasts a day or two and sometimes 5 days. I'm hoping this is a 1 day thing! :-)

I will keep you all updated.

Comments

  1. I appreciate your telling it like it is with your experience including the not so fun stuff like pain. Will be sending you good vibes for your performance tonight and crossing my fingers this is one of the 1-day sessions!

    ReplyDelete
    Replies
    1. Thanks! yeah, the point of the site was to be honest about what its like for me to have CF. Ps. your vibes worked. I was only a little stiff and not much pain at all today; I performed at my full 100%!

      Delete

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 ...

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! 

Exciting News, even in a Hospital!

Exciting News: Even in the Hospital: 3 Exciting things!! Yes, I know. exciting news in the hospital...Nope, I don't get to go home. Not yet. BUT, I'm excited to share some othe GREAT NEWS! First, of all since I was admitted last Thurirsday morning, I have gained weight. 1. because I don't have time to make food and eat at home as much as I need and 2. Who wouldn't devore a meal of roast beef, potatoes, veggies, fruit, and pudding at 6pm then order anothertray with shrimp and rice, and more dessert at 7pm? 1. So as of today I am 107.4 lbs! This is the highest I have been in a very long time. To check out my weight and lung functions changes over the years click here- Clinic-My Health Page! Only, down side...I need to buy new pants and running shorts, none of them fit me...I'm cheap and picky with clothes..so it may take a while. However, I'm sure a trip to Delia's will change my mind. Ps. for some reason Delia's usually fit, when others are t...