Skip to main content

Oh lungs...

High School reunion and Clinic Update:


I had a busy weekend. I worked Friday night, then we drove the 2 hours back to my hometown and Saturday was packed full. I (along with 2 other classmates) put together our 10 year reunion.  It all came together and turned out pretty nice. We had the parade at 1pm with the reunion that night at 5-10pm.  I had a great time and really hope all my classmates enjoyed it too.

Then Sunday we returned home. Monday I had classes and CF CLINIC!!!

Here's the update. We re-tested my liver function. I won't know results until later this week. Also, we discussed my issues with insurance and receiving meds. My weight was VERY good at 102 lbs. I haven't been triple digits for a year and really have been struggling. However, I realized last week that my high as calorie powder has been disappearing quicker. Andrew is tricky. He has been putting a ton apparently in the hot cocoa that he keeps offering to make me.

So yay! However, the last two weeks I have been wheezy and raspy. My lungs have been really full feeling and crappy. I figured allergies... This clinic my lung function FEV1 went from 54 to 49... Ugh. Last year I was 61. How defeating feeling.  I guess everything is catching up to me. I'm going to school full-time (15 hours a week), working 16 hours at my Internship (Hospice Care-Social Work- note my director understands my immune system and health needs), and working 12 hours at Family Video. So on top of that 43 hours I'm doing research, homework, running errands (and commuting 40-80 minutes a day between work/school)... I'm doing my minimum needed therapies (2 abluterals, 2 hypertonics, 1 pulmozyme, and 2 Tobi).. BUT I need to do more.

I need to do the extra stuff. Like get enough sleep, exercise, etc. Doc. B has me taking prednisone for the next 5 days. If I don't start to respond and feel better in the next two days I will go on Cipro (since I'm allergic to the main other antibiotics) for 14 days. If that doesn't work hospital tune up. However, Dr. B thinks it could be a small infection and allergies and I will bounce back without need of IVs :-)

So hopefully my lungs feel better by Friday. I will not let myself continue to decline. The only time in my life I seem to increase in lung function is when I'm not going to school and not working more than 20 hours a week. It's really frustrating. I want to go to school, I want to work full time. BUT I want my health to go up.

So Andrew and I are going to start a more scheduled approach to our days. Hopefully we can keep up with it and it will pay off.

Lot to implement, lots to change, and a lot of work. Hope it works :-)

Comments

  1. Take time to smell the roses or if your allergic try freshly baked cookies! Don't stress yourself out! Take time to relax! Make sure you have Cheriz time!

    ReplyDelete
  2. yep, I don't have as much this week, so that's what I'm gonna do! Thanks Martha! ps the banana walnut pancake was amazing!

    ReplyDelete

Post a Comment

Popular posts from this blog

First blog: Hello

My first Blog: A little About Me I'm not sure why I have decided to start a blog, however, here I am.  I have honestly thought about writing about my life for years, but have always chickened out. I have finally decided to share the experiences life has thrown at me. The biggest reason I have been asked to blog by people is because of everything I have dealt with medically. I have Cystic Fibrosis and a few other medical problems...This is probably the best reason why I should blog. I can relate to others who are dealing with medical problems, however,my CF is also why I did not want to write this blog. CF can be embarssing and annoying sometimes... but it  has helped define who I have become to be as a person. Therefore, (yes, even though I want it cured) I don't hate having CF. Let me start off with some basic info and statements. I'm 26 yrs old and have dealt with CF all my life. In this blog you will hear recent stories (good, bad, embarassing); a...

Holding Down the Fort

My husband, Andrew, is currently at Wartburg Theological Seminary and is starting his first week of his second year there. Every year he lives on campus for one week. He enjoys starting each semester on campus where he can build friendships with other students and professors. It's the only time he is on campus. Usually he does long-distance learning, online, from home. It was the only way we could manage him doing a four year Master degree program while working. This week is the hardest for us. However, we have something on Thursday and Friday this week, so Andrew will only be gone 3 days instead of the typical full five. So that will make this week a bit easier than the other semesters. It's hard for Andrew to be away, although I know he is having a blast. We send random pictures back and forth like a book he may be reading or a game I may be playing with our kiddo. It is hard for the kid(s) to not see Andrew every day. We are foster parents and stability is a BIG issue for ...

Close to a Cure?!?!?! and Thank You!!!!!!!!

Help Us Find A Cure & Thank you! Lots of new meds and treatments are being researched thanks to the CF Foundation and the people who support it! Thank you soooo much everyone for supporting me and the CF GreatStrides Walks! I hope you enjoy hearing about the cool new ways steps are being taken towards finding a cure for CF and how everyone has helped me and us (the cf community)! New Treatments And Break Throughs: As you may know, from reading my last couple blogs. Some exciting news was released!  VX-809 + Kayldeco Phase 3 (6 month clinical trials) has started! Which means if all goes well, this could be on the market in the next year or two. This drug helps target the actual faulty gene. It will help improve our lung function (hopefully gain some back, the part that isn't damaged) and will help us to slow the decline of our lungs health tremendously! This is the treatment for my mutations!To read more about this new treatment click Here! Also, there are other medic...