Friday, July 29, 2011

Compliance, Judgement & Progression

A fellow blogger, Piper, over at A Matter of Life and Breath wrote an amazing blog post yesterday and extended a challenge to others to write about their thoughts on CF control and progression.  So here goes...

 I am an old CFer, who has by luck or biology or by the grace of God, had an easier road than most with this disease.  It has limited me little up to this point and for that I am extremely fortunate.   However, I don't ever feel like I have "control" over my disease.  Instead, I feel like I do what I can to "manage" my disease(s) on a daily basis.  It takes A LOT of work.  It take enormous amounts of patience.

Sometimes, it even takes giving yourself a break.  Allowing yourself to not be perfect.  Treatments are crucial...compliance is so very important...  Yet, sometimes, life gets in the way.  My personal definition of compliance involves working hard and doing your best.  Everybody's best is different.  I think people in the CF community like to compare each other.  If this one is running a marathon, while that one walks around the block for exercise, the one who walked is not doing "good enough".  My wish is that people would stop making these comparisons.  There will always be someone doing more than you.  There will always be someone doing less.  I think each of us should only judge ourselves when it comes to self-care. 

I also think that sometimes a person can do everything by the book, yet still decline.  This is the nature of the disease.  I think judgement coming from others regarding this decline is harsh.  That person who is declining is often judging themselves harshly enough already, even if they have done everything in their power to stave off the progression. 

This is going to sound odd to some people, but I honestly feel judged for being "too healthy" within the CF community (no, I'm not complaining about being a too healthy CFer...I'm fortunate!).  A lifetime of doctors, hospitals, pills and daily treatments doesn't make me a card-carrying CFer in some people's eyes.  Yes, I have been told this directly.  My lung function is not low enough to qualify.  I haven't needed IV's enough times.  I have been told that I shouldn't have feelings regarding my CF, because my road has been easier. 

Here's the deal.  This is MY experience.  This is MY journey.  These are MY feelings.  I admit that my road has been easier, but I am entitled to my feelings, fears, worries.  Just as I am entitled to celebrate successes without being judged.  I wish more people were accepting of that fact that EVERYONE has a unique experience...all of them valid.  Yet, I know that the judgement will continue to exist.  Honestly, it's human nature.  There are people who feel better about themselves when they put down others.  I consider that the judges problem, not the problem of the judgee.
So, I have been feeling excellent lately!  So much so, that I have had very little health-related news to blog about.  Yet, the MAC infection persists.  I have an appointment in a week in a half, where I will be cultured to see if the MAC has been suppressed at all.  If not, we may need to switch things up again.  I struggle with the unpredictability of this disease.  I think I keep motivated to exercise regularly and be compliant with my treatments to give myself a sense of control.  It makes me feel like even if nothing is going to change, at least I'm doing something.

These are my jumbled ramblings about compliance, judgement and progression.  If you wish to take the challenge, read below...
1. Write a blog explaining your personal thoughts and experiences in dealing with CF control and progression. This could include your views on whether CF is in fact a "controllable" disease, your personal definition of compliance, your thoughts on whether (or how) someone with CF should be judged in terms of "good enough" self-care (what makes you feel judged? do you think those fears are justified? is judgment ever useful in this context?), your own struggles with control vs. unpredictability, and how you keep motivated in the face of so many questions. Or, you know, whatever you want to write about really. It's your blog.
2. Comment below with a link to your blog so that all of us can read your response. YOU DO NOT NEED TO LINK TO MY BLOG IN YOUR ANSWER. If you'd like to do so, please feel free, but this is about starting a discussion, not publicity.
3. Encourage your own readers to get in on the conversation by posting the same instructions on your blog. Remember, the more responses, the better the conversation. Let's see if we can get this one going as much as with past challenges.
4. If you don't have a personal blog (or just don't feel like going through steps 1-3), feel free to still make yourself heard by simply leaving a comment with your thoughts below.
5. Non-CFers are 100% welcome to participate, either by pulling from their own experiences or simply by offering their perspective as people, friends, and loved one's.

13 comments:

Piper said...

oh my goodness, I LOVE THIS! please please please give me permission to repost a quote or two from this VERY insightful and much-needed post??? i'll love you forever...(well, i'll love you forever either way, but i'd be super grateful!).

Specifically, i swooned when i read this:
"This is MY experience. This is MY journey. These are MY feelings. I admit that my road has been easier, but I am entitled to my feelings, fears, worries. Just as I am entitled to celebrate successes without being judged. I wish more people were accepting of that fact that EVERYONE has a unique experience...all of them valid."

gorgeous.

keep up the good fight, stacey. i'm proud of your dedication to your disease, proud of your outlook, and most of all just proud to call you "cyster"!

Stacey said...

Thanks, Piper! That means a lot! I was hoping this didn't come across like I was complaining for being "healthier". That certainly wasn't my intent. Take whatever you would like!

Huge hugs!

Jamie said...

I love this! And I think I will take the challenge, mostly because I just had an experience with being judged. Love your blogs, and girl your being a "healthy" CFer is something to celebrate!

cindy baldwin said...

I am definitely going to blog on this if I have time! (I'm going out of town tonight, so we'll see.) I completely agree with just about everything you said. Also, on the exercise front - for some of us, exercising harder/running marathons/etc. etc. etc. is simply not the option. My body wears down really, really fast. I make exercise an important part of my life, but I probably will never be one of those "CF runners." When I wear myself out - I get sick. I make sure that I'm getting my heartrate into the target zone that the therapists want it in, and make sure I'm active and living a "healthy" lifestyle. But for me... pushing myself harder, trying to run marathons, will not only NOT make me better, it will make me WORSE. I get so frustrated with so many peoples' attitudes that are like "Well, if you're having problems, you obviously aren't working hard enough." Everyone's experience of CF is different. One size does not fit all. And often, even when you're doing the best you can, you decline. I've actually had some of my worst lung function when I was exercising most regularly!

Anyway - thanks so much for writing about this!

Jamie said...

Here's my version :) And to Cindy, I agree with everything you said!
http://letmefly-jamie.blogspot.com/2011/07/im-taking-this-challenge-that-was.html

amybraid said...

Great blog!!!!!!!

I can't believe some have said that you can't have feelings about CF because you are healthier. What douches! I consider myself very lucky when it comes to CF. I may never have had great lung function and was under weight for years, but now I am at a decent weight and I don't have the issues that so many have with digestion and sinuses. Everyone's CF is different and to judge others based on your own is downright selfish. Life is very individual - healthy or not <3

Teresa said...

Wow, I love this post! Thanks for sharing your thoughts. I agree with Piper, in that I thought the quote about "This is MY experience..." was especially great.
I am glad you have been so healthy and feeling so good lately.

Anonymous said...

I am so glad you posted! When I saw the challenge I thought to myself, "I hope Stacey writes a post because her perspective needs to be heard." based on our conversations on the topic. Even though our situations are a little different, I am not sure I have anything to add - your post was very powerful and beautiful - as always... and of course, just like you!. Great job!

Rachel Olimb said...

Love this! Just can't believe someone actually said that to you!!!

Emilee said...

I love it Stacey! I'm going to do it, we'll just see how long it takes me to actually get it done:). I'm glad you are doing so well. I hate the judgements that can come from other CFers. As if this disease weren't hard enough. I love getting to know you and your journey better. You are amazing!

Stacey said...

Thanks, friends, for your support and comments! I always appreciate your love and support. I have really enjoyed reading the other blogs on this topic!

LS said...

Stacy! I love the blog. I swear I could have written that blog myself because I feel the EXACT same was as you. I often feel like I should not be complaining about anything because I have had an easier road than most, but at the same time there are days when I am so down about the way I am feeling that I want to reach out for support. But just because our life has not been as 'challenged' up until now does not mean that we don't have the same problems, fears, and concerns. Our life is still very unpredictable and there is no control. That is why I try to live my life the best I can and enjoy those moments whole-heartedly that I am able to play sports, watch my kids run in the sprinkler, and work full-time.

Love your blog!

Emilee said...

I did it. It didnt take me as long as I thought. It's over at emileepehrson.blogspot.com