Sunday, February 13, 2011

28 years old and one regret. Not bad.

by Michelle Matta

When Ronnie asked me to do a guest post I was excited to do it immediately. I have a lot of disability-paid hours to spare, tons of time during treatments for my 24% lungs, and a mind that needs a break from anticipating a call that is coming anytime. A call to tell me whether the doctors think its time to list for transplant following the assessment I did 3 weeks ago.

The delay in my post-writing was a combined result of the stresses of waiting for that fateful call, and the urgent desire to find a way to convince anyone out there to avoid my fate at all costs.

I had 80% lung function until I was 19 years old. No admissions until I was 23. In the years from 19 to 23, I lost 40% of my lung function, and I didn’t smoke or do drugs at all, or drink or date much. It was a direct result of a lifetime of little to no physio, and putting life before CF always. University, part-time jobs, socializing, everything typical of a young adult. I saw my numbers fall at clinic and forcefully proclaimed that I felt “fine”. Which was true, until I went below 50%.

I want you all to consider that you may have things going on right now that feel really important. Maybe you go to school, maybe you work, or both. Maybe you like going dancing all weekend and find it hard to squeeze in treatments. Whatever it is, take a moment to live slower. Physio is not as time-consuming as it feels. Spend 15-30 mins on facebook with your vest on. Watch your favourite show with the flutter in your mouth. Get a puppy and take him for a run every day. You’ve heard it all before, but trust me, the way it feels to wonder if you could’ve helped yourself have just 10% more lung function is too difficult to explain. 10% that could’ve meant pursuing surrogacy with my husband and having a baby on the way instead of living in the limbo of pre-transplant. 10% that would mean no oxygen concentrator chugging at night, or beside you in the mall, or preventing thoughts of winter trips to Florida. Maybe even 10% that would’ve let you be healthy enough for the most fabulous drug trial to stabilize your pft’s and save you from transplant entirely. It’s possible. It’s not about saving yourself from CF, its about making your life better. Just the little bit that you have the power to control, means a complete difference in your future at 25, 30, 35, and beyond.

And that university load that’s holding you back? That job you’re always stuck overtiming at? You know what happens to them? They become a terrible math equation. My 4 years at university bought me only two and a half years at my job before I had to stop working. Please remember that slow and steady wins the race, and unfortunately with CF, our best bet is to sometimes compromise living so busily in order to make it to the next step with good health.

If only I had known that my dreams would come true, and I would fall madly in love and ache for the rest of my fairytale. I would’ve never EVER missed a single physio session or chance at exercising. If only I had known that feeling fine is not enough. That’s my one regret.

Note from Ronnie: Thank you SO MUCH Michelle for taking the time to write this pointed and powerful guest blog. I've had the opportunity to share various emails with you and one thing is for sure, your desire to help others is very clear. You explicitly said to me "I hope my story helps someone out there". Well Michelle, I can guarantee you that this will help more than one. Sometimes, sharing our one regret can be more powerful than sharing our many accomplishments. Thank you.

Comments (14)

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This post couldn't have come at a better time for me. I am a CF patient who currently works in a hospital where I've been for over three years and also where I just recently caught pneumonia that landed me in the hospital for two weeks...And I'm hesitating leaving, despite strong urgings from family, friends and especially my CF doctor because my job, my boss and my patients seem more important to me than my own health and vitality. Sometimes we spend so much time fighting to appear normal that we even convince ourselves. May God bless you with a transplant and a second chance so that one regret can turn to none.
I got passed the first paragraph, slapped my laptop shut and went out for a 30 min run for the first time in 7 months.
I owe you one, Michelle.
1 reply · active less than 1 minute ago
And how'd it go? :)
michelle, i am proud of you, i know how hard this was for you to write....after transplant the idea and dream of surrogacy becomes an option again!
also if you want to check out this awesome girls blog you can find it at http://heartofthematta.blogspot.com/
You have no idea how much I needed to read this. Just perfect.
Thank you guys. Keep pushing. Proud of you all and your words meant the world.
This is a very thoughtful and well written article. CF folk often say, "let's live in the moment", but it seems like you're arguing that we must live in the future, and with hope: for to have CF means to confront the potential of bacteria in our lungs, the potential of developing diabetes, the potential of being hospitalized. And we must do so my protecting ourselves from the very beginning. You are calling for us to not deny our situation, but to confront our illness - even though we might be "feeling fine". And in confronting our illness, you argue, this is the only way we can do something as powerful as falling in love. To have CF, one must think, "I am not in love now, but maybe one day I could be in love. So, today, I run for 30mins so I might add add 30mins to my life, so I (might) have 30 mins with the person I love (whom I haven't even met yet). To most "normal" people that sounds insane: you're going to work for something that might never come? Yes! you say. This is what we must do.
I just want to say thanks for this great opportunity to meditate on the future to come, and the importance of cultivating care of oneself.

I hope you'll accept the sincere best wishes of a stranger. I'll be thinking about your words here for a long time to come!
wonderful blog post!
Very good to hear these words from someone with experience! I am a freshman in college this year and am scared to death of my health getting worse. Thanks so much for making this even more of a reality for me! Good way to boost someone's motivation for sure :) Thanks Michelle!
Thank you so much for sharing this Michelle. As a freshman in college, this is exactly what I needed right now. I can't seem to slow down, but it makes so much sense hearing it like this. I am going to make some serious lifestyle changes. Thank you so much.
Samreen Salim's avatar

Samreen Salim · 678 weeks ago

Thanks Michelle for sharing with us..It's an eye opener for all cfers :)
julie a. katsiris's avatar

julie a. katsiris · 604 weeks ago

Aunty Julie , stumbled across this for the first time, Sept 3, 2013. Excellent article, with true insight, and hope. You can truly help others, and you have a wonderful ability to be an author too Michelle. Don't stop writing!!!.

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