Skip to main content

Health and 5K

Getting my Health Back:

I was at my healthiest in 2012. I was walking every day and jogging some parts of that. I was in a musical where we had dance rehearsal at least 2x a week. And I did a 5K where I pushed the hardest I could, finishing in 42 minutes. Well, I did another 5k last Saturday (on my mom’s birthday) and power walked the entire thing finishing in 53 minutes. 

( Picture to right: Ada & I at the 5K)

I knew I couldn’t jog, since my hips now like to pop out of place and it is too hard on my joints. My arthritis has gotten a lot worse in the last four years. While I know I will never will get back to level of health I had in 2012 (due to normal progression of my disease), I think looking at how I achieved that level, will help me to reach the best health I can today. I had a steady hourly job that allowed me to schedule out my day. Routine is what has always worked best for me, which is why I struggled in college and with jobs where hours changed a lot. In 2012, not only did I have the time to walk every single day, but also the motivations. I also started out slowly and gradually added more distance with time.
I had someone who walked with me 2-3 x a week. Those were my walking days, I’d usually push myself to jog walk 2-3 nights. So I’d be active walking or jogging typically 4-5 nights a week. They weren’t long periods of time or very long routes, just a 1 mile or so at first. I started this in late February and by July was jog/walking 2 miles at least 2 x week. Then I built up to do the 5K in September. 

Having someone walk with me 2x a week really helped keep me on track. My 2nd major motivation was my health in general. My lung function was around 56-58%. Whereas, now I struggle to hit 50% at clinic. I’ve lost 10% lung function in the last 3 years. I’m hoping being more active (with the help of “hopefully” Orkambi) will help me increase my lung function again. In 2012, I actually hit 64% at one clinic. While I think 64% is a pipe dream, I’m trying to 58% again. Which will be hard, but I WILL do it! My 3rd motivation was Laura. My best friend Laura (who passed in 2014 and also had CF) was being evaluated for a lung transplant in 2012. We were hopeful and she’d tell me how hard it was and that I needed to push to stay healthy. She was honest and open. She wanted me to succeed more than anything. I was also motivating her to keep her health stable until she could get her new lungs. [Note: Laura was denied transplant listing and therefore, had to try to make do with her 18% lung function]. Her living 2.5 years with 18% lung function was amazing, especially considering all her secondary problems, like diabetes, gastroparesis, etc. She was one tough lady.

While Laura isn’t here anymore to cheer me on, I can still hear all the words of wisdom and motivation she gave me. I have a playlist I put together that reminds me of her and my future for while I go out walking.  My new motivation is my future with Andrew, in our home, hopefully with a family. The biggest motivation is wanting to be a mom (via surrogacy/ foster/adoption) and to have the ability to run and play with them. I want to be able to pick up my child and carry them if they are scared or hurt. I don’t want to drag an oxygen tank with me to their games or recitals. I want to be healthy for them. I want to live to see them grow up.
I can not jog anymore due to arthritis, but I can power walk. So I’m going to keep walking and try to do another 5k for a good cause later in the year! I loved that the one I did last week. It was for ALS research. I have a friend, Sean, who has ALS. It is a truly horrible disease and I seeing him continue to fight it, is some powerful motivation right there. Perhaps I will powerwalk the CF Walk in October!

Anyway, fighting for my health and trying to get to a point where I feel healthy and not sick is where I am right now. I will continue to update you as I go along. Also, if anyone has a Fitbit add me!

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...

Calling All Who Care!

     Please Read : Okay, so first off I want to say that this post is tough. It's tough to think about and write. However, it is extremely important and a huge topic in the CF Community, and is VERY NEAR AND DEAR to MY HEART!  First I want to ask you... What if I told you I needed a Transplant. That I needed to reach a certain weight, get my kindeys functioning better, get a higher pain tolerance, and get off a couple medications I take right now. What if I said I couldn't receive a 2nd chance at life unless I reached these goals and I raised a certain amount of money that seems impossible to raise. What if I had been in and out of the hospital off and on for the last year, with many surgeries, had multiple infections and my lung function dropped from 40s to the teens and now is slowly dropping still. What if I was starting to wonder if my decision to go through the grueling Transplant tests was worth it. What if I start to get down about my cf and wondering why ev...

A Hospital at Home

Coming home from the hospital takes a balance..... Wait.... Did I just say home from the hospital??? That's right!  I get to leave Wednesday the 18th, after 8 days in the hospital. It was a logistical thing. I have a super important court date on for "Shoes (our AMAZING foster son) soon." So Doc knew before he admitted me that I would be leaving by that day... So what does this mean for me and my health??? Well, I need to make sure I continue the same treatment schedule I would in the hospital. So 4 sets of nebs a day. 8am, noon, 4pm, 8pm. Which means I finish my course of IVs at home. I will be on IV's at least until 27th (so 1.5 weeks left). I came into the hospital on Tuesday the 10th, but we didn't realize until Friday the 13th that my Psuedomonas is resistant to all of the antibiotic options for IVs except one med. So on the 13th we switched to Avycaz, which is a newer, hard hitting antibiotic that was brought to market less than 3 years ago. We were hoping I...