Skip to main content

All the details of my 5K

My 5K


I ran my first 5K on Saturday. I finished and that was my goal. I've been jogging over the summer, but stopped in August when I was having my "mummy disease" AKA CFRA (CF-related Arthritis). Then I went on vacation, came home and I decided to start again. So I signed up for a 5K. But I didn't get around to jogging at all before the ACTUAL 5K. Which meant sunday my legs were sore..lol

Oh well, I did it, I still am in awe that I was able to finish. I had to walk the two hills (both up and down them), the hills were too much for me. But that's okay. I walked more than I had been earlier in the summer. Which means I need to get back on track. Now, my doc has me on a new med that is supposed to help more with my CFRA. I'm really hoping this new med can control it so I can continue to jog.

It took me a long time to work up to a 5K. I walked a mile in Feb every day. Then added another mile, then eventually my friend and I were walking 2.5 miles 3 times a week. In May I started adding bits of jogging here and there. Then June and July I started jogging on my own with a mile at first, then towards end of July I'd do a 3 mile jog once every two weeks and 1 mile or 2 mile jogs every other night. ( Note I can jog about 3/4 mile straight, then walk, then jog 1/2 mile, etc; I still can't straigh out jog the whole thing)



DAY OF 5K

I was excited to be doing a 5K, but also nervous to be running it in my hometown. Everyone knows me there. I was worried I start coughing a ton or I'd sound like a panting dog, I was also nervous not to have my headphones!!! My headphones keep me from hearing my breathing, which I like. I keep it more steady when I don't hear it. When I can hear my breathing I psych myself out. So at the start of the 5K I'm terrified. People know me, I have no headphones, I have some family and a friend at the end waiting for me with cameras...GOOD GRAVY! So we start and at first, I keep up pretty well, but about 3/4 miles into I start falling behind the "pack" and when you reach the 1.5 mile mark you turn around and jog past people behind you. So of course, I see up head people turning around and now facing me. They are jogging closer. And I'm like "CRAP, everyone jogging the 5K in town is going to see me struggling, I'm already out of breath, half gasping (due to the chilly morning air- which really hurt my lungs), half panting,  So I'm pretty self-conscious.

But to my Surprise, everyone who knew me (and saw me) cheered me on! My friend's Dad started the positive remarks "Keep going, you got this" and it just continued, even those out of breath would say my name and wave or give me a thumbs up! I guess, my thought process was completely wrong. I should of realized nobody would judge me, I know my hometown and friends have always been supportive when it came to anything dealing with Cystic Fibrosis. I was just afraid.

Which was silly. I was surrounded by people who know me, know I have CF, and have always been there for me.

FUTURE 5KS

I'm hoping to run the Turkey Trot in November. Depends how my lungs do with the cold air, the chilly air last Saturday really hurt, so we will see. I will continue to run outside and see if it gets better. I'm definetly looking forward to running more 5Ks! I want my lung function to continue to climb as it has been the last year!

My CF Walk to raise awareness and funds for research for CF is coming up in LESS THAN A MONTH! it is the same distance as my 5K, but we walk at a nice leisurely pace! So please come join us! If you are walking with my team PLEASE register and set your "goal" for fundraising. It can be anything, you can try to reach a large amount or set it for what you can contribute yourself. If you have ?s contact me on Twitter, FB, or email me! Walk info: WALK WEBSITE HERE!

I will keep you posted on how my exercsie affects me and my lung function too! Next Clinic is in November!







Comments

  1. Way to go Cheriz!!!! It doesn't matter the time you did the run in it just matters that you DID it!! Congrats again and keep on running.

    ReplyDelete
  2. Thanks John! And yes,I plan to keep at it!

    ReplyDelete

Post a Comment

Popular posts from this blog

Planning ahead (yay, for being organized).

Organization: it is a great thing! I'm doing another CF Walk in October! It's on the 6th at 9am. Why am I posting this now? In the past I wasn't organized. I would end up asking a couple friends to walk it with me. I didn't fundraise much, but I want that to change! I've had people tell me they would have walked if they knew about it. I'm blogging now, being more active on CF communities online, and there is no reason why I shouldn't invite others to do the walk. Everyone knows I have CF, why did I never invite more people?? No clue. So here I am inviting everyone to come and walk with my team! Here is the link the Facebook Event: Cheriz's CF walk FB event Also a link directly to my GreatStrides Walk page is on the upper lefthand side of the blog! I want to start to be more active in fundraising walks (along with 5ks). I'm planning on doing 2-3 CF walks a yr, and the ALS/PLS Walk every year! If you want to cheer me on at my first 5k i...

End of Summer -Updates!

Wow, I can't believe it's been a year since we moved our blog to www.MoreThanDNA.org! A lot has happened in that year. My husband and I became Foster Parents to some amazing kiddos and still have one of those kiddos living with us. We have loved having "Shoes" with us and can't believe how much he has grown and learned in the year!I'm so proud of him! We have court next week, so prayers that it goes okay (and doesn't get continued again- that just drags it out longer for the kids). He is now 39 months old and starting Pre-K this month! Other big changes include: Some renovation to our home (complete Bath rehab & updated plumbing throughout), I started a new gene-targeting medication (symdeko) that is helping to keep me stable these last 3 months, and I got an AffloVest! I'm loving my new portable vest! Also, career wise...we both switched jobs! Andrew also started Seminary this summer to get a Masters Degree in Divinity. He has always wanted to be ...

Why I Hope this Hospital Stay is Different

Typically, I've been very stable as an adult. I'm very lucky for that stability. However, 2018 started out nowhere near where I wanted. I was admitted mid March for a virus. We aren't sure what virus I had (every test came back negative). However, I had a consistent fever over 102 the entire 5 days I was in the hospital. Once I was fever free for 24 hours and I started eating better, they let me return home. I was excited to leave and get back to my everyday life. But, considering now a month later (and re-admitted), I think I should of just done a two week tune-up last month while I was in already. Live and learn. As you know (I'm sure) I have been trying to get my lung function back up to around 55-60%. 60% is my goal and it really is the highest my lung function can get, due to all the permanent scarring. I started Orkambi in October 2016. At that time it was the newest gene-modifier drug on market for CF patients (with my mutations).  After going on Orkambi I droppe...