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

How Fostering and CF impact my work

I haven't been on my blog much.... I think that is because most of my blogging is currently been done on Health Union's Cystic-Fibrosis.com (here is link to all my posts on their site: https://cystic-fibrosis.com/members/cherizkunkel/ ). I decided last fall to step away from real estate after 3 years in the business. It was tough to say good-bye, especially since I had tripled my volume and business in the last year. However, I didn't have time to add any new clients; I kept saying, maybe next week, next month I can fit more work into my schedule. The truth is fostering takes a lot of time. We have between 5-8 monthly visits at the agency, 1 court ate a month, 2 home visits from the caseworker a month, plus e have 2-3 doctors/specialist appointments for our current kiddo. We have lots of paperwork we fill out, gas mile logs, receipts to add, and more! Our kiddo also participates in gymnastics and dance two nights a week. We go to a fosterparent support group with our kid ...

Oh the Joys of a Colonoscopy!

Colonoscopy, Fun: As you may remember from reading my October Posts (  Oct Post #1   &  2nd Oct Post ) that I was admitted a second time that month for Gastrointestinal issues. I was having stomach cramps and what was believed to be Antibiotic Associated Diarrhea. However, CT scan revealed my colon and intestines were inflammed.  After having a rough 2 months of GI issues, and cuting out most food (diary, meat, grease, carbonated beverages, and sugar). I finally am getting a Colonoscopy to see what in the world is going on! I'm been taking Probiotics, was on meds for both C. diff and AAD. I even added driking Kefir to add to the probiotics and good bacteria.  Only now am I seeing any changes, less stomach aches, etc. I add a 1/2 cup pf the Kefir to my smoothie, its not bad -yum! I really reccommend it and Probiotics (so talk to your doctor about it), it could really help you out! Read about Colonoscopies here! So I'm glad to be g...

What Else Should I Do?

Need Some Feedback.       May has almost come to an end. I love May, nice weather, summer starts, AND its Cystic Fibrosis Awareness Month! A lot of the CF walks are in may and its a great time to raise funds and awareness for CF! However, I'm also excited that it will be June soon! June 28th is the Princeton Cystic Fibrosis Walk. I've helped organize other events in the past. Whether for school or other non-profits I've volunteered at, but this CF Walk is a little different. It is the first time, I've put together a City event. Or put together an event that is so near and dear to my heart. I'm so thankful that I had so many people sign up so quickly. Pretty much everyone family member I have on my mom's side signed up the first day. And I've have had some family and friends help me (giving me ideas, helping me recruit, etc). But, Its the first time I didn't have a committee or team behind me to help execute the ideas and actually plan the event. I lo...