Skip to main content

Swimming is Tough

My Much Needed Health Rehab:

As you know, I've had a lot of health issues in the last year. Liver being elevated, pancreas not working as well, which resulted with me now being on a permanent low-fat, therefore, low-cal diet. So of course, I'm losing weight. But also, I'm struggling breathing wise more. My lung function has been fluctuating between 48-60 since 2012. However, I've have really struggled since last year to keep it at mid 50s. I didn't respond to IV antibiotics in Jan-March this year. I'm now currently at low 50s. Which would be okay, if I couldn't tell the difference it has made on my body.

Because of my lower lung function and energy, I haven't been able to do simple things like carry laundry or groceries.  As I've talked about in a previous blog here, I'm wanting to get back to my 60% lung function, 110 lb self, the girl that had energy to work part time, do theatre at night, and still come home to jog 1 mile before bed. I want to be able to not only ACTUALLY finish a 5k, but be back to my jogging/walking them.

I want to be healthy and I'm tired of not being able to keep up. Being a healthy wife for Andrew is more than enough motivation to get me back on track for working out. But it is sooo tough. If I lift weights I'm sore for 3 days after and I get tired after seriously 5 minutes... If we go for a walk I only make it 1/2 mile before we'd turn back. Bike riding is worse, I make it around the block before panting like a dog. So we try to switch up my "working out" so it's more fun & I don't notice how hard it is. We have lifted weights a few times, gone on walks, done short bike rides, and today we went SWIMMING!!!!

Why is it a big deal that I went swimming? Well, I like swimming at my parent's, cuz it's private. But, I don't like to swim in public pools. I get out of breath easy, have asthma attacks, lifeguards look at me weird, and I've never liked how I look in a swimsuit.

Now don't judge, it has nothing to do with how big/skinny I am. BUT, I have scars everywhere. And one pieces tug on my mediport and my stomach tube, so I was super uncomfortable in them, but didn't want people to see my stomach tube or scars in the past. Hence, not swimming much in public. BUT guess what!!!!! I don't have a stomach tube anymore (read about that here) & I can deal with just scars now!

So here is a picture of me today SWIMMING for the first time in public in a bikini!!!!

We had a pool in our backyard, so even though I get cold fast, I used to swim a lot and rather enjoyed it (or at least floating on rafts...lol). But I haven't been swimming since 2012 at my parent's house. And today I did. But, whew... I can tell how out of shape I am. Never before have I been sore after swimming. I couldn't hold my breath hardly long enough to dunk under the water. It was sooo sad and pathetic. I only swam for 15 minutes, Andrew swam with me and it was fun though. It didn't feel like work at all, so I think it will be a great way for me to work out. I look forward to seeing if I can make a difference in my health.

It's like my own personal rehab. I go to Doc's on Wed, so we'll see how I did weight wise this week :-)

Comments

  1. Swimming is my favorite exercise! I swam regularly until I graduated college. Last year when my lungs were giving me a horrible time and I was so short of breath that exercise felt impossible I joined water aerobics. I was the youngest there by 30 years and could hardly keep up. I kept at it and eventually "graduated" to laps on my own and thankfully am keeping it up. I find my lungs are healthiest when I swim.

    ReplyDelete
    Replies
    1. I was surprised how much of a work out it gave me, especially considering I was just goofing off and swimming around the pool. I actually never learned how to "swim"..., I'm looking into water aerobics. Plus my joints didn't hurt after, my arthritis makes other exercise tough. I think you're right swimming will be the perfect fit for me. :-) Glad it helped you so much and nice to know if I keep with it, I can look forward to some results. Thanks for sharing :-)

      Delete

Post a Comment

Popular posts from this blog

CF isn't all tears and saddness. Get a Full Picture.

  CF and Laughing Cystic Fibrosis can bring sad times and times of tears (like losing a close friend with CF, etc) BUT, it can bring so much joy and love. I've noticed most people love to talk about the people they meet while traveling. This is usually, because they have learned something from the person. Or the person is considered unique to them. I can do the same thanks to my Cystic Fibrosis. I may not have traveled much in my life thus far, but I have learned mountains of lessons from my CF. [Picture right:  Me ready for surgery in 2nd grade!] Forgive my shoutouts (but I must recognize a few amazing people) I have met some of the most amazing doctors: Chatrath, Dr. B Nurses: Sara & Marie (from Clinic), Lizzard, Melody (best IV stick ever), Deb, and Kris (you know a nurse is amazing if you love her after putting tubes down your nose!) Respitory Therapists: Jeannette, Lanell, and Don (you da Man) And Cookie Marrow (Musical Therapist- She would sing to me a...

Video Blog: Life in the hospital (as a child)

The daily life in the hospital! Most people cringe at the idea of a hospital. However, when I was little I never minded going into the hospital. I usually would have at least one other friend with Cystic Fibrosis to hang out with there (before we knew about the "CF Bugs"). I didn't love being sick, but I loved my CF friends that I would hang out with. Also the hospital, nurses, and my parent's tried to make it a "normal" environment. I got up and put on cute clothes, "walked to school", flirted with a couple CF boys, did homework, came "home" (back to my room), my friends would ask my parent if I could go play with them. We'd hang out in the play room or go on a walk with one of my parents! My dad loved taking me on walks and I LOVED going on our walks! Here is a video blog of the route we took and bit of information on what is was like growing up (for a chunks at a time) in the hospital! (it is posted via youtube, let is dow...

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 ...