Skip to main content

Cystic Fibrosis= a lot of recycling


CF and Recycling:

I never realized how much I recycled until I moved to a town where I don't receive curb-side pick up. Instead we fill up our trunks and drive it 20 mins to a neighboring town's recycling center. Also, my pharmacy is in this town, just a few blocks away.  It's meant to be....

I've always recycled a lot and have been earth friendly. I have convinced quite a few others into being "recyclers" too. Most of my college roommates and friends learned early on it was easier to break down the  boxes, rinse out the cans, and recycle, rather than here my 20 minute "soapbox" talks every time I found a recyclable product in the trash. Just ask them...lol

So I've heard people discuss the fact my recycling container in the kitchen is your average 13 gallon can, whereas my trash in the kitchen is small (like a bathroom or an "under the desk" size can) is beyond weird looking. They may look funny next to each other. But the truth is in my picture below:

A couple days worth of recycling on the left opposed to my trash on the right.



How could I have that much recycling?

Easy. I have to eat an enormous amount everyday. I empty multiple pill containers a week, I use 4 cans of feeding at night. That is around 30 cans a week. The wrapping/ packaging my meds and equipment comes in. Plus, the typical food boxes, cans, plastic. 

How could I not recycle? 

I really hope other CFers think about this too! It can make a difference. Its not that hard to rinse out the cans. At first I hung a big poster in front of the recycling can with pictures and lists of what can be recycled. My roommates soon were recycling without even thinking about it and I know that even after I moved away they continued.  So if you don't. I challenge you to a month of trying. After one month I think you will be used to it and it won't seem so weird. 

I can't wait until I have my own home and yard! Then I can compost, garden, etc :-)


Not sure where to take your recycling? Don't have recycling in your town. Think you can't find one? click HERE to find your nearest recycling center!

If you have to travel far (I know some small towns around my hometown have to drive over 20 mins). Get  more people in the community involved, go to a city "board" meeting. Or even just ask your neighbors and friends. Take turns driving it there :-) 

I definetly think my CF has helped my roommates, family, and friends realize how much we really do recycle!


  

Comments

  1. Aaah spot on!! Since I started with tube feeding, 2 months ago, I've got so. much. stuff to throw out! Here in the Netherlands most people recycle paper and glass, but thats it. Where I live now there is a big container for plastic as well, next to the supermarket where I do my groceries so it's perfect! My boyfriend used to make fun of me being so into recycling, hehe, but once he saw the amount of waist that I have now, every day, I think he gets it! He certainly does it a lot more himself now too ^^

    Saw the link to your blog on the cf page on facebook. It's great, I like your attitude and recognize a lot, next to the recycling ;) Take care and kick ass with your next clinic visit! Hopefully those lungs are acting a bit nicer again by then.

    xSarah

    ReplyDelete
    Replies
    1. Thanks Sarah! Glad you found the blog. I've been made fun of for recycling too. But eh, that's okay. And my follow up clinic is in one month. (fingers crossed) Once I get settled with jobs/school- it should be okay. you on the FB group or CysticLife?

      Delete
  2. Kudos to you for being earth friendly, Cheriz! If only each and everyone of us is practicing the process of recycling, our environment will surely be preserved. I really admire people like you who are concerned and aware about our surroundings. In any way, just continue doing that project and never stop encouraging people to do the same. I hope you are faring better now. Thanks for sharing that! Kudos and all the best to you!

    Clarence Rios @ Bins By Jo Ltd.

    ReplyDelete
    Replies
    1. Thanks, and I totally agree with you. It's so important!

      Delete

Post a Comment

Popular posts from this blog

Today's BIG Appointment

 I discussed last week about my recent struggles & goals. I have been dealing with a lot all at once! Family planning (update on that in 2 weeks), my Grandma's funeral, lower lung function. Through it all I have remained very compliant with my meds! My health is VERY important to me. So this last weekend I took my vest machine, wabi sterilizer system , and packs of ensure to my parent's for the weekend. I wanted to make sure I did everything. While it was a sad occasion, it was still pleasant seeing almost all of the family together again. Actually 27 out of 29 of the cousins made it to the funeral. Grandpa is in the middle of the picture (can you find me?) LOL   On top of my medications I have been doing some dancing & walking, but no jogging or anything. I'm still counting calories on my fitbit (hitting over 3000) a day (& 40 grams of protein, 50 grams of fat at least). I knew I was feeling a bit better than before, but wasn't sure what to expec

Post- Surgery Appointment

Post Surgery Appt: As you prolly know, I had Laparoscopic Triple Hernia Surgery last Tuesday. Here was a picture of me devouring a piece of bread so I could go home afterward the surgery (4 hours post surgery and 20 mins post waking up from recovery). I was ready to go home! Today I had my post surgery check up. He said everything in the surgery went well and besides the finding the 3rd hernia there were no surprises. He pointed out where the staples/stitches (they are holding the mesh in place) are in me. I have two on each side at the end of the mesh (so 4 on top) and two down farther in my groin. Apparently, I just have one huge piece of mesh that runs the width and length of my whole abdomen/groin area. Bahaha. I am Inspector Gadget after all. He said a few more weeks before I can lift stuff or exercise. Also, he said the area where the staples are will hurt when bending or twisting. However, I only notice really when I twist or turn too fast. Overall, it was a nice appointment

Theatre and Life...how to fit in CF?

Fitting CF into my life: Cystic Fibrosis won't be hard to fit into my schedule right now. As I just finished my job watching my babysitting kids for the year. I'm currently job hunting and taking classes on Mondays at the local community college (as a pre-req for Grad programs/and for fun). Mulan Jr, just ended today. We had two shows. Back-to-back performances are harder, since I had a busy day before the shows, I didn't get a chance to do my meds before the shows. Therefore, I end up bringing my therapy machine along.  Yep, sitting in the light booth and doing my meds, while watching people take their seats. [Note: I turned my therapy machine off when the house lights had to go out.] Its not that hard to fit them in. You just have to be willing to do them sometimes in unexpected places and be willing to have others find out about it. I had two people in the light booth with me, neither knew I had Cystic Fibrosis, but neither were bothered by the nebs. So bottom line