Skip to main content

About Us


👩🏻‍💻The Mama:  Cheriz, is a foster parent with Cystic Fibrosis, with passion for (freelance)blogging & social media and works for Health Union Inc. she is a consultant for Norwex and Tastefully Simple! She loves Real Estate, Design & Decorating, Home Remodel projects. In her free time she loves cleaning, cooking, and spends lots of time fundraising and volunteering for the Cystic Fibrosis Foundation.

👨🏻‍🍳 The Dadda: Foster Dad, cook, avid book reader. Andrew, works as Meat & Seafood Department Market Manager for Hy-Vee. In his spare time he likes to cook (culinary school degree) and enjoys playing guitar and singing. 

❤️Our love story: The two met while dancing and singing in a local theatre group and got married a few years later. They have been fostering kiddos for 3+ years

📖 Our Blog: Is a way to share our lives with you! Open the doors to our homes and show what our life is like fostering with CF, including our hobbies, passion, and work! 



Comments

  1. CherizOctober 23, 2013 at 3:07 PM

    That would be awesome. But.... It's a lil expensive... So not sure, but I will go at some point in my life..that is not negotiable. lol! Do you live there?

    ReplyDelete
  2. UnknownMarch 1, 2015 at 11:50 AM

    Cheriz, you are truly beautiful and strong, hopeful and mightily encouraging. Thank you for following me on twitter@AbundantBreath. You inspired and encouraged me greatly. I forwarded the link to your website and a brief summary of your story to my older son, who is going through a CF related mentally tough time lately.
    Michelle
    thecfofcf@blogspot.com

    ReplyDelete
    Replies
    1. CherizMarch 1, 2015 at 9:51 PM

      Thank you Michelle, that's so nice of you to say. We all do have days where we wish we had it a little easier, but most of the time I'm just thankful. I'm glad we connected on Twitter. I'm gonna jump over to your blog in a minute :-) Thanks for reading my history, hope my blog provides a lil comfort for him. Sorry he's going through a rough time. Keep in touch! and you both take care :-)

      Delete
  3. AnonymousOctober 25, 2015 at 4:12 AM

    Love your blog Cheriz, good job!! I would love for you to share your blog link with our CF community on www.genefo.com- I'm sure you'll find some fans there who need inspirational messages like yours....

    P.S. As for 'Travel to Europe' in your bucket list- If you need a place to crash, I'm in Paris! :))

    ReplyDelete
    Replies
    1. CherizOctober 30, 2015 at 10:08 AM

      Hi,
      I'd love to share it, that's what it is here for :-) It looks like a great site with lots of resources. Love your tip about heels! I'm signed up. And yeah I'd love to travel overseas, but its pretty pricey. One day I will though. Thanks for the info about the site!

      Delete

Post a Comment

Popular posts from this blog

First blog: Hello

My first Blog: A little About Me I'm not sure why I have decided to start a blog, however, here I am.  I have honestly thought about writing about my life for years, but have always chickened out. I have finally decided to share the experiences life has thrown at me. The biggest reason I have been asked to blog by people is because of everything I have dealt with medically. I have Cystic Fibrosis and a few other medical problems...This is probably the best reason why I should blog. I can relate to others who are dealing with medical problems, however,my CF is also why I did not want to write this blog. CF can be embarssing and annoying sometimes... but it  has helped define who I have become to be as a person. Therefore, (yes, even though I want it cured) I don't hate having CF. Let me start off with some basic info and statements. I'm 26 yrs old and have dealt with CF all my life. In this blog you will hear recent stories (good, bad, embarassing); a...
Read more

Holding Down the Fort

My husband, Andrew, is currently at Wartburg Theological Seminary and is starting his first week of his second year there. Every year he lives on campus for one week. He enjoys starting each semester on campus where he can build friendships with other students and professors. It's the only time he is on campus. Usually he does long-distance learning, online, from home. It was the only way we could manage him doing a four year Master degree program while working. This week is the hardest for us. However, we have something on Thursday and Friday this week, so Andrew will only be gone 3 days instead of the typical full five. So that will make this week a bit easier than the other semesters. It's hard for Andrew to be away, although I know he is having a blast. We send random pictures back and forth like a book he may be reading or a game I may be playing with our kiddo. It is hard for the kid(s) to not see Andrew every day. We are foster parents and stability is a BIG issue for ...
2 comments
Read more

Close to a Cure?!?!?! and Thank You!!!!!!!!

Help Us Find A Cure & Thank you! Lots of new meds and treatments are being researched thanks to the CF Foundation and the people who support it! Thank you soooo much everyone for supporting me and the CF GreatStrides Walks! I hope you enjoy hearing about the cool new ways steps are being taken towards finding a cure for CF and how everyone has helped me and us (the cf community)! New Treatments And Break Throughs: As you may know, from reading my last couple blogs. Some exciting news was released!  VX-809 + Kayldeco Phase 3 (6 month clinical trials) has started! Which means if all goes well, this could be on the market in the next year or two. This drug helps target the actual faulty gene. It will help improve our lung function (hopefully gain some back, the part that isn't damaged) and will help us to slow the decline of our lungs health tremendously! This is the treatment for my mutations!To read more about this new treatment click Here! Also, there are other medic...
Post a Comment
Read more