Skip to main content

About Us


πŸ‘©πŸ»‍πŸ’»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.

πŸ‘¨πŸ»‍🍳 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

πŸ“– 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. 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. 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. 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. 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. 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

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...