Skip to main content

Little Over a 1 Year of Marriage!

Thank you to my Husband:

 As of August 16, 2016 Andrew and I have been married for a year! (click here to read our 2 wedding blog posts) It is hard to believe a year went by already. It was an exciting year, that's for sure! Andrew got a promotion with the company he works for and we moved the week of our wedding for the new opportunity. Even though it added a bit of stress to our wedding week, we didn't mind because we knew it would be worth it! We got to move to the same town my sister lives in and a big bonus factor is my Cystic Fibrosis Center is in Peoria too! After moving to Peoria, I decided to finally become licensed as a Real Estate Broker. The career choice wasn't new, I had always wanted it. I just couldn't be a Real Estate Broker, because I needed health benefits. Both our careers are going really well  and we decided to buy a house this June!

So it has been an exciting year thanks to all the milestones we have achieved.  I just wanted to take this time to thank everyone for encouraging us and always being there for us!


This past year I have really been focused on my health with the future goal being us becoming a family somehow. I've been a lot more active this year. I have done 4 5Ks since July 2nd and I'm going to try and keep it up. Exercise, never skipping meds, eating more then I need in calories....That's my goal to continue. Obviously, all this hard work is paying off. Granted my life is a little hectic and my arthritis is a bit worse (which is why I believed I was lower in lung function). BUT, it is sooo worth it! I was 49% in lung function in May and now I'm around 58%

At my last clinic I misread my lung function numbers and thought I hadn't increased. They said I went up a bit, and with the doctor talking about how my lungs might not react well to the anesthesia, when I glanced at the numbers I just assumed the 49% was my lung function. But that was from the time before. Dropping to the 40s in lung function was scary. I'm so glad to know I'm back to where I usually am :-) I thought I felt healthier, so I freaked when I didn't think it went up. WHEW!

We can finally start focusing on becoming a family. We are meeting with FosterCare, Adoption and a Surrogacy Center this Fall to start looking into our options! I never thought I'd have a family of my own some day, but with Andrew it all seems possible!

Happy 1 year to my Super-Man of a Husband, Andrew! I can't wait to see what year two will bring us! Whatever it brings I know I can look forward to it with you, Andrew!
Labels:

Comments

Post a Comment

Popular posts from this blog

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 ...
6 comments
Read more

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...
Post a Comment
Read more

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...
2 comments
Read more