Skip to main content

Wedding Storytime

My twin sister got married Saturday, June 18, 2016. What. A. Day. Katie truly deserved the best day ever, and I believe she got that! You see, when you have a twin sister with a chronic disease, you have to grow up pretty fast.  I know that even though I'm the one with the disease, growing up wasn't easy on her, either. I got lots of extra attention she didn't get (not good attention, but still attention). I needed her to be strong many times, even when it was hard. And I counted on her to help me stay healthy, help me catch up on school work, and sometimes miss out on fun stuff to be with me. Katie is the most supportive, most protective, most caring sister I know. There was never a time she refused to step up and be there for me. My sister is truly incredible, and I'm so glad we could make her day so special.

I was feeling pretty good during the whole rehearsal and getting ready the next day. However, the second I walked into the chapel heading down the aisle before Katie's grand entrance, I started bawling. I mean, big, fat, ugly tears. I completely and totally lost it. Part of the reason is because Katie's now husband was at the front, crying and looking so happy. Another huge reason is because I saw the faces of the 200 people in the chapel, many of whom I knew, gazing back at me with the biggest smiles on their faces and the proudest looks. These are people I knew from my parents, from our growing up days, or through Katie's college experience. Through every stage of life, these people had been there for different bits and pieces of it (and some for every step of the way!), and they had helped shape the woman Katie is now. Regardless of how I knew them, all of the guests were there for Katie and Brice, and they were so wonderfully happy and proud of the couple. It's an indescribable feeling to be surrounded by so many loved ones, cheering a couple along and celebrating a new commitment. I was flooded by this emotion and the realization that Katie was no longer going to be just my twin sister, she was about to be a wife as well. I was overcome by emotion, and tears flooded down my face. Pretty soon the rest of the bridal party was crying, as were many people in the audience (sorry to start the tears, guys!). I'm sure once we get the pictures back from the photographer, he'll have some good evidence of the ugly cry going on.

The rest of the wedding was beautiful, and I managed to hold it together somewhat. The reception was fun, as well! Such great food, yummy cake, and awesome dancing (I posted my written copy of my MOH toast in the previous blog--have a read if you want :)). It was so fun to be with friends and family celebrating such a lovely couple!! Katie and Brice are now on their honeymoon. I can't wait for them to get back because I am already missing them! Congratulations to my wonderful sister and new brother-in-law! So much love for the happy couple.

Comments

Popular posts from this blog

CF Letter 2020

Dear friends and family, It's May 2020, which means it is another CF Awareness month and another time to talk about all the amazing things happening in the CF world! This has been a very good year in the CF community. In October of 2019, Trikafta was approved by the FDA for all people with CF with at least one copy of the dF508 mutation. 90% of people with CF have at least one copy of this specific mutation. This is a HUGE deal in the CF community because it is one of a handful of drugs that addresses the underlying cause of CF and the only drug that such a huge percentage of people with CF can take. Trikafta is a total game-changer for so many, including me. I have gained stability, I require fewer IV antibiotics, I gained lung function I thought was long gone, and I feel like I can plan things in my life again. The hard work of the CF Foundation, willing researchers who continue to search for a cure and medicines that will increase quality of life, and the generous donations fr

CF Letter 2019

Dear friends and family, I hope you all are having a happy and healthy 2019! The Great Strides CF Walk is just around the corner, and we are gearing up for a great walk day! Since my last CF Walk letter, my health has had its ups and downs. Just before the CF walk last year, I got the sickest I have been in awhile and had to fight off pneumonia with the help of 4 weeks of IVs. I also had to do IV antibiotics in August and November. However, I have stayed relatively healthy in 2019, and for that, I am extremely grateful! Although I’ve had to fight off 2 colds, my body has been able to get through it without needing IV antibiotics. While I know I will need another round of IVs eventually, I am thoroughly enjoying being IV free. I credit this to the amazing CF therapies available to me, my compliance to my treatments, and all of your prayers for my health. I continue to take 30+ pills a day including enzymes to digest my food, vitamins and supplements that my body cannot absorb

The spirit of giving

It’s the end of 2017. That means it’s time to send in those end of year donations. Want to give to some amazing charities actually doing good in the world? I’ve compiled a list for you!  The Cystic Fibrosis Foundation- Obviously, I’m biased toward CFF. They fund amazing research that is saving people’s lives! Don’t you want to be part of that? Not only that, but 90 cents of every dollar goes directly to advocacy and CF research. If you donate to the Cystic Fibrosis Foundation, you know your money is going to be spent wisely and is going to make a difference. Since cystic fibrosis is an orphan disease (that means it’s really, really rare), people with CF rely on your donations to fund research. As well, Congress just cut the orphan drug tax credit, meaning companies are not going to get as much incentive for studying orphan diseases and creating drugs to treat them. The CF Foundation needs people like you to donate to CF research so we can find a cure for CF SOON. —www.cff.org