Skip to main content

Happy Anniversary

Twenty-five years ago today, my parents stood before God and 400 of their closest family and friends, pledging their love for and commitment to each other always and forever. I am beyond blessed to have these two as my parents. As society has changed and become much more self-centered, my parents have continued to focus on their marriage, their family, and their God. They care for each other immensely and are such a testament to God's design for marriage. They take the vows they made August 15 seriously, no matter what.

My parents' example of love is amazing in and of itself. But they have had an awful lot of challenges in the past twenty-five years--the biggest burden of which is my CF. Most people don't realize what a strain a chronically ill child is on a family, and even more so on a marriage. Many people with this extra issue end up with a broken marriage due to the excessive stress caused by the illness. Being the parent of a chronically ill child is draining-financially, emotionally, and spiritually. You don't know how you're going to live from paycheck to paycheck with all the medical expenses. You are exhausted beyond belief from trying to stay strong and provide emotional support for the family. You start asking God why or even trying to solve the crisis on your own. Yes, dealing with a chronic illness can certainly break a marriage. Yet my parents refused to give CF that satisfaction. They rely on the Lord to get them through the challenges and trust in each other for life.

I am so grateful for my parents' twenty-five years of wonderful marriage. Yes, there have been challenges. There have been fights and disputes. They are both imperfect people. But God united them as one, creating a cord of three strands that will withstand it all. Happy anniversary, Mom and Dad! I love you both so much. Here's to the rest of y'all's life together!

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