Faith's Blended Diet and Other Things that Help with Her Digestion

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This page contains affiliate links and Faith's Mom may earn a commission if you use them. As an Amazon Associate, Faith's Mom earns from qualifying purchases.  Learn more.   Ever since Faith was born, she has struggled with her digestion. When she was in the NICU, she would spit up after eating even the tiniest amount of formula. Her dad and I were convinced her tummy was too small to handle large volumes of food. Sometimes when she ate, her heart rate would drop really low, which is why she needed to be in the NICU for longer. She just could not get the hang of eating and breathing at the same time!  Faith receiving food through an NG tube in the NICU.  Grandma giving Faith a bottle when she was 2 months old.  After finally bringing her home, eating continued to be an issue as she struggled with severe reflux and constipation. We tried various formulas, but she was never able to drink enough formula to gain a lot of weight. She also had trouble burping, and she...
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God's Little Reminders

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I remember very well the day in April of 2004 when we got the news that Faith had health issues that could lead to cerebral palsy. It was one of the most heartbreaking days of my life. I wondered how this smiley, happy little girl who would lie on her back and move her arms and legs around could possibly end up with CP?

Faith as a baby. 

When we returned home to Watford City after seeing Faith's pediatrician in Bismarck, there was one day where I opened up my Bible to Hebrews 11. For some reason, though, I skipped over to Chapter 12 and started reading it aloud to Faith. I couldn't believe my eyes when I came across verses 12 and 13.


Therefore, strengthen your feeble arms and weak knees. Make level paths for your feet, so that the lame may not be disabled, but rather healed. Hebrews 12:12-13

I was so excited, I said, "Faith did you hear that?" and I read it again. I really truly believed that the Lord had given me that verse at that particular time for a reason.

As time went on and we learned more about Faith's disability, I became disheartened. I wanted to believe the Lord could heal her, but I think I wanted Him to heal her more for my sake than for hers. I didn't want to go through life with a special needs child. I also thought it was so unfair for God to give me a special needs child when I myself had a congenital defect.

Through time, patience, prayer, emotional healing, perseverance and the Grace of God, I was able to accept my daughter's disability. My belief for her healing has waned at times but remains strong at others.

Sometimes when I'm going through a period of doubt, I start thinking about what it's going to be like years down the road. Faith is growing and while that is a good thing, I worry about the inevitable day when I'm not able to lift her. How am I going to get her in and out of bed or in and out of the bathtub especially when I have a 50-pound lifting restriction? What's it going to be like when she reaches puberty? Am I going to have to shave her legs and armpits for her?

Faith today. 

I believe we have seen God's healing work in her already and I know God can heal her completely. But I also know it is in His timing, not mine. So, when these thoughts start crossing my mind, the Lord reminds me of Jesus' words in Matthew.

Do not worry about tomorrow, for tomorrow will worry about itself. Each day has enough trouble of its own. Matthew 6:34

Not only do I have to remind myself of this, but also the fact that God has given me everything I have needed to get through the past six years, and I know He will give me everything I need to make it through the next six and all of the years following.

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