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

-
Image
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...
2 comments

Making Faith's Orthotics

-
This week Faith had two appointments. One of them consisted of getting her fitted for new orthotics, which by the way are also called AFOs or SMOs. The whole process took over an hour and Faith did great the whole time! She loved seeing her physical therapist again, whom she doesn't see on a regular basis anymore because she gets all of her PT at school. 

As the therapists worked hard to get the molding on her feet just right, they asked Faith what color of padding she wanted, what color she wanted for her straps, and if she wanted a picture on the back. Faith responded, "You can never have too many accessories!"

Jackie and another physical therapist work to get the molding just right for Faith's long, skinny feet.

The therapists have to repeatedly fit Faith's foot in the mold, make some adjustments and fit it again. They did this several times before finally getting it perfect.

Next, it's time for Tate from MedEquip to come and do his thing which is wrapping Faiths' leg in casting material to get the general shape of the orthotic.

Tate has to squeeze really hard to set the molding in place for Faith's foot.

It's important for Faith to be as relaxed as possible during the fitting but here she is uncomfortable because she's fighting hard against her tone.

Finally, the last step takes place as Tate cuts away the casting. He will then take the orthotics to his shop to finish putting them together.

The final product will be an orthotic with pink and purple padding, purple straps and a picture of a yellow butterfly on the back, all which Faith picked out herself. After Tate puts them together, it is a matter of seeing how they fit and then possibly making some adjustments so that they fit her as best they can. I will be sure to post a photo of what the final product looks like.

Comments

Post a Comment

Most Popular Posts

Guest Post: Who Needs Sympathy?

-
Image
Guest Post by Stephen Gallup Last week, a columnist for the local newspaper interviewed me in connection with a memoir I wrote that’s being published this year. It was a comfortable, low-key discussion in which he asked about the basic facts regarding my disabled son Joseph and what I’ve learned that might be of value to other families. It was the sort of dialog that required no special preparation in advance. I just sat down with him and talked about the subject closest to my heart. But looking back on it now, one thing bothers me. In concluding the interview, the reporter expressed heartfelt sympathy for everything I’ve endured. He was being more than polite. I mean, he laid the compassion on with a spatula. Startled, and already thinking ahead to what I had to do next that day, I just thanked him and said goodbye. But now that final note troubles me. I don’t want sympathy! First of all, from the point of view of a new author hoping to promote his book, sympathy...
Read more

Our Review of Wheel of Fortune: The New Era

-
Image
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.   Last year, when I heard the news that Pat Sajak was retiring from Wheel of Fortune , I knew I better prepare Faith. When season 41 began, I told her, "This is Pat's last season. Next year, there will be a new host."  Faith likes Vanna but loves Pat!  Faith and I have faithfully watched Wheel of Fortune every night since she was about 5 years old. It's how she learned that AEIOU were vowels. The show was also a great way to reinforce the rest of the alphabet. Counting was reinforced, too. When Vanna turned the letters, she counted how many T's, N's, or other letters there were.  She also learned some geography skills with the different trips they gave away. Upon winning a trip to Aruba, she would ask, "Where's that?" Sometimes I honestly didn't know and had to loo...
Read more

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

-
Image
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...
Read more

Cerebral Palsy Awareness Month: Reflecting On Our Journey So Far

-
Image
Did you know there are 1 million people in the United States who have cerebral palsy? I guess that means Faith truly is one in a million!  Faith was diagnosed with cerebral palsy when she was six months old. Prior to that, she had been given the diagnosis of Periventricular Leukomalacia  (PVL). During her premature birth, there was a lack of oxygen to her brain, which resulted in damage to the white matter, or inner part of her brain.  I will never forget receiving that news. Faith's Dad and I were told that nobody knew what the long-term effects of PVL would look like for her. All I could do was stare at my tiny daughter lying in her isolette, hooked up to all kinds of tubes and lines, and choose to believe she would be okay.  Faith in the NICU a few days after she was born. After over 70 days in the NICU, we finally took her home to Watford City. There, she would receive regular visits from an Early Intervention team who would assess her and ensure that she met al...
Read more