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

Faith the Soccer Star

-
Faith was so excited last weekend when I told her they were having wheelchair soccer again. Her first question was, "Can Adam push me again?" 

I told her I had no idea if he even went to school at the University of Mary anymore. When we got out there, she was disappointed to learn he had another obligation that day. Everyone assured us Adam would be there the next time. She still had fun with a few other guys from the college soccer team who pushed her around to help her play.

In wheelchair soccer, they don't actually use a soccer ball, instead it's more like a beach ball. Normally, the soccer players who push the kids around throw the ball to each other and then help the kid they are pushing hold onto it as they try to get into the net. She had so much fun and the faster they pushed her, the bigger the smile on her face.

Ramsey helps Faith with the ball

Faith making friends
Faith having fun with Garrett the goalie

This weekend, despite the fact she was suffering with a terrible cold and hadn't gotten a lot of sleep, she still wanted to play. She was thrilled to be reunited with Adam, who I found out was a junior in college and had come to Bismarck all the way from Ireland.

Although the organization, Dreams in Motion, has other adaptive sports throughout the year for those in wheelchairs and other mobility challenges, I can't convince Faith to try them. (Although, she did try curling once.) They also have basketball, tennis, skiing, sled hockey and dance. 

Soccer is her favorite but unfortunately, they only have it a couple of Saturdays a year, although they might try to get an outdoor game going in the Spring. We also told Adam we would love to see him play when his soccer season starts at school in late summer.

Faith taking a break
Faith and her all-time favorite soccer player
Everyone's a winner!

Dreams in Motion is a great organization for planning these events. I was also impressed with the dedication of the soccer players from the University of Mary who took time out of their Saturdays to help out and spend time with the kids. You can click on the video below to see everyone in action!



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