Our very first Buddy Walk! I really hope we make a yearly habit of doing this fundraiser. It was neat seeing all of these people come together to raise money for Down syndrome awareness, acceptance & inclusion. Our team raised $845.00! Thank you Paul & Sylvia, Dad & Margaret, Mom & Tim, Debra, and Rebekah for all of your donations. You guys totally ROCKED IT OUT!
Although it was a teensy bit chilly outside, we had a ton-o-fun. Melanie played all sorts of games and won prizes. We wondered around checking out all the venders. We even saw a few friendly, familiar faces from a previous Down syndrome function. That's what I enjoyed most, being able to connect with people. You guys helped us raise enough money to have a poster of Sean set out on the Buddy Walk grounds. When I first spied it I got very emotional & teary eyed. Sometimes I just can't believe God has entrusted me with loving, nurturing, guiding & raising this super sweet baby boy. He Blessed me (us)
with a Down syndrome child. I am for certain, the lucky one. Thank you Lord. I am beyond grateful. (even when he wants to be awake at 3AM!) LOL!
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This BLOG is a window into our life for our family & friends that can't always be with us to see our ever changing world.
Tuesday, October 21, 2014
Monday, October 20, 2014
Super Sweet Down Syndrome Video
Thursday, October 16, 2014
Tuesday, October 14, 2014
Monday, October 13, 2014
Down Syndrome: Hypotonia and Physical Therapy
Quotes from the book Gross Motor Skills for Children with Down Syndrome
Patricia C. Winters, PT
- Hypotonia: "Not a decrease of muscle strength, but a decrease in resistance or stiffness of muscles in resting tension or relaxed state."
- "The degree of hypotonia can be mild, moderate, or severe. It can vary from one area of the body to another, and from the right side to the left. Hypotonia in the arms makes it harder to learn to combat crawl. Hypotonia in the abdomen makes it harder to move onto hands and knees and creep. Muscle tone will improve over time. When your child is school age you will only see subtle remnants of it."
- The goal of physical therapy: "The goal of physical therapy is not to have children with Down achieve gross motor skills more quickly. The goal is to have (your) my child achieve maximum physical potential and to build a body that is fit and functional throughout life and minimize compensations."
Bumbo Seat For Children With Down Syndrome
The Bumbo Seat is very controversial. Most people either love it, or hate it. Regular ole moms, OT's and PT's alike, can't decide if it's the greatest thing since sliced bread or detrimental to a babies well being. Although the leg openings could be a little wider to accommodate those babies on the husky side, the ability of the seat to assist Sean in sitting up and being involved in our world a little easier vastly outweighs that minuet discrepancy. So, as of right now, I'm leaning towards lovin' it! Just look at the alignment of his body now compared to the previous post. He has the ability to use his hands to reach for toys all while using his core. At first he was a little wobbly, but never falling over like I've seen others doing in videos. I think he is at the right age and was ready to start making this transition. We have been using other methods for sitting him up to slowly build up his stomach and back muscles so this is a good time to introduce the Bumbo Seat. About 10/15 minutes every hour or two throughout the day and he's good. I'm sure he'll be sitting up before we know it!
And by the way, I would never actually advocate a container for a baby because babies will learn to sit up no matter what. But in Sean's case we definitely thought he could benefit from it. :-)
And by the way, I would never actually advocate a container for a baby because babies will learn to sit up no matter what. But in Sean's case we definitely thought he could benefit from it. :-)
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