This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like.
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Caring for Cole | caringforcole.blogspot.com Reviews
https://caringforcole.blogspot.com
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like.
caringforcole.blogspot.com
July 2009 ~ Caring for Cole
http://caringforcole.blogspot.com/2009_07_01_archive.html
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like. Thursday, July 30, 2009. Special Friends at Special Care. I have mentioned before how much Cole loves being at Special Care School and we love the services they provide. While Cole is at school they work with him and he is seen by his team of therapists. They are truly amazing! Costa, a 2-year-old blac...
Special Friends at Special Care ~ Caring for Cole
http://caringforcole.blogspot.com/2009/07/special-friends-at-special-care.html
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like. Thursday, July 30, 2009. Special Friends at Special Care. I have mentioned before how much Cole loves being at Special Care School and we love the services they provide. While Cole is at school they work with him and he is seen by his team of therapists. They are truly amazing! Costa, a 2-year-old blac...
5 Little Monkeys Jumping on a Bed ~ Caring for Cole
http://caringforcole.blogspot.com/2009/08/5-little-monkeys-jumping-on-bed.html
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like. Sunday, August 23, 2009. 5 Little Monkeys Jumping on a Bed. Cole is now 2 1/2 years old and he still can not talk. I love this video of him playing the “5 Little Monkey’s Jumping on a Bed” game on the Dynavox. You can see he is so excited and he wants to interact with it. He is squealing in delight.
August 2009 ~ Caring for Cole
http://caringforcole.blogspot.com/2009_08_01_archive.html
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like. Sunday, August 23, 2009. 5 Little Monkeys Jumping on a Bed. Cole is now 2 1/2 years old and he still can not talk. I love this video of him playing the “5 Little Monkey’s Jumping on a Bed” game on the Dynavox. You can see he is so excited and he wants to interact with it. He is squealing in delight.
March 2009 ~ Caring for Cole
http://caringforcole.blogspot.com/2009_03_01_archive.html
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like. Monday, March 30, 2009. Today is the last day of CEREBRAL PALSY AWARENESS MONTH. I wish I had all the answers to the many questions about cerebral palsy. I still have SO much to learn. Not only about CP but what I can do (or have Cole do) to improve his quality of life. Well, this all changed when I bu...
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Lieck Triplets: The Good Mommy
http://lieck3.blogspot.com/2013/12/a-really-good-mommy.html
Monday, December 2, 2013. Overhead last night at our house. Hello, yes, I'm calling about my daughter. I would like her to not use her walker and wheelchair as much as she has been. She is doing really well with her walking and I'm so proud of her.". Yes she can use her pink canes but her walking is getting so much better and I would like her to walk on her own as much as possible.". The talking begins again but I'm lost in the first part of the conversation. The one that needs her the most. I am a mothe...
Lieck Triplets: Just Another Dream
http://lieck3.blogspot.com/2013/05/just-another-dream.html
Wednesday, May 22, 2013. I'm a dreamer. Literally. I dream very vividly. Sometimes there are nightmares but most often just puzzling events that stay with me much of the day. I had such a dream last night. In this dream I was back in my twenties, unmarried and no kids, but there was Grace. Everywhere I went I was trying to bring her along.make her comfortable in whatever situation we were in. How was she there? Will she always be there? What does this mean? For if you can dream it, it can be done. I neve...
Lieck Triplets: Seven
http://lieck3.blogspot.com/2013/04/seven.html
Friday, April 26, 2013. Seven I've always liked the number 7. What's not to like? You have.Seven Wonders of the World, Seven Brides for Seven Brothers, The Seventh Day of Creation, Seven Jeans, Seven Layer Dip, and my birthday's on the 7th. Seven was the magic number. (I guess there are the 7 deadly sins but that's another post.). Be strong and take heart, all you who Hope in the Lord. Psalm 31:24. And one day our kids will soar on eagles wings. Blessings to your family. April 28, 2013 at 9:38 AM.
Lieck Triplets: April 2013
http://lieck3.blogspot.com/2013_04_01_archive.html
Friday, April 26, 2013. Seven I've always liked the number 7. What's not to like? You have.Seven Wonders of the World, Seven Brides for Seven Brothers, The Seventh Day of Creation, Seven Jeans, Seven Layer Dip, and my birthday's on the 7th. Seven was the magic number. (I guess there are the 7 deadly sins but that's another post.). Be strong and take heart, all you who Hope in the Lord. Psalm 31:24. Sunday, April 21, 2013. Remember to Be Thankful. Subscribe to: Posts (Atom). Barely Sane Mother of Triplets.
Lieck Triplets: May 2013
http://lieck3.blogspot.com/2013_05_01_archive.html
Friday, May 24, 2013. Stop Complaining and Just Keep Trying. Grace begins an intensive therapy session next week. It's 3 hours a day, every day for 3 weeks. It is one of the best things she does to get stronger. However, it's not always easy on our family. We drive back and forth to Dallas every day. I have to juggle our schedule.make provisions for Mack and Sophia. Grace is tired and grumpy. I am tired and grumpy. Wednesday, May 22, 2013. Will she always be there? What does this mean? Recently I was hav...
Lieck Triplets: What Might Have Been
http://lieck3.blogspot.com/2012/10/what-might-have-been.html
Wednesday, October 3, 2012. What Might Have Been. There is a song by Little Texas from the 90's that keeps popping in my head lately. The title of the song is What Might Have Been. If you listen closely to the words, they don't really apply to my situation but I often think of what might have been. So why the questioning lately? What if we didn't have to spend so much time and money on therapies and equipment? What if our lives were typical? There are no words. October 3, 2012 at 9:32 AM. Im so proud of ...
I am fearfully and wonderfully made: Those motility issues
http://braydenandmommy.blogspot.com/2015/04/those-motility-issues.html
Thursday, April 23, 2015. Brayden has not had a bowel movement on his own for over 9 months. It requires a lot of help on our part for him to actually go. We talked with Brayden's GI doctor. Brayden's GI system has gone through a lot in eight years. Scopes, testing, studies, g-tube, g-j tube, j-tube, suctioning, draining, medications. I hope to put together a summary of Brayden's GI history to send to the motility clinic in DC before we meet with them. We will see what the clinic at Children's National i...
I am fearfully and wonderfully made: Bone Clinic
http://braydenandmommy.blogspot.com/2015/03/bone-clinic.html
Tuesday, March 17, 2015. A warning for today (on St Patrick's Day):. A day of bone scans and x-rays, then meeting with a team of doctors. The bone team also wants his legs more active; have more impact to help with bone health and growth and help his hips (which always seem to be teetering on the edge of having problems as he grows). He does a stander at school. But the bone team want him to do more. They want us to work towards this: http:/ www.fireflyfriends.com/upsee. April 20, 2015 at 10:45 PM. G-J t...
I am fearfully and wonderfully made: The Unexpected Gift
http://braydenandmommy.blogspot.com/2009/12/unexpected-gift.html
Thursday, December 24, 2009. Let me tell you about one of the most memorable Christmas presents I ever received (my parents will remember this one and get a good laugh out of it). I was in high school. Just like many of us (if you are truthful), I survey the gifts under the tree days before Christmas. As an experienced gift looker, I kind of knew what was clothes or certain things that I asked for that year. Of course I went for the brick.dying to know what was inside. I tore in to that gift. As I was si...
I am fearfully and wonderfully made: The Birthday Boy
http://braydenandmommy.blogspot.com/2015/04/the-birthday-boy.html
Friday, April 17, 2015. He had to go to school on his birthday, much to his dismay. In protest he would not open his eyes or even acknowledge me. After school he did get some good cuddles from daddy and licks of an ice cream cake. Subscribe to: Post Comments (Atom). Follow us on Facebook. Follow Jenkins Enterprises on Facebook. Jenkins Enterprises, LLC. At the White House. Click here to see the photos. Brayden's White House Christmas 2014. To understand a little more about Brayden Jenkins. Special Needs ...
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Caring for Cole
This blog is for family and friends to stay updated on the progress of my third child that has cerebral palsy and hopefully it will inform others about what the life of a child with cerebral palsy is like. Monday, February 28, 2011. All images ©2011 Bobby Acree. Have you come to visit Cole? Well, come on over to his new home. We would love to have you visit with us all! Cole's new address is over at http:/ leannakeathley.com/category/caring-for-cole/. We hope to see you soon.and often! TEFRA, a Medicaid ...
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