rkjenscoliosis.blogspot.com
Our Journey through Progressive Infantile Scoliosis: March 2013
http://rkjenscoliosis.blogspot.com/2013_03_01_archive.html
Our Journey through Progressive Infantile Scoliosis. This blog is to chronicle our scoliosis journey with our son. Monday, March 11, 2013. EMG at PCMC on Feb 25, 2013. Since Scott went with Russell to do his EMG, I don't know as many details as I normally do. This is so totally fine with me. I am so grateful that he went with Russell, so I got to skip alot of the stress of that day simply by not being present. Thursday, March 7, 2013. Details of Russell's fourth cast on Feb 21, 2013. He’s supposed ...
sticksandrocks.blogspot.com
Sticks and Rocks: The Rigo-Cheneau System Brace, and The Short Version of Treatments Til Now
http://sticksandrocks.blogspot.com/2010/03/the-rigo-cheneau-system-brace-and-short.html
Monday, March 29, 2010. The Rigo-Cheneau System Brace, and The Short Version of Treatments Til Now. Apparently, I needed a little time to live with the new brace before posting about it. We got home with it a little over two weeks ago. So here's a little sum-up of his scoliosis treatments to date, to give you the picture of our journey thus far. So we stayed the course with the Providence brace until we learned it was not holding him. We were scheduled to go get this brace made last month, but Snowmagedd...
lifeheartandsong.blogspot.com
I LOVE MY LIFE: FREEDOM!!
http://lifeheartandsong.blogspot.com/2009/08/freedom.html
I LOVE MY LIFE. Thursday, August 6, 2009. For the past nine months, our little girl has had on, what she calls her " armor. To correct her Progressive Infantile Scoliosis. On November 14, 2008 Will walked her down the hall as we prepared to get her armor on. . . . Nine months later on July 30, 2009, after 4 cast and alot of prayer, he walks her down the hall in preparation for FREEDOM! We believe it's completed! What the caterpillar calls the end of the world, the Master calls a butterfly. ". I do, I lov...
fancastickids.com
Noel Industries
http://www.fancastickids.com/fancasticfriends.html
Middot; Fancastic Friends. Perfect pals for kids in casts! Each animal is hand casted using real casting materials and techniques including:. Moleskin petaling on the cutout edges. All animals will have a white, plain plaster of paris edf cast unless a decoration option is specified. Animals can be decorated for a boy or girl for only $5.00 more. 200 from each Fancastic Friend sold will be donated to the Infantile Scoliosis Outreach Program. Is your hospital in need of an EDF casting frame?
infantilescoliosis-diary.blogspot.com
Infantile Scoliosis - J's diary: February 2012
http://infantilescoliosis-diary.blogspot.com/2012_02_01_archive.html
Infantile Scoliosis - J's diary. Diary of my son's treatment for infantile scoliosis. Wednesday, 29 February 2012. J asked for a purple cast yesterday! Yes - you read that right - he. He can say 'purple' and knows the corresponding colour! He also pointed at the earrings of one of the keyworkers at the nursery today and said "purple" (which they were). Tuesday, 28 February 2012. Cole and the Crooked Flower. Http:/ shop.earthycrunchymama.com/products/cole-the-crooked-flower. From the back cover:. The Infa...
infantilescoliosis-diary.blogspot.com
Infantile Scoliosis - J's diary: October 2014
http://infantilescoliosis-diary.blogspot.com/2014_10_01_archive.html
Infantile Scoliosis - J's diary. Diary of my son's treatment for infantile scoliosis. Wednesday, 1 October 2014. How to contact C.A.S.T. I've been asked how to contact the C.A.S.T group. They used to have a Yahoo group, but have now switched mainly to Facebook. If you go to the infantile scoliosis website http:/ www.infantilescoliosis.org/. There is a facebook link on their homepage to "join" them. Best wishes to you and your family. Subscribe to: Posts (Atom). How to contact C.A.S.T.
theinfantilescoliosischronicles.blogspot.com
The Infantile Scoliosis Chronicles: "Brace" yourselves ;-)
http://theinfantilescoliosischronicles.blogspot.com/2013/07/brace-yourselves.html
Chronicling the experiences we are going through as a family with a child diagnosed with infantile scoliosis. Thursday, July 4, 2013. Brace" yourselves ;-). Greetings and a Reminder:. I write this blog as we go through ET Mehta Casting with our daughter Olivia. The blog is intended to inform, possibly inspire, and raise awareness of Infantile Scoliosis and its treatment/cure. Please share our story. For more information please check out http:/ www.infantilescoliosis.org/. Olivia loves her brace. She ...
sticksandrocks.blogspot.com
Sticks and Rocks: Bodywork: an Introduction (Not an Intervention)
http://sticksandrocks.blogspot.com/2011/03/bodywork-introduction-not-intervention.html
Saturday, March 5, 2011. Bodywork: an Introduction (Not an Intervention). For years, I have struggled with finding a way to help The Dude strengthen his muscles, counteract the scoliosis, and assist him in living pain-free. Yes, he does have pain and discomfort. He can tell me where and what hurts, and has for several years. Physical therapy does wonders for so many people, particularly the Schroth method. And a marvelous anatomy text recommended by one of our Schroth PTs: Atlas of Human Anatomy. When I ...
fancastickids.com
Noel Industries
http://www.fancastickids.com/index.html
Middot; Fancastic Friends. A cool new way to beat the summer heat! My son Cole wears a scoliosis brace 23 hours a day, which can get very hot and sweaty in the summer. He loves his Fancastic Kids cooling vest and asks to wear it when we go outside. It is comfortable and stays cool for hours, allowing him to participate in all his normal toddler activities! Cooling cells are placed in front and back pockets. Cooling cells held in the vest with neoprene. The vests come in 2 sizes: small and large.
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