Archive for 'Glycogen Storage Disease Type 1A'
The School is “Fixed”
Posted on 18. Jun, 2007 by Jillian.
Anyone who has read previous posts on Starchwars may remember the difficulty we have been having trying to get our oldest son appropriate services at his public school. For him, this would include an aide assigned specifically to him and trained to recognize and treat hypoglycemia as well as administer his cornstarch “medicine”. The school [...]
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Florida Trip Tips and Tricks (try saying that 10 times fast)
Posted on 01. Jun, 2007 by Jillian.
We just got back from seeing Dr. Weinstein at Shand’s Hospital/ Univerisity of Florida in Gainesville. Last year just getting there was extremely difficult. Anything that could go wrong, did. This year was incredibly smoother, mostly due to the extra set of hands AKA Aunt Bonnie (we will NEVER be able to thank her enough) [...]
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Bloodless Glucometer
Posted on 07. May, 2007 by Jillian.
CNN just wrote an article on a new device that can test blood sugar without pricking the finger! Apparently the device penetrates the skin with near-infared rays eliminating the need for an actual drop of blood. Of the five clinical studies already performed, the new device has tested 85% accurate, whereas a glucometer has an [...]
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Medic- Alert Service Dogs
Posted on 30. Apr, 2007 by Jillian.
Last year when my boys were staying at Shand’s Hospital/ University of Florida, our favorite physician mentioned they had some Malteagles (a maltese/ beagle) that needed a good home. We like dogs, but with (at the time) three small boys with a chronic medical disease, we felt it best to not even consider it. However, [...]
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Emergency Preparation
Posted on 20. Apr, 2007 by Jillian.
What if there was another tragedy like 9/11? Another natural disaster like Hurricaine Katrina? How would we be able to leave without any notice? It’s important for everyone to be prepared for an emergency. It’s especially important for someone with GSD, and it’s extremely important for four boys with GSD. There are many good resources [...]
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GSD Vs. Small School Districts
Posted on 05. Apr, 2007 by Jillian.
Our eldest son began preschool at the local elementary school (commonly referred to as head start) due to developmental delays. In the beginning of the year, I held a meeting with the school staff to discuss his Individualized Education Plan (IEP). I had NO IDEA what I was doing, and I write this post not [...]
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Shaken, not stirred.
Posted on 29. Mar, 2007 by Jillian.
I often have people ask “Cornstarch? Really? Why? How?”. So, I thought it might be nice to write a post in response. Glycogen Storage Disease type 1a kids like mine cannot regulate their own blood sugar. So we give them cornstarch every 4 hours, 24 hours a day. Even in the middle of the night. [...]
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Weird Ice Cream that’s GSD 1A Friendly
Posted on 25. Mar, 2007 by BMW.
I ran out of ingredients that I normally used for makign our boys “special ice cream”, so I decided to improvise and see what I could come up with. I ended up with an ice cream that had the best texture that I’ve been able to make so far. I was dissappointed with the flavor [...]
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Recipes
Posted on 21. Mar, 2007 by Jillian.
One of the hardest parts of GSD is finding recipes to match the diet- especially for special occasions such as birthdays or holidays. So, we’ve started a “recipe” page. PLEASE feel free to e-mail me ANY sucrose, fructose, or lactose-free recipes you come up with. I would particularly like to post a frosting recipe. Wink [...]


