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Meet Alyssa, a 20-year-old living with glycogen storage disease type 1a, a rare and life-threatening genetic disorder that changes how the body stores and uses glycogen, a key source of energy. Alyssa’s daily routine looks very different from most of ours, yet she navigates it with remarkable grace and strength. Read her story, told in her own words, https://bit.ly/4lDU9gA #GSD #DayintheLife #ConnecticutChildrens | Connecticut Children's Foundation
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Meet Alyssa, a 20-year-old living with glycogen storage disease type 1a, a rare and life-threatening genetic disorder that changes how the body stores and uses glycogen, a key source of energy. Alyssa’s daily routine looks very different from most of ours, yet she navigates it with remarkable grace and strength. Read her story, told in her own words, https://bit.ly/4lDU9gA #GSD #DayintheLife #ConnecticutChildrens | Connecticut Children's Foundation
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Understanding Glycogen Storage Disease Type 1b and its impacts. Glycogen Storage Disease Type 1b (GSD1b) is a rare genetic disorder that has a huge impact on patients’ lives and the lives of their families. People with GSD1b cannot effectively access the glucose needed to fuel themselves, leading to severely low blood sugar and life-threatening infections among other complications. Current treatments, such as frequently consuming cornstarch, provide some help to those with GSD1b, but new treatme
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