Elise was diagnosed with type 1 diabetes (T1D) in 2008, two days after her first birthday. Team Elise started three weeks later when we participated in the JDRF Walk in Dallas. Elise is now 10 years old.
In the last nine years, we have had over 1,500 people walking for Team Elise in Dallas, Toronto, Lisbon, Maputo, Little Rock, Abu Dhabi and New York City and we have raised over $100,000 for JDRF!
T1DT1D is an autoimmune disease in which a person's pancreas stops producing insulin - a hormone essential to the ability to get energy from food. It strikes both children and adults suddenly and changes life as they know it forever. T1D causes lifelong dependence on injected or pumped insulin and carries the constant threat of complications. T1D cannot be prevented and there is no cure.
ELISEElise has grown into such an amazing little girl. She has the sweetest heart and is probably stronger than most adults. Perhaps it's because of T1D, but we like to think it's just who she is; strong spirited. Elise is beautiful; inside and out. And while most people comment on her outer beauty, she is kind, generous, loving and the best big sister to Mattias and Lucas. Elise is a quirky, fun princess with a huge imagination and a heart to match. She is now also a published author - check out The Mouse Who Ate The Moon at www.themousewhoatethemoon.com (the Portuguese version is available at www.oratoquecomeualua.com).
It has been nine years since Elise was diagnosed. T1D is tough, especially when you're a child. Every day, Elise gets her fingers poked 5 to 10 times, sometimes more. She had at least three shots a day for over three years. In November of 2011, she started using an insulin pump (Omnipod) which means that she only gets shots if we run into an issue with the pump, which now delivers her insulin. The pump has to be changed every three days. We weigh almost everything she eats (since almost everything has carbs) so that we can give her the right amount of insulin to cover the carbs that she eats. T1D is a 24/7/365 disease. Not only do we check her blood sugar during the day, we also get up at least once a night at around 3 AM to check her blood sugar and give her carbs or insulin, if needed (there are nights where we get up as many as 6 times). Elise also has a continuous glucose monitor (Dexcom) so that we can know what her blood sugar is at all times and if it's stable, going up or down and how fast it's rising or dropping.
In 2014, Elise was the youngest kid, at age 6, to enroll in a clinical trial for the bionic pancreas, a system that uses a continuous glucose monitor and an insulin pump to deliver both rapid-acting insulin and glucagon as directed by a computer algorithm.
Check out www.deathofapancreas.com where Joanne blogs about Elise and T1D.
JDRFJDRF is the leading global organization focused on T1D research. Driven by passionate, grassroots volunteers connected to children, adolescents, and adults with this disease, JDRF is now the largest charitable supporter of T1D research. The goal of JDRF research is to improve the lives of all people affected by T1D by accelerating progress on the most promising opportunities for curing, better treating, and preventing T1D. Since its founding in 1970, JDRF has awarded more than $1.6 billion to diabetes research. Past JDRF efforts have helped to significantly advance the care of people with this disease, and have expanded the critical scientific understanding of T1D. JDRF will not rest until T1D is fully conquered. More than 80 percent of JDRF's expenditures directly support research and research-related education.
WE NEED YOUR HELP
Our goal is to create awareness about T1D and raise money to cure, treat and prevent T1D. If you would like to become a Team Elise sponsor, go to the Sponsors page to view the sponsorship packages available and email email@example.com for more information.
A big thank-you to everyone who has supported us over the years. It means a lot to us!