Elise, our 5-year-old daughter, was diagnosed with type 1 diabetes (T1D) when she was 12 months. Team Elise started three weeks later in September of 2008 when we participated in the JDRF (Juvenile Diabetes Research Foundation) Walk to Cure Diabetes in Plano, Texas.
In the last four years, we have had over 600 people walking for Team Elise in the United States, Canada, Portugal and Mozambique and we have raised over $58,000 for T1D research!
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.
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. Elise is a quirky, fun princess with a huge imagination and a heart to match.
It has been over four 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 and 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).
WE NEED YOUR HELP
Our goal is to create awareness about T1D and raise money to cure, better treat and prevent T1D. You can still make a donation to JDRF by clicking on Donate.
A big thank-you to everyone who has supported us over the last four years. It means a lot to us!