Technology is an ever changing part of diabetes care. We have compiled resources from technology providers that will help parents, schools, and other caregivers use the latest tech safely. View the different diabetes tech resources HERE.
Ready to get back to school? Make sure you are prepared for T1D in the classroom by following our back to school checklist for both the school and parent. Don’t forget to pack extra pump supplies and insulin! You can access the check lists by CLICKING HERE.
Diabetes Youth Services suggests every child have a 504 plan on file with their school, in addition to the diabetes care plan from your physician. THIS GUIDE, designed by the ADA, can help you put together a good 504 plan for your child. If you have questions about what should be part of your 504, please ask your health care provider or other expert.
The Smart Sitters Guide can help you prepare sitters or other caregivers for tasks they may need to do and situations that may arise while they take care of your child with T1D. THIS GUIDE, covers basic information about T1D, current tools to manage diabetes, along with plenty of practical advice and tips for parents and sitters. It is not intended to serve as a complete guide to managing T1D in children and young adolescents. Developed with support from Omnipod.
T1D Everyday Magic created a printable Diabetes Plan that you can fill out with your child. Hang the form where you can always see it. Make copies so every member of your family can keep one in their backpack, wallet, purse, or car. It is also a good idea to give a copy to teachers and coaches. Click HERE to print the form.
Classroom and birthday parties are full of excitement, fun, and of course SWEETS! Birthday parties and classroom parties just involve more of the same good planning you’re already doing, plus a few creative ideas. T1 EVERYDAY MAGIC and BEYOND TYPE 1 wrote articles on how to survive the school and home birthday parties so your T1D can have the best time with their friends and family.
Bright Horizons is a proud partner of DYS. If you have a problem with school, athletics, childcare or any other similar entity working with you and your child’s diabetes, this organization can help you out. They are a non-profit 501 (c) 3 and offer their services on a sliding scale based on your personal financial situation. Call Jennifer or Victoria for more information at 419.318.9636 or CLICK THIS LINK to view their website.
Michigan Alliance for Families provides information, support, and education for families who have children and young adults (birth to 26 years of age) who receive (or may be eligible to receive) special education services. This website can help you with finding information on special education issues as well as disability specific information. CLICK THIS LINK to view their website.
Disability Rights Michigan advocates and lawyers advise individuals with disabilities of their rights and responsibilities and advocate for their human, civil and legal rights within the state of Michigan. DRM has broad access authority to monitor institutions and advocate for people with disabilities who live in them. Their services expand from having trouble with schools, coaches, sitters, to helping with medical care and beyond. All services are free of charge for families and adults. You can call 1-800-288-5923 or visit their website CLICK THIS LINK to view their website.
People living with Type 1 diabetes must take insulin by injection or infusion every day. Insulin is life support – we all need it to stay alive, as much as we need oxygen, water, and food to eat. If you are in emergency need of insulin right now, always go to the emergency room. If you are struggling to afford the monthly cost of insulin CLICK THIS LINK and visit Beyond Type 1 to view resources you can use not only for insulin but other diabetes supplies, insurance coverage, and information on exploring tools and actions you can take to get involved with access advocacy.