Stella was diagnosed in 2014 and has been fiercely independent for years, taking care of all the day to day Type 1 tasks while living her very busy active life. We admire Stella’s perspective on Type 1, she incorporates it into her life and doesn’t let it stop her pursuing her passions. 

We met Stella at Friends for Life in 2016 and have looked forward to seeing her there every year since!

Isabella was diagnosed in 2017 with Type 1 and immediately her whole family jumped in to learn as much as possible so she could thrive living with Type 1.

She’s been attending Friends for Life for many years and looks forward to her annual selfie with EBK’s mom (this page could be filled with their selfies)! She’s a superstar cheerleader, one of the friendliest & most social teenagers you will ever meet. We are so lucky to have Isabella in our T1D community!

Zoey was diagnosed on Halloween 2022 when she was 3 years old. It was a very scary 3 days in the hospital. When we got home, Zoey began her journey and learned what happy tears were when she let mom Kim do a finger stick without any tears or hesitation. She's been a Rockstar ever since and absolutely thrives living with Type 1 Diabetes.

Zoey is a frequent attendee at Elbowbumpkid Inc events, especially girl power. She does eat something other than watermelon pictured but it’s clearly one of her favorites! 

vy & Hannah are our 2025 college scholarship recipients, in fact Ivy is a second time winner! The EBK team recently sat down with them over breakfast to learn more about their experiences navigating college life with type 1 diabetes (T1D). They shared valuable perspective for families preparing to send a student with T1D off to college.

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Both students have advocated for and received testing accommodations, though they haven’t had to use them yet. Instead, they focus on careful planning to keep their blood sugar in range on test days. Ivy emphasized the importance of staying ahead on supply management—making sure you never run out while at school & planning for trips home to coincide with supply deliveries. Hannah reflected on how she’s come to accept the unpredictable nature of T1D, noting that even with a consistent routine, outcomes can still vary from day to day.

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One message they both strongly believe in: the importance of community. That includes the T1D community and also being active and connected locally wherever they are.

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Ivy is a patient at Connecticut Children’s Endocrinology clinic who are longtime Elbowbumpkid supporters & appreciate the programs and support we provide. Hannah is a patient at Hasbro Children’s & already dropped off our community postcards at her last appointment to inspire them to share our programs with their newly diagnosed Rhode Island families.

We can’t wait to hear how their school year goes & we congratulate them again for their accomplishments!

Our July Thriving Thursday post features the original Elbowbumpkid. Saige, this month Saige celebrates their 16th diaversary! Happy diaversary Saige, keep being a superstar!

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Saige runs our diaversary program, helps at events, mentors newly diagnosed children and helps coordinate any kits/mailings for programs. Saige is always in the background giving feedback and helping families connect. That includes being silly with other teenagers at events too!

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Saige has learned to never let T1D deter from anything and to adapt it for school/sports/everyday life.

Thanks Saige, keep up your fantastic community work!

Audrey  is at many of our local events and while we hate that she has to live with T1D, we are so glad we have her light in our community! She has such a positive outlook, here's a little poem from her to brighten your day:

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Find ways to love your diabetes even if no one around you has it

We are all just sweet

We are the sweetest people around

There are highs and lows and party's

Live like diabetes was yesterday and you are today

Diabetes doesn't define you but being sweet does

Stay strong and always remember you are the hero

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We call Amelia “amazing” Amelia because she’s an incredible kid. Diagnosed with T1D at age 2, now 11, she lives with multiple diagnoses including celiac disease & seizures.

She’s been attending Elbowbumpkid Inc events for years, even before we were an official nonprofit. She’s a passionate podder & is always smiling. She gives the biggest hugs, is super friendly to every kid she meets and is just a joy to be around. Amelia loves being around other kids living with Type 1 and we feel incredible about our mission every time we see her!

Brooke has been living with Type 1 Diabetes for 18 years and just started using an insulin pump for the very first time, brand new Podder!

Brooke sent her pic in to us and we chatted that you are never too young or old for Barbie and a pump. Brooke also has a T1D son diagnosed at age 3, living with T1D for over 10 years.

Fun fact, Brooke designed our initial EBK logo!

Kaylee was diagnosed with T1D at age 4 and is serving as the Director of Inspiration for TK.Type 1, a nonprofit in NY empowering families impacted by T1D through comprehensive education, compassionate support, and vital resources, all aimed at significantly improving their quality of life.

The Elbowbumpkid Inc team met Team Kaylee several times & we are truly inspired by her passion to help others thrive with their T1D diagnosis. Team Kaylee attended our 2025 Legoland outing & had a fun day making connections with others just like her, including a new friend in NY.

We thank Team Kaylee for supporting Elbowbumpkid Inc & the community!

"I was diagnosed with T1D on july 2 2021. I felt really sad because I thought my life would change forever. I really wanted to leave the hospital and go back to my normal life with no insulin injections.

Realizing a new normal was ahead of me I decided to get busy learning about the disease and helping others. The first thing I did was create a team, Taylan's Tricks or Treats, and do a Breakthrough T1D (formerly JDRF One) Walk. My mom then met Miss Samantha and connected me with Elbowbumpkid Inc where I met other kids with T1D. I then decided after my first year of diagnosis, I could still lead a normal life. I started playing basketball in my first year back, and my team won the championship.

I didn't stop there, I decided to push myself in my education and apply for the  Aerospace and Engineering program at my school. And by the grace of God... I made it in. After completing the aerospace program in middle school, I decided to push myself further and apply to EC Goodwin Tech to continue the engineering curriculum...and I got accepted!!!

By accepting that T1D is a part of me until a cure is developed, I have decided to thrive despite the diagnosis." 

Kaitlin and Ivy both won our college scholarship this year - their applications clearly demonstrated their commitment to the community. 

Ivy was diagnosed at age 7 and Kaitlin was diagnosed at age 9, so both remember live before T1D. Both women have supportive networks at school and in sports that are knowledgeable about T1D. In fact, both have tips for parents whose kids play sports: make sure the coaches and friends playing know what to do when they are low. Ivy is an amazing softball player and says: "set the expectation when educating Coach that just because you are low for 5 minutes doesn't mean you can't keep playing the game!" Kaitlin says: "don't forget to educate your college roommate about low blood sugar protocol as well."

Both students are patients at Connecticut Children's and appreciate the consultative relationships they have with their providers.

Check out Idan's video discussing his Type 1 Diabetes diagnosis and if he could turn back time and choose his life as a T1D kid or not, what he would choose... you might be surprised!