Living with diabetes is a challenge for anyone, but imagine caring for a family in which six of eight children are living with type 1! Yes, that’s right: A family in Utah has six of eight brothers and sisters living with diabetes, and that could very well be a record (!), though not one that any family desires.
Amazing D-mom Kirsten Schull has been advocating on behalf of her six children with diabetes (CWDs) since the first diagnosis came 15 years ago. Since then, they’ve gone through every level of schooling and just about every type of D-situation imaginable. Not to mention the basic issues of differing D-routines and what must be the extraordinarily high cost of medical supplies for the family.
We are truly in awe — and delighted to be sharing their story today, via our correspondent Mike Lawson:
Special to the ‘Mine by Mr. Mike Lawson
I struggle to find matching socks. It’s not that I don’t own many pairs of matching socks and therefore the task is challenging. My problem is that on many mornings, before drinking my coffee, the act of opening the sock drawer and using my mental energy to pick out two identical socks is just too much to bear.
For this reason, I am blown away when I hear about parents who wake up each morning and not only remember to feed their children and put matching socks onto their young feet, but even sometimes manage to find a matching pair for themselves.
Now throw diabetes into this mix, and I’m dumbfounded.
There are many great diabetes advocates who have became engaged and involved because their children have been diagnosed with diabetes, but what’s even more astounding to me are the super-parents out there who juggle multiple diagnoses in their families.
Did you know that having one child with diabetes statistically raises the risk of your other children developing diabetes? Yes, according to Joslin Diabetes Center, if an immediate relative (parent, sibling, son or daughter) has type 1 diabetes, the risk of a child developing type 1 diabetes is 10 to 20 times the risk of the general population.
D-mom Kirsten Schull living in Utah has seen the impact of these stats firsthand. Kirsten has eight children and six of them have been diagnosed with type 1 diabetes. She said that she was unaware of the increased risk of subsequent children developing diabetes after her 7-year-old son received the family’s first diagnosis about 15 years ago.
Her kids are currently ages 21, 19, 16, 13, 11 and 7. She actually told us that HIPPA privacy rules prohibit her from saying when each of the kids was specifically diagnosed (?), but the D-mom says all the diagnoses came between ages 5 and 13 years old. One of her kids is still “honeymooning” after being diagnosed a year ago, and it’s been “a long, slow decline into the disease” for that child, who took part in a TrialNet study for five or six years before crossing the blood sugar threshold of 200 mg/dL after a two-hour fast (wow!).
The last three Schull kids were only diagnosed because of the TrialNet study that tested first for antibodies, and indicated all six kids had antibodies as early as eight years ago.
“I feel so sad when I think about it,” Kirsten said. “But honestly, to keep up with our crazy life, I put deep contemplation on the back burner, deal with each day and each new situation as it comes. I’ve mourned the loss of their freedom and health and simplicity, and each child has had to do that for him or herself as they’ve come to the edge of the abyss.”
Guinness Book-worthy?
Curious about whether the Schulls really hold the record for the most children being diagnosed, we asked Kirsten. “We don’t know of any other family with 6 kids with diabetes. Our doctors don’t either, but I wouldn’t know where to look for a definitive answer on that. Not a great record to hold, frankly, if we have the most, but my kids are awesome, and deal with it very well. They are very supportive of each other, and it’s a rare dare they complain about having diabetes,” she says.
We also took the question to a handful of experts with some insight into families with large numbers of CWDs. No one seemed to know of any other families with six of eight kids, although no group or institution appears to track that information.
Founder of the Children with Diabetes community Jeff Hitchcock who’s met thousands of families dealing with type 1, says he hasn’t heard of other cases with so many CWDs in a single family. An online TuDiabetes discussion group on the topic doesn’t list any info on that many CWDs in one family, while nationally-known experts and D-advocates like Lorraine Stiehl, who worked with JDRF, and prominent CDE Gary Scheiner, who’ve both traveled the country on the type 1 circuit say they also haven’t. Neither has Joslin Diabetes Center, which reports it has neither stats nor any anecdotal knowledge of that many D-kids in one family.
Even TrialNet’s Clinical Research Administrator, Christine Webber, hasn’t heard of that large amount of CWDs in one family either. She says the closest she knows of is the Gould family in Tennessee (who the ‘Mine interviewed in 2009), in which four of eight children have diabetes. Webber said a few years ago, a study called the Type 1 Diabetes Genetics Consortium studied families with two type 1 siblings, but it didn’t track how common these families are among the general type 1 population.
Challenging!
Through the years, Kirsten and her family have faced myriad challenges when caring for six CWDs. But they’ve also found positives in learning from each kid’s experience and applying that to the others — especially when it came to school. They’ve been in every grade level from kindergarten to college, and Kirsten says each age group and grade level has its own unique challenges.
“The younger they are, the more support they need, but the older kids need reminding, love, support and encouragement as well,” she says. “I find that a lot of what each child needs is personality-dependent. For example, one child has never wanted me involved at school in her diabetes care, and as long as she does well, she is free to handle it herself. The youngest would like me to take care of it completely and never ask him to think about it. Each parent needs to fine-tune what they do with their child, make it work for them, and give their child the responsibilities and rewards that go with good care.”
For mom Kirsten, she’s found help in knowing how to manage her children’s diabetes by turning to local JDRF chapters, support groups and online sites.
Many of the problems the Schulls have faced are financial ones, and they often cut corners to help stretch their medical budget — like refilling just one insulin prescription at a time because of high co-pays, and dividing that insulin up between the kids.
“One person with diabetes is expensive,” she says. “Now multiply that by six.”
Kirsten’s husband is a safety director for a manufacturing firm, while she is self-employed as a legal deposition proofreader, giving her the ability to work from home and provide the necessary on-call support for her CWDs.
“I tip my hat to families that manage work and school seamlessly, but we seem to have a crisis or two each month, so working at home suits me well,” she said.
All PWDs are unique, and according to Kirsten that is still very much the case when it comes to siblings with diabetes. Kirsten said that she doesn’t go out of her way to prepare “diabetes-friendly” or low-carb meals at her home because each of her children has a unique management plan. “I make what I’m going to make and then they count carbs and adjust.” Four of Kirsten’s children are using insulin pumps, one is doing multiple-daily injections and the one still in the honeymoon phase has not yet started to inject insulin.
Kirsten has become a passionate diabetes advocate and has written articles about raising children with diabetes. Because of her extensive knowledge on educating educators about diabetes, she often writes about the difficulties children face when dealing with diabetes at school. She has also collaborated with Lilly Diabetes and Disney to help create content for a website that assists parents that need help raising CWDs.
More Multiples
Unfortunately the Schulls high number of children with diabetes is not as unique as it might sound. We have been hearing more and more stories of families with multiple type 1 diagnoses. Another D-mom dealing with this, who’s familiar to many active in the DOC is Meri Schuhmacher; three of her four sons have type 1.
Meri has compared raising multiple D-kids to a Hunger Games challenge: “The odds are never in our favor. It’s so rare for all three boys to have dialed-in basal rates and for all of us to get a good night’s sleep.”
Both Kirsten and Meri can talk about the challenges of raising multiple children with diabetes, but they also were both quick to point out some of the upsides of having multiple diagnoses in the family.
“Around here, diabetes is normal,” Meri says, noting that when her most recent son was diagnosed, he expressed happiness because it made him more like his older brothers. “There is no ‘poor me’ attitude since it’s just a regular thing.”
Kirsten says she thinks diabetes has helped her children be more supportive of one another and more realistic about money. “My kids know that diabetes is expensive, and they don’t complain or ask for a lot.”
If you have multiple children and one of them has diabetes, you might consider signing up for the TrialNet clinical study, an international network of researchers exploring ways to prevent, delay and reverse the progression of type 1 diabetes. They offer annual screenings to children for free, to look for diabetes-related auto-antibodies that usually appear years before type 1 diabetes develops. Your participation will help further the research, of course.
While it’s clearly a struggle to raise children with diabetes, we’re in awe of Kirsten and Meri for finding a silver lining. They both have really great, grounded kids, and wonderful relationships with them.
“There is sorrow and chaos and anger with this disease, inconvenience and huge expense, but there’s also hope for the future,” Kirsten says, noting that she’s confident a cure will be found and there will be amazing treatment improvements along the way.
After learning about the kind of preparation and work they have to put into each day, I think that I can muster up some more energy to match up my socks each morning.




WOW, these families are amazing! A houseful of PWDs is always interesting and always presents challenges and these parents allow me to peak into a window to better understand my own parents.
These D mamas show me what my parents dealt with on a daily basis in the Diabetes Dark Ages. Pre insulin pump, pre meters, pre carb counting, pre Diabetes On-Line Community. I come from a family where 3 out of 6 children (including myself,) were dx’d with t1, as was my father, my nephew, 2 aunts and a cousin.
THANKS LADIES!
My brother was diagnosed 42 years ago with Type 1 and I got an unexpected gift at the beginning of middle age: It’s Type 1! It hasn’t helped me any having a brother who has it as well except that I knew it was dead serious. I’m also in awe of people who dealt with diabetes with no meters, injecting animal insulin and testing urine (and then trying to decipher the color on the strip.
It’s also strange for someone who’s had Type 1 for three years to know what an older diabetic means when they say they’re having a reaction. (It’s old dia-speak for a low).
Thank you for sharing your family stories, Kirsten and Meri. I hope you realize just how inspiring you are. For families considering participation in TrialNet, here are some details I learned when my family got involved: http://www.forecast.diabetes.org/welcome-dec2012. As Wil Dubois notes in his article about the ADA’s Standards of Medical Care in Diabetes, http://www.diabetesmine.com/2013/01/fresh-new-ada-standards-for-you-yes-type-1s.html, practitioners are encouraged to refer relatives of people with type 1 to clinical trials that do antibody testing and type 1 screening, because knowing there’s a heightened risk of developing type 1 can help people who progress to diabetes get treatment before life-threatening ketoacidosis occurs.
Wow. I know Meri and consider her one of my heroes , now ill add Kristen to the list. I can now say only 2 of my 3 girls have diabetes. 6 out of 8, much deep respect I have for you and your family, Excellent article Mike, thanks for sharing this story my friend.
We just returned home from the hospital where now three of our five children have been diagnosed in the past three years with type 1 diabetes. It helps to know others have been here. Thanks for the encouragement.
Having a family member with diabetes specially kids is quite difficult coz they need a lot of attention and focus. But there are so many natural ways to combat it and they should live a normal lifestyle. My kid has diabetes but i make it a point not to let him feel he’s sick with so many limitations specially on food. Discipline is what they should learn best.
We have four sons aged 17-8, the older three of whom have diabetes, diagnosed aged 16 months, 4 and 11 months. There is no history of Type 1 in either our parents, grandparents, and neither myself or husband have diabetes, we are 47 & 43. They all transferred to insulin pumps last year from four injections daily, and all agree they find it easier. All four boys get on very well together and support each other, and are very happy and positive, and generally healthy children. One also has Marfan Syndrome and chronic urticaria, and our youngest is dairy intolerant. Obviously life is very hectic, as it would be with four kids, but the boys just tend to get on with school life, music clubs, cricket, fencing, swimming etc with a lot of background support from us and we educate them how to deal with diabetes issues as part as daily life as they grow. Thinking of you as the early days of building routines etc are tricky and wishing you all the best.