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Sweet Talk for Parents of Kids with Type One Diabetes

JoAnne Robb, T1D Mom and MFT

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The answers you’ve been waiting for! We all know that raising a type 1 child is filled with stresses and uncertainties that go beyond regular parenting. In this podcast, host JoAnne Robb, a psychotherapist, diabetes coach and T1D mom herself, brings her expert knowledge and experience to give you practical and sane answers to the questions you have about the emotional side of living with a T1D child. She will tackle your real-life questions so you can get the help you deserve to manage the c ...
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In today’s latest episode, I answer a listener question that will resonate with most parents of T1D kids: the emotional and practical considerations of testing siblings for diabetes markers. The decision to test siblings for diabetes markers is one that many families, including my own, approach with trepidation. The anxiety surrounding this decisio…
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Today’s show touches on a topic that’s close to many of our hearts—preparing our little ones for big life transitions. But as you know, when you’re the parent of a kiddo with type 1 diabetes, those transitions take on a whole new layer of planning and care. In this episode, I had the pleasure of speaking with Rachel, a proactive mom who’s thinking …
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In today’s episode, I’m joined by Sveltana, a mother who’s navigating the bumps of diabetes management with her 9-year-old snowboarder and athlete. While we do spend some time strategizing management and I talk to this mom about questions she could put to her endo, we’re actually having an important conversation about the values that she might be c…
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I feel so lucky to have been part of the conversation that makes up this week’s episode. My guest is Stacey Simms, herself a big name in the diabetes world, and the host of the Diabetes Connections podcast. At one of her Mom’s Night Out events, she had told me that she had a question about her T1D son’s transition to college — and here she is to ta…
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On today’s show, I welcome back Kaylor Glassman, founder of Diabetes Support Partners, to talk through a question from a listener. The question has to do with an 11 year old, who the parent feels isn’t being as responsible about diabetes management as mom thinks she should be. Mom is concerned that this kiddo isn’t tracking the insulin in her pump,…
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Today’s mom has a wish to go away with her husband for a weekend — and leave her T1D son behind. The grandparents have offered to take him for that weekend — they are more than happy to help — but mom is nervous, worried not just about her son’s numbers, but also about how asking for what she needs might impact her relationship with her in-laws. As…
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This week’s guest is a mom of a relatively newly diagnosed 10-year old girl. Mom describes her daughter Maisie as having always struggled with some anxiety — but now that diabetes is in the mix, Maisie's anxiety is higher and more dramatic — and mom is at her wit’s end. Together, this mom and I dig into what she’s seeing with her daughter and come …
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Thanks for listening to Sweet Talk all year long! I’m closing 2023 with a recap of some of my top recommended episodes to tune into this holiday season. These episodes will serve you as you brace challenges with food, family, and friends during this season. 57: What To Do When People Have No Idea What Your Life is Like 37: When Family Doesn't Under…
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The mom who joins me this week — Michelle — doesn’t have a specific question; instead, she wants to face off with the broad challenge of how lonely it can be to have diabetes, both for her and her T1D daughter. Ultimately, she’s bothered by the ways other people misunderstand what her daughter lives and struggles with. She’s frustrated that people …
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On today’s show, a mom joins me to talk about her nervousness about having a new driver — and to think through any issues that she should be on the lookout for because of diabetes. Mom is understandably anxious about her daughter starting to drive, but can also see that her daughter is pretty responsible about diabetes management. That said, we loo…
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This remarkable grandmother came onto the show to get some support for her newly diagnosed grandson. In the last few months, this 12-year-old boy — who was adopted by this family through the foster-care system — has been living with grandma. She’s observed that the higher his blood sugar, the more volatile his moods are. She notes that it’s hard to…
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This week, I’m honored to have Kaylor Glassman back on the show. As a reminder, I know Kaylor from DYF, the organization that runs camp in my neck of the woods in Northern California. She used to work there as the Director of Programs. Now, she’s started her own business called Diabetes Support Partners, which provides support to people in the firs…
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As T1D parents, most — if not all — of us grapple with some pretty significant anxiety about keeping our kids safe. The parent on the show this week shares with us about how she’s fighting with that anxiety in the quest to get things right with diabetes. Frankly, the parent has one of the hardest diabetes scenarios: Her daughter, now four, was diag…
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This week a mom came on the show to talk about her son who was diagnosed a little less than a month ago — but, amazingly, she didn’t have a question about him! Instead, she wanted to think about her 5-year-old non-T1D daughter who had come to her, saying that she feels “left out” of the family since the diagnosis. I am so impressed that this mom no…
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This week, a mom joins me in a wide-ranging conversation about the way her son can get sassy — and be difficult to parent — when his blood sugar is high. But before we ever got to that issue, we hit on a few other important topics. First of all, this brave mom talked about how dysregulated she gets when she is following diabetes all, all, all the t…
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This week, I’m talking to a mom with an all-too-familiar problem: Her teenager, diagnosed for years now and a conscientious diabetes manager until recently, has basically given up on bolusing. Mom is at her wit’s end, trying to figure out how to help her daughter pick this habit back up. She’s tried lots of strategies: motivational talk, discussion…
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This week, I talked with a mom whose T1D son recently left for college. It’s clear that mom trusts her son – and that they have a good relationship – but she’s also nervous about him being on his own. A lovely priority for her is to make sure that he knows that she’s there for him. We discuss how important it is for her to take a step back and make…
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For today’s episode, a mom came on to share how her 9-year-old son has become increasingly and newly worried anytime his CGM shows a high reading. We were able to trace this new anxiety to one particularly traumatic experience when he was over 400 for several hours and his parents (and grandparents) weren’t sure why he was high and were pretty anxi…
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I’m so lucky this week to have Kaylor Glassman on the show. I know Kaylor through DYF, the organization that runs a diabetes camp in Northern California; she used to be the program director there. Now she has a business called Diabetes Support Partners, which is specifically designed to help families with a newly diagnosed child. The question we’re…
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What a dilemma! To stay or to go? In this episode, I talked to a lovely mother who is debating whether she should move to live near her family who she knows can and will support her and her newly diagnosed daughter. The sticking point is that she also loves her job, feeling like she won the “career lottery” – and she isn’t sure she wants to give th…
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This week, I had a wonderful conversation with my old T1D mom friend, Tamar. Tamar and I met at camp a million years ago and our children were diagnosed on the same day! She’s a veteran, so you’ll hear a robust conversation about the question. A parent wrote in, saying that her son wants to eat “normally.” Together, Tamar and I think about both how…
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What a complex issue! This week, a mom came on the show, talking about how her somewhat-newly diagnosed 7-year-old has been pulling off her pump. Mom has been working hard to stay calm in the face of all these pump “failures” but really wants to get at the root of the problem, so her daughter stops derailing her own treatment. She’s thinking about …
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I had an interesting conversation this week with a mom of a T1D pre-schooler. Because she’s managed to keep dosing pretty invisible and seamless for him thanks to tech, she’s worrying that he doesn’t understand that he needs insulin to eat. As we explored the issues of how she could introduce the idea to him about this, we also were able to better …
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Sure, we want our kids to like their low supplies — after all, they sometimes need to eat them when they don’t want to eat a thing. But we don’t want them to like them so much that they eat them for fun. That would equal a blood sugar disaster. In this episode, T1D mom Julie comes to talk about just that: Her four-year-old was high for several days…
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Diabetes anniversaries! If you go onto Facebook, you’ll see a lot of photos of kids with cakes celebrating this milestone. But not everyone wants to take that on. In fact, some people just feel like diabetes is a bummer, and not something they want to celebrate in any way. In this episode, fellow T1D mom Annie and I discuss a question from a listen…
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With diabetes, there’s the independence dance: Sometimes our kids want to learn and grow into new tasks and responsibilities with their own self-care — and sometimes they’d rather hand it back to us. What makes this particularly hard is the chatter in our own heads. We parents worry when our kids take a step backward, thinking that we need to hold …
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We all remember what it was like when our T1D child was first diagnosed: The shock and sadness — and the steep, steep learning curve to trying to get diabetes “right.” As we watched each reading and each bite of food, we worried about being away from our child, and we wanted that CGM as quickly as possible. In this episode, the mom of a newly diagn…
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Another listener wrote in with a question about drug use for their T1D kid so I asked Dr. Justin Altschuler, a T1D and addiction doc, back onto the show to provide answers. In this episode, we tackle issues that come up around experimenting with “harder” drugs, like cocaine, hallucinogens, and opiates. Dr. Justin leans into his experience as a subs…
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Getting help and feeling misunderstood: the bane of a T1D parent’s existence. But what happens when we feel misunderstood by the people who are supposed to be closest to us, like our own family? Because I’ve heard these challenges from so many parents, I took this question from a listener who’s struggling with family misunderstanding about their ch…
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This episode surprised me — it’s the first time I’ve had a couple come on the show together to help them navigate the stress and challenges that come up because they have a type 1 child. It’s like a sneak-peak into a couples therapy session. In Colleen and Wesley’s case, their disagreement centers around food and eating. Since we know that diabetes…
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One of the ways so many of us manage our nighttime anxiety after our kids’ initial diagnosis is by pulling them into bed with us. We have a magical belief that we will keep them safer if they are right next to us as they sleep. And while that’s a reasonable strategy for a time — until we can get our own anxiety and shock under control — it’s not an…
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Parents know that mixing alcohol and type 1 brings extra challenges. Although we’ve tackled this topic before, Dr. Justin Altschuler is back to answer more listener questions about how to navigate the tricky territory of drinking with T1D. And just as a reminder: Not only does Dr. Justin have a private practice that specializes in addiction and T1D…
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Sending our T1D kids to school can be hard, but we know we have to find a way — after all, they need to be there and we know that the school needs to help us make that happen. It can feel really different, though, when we need to lean into our community to ask friends to take care of our type 1 kiddos for something like a sleepover. Sure, our kids …
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Camp! If you’ve come to almost any event I’ve hosted or been part of, you know that I’m a big proponent of diabetes camp. There are so many good reasons for this but the biggest is that our kids benefit from being in a community with other people who also have diabetes. So what to do when you tell your T1D child that you’re planning to send them to…
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We all know that how we experience our kid’s type 1 is very different from how the rest of the world sees us. People on the outside might see us calmly dosing for a meal or picking up prescriptions at the pharmacy. They have no idea that we’re up nights, checking the Dexcom through the day, or on the phone with insurance for hours on end. That said…
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Another mother coming on the show, concerned because she’s finding food wrappers and feels like her child is “sneaking food”? Yes! But food and eating is such an important topic that I wanted to let you listen to lots of different ways you can think about and approach the issues if (and when) they come up with your T1D child. In this episode, we me…
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It’s so hard to stay level when you’re parenting – and adding type 1 to the mix can really turn up the temperature on feeling out of control. In this week’s podcast, Annie and I talk together about a question from “Feeling out of control in Albuquerque” who is struggling with the anger that can sweep over her when something goes sideways with diabe…
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For many parents, with or without T1D, food triggers so much baggage and confusion. On the one hand, we want to serve what’s healthy and limit “junk” food. We also don’t want to be overly restrictive: We know that as children get older, it’s going to be up to them to start making their own smart choices. And if we never give them chips or ice cream…
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It is not an easy thing to let go of our kids as they grow up and become more independent. Having a T1D diagnosis only makes that process more difficult, and there is much anxiety, frustration, and fear in relinquishing diabetes management to other people. What if something happens and I’m not there? Will the caregiver know what to do? These questi…
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Being skeptical and fearful of the new technology of an insulin pump is real for many T1D parents. Is it reliable? Will it do what it’s supposed to do? Annie, a friend and fellow T1D mom, joins us to read a listener question from “Resistant” in California. Join us! Show Highlights: Listener Question from “Resistant”: “I’m feeling a lot of pressure …
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Dealing with your child’s additional health diagnosis on top of T1D can ramp up the stress and anxiety for parents. Today’s question comes from a parent who is navigating this difficult road with her teen. Join us to hear the conversation. Show Highlights: Guest: Janelle, whose daughter Michaela (16) was diagnosed with T1D at age 12 Testing has rec…
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Worrying about how your T1D child is adjusting to the new routine of diabetes management is common. How do you convey the seriousness of diabetes management while not overwhelming them with anxiety and fear? Is there a way they can take a “break” without endangering their safety? I’m joined again by Annie, a friend and fellow T1D mom, who will read…
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Nighttime alarms for your T1D teen’s blood sugar levels are difficult. They bring fear and stress, besides robbing the family of good sleep. How much should the parent be involved in nighttime dosing, and how much ownership should the T1D teen take? Join us for today’s listener question about how that partnership might work. Show Highlights: Guest:…
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Leaving your T1D child for an overnight or weekend trip for the first time brings up many anxious thoughts and concerns. The multitude of fears and “what ifs” can spiral out of control without a solid safety plan, but how do you put that in place? I’m joined today by Annie, a friend and fellow T1D mom, who is here to read and discuss a listener que…
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As a T1D parent, you go through a flurry of activity and adjustment when your child is diagnosed. The years that follow can be very difficult with daily management and monitoring, and it may look like you have it under control. The truth is that we all need the support that comes from other T1D parents and other friends and family members—and we ar…
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I’m honored to be joined by two guests today. One is a mom who has questions about substance use and her T1D teen. Because I’m not an expert on this topic, I invited Dr. Justin Altschuler to join us. Besides having T1D himself, he has a private practice that specializes in addiction and T1D, and he is the medical director of Diabetes Youth Families…
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Welcome to another episode! Today’s question comes from a listener who wrote to me, and I have a friend and fellow T1D mom, Annie, to join the discussion and offer her perspective on this difficult situation. Join us! Show Highlights: Question from “Feeling Powerless”: “I need help in supporting my T1D daughter, who is in 3rd grade and was diagnose…
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Coordinating your T1D child’s care with school caregivers can vary from one extreme to the other. Some parents have wonderful support in place, and others feel like they are constantly battling and advocating. The truth is that parents, teachers, and school staff CAN and SHOULD work together to keep the child safe–that’s the bottom line. All the nu…
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As with many medical issues, testing can be done for T1D markers. The problem is that those testing results give a measure for a particular point in time, and a negative result does not mean that someone will never be diagnosed with diabetes. For parents, it can be a real dilemma whether to test a child for these markers. Today’s question comes fro…
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We are talking about T1D from a perspective other than that of a parent, which is our usual format. I’m talking to the care provider who helped both of my children when they were in elementary and middle school. Cassandra shares what it’s like to be a care provider, along with what worked best (and what didn’t), and how she coordinated with school …
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