Diabetics Doing Hollywood 2 with Jen Bartels


Episode summary
Jen Bartels, an actress known for playing Diana on American Woman, was diagnosed with type 1 diabetes about a year before this conversation while filming the show. She noticed weight loss and frequent urination and assumed it was the toll of acting life until blood tests showed high blood sugar. She already had Hashimoto's. She describes mourning her old life, learning to dose for meals, and a scary low blood sugar episode while traveling in New York. She talks about the stress of performing with diabetes, body image and costumes, her choice to stay on multiple daily injections instead of a pump, and finding support online after posting a photo of herself giving an injection. She credits therapy and exercise for managing stress.
Key takeaways
- Jen says she first dismissed her symptoms as just the toll of being an L.A. actress until a fasting test put her blood sugar around 210.
- She still uses multiple daily injections with pens rather than a pump, partly because of how a pump would show under costumes for acting work.
- On a trip to New York she dosed for a late-night grilled cheese before it had digested and dropped to 40, needing a friend to bring her test strips.
- Posting a photo of herself giving an insulin injection on Instagram connected her to the online diabetes community and eased her sense of isolation.
- She credits consistent workouts and therapy with helping her manage the added stress and anxiety that came with her diagnosis.
Show notes
You may know her as Diana from American Woman on Paramount Network, but the woman in character is Jen Bartels (@jenbartels on Instagram); today we’re bringing Hollywood to the booth as Jen joins us on this episode of Diabetics Doing Things.
Jen and I dive into her diagnosis story and she explains how she asked herself, after noticing some weight loss, “Is this the life of an L.A. actress, or is it diabetes?” For Jen, it was Type-1 Diabetes. Throughout the episode, we talk about what it means to be a T1D and how big of a role the diabetic online community plays in encouraging you to go above and beyond and connect with others. The more we share, the more we learn, the more we know.
Jen and I discuss the implications of T1D, how there are no off days and how it’s more than just not drunkenly eating pizza on a Friday night. Further, we talk about being diagnosed later in life and the changes that it brings. As Jen says, it’s like "packing a diaper bag for a child that never grows up."
Be sure to give this episode a listen and reach out to Jen if you need some advice or just want to chat.
Questions this episode answers
How was Jen Bartels diagnosed with type 1 diabetes?
She noticed weight loss and frequent urination while filming American Woman and assumed it was just the demands of acting. A doctor sent her for testing, her fasting blood sugar came back around 210, and antibody testing confirmed late-onset type 1 diabetes.
Does Jen Bartels use an insulin pump?
No, she uses multiple daily injections with insulin pens. Her endocrinologist has pushed her toward a pump, but she says she isn't ready, in part because of how it would look and fit under costumes for her acting work.
What CGM does Jen Bartels use?
She tried the Freestyle Libre and documented putting the sensor on for the first time in an Instagram Live video. She says it works well for her when the sensor is functioning correctly.
How did Jen Bartels get involved in the diabetes community?
She followed other people with type 1 diabetes on Instagram before going public herself. About a year after her diagnosis she posted a photo of herself giving an insulin injection, which she says connected her to a supportive online community.
Full transcript Searchable, with timestamps
Rob Howe: Welcome to the Diabetics Doing Things podcast. We've been telling the amazing stories of type 1 diabetics all across the world since 2015, and we have over a thousand years of living with T1D on the podcast. The interviews range from incredible feats to everyday victories, and we celebrate them all just the same. Thanks for listening, and if you want to get involved even further, just send me an email at rob at diabeticsdoingthings.com. Hello and welcome back to another episode of Diabetics Doing Things. We're telling the amazing stories of type 1 diabetics from all across the world. And my very special guest today, calling from Los Angeles, California, you might know her as Diana on American Woman TV on Paramount Network, but I know her as Jen Bartels. Jen, welcome to the show.
Jen Bartels: Hi, thanks so much. Thanks for having me.
Rob Howe: I'm really excited for this. I've been looking forward to it for a while. And I know you're super busy and just like seeing just the week you've had on Instagram. I'm very grateful that you've come on the show today. And I'm excited to not only talk to you about your diagnosis and your life with type 1, but also just do some skits and bits and have a fun conversation with a very funny person.
Jen Bartels: Oh, I hope I can be fun and funny. Thank you.
Rob Howe: Well, I have no doubt that you will. But to start out with always the least fun and funny part of our show, how did you end up as a part of this type 1 diabetes family? Because this is somewhat of a new thing for you.
Jen Bartels: Yeah, it's a really new thing. And I don't have any family members that I know that have type 1. But it gets lost in the mix history-wise. So I just was me up until a year ago. And then I had autoimmune. I have Hashimoto's, hypothyroidism. But I feel like one out of every one person has that. Yep, same. I have that. Yeah. So it's like that's just everyone's thyroid is horrible. But then I was shooting American Woman. and during filming I noticed I was losing a lot of weight not a lot of weight but a few pounds and I was being so much I was just like every night I was like do I just have chronic utis like how much cranberry juice can a girl drink and I was like no this feels weird it feels different and I was like but I also look good so I was like I guess this is being an actor you just lose weight and feel like you're dying and I really thought that for a few weeks and was like this is LA Jennifer um and then I went to the doctor and they were like you're we need to send you right away to an endocrinologist your sugars are really high and I was like I don't even I don't know I just I kind of was like diabetes I thought about it a little and sure enough I went and did a fasting test and my sugars were like 210 or something and uh then and then I I researched very heavily very quickly I'm like what other tests can you do and so they did that antibodies test to ensure that it was my own body attacking my pancreas and that it was type 1 late onset. And that was it. And then I kept filming. I had a weird hiatus. Like it just was like the universe lined up. I went on break from filming. We took a few weeks off and I was able to mentally and physically kind of accept. I don't know if I accept it, but like, I guess address it. And and the first weekend I planned a trip with uh my family um and I knew I had to start taking metformin they started me on that because my pancreas was a bit and I was like I looked at my family and I was like I get two more days I get two more days of old gen carb chubkin gen I'm eating whatever I want I'm drinking whatever I want and I went to Palm Springs and then Monday I started the meds and and that's that was the start of the journey it's interesting kind of how
Rob Howe: those things line up, right? When you're, when you get diagnosed and you have either like, for me, I was on Christmas break. So I didn't have to go to school. And you know, in high school, is that weird? Like you get Christmas, but also like the first few days of the year, depending on when the first Monday is. And so I was in the hospital from New Year's day through that like Sunday night. And then the next day, my mom was like, all right, well, you're going to school. so it was sort of this like oh yeah everybody's heard now that I was in the hospital but on day one like I'm there and I just have diabetes now like that's the thing
Jen Bartels: yeah and I think it's I don't even think I realized I think I'm still realizing the gravity and the weight that diabetes has on a person's health and physically and socially uh and I think real quickly I was like I guess I just have diabetes and I was like well here we go and only through time do you realize when you have a really bad low or a series of highs where your head is pounding or you're getting night sweats, you're like, oh, man, this is a forever little elf on my back, a little whatever. It's not going away. What were your symptoms?
Rob Howe: Very similar to yours. My blood sugar was a little bit higher. I think I had had type 1 for a little bit longer. But, yeah, I was real tall and skinny and lost like 20 pounds in two weeks and was peeing nonstop. I think I went and saw The Aviator. I always joke like, and the thing I did when I was 16 was I, and I went to the movies, I'd get a big popcorn and a big Coke. So I was drinking those and my blood sugar was probably just climbing super high. So I went to the bathroom probably every three minutes in that movie. And I was like, this movie sucks, man. Leonardo DiCaprio is overrated and all this stuff. And then I realized like, Oh, the movie's actually not that bad. I just had terrible chronic diabetes, type 1 diabetes.
Jen Bartels: Yeah. Yeah. So, yeah, go ahead.
Rob Howe: It's always, it's always interesting. You know, like you said, like, Hey, I don't feel that bad. I look great. You know, I'm, I'm just dealing with this. And then you learn, you start doing your research, right? Like, Oh no, what is, what is all this? And then you, not only do you get diagnosed, then you get told, okay, well, here are your treatment options for the rest of your life. And then you say, Oh, you have, you accept that. And then you kind of go through and you understand the day to day, like really living with it. And that's sort of where the burden really kicks in. Did you have any of that like early on where you're like, oh, no, like this is a real chronic lifelong type thing?
Jen Bartels: I think it said in over time because I was in a honeymoon phase for a while. So my blood sugars were flirting with like the 200s, which I was used to running high. So it wasn't that problematic. And and I didn't really know that, you know, running years on end can cause horrible complications down the road. So I was eating lower carb and I was taking, I wasn't even short-term insulin. I was just doing basal in the morning and at night. And then just eating low carb, I wouldn't go above 200. So I was, and I was really active because I've always worked out a lot. So it was fine until the end of last year. I got, it was just a stressful time, holidays and everything. And I think my pancreas was like, I'm good, and then peaced out. And now it's been much more I have to, unless it's really truly no carbs, my ratio, like I have to shoot for meals. And I have to monitor when I want to have a glass of wine or three and, you know, things like that. It is, yeah, I mean, there's just no taking the day off. There's never a day off. It's like, that's, what's I think frustrating that with time settles in, you're like, uh, no matter what you're, you have to deal with this. So that's, that's a realization.
Rob Howe: And I think it's really different to, you know, for people like you who were diagnosed later, later in your life, like already, you know, late twenties, early thirties, like you've lived your life, like a large portion of it with, without diabetes. So, you know, I mean, you still, right now you can remember life like old Jen, carb Jen, like you described her. I remember basically kind of not having diabetes, being diagnosed at 16. And then I have a friend named Austin who has had diabetes since he was two and doesn't know the difference. So, you know, creating that adjustment for in the middle, you know, in the middle of your very active life, you know, where you don't really have time to think about how now you have to change the way your body's going to respond to things. What is that like? What's that sort of stark line in the sand moment like oh things are different now well it's interesting
Jen Bartels: because I I think of all the children you know that uh oh my gosh I don't know what I sound like like I'm here to save everyone I think of all the children no but I do I think of all the kids that are just you know a few years a few months of being born or diagnosed with type 1 and they don't know any different and I feel like this this sympathy and this empathy for them and then I'm I'm like, but wait, in a way, they just don't know anything different. So for me, there was a mourning of who I used to be and now who I am. And it's like it's not just drunkenly eating Pizza Hut on a Friday night. Everything changes. Like I've had lows now that have made me so scared I'm going to have a seizure or no one's going to find me. And I've had highs where I'm like, well, if this goes on for days, you're going to lose a finger. Like these are things that now I'm realizing. And because I've experienced what it was. A year before, my blood work was fine. totally fine I'm so I'm hypochondriac so because of Hashimoto's and me being me and I have anxiety at times I'd go the doctor and they were just they were everyone was kind of like wait a minute you have type 1 so it was just it was a different kind of jolt that I think I had to come to term with um because I did get it later in life uh so that's that's been it has been an adjustment and so I'm like should I have would I have liked it as a kid and I'm like no it everything the universe works the way it's going to but it has been shitty can i say shitty yeah okay shitty
Rob Howe: i said the f word on the podcast a few episodes ago um i just describing myself and it was a really weird like moment i was like oh now i know what my guests feel like when they don't know that they can you know curse there's no like explicit content next to my podcast on itunes yet i think
Jen Bartels: It's like 2018. So an occasional shit or fuck is fine. I think it's turning into a Tarantino podcast about diabetes, which could be amazing.
Rob Howe: It might be. It would be awesome. It would be really gory. There'd be a lot of lost limbs. Yeah. But yeah, I mean, the kids have Instagram. They've seen shitty. They follow Kim Kardashian. Yeah. They're in numbers, right? So let's talk a little bit about your life as an actress and a comedian. You, you know, for those people like you're you. We've had actors on this podcast before. we've had Derek Theler on talking about days on set, traveling, you've just been doing a press tour. Any sort of challenges now that you have to think about outside of the general, oh yeah, don't forget to pack your insulin, that you didn't have to think before? Oh, definitely. Well,
Jen Bartels: there's such a stress being a performer. I mean, you're a performer, you know, like you're creating your business as yourself. So there's like your storefront is you. So mentally, physically emotionally you have to be ready to go at any moment and and there's so much pressure um and it's wonderful but there's a lot of there's a lot of and there is stress with it with traveling and landing safely and getting there and what's going on and itinerary and performing in front of people and then when you throw the diabetes into it uh new york was a little stressful just the last thing you know last um you know you go to these big events and these dinners and then you have to ask for a modified plate and like then it's like you want to explain why I know for me I shouldn't care but I do it's just who I am I don't want to even want to go to a restaurant when I was in New York or anywhere where I'm like can I just get no carbs or can I just get double veggies and I get like an eye roll look not that person I type 1 thanks like this isn't a joke um and then I there was a few nights with sleep and with blood sugar just because I was traveling um Um, like on the last night there, I went out with friends. I had worked, I did, I did two photo shoots and three dinners and a community day to support Viacom, which was so wonderful. And I over insulated because I'm still learning about it. So I wanted this grilled cheese from this hotel I was staying at so bad. I gotta have a wine and get that grilled cheese. And I was like, tonight's the night. Cause normally I just don't do it. Um, it's just easier. And so I shot for the, the mac and cheese cheese. Cause I really went hard. and then I was like you know what precautionary let me shoot and I hadn't even digested it and I overcompensated and I checked my blood about an hour into hanging out with my friends and it was like 57 and then it was 40 and I just started sweating profusely and I was like I'm gonna die on this trip because I've never gotten that low and my friend had to get me blood strips because I had just run out and then my friends are like are you sure you're taking care of yourself and I'm like no I am I just happen to run out of blood strips this normally doesn't happen And I'm just fun. And fun for me is like packing a diaper bag for a child that never grows up. That's what it feels like now. And then still being like, cool, fun, ready to go. So it's an extra stress.
Rob Howe: It is. And I think even more so like the friend thing, I think that just really stood out to me when your friend's like, hey, are you sure you're all right? Like, are you sure you should be doing this? And I think, you know, at least in me, like I have this like confidence and life is a confidence game and all this stuff but like i'm gonna be fine i'm choosing to do this i'm in control of my choices whether it's going out and drinking or eating a big slice of cheesecake i remember i was at our dallas comedy house maybe two and a half years ago and they had this cheesecake thing on the food menu that they added for some reason because everybody wants cheesecake from a comedy club but i was like i'm gonna eat this tonight i'm gonna show you guys and like one of my friends came up and met well i was like is that okay for you and you know so there's always those moments where, yeah, it's okay, but afterwards I'm the one that's going to have to deal with it, whether that's a big spike followed by a long crash or, hey, maybe I managed to get the first spike right but didn't dose enough and I go high in the night because I'm asleep and it's sitting there in my stomach or whatever the case is. And you can kind of spiral down the decision tree there and by the end of it you're like, wow, was this even worth it? And that's kind of the tough thing that they don't tell you when when you walk out of the hospital on day one in a world we could
Jen Bartels: all be better and we could all be to the book a lot more uh but there has to be a point where you're like i have to just live my life and i'm going to live it with these adjustments i'm going to do the best i can the majority of the time but there's going to be mistakes and my mistakes is someone else's mistakes in regards to something else so i can't i can't let it dig me and that's something we kind of talked about before we started this podcast is this idea that it defines you and And I don't think it does. It's a crappy thing that happens. But crap things and suffering happens to everyone. That is life. Then there's just pops of brightness. So you just try to run, chase, and absorb and be in those moments. And you just deal with the shit you're given because everyone at any level is given shit.
Rob Howe: I do want to say I'm thankful that you reached your only two shits per answer. Yeah, thank you. In your contract and replaced the others with craps. It was good.
Jen Bartels: thanks i mean satan island sometimes just pours out of me sorry about that no it's fine i'm just
Rob Howe: uh giving you shit um so let's talk a little bit about i'd give a talk called tools of type ones um and i've been kind of going around the country doing that this year and one of the things i try to get up at the beginning of the presentation is that you are not a burden to anyone uh that in you described your feeling in the restaurant whether it's the maitre d or the chef saying, Oh God, another person who wants more veggies and no beautiful potatoes or whatever that I made. Um, but that you, you're worth it. You are like your life with diabetes is your life and you have to assign value to that and, you know, make sure that you're taking care of yourself. Um, how do, how do you manage that? Um, with so many expectations on you as a performer and, uh, taking care of managing other things, um, how do you make sure that you prioritize like taking care of Jen and Jen's life with type 1? Well, I think like you said, I think a lot of people don't
Jen Bartels: invest enough time in self love and self care. I've been guilty of that, too, where you just, you know, you're just not the kindest to yourself, either physically or emotionally or mentally. And diabetes kind of forces you to take better care of yourself to put yourself first, because it is a life or death situation. And, and that's not dramatic, that definitely can happen with the way our bodies work. So I've always worked out. That's really important. Physical fitness is, um, is number one to me. I've always been active because not even factor in weight and trying to, you know, of course my body is my part of my job. So I want to maintain healthy and a good size and a good role model to people. Like I think you can eat and just be healthy and strong, but, um, working out's always been big. And I think therapy too. I'm really big into therapy. Like Like I just to have someone to springboard ideas or anxieties or concerns with that isn't my mom who's like, Jennifer, I don't know. It's fine. Just don't eat. So like whatever it is, like to have someone that can have a different perspective, I think that's important as well. L.A.'s been great, too. I think L.A., for all the judgment on L.A., whatever, it's a really positive place to do work on yourself if you want to. There's just a lot of opportunity to do that out here. So just try to just not anymore to do the things that a few years ago was like, I can't miss this spin class. If I do the spin class, my insulin resistance is or my insulin, I need less insulin. So of course I'm going to do a spin class, you know?
Rob Howe: Right. I think it's that's one of the first things that I notice as well. I think it's just because my life as an athlete or, you know, and, you know, insulin absorption and just feeling good and getting endorphins flowing. if I don't work out two or three times a week consistently. And I do, I have for a while, shout out to my friend Andrew, who's been waking up with me at 5.30 in the morning for the last year and a half. But yeah, you need people like that. And if he's not there, I never show up. So it's just like, because my anxiety wakes me up to not be a bad friend, basically. So you got to know yourself. But if I get a workout in three times a week and it's good physical exercise, then my blood sugars are perfect and right in line, right where they want them to be. Never perfect, but right where I want them to be. And if I miss that or my routine is off, it's such a noticeable difference. And, you know, that just creates other stress. You know, it just adds to the weight of chronic stress that the world kind of gives us today anyway. And that can be challenging, I think, especially in, you know, a world, you know, I think for women especially, like that just gives us a lot of – there's so much negative energy. There's so many expectations that are set for people that if you don't create space for your self-love and create things that you know are good for you, you can find yourself upside down on the wrong end of that pretty quickly.
Jen Bartels: If you don't do it for yourself, no one else will. Not your mother, not your father, not your partner, not your bestest friend. Like I thought that I was like pretty hungover during Christmas break. And I was like sitting there and I was like, oh, my God, what did I do to myself? And I was like, well, I can't blame anyone else for this horrible feeling. and my sugars were all over the place. And I just felt, I was just like, what am I doing? And I was like, you are the only one that can change and direct the way and choice, like the choices you want to make. Because a lot of times too, people love when you make bad choices because like wounded or weak love to hang with wounded and weak. And sometimes that's fun. You know, too many drinks on a happy hour and we're like, fuck it. Like that's fine. But overall you have to put you first. And like I said, this disease, uh, raises that bar. Like there is there's less choice and and and if that comes across as confident or or like people have been like Jen your energy is so great and I'm like yeah I had to step my game up like there was no choice for me so you know it's been a blessing and a curse you know yeah because it sort of makes
Rob Howe: you answer the call every day answer the bell right you got to go out and fight because if you don't you might be in trouble yep exactly exactly um so for you somebody who's been diagnosed so recently. I like to talk about this sort of time we're living in as it's definitely the best time to have ever had type 1 for a number of reasons, one of which I think is the social media community and kind of being able to get connected. I know that you have been more outspoken recently about, you know, diabetes activism and creating awareness and sort of using your platforms to do that. What did you find when you were diagnosed and you sort of looked and said, okay, where do I go for information and community? What was that like for you?
Jen Bartels: I felt pretty alone. I felt really alone. And you're just kind of left with these tools and this diagnosis. And my endocrinologist is great, but they speak to you like you should know. And I'm like, I don't know what's going on. I don't know. I have to shoot myself up every day. And I had to start poking myself. And then I had to watch carbs. And I was like, what does this all mean. So, um, and I was in the middle of shooting and my family was here. I didn't have time to just go to a support group and like, here we go. So I did a lot of like researching online and I was like shadowing you and other people. And then through other people through time on Instagram, like kind of a weird diabetes stalker because I was like, well, I can't come out that I have type 1 diabetes because people are going to think I'm weak or people are going to think I'm sick. act, I don't know what people are going to think because I totally don't look at it the same way anymore. But, um, I felt like it was a weakness. Like it was why me? And, um, and then I was following, uh, you know, just my type or you're just my type. And I was following happy pancreas and all these people. And I was like, they seemed like they really got it together. And, and then I think was at the beginning of this year, I, I had this photo shoot I did for myself. it was kind of cathartic at the end of last year. It was like this sexy bardois or boudoir thing. But I was like, I want to get a shot of me shooting up. But like sexy and fit and tone and strong and a woman. Also, I have diabetes. Also, that's something I have. And then I posted the picture. Like I had I was like, I'm doing it. I'm going to also be an actress that's a performer, a sister and then a friend. And I have type 1 and I posted it and everyone like loved it. And I and I was so surprised and I felt so supported and people you came everyone was coming out and being so kind to me and then I really started to see the community that is online and that's been the most helpful is is feeling not alone by seeing the journeys that the other people are not you know are willing
Rob Howe: to share so that's been great I want to I mean you're a performer and you know vulnerability is just part of what you do um in that moment though that like that posting that photo like first of all like coming up with the idea making the photo shoot happen like and doing it that takes a little bit of like a certain mindset like you that's obviously I think part of the acceptance process um for you like for you what what made you decide that that was the thing
Jen Bartels: well I feel like a lot of times as performers we are given a platform and we I think maybe not everyone, I can't speak for everyone, but a lot of the people I surround myself with have a great platform and like, or excuse me, have a great cause that they're really passionate about. And I'm, I'm a lover of so many things. I was like, what is my voice? What is my thing? And then I kind of just woke up and was like, I think type 1 is part of my thing, raising awareness for kids and performers and people that get it late in life and people that are down and out or depressed for the day and, and to show them that, yeah it sucks but it's okay and this look what else I'm doing and look what else you can do um I'm putting a face to it uh while it not defining you so like I think I just was like this might be one of my things that I as I hopefully gain momentum and acclaim for my work and my art I can help like the brilliant things you do and the brilliant things other people do that I care about that have type 1 and raise awareness and and step up our technology because when I became type 1, I was like, I'm sorry, are we in the eighties? I just like, I don't understand why we are where we are with like these big ass pumps and, and, and the Libre, which works. But then sometimes I'm like, this is lying to me. It's just this whole thing. And, um, unless you're in it, like we could just be farther and I know why we're not, but we,
Rob Howe: it's a business, but anyway, what did they give you? What did they give you when you got diagnosed? What was your, like, do you remember your meter and you're like, you're on obviously syringes and and vials and multiple daily injections?
Jen Bartels: I still do MDI. So I do multiple injections. I do the pens. So the pens are fine, but they get sticky. So I always have to waste one shot, one little thing with, please don't be plugged. And then I like-
Rob Howe: I guess that's what you, do you play with Gak a lot? Is that like, what kind of sticky lifestyle? Do you live a sticky lifestyle with your- What does that mean? I don't know, with your pens getting sticky. I don't know. I'm just-
Jen Bartels: Oh yeah. Oh no, no, no. I mean, yeah, I guess they, They get sticky, and then they stick me. That's all I know. I try not to think about it. But I have the OneTouch, the little meter, and then I just do the MDI, basal, and bolusing, and all that jazz. And I'm not going to do a pump for now. My endocrinologist is like, pump, pump, pump. And I'm like, no, that's not what I want to do right now. And it might be a little stressful for me, but it's just everyone has their own choice of what they'd like to do. And I think as a woman with fashion and with costumes, yeah, I'm not there yet. And I hope we can keep improving so maybe none of us are there. And then I did the Libre, and I documented it on a live Instagram video. I did the Libre doing it the first time because I was so scared to do it. I was like, I went live. I've never gone live. And I went live, and everyone was being supportive. And then I did that. And I actually enjoyed the Libre sensor when it works. It's great.
Rob Howe: yeah I think it's it's always interesting backing up to what you said before about hey type 1 is who I am like because I had a very similar type of reaction when I decided to to get more involved in the community it never occurred to me before that me having diabetes was like a and it made me accessible to this community or was anything worth writing home about that was never I don't know I just didn't look at it that way and then I was just thinking like oh I really love helping people, that's when I'm probably the happiest. And I was like, Oh, actually, this makes sense. Like, it's like authentic, it's real. It's like what I know, and I can maybe help people. And then I just discovered like, if you're having a bad day, or you have something to say, like you can just, even if it's as simple as sharing a, you know, installing a sensor or a bad blood sugar, or a high blood sugar, low blood sugar, and people are just talking about it there. And there, I much more open to vulnerability than I thought they would be. Maybe that's just fear, you know, creeping and telling you lies anyway. But man, just like I, the community is so open and I think so supportive. And it's one of those things that doesn't get talked about as much in the social media realm, because I don't think a lot of people know about it. Unless you're plugged into it, you don't know. And so, you know, being welcomed into that, I think is a great way to, you know, learn about technology. I got a Dexcom for the first time last year, and I don't use it anymore. Now I'm on Medtronic 670G. But because somebody after an interview was like, hey, you don't have a CGM. Why? And I was like, oh, well, I don't think I want another site on my body. And I fought the pump for years because it wasn't sexy. And I was 19. And I was like, bro, I've got to have abs and girls and stuff. And so that was super important to me. And I also thought you had to have surgery to put it on. It was a, it was a long story, but I kind of felt the same way. I was like, I don't know if I want another thing in my body. And she's like, you should try it. You'll love it. And she was right. And I was like, well, if I hadn't been plugged into the community, would this have ever happened with this conversation? Have you ever happened? And so, you know, it's kind of an interesting thing. It's like, I almost feel like I benefit more from the help of others than they benefit from anything that I do.
Jen Bartels: Oh, well, I think you've done, I mean, just the foot, the stuff I've seen that like the footprints you've made, I think it is so amazing. But I, I think, yeah, including you, this community has been so open to even the Libre. I was like, what is that? What is this little quarter thing? And then how do you do it? And then I just asked my doctor and I was like, what's this new sensor? And then I reached, we're, we're, we're tapped in as a community and everyone is not afraid to put out there. Like you said, I also think it's really cool because everyone is kind and welcome for the most part and like we're kind of all in this together and it helps break this stigma. Like, you know, we're performers, we're photographers, we're running businesses, we're fitness people, nutrition people. Oh, we also have type 1. And so it's changing the face of diabetes, especially type 1, which that's a thing too. I try to rise above that. But when someone's like, oh, but you look great. You have diabetes. Just did you not eat well? And I'm like, OK, there's so much to unpack right now and what you just said. you don't even realize that it's very offensive. So then I have to try to sit with that. And so again, it's nice to have a community where you're like, oh, I've been there. Yeah. And like, this is how you can talk to people about it or it's not worth it, you know, or just you feel less alone. I think that's the biggest thing is when you're given something like this that a lot of people around me don't have. It just makes you feel like people get it. And it's like, fine, it's better. It's okay.
Rob Howe: What do you, you know, what are you hopeful for? When you think about your life with diabetes, obviously like a cure, none of us want this anymore. We obviously want devices that are less intrusive and better care and better awareness. But for you, for Jen, like what is your successful life with diabetes? Like what do you dream of with that? How does that look? That's a big question.
Jen Bartels: Go ahead. I'm sorry.
Rob Howe: I said that's a big question. I get it.
Jen Bartels: I like my life now. um it's been it's interesting that with diabetes and all of the fun but crazy success and coolness of this career that's like in a different level now or taking me to another level it's just so wonderful I'm so thankful but like I feel stable and I want to continue to create opportunities for myself and others uh like I've written and produced stuff that's really important to me as a performer and I don't want diabetes I don't even want to say that to get in the way of that because that to me means I hate it and I have to accept it. So it has to just come along with me on this journey and my hope is that I can bring it along and shed light on it and gain enough power or voice within this world to have someone, like have people, like I can shed light so we can get somewhere with technology. Of course we'd love a cure but realistically, I'm honest with myself, I just think we can be farther than where we are with technology. I'm just, I was so appalled. I was like, wait, what, what is that big thing on you? And it just, it's like the technology hasn't changed as much as it should have when I feel like we're, we have flying cars. I don't understand. Or, you know, cars that drive themselves, excuse me, whatever. You know, like it's, I get it. I see the ugly side of big pharma and all of that. But if there's anything I can do to shake hands or smile or attend an event or speak to people that can help all of us, I'll do it. I want to do it. I want to do that.
Rob Howe: Yeah, and I mean, we need that. I think now representation is something that's new for type 1 as well. Certainly, we've had people in the past, and now we have Nick Jonas, and he wears a Dexcom on his six-pack. And we have, you know, Victor Garber, who's, you know, does has done other stuff besides Without a Trace. And I think, you know, we have Derek Theler now and he's a real life superhero and a great role model for kids. And these people are speaking up and hopefully, like you said, like changing things and creating or meeting the right person or shaking the right hand at the right event and making a difference at a macro level. but you know all of us as well like newly diagnosed like you mentioned it's only been like a year and a half right for you a year yeah about a year actually so about a year and like the amount that your life has changed and i think even just mindset in the last year um we all go through that at some level and so what i like now is that there are people like you who are in that first year they're already stepping forward and using their voice for good and that's something this wasn't possible 10 years ago, 20 years ago. And it gives me a lot of hope, I think, for where we're going to be in 10 years, where we're going to be in 20 years. And hopefully we can just have some big Jamaica sandals retreat with a bunch of people that used to have diabetes and we can all, you know, jump around a campfire or something. Yeah, I used to have it. So we're just pounding
Jen Bartels: pina coladas and pizza. Yeah, I want to be a part of that. And I do agree, like it really is breaking this stigma or this idea. And there's not enough people. Like I remember the first thing I Googled was working actors and Hollywood people who have diabetes. And like I couldn't find much. And there were some people that were like, yeah, but it's type 2. But they got it from a role because they gained weight. And I'm like, why is everyone being so vague? Like I don't. And then I was like, and that's when I kind of reverted. I was like, don't say anything because maybe no one talks about it. And, you know, you're doing a stuff with this show. And I'm like, I just, like I said, I woke up. I was like, nope, no, no, I have to. Like, I read a few books from Mary Tyler Moore, and that really moved me as well. And what she did for type 1, but also just being a comedic, funny, brilliant, empowered woman who happened to have type 1, you know, and wasn't perfect by any means. But that's what I want to do. So it's cool to talk about this.
Rob Howe: It is. It's good. It's cool to hear people get fired up Especially badass cool people like yourself I love it It's one of my favorite things about The decision I made to get involved I ask this question to everybody And it's context is important But you can totally reject the context if you want Because people have and it's fine It's basically I just get dunked on in my own question Which is how I look at it But You're in an airport And you're about to catch a flight and they're about to close the door to your gate and you bump into somebody with type 1 who's either been recently diagnosed or is struggling and kind of maybe struggling with acceptance and you can't miss the flight. Whatever's on the other end is super important. What's the one thing that you say to them in that 30 seconds before they close the door to the gate?
Jen Bartels: I would say that you, what my late grandmother said, you can only take one day at a time. And the biggest thing you can do to yourself is to stay present because when you think ahead about anything personally or health wise or professionally it creates anxiety and whenever you think about the past even things that you loved about the past it makes you sad and it can bring on depression so stay mindful and stay present and that puts things in a perspective and then I'd probably give them my contact information and say when I land go ahead and reach out to me and I'll get back to you and we can take this conversation offline or I've done that for a lot of people if I connect with you know if you seem like a crazy you know let's be real i gotta watch my stuff here but uh but yeah no if there's something that we're connecting on and they're looking for guidance or um trying to align with someone and i can be there for that yeah and i'll probably be realistically a half a xanax and a half a glass of wine in because if this is a true plane ride i'm already gonna be a little looped out and listen to some hip-hop on my beats and then i'll be like really nice probably overly nice and then i'll get on my plane
Rob Howe: uh and let's let's be honest there are certainly super crazy people with type 1 and a lot of them listening to this podcast and I'm so grateful for you guys and y'all scare me. Jen, thanks so much for coming on the show. Thank you. It was my pleasure and I'm glad we were able to make it happen. I know you're super busy and, but you know, for you to be here with us and be present, to be here now, shout out Ram Dass. And then, you know, to really be, you know, only a year into this lifelong journey that we're all on and to be as inspiring and empowering as you are. It just says a lot about you, and we're happy to have you in this family.
Jen Bartels: Well, thank you so much for opening. You've just been so kind via social media, and thanks for everything you're doing, and kudos to you for being an awesome performer and making this one of your causes in life. Yeah. Oh, and can I plug my show? Is that gross and hollow? No, no, no.
Rob Howe: Please, I was literally going to ask you to plug it and plug your Instagram, plug everything. Plug your side projects, plug your, you know, anything you want.
Jen Bartels: Well, I'm really proud of this one, guys, because it's been a long time. So American Woman comes out on Paramount Network on June 7th at 10 p.m., and I'm very excited. It's with Alicia Silverstone and Mena Suvari, about three women trying to find their voices in the 1970s. uh side wise i'm just really focused on the show and writing new materials to sell as tv shows to give opportunities to other people and my handle is at the jen bartels j-e-n-b-a-r-t-e-l-s and i'm here if you need a fellow type 1 to talk to or connect with or feel supported by
Rob Howe: oh that's awesome and i hope people will take you up on that offer and we'll definitely watch American Woman as it comes out later this summer. That's super exciting.
Jen Bartels: Thank you. Thanks so much for taking the time.
About Jen
Jen Bartels is an actress who played Diana on American Woman on Paramount Network. She was diagnosed with late-onset type 1 diabetes about a year before this episode, while filming the show.
