Jeanne Martin as a teenager

[podcast src=”” width=”100%” scrolling=”no” class=”podcast-class” frameborder=”0″ placement=”top” primary_content_url=”″ libsyn_item_id=”15989381″ height=”90″ theme=”custom” custom_color=”3e9ccc” player_use_thumbnail=”use_thumbnail” use_download_link=”use_download_link” download_link_text=”Download” /]Jeanne Martin was diagnosed with type 1 diabetes at age ten, in the 1950s. Technology was very different back then, of course, but so was the medical community’s reaction. Jeanne was told she would never have children and if she did, she wouldn’t live to see her children grow up. Today, Jeanne not only has a daughter, she’s also a grandmother. She shares what she’s learned along the way. We also talk to Jeanne’s daughter Jessica, who talks about growing up with a parent who has type 1.

In Innovations, find out why when it comes to keeping track of long and short acting insulin, a CDE says invest in rubber bands.

This podcast is not intended as medical advice. If you have those kinds of questions, please contact your health care provider.


Other episodes with amazing people living long and happy lives with T1D:

Richard Vaughn was diagnosed in 1945

Judith Ball was diagnosed in 1941


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Episode Transcription

Stacey Simms  0:00

Diabetes Connections is brought to you by One Drop created for people with diabetes by people who have diabetes. By Real Good Foods real food you feel good about eating and by Dexcom take control of your diabetes and live life to the fullest with Dexcom.


Announcer  0:24

This is Diabetes Connections with Stacey Simms.


Stacey Simms  0:30

This week, Jeanne Martin was diagnosed with type one at age 10. Back in 1955. She’s had to fight a lot of doctors along the way, including one who told her she would not live to see her child grow up.


Jeanne Martin  0:45

And my reaction was I told my husband that guy can go walk up the street and get hit by a bus tomorrow. I’m not going to go along with that. That’s was my reaction. I got mad. I didn’t buy into it. I didn’t get depressed because I Just thought he was full of baloney.


Stacey Simms  1:00

Jeanne was right. She’s now a grandmother. And she shares what she’s learned along the way that made her question and stand up to doctors like that. We’re also joined by her daughter, Jessica, who shares with like growing up with a parent who has type one

in innovations this week why a diabetes educator says invest in rubber bands. This podcast is not intended as medical advice. If you have those kinds of questions, please contact your health care provider.

Welcome to another week of Diabetes Connections. I am so glad to have you here I am your host, Stacey Simms, and we aim to educate and inspire about type one diabetes by sharing stories of connection. My son was diagnosed with type one right before he turned two that was back in 2006. My husband lives with type two diabetes. I don’t have diabetes. I have a background in broadcasting and that is how you get this show. I spent 20 plus years and local television and radio news.

I’ve been doing this show for more than five years now and I don’t remember Ever putting the topic of the show to a vote, but I did that for this week, I put up a poll in our Facebook group, it’s Diabetes Connections, the group, I have a couple of interviews. I’m usually a few weeks ahead with interviews in the can. And I asked the group to vote on which interview they wanted to hear next, and everybody chose Jeanne, I cannot say blame you. I am always amazed at the strength of these people, the stories of people who are living well with diabetes for 50 60 70 years. I mean, you think about it, before blood glucose meters were a thing. I mean, they weren’t available to the 1980s. And this was a time that we’re talking about with Jeanne before some doctors would even know about different types of diabetes. I was shocked to learn that that for a very long time, it was just diabetes and you treated it with a one shot a day, or then they would say juvenile diabetes. And you couldn’t possibly have that if you were an adult and you’re just on and on.

And if you’re new to the show, I’ve done several interviews with people who were diagnosed in the 50s in the 40s. And they’ve lived with type one for 70 years. And I will link those up with this episode. You can also search with a very good search engine at Diabetes We’re up to more than 320 episodes. So if you want to Google keywords like living long or 60 years with diabetes, that sort of thing. You can find that on the website.

Before I get to the interview. I want to read something that was sent to me it’s actually a review on Apple podcasts. I’m really bad at asking for reviews and keeping up with reviews. If you want to leave one up man, I would love it. Whatever podcast app you listen on, there is a way to leave a rating or review. This one came in from Shelley. Now her name is not on this but I know who this is because we featured her. We featured her son in a recent show. So Shelley wrote I love this podcast so much. I learned so much from listening especially enjoyed the tech episodes with Dexcom and Tandem etc. As the mom of a newly diagnosed four year old. I have found much needed encouragement and tips for helping and thrive with diabetes. Also, cannon was excited to hear you mention him swimming in the lake. Surely thank you for writing that. Yeah, we talked about cannon she had sent a picture into the Facebook group about him burning off the glucose. She said swimming in the lake pan swimming is one of those ways where Benny used to just those little kids just swim with every part of their body. They used to go low all the time in the pool. It’s a little bit different. Now you know, a 15 year old does not swim like a four year old. But surely thanks for sending that review in. It’s always nice to get reviews like that. And if you like the show, truly the best thing to do is to tell somebody about it tell somebody in the diabetes community. That’s the best way to get the word out.

All right, Jeanne and her story in just a moment but first diabetes Connections is brought to you by One Drop, getting diabetes supplies is a pain. Not only the ordering and the picking up but also the arguing with insurance over what they say you need and what you really need. Make it easy with One Drop. They offer personalized tester plans plus you get a Bluetooth a glucose meter test strips lancets and your certified diabetes coach, subscribe today to get the test strips for less than $20 a month delivered right to your door. No prescriptions or co pays required. One less thing to worry about. not that surprising when you learn that the founder of One Drop lives with type one, they get it One Drop gorgeous gear supplies delivered to your door 24 seven access to your certified diabetes coach, learn more, go to Diabetes and click on the One Drop logo.


I feel like I’ve known Jeanne Martin for as long as my son’s had diabetes. That’s almost 14 years. And that’s because while I have never met Jeanne in person, I have been friends with her daughter Jessica Graham for even longer than those 14 years. We met when Jessica was in public relations here in Charlotte, and I was working as a health reporter for a local TV station. And later we were on the board of our local JDRF chapter together. I cannot believe it has taken me this long to share Jeannes story. She is just incredible. I was able to talk to Jeanne and Jessica, about living well with type one for 66 years. Jeanne and Jessica, thank you so much for joining me. I’ve known Jessica for so long, but I don’t know so much of this story. I’m so excited to talk to you both. Thanks for coming on.


Jeanne & Jessica  6:17

Thank you for having us. You’re very welcome.


Stacey Simms  6:20

Jeanne, I got to start with you. Because you have lived with type 1 diabetes now for more than 65 years. Let me just start out by saying How are you? How are you doing?


Jeanne Martin  6:30

I’m doing great. I think I’m doing just fine.


Stacey Simms  6:35

What do you mind if I ask what technology you use how you manage anything you’d like to share?


Jeanne Martin  6:40

Well, I checked my blood sugar with little contrast test strips. And I shoot nice. Well, I take shots


Stacey Simms  6:49

you can say brands, we’re all friends here.


Jeanne Martin  6:51

Yeah, I say I shoot myself


four times a day. I see my doctor every six months. Well, that’s about it.


Jessica Graham  7:01

She does not use a pump or


Stacey Simms  7:04

any of that. No, if you don’t mind, let’s go back. Do you remember what it was like when you were diagnosed? You were 10 years old. Do you remember anything about that time?


Jeanne Martin  7:13

Oh, yes, I do very much. We lived in a very small town, not far from the Mayo Clinic. We just lived there a couple years. My friend’s mother mentioned to my mother that I was drinking a lot of water and going in the bathroom a lot and she thought maybe my mother should have me checked out. So we did in the small town with the with the doctor there said, Well, she’s either got diabetes or TB. Well, I didn’t know what diabetes was. And I knew what TB was. So I thought, Oh, please don’t i don’t want TB. I’ll have the other and so so the little basically country doctor didn’t know what to do. So anyway, so they sent me to St. Mary’s, which is public Have the Mayo Clinic. And they tested me and for sure that’s what I had. So I had to stay there. I think it was five years. I didn’t do all this stuff with the diets. And they wouldn’t let me leave until I could get myself a shot. But I was active. And I don’t really remember too much about it. The doctor were very nice, and everybody was very helpful. And back then you had glass syringes and needles and you couldn’t check your blood sugar. You had to pee on the stick, and they sent me home and my mother had to weigh everything, and I had to watch what I ate. But other than that, that’s about it. Then I just basically went on with my life. Did you


Stacey Simms  8:46

really? Were you able to jump back in go to school, do all the things you wanted to do with that time?


Jeanne Martin  8:51

Yeah, I did.


Stacey Simms  8:52

Mm hmm. It seems like such a different time, right. I’m just trying to think,


Jeanne Martin  8:55

Oh, yeah, it was a very different time and when I first got married, Remember, I had to boil my syringe once a week, we had to do that. And I was still peeing on a stick. And I only had one shot a day back then all through, you know, school. And of course, I didn’t want to tell my friends when I was in high school. That’s what I had. But of course, my mother told my best friend’s mother. So everybody knew it, but I didn’t know they knew it. Oh, wow.


Stacey Simms  9:25

Anyway, moms are sneaky that way. But yeah. The you know, the regimen was so different. You had one shot a day, right? And then you had to kind of eat around that shot. Did you have problems as a teenager? Did you do remember, you know, any issues or were you able to buy I would assume by routine and by figuring out what to eat, you know, how did it work out for you?


Jeanne Martin  9:47

Well, I didn’t run into any problems when I was a teenager. And I do remember I don’t know how I would go not very often, my friends and I and I would have hot fudge sundaes. Believe it But other than being bad like that, I lived at home and my mother, kind of watch what I ate. And I didn’t need a lot of sweets. You know, it was my mother’s management, not mine. And I came home for lunch all during school. And I didn’t start taking more shots until about, oh, I don’t know, maybe 45 40 years ago.


Stacey Simms  10:23

Yeah. It’s so different to think about because we’re talking about I mean, if doing my math correctly, you were diagnosed right? In the early 50s 1950s.


Jeanne Martin  10:30

Right? And 1955


Stacey Simms  10:33

Yes, so the routine was completely different. I mean, as you’re listening, you got to understand not only one shot a day, but no blood sugar home meters, right. You’re still checking. How often did you check done by check? We mean, pee on the stick.


Jeanne Martin  10:50

I probably did it maybe once a day. I honestly don’t remember that. Not a lot. It’s very different now. And somehow, I think my pancreas has always worked a little bit because I don’t take much insulin. And I’m very, I don’t want to say touchy with it, but I don’t have to take a lot. And when I was diagnosed at the Mayo Clinic, they said that yes, my pancreas was working a little bit. That’s what they thought. And I still think that’s the case because I just don’t need much insulin. And and I watch what I eat. I do, but you know, I’m not 100% I mean, I do have cookies,


Stacey Simms  11:30

but you’re told us you were eating hot fudge sundae. So the cat is out of the bag…


Jeanne Martin  11:35

That was in my youth. You know, I do take care of myself. Now. I check myself four times a day, shoot up four times a day and I watch myself better now because I know better. I’m more wiser.


Stacey Simms  11:48

I’m curious to growing up. Did you know anybody with Type One Diabetes and if not, when did you meet somebody with no,


Jeanne Martin  11:55

I never knew anybody. I didn’t know anybody with any kind of diabetes. It wasn’t in my family, so none of my relatives had it. No, during high school I did not know, as an adult. I have met very few type one diabetics, I know they’re out there, but very few. And it’s kind of fun when I do just to kind of say, Well, you know, compare notes, so to speak. Sure.


Stacey Simms  12:21

Just let me ask you a couple of questions. Because the perspective of a kid, you know, we’re all adults now. But a child growing up with type one in the house and the type one is in the parent is not something that I’ve talked a lot about on the podcast. What’s your earliest memory of your mom and diabetes?


Jessica Graham  12:38

Well, I don’t ever remember it not being there. And that was more because I worried about her than it was her. There was never literally and I’m, I mean, this literally, there was never a day when my mom said, Oh, I don’t feel well or Oh me, you know. My sugar is off, or I just don’t feel good today, never. And so it was nothing that she did. I just knew that if mom started acting funny, I needed to get the orange juice. So I remember that I never had a problem with shots. And I think that’s because I always saw you give yourself a shot. So it was just, it was always there. The other thing that I remember is that I was always told that it skipped generations. And so I do remember I don’t even know if you remember this. But I remember at one point when I was little, I told mom that I didn’t want to have kids until there was a cure, because I didn’t want my kid to have type one. And I she got really mad. My mom never got mad. But she got upset at that and told me that was absolutely you know, the wrong attitude to have and that she had a great life and it didn’t have any impact. And so that was the end of that but it was just always there. So just always a part of life. Jeanne, I’d love to hear your perspective. On when Jessica who now has a I want to say a tween a teenage Yeah, yeah. just turned 13 Yeah. Wow.


Stacey Simms  14:07

I want to hear your reaction Jeanne to when she said that!

Right back to Jeanne answering that question but first Diabetes Connections is brought to you by Real Good Foods. True story from my house. Benny came downstairs the other night, open the freezer door, looked in it close the door and said who ate the mint chocolate chip ice cream. And I had to say it was the I finished it off. Sorry, Benny. But they’re Real Good Foods. Ice cream is really good. We had a vanilla chocolate and mint chip this last time I promised him I would buy more and I have to get the peanut butter kind as well. We haven’t found the ice cream yet in our grocery store freezer so I get that online but our grocery store carries a lot of the meals and they are so good and super easy and basically just heat them up. If you have an air fryer. It’s even better They have everything from pizza to breakfast sandwiches to bowls, these new bowl meals that are really nice entrees. Find out more, check out that mint chocolate chip ice cream for yourself. It stays frozen. They they package it up the right way. I was worried about that, but no need to worry should have known. Just go to Diabetes and click on the Real Good Foods logo.

Now back to Jeanne answering my question about her reaction. When Jessica told her she was really concerned about having children.


Jeanne Martin  15:33

Well, I didn’t want her to dwell on it. And I didn’t want her not to have kids. You know, it’s so much more advanced nowadays. And there’s so much more that they can do. And I always do hope for here. I mean, I’ve been hanging on that for a long time, but you never know, one of these days. No matter what your problem is. You just have to get along and do the best you can and get along with your life and not dwell on it. And I’ve never dwelled on it.


Stacey Simms  16:02

Well, I’m curious too, because now we know and I’ve heard that too. it skips generations. We know it absolutely does not. But I’m curious Jeanne, you know, when you decided that you wanted to have children? Did anybody try to talk you out of it? This was a very different time for diabetes.


Jeanne Martin  16:14

Well, I was told that I would have a hard time having a child. And so we put up for adoption. And we were waiting to hear and I went to the doctor and thought I had a tumor but the tumor was Jessica. So I thought, okay, so we said, you know, we were going to have a baby so we don’t need to adopt and they said, Well, why don’t you wait to see if everything is okay. And I said, okay, because the doctors told me that Jessica only had a 40% chance of being born alive. So we waited and she was screaming and kickin, so she was Fine. So we stopped the adoption because we didn’t need two babies at one time. And I didn’t see her for I think it was like two or three days. She was in an incubator because her blood sugar was low when she was born, but then after that, she was fine. And I was fine. And that’s it.


Stacey Simms  17:19

I’m sorry. I’m still on the tumor.


Jessica Graham  17:24

Well, and I’ll add to that, because, you know, she won’t tell you this part, but because she was diabetic, she couldn’t have any medicine or or painkillers. When I was born, and you were in labor, what, 24 hours? No, no,


Jeanne Martin  17:39

it was, I don’t remember 13 hours. So it was a


Jessica Graham  17:42

ridiculously long and I was stuck behind a piece of cartilage. And so I wasn’t coming out. So she went through hell delivering me. But it all worked out. Yeah.


Stacey Simms  17:54

Oh, worked out. things really have changed. I mean,


Jeanne Martin  17:58

Oh, yes. And I also was I would not live to see my child grow up. Now I’ve got a 13 year old grandson.


Stacey Simms  18:07

But let’s talk about that, because I’ve heard that from so many people diagnosed not only in the 50s, but even as late as like the 70s and 80s. This Doomsday of you’re not going to live past 30. And I know that for many people, that unfortunately was the case, there was not the care. There was not, you know, whatever they needed, but it seemed as though in some ways, the doctors, I don’t know, I don’t want to editorialize here, but they seem to have this Doomsday approach. And when you were told that Jeanne, what was your reaction? I mean, I think a lot of people would have said, well, what’s the point? Oh,


Jeanne Martin  18:37

I’m kind of stubborn.


And my reaction was, I told my husband, that guy can go walk out in the street and get hit by a bus tomorrow, and I just, I’m not going to go along with that. That’s was my reaction. I got mad and he did die. A younger The age that I am now is a matter of fact, the guy that told me that I didn’t buy into it. I didn’t get depressed because I just thought it was full of baloney. I love it.


Stacey Simms  19:10

All right, this is getting interesting now. I do love it. Jessica. I know your mom is sitting right there. But you’re doing great Jeanne, obviously with with your shots and with your checking, but the technology has advanced. I’m going to assume, Jessica, that you guys have had a lot of discussions about this. And your mom has said no. And you’re respecting that don’t put words in your mouth. But I’m curious how have those conversations happened?


Jessica Graham  19:36

Oh, yes. And I don’t mind saying it with her sitting right here. So I don’t mind that she doesn’t do the pump because I understand. I mean, she’s had incredible control for 60 some years and so i don’t i don’t blame her that but I want her to have a blood sugar monitor because she tends to go away Low, and she goes low at night. And it’s been a problem as I call it a problem. Whenever she goes low it to me it’s a problem. And so while she keeps great control, and I mean, it’s her life, right, and it’s her decision to make, I wish that she would get some of that electronic help with the monitoring of it. So yeah, we have that conversation a lot. But I lose.


Stacey Simms  20:26

That’s a difficult situation. You know, we, as parents of children with type one have these conversations, especially once there were certain age, and I’m going to say, as young as four or five years old, where it really has to be up to the person to buy into it and say, Yes, I want this technology. And I would imagine and I’m just imagining having this conversation with my mother, who I think you have a lot in common with with Jeanne. And I think it would go that well. Yeah, well stubborn, but also you’re doing very well.


Jessica Graham  20:52

Yeah, and Exactly. That’s why I mean at the end of the day, what am I going to do right now I can only put in my two cents but that that is is the one thing that I wish you would do. And my dad to his credit. I mean, he’s kind of grown up with this too, right? And so he’s a great monitor strangely, he knows when it’s the middle of the night and she’s having a hard time. But I don’t like to rely on that.


Unknown Speaker  21:17

But again, I lose


Jeanne Martin  21:19

stubborn. Well, let me cut in here. But the doctor prescribed a new kind of insulin that I’ve been taking. I don’t know six months now and I have not had any trouble at night. Oh, good.


Stacey Simms  21:32

We don’t have to use it in the show. Are you taking Tresiba?


Jeanne Martin  21:34

It’s Tresiba. Yeah. And I have not had any trouble at night. Since I’ve been on that. Yeah, that’s a good thing.


Stacey Simms  21:41

But my son uses an insulin pump. But long story short, we had him on Tresiba with the pump for a while because teenagers use the most ungodly amount of insulin that you could imagine. He’s coming out of it. So we did away with the trusty bow, but boy, it’s like the best long acting we’ve ever used. I’m curious too, and the bridge kind of skipping around chronologically. Hear but I mentioned earlier that there were not blood sugar meters for home use when you were diagnosed. Do you remember when you started using one of those maybe the 80s


Jeanne Martin  22:09

Well, I thought it was great because then I really knew what was going on. I mean it just it was very helpful because and that’s why I checked myself a lot because you can’t guess how much it’s I mean, you can guess kind of how much insulin but you really can’t without knowing what your blood sugar is to my mind. I mean, I think that’s what’s helped me keep control in Yeah, I don’t like to stick my fingers but I mean, I’m so used to it now just comes second hand to me, so it made a big difference. What really made a big difference to is having plastic syringes that don’t have to boil. Tell me


Stacey Simms  22:49

more about that. When did that switch? Not Not Not necessarily like what year but tell me more about that. What do you remember kind of the transition? Did you just one day throw all the glass ones out? What happened? Right


Jeanne Martin  23:00

Yeah, I did. I guess the doctor told me that these were available. And so I bought them and and use them. And then you know, he used it, throw it out. And it just, it made a big difference. It’s just like, oh, gosh, you know, this is getting easier. Well, and you know, it was a lot easier. I mean, it sounds like a small thing, but it was a no to boil, you know, syringes once a week and needles once a week. And so this was great.


Jessica Graham  23:28

When did you I don’t remember you ever boiling? Was that in the 60s or


Jeanne Martin  23:32

70s? No. Well, I must know. I don’t think when you were born. Other times, I must have used the plastic ones. Yeah. Because I don’t remember doing that either. When you were born.


Stacey Simms  23:43

You know, Jeanne, it’s interesting. You said it seems like a little thing. I think for someone who has my perspective. My son was diagnosed in 2006. When we basically have I think we have all of the technology. At least it was on the drawing board if not available at the time. It wasn’t as good as it is now. Just 1314 years later, but it was there. And so to think about transitioning from peeing on a stick to a blood sugar, meter glass syringes, to plastic syringes, these are monumental changes. I don’t think it was a little thing. I can’t imagine how much of a difference that made. I mean, the needles had to even feel different. They were more comfortable, I assume.


Jeanne Martin  24:20

Oh, well, it was it was like one size needle with the glass syringes, and they weren’t that small. And now, you know, you can get all different kinds of sizes. Jessica, do you remember growing up?


Stacey Simms  24:32

It sounds like your mom’s diabetes was not front and center, as I’m sure she would not have wanted it. But are there any things that stand out? You know, when you were a teenager? I’m trying to think his parents are just super embarrassing to begin with?


Jessica Graham  24:44

Honestly, no, because it just my mom wouldn’t let it be the center. I mean, you’re absolutely right about that. She she would never have wanted that. And I don’t remember there being anything that happened when I was a teenager. That was odd. She She had one episode. I guess I was a teenager when you broke your ankle. She was we discovered that she couldn’t drink champagne. She had a glass of champagne. I mean, literally a glass and the next morning passed out and broke her ankle because it messed up her blood sugar so badly that I don’t remember anything ever. Embarrassing or weird or no, not not at all again, I I remember when I was a younger teenager, like if you started acting strangely, I needed to get you orange juice like I vaguely remember that but and that went for anybody. Like I think if anybody started acting strangely, I would have ended them. Shoes. But


Stacey Simms  25:43

  1. Jeanne, did you have a career did you work? Did you work at home? Tell me a little bit about what you you know what you did?


Jeanne Martin  25:49

You know, I work during high school, I worked at clothing stores and I worked at a bakery. And then after school, I worked at a real The state office. And I guess that was it because it was the board of realtors, because I had to quit them when I got pregnant with Jessica. So that was it. And then when my husband started his company, I worked for him. I did the payroll and things like that.


Stacey Simms  26:19

Jessica, what led you to JDRF? I mean, we had met Previous to that, but we connected again at the Charlotte chapter.


Jessica Graham  26:25

I led community outreach for Harris Teeter, but didn’t formally get involved. They were supportive of JDRF, but didn’t formally get involved in a board capacity until I got to Time Warner Cable, and they were also involved with JDRF. And so I joined the board at that point, and was on the board for, I don’t know, six or seven years, I think, and shared it in there. But I think I knew about JDRF through mom, like I think you just always supported them. Yeah, um, if I’m not mistaken, the world. organization was born the year I was born. Just another thing that has always been a part of my life. And I was really excited to get involved with the chapter because yeah, as you sort of already mentioned, the parents of type one diabetics are really involved. But there really aren’t many children of type ones out there. There weren’t at the time. It meant a lot to me to be involved and to be part of it.


Stacey Simms  27:24

I’m just curious, your mom, Jeanne, you just seem so laid back. And I’ve talked to several people who have lived with diabetes for this long who are I want to say relax, because obviously you’re not, but who are more of the, hey, I’m taking care of it. We don’t need to talk about it. You know, I’m not surrounded by people with type one. And then there are people who are younger, or we’ve been diagnosed more recently, who are really a big, big, big part of that community and want and need to kind of breathe that air. And I was curious, Jessica, was it surprising for you to kind of be involved in JDRF and be around people who were more like well, I am talking about every day and I am going to tell you more about it.


Jessica Graham  27:58

Yeah, I mean, it was it was definitely Different, because that’s just not how it was in my house. I mean, it wasn’t a big secret or anything. But Mom definitely didn’t advertise it. And it certainly wasn’t part of her identity. It was very, very different. And I really loved to one be involved that I really loved getting my mom in that community, like I would take her to the gala and that kind of thing. And she really is such an inspiration to a lot of people, especially those who are newly diagnosed because they can see somebody who really, I mean, has had a full, long, wonderful life with it. And so it’s not this Doomsday message. And so she’s really, I think, a real inspiration for that. And I think too, she’s a great inspiration for how important attitude is an outlook is because she’s never let it define her and she’s never really Let it limit her. And I think she’s really inspirational. So yes, it was very different to be around different people with it. But also it was really exciting to just to be able to share her with that community.


Stacey Simms  29:12

Jeanne, what’s your reaction to have your daughter sitting next to you and saying, what an inspiration she thinks you are?


Jeanne Martin  29:17

Well, I think that’s very nice. It’s very complimentary. I never thought of myself that way. But I’m glad she sees me that way.


Stacey Simms  29:26

I know my listeners are going to want to know, a few more little details. Jeanne, do you exercise a lot? Have you always been active? Are you more kind of laid back about that too? You know, that’s one of the things that people always ask me about.


Jeanne Martin  29:37

No, I say I’m pretty active. Well, since we’ve lived here almost the whole time. I would go to the why three days a week. I don’t do that now because I suppose and when I was younger, I played golf, and did a little bit of tennis. I’ve always gardened Well, not always but for a long time I went out in the They are dug in the dirt and that type of thing. And I try to walk about a mile a day. I mean, I walk more, but I go for a mile walk, or more. I tried to do it every day, unless it rains. I do it early when it’s hot, because the heat affects my blood sugar. I run into trouble easier. And I don’t know if that’s the same with other people. But anyway, that’s what it is. Yeah, I think I’m pretty active.


Stacey Simms  30:27

Yeah, you’re very active. Jessica, I’m curious, have you. You mentioned that you were worried about your son having type one and he’s 13. Now, do you still think about that? It’s in the back of your mind. Is it something that you’ve ever had checked out? Anything like that?


Jessica Graham  30:41

Um, yes. So I worry about it every day. But I don’t


I try not to think about it. And I certainly have never mentioned it and


Unknown Speaker  30:49

we had


Jessica Graham  30:50

it chat once and I forget why you’ve charged it. Yeah, maybe. Maybe you were the one anyway. I feel like I had it checked once and I don’t remember why maybe he was thirsty that day. But I do worry about it a lot. And I mean, literally every time he says I’m thirsty, because I’m just a little neurotic that way, but I don’t talk about it at all. Like he would have no


Unknown Speaker  31:14

idea. I don’t


Jessica Graham  31:16

think anybody would know that. But yeah, I worry about it a lot. But then again, I think, well, if he ever were to develop it, oh, my gosh, he has the world’s greatest teacher to help him navigate it. So that puts my mind at ease. When he was very, very small. I found a test that he could have done. It might have even been when he was born. I mean, it was he was really, really young. And I think it was down in Florida, talking about TrialNet Yes, that must be what it was. And we just decided


Stacey Simms  31:49

not to do that. And I think I talked to you about it and talked to my mom about it. And she, I think suggested that we not do it and I decided not to so Well, Jeanne, let me then ask you about that because you would, as Jessica said, you know, he would have such a great role model and teacher, God forbid something would happen like that. So let me just ask you, what would your advice be for a newly diagnosed adult or a newly diagnosed family facing something like this now in in 20?


Jeanne Martin  32:19

Well, it depends the age of the kid. I think when you’re a teenager, I think it is be harder on the kid because, you know, you don’t want to be and maybe it’s because I’m a girl and maybe it’s back then you don’t want to be different. I mean, you know, you want to blend in as a teenager, you don’t really have enough self confidence to just say, Okay, I’ve got this and I’m gonna deal with it. I mean, I’m not saying that kids don’t but I would think that’s a harder age. But I guess I would just be very positive and all the things that can help. At the same time, it was would be your his responsibility to see He does try to do what he should do with diet and exercise and taking this medicine. I have a niece who came down with it when she was 10. And she never did well with it. She didn’t do what she was supposed to do. And over the years, she’s had all kinds of complications. And she just got very depressed with it. And you have to be positive. But you the kid himself, has to take responsibility for himself to do what he should do. And I strongly believe in that.


Stacey Simms  33:36

Thank you both so much for joining me today. It was amazing to learn about your story, Jeanne, and I’m so glad, Jessica that we were able to do this. Thank you for being on the podcast.


Jeanne Martin  33:45

Thank you for having us. Yes, thank you. It was nice meeting you via the computer.


Announcer  33:55

You’re listening to Diabetes Connections with Stacey Simms.


Stacey Simms  34:01

I shared some photos in the Facebook group that Jeanne and Jessica sent me, I was so happy to finally get a chance to talk to her. And you know what, after that interview, she sent me an email with some advice for Benny, which I thought was really, really nice. Now he is, as you’ve heard him here on the show, he maybe he’s a little too confident, but he’s very independent and very confident. But Jeanne has some really nice words just about you know, not letting diabetes stop you and keeping a good attitude that has served her well. And I really appreciate that she took the time to do that this community is just great.

All right, innovations is up next. And we have a very low tech solution to a very scary problem. It has to do with rubber bands. All right. I’ll explain that in just a moment. Diabetes Connections is brought to you by Dexcom. And we started with Dexcom back in the olden days before share. So trust me when I say using share and follow apps make a big difference. I made a lot of people who don’t realize that when Dexcom launched you could not see numbers not only on your phone, but you could not share than with anybody else. But now it’s such a great system. And Benny and I set parameters about when I’m going to text him or you know how long to wait all that it helps us talk and worry about diabetes less when he is at asleep over or goes on a trip. It gives me peace of mind. It also helps if I need to troubleshoot with him, because I can see what’s happening over the last 24 hours and not just one moment. The alerts and alarms that we set help us from keeping the highs from getting too high and help us jump on lows before they’re a big issue. Internet connectivity is required to access separate Dexcom follow app. To learn more, go to Diabetes and click on the Dexcom logo.


As you know I am the queen of diabetes mistakes I wrote a whole book about why I think mistakes are great. It’s the world’s worst diabetes mom real life stories of raising a child with type one. But I will say that making mistakes is also incredibly scary at times. And the one mistake that I think almost everybody with time wonder who’s a caregiver for someone with type one has made is mixing up the long acting and the short acting when you’re on MDI, whether it’s the beginning or you’ve been doing this for a while, I’ve been enough Facebook groups where I see this happening. It’s once in a blue moon for the individual. But it seems like almost every week somebody is coming in and saying, Oh, my gosh, I did this. I’m so scared. What do I do? Right? Well, one of the best tips I ever heard on is so simple. And I heard it from a CDE.

And I’m so embarrassed that I don’t know their name. And I’m so sorry, if this was you, email me Stacey at Diabetes And I will give you credit, but what you do is this, whenever you have a new vial or a new pen, have long acting and do this on the long acting only take a rubber band and wrap it around the pen or the vial. Just wrap it around a couple times. You know, make sure it’s not loose, it’s not sliding around. And then every time you pick up your long acting, you will know that it feels different. It’s got those rubber band bumps on it and If you do this often enough, really doesn’t take that long, maybe two weeks, your fingers will start to associate that feel with the long acting. So if you make a mistake if you accidentally grab the wrong pen, your hand and your brain will instinctively know that something is wrong. Now, this is not proven. I haven’t seen any studies on it. But this is advice that was given to me that I’ve heard other people use. And it really does make sense.

It is incredible that after all this time was different kinds of insulin, that the pens are pretty much exactly the same. The Lantus vial, I remember might be a little skinnier, right? It looks a little bit different. But when you’re moving quickly and automated, like a lot of us are, I mean, I could do that Tandem cartridge in my sleep, whereas when we first got it, I thought, oh my god, this is so complicated. I’ve got to lay everything out on the table. We did the Animas pump for 10 years, I could definitely feel that thing blindfolded. You just get used to your routine and how things are Feel so if you just wrap the rubber band around the long acting, you will get used to the feel of it.

Let me know what you think. Does that make sense to you? Has anybody tried that? And if you’ve got an innovation like that This segment is for everything big and small. That makes living with type one just a little bit easier. Let me know I would love to hear from you.


Just a little personal update before I let you go, this has to do with insurance. We’ve had some employment situation changes around my house, which means I have already spent far too much time on the phone. I decided to start taking advice from one of our previous guests from Melissa Lee, who said when you have insurance issues, you should start with the diabetes companies and work backward. So I called Dexcom and Tandem and I said hello, I have changed insurance. What do I need to do? And they were very helpful. The bad news is my new insurance means we have to order from a third party supplier and it’s Edgepark. Edgepark. If you’re listening, please, please handle this.

Well, we were with Edgepark years ago and I hate to disparage anybody. But let’s just say let’s turn this into a positive. I felt that it was such a gift for the last five and a half years to order directly from Tandem and directly from Dexcom. I am sad to see those days in my rear view mirror. So I will keep you posted on how it goes. I’m currently as I’m recording in the limbo of an Edgepark representative, we’ll get back to you. We have plenty of supplies. I have a great support system if I need anything, so I’m not worried about Benny. But man, although I’m a liar, because I did say to him, you know, before you rip anything off your body, so bad before you take off that sensor or that inset, come talk to me, and make sure that it’s okay to do so. Isn’t that terrible? I mean, I’m laughing because we really are fine. But it just makes me crazy how expensive this stuff is, and how difficult the process is to order what you need. So I will keep you posted on that. Hopefully, it’ll all go smoothly. But this is not my first rodeo. So I’m anticipating navigating a not so smooth road. I’ll let you know.

Thank you so much to my editor, John Bukenas from audio editing solutions. Thank you all so much as you listen, I’m Stacey Simms. I’ll see you back here. Next Until then be kind to yourself.


Benny  41:07

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