#1303 Two Cans of Beans
Rebecca and Mel are mother and daughter T1s.
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Scott Benner 0:00
Hello friends and welcome to another episode of The juicebox podcast.
Rebecca is 57 diagnosed at six. She is Mel's mother. Mel is 34 diagnosed at 32 and today they're both on the juicebox podcast. Please don't forget that nothing you hear on the juicebox podcast should be considered advice medical or otherwise, always consult a physician before making any changes to your healthcare plan or becoming bold with insulin. Don't forget to save 40% off of your entire order@cozyearth.com All you have to do is use the offer code juicebox at checkout. That's juicebox at checkout to save 40 percent@cozyearth.com when you place your first order for ag one, with my link, you'll get five free travel packs and a free year supply of vitamin D drink, ag one.com/juicebox I know that Facebook has a bad reputation, but please give the private Facebook group for the juicebox podcast, a healthy once over juicebox podcast, type one diabetes, and if you're a US resident who has type one or is the caregiver of someone with type one? I'm reminding you to take the survey AT T 1d, exchange.org/juice, box. This show is sponsored today by the glucagon that my daughter carries, gvoke hypopen. Find out more at gvoke glucagon.com, forward slash juicebox. Today's episode is sponsored by Medtronic diabetes, a company that's bringing people together to redefine what it means to live with diabetes. Later in this episode, I'll be speaking with Jalen. He was diagnosed with type one diabetes at 14. He's 29 now he's going to tell you a little bit about his story to hear more stories with Medtronic champions, go to Medtronic diabetes.com/juice box, or search the hashtag Medtronic champion on your favorite social media platform. The episode you're listening to is sponsored by us med usmed.com/juice box, or call 888-721-1514, 887211514, you can get your diabetes testing supplies the same way we do from us. Med,
Speaker 1 2:29
Okay, hello, I am Rebecca and I am her daughter. Mel, all right, so
Scott Benner 2:36
we have Rebecca and Mel here, and it's not something we normally do. So Mel, can you tell me why you and your mother are here together?
Speaker 2 2:43
Well, I will take any opportunity given to talk about myself, but I also think that we have kind of a unique story together with the diabetes and but we were both diabetic, and I wasn't diagnosed until my 30s, and I'm also autistic, so that adds another level of struggle with the diabetes.
Scott Benner 3:13
Okay, so, Mel, exactly, how old were you when you were diagnosed? It
Unknown Speaker 3:18
was right before my 32nd birthday.
Scott Benner 3:20
How old are you now?
Unknown Speaker 3:22
I am 34
Scott Benner 3:26
and Rebecca, how old were you when you were diagnosed?
Speaker 1 3:28
I was six years old, almost seven.
Scott Benner 3:32
And how old are you now?
Unknown Speaker 3:33
I am 57 Okay, been diabetic 50
Speaker 2 3:38
years we were both diagnosed right before our birthdays. Oh,
Scott Benner 3:43
okay. My daughter was diagnosed right after her birthday a couple weeks later, and she was two when she was diagnosed. Oh, so, okay. So let me just find out a little bit about both the I'll start with you Rebecca, because you know Age before beauty, right? And so let me, let me ask you, 50 years that's you were like animal insulin, right? Or, Yes, yeah,
Speaker 1 4:06
I was on a it went and it was a mixed insulin. So I got two shots a day. It was pig insulin, and it was a 7030 mix of regular and NPH. So how long
Scott Benner 4:19
do you reckon you did that before you moved on to regular and just the regular mph, like, when did the
Speaker 1 4:27
port go away? Oh, gosh, um, not until I got pregnant with Mel, really? Yeah.
Scott Benner 4:34
So how many years did you do that mixture? How old were you when you got pregnant?
Unknown Speaker 4:39
I was 2222
Scott Benner 4:42
so you were 722. I'm gonna do some math here real quick. I don't want anybody to be, uh, like it's five. Carry the one. You had diabetes for 15 years, and you were using that regiment. Yes. Okay, yeah. Do you remember why they had you change? Not
Speaker 1 4:58
really, other than. I, I think it was about the pregnancy and then I was on, I don't think they had Lantus back then.
Scott Benner 5:09
I don't, I mean, yeah, that's 35 years ago, so yeah,
Speaker 1 5:13
I honestly, I don't. I don't remember that much about that, other than I switched from getting two injections a day to I would get one before I ate, and then the long acting, whatever it was at that time. Okay,
Unknown Speaker 5:29
all right, so
Scott Benner 5:30
how do you recall your management being up until your pregnancy? Do you remember what your a 1c were, or what you were considering an accomplishment back then,
Speaker 1 5:41
honestly, just staying alive was pretty good for me. Back then I had it was not good control. I don't really know how to answer other than I don't remember my a one C's, but I think they were pretty good because my blood sugar swung so much that it evened out that number. So,
Scott Benner 6:02
so your a 1c didn't look terrible, but you were very high, very low, kind of fooling the a 1c test, basically, yes, yeah, did you get low to the point where you needed help?
Speaker 1 6:13
The same right around the same time I got pregnant, I started to have hypoglycemic unawareness, and I I couldn't even remember certain things I would come out of it with somebody, usually my husband at the time, ELS dad, helping me, uh, eat something and get out of it. And I, I just at that point in my life, I didn't, I didn't really think, I think I'm kind of low now, so I'm not making a lot of sense in my gravy juice here, you
Scott Benner 6:41
check your are you wearing a CGM? By any chance I am
Speaker 1 6:45
and I'm I'm hovering right around 92 but I think it's a slow drop. Okay, some of it might be nervous. Do you
Scott Benner 6:52
find yourself reaching for words you can't find when you feel like this? Yes, yeah, yes. Mel, I'll jump to you while your mom drinks a juice box on the juicebox podcast, I will jump. Do you know this story about your mother? Do you guys talk about this stuff? Oh
Speaker 2 7:08
yeah, her diabetes was a huge part of my childhood. I think it definitely impacted our relationship a lot because of her blood sugars being so erratic, I kind of learned to there's a certain look in her eyes that I could recognize when she was going low, and I knew, Okay, that's not really my mom. I need to, you know, help her out so that I can get my mom back. And so a lot of my earliest memories are of hypoglycemic episodes with her, and so it definitely had a very big impact on my childhood. Hey,
Scott Benner 7:55
Rebecca, do you have a meter with you? I'd love to know what your blood sugar is versus what the CGM said.
Speaker 1 8:01
Oh, I do. I'll have to go get it. Would you mind? Yeah, no, no, I'm
Scott Benner 8:05
gonna keep talking about when take it back. Okay, sure thing. So, Mel, when you say that it had a big impact on your childhood. Was she low a lot?
Speaker 2 8:13
I was so little. I mean, she had it my whole life. And so it's kind of, I'm thinking of my whole entire childhood, and kind of condensing it down, yeah, and so I'm not sure if it was, if it was really extremely frequent, but I I remember it happening quite frequently in your head,
Scott Benner 8:36
yeah. Then was your father? Were your mom? Are your mom and dad together now?
Speaker 2 8:41
No, they're not. They divorced when I was 10.
Scott Benner 8:45
Okay, so there was some time with him there, and then there was time without him. Yeah. Did it get harder when he was gone?
Speaker 2 8:52
Absolutely, yeah. There was an incident where my mom and I, thank God. We were sleeping in the same bed together, and she had a seizure from below, and she woke me up seizing, and so I was able to call 911, and get her help. But that was a really terrifying thing to experience. I think her, her blood sugar was 12 or something, oh,
Scott Benner 9:28
oh my gosh. So you just called 911, and sat with her until they arrived.
Speaker 2 9:32
Yeah, my we were staying with my grandparents at the time, because it was very recently after my parents got divorced, and so my grandparents were there to help out, but they honestly didn't know the day to day. And so when the paramedics came in to help, they were asking questions, and my grandparents were answering them incorrectly, and nobody was listening to me, because I was 10. 10. So that was frustrating. Rebecca,
Scott Benner 10:03
you can hear me again,
Speaker 1 10:04
yes, yes, 20, and I'm at, yeah, I'm at 114, so I'm, I'm fine. You weren't
Scott Benner 10:09
low. You think you're just nervous? I think I'm just nervous. That's okay. Well, now you might have the bowlers for that juice.
Speaker 1 10:15
Yeah, that's what I'm thinking. I'm keeping an eye on it, not accusatory,
Scott Benner 10:19
of course, Rebecca, but 25 years into diabetes, you were still like seizing in your sleep. I don't know how you guys order your diabetes supplies, like CGMS, pumps and testing equipment, but at our house, we use us Med, and I'm gonna walk you through the entire process right now. I'm looking at the email from us med. It says it's time to refill your prescription, dear Arden, please click the button below to place your next order. Then you click the button that was it. Two days later, I got this email, thank you for your order from us med. We wanted to let you know that your order and it gives you an order number was shipped via UPS ground. You can track your package at any time using the link below, and then there was a link, and then it showed up at our house. Now I'm going to walk you through the entire chain of events. On the 29th which was a Saturday, I clicked on the email on that Monday, the first I got an email that said the order had been sent four days later on the fifth the package arrived. If you can do it easier than that, you go get it. But if you can't, us, med.com/juice, box or call 888-721-1514, get started today with us. Med, get your diabetes supplies the same way we do. This episode is sponsored by Medtronic diabetes. Medtronic diabetes.com/juicebox and now we're going to hear from Medtronic champion, Jalen.
Speaker 3 11:50
I was going straight into high school, so it was a summer heading into high school. Was
Scott Benner 11:54
that particularly difficult?
Speaker 3 11:55
Unimaginable? You know, I missed my entire summer, so I went to, I was going to a brand new school. I was around a bunch of new people that I had not been going to school with, so it was hard trying to balance that while also explaining to people what type one diabetes was. My hometown did not have an endocrinologist, so I was traveling over an hour to the nearest endocrinologist for children. So you know, outside of that, I didn't have any type of support in my hometown.
Scott Benner 12:23
Did you try to explain to people, or did you find it easier just to stay private?
Speaker 3 12:28
I honestly, I just held back. I didn't really like talking about it. It was just it felt like it was just a repeating record where I was saying things and people weren't understanding it, and I also was still in the process of learning it. So I just kept it to myself. Didn't really talk about it. Did
Scott Benner 12:43
you eventually find people in real life that you could confide in? I
Speaker 3 12:47
never really got the experience until after getting to college. And then once I graduated college, it's all I see. You know, you can easily search Medtronic champions. You see people that pop up, and you're like, wow, look at all this content. And I think that's something that motivates me. Started embracing more. You know how I live with type one diabetes, Medtronic
Scott Benner 13:08
diabetes.com/juicebox, to hear more stories from the Medtronic champion community.
Speaker 1 13:16
Yes, and I'm gonna after, after the divorce, after I started living on my own and taking care of myself, I started seeing an endocrinologist, and he that man. I appreciate him, but not everybody, not everybody did. But he looked at me and he said, I cannot believe that you've been diabetic this long and you know nothing about it. And he basically shamed me into learning the technology. And I'm gonna, I'm gonna give myself a little bit of a a pass on it, because when I was diagnosed when I was seven, yeah, they told me it was going to be cured, you know, before I was 10, before you were 12, before. So I heard this, and I looked at every newspaper article. I've got a scrapbook with things from 1978 about advances in diabetes, and it, it didn't change. It didn't change. And then I got to be a teenager, and I just completely, I'm like, nothing ever changes. This is just what my life is so I didn't, I didn't try. I stopped trying. Dr Whitey, I will use his name. His name's Lamont Whitey, and he was paramount in helping me get onto a pump. It was before I got my pump, before they had continuous glucose monitors, but that helped, and once the Dexcom came out, like that was life changing for me. It I don't worry about not waking up. Dexcom has changed my life, but, but Dr Whitey was the one that really, he told me, yeah, I can't believe you don't know anything about this disease. Like, oh. You
Scott Benner 15:00
really do attribute that to just being told at such an early age, this isn't going to last very long. Don't worry about it. I
Speaker 1 15:06
did try back in the day, but I was peeing in a cup. Okay? After school, I would go home, I would pee in a cup. I'd go pee because he wanted fresh urine. So you'd go pee. I'd watch Gilligan's Island, and then I would pee in a cup again, and if it was blue, I was supposed to eat four vanilla wafers. And that was what it was when I was seven. So as time went on, you get to be a teenager, and you don't even care. I just I didn't do very well, and it wasn't until after I, I was divorced, that I actually started caring for myself without help and
Scott Benner 15:48
without the doctor. Do you think you would have even begun then? I
Speaker 1 15:51
think so. I think if I, because I was still, I still saw an endocrinologist, I just didn't care. Yeah, you know, it was like my insulin supplier, so it didn't, you know, I didn't want to get on a pump. They talk about me getting on a pump. I'm like, I don't want one of those. I don't want something attached to
Scott Benner 16:07
me. Try to explain to people listening. It's not apathy, right? Like it started off with, this isn't actually something I have to worry about because it's going to be over soon. But then it turns into like, you're a young kid and you're just not paying attention to it. Are you not having physical symptoms? Something that you would say to yourself, I need to stop this. Like, this is happening to me all the time, or my numbers are crazy, or whatever. Like, why didn't something happen to shock you before the doctor said, I can't believe you don't understand
Speaker 1 16:34
this. Well, things were happening, but I thought that was just my life. I never stopped taking insulin. I took sugar or glucose when I was low, but I just couldn't figure out how the food and the insulin worked together, so I just thought it was a crapshoot. Gotcha. Sometimes I'm low, sometimes I'm high, and I get insulin when I'm high, and I eat sugar when I'm low, and I
Speaker 2 16:59
I just want to jump in to I watched, you know, growing up, my mom always took her diabetes serious. I mean, there was never a time she would complain, you know, oh, I don't feel like taking my insulin, but she always took her insulin. And so there was never, there was never a lack of effort, but it was just, it was almost like you didn't realize that you that it was possible to do better.
Scott Benner 17:31
Yeah. So this, this chasing. It was what she thought it was. Yeah. Okay, Rebecca did the so the pump helped a little bit when you got your first pump, but not completely you're saying the CGM is what turned it around. So how long have you had a CGM?
Speaker 1 17:47
I have had a CGM since. When did they first come out? I got one early on, and then I lost my job, and I did without it for like, two years. And artist, artist, two years after having something like that taken so I just recently got back on it within the past probably seven years.
Scott Benner 18:09
So how many, like emergency low blood sugar incidences with just the pump? Did they go completely away, or did they just the number go down?
Speaker 1 18:20
The number went down. It it I stopped going as high and as low. I remember once, once I wanted to get on the pump, and I didn't have the CGM before they were a thing. I was told by my doctor, you need to stop checking your blood sugar so often, and you need to gain some weight. And because I was checking every hour, I checked my blood sugar every hour that I was awake, but I didn't know what to do with the numbers, until I I heard this guy. His name's Scott and Keith really helped me realize what I could do with those numbers. Wait, really, yeah, oh yeah, it was you. Oh, let me
Scott Benner 18:59
sit up. I didn't know I was going to be congratulated on a second I was leaning back. No, honestly, just that you'd had diabetes for so long. I just, I guess I just assumed that you had gotten it worked out on your own, Ben and found the podcast later. But that's wonderful. I'm happy. So do you think that what was happening before is like you probably weren't pre bolus in your meals, you were shooting up high, testing, seeing a big number, putting in insulin, then crashing down low after the food was digested, exactly that. Yeah, you were just chasing the whole time about that. What makes you find me? Is it your is it Mel's diagnosis? Did you think, Oh, I can't let her live the way I lived.
Speaker 1 19:38
Actually, it's not even that when Melanie was diagnosed, she researched and she told me about you, and I started listening to the podcast, you have literally changed my life as much as the Dexcom did, sir. And I can't say enough good things about you. That's so
Scott Benner 19:56
nice. Thank you. Incidentally, a couple of years ago, a web. I ran one of those, like, you know, the brackets they do in March Madness, but they did it with diabetes stuff, and it came down to the final two. It was me and Dexcom, and I beat them. I was very proud of that. I don't know why it was an online poll. It wasn't really that specific, but that's awesome, yeah, but so well, first of all, that's terrific. And secondly, Melanie, how did you also I love Mel, that your mom calls you Melanie, but you want to be called Mel. Oh, yeah,
Speaker 2 20:29
she gets the pass because she gave me the name. Yeah. No,
Scott Benner 20:33
no. It's funny, though. But every time Rebecca, every time you say Melanie, I think am I supposed to be saying Melanie?
Unknown Speaker 20:40
You can we can use Melanie. If that's easy.
Scott Benner 20:44
Let's see if I can't figure it out. So how do you find a podcast? Then what's the path that leads you to it?
Speaker 2 20:50
After I was diagnosed, I Well a lot of the first fear I had when I saw the 600 on the glucose meter and we went to the emergency room, was I've ruined my family's financial future. And then once I kind of got over that, I'm like, I didn't want to have a seizure in front of my daughter. I didn't wanted to be able to avoid a lot of those things, and so I'm like, I'm gonna do everything I can. And so I I found the podcast on a Facebook group, okay? And so that's how I that's how I got, got into it, and I started sharing some of the information I found with my mom that I thought she might find helpful, gotcha.
Scott Benner 21:42
And then, then Rebecca, did you start hearing things that you're like, This is completely different. Is that what happened
Speaker 1 21:49
when I was a child and we pre bolus? It meant getting your shot. And, you know, was an injection, getting your shot before you ate, which to my mom. And you know, it was 1974 Yeah, but it was get your shot, and then you eat immediately, right? And now I did not understand how much pre bolusing could help my after, after, I ate numbers I had no idea until your podcast. And I mean, I maybe that sounds dumb, but nobody, yeah, they talk about pre bolusing, but they don't. I've finally figured out oatmeal, and it takes four four units is typically what I get 15 minutes before I eat it, and I rarely will go I still kind of Spike, but it's like 181 90, if I go up to 200 after oatmeal, and I never could eat it before, I'd have double numbers going straight up. It's 400 because I felt like But understanding pre bolus. And one other thing I want to really again, give you credit for like, I feel like it's the yay Scott show
Scott Benner 22:59
here, but just for a couple more minutes. Go ahead.
Speaker 1 23:03
It's fine. It's fine. Part of the reason I never felt like I could be good at being diabetic was I felt like any time I had to make an adjustment, if I didn't do the carbs right, and I went high later, and I took insulin, I felt like I had failed. If I had to get a bolus because I was high in the morning, I felt like that was a fail. And so now, when I before I put my feet on the floor, I will get between a half a unit and one unit of insulin, depending on what I'm planning on doing in the morning and what my blood sugar is when I wake up and I'm fine the rest of the morning. And I felt like that was a cheat, like I was I wasn't good at it because I had to do that. I'm like, It's no worse than getting insulin at all, really.
Scott Benner 23:54
And that's something if you take insulin or so final ureas, you are at risk for your blood sugar going too low. You need a safety net when it matters most, be ready with G voc hypo pen. My daughter carries G voc hypo pen everywhere she goes, because it's a ready to use rescue pen for treating very low blood sugar in people with diabetes ages two and above that. I trust low blood sugar. Emergencies can happen unexpectedly and they demand quick action. Luckily, jivo kypopen can be administered in two simple steps, even by yourself in certain situations. Show those around you where you store jivo kypo pen and how to use it. They need to know how to use GVO kypopen before an emergency situation happens. Learn more about why GEVO kypo Pen is in Arden's diabetes toolkit at gvoke, glucagon.com/juicebox, gvoke shouldn't be used if you have a tumor in the gland on the top of your kidneys, called a pheochromocytoma, or if you have a tumor in your. Acre is called an insulinoma visit, gvoke, glucagon.com/risk, for safety information. So you just had these years and years of preconceived notions that were close to right, but not not exactly right, and then you just didn't see the big picture enough to make adjustments to the timing of the insulin. Yes, and that's exactly it's so it feels so simple now in retrospect, doesn't it? Yes, yeah, it does. What could somebody have said to you all those years ago that would have, would
Speaker 1 25:35
have changed things for you? Honestly, I don't think anybody could have said anything at that time, because without the Dexcom, the continuous glucose monitor, I still don't think I could have done a very good job.
Scott Benner 25:48
I have to agree, seeing seeing it happen, is it's transformative. It really does teach you on a different level.
Speaker 2 25:54
I'm incredibly grateful to have been diagnosed when I was within about a week of getting my official diagnosis, I had the Dexcom, and then I was able to get on a pump very shortly after. And so I I think about that all the time, just how grateful I am that I've I've never had to deal with well for about two weeks, I had to deal with, you know, just the the finger sticks, yeah,
Scott Benner 26:26
I have to ask Melanie. I need a little more context here. So you have a child? One, yes, one, yeah. And are you married?
Unknown Speaker 26:36
Yes,
Scott Benner 26:37
you are okay. I'm just gonna dig into this, because I don't know another. I can't find a another route to it. But how do you get an autism diagnosis as an adult? What
Unknown Speaker 26:46
leads to that?
Speaker 2 26:47
I had dealt with various kind of it was described as anxiety. And when I was really, really young, I had a lot of issues with anxiety. I was told all of the doctors I went to, I would describe what was going on with me. I also have narcolepsy, which I've always had, and every time I went to a doctor, they would say, oh, it's anxiety and depression. When I got older, I got a therapist and started really talking about anxiety and how that works. And as we were talking about that, my therapist said, that doesn't sound like anxiety. That's not and so after doing some more research, I found out that there are a lot of comorbidities with narcolepsy and autism and Ehlers Danlos Syndrome, which I also have. Okay, so I already had kind of an alphabet soup of issues before the diabetes. I was accommodated really well by my family when I was little, and so I didn't struggle as much until I got older and didn't have those accommodations anymore day to
Scott Benner 28:09
day. What did it look like for you before you had a diagnosis? Where were the where were the places you struggled?
Speaker 2 28:13
I hadn't been able to go to I can't go grocery shopping. I've never really been able to because all of the the visual stimuli is too much for me, and so even if I have a list, I'll, it's like my brain just kind of blue screens, and I don't know what's going on. And I'll it's I almost black out, and I would come home from the supermarket with like, two cans of beans and absolutely nothing that I had actually gone to the store for. Okay, fell asleep at work a lot because of the narcolepsy I have arfid, which is a it's a sensory based eating disorder that's often associated with autism, and so I really, really struggle with eating. Used to get called into the counselor's office at school a lot because they thought that I had some sort of, like image issue, like I was trying to be thin. But I really, I just, I struggled terribly with eating. Yeah. I
Scott Benner 29:22
think you might have named the episode two cans of beans, by the way, because, in my mind, in a panic, you ran out of the store, but just, and you just grab two cans in front of you, like, I get these, and
Speaker 2 29:34
I'll go, yeah, that's, that's exactly it. That's what I
Scott Benner 29:37
figured you just standing in front of the beans when you decided to get the hell out of there. Yeah. How long were you married before you had the diagnosis? We
Speaker 2 29:43
have been married for it'll be 12 years this year, so I guess we've been together about 10 years when I got the diabetes diagnosis, and eight years for the Oh, yeah, three years into the marriage. Age is when I got the narcolepsy diagnosis, the autism was about 10 years in. Got you,
Scott Benner 30:09
I'll tell you what. I didn't get any sleep last night, so there's a reasonable chance I'm gonna nod off at some point today and not mean to, but, but, but, well, I'll understand. Yeah, you, you will be if it happens now you like, that's fine. It happens to people. Melanie, I'm just gonna ask you a very direct question, okay, you grew up all that time like, so you had issues. That's fine. You thought you were anxiety, you know, etc. But once you're living with someone that your husband never looks at you and goes, Hey, like, are you autistic? Or, like, you know what I mean? Like, doesn't even come up in a joking way sometimes. Or, like, you know, are you always like, you know what I mean? Like, how does that? I'm just fascinated that that slips by for so long, I guess is what, what I'm asking about.
Speaker 2 30:55
It's a little bit embarrassing, because he actually had, he is also autistic, and he brought up to me a few years into our marriage, hey, I think I might be autistic because I've been looking into it, and I was not very he I was not receptive to it. I thought that you're so much like me, and there's no way I'm autistic. So you can't be autistic because we're so much alike and super interesting.
Scott Benner 31:27
Yeah, and Rebecca, before she goes on, yes, I know autism was not a big diagnosis when she was little, right? But she was growing up, did you? Did you have other kids? No,
Speaker 1 31:40
just, just Mel, and I, honestly, because I only had the one kid, and I was, I, my blood sugar was so out of control, there were a lot of mood swings and stuff. I was just kind of doing the best I could. And in our we, I come from a big family, and nobody thought Mel was any weirder than any of the other kids. So it just,
Speaker 2 32:07
yeah, we're a strange family. And so there, there didn't seem to be, I wasn't that much weirder than anyone else.
Scott Benner 32:15
Well, Mel, like, are you just related to a bunch of people with autism or or that are on the spectrum somewhere, or is it just, it just didn't. It's such an odd thing not to recognize, like, that's all I'm saying. You know, I'm not, I'm again, I'm not coming down to anybody. It was just like, You're freaking me out, that this is the story. Just,
Unknown Speaker 32:33
it's, yeah, it
Speaker 4 32:35
feels like somebody I don't know. It almost feels like somebody comes up to me, you know, on my 30th birthday and says, Hey, you know you're actually Puerto Rican. And I go, what I am? Oh, okay, like, I didn't know. Like, it almost feels like that, you know what I mean? Like that, that kind of outlandish.
Speaker 2 32:51
It was there. It was mind blowing when I finally accepted it, because it put so much into context. And if I think that if we had access to the kind of information that we do now, when I was younger, looking back, I was a textbook case, and it it almost kind of shocks me that none of my teachers or anyone ever suggested that I go in for an assessment. I feels
Scott Benner 33:24
like the public school system let you down pretty well too. Yeah, I
Speaker 2 33:28
had to have my own special classroom for when the fluorescent lights got too overwhelming for me, and so they would they would send me in because I would have what they were calling panic attacks that I now know were autistic meltdowns, but so they knew enough to put me in a separate classroom, but not enough to say, hey, maybe you should look into this more.
Speaker 1 33:55
I'm going to jump in right here, because, again, the public school system did not notify me her mother that this was happening, so I, you know, she'd come home from school, and when she was a teenager, we weren't, we're very close now, but we weren't as close back then, so we didn't have the same kind of relationship we do now. And I, I just didn't know. I thought, yeah, she's doing okay in school. And one of the things she said to me, because Mel did very well in school, but she she said, I literally slept through high school, and after the narcolepsy diagnosis, it was even funnier. I
Scott Benner 34:32
did, by the way, I did too Mel, but not because I had narcolepsy. I was just like, I hate this. Wow. Okay, so I want to say, admittedly, I don't understand the entirety of the autism spectrum, right, but, yeah, you're beyond high functioning, I would imagine. Well, I,
Speaker 2 34:51
I haven't been able to work in several years. I think it's, it's a little bit difficult. Able to put, you know, what's the autism and what's the narcolepsy, and what's from the Ehlers Danlos Syndrome. So I don't know, like, what percentage of my disability comes from autism, specifically, because I know that narcolepsy makes the symptoms a lot worse, and then the sensory issues adding diabetes onto it, now I have things stuck to me all the time, and so that's kind of lowered my capacity overall for other sensory input.
Scott Benner 35:40
Okay, tell me about the sensory stuff. What bothers you?
Speaker 2 35:44
My mom can remember when I was getting dressed in the morning for school, putting pants on was physically painful for for me, it cold. Fabric would was like a electric shock all over my body, makes my teeth hurt, just genuinely painful, and I didn't have the words to really describe that back then. But autistic brains process a lot more information than a neurotypical brain, and so my body is just more aware of everything that's happening. I can, you know, being outside can be overwhelming if it's a little too windy, because I'm like, oh, there's too much air on my skin. And so that's why I have the the tea slim pump, because it's a smaller thing that's actually stuck to me, because I feel like I would kind of panic with the the OmniPod, I
Scott Benner 36:55
don't know, Yeah, but you're doing it though, right? Like you're making your way through it,
Speaker 2 36:59
yeah. I really want to credit my mom, because even though her control was not good when I was growing up, she taught me so much. And after I think about all the people who are diagnosed who have no idea about diabetes, never even heard of it, and they're learning all these new things. And for me, I watching my mom. I was just like, okay, that there was a grieving period, but I had seen my mom she keeps pointing to I wrote a note she wanted me to say that my husband bought me condolence flowers for the passing of my pancreas. That's very funny.
Scott Benner 37:55
What kind of bow? Was there a lovely bow on it, or anything?
Speaker 2 37:57
Yeah, it was, it was a, it was a gorgeous, it was a gorgeous bouquet. I cried. Oh, that's very nice,
Scott Benner 38:04
well, but Rebecca, I mean, I think what we're really hearing here, and it's not, it's not an apples to apples comparison. But you know how sometimes you grow up with a parent who's the, you know, an asshole, and you think, either I don't want to be like that, and you work hard not to be like that, or you end up being an asshole and like, it sounds like Melanie saw what happened to you, and was like, Well, I don't want that to happen to me. And so you really, you kind of did help her. It's not how you think of it's not how you think of setting an example. But you really, you ended up being very valuable for her still.
Speaker 2 38:40
Yeah, it was, it was her, her attitude a lot to more, more so than I don't want to be like that control. Was she, she never like it was just a normal thing. She would complain sometime. You know, of course, you don't feel like taking your insulin all the time. And she'd be like, Oh, I don't feel like it, but there was never any like self pity, or it was just treated like such a normal part of daily life, and
Scott Benner 39:11
you took her attitude up, then, yeah, okay, yeah. That's nice. That's lovely. Radical
Speaker 2 39:18
acceptance is the a term that I like, that I think fits pretty well, is just, you know, well, like she said, she didn't think that things were gonna get better, you know, she didn't see really room for improvement. But at the same time that didn't you weren't hopeless about it, that didn't make that didn't make her like, Oh, my life is over. My life is going to be terrible forever. It was like, well, this sucks, but I can deal with it. And so that's just kind of been my attitude. And I'm, I'm so grateful for that, because especially with. With my other health issues, I could see myself absolutely spiraling with a new diagnosis like this, but Well, I was saying to my mom earlier that it was less of an adjustment for me, because there was never a time in my life that I ate food without thinking about diabetes long before I was diagnosed, every time I ate anything, I would think I'm so thankful that I don't have to worry about how this is going to affect my blood sugar. And so now I've I'm still thinking about thinking, Oh, I'm sick, but I still have to think about it. It's not in the positive, grateful way anymore, but at least I don't forget to bolus. Yeah, Rebecca,
Scott Benner 40:48
why do you think you held on to that attitude when things weren't going well for so long?
Speaker 1 40:54
I I believe I am pretty much just an optimist, and always have been I. My mother used to tell me that you're like your grandma. You can get knocked down, but you always get back up. And I don't. I don't know if that's just the way I'm built or because it was never a conscious thing, but I have always felt incredibly lucky. Not lucky like I could go win the lottery if I play it right, but just lucky in that I my kidneys work. I'm not blind. I haven't had any amputations, and I'm still diabetic. I've been here for 50 years. I had a baby, yeah, and I've always just felt really lucky. And so when, you know, I talk about how crappy my control was, but it didn't seem to now, I don't think about being diabetic as much as I used to, and I used to think about it, and I was trying to do something with it, and I really couldn't. I did not know how. And I took classes, I talked to people, I went to doctors. I just couldn't really do it. It wasn't, I feel like I kind of had the spin of, I was just didn't care, yeah, I did care, but I just
Scott Benner 42:14
couldn't, there's nothing left to do for you. Didn't feel like, yeah,
Speaker 1 42:17
yeah. It's like I was trying to dance, but I didn't know the steps, but I still, I still got out there and made up, made a fool myself very every time I was dancing, but I was still trying to dance. And now, with this technology, and you It's you can hear
Scott Benner 42:33
the music now, yeah, right. You can hear the music. You're on the beat. Yeah, yeah,
Speaker 1 42:37
exactly. My, my hemoglobin, a 1c, I went, what, a couple months ago, I guess, and it was a 5.8 look at you. And it's not because of highs and, you know, lows. It's
Scott Benner 42:51
Rebecca good for you. Can I ask a question? It's gonna sound self soaring, I promise it's not. What did I do? This is really me asking, Okay, look, I'll just preface it by saying, I just sit down here and I record. I don't prep, I don't have notes. Somebody comes in, I talk to them, Jenny and I made all that stuff that I'm assuming you listen to Pro Tip series or bowl beginnings, or whatever you listen to, defining diabetes, all that stuff, the variables. I had a list of things I wanted to talk about, but I mean, just a bullet point header, and then we just talk. And so I'm not lying to you, and I say I'm doing this on purpose. It's not planned the way you might think. It's just what falls out of my head. So my question is, and this is more for other people who are trying to help others, but a little bit for me, so I can, I can figure it out. And again, this is going to sound strange, but what did I do that helped you? Like, what did I say or do? Or was it how I said it, or was it the repetition of it? Like, I don't understand why you tried all those other things, and then you listened to me, and then it all worked out for you.
Speaker 1 43:55
I have to answer it the same way I answered what? What made me have the attitude I did. I, I think it's just you. I think you are, you were handed this problem when, when your child was diagnosed, and you, you jumped into it, and you did what you did. And I, I'm not a real religious type person, but I just I, I think the way your your brain works, and the way you're able to communicate with people this way, and and you're wanting to help them, all of those things led to me having an A 1c of 5.8 and part of it maybe was a repetition. Part of it was, you've got a good voice for a podcast. You know, you'll joke with people. And it's you're just easy to talk to. I've heard you talk to other people. That's why I wanted Mel to come. On and talk to you, because I felt like maybe she could share some of her story, but and, and maybe that, yeah, the self serving thing or whatever, but I you're one of my most influential, maybe the most influential per person in my, my journey with this disease. What about me? Wait, wait,
Scott Benner 45:21
that's you doing? Don't step on my moment. What the hell.
Unknown Speaker 45:28
Well, Mel, can I be a guru? Introduce me.
Scott Benner 45:31
I would like to be a guru. If I could. I think that's what I would like to ascend to guruism. Well, listen, I appreciate your explanation, and I want to tell you, like as a human being, it's lovely, and it meant the world to me, as a person who is trying to understand why this is like working for me, it was very unsatisfying.
Speaker 2 45:52
Well, I actually have for me. I think the the biggest thing that listening to you helped me with was just realizing how many different Well, first of all, learning how well we can control, I didn't know, like, how, how good it was possible to get. So just knowing that and that you, there's no, you're not, like, dogmatic about this is how you have to, yeah, not at all do. And so just knowing that there are different options, and especially with my sensory issues with food, a lot of that can be really tricky for me. And so you just, you offer such a wide variety of tools and explain them so well, okay, because this disease, it's not one size fits all. You know, one one thing isn't going to work for every single person. And so there's, it's the the wealth of ideas that you put together is just tremendously helpful, I'm glad. And the lack of judgment,
Scott Benner 47:08
if I'm being honest, I think most people who create content, which I guess is technically what I am, but I think that they're trying to be on a team so they can fervently get people behind them. And actually, when you cause a little bit of strife, it drives numbers. And I'm just not into that. I just think however you eat is how you eat. And you know, the goal here in the key to it is obviously to use insulin correctly, understand the timing and the amount and and see the variables that kind of stuff. But I appreciate, I really do appreciate both of your perspectives. If you said to me, write down the recipe for this. I think I would get it close, but I just don't know it. And I guess you just described Rebecca that the rest of it's intangible stuff that you can kind of say maybe it's this, and maybe it's a little bit of that, but you don't know the measurements of it. I actually told somebody yesterday. Somebody asked me privately, why do you think your podcast is popular? And I ran through a few things, and one of them I said, was I have a deep voice, yeah, and I actually think that helps. I know what I'm talking about, and I have a deep voice, and I talk in pictures too.
Unknown Speaker 48:13
So you do have a pleasant voice. Thank
Scott Benner 48:15
you mellow. Thank you very much. It's just true, like if I was screechy or shrill or, you know, it just wouldn't be the same. It sounds commanding that you have a deep voice. You sound like, you know, what you're talking about, just sort of what it is, you know, yeah. And I think people are tuned in to listen to this as well. Like, again, like people's voices being deeper Anyway, okay, well, this is wonderful. Let me ask you, I want to make sure we're covering the things you wanted to talk about. So Mel, do you have more that you'd like to say about your life, or anything you want to fill me in about
Speaker 2 48:46
there's not really a small snippet, I guess, just the my mom being that my mom and my uncle are both diabetic, and I have a great aunt and a great great aunt who both passed away from diabetes, so I'm from a long line of diabetics. Yeah, I feel so, so grateful, and not a lot of people get that, but I feel like I think about the family members who I never got to meet because they didn't survive it, and I get the opportunity to live on for them and my mom as well. And I just, I think that's incredible, beautiful. Yeah.
Scott Benner 49:35
Hey, so five members I counted, including you and your mom with type one just there, and you have, I can, I never say it correctly, uh, Dan ears. Say it for me that danlos Ehlers, danlos, danlos. And that's like, hyper extended joint, like you can hyperextend your joints,
Speaker 2 49:53
yes, yeah. It has to do with the connective tissue. So I actually had, um, gastroparesis. Is long before my type one diagnosis,
Scott Benner 50:05
just slow digestion in general, yeah. How did that impact you? Trouble picking up nutrients,
Speaker 2 50:11
lot of absorption issues. Iron get low. Yes, yeah, I have to take a lot of iron with the I can't really pre bolus, my a 1c is 5.3 and I have a 92% time in range. Sorry to brag for a minute, but I'm very proud. Don't apologize for that. I'm, I'm I'm doing well, but it in spite of the gastroparesis, but it's definitely it adds its own challenges. But my endocrinologist is always thinks it's really interesting that I had pre existing gastroparesis well before the diabetes. What
Scott Benner 51:00
other autoimmune stuff is in the extended family, any thyroid, celiac
Speaker 2 51:05
My uncle has on my maternal side, a different uncle from the diabetic one has celiac, and I have a grandmother with MS, and I, other than the the long line of type one I can't really think of,
Scott Benner 51:28
yeah, Rebecca is the last name I'm seeing here. Is that your maiden name?
Speaker 1 51:32
Yes, I, when I got divorced, I I got my maiden name. Yeah. So you
Scott Benner 51:38
pull you polish, descent, yes. Okay. And what do we mixed with? What was Mel's Dad?
Unknown Speaker 51:45
What is your dad? Rebecca, he
Scott Benner 51:48
had a job. That's all. I know.
Speaker 2 51:51
I love my dad, but I don't. He didn't come from the greatest family, so I just kind of pretend that I'm just coalition.
Scott Benner 52:02
Oh, I see you don't. But, I mean, is it Irish, Italian? Like, do you know what it is?
Speaker 2 52:08
I think, like a just my various places in Europe, I don't know that there's, I think the last name is Scottish,
Scott Benner 52:19
okay. Oh, that makes so that's what I'm trying to get at, because there's, there's definitely pockets in Europe and places where you see, like, more autoimmune type one come from. That's what. That's all I was trying, yeah. So I was trying to get at, yeah,
Speaker 1 52:31
okay, your dad has Ehlers, danlos as well. He does. Yeah.
Scott Benner 52:37
What's the day to day impact of that? Mel
Speaker 2 52:40
basically had to adapt my whole entire life around it, and so now it's like the day to day. It's just kind of like how I live my life, but I have to do physical therapy. I can't miss more than two days of physical therapy, or I will be unable to move. My joints will lock up. Things pop out of place. I had an issue once where I was driving and my wrist and elbow both dislocated at the same time, and I almost crashed the car. I had my elbow dislocate while trying to hold a door open for some poor man, and I slammed it right in his face. And I was so embarrassed that I didn't even
Scott Benner 53:32
say anything I haven't already Munich, you're sorry, yeah,
Speaker 2 53:35
I didn't like, how do I explain that I've held the door, and then I just slammed it in your Oh, sorry, my elbow dislocated.
Scott Benner 53:44
Have you ever used autism as an excuse for something? Have you ever been like, It's not my fault I have autism?
Speaker 2 53:49
I don't think I've known I might have when I was younger, if I would have known that that's what was going on. But yeah, not, not yet. I'll keep it in the back pocket. Gotcha,
Scott Benner 54:03
there was a term that we used to use, God, why can't I think of it? I think it started with a P for somebody who was,
Unknown Speaker 54:14
Are you thinking of Asperger? Oh,
Scott Benner 54:16
wait, yeah, Asperger's, thank you. When I say p, is that just a word that doesn't get used anymore?
Speaker 2 54:22
Yeah, they just changed the in the DSM, there's now three autism, level one, two and three. And so what previously would have been classified as Asperger's is now level one.
Scott Benner 54:38
Do you think you would have been Asperger's back then.
Unknown Speaker 54:40
Yeah,
Scott Benner 54:41
I think so, okay. Oh, interesting. Oh, that's so interesting. Actually, that's a personal story I can't tell. Oops. I almost said something I can't say that doesn't happen often. It's the person that I know that I'm not connected to enough to think that I would be okay saying what I was gonna say. Oh, yeah, but oh, that's just, it's so. So I don't know the whole thing is fascinating to me. Tactile problems with food. Yes, what kind of stuff bothers you? Textures.
Speaker 2 55:06
I'm I'm very, very sensitive to textures. If there is any sort of unexpected like meat, is tricky for me, because if I bite down on a piece of bristle. That's it. It's not a picky eating thing. It's my it's physiological, my I'll be I can be eating something and be like, Oh my gosh, this is delicious, and I'm really enjoying eating it. And suddenly, midway through my throat will just say, Nope, we're not I can't swallow anymore. Physically, I'm not able to force myself to swallow, even if it's food that I am enjoying. Sometimes my brain will just say, Hey, this is poison and not let me continue. Okay, interesting. So that's that's been sometimes when I bolus, I'll bolus for, like, less than you know what the actual meal is, just in case I'm not able to finish it, or I've got to, like, always have, you know, juice and stuff on standby because of how frequently I will bolus for something that I normally am able to eat and then discover, oh, it's an off day. I'm not able to my brain's not liking this food. Now, there's no rhyme or reason to any of it. Okay, it's, it's absurd and ridiculous, but enjoy something
Scott Benner 56:44
though. I mean, honestly, I look, have you heard me say on the podcast, like I don't like broccoli because it feels like the florets are little, tiny balls in my mouth? Yeah, I don't like that at all. I'm just, I now it doesn't like I could eat it if I had to, but that it is, what about it makes me go, what are we doing here? You know what I mean? Like, I'm not okay with this. The gristle things interesting, like, just shuts you down, huh?
Speaker 2 57:10
Yeah, any kind of unexpected texture and flavors are really I'm not super sensitive to flavors. I can I'm not a fan of spicy food, but I don't get, like, the visceral throat, the throat closing up reaction to it. It's really just just
Scott Benner 57:32
textures, yeah, and you have a little Oh, I'm sorry, Rebecca, go ahead. Well,
Speaker 1 57:35
I was just gonna say, tell Scott about yogurt and Greek yo, about yogurt that much and and then she tried Greek yogurt, and it was she said, What was it? A food has to commit to a flavor?
Speaker 2 57:53
Yeah, I didn't like I wanted to like yogurt so badly, because I'm like, that's such an easy, you know, simple, quick thing, and I never liked it because it's a little bit sour. And someone suggested, suggested I try Greek yogurt, and it I'm like, but that's more sour. So wouldn't I? But then I realized that I just have a preference for, like, a really strong flavor, because if it feels like the flavor. If a flavor is subtle enough, then my brain tells me that it could be an accident and the food has been contaminated or gone off somehow. So if it's gonna have a flavor, it needs to be a strong flavor. I
Scott Benner 58:37
gotcha. Mel, you have a little boy or a little girl? A little girl, how
Unknown Speaker 58:42
old six?
Scott Benner 58:44
Does she have any autism signs? Not because we can't leave it to you and your husband. You guys couldn't figure it out when you were together, so I'm not sure. Yeah,
Speaker 2 58:54
she hasn't had any issues in school or anything. So far, we're staying in communication with her teachers about it. I do see a lot of traits that I have in her, but I I don't want to project too much. But yeah, I figure that's that's something that we're going to have to kind of stay on top of and, yeah. But so far, she's doing well. So
Scott Benner 59:25
you're trying to balance the line between paying attention but not putting it in everybody's head so that they start seeing it if it's not there.
Speaker 2 59:32
Yeah, yeah. I don't want to see little normal things she because
Scott Benner 59:38
she doesn't like carrots, and all of a sudden she has autism or
Speaker 2 59:41
something like that. Yeah, I try really hard not to jump to conclusions too fast.
Scott Benner 59:48
I see if I just met you in, like, day to day stuff, would I know if you and I bumped into each other at, I don't know target, and you were like, you're the guy from the. Podcast, and I'd be like, I am the guy from the podcast. And you were like, Hey, I'm Mel. And I'm like, I know you. And then we chatted back and forth. Like, would I know that you're on the spectrum? Or you don't think I would be able to sniff it
Unknown Speaker 1:00:10
out? Um, I, I don't.
Unknown Speaker 1:00:14
I'm
Speaker 2 1:00:15
told that I'm a little strange. I've always been a little odd, but I don't know that I read specifically as autistic. I might seem like a little quirky, but
Scott Benner 1:00:33
who told you were strange?
Unknown Speaker 1:00:36
What I think? What
Scott Benner 1:00:37
the hell are you after that? Okay, all right. Literally, everyone, yes. Rebecca's like, yes, all, yeah, D everyone, Oh, I see. Okay. Well, can you tell me, Rebecca, tell me something she does that you think, that people think is strange
Speaker 1 1:00:55
one? Well, I was just thinking of one of these. I once asked her, Oh, I she was listening to the radio where we were together, and it was David Bowie. And I'm like, Oh, you like David Bowie. And she reacted in such an angry she's like, of course, I like David Bowie. And when she is confused by a question, it comes across as anger to other people, but I'm aware of that because it's my daughter, and we can joke about it, but it's one of the things that is kind of, it's kind of off putting for other people. If she's confused, it seems like she's angry,
Speaker 2 1:01:33
and I didn't know why that I really, I really was. It made me even more confused when people would react like I was trying to pick a fight with them, because I was genuinely just trying. I didn't find out until my late 20s that I was coming across as really rude, and I'm like, Oh no, why didn't everyone tell me that I was seeming like that?
Scott Benner 1:02:00
Rebecca, if you would have told me that story, and it would have been like, I said, Hey, you like David Bowie. And she said, Of course, I like David Bowie, and you would have responded, I'm afraid of Americans. I think I would have peed myself and fell on the ground just now. Rebecca, do you have any of this Autism Spectrum thing, or your or did Mel's father,
Speaker 1 1:02:23
we've been apart so long now. We were, we got married very, very young, so we've been apart so much that I don't, I don't really remember, but the more I know about autism, the more I kind of think I'll yeah, maybe gotcha, because we're Mel, Mel and I are very I don't know what the word I want to use. We're, we're not, we're not exactly like just a light, but we understand each other on a level that I don't think she's able to get that with other people, because I know that if she looks, you know, she's she's angry about what I offered her as food. That's not, she's not angry with me. And we have kind of a it took us a while to get here. I wasn't the best mom when she was little, and when I split up, you know, her dad and I split up, but we we've come to really appreciate each other. So I don't know if it's because I'm autistic somehow too, or just that I understand my daughter and so I'm more accepting of things. Yeah,
Scott Benner 1:03:34
what do you think? Well,
Speaker 2 1:03:35
I think that there's, I mean, it's, it's a spectrum, and I think she might be like on the like, maybe not quite like a subclinical or something, but definitely more toward she's always just understood me in a way that because I I wasn't able to explain what was going on, and my mom was sort of the only person who would try to understand me. She, instead of just getting frustrated with me, she she was always, always showed curiosity in if there was something she didn't understand about my behavior, she would try to understand it, which was not my experience. I was disliked by a lot of teachers because of how my curiosity came across, and I was assumed to be sarcastic when I wasn't things like that. And so she's always kind of gotten me there and I and the last name, so I'll just say that all of her siblings, all my aunts and uncles, they're all on the spectrum, most of my cousins. Not a Not, not all of them know it, and not all of them might want me to say it, but I'm, I'm fairly convinced I
Scott Benner 1:05:08
see. Okay, all right. Well, it's a family thing. Got it. Well,
Speaker 1 1:05:11
it just saw when that big family everybody knew if Mel would go somewhere and take a nap in the, you know, my parents house, where's Mela? She's taking a nap. Well, we didn't know she was narcoleptic as a child, but if that was normal, if my brother went next door because he just couldn't take the noise anymore, he'd come back after a while. Nobody, nobody made a fuss about the things that were
Scott Benner 1:05:38
adaptive. Yeah, it's adaptive, yeah. And it seems like, at least in your situation, Rebecca, like, a very, like, don't give up attitude too. That is what you described about your about your time with diabetes being rough, and then, like, how come you didn't just, like, throw in the towel at any point you told that story about your mom's head. You're like, you're great. I think your great grandmother, right? Like, you just get knocked down, stand back up again. But that's, that's the little bit of wiring, that's a little bit of personality. It's a little bit of, you know, being able to regulate your emotions, the whole thing there. So maybe your family's just a tough bunch of people who are slightly on the autism spectrum, you know what I mean, kind of just fight their way through it.
Speaker 1 1:06:19
Very, supportive. I lost my my brother, my father just it's been about a year now, sorry and thank you and my I know that I heard that your mother had passed too. I was very sorry to hear that. But in losing my my parents it they were such a supportive couple, my dad was pretty weird. I'm convinced my dad was autistic just at the end of his life. I was his primary caregiver, but my my parents together, they were just such a dynamic couple. My mom was half deaf and my dad was blind, and between the two of them, they they made a full person. They used to make that joke about themselves, but I grew up in a house with disability, and then I was diabetic at a young age, and so I think it Yeah, there was Dad obviously didn't drive. He was blind, and mom would do all the driving, and so we Yeah, it was adapting to whatever was. You don't throw something to dad. You go and put it in his hand. You You don't yell at mom, you look her directly in the face and talk to her that way.
Scott Benner 1:07:34
The perfect Marco Polo team. Do people play that still? I don't think so, right? Oh my gosh. Okay, well, I feel like I've gotten a really good look into into your situation, and I love how far you've come. Rebecca, that it's really a triumph, honestly, to get to an A, 1c, in the fives after all these years. And then Mel just starts off that way. So she's got a great start for her, her time with type one. And it's, it's inspirational. It really is. My gosh, I don't even know what else to say. It just, uh, I didn't expect this, I guess, I guess I'll, I'll finish up, and then I'll ask you if you have anything else. But, like, I read your note, and I have to admit, like, I didn't know what the hell today was going to be and and here's why, like you said, I said, what are some of the themes you hope to cover in your episode? And it starts off by saying, well, all the contact information is mine, but this would be an interview with my also type one daughter, who was recently diagnosed as autistic, and she's interested in discussing family history as a unique, positive. Okay, so that's your description. I swear I thought Mel was gonna be young from your description. And Mel like, I know you're in my group, like now, but I didn't like, I didn't search your name when your mom sent it to me. I just, I just, I just went with what I read, and when you jumped on and you were like, I'm in my 30s, and I was just, I was like, Oh, what the hell yeah. Like, I really thought that I sat down today to have a conversation with like, a teen, or a pre teen, or something like that, who had autism and whose mom was going to sit next to them and kind of help them through it. Yeah. And so even when you started talking, Melanie, I thought, this woman doesn't need help talking to me what is happening. And then I realized, Rebecca, you had type one also. I was like, Oh, I'm like, this is, like, a fantastic opportunity to talk to the two of you, but just not what I was expecting when I started. So really, really,
Speaker 2 1:09:39
I I think that our family dynamic is, is a it's a big part of it for me. Yeah,
Scott Benner 1:09:47
yeah, no, you guys seem very close.
Speaker 2 1:09:51
Oh, yeah, yeah, that we really especially we were already close before my diagnosis, sure, but I. Since then, I was misdiagnosed. Because of my age, I was misdiagnosed as type two, and the doctors were really not taking it seriously, and so she, like I, used her insulin for a while to keep myself stable until we were able to get into her endocrinology. I went to a diabetes class, and I think I was supposed to go to three of them, but I was so annoyed after the first one. I'm like my mom. Can I learned everything from her? I mean, the first day, you know, as soon as we saw the 600 on my blood stick thing. She brought her monitor over. You guys were on your way. Yeah, from that moment on, really, most of my education has been through my mom and through juicebox. About
Scott Benner 1:10:54
that, that's really something. Well, I You guys are delightful. I really enjoyed this. I want to make sure we're not missing anything though I did, I not ask anything I should have, or is there anything left that you didn't get
Speaker 1 1:11:04
to talk about? No, the only, the only thing is her diagnosis story was the only thing that I and she already went over some of that, but she was thirstier than she'd ever been, and I said, Okay, I'm bringing my meter over. I did that, and she didn't want she didn't want to get stuck, so remember, I had to pee on the little keto sticks. I said, If this turns purple, then I'm sticking your your finger. So of course, it was purple. But we went to the emergency room, they gave her insulin and IV drip, and then they sent her home with metformin. And I knew that wasn't adequate. It took, it took such a fight, and I was crying, and I was ready to put a box knife in my purse and bring it with me to these appointments, because nobody would listen. And I finally was able to get with my endocrinologist.
Unknown Speaker 1:12:00
He was also type one. Yes,
Speaker 1 1:12:02
I love him so much. He is. He's just the best. But I, I emailed him, I said my daughter went to the emergency room with this, and you know, she would like you to be her doctor, but they said she needs a referral. They gave her Metformin if you if you think this is okay, I trust you. And they okay my narcoleptic daughter. They worked her into an appointment at eight o'clock in the morning, and I had to go go, you know, sneak in the back door make sure she was awake. And I got her to that appointment. But he just, yeah, he's just like, I don't agree with that. And he's type one as well. And just, just a gem. He is awesome. But yet, as as an adult, being diagnosed with, I guess it was La da really, not really type one, right? Just getting her diagnosis. When I talked to the diabetes educator about her needing to have some insulin. And she said, Oh, it was, you know, she we're pretty sure she's type two. Is she a big girl? I said, I laughed at her. I said, I'm hoping that she weighs 100 pounds, because
Speaker 2 1:13:16
I was very, very thin. You were really thin at that time, yeah, I
Scott Benner 1:13:19
imagine, yeah. Because I know what you look I know what you look like, and you're, you're a lean person to begin with, yeah,
Speaker 2 1:13:24
and I had, I was very, very active at the time, peppered off a little after the diagnosis, because I struggled a little bit to figure out how to keep from going low. And so now I've kind of gotten back into that, but yeah, at the time, I was very fit, very active. The only reason to assume type two rather than type one was my age.
Scott Benner 1:13:52
That's a common mistake they make.
Speaker 1 1:13:55
Honestly, yeah, it is and frustrating. Yeah, at
Scott Benner 1:13:58
least you, your mom was there, and it didn't have to go on for a long, you know, yeah,
Speaker 2 1:14:02
I'm, I'm so thankful for her, because with I already have medical trauma, just because of, you know, being in and out of hospitals with all of my different issues and not knowing what was going on, and I don't know how, like my mom did all this stuff. She was calling people for me because I was just it. I was completely shut down. I couldn't, couldn't handle it. So can
Scott Benner 1:14:34
I ask Mel, this is like, How valuable is your husband in personal moments like this, like, do you guys have incredibly he is okay? Because that's what I'm wondering, because if you're having trouble, if you're shutting down, does he shut down too? Or do you guys have different reactions? Well,
Speaker 2 1:14:50
he was working from home when my mom came over to check my blood sugar, and he was actually in the middle of a meeting, and we were in the same. Same room, and I start hysterically crying once I saw how high my blood sugar was, because I knew what that meant. And he's just trying to finish this work call, and like looking at me like, you know, because obviously he wanted to get off the call and talk to me, but he he doesn't always immediately know the the best thing to do, but he is really big on research, any any kind of, I mean, with the the narcolepsy and the EDS too, as soon as I got those diagnoses, he would do a lot of time, you know, researching, and I used to do all of the cooking for our family. And since my diagnosis, I've, I've started cooking again now a little bit, but he took over all of that. I did not cook at all for about a year and a half because it was, I was dealing with the, you know, adjusting, and he would memorize the carb counts and tell me, and yeah, he's, he's absolutely fantastic, good.
Scott Benner 1:16:13
I'm glad that's great. Are you able to help him when he needs it?
Speaker 2 1:16:16
I try to. He is someone who doesn't ask for help. And so I kind of like, if he's sick or something, I have to be like, Get in bed, right? Like, I'll go make you soup. Why are you, like, dragging yourself into the kitchen? Like I can do it. So I kind of have to to force my help on him a little bit.
Scott Benner 1:16:39
That just sounds like you're married to a boy, but Okay, all right, I got it. I understand, ladies. I really appreciate this very much. I can't tell you how much actually, you were very kind and lovely throughout. And I think it's a terrific story. I appreciate you sharing it with us. Thank you. Yeah, my pleasure. Hold on one second. Okay, a huge thank you to one of today's sponsors, gevok glucagon. Find out more about Chivo hypopin at gvoke, glucagon.com. Forward slash juicebox. You spell that, G, V, O, k, e, g, l, U, C, A, G, o, n.com, forward slash juice box. US med is sponsoring this episode of The juicebox podcast, and we've been getting our diabetes supplies from us med for years. You can as well. Usmed.com/juice box, or call 888-721-1514, use the link or the number, get your free benefits, check and get started today with us. Med Jalen is an incredible example of what so many experience living with diabetes. You show up for yourself and others every day, never letting diabetes define you, and that is what the Medtronic champion community is all about. Each of us is strong, and together, we're even stronger. To hear more stories from the Medtronic champion community, or to share your own story, visit Medtronic diabetes.com/juicebox and look out online for the hashtag Medtronic champion if you have type two or pre diabetes, the type two diabetes Pro Tip series from the juicebox podcast is exactly what you're looking for. Do you have a friend or a family member who is struggling to understand their type two and how to manage it? This series is for them seven episodes to get you on track and up to speed. Episode 860, series intro. 864, guilt and shame. Episode 869, medical team. 874, fueling plan. Episode 880, diabetes technology. Episode 885, GLP ones, metformin and insulin. And in episode 889, we talk about movement. This episode is with me and Jenny Smith, of course, you know, Jenny is a Certified Diabetes Care and Education Specialist. She's a registered and licensed dietitian, and Jenny has had type one diabetes for over 30 years. Too many people don't understand their type two diabetes, and this series aims to fix that. Share it with a friend or get started today. Hey, thanks for listening all the way to the end. I really appreciate your loyalty and listenership, thank you so much for listening. I'll be back very soon with another episode of The juicebox podcast. Hey, what's up, everybody? If you've noticed that the podcast sounds better and you're thinking like, how does that happen? What you're hearing is Rob at wrong way recording doing his magic to these files. So if you want him to do his magic to you. Wrong way recording.com. You got a podcast. You want somebody to edit it? You want rob you.
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