To round out season 3 of Period Story, I’m really excited to share today’s episode with twin sisters Lauren Lee-Crane and Catherine Lee. They are the founders of Semaine, a health and wellness supplement for people with painful periods. I loved our conversation and am really grateful they shared their story of living with endometriosis, going through various surgeries, being Asian in the ballet world and of course, the story of their first periods.
Catherine said that her first period was very memorable because her mom made homemade Frappuccinos to toast the occasion! Within a few months, she said that she was already asking for a hysterectomy. Lauren says she got her period after Catherine and really didn’t want it.
We talked about being bunheads, which is the term for girls who do ballet at a relatively high level and how they navigated this very structured, hierarchical and rigid world. They were often told that they were too exotic for the ballet world and that they didn’t have the right ‘look’.
Lauren talks about how as ballerinas, they learned to suppress and numb themselves to any pain they experienced and this translated to the endometriosis pain as well. Lauren says they thought of it as just another pain they had to deal with.
Both Lauren and Catherine shared their endometriosis journeys, with Lauren getting diagnosed with stage 4 endometriosis and Catherine getting diagnosed with stage 2 endometriosis. Lauren described the pain she experienced as ‘a bouquet of knives sort of sitting up in her pelvis’. Catherine describes her pain as ‘feeling like she had a bowling ball in her uterus’.
Catherine and Lauren shared stories of their pain being dismissed by doctors and health professional in quite critical moments and how they’ve learned to advocate for themselves in health situations. Catherine says that it’s important to become an expert in your body and Lauren says to trust yourself and advocate for yourself. Thank you so much, Lauren and Catherine!
Get in touch with Lauren and Catherine:
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CATHERINE AND LAUREN’S BIOS
I’ve had painful periods since I was 15. After decades of believing the immense pain I experienced was normal, I was diagnosed with endometriosis and underwent multiple surgeries. I don’t want other women who have painful periods, endometriosis, adenomyosis and PCOS to go through what I have. Finding a natural way to support women’s health and voice their stories are the reasons we started Semaine: a health and wellness supplement for people with painful periods.
In my late twenties, I started to experience worsening symptoms from endometriosis. In 2015 I elected to have surgery and was diagnosed with stage II endometriosis. I see learning to live with endo as a journey – taking care of myself, listening to my body, and voicing what I need to be healthy. Normalizing the conversation around periods and period pain, is exactly why I wanted to start Semaine with Lar and her husband Matt.
Le’Nise: On today’s episode, we have Lauren Lee-Crane and Catherine Lee. They are the founders of Semaine, a health and wellness supplement for people with painful periods. They started Semaine after both being diagnosed with endometriosis and undergoing multiple surgeries. Lauren says that she doesn’t want other women who have painful periods. endometriosis, adenomyosis and PCOS to go through what she did. Catherine says that normalizing the conversation around periods and period pain is exactly why she wanted to start Semaine. They wanted to find a natural way to support women’s health and voice their stories. Welcome to the show.
Lauren: Thank you so much, Le’Nise, so happy to be here.
Catherine: Thank you, so excited.
Le’Nise: So can you both start off by telling me the story of your first period?
Catherine: Yes, this is Catherine. I will tell my story first because I got my period first, which, I was very upset because I thought as twins we were supposed to do everything together.
And I think I got my period almost like 6 to 12 months before Lauren did. And I remember it very vividly. We were, so we grew up outside of Washington, D.C. and Maryland. And every summer, our extended family had a beach condo in Ocean City, Maryland, which is on the eastern seaboard.
So we were at the beach, of course, so we were at that condo. And I still remember there were two bathrooms in that condo and the bathroom where I discovered I had my period. It had all these like orange and brown daisy wallpaper that I feel like that’s like stuck in my mind. But anyways, so I was like I started my period and I was like, oh no. And I remember I told my mom and she was like, so excited, at least that’s the impression I got. Like, maybe she was like, oh my gosh, what’s going on? But I remember it was when this is gonna age us for sure, but it was like a couple years after Frappuccinos came out in Starbucks and there were no Starbucks in Ocean City at the time. But my mom had found like a recipe to make Frappuccinos at home. So I remember she made, like, took out the blender at the beach condo and like made Frappuccinos. And we all, like, cheered to my womanhood. I was mortified and I was just like, I don’t want this. And I think eventually, like within those first couple of months of having my period, I think I asked my mom for a hysterectomy. Like, I don’t really know what it was. I just thought it was like it meant you didn’t have to bleed every month. So my mom was like, “but you’re going to want to have babies and all the things” and I was like, “Not worth it, don’t want this, get it out my body.” And I was just like, not. And I had I remembered, like, you know, with reading like articles like reading teen magazines and stuff and books like women were or young girls were so excited to get their periods and I was like, I can’t really I don’t I don’t want this at all. And I know, like, Lar, you can talk about it, but I know you were like, equally mortified for me.
Lauren: I remember. Oh Cath was twelve. Yeah. So we were a little bit older, I feel like when Cath got her period, I remember I was just like, ‘Oh my God, thank God I don’t have mine yet. And I, I think the reason why we felt that way is we were both dancers. We wanted to be ballerinas. I feel like most little girls at some point want that. We continued to want that until we were 18 and we danced all the time. We, we did like twenty five hours of ballet every week. That was our life. And as a ballet dancer, anything that’s going to cause you inconvenience or make it harder for you to be a ballet dancer, whether it’s to develop breasts, you know, you just want to be skinny. You just want to be able to move the way that you’re used to moving when you’re 11 to 17. And I remember, it’s like a period is going to be such an annoyance because, you know, you have to wear a tampon, you have to wear a pad. So I remember when Cath got her period and she was saying like she was so embarrassed. It was just me and my mom and my dad there. It’s not like we had other people at the condo with us. And I was so embarrassed for her, like, ‘oh, my God, why are we talking about Catherine’s period? I’m so glad I don’t have mine.’ Catherine’s right. I did get mine six months after her and I actually had mine when we were doing The Nutcracker. So every December, you know, every bunhead in the world does The Nutcracker at some point. And Cath and I were getting changed. This is a, you know, a couple hours before you went onstage and I was putting my costume on and I notice there’s like a little bit of blood on my tights.
And I was like, “No, I think I know what this is though. Why is it happening now?’ Cause of, you know, happening right before you’re going on stage. You’re already sort of like nervous and excited and then getting this thing that, Catherine and I obviously we never wanted. I know there are women you’ve had on your podcast and our friends who are excited to get their period, that was never our experience. And I think a big part of that was being ballet dancers and being so focused on on wanting to do that in the sort of strange culture that the ballet world is.
You know, I mean, it’s not like our ballet dancer teachers ever said, oh, getting your period is bad. I just remember hearing older ballet dancers talking about it and how painful it could be and how, you know, like I remember the Sugar Plum Fairy one year having to ask the costumers just to keep taking her out of her tutu because she had to go put a new tampon in. And I remember I was like, oh, my God, that sounds like such a headache. So that was that was our experience with with periods and ballet.
Le’Nise: Talk a bit about being bunheads. So for people who don’t know what that expression means, typically it refers to girls who do or who do, is it ballet and does it include gym, gymnasts as well? Or is it only ballet?
Catherine: I think I’ve only heard it used with ballet and when you’re a, if you’re doing ballet at a relatively high level, like a pre professional level like you, it was until like probably we were 16 that we just assumed we weren’t going to be going to university, that we would immediately go into a company or if if we were lucky enough, maybe we’d apply to Juilliard, you know, which is a very well-known school. But if you did ballet specifically, not modern dance or something like that, you essentially go in to a company as early as, like 16, depending on where you are.
And it wasn’t until we were 16 or 17 that we realized maybe we should get a college degree.
Le’Nise: Tell me a bit more about the ballet world. I did ballet when I was really little. But the only thing I really know about ballet is Christmas equals Nutcracker or. And then Black Swan, the movie. That’s it.
Lauren: That is totally understandable. I feel like that’s most people’s experience with ballet. And to be honest, Catherine and I have never seen Black Swan on because we were like, ‘it’s going to hit too close to home.’ So we’ve never watched it. But really, I feel like how it changed for us is when we were about eight years old, we decided, you know, this is our life. We started when we were about 3 because we had seen Baryshnikov, famous male ballet dancer dancing on television. And I thought he was flying. And I was like, yes, that is what I want to do. So I think a lot of people assume it’s like the pretty tutus or the pointe shoes. But for as we saw Baryshnikov and we like. That’s it. That that is life. And so we took like sort of the classes everybody takes when you start ballet and there’s like tap and jazz when we were younger and when we were eight, we went into this pre-professional academy. And so we would go to ballet anywhere from like when we were younger, it’s like three days a week, by the time we were in high school or about 13 – 14. We were going, you know, five to seven days a week and even leaving school early in order to go to class longer.
And it’s a very it’s a very, very structured, very hierarchical and very sort of rigid world. So each year, you’re trying to progress to sort of the next year. And within those years, you’re also doing performances. So The Nutcracker is the big one in the winter, but we’d have multiple performances in the spring, in the summer as well. And then in the summer, you’d also be applying for workshops with bigger companies like the Royal Ballet, if we were in the UK or American Ballet Theater, we would do workshops with the Joffrey Ballet Theater. We were often considered a little too exotic for the ballet world. We were told that multiple times. So we didn’t have as much luck with some of the bigger companies because we didn’t have the quote unquote look. This was in the 90s. Things have definitely changed now. Not as much as they should. But, you know, Misty Copeland’s out there, which is awesome. But that was very different for us. And sort of the mid, late 90s, we were just told we wouldn’t fit into the corps very well. So this was happening when we were sort of in our later teenage years. And one of the reasons why we ended up getting out of ballet and going to university instead just because of some of the discrimination we faced. But it’s in when you’re in that world, it just seems like even though you see that discrimination, you see, you know, the body dysmorphia that can happen. And obviously the way we thought about our periods was not particularly healthy. It was still such a dream for us like that, still having such a passion for something that almost nothing else mattered. You knowing you were just going to do whatever it took to get to where you wanted to be. And Cath and I were lucky to have each other because it’s a very, very competitive atmosphere that, the teachers are not particularly supportive. And we never competed against each other as twin sisters. It was like if Cath did well, I felt like I was doing well, even if she got a better part than me. But for the most part, you know, it’s not like a team sport. You are very much sort of alone in trying to be better than the next person next to you. So it’s it’s a very yeah. It’s as sort of a strange way to grow up because that, you know, we weren’t focused. We always had to do well in school because our parents were like, if you don’t do well in school, we’re taking you out of ballet. So we, we got the straight As or whatever we needed to do in order to stay with ballet. But really, that wasn’t important to us. It was just, do as well as you can at ballet. Nothing else really matters. And that’s you know, most people are going to parties when they’re teenagers or doing things like that. And we didn’t. It was just like ballet, ballet, ballet all the time.
Catherine: And a big part of it, too, was like Lar was saying about the teachers. Like, a lot of it in that world is just like you’re so desperate to get approval from all the teachers that you have, because they’re the ones who, like, you know, can help push you into a company. They’re the ones that give you better roles and different ballets and stuff like that. And then along the same side, of course, and you have the whole, like, body image aspect of it, which you always hear about with ballet.
Lauren and I were very lucky, we never had to worry about weight problems. I think that’s the Asian side of us. You know, we were naturally skinny, so we were very lucky in that. But we also didn’t have, like, Lar said there, we didn’t have the looks and we weren’t blond and blue eyed. And then on top of that, we didn’t really have the body type either. We’re tiny, we’re like 5″3 on a good day and and ah, you know, our pointes, our feet weren’t exactly like perfect. Our legs didn’t come up to our shoulders. We didn’t have super long legs. I think our torso and legs are kind of even. So it was all these things. It was funny because it was like we were very lucky. We had friends that, you know, suffered with anorexia and stuff and we didn’t have that. But for us, it was like growing up, knowing our bodies weren’t quite right for that world. So, like. And then on top of that, you have you get your period at 12, 13.
You know, and so it’s like one more thing to contend with. And the worst part was when, like, bloating started. I don’t think I started bloating. I don’t know. I can’t really remember. I was not in touch with my body at all at 12 and 13. But, you know, you can’t like suck in your stomach. And I remember dance teachers, you know, you want to tell them you were on your period and they would constantly tell you if your stomach was sticking out, you know, you’d be like, this is not my stomach. This is my uterus.
Le’Nise: Can you guys both can you both talk about how you feel if you start thinking back to what you went through and the comments that were made about your body so to the bloated belly, from what we know now, is endometriosis and the comments about you being, quote unquote, exotic, talk about how you feel looking back on that now. And whether that had any lasting effect on your, the way you view yourself.
Lauren: Yeah, absolutely. It definitely does. We are now in our 30s, so it’s been almost 20 years since we’re in that very dysfunctional world. But for sure, I still, I still remember the comments that the teachers made either when we were on our periods. And I remember the times when I had such painful periods. But you still had to dance.
And I remember the idea was you just shoved down whatever pain your body was feeling and you did what you had to do. And that is still the idea that stuck with me, I think, through my 20s for sure. So even when my endo pain was getting a lot more acute, it wasn’t just super heavy, painful cramps anymore. I was getting sharp jabbing pains in my pelvis. I remember just thinking, ‘OK, this is another pain I have to deal with. You just take some painkillers and you go to work. You know, you just keep doing what you have to do.’ And, you know, part of ballet is, is discomfort and pain. You know, whether it’s pointe shoes, you know, your feet always hurt or just what you’re how you’re using your body is. You know, it’s like any athlete. You’re, you’re also creating a lot of wear and tear on your body because of how demanding it is. But that sort of pain and rigor is sort of, it feels normal. It feels like part of what you have to deal with. And for me, painful periods. And because I feel like a lot of the women who were dancing with also had painful periods. And I don’t you know, I don’t think most of them had endo, but I don’t know if it’s like a body fat thing. You know, you had really irregular periods because you didn’t have a lot of body fat on you and you were probably stressed out a lot. Your body is physically stressed a lot. So I remember just thinking periods were horrible and painful and abnormal and could be super heavy one month and then you wouldn’t get it the next month. And now that just seem like a normal thing to me. And we definitely never talked about that side of our bodies with our teachers. You know, the teachers. It was all physical appearance, like superficial appearance. If you were looking a certain way and I think you know, the other ways that they told us, you know, being too exotic, being too short. And I remember they said our legs weren’t straight enough. And that’s always stuck with me cause my legs were slightly bow-legged, which I don’t think you would normally think about if you were a normal person who had done ballet. But I remember one of our teachers being like, we could have fixed that if you had told me about this when you were younger and now you always have bowlegs and no company is gonna take you. I remember thinking, just like…
Catherine: If you look at Lauren and she does not, I don’t, I don’t think you have bowlegs. That’s the thing, it’s like these little things that get stuck in your brain. You know, for mine, it was like, you know, our arms didn’t straighten all the way or in the right line and our legs didn’t. But like, I didn’t know you had that bowlegged thing. She also has, like, very subtle scoliosis. And it was so subtle that teachers just thought she was not stretching her neck out enough so she couldn’t turn her head. So it’s this constant thing where it’s like it’s on you, you know, to fix things that are wrong with your body. The responsibility is on you. Obviously, we couldn’t do anything about our ethnicity. We never felt ashamed of the way we looked. But it but it was just accepting. There’s a lot of stuff we accepted back then, I think, because we were kids and it was the 90s that nowadays I don’t think they could have gotten away with it, like, you know, just accepting like, oh, yeah, we’re we’re not blond and blue-eyed. So that’s we’re not going to get certain roles, are, you know, or since their bodies aren’t exactly right, we’re not going to be the teachers aren’t gonna pay attention to us the same amount away. And that was just accept, that was to us that was part of the world. We just stayed focused on it.
Le’Nise: You both have mentioned pain quite a lot, and something I find quite fascinating about ballet dancers is, you mentioned the pointe shoes and how you just have to, it’s painful and you’re putting your foot in a really unnatural way and basically balancing on your tip toes for like, what, 5, 6 plus hours, however long you’re dancing that particular day.
And do you think that that going through, having to go through that or deal with that pain on an ongoing basis, kind of numbed you to the endometriosis pain in the beginning?
Lauren: Yeah, absolutely. I just remember thinking that, you know, as a dancer, you know, your feet are sort of shaped a certain way and you have a lot of pain. But it’s also something you learn to sort of pull out of a little bit. There’s ways that make it a little less intense. But I think you’re absolutely right using that word numbing because it’s kind of a weird contradiction, because as dancers, you are very self-aware about your body, you know, just in the ways we were saying, because your things are constantly pointed out to you, but also just moving your body and being able to move through space a certain way and control it a certain way. You’re very aware of your, the way your muscles move and the way your centre of gravity is. But at the same time, you do numb yourself out to any discomfort or any pain because that isn’t going to help you, you know, perform. So it is it’s this weird dichotomy of, of being very aware of your body. But at the same time, if there’s pain, or things that are hurting, that’s something to ignore or push down rather than say, I wonder why I have really painful periods. I wonder why my cramps are so intense or is I didn’t even ever question if that was normal. Our mom also had a really, really intense periods and right, I’m sure she had endometriosis. It was probably not the same stage that maybe I had it, but that was another thing. You know, in our household, it was sort of normalized that periods were painful. And my mom is also a very stoic person. But I wouldn’t say I’m stoic. She is a stoic person. And so she never really complained. She would just say, oh, you know, my period’s really hurting right now, but I’m going to continue to cook food for our entire family during Christmas or, you know, clean the house. It’s just part of what you have to deal with this pain.
Le’Nise: Can we talk about your both of you, your individual endometriosis journey?
Because so, Lauren, you said you had painful periods from the age of 15. And then, Catherine you said that in your late 20s, you started to have worsening symptoms from endo. Can you talk? So you both had endometriosis, but very different experiences. So can you individually talk about what happened to you?
Lauren: Yeah, so my endometriosis story is like a lot of women with endometriosis. It took a really long time to get diagnosed. I think the average time for women to get diagnosed is about 7 to 10 years. For me, it was about 15 years. And the reason why is because I think, culturally, we normalise period pain and a lot of ways, you know, not just in the ballet world or not just in our family, but I feel like whenever I went to a doctor and said, oh, yeah, my periods are very painful, they be like, oh yeah, that’s too bad. You should you know, you can go on birth control or, you know, just keep taking ibuprofen. Like, that’s all you can do. So even at the point when, you know, being fifteen years old and my periods were starting to get really painful and it was for me it was mainly really, really, I could have really heavy periods and then I’d have really, really intense cramping where you had to lay down like, I just could not sit up straight. I mean, my body was just like bent double and that didn’t happen every single period. But it happened, you know, often enough. And I always dreaded getting my period. It was never something I was excited about or just thought, oh, hey, I’m bleeding now. I always knew when I had my period and it was painful. I didn’t, I don’t remember skipping school or anything because, again, I thought you just keep doing what you need to do. So, you know, this is something that’s going to happen every month or every other month. If it was erratic and you just had to deal with it and then like Cath and I both had the experience, we were as we move through early 20s, that pain sort of shifted from really heavy cramping. To me, it was a lot of sharp stabbing pain. Like I explain it as sort of it feels like you have a bouquet of sharp knives sort of sitting up in your pelvis. That’s how endo felt to me. And I was lucky in the sense that I’ve only ever had the pain during my period. I know a lot of women with endometriosis, you have pain throughout your whole cycle. And I felt so lucky that it was just that week. But then you have a quarter of your month is something you absolutely dread. And at the time, my husband and I were moving abroad. We went to the UK to live in Edinburgh. And at that point, I was like, you know what, I I’m pretty sure I have endometriosis. I Googled it. I talked to my doctor about it. She’s like, “Oh, yeah. I think that’s what you have.” I mean, that was the conversation. That was it. And so, again, it was something where it’s like, OK, I just need to deal with it and figure it out on my own. And so I tried changing my diet. I went vegan and gluten free, dairy free, all the things. And my pain just kept getting worse because I think at that point I had so much scarring with my body. I also had an endometrioma, which I didn’t know about, which is a specific type of cyst you can get with endometriosis, especially in the later stages. So endometriosis, for those of you that don’t know, are stage similar to cancers of stage one, two, three and four. And I ended up having stage four. I didn’t know that at the time and no one had told me about these different stages. But as I was experiencing worse and worse pain, I would go to my GP in Edinburgh and tell her like it’s getting worse and I don’t know what to do about it. And then at the point that it was about six months before my first emergency surgery, I remember feeling a lump on the left side of my body around where my left ovary would be. And of course, that freaked me out. I just assumed it was ovarian cancer. And I told my GP and she said it’s not really anything to worry about. I don’t think you have to worry. And I really had to push her to get me an appointment to see an ultrasound technician. And I finally got that like, a couple months later. And the technician was like, “oh, honey, I’m so sorry. You have an endometrioma.” And I was just so happy it wasn’t cancer. I was like, I don’t know what that is, but that’s I was fine. And she’s like, but you’ll need surgery. And I was like, okay, you know, I’m OK. Take it out. And I had no idea what it was like. I just I just was like, OK, it’s not cancer. We’ll schedule surgery six months from now. Great. We’ll get it done. And I don’t know if it’s just like experiencing pain. You’re just like, oh, surgery. Yeah. Massive surgery doesn’t sound like a big deal because let’s just let’s just do what we need to do. And before I could have that surgery, that endometrioma ruptured. Again, I didn’t know that’s what was happening at the time. But it it felt like something had kind of broke or snapped in my body. And I just had so much pain flooding into my pelvis at that point. And I remember this is really early in the morning and Matt had to call, my husband had to call 999. And the EMT came and I was lying on the floor. And the guy was like, you kind of look OK, essentially, like he took my vital signs or whatever. And he is like, You look OK. And I was like, I can’t get up off the floor. And he was like, well, you know, you probably have like a sore tummy. Like it was it was a really odd experience. Like I was like, no, I literally like, I’m in so much pain. And he started to like, get ready to leave. And I was like, I have a heart condition, cause I have mitral valve prolapse, which is very common for a lot of women, and it’s never something that bothered me. But I knew if I said I had a heart condition, they had to take me to the hospital. And so he was like, oh, OK. So then they took me to the hospital and they even though I told them I had to be an endometrioma, I have endometriosis. They were like, we think it’s appendicitis. And I was like, OK. So it took them about 24 hours to decide what to do with me. And I finally ended up in the gynecological ward. And I think they thought I had an STD like I was in so much pain. And they did an exam on me with like a speculum. And it hurt so much. And they still kind of didn’t believe what was going on. And I started running a really high fever. And that happened over the course of a couple days. And then during those couple days where they still couldn’t figure out what was going on, my stomach swoll up because of all the fluid that was pulling into my pelvic cavity. They basically it was the endometrioma had ruptured and was like irritating everything. So my body was trying to protect all my organs. I looked about six, seven months pregnant, and that was when they were finally like, oh, OK, we need to do an ultrasound and see what’s going on. So this is like day five of being in the hospital. And they were like, oh, OK. You have 500 milliliters of fluid. You need to go in and do emergency surgery and pull all that out. And after the surgery was when they were like, yes, you have endometriosis. It was a ruptured endometrioma. This is what happened. And so I was in the hospital for two weeks, and that was after the EMT almost didn’t take me to the hospital. So it’s such a bizarre experience to to by your GP, by everyone being told like it’s no big deal. You know, and then this thing happens. It’s very traumatic, big experience happens. And so that’s, it’s just it’s been a hard, hard journey. And since then, I’ve done a lot more research. And a year after that first emergency surgery, I learned about excision surgery, which is, quote unquote, the gold standard for endometriosis treatment. At this time, there’s no cure. Where they go in and they essentially I’m sorry, probably saying this wrong, but laser out sort of like cut through even healthy tissue to get out a lot of the endometrial tissue that’s where it shouldn’t be. And we found an excision specialist in Atlanta. And I had my second surgery about six months later. And since then have had way less pain, you know, instead of being a 10 plus off the charts. Now, my period, I have about like a three or four, which is amazing to me because I never, never thought that would happen. But it’s been a very long, painful road.
Le’Nise: What you’re saying about how the EMT didn’t, didn’t. He said, you look normal, but you’re, yet you’re saying to him: “I am in so much pain. I need to go to the hospital.” And every single time I hear a story like that, it never fails to just make me really angry at it.
Just believe women, believe women when they say that they are in pain. And it so absolutely enraged and enraging.
Lauren: Yeah. And I know that. Yeah. That’s not an uncommon story to hear, you know. And even if it’s not as extreme and you get to the hospital even talking to your GP and saying this is what’s happening, I never had a doctor say, oh, maybe you have endo or maybe there’s some other complication we should look into, even though my my pain was extreme. That was all my own research. And at that time, there weren’t. I’m so glad there’s so much more out there on the Great Interwebs right now about endometriosis. But at the time, there wasn’t that much. And I remember just trying to scour through pages and listen to, especially chat forums where other women were talking about this. I was like, OK, so I’m not crazy. I’m not alone. This is an actual thing because I didn’t get that experience from any doctor that I saw. And and sometimes people ask, like, oh, was it a male gynecologist? I’ve had tons of gynecologists. They’ve all been women. And none of them none of them took my pain seriously.
Le’Nise: That I mean, I it’s not you would say it’s unbelievable. But it’s not. I like it. I’ve heard this so often. Cath, can you talk about your story now?
Catherine: Yes. Mine is slightly less or significantly less traumatic than Lar and I, it’s a lot of that I give credit for Lar for basically being the guinea pig between the two of us because her, we don’t know if it was partly because she did get off birth control. And that’s kind of what triggered more of an endo pain because I never got off birth control. So when she and her husband had moved to Scotland, I was still on birth control. And by my late 20s, like Lar, I started developing more pain that wasn’t just cramping. I mean, all throughout my teens and twenties, certain periods would be, the cramps would be so bad I would feel like I had a bowling ball in my uterus, like, you know, like it’s such a weird sensation. And I just assumed, especially with our mom, who had painful periods, I was like, wow, this is what every woman goes through when they say they have cramps. So like that, I never even though it was hard to like stand for long periods of time with that sensation, I was like, this is just being a woman. And then by my late 20s, it was actually when I would have my period, on my period, like, wow, I was lucky I didn’t have pain off my period, but on my period when I’d have a bowel movement, the pain like in my pelvic region and I guess around my colon was so extreme that I thought I would pass out. And what’s funny is like, you know, you see movies and stuff. People get so much pain and then they pass out from the pain.
Like, I was like, why couldn’t that happen? I could not pass out. I would just have this extreme pain, you know, like where I would see stars and. And so that’s. And this is all while Lar was going through everything, which was horrendous and it was horrible too not being close to her and and not understanding the NHS system too, I was so confused by that. They didn’t let her have visitors at night. Like also like in the US, which, by the way, has a very broken medical system, too. I’m not like, I think the NHS is great compared to us, but in the States because everything’s charged to you. And they try to get you out of the hospital as soon as possible. They do like a million scans that first night. You know, they would have realized what she had sooner if she had been in the States. But that being said, she would have still been dismissed. So. So that was very like hearing from a distance, hearing her whole experience was kind of mind boggling to me. And I was, I remember being like, well, I just got to keep my periods not super painful. I don’t know what I would say. I mean, obviously, I couldn’t do that. I would take ibuprofen when the pain got really bad. I did start taking one or two days off of work. And that’s when I was like, OK, this is this is affecting my lifestyle. Like, I had to accept it. And then it was when the pain was getting so bad by my late 20s. And by then I think it was right before Lar had discovered that the Center for Endometriosis Care, which is in, which is in Atlanta with a great surgeon, that that’s when I was like, OK, you know, I think I’m going to have to do this, too. So it was a whole year after Lar had her excision surgery that I got it done too. And I have stage two endometriosis. So a significant amount of endometrial growth in my body, but obviously nothing to the extent that stage four would have. They did remove my appendix, funnily enough, because they did see endometrioma cells on my appendix. So I still remember, it was like they had given me that like horse tranquilizer right before my surgery. And then they come with this clipboard and they’re like, oh, just sign here. It basically says, we’ll take your appendix if it looks kind of weird.
And I was like, oh, you know, I’m high on drugs. I did. I was like. But the other thing that you like for the surgery prep, especially as I told them, I had so much pain around my colon, was there was a potential for colon resectioning which like by the time I was getting my surgery, I had so much pain, I was like, do it. I don’t know, you know, not really thinking the ramifications. And surprisingly enough, I didn’t, I think they found some endometrial cells around my colon, but not to the extent that they had to do any type of resectioning. So I was very lucky in that sense. And like Lar, since that surgery, I have not had that pain. When I go to the bathroom, the pain is definitely instead of being like a 10, it is now during my period, it is like a 3 or 4, nothing to the extent where I feel like I have to take off work or just lie down. Ah, I don’t even need to use heating pads, which is kind of amazing because it’s like I feel like I always had to use those beforehand. So definitely Lar kind of paved the way for me. We we both grew up knowing somewhat what endometriosis was. We had heard it because our mom had kind of self diagnosed. But we it to us that just meant like literally you just had painful periods. And so it wasn’t until Lar did all her research and she was telling me about it. I mean, I for me, I think maybe it was because of ballet. Maybe it was just growing up as a woman in the 90s, as a teenager. Like, to me, it was just like deal with it, press it down, kind of what Lar said, not being in touch with my body in the sense like I always use tampons, so I won’t even have to, like, feel myself bleeding, you know, like all that stuff. And then.
Yes, so similar to what Lar was saying, like pushing the pain down, trying to ignore it or just like, quote unquote dealing with it. To me that was like from that all the way to, like, even using tampons all the time instead of pads. So I don’t feel myself bleeding and stuff. And it wasn’t until my pain got so bad. And I think my, I was just so inflamed. Every time I was on my period, I could almost, I couldn’t really use tampons or if I did, I could only use the light tampons. And before we went on birth control, I think we went on, I can’t even remember. I think it was in our later teens and it was mostly for acne and it didn’t do anything for me. But once we started birth control pretty consistently, our periods weren’t super heavy. But when we first our periods first started and we were doing ballet so much, our periods were so heavy. I remember classes were like an hour and a half to two hours and I would have to use the bathroom at least once or twice to change out like a super tampon. But by the time it got to my surgery, which I think I was 29, I can’t do the math right now, but late 20s. I wasn’t even able to use tampons at all. So that’s, I mean, that alone, I was like, okay, something’s more serious here, but yeah, just the whole experience. I mean, it was traumatic. Lauren and I, actually one of the similarities we did have is after surgery, we both got post operation infections, which even our surgeon, who was a great guy, he was like, oh, you have less than one percent chance of getting a post up infection. And I remember Lar had gotten one after hers. And I was like, oh, I bet I’ll get, I’ll get one too. And the doctor was like, no, no, no, there’s no chance. Totally did. And once again, it was that that experience of being dismissed. I remember the doctor they kind of put me with after the surgery. It’s not the surgeon. You know, I would constantly call him because my, I had this low grade fever that just won’t go away. And something felt wrong. I think this was like a week and a half after my surgery. And I would call the hospital and be like, this is, I would call the doctor and say, you know, this isn’t right. Why am I having a fever? I can’t really keep food down. And I remember he just kept saying, oh, this is part of, like, surgery recovery. And he would brush it off and brush it off and brush it off. And then finally, I was talking to my mom. I was like in tears. My mom was like, that’s it. We’re just going to the emergency room. And sure enough, they like, there was an abscess. They had to drain an abscess. And I was in the hospital for another three days, which in the US, being in a hospital for three days is a long time, like Lar was in the hospital for two weeks. You know, the NHS, that’s a long time. But like three days in the US, they try to get you at a hospital as soon as possible. And it was just recovering from that. And I remember it. And the antibiotics that I had to take from that probably made me feel much worse than any surgery ever did. And I couldn’t eat. But you had to take the antibiotics and stuff. So we both, Lar and I both had that experience, too, which was us, so we, our recovery took a lot longer, I think, than most women. But just, you know, that’s another example of being kind of ignored, like after you’ve been through this very intense surgery. And like knowing your body, knowing like this doesn’t feel like just a recovery. Something’s going on. Like, my head felt like I was on fire 24/7, I think from the fever and just being dismissed after having gone through all of that, you know, and it, it just blows my mind. And then even today, like Lar was telling you, you know, I’ve had male and female gynaecologists. Before my surgery, I would tell them I had endometriosis and they would always say the same thing like Lar said, just take birth control, take pain meds. And then even after I had my surgery where I was like I have proof I have stage two, you know, and I would tell different gynecologists. I specifically remember when he was just like, oh, yeah, that’s oh, that’s rough. Like, that was literally the response. It wasn’t like, okay, well, like we understand that you stayed on birth control to kind of manage that and, you know, talk. There was there’s no discussion. I even had, I have some scar tissue. I think it’s up towards like the top of my vaginal wall. So it makes penetration with sex very painful, like full penetration. And that I didn’t start feeling until like six months after my surgery. And I remember going to the gynecologist and just, like, crying, because I was like, I don’t know what to do about this. And like the for some reason, it wasn’t my normal gynecologist. It was another woman in the practice, who was like, I think a robot. And she basically was like, well, you’re just going to have to get surgery again for that scar tissue. And I was like, but cutting away scar tissue causes more scar tissue. And she’s like, Yeah. And that was it. She was just like, you need to talk to your, and this is after and in the US, like our surgeon wasn’t covered by any insurance. He was outside that. So you’re paying so much money. I mean, a lot of women can’t get the surgery in the first place in the US because they can’t afford it. Their insurance obviously is not going to cover it. Or they cover a specific surgeon who maybe doesn’t do full excision surgery. They just do ablation and that’s not getting to the root of the cause. So, I mean, there’s all these things where you’re dealing with this medical world, too, that does not want to support you at all. But then, like, when you’re going to a gynecologist who’s supposed to be, you know, knowledgeable and be focused on female bodies, there’s like there’s it’s more like indifference than anything, which just blows my mind.
Le’Nise: I mean, I’m nodding along as you’re talking and everything you’re saying. I am. I keep thinking it’s just trauma and then more trauma and. I want to know, everything you’re going through now. And I want to talk about the company you founded to help women have better periods. But before we talk about that, I just want to talk about how you have gotten past or if you’ve gotten past the trauma of the surgeries and everything and dealing with the various doctors and medical professionals who questioned professionals who dismissed your pain or tried to downgrade your pain.
Lauren: Yeah, I would say that I’m still working through that trauma in a lot of ways, I think it’s almost been one of the unexpected advantages to starting a company sort of about period pain is I’ve had to think about my experience more, which has been hard, but also a really positive thing, because otherwise I would have reverted back to my usual, just push it down, don’t think about it. And I still like, I think on a day to day basis, like now Cath and I talk about it so much and we have a whole community of other women who have endometriosis pain in Atlanta, but just also online and just talking to women about their period pain in general. It’s so like life affirming and empowering in some ways because you don’t feel alone. You realize everybody is different. You know, you experience pain differently. Even if I talk with another woman who has stage four endometriosis, their experiences are completely different. So there’s, there’s so much good that’s come out of this, too. But Cath and I still talk about how before we go to gynecologists, even for just a normal routine exam, like we’re like we know we’re gonna cry in the office. Like, I don’t generally especially you, Cath, I don’t think you’re a big crier, but like, I just know I feel so vulnerable in that situation. And even if I talk through with my gynecologist and I usually bring my surgical like photos, like photos from inside of my body and I’m like, this is what I had. I’ve had the experience like Cath, where it’s still sort of worn off. And so you just always feel the sort of vulnerable existence when you’re in the doctor’s office and that you have to fight like, okay, I need to get my fighting face on because I need to make sure they believe me. I need to advocate for myself. But at the same time, I’m not completely over the trauma that’s happened to me before. So I know I’m going to feel really sort of teary eyed and then the doctors aren’t going to take me seriously and all this stuff that’s usually still was playing through my head. So, yeah, I would say I’m still working through the trauma, still working through some of that pain, but there’s been a lot of positive having to go through it.
Catherine: And I think the other thing, too, is that it seems sort of like the dark ages, but like any an gynaecologist you go to, their focus is on fertility.
And if they you know, they they, most gynaecologists have very little experience or got very little education on endometriosis. My guess would be the same with adenomyosis and PCOS and all the other things, PMDD. And to them, it’s at least the ones that I’ve met, it to them means potentially could affect your fertility. And so even when I try to have these conversations with the gynecologist, they always turn it around to like, well, I think you could get pregnant, or especially now, since we’re with, like, geriatric moms if we ever got pregnant. Right. We’re 37, 36, 37 in two weeks. We’re 36. And so, like, when I go to the gynecologist, every discussion, it’s always like, do you want to freeze your eggs?
Which in the States takes I think it’s like at least $20,000 to start out and like they talk about it so casually, like everybody has that amount of money, but also that that’s always how they focus on your body as basically as a baby making machine. And it I feel like even the surgeon too who we loved it, it’s still like he’s very used to having the conversation around fertility. Like, how does your endometriosis, how will that affect your fertility in that kind of thing? And both obviously, neither one of us have kids. We’re not. Neither one of us have decided whether we want kids, even though, you know, it’s getting a little late for us. But to me, it was always like, no, I. I want to focus on fixing my body first before I could even think of having, you know, a parasite. You know what I say? I was like, why? Why, why am I going to focus on kids now when, like, I’m in so much pain? But it’s just funny. The whole like the whole dialogue around it, even at doctors offices, even if they like, you know, kind of ignore your pain. It is always about fertility and how you’re basically worthy as a woman because of your level of fertility. That’s how I see it. And like Lar, I always have to prep myself before I, actually have my annual is on Monday. And I know, like, I’m going to get there early, I’m going to do breathing exercises. I’m going to be ready for the doctor to just dismiss me. Ah. You know, I want to talk about freezing my eggs again, even though I told her last time I saw her I was like, you need to write down in my file do not talk to me about freezing eggs. And even when I said that, even when I met with her last year, she was like, Really? Are you sure?
And I was like, come on, lady. You’re educated, listen to me.
So, like, it is still is like it’s something we deal with. And I think Lar said starting Semaine has kind of forced us to have those difficult conversations and revisit it. But I think that’s very healthy and something that we need to do. And it’s been so empowering and hearing other women’s stories and knowing that we’re not alone. And the fact that we could we could create this thing with Lar’s husband that actually helps women through their pain.
Le’Nise: What you’re saying about having to prepare to go and see your doctor, to see your gynecologist. I, you know, I think it’s really important because in an ideal world, we wouldn’t have to do that. We could go and our doctors would have the time to spend with us and have the time to ask questions and really figure out what’s going on in the moment. But certainly in the UK, there’s 10 minutes and you have to make the most of those 10 minutes. But I love what you’re saying about, you know, you do your breathing exercise. You’ve got your notes. Lar, you were saying you take the photos of your prior surgery. You know, you you you tell them to refer back to the notes you ask them to make on your file before. I think all of those are really important for women to remember. They have to go in prepared and be prepared to advocate for themselves. And if they don’t feel comfortable doing that, bring someone with them who can do that for them. I want to go on to talk about your company. So is it Semaine? Because I’m thinking French Semaine means week or how do you pronounce it?
Lauren: You’re completely right and you’re saying it correctly. As Americans, we say Semaine. So, yes, it is. It is the French word for the week, but, we, we, we. But you’re an American French. Oh, yes. That is the name in it. It came from from the fact that the supplement that we created, which is a plant based anti-inflammatory, is just for the week of your period or whenever you have the most pain on your cycle. Generally, even women who have sort of pain throughout their cycle, that might be the worst pain is during ovulation, maybe or maybe it’s right before your period. But for me personally, I’ve always been really bad about taking supplements continually. And so when Matt, my husband and Cath when we were creating this, I was like, I am not going to take something every single day. I won’t remember. And I don’t like the idea of having to take a pill every single day, even if it is all natural and plant based. And so because we were focusing on the inflammation aspect of period pain, rather than balancing hormones, making sure you have more estrogen or less estrogen, we we could really focus lowering that inflammation when you need it the most on your period. So in general, this is something that I had no idea about before we started Semaine. My husband did, he’s a research scientist. He has PhD in bioengineering, that on your cycle over the course of 28 days, roughly. Of course everybody’s different, but that your immune system sort of works that quickly as well. So when you’re moving into your ovulation period, your immune system pulls back a little bit, just in case you are you have foreign DNA that enters your body, you know, and you’re impregnated. So your immune system’s like, okay, we don’t we don’t want to attack that. Let’s pull back. And then if you’re not, if you’re not getting pregnant, your immune system kind of comes roaring back in the next two weeks and reaches its peak as you start to bleed. And a lot of the times with that immune system, that that causes a lot of inflammation, that your immune response and inflammation is connected. And so those of us with painful periods, not just with endometriosis, but with just painful periods in general, you’re having sort of a stronger immune response and more inflammation. So the thinking behind creating an anti-inflammatory is we’re lowering that inflammation levels So it’s all about, you know, like helping your body do its thing, have its period, but with sort of supported help of lowering the inflammation markers that are happening and causing a lot of pain. And that has been tremendously helpful for me because I know I was always sort of nervous about taking different things that regulated my hormones because there’s not a lot of research behind endometriosis, behind PCOS, behind any of these period related conditions. I think there’s not a lot of understanding of exactly how our hormones are sort of out of whack and that that can vary from person to person. So I really wanted something that could address the pain without having to be like, I don’t know, is my estrogen too high? You know, a lot of people do think endometriosis is estrogenic. So there is a link there, but they’re still not sure. I mean, again, because this is a, quote unquote, woman’s disease. The research is starting now. There’s a lot more research than there used to be, but there isn’t a lot of you know, there hasn’t been in the past. And just generally in medical history, you know, there hasn’t been a lot of research on women. I think a lot of people probably heard that that study about how women experience heart attacks different than men. But the symptoms we’re taught to look elsewhere are the symptoms that men usually have. And I remember reading, this is a study done like, you know, ten or fifteen years ago on cervical cancer. And they they tested the drug just on men who don’t have cervixes, you know, so it’s like. It blows your mind when you learn about this stuff. We were like, wait, you have to be doing these studies on women. And a big reason they don’t do the studies on women. And then prior to human subjects, why they don’t do it on on like female rats is because the hormones and having menstrual blood is very complicated and it complicates the results. And you’re like, yes. But the people taking it 50 percent plus are going to be people who have menstruated at some point and have these complex hormones. I, even when I was in the hospital actually in Edinburgh, it was a female doctor who was super sweet. But I remember at one point she said, you know, it be so much easier for us to figure out what was going on with you if you were a man, because all your bits are on the outside.
And I was just like wait what? What is it? Oh, my God. Like, this is the extent of of medical knowledge. Sort of like really a big community. I was like, we don’t have a chance in hell. Like, how is this, this is like the the response? In starting Semaine, we’ve learned that up to 80 percent of women have painful periods in their lifetime. So this isn’t abnormal. You know, it’s like everybody has has pain and you experience at different levels. Definitely our stories are a little more acute. And having endometriosis is is something that not all women have, though. More than 10 percent of women do have endometriosis. So none of these things are super unusual. And the fact that there aren’t hardly any pharmaceutical drugs specifically for women’s pain or even a lot of like natural things that we can do on the market right now, is really telling to me the fact that women’s pain isn’t taken seriously. If there’s, if PMSand endometriosis and all those conditions were something that men experienced, we’d have gobs of research. We’d have so many, you know, if they’re 5,000 pills for erectile dysfunction but nothing for, you know, period pain specifically, except for maybe Midol or Pamprin, which hasn’t changed in the last twenty five years. Something’s wrong. Something’s broken with with innovation in health care for women.
Catherine: I always think of that line in the show Veep.
Did you ever watch it? I don’t know. It was. I don’t know if it would come if it was in the UK at all. Because it is very specific to the US. But it’s the main character at one point. She was like, you know, if men got pregnant, you could get an abortion in an ATM by now, you know, and that’s what I always think about. It’s like it’s like it’s so true. What I think is so cool about Semaine is that so, Lauren and Matt, after Scotland, they moved to Seattle and that’s when Lar was especially, even now, when we get cramps and stuff, I think we’re a little triggered by experiences before we had our surgery. So even though we know the pain is not going to get as bad, it’s still very triggering. And so Lar’s husband, he’s a scientist. He has a PhD and was working for the University of Washington at the time. And he started doing research and reading up on white papers and peer reviewed papers on anything that could possibly help. So he started getting all these like extracts like in powder form and adding them to her smoothies. And it was I always joke that like the few times I would like go and visit them and see had all come to their kitchen. They had all these like jars of random powders or things going on. So he played around with the formula, I would say like that two years. Right. So and Lar was telling me how much of a difference it was making and I was like, send it to me because I, you know, I’ve been in Atlanta this whole time. And they literally sent me, it was a jar you sent me like a little scoop. And with like Lar’s handwritten instructions like how many scoops they should put in a smoothie each day. And I remember the first period I had using it, like my pain was reduced so much. And when I was and it wasn’t until we started talking about it, we were like, well, if this works for us, then maybe it’ll work for other women. And that’s how it got started. Like literally from them having a kitchen full of jars with powders in them.
Le’Nise: Wow. And so then you found that this worked for you. And then what was your, talk about the process of getting it onto the market?
Lauren: Yeah, that was that. That’s been a long journey because we started, Matt and I started testing those different plant extract powders. So it was like powder of green tea and curcumin. And I feel like those people have maybe heard of us as far as being good anti-inflammatory as are antioxidants. But we were testing other things, like some thing called resveratrol, something called boswellia, which is from frankincense. Matt had been doing research at the University of Washington about chronic inflammation and aging. So that’s how it was sort of in his mind already about like maybe we don’t address hormones, but we address the inflammation that’s happening every month when you’re on your period. And so after about two years of trying this and Cath and I being the guinea pigs, we opened it up to a larger test group of about 10 women who had period pain. So a couple of them did have endometriosis, but most of them just had general period pain. So not just pelvic pain and cramps, but maybe they got migraines or leg pain. You know, there’s lots of different types of pain that are associated with getting your period. And we had really good results from from that test. And so after getting those results, we’re like, okay, let’s start this as a business and let’s see if we can launch this as a product. And so originally it was, we were just putting the powers in pills ourselves, but we found a manufacturer and we, Matt and I quit our jobs in Seattle, moved to Atlanta, where we’re now living with Cath, so fun. And we focus on this full time. And we started an Indiegogo campaign in the fall to just sort of raise awareness and also a way to raise a little bit of money, but mainly to get sort of the name out there and make sure people are hearing that we’re doing this thing for period pain. And then in February of this year, we launched full time. And so right now, we sell Semaine directly from our web site: semainehealth.com. But we’re hoping to branch into retail so it’s more readily available to everyone. We do ship internationally, but most of our subscribers right now are in the States just because international shipping is really expensive. But we’re hoping, you know, eventually to expand and we could have distribution centers in the UK and Australia specifically because we get a lot of great feedback from those countries. But that’s how that’s how it started. It was literally trying to find something to fix my pain. We weren’t thinking of it as a business at all. But then when Catherine was like, it’s working for me. And the woman we had in our study was like, yes, you need to make more of this. We were like, OK, we want to help other women. You know, it was such a relief to have less painful periods, the fact that we are now helping other people have less painful periods, like I couldn’t ask for a better purpose in life, really, because I just never thought that was possible. I don’t know if it was because of years of being told that, oh, this is the only thing you can do. You can go on birth control. You can take ibuprofen. That I just thought that was kind of it. It didn’t even strike me that, why aren’t there more products out there for women? You know, and I think it’s such a great time now because people are talking about periods more openly. You have this wonderful podcast where people are talking about their first periods and hearing the differences and those stories are amazing. I think it’s so great to normalize those conversations. And I think that will change the way innovation help, that happens around women’s health care. Just the fact that, you know, people are making organic pads or reusable menstrual cups and like all of like The Honeypot Co. I don’t know if that’s big in the UK yet, but it’s here in Target that, you know, having said feminine care wipes like that, you know, something that’s in like the vernacular that we growing up, you know, we’ve never talked about that sort of thing, you know, and that wasn’t on the shelf at Target. And now you see that and women are interested in trying more natural solutions or just any solutions to try to make their periods better or more manageable and not this hush hush taboo thing that you can’t talk about.
Le’Nise: I think it’s incredible what you you both have done. And I love that you you took an issue that you had and you then created something that would not only help you, but would help loads of people with the same problems. So amazing. I can’t wait to see it here in the UK, but to round up our conversation. You both have said so many amazing things. What would you want someone to think to take listening to the podcast, to take away from what you individually have said?
Lauren: Such a great question, Le’Nise. I would say, as hard as it is always trust yourself and advocate for yourself. You do know your body better than anybody else. Better than any doctor. Better than anybody in your family. Being in tune with your body and knowing something doesn’t feel right. Push your doctor, push your health care provider to give you answers. If I had known that when I was younger, I know I just always assumed, oh, this person went to medical school and is a doctor, they know way more than me. If something was wrong, they would tell me. And I think, you know, doctors are amazing and they’re great. And I’m so glad we have the health care available that we can go to them. But that doesn’t mean that they know you better than you know yourself. Listen to your body if something feels wrong, you know. And also listen to yourself and not just assume that because one treatment works for one person, that that’s what you need to do. I think a lot of the time in the health and wellness space, we’re like, oh, I found this diet that cured me of this thing. You know, my endo is so much better because I stopped eating gluten. That is amazing. And that works for a lot of people. But that doesn’t necessarily mean it’s going to work for you and you have to do that same thing. If birth control works for you, if you need to be able to take that in order to get to day to day life, you know, do that. Don’t ever feel ashamed because people are pushing a certain solution on you. I think that’s so important.
Catherine: At the same exact thing, reiterate, advocate, advocate, advocate for yourself. I think that’s the big thing.
IF I could go back in time and talk to my 12 year old ashamed self with my period, just giving myself grace, but also telling myself, like, you know, trust yourself and be comfortable with your voice, especially when you’re with doctors. And then the other thing. What Lar said exactly, we’re identical twins and we’ve had very different experiences. You know, I compared to Lar, I eat garbage, you know, like I’ll eat fast food. I love I love to drink Coke. But Lar is much healthier than me. And part of that is driven by the pain that she had and kind of the PTSD left over from her experiences. But for me, diet does help. Absolutely. Without a doubt. But if I had just started looking into not just endometriosis but period pain and seeing all these like wellness warriors who can, you know, eat just kale for a day and, you know, that works for them, that I would feel kind of alienated from that. So I think reiterating what Lar said, like you figure out what works for you and then give yourself grace. You know, you’re not going to be this perfect pinnacle of health and you’re gonna have bad days and good days and and just celebrate the things that do work. But, yeah. That that some women don’t want to use tampons or don’t want to use hormonal birth control. And that is great. But some women would do. And that’s also great. So giving yourself grace and and figuring out, like Lar said, become an expert of your own body and what works for you.
Le’Nise: Thank you so much. I honestly feel like I could talk to you guys for another hour. It was just so brilliant.
Lauren: Thank you so much, Le’Nise. So much fun.
Le’Nise: You mentioned the website URL before. Can you just mention it again? So listeners know where to find out about Semaine.
Lauren: Yes, thank you. It’s semainehealth.com And we’re also very active on Instagram. So and that’s just @semainehealth. So thank you so much , Le’Nise. Yes, that’s where you can find us. We’re there all the time. We also have a chat on our web site, and that’s us answering questions. We love when people pepper us with questions about Semaine. So please feel free to do that.
Le’Nise: Thank you so much.