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EPISODE 12 · Oct 1, 2026

My Breast Cancer Story

Bree Allred shares her breast cancer story: a lump found after weaning twins at 28, biopsy and surgery choices, chemo, and why to trust your instincts.

Hosted by Bree Allred, PT, DPT, PRPC

30 min

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Most people expect a breast cancer story to start with a mammogram. This one starts with a clogged milk duct, a set of one-year-old twins, and a mother who knew her own body well enough to notice that something had changed and stayed changed.

In this episode of Healing At Your Core, host Bree Allred, PT, DPT, PRPC shares her personal breast cancer story. She was 28 years old, pumping for twins, and diagnosed with ductal carcinoma in December 2011. Her purpose in telling it is not to alarm anyone. It is to encourage you to listen to what your body is communicating and to follow that instinct when something does not seem right. Below, you will find how her lump was first noticed, how the diagnosis unfolded, the decisions she weighed around surgery, fertility, and chemotherapy, and what survivorship has looked like almost fifteen years later.

A Lump That Did Not Go Away After Weaning

Bree had struggled with infertility, conceived her twins with Clomid, and ended up pumping because breastfeeding never went smoothly for her babies. Because she was massaging her breast tissue regularly to express milk, she was deeply familiar with how her breasts normally felt.

In September 2011, she developed a significant clogged milk duct. She was eventually able to clear it, but a lump remained. She described it as feeling like a marble she could chase underneath her skin, moving a bit like a kneecap slides side to side.

She waited and watched. Her twins were nearing a year, so she weaned in mid-October, then gave her body another month to settle. By late November the lump had not changed size and had not gone away. That is when she went to her OB's office and asked for an exam. Breast changes are common during and after lactation, and many lumps are not cancer. Persistence is what made this one worth investigating. Not every lingering symptom after weaning is serious, and the same principle applies across postpartum recovery: a body that keeps signaling deserves an answer rather than an assumption.

From Ultrasound to Biopsy: How the Diagnosis Unfolded

An ultrasound came first. Bree was told the lump had smooth edges, which was encouraging, because jagged edges are more typical of cancerous tissue. She was then referred to a general surgeon, who suspected a fibroadenoma, a benign finding that is common in pregnant and postpartum women. But because the tissue had some solid quality to it, he recommended a biopsy.

The biopsy was on December 16th and was largely painless. Three hollow cores were taken under ultrasound guidance so the needle could be confirmed inside the mass, then sent to pathology.

When the surgeon himself called after hours to schedule a morning conversation, she had an inkling. That night she finally got her results to load online.

I've never had the experience quite like reading ductal carcinoma on a report that had my name at the top.

Ductal means the milk ducts of the breast. Carcinoma means cancer. Her tumor was high grade, meaning it was dividing and developing quickly. The initial biopsy did not show estrogen or progesterone feeding it.

The Decisions: Surgery, Fertility, and Chemotherapy

Her surgeon walked her through the full landscape: possible chemotherapy, possible radiation, surgical options, further imaging, and a lymph node biopsy to check for spread. One thing he said gave her room to breathe.

Breanne, the research that we have really shows that you've got six weeks without this changing survivability.

Because she was young with dense breast tissue, she had an MRI, timed to a specific point in her menstrual cycle since breast tissue changes across the cycle. The MRI showed another questionable spot in the same breast. Her lymph node biopsy came back clean, so the plan became surgery first, then chemotherapy. She also connected with the Huntsman Cancer Institute and learned about tumor boards, where physicians present complex cases to colleagues to determine the best approach.

Choosing a unilateral mastectomy

Given her tumor size relative to her breast, and the second questionable spot, she chose mastectomy over lumpectomy. She chose a unilateral mastectomy on the right side because she hoped to have more children and wanted to preserve the ability to breastfeed. Her nipple was saved after the tissue beneath it tested clear, and a tissue expander was placed, later exchanged for a silicone implant. The surgical drains, she said, were the hardest part of recovery.

Weighing embryo preservation

Her recommended chemotherapy carried a likely risk of infertility. She was offered one cycle of IVF to freeze embryos during the month between surgery and chemotherapy. After a great deal of consideration with her husband, she declined, knowing she could not put her healing body or her mind through it at that moment. For her, it was the right choice.

Chemotherapy, Community, and Survivorship

A Port-a-Cath was placed under her left collarbone about a week before treatment. Her regimen, which she called ACMT, included Adriamycin alone and then Cytoxan with Taxol. Bloodwork before each infusion confirmed her body could withstand the next round. Nausea, GI upset, profound fatigue, and deep bone aches from the follow-up shot defined roughly five to seven days of every other week. She is direct about it: she does not wish chemotherapy on her worst enemy.

On day 14, her hair began falling out, so she held a head-shaving party. Her husband and his friends shaved with her. A friend cut her hair into a pixie. Neighbors tracked her chemo schedule and brought the few foods she could keep down.

She also holds onto a reframe her uncle offered when she asked why this was happening to her.

Of course, why not you? You have incredible family support. You're young and healthy and you can fight this. You have two beautiful babies.

Survivorship brought its own mental work. Every lingering headache or slow recovery from illness raised the question again. Over time that quieted, and she now gives herself permission to worry at her yearly oncology visit. Chemotherapy put her into temporary menopause for about a year and a half. She later had two more children without fertility treatment, breastfed both under close oncology monitoring, and about twelve years out chose a prophylactic mastectomy with symmetry surgery on the left side. That tissue came back free of cancer.

Action Steps

  • Get familiar with what your own breast tissue normally feels like, so a new change stands out to you.
  • If a lump persists after a clogged duct clears or after weaning, ask your provider to evaluate it rather than continuing to wait and watch alone.
  • Bring your questions in writing to appointments. Ask about imaging, biopsy, surgical options, and timelines so you understand the plan you are agreeing to.
  • If chemotherapy is being discussed and future pregnancy matters to you, ask about fertility considerations early, and give yourself room to decide what is right for your body and your mind.
  • Let people help. Meals, childcare, and rides are practical care, not an imposition.

Bree is clear that breast cancer no longer defines her, though what it taught her remains part of who she is. If something in your body has changed and stayed changed, that is worth an answer. You can hear more of her story behind founding this practice in Why I Created Aylara Pelvic Health, and when you are ready for support with your own recovery, you can request an appointment.

READ THE FULL TRANSCRIPT
We here at Healing at Your Core and at Aylara Pelvic [00:00:30] Health are very passionate about women's health, and we feel that it would be a [00:00:35] disservice if we didn't spend some time talking about breast cancer. It's something that's near and dear to our [00:00:40] hearts here, as I am personally a breast cancer survivor. It's been almost 15 years since my [00:00:45] diagnosis, and, um, something that I really want to [00:00:50] discuss and share a little bit of my experience, and also encourage others [00:00:55] to listen to your body, to listen to what you know, and to follow those [00:01:00] instincts when things just don't quite seem right. So [00:01:05] starting my journey, um, it was [00:01:10] September of 2011, and I was [00:01:15] a new mom to one-year-old twins, almost one-year-old [00:01:20] twins, boy and a girl, and we had prayed vivaciously for these little [00:01:25] babies. We struggled with some infertility and had to take [00:01:30] Clomid in order to get pregnant, and ended up being one of the [00:01:35] 3% increase that get twins when we're on Clomid. And it was such a [00:01:40] crazy and hectic time. My kiddos never did do great with [00:01:45] breastfeeding, so I ended up pumping, uh, breast milk for them. Um, I [00:01:50] remember that I got a clogged milk duct, and this clogged milk duct, [00:01:55] um, was a pretty significant one, but I was finally able to get it to clear. And [00:02:00] once I got the clogged milk duct to clear, there was a lump in my breast that I never really [00:02:05] did get to go away. But I was just watching it and monitoring it. Um, [00:02:10] as I'd been pumping, I was massaging my breast tissue quite a bit in [00:02:15] order to, um, help express more milk, so I was pretty familiar with what my breast [00:02:20] felt like at this time, and I knew that this lump was new. But being that [00:02:25] my twins were almost a year and I was going to be working on weaning down the amounts of milk that I [00:02:30] was, was providing, um, I decided to just wait. So I waited [00:02:35] and right in October, kind of middle of October, we, we weaned, and then I [00:02:40] waited a month after we had weaned in order to kind of assess things. [00:02:45] So come to like end of November, I believe, I was [00:02:50] like, "Okay, this lump is still here, and it hasn't changed size," and so I went to [00:02:55] my OB's office to get it checked out. And I went in for the exam. They [00:03:00] did a breast exam and found the lump and knew what I was talking about. For me, [00:03:05] um, it sounded silly, but it was almost like a marble that I could chase underneath my skin. [00:03:10] Um, kind of like you move your kneecap back and forth, like it would kind of wiggle and move, um, [00:03:15] and it felt like about a marble size, like a standard marble. That's about what mine felt like. [00:03:20] And, uh, they sent me for an ultrasound, and I got the [00:03:25] ultrasound done, and I remember the ultrasound tech, um, giving me some guidance to [00:03:30] where it's like, "Okay, it has smooth edges. Um, it's looking pretty good." Cancer tends [00:03:35] to have more jagged edges. But they did say that there was-- that they would send these back, [00:03:40] um, to the physician and, um We actually-- [00:03:45] trying to think. They had me follow up with a general surgeon, so I did the ultrasound, and then they scheduled an [00:03:50] appointment with a general surgeon for me. And the general surgeon looked at the results, and he's like: "Well, the edges here are [00:03:55] pretty smooth. It looks like it's pretty localized and encapsulated." Um, edges on [00:04:00] cancerous tissue tend to be a little bit more jagged, and it was encouraging. He's like: "It's probably a [00:04:05] fibroadenoma, especially given, um, that those are common after breastfeeding and [00:04:10] in kind of pregnant postpartum women." And he was like: "But there looks like there's [00:04:15] some solid nature to this tissue, and so we probably ought to get it biopsied." So I [00:04:20] remember going in for a biopsy on December 16th, [00:04:25] and the biopsy was generally painless. [00:04:30] Um, I'm pretty sure they took three hollow cores, so meaning that they've got a needle [00:04:35] that has a hole in the middle, and they just puncture it through. And they did mine under ultrasound. I don't know if that's [00:04:40] standard for people, um, but they did mine under ultrasound so to make sure that they got the needle [00:04:45] through the mass that they were looking at. And they took three hollow cores, meaning they [00:04:50] cored out, um, three different spots in that and sent it off for, [00:04:55] uh, the pathologist to take a look at. And I remembered [00:05:00] not really thinking much. It was a little bit sore afterwards, but I remember not really thinking much about it. [00:05:05] And then come Monday, around five PM, the general surgeon [00:05:10] called, and, um, I was still with patients in my physical therapy [00:05:15] practice and wasn't able to answer the phone call, but he said that, um, [00:05:20] he wanted to chat with me, and he would be calling around nine o'clock the next morning [00:05:25] and to see if I could be available. And I was like, "All right." Uh, I knew then that that [00:05:30] meant that my biopsy results were likely back. And typically, when [00:05:35] the surgeon themselves is calling, uh, I just had an inkling that it probably [00:05:40] wasn't good. But I remember, um, then we had a Christmas party [00:05:45] that night with some friends, and I kept trying to look up my results online on the [00:05:50] online EMR results. And they wouldn't load and wouldn't load, and so [00:05:55] finally we went home. We put our twins to bed, um, and then I went and was able to [00:06:00] get on the computer, and finally those results loaded. And I will tell you, I've never had the [00:06:05] experience quite like reading, um, ductal, ductal carcinoma [00:06:10] on a report that had my name at the top. And ductal [00:06:15] means that it is in the milk ducts of the breast, and carcinoma means cancer. That's [00:06:20] the medical term for cancer. And I was like-- My husband looked at me, and he's like, "What?" And I'm like, "I have [00:06:25] cancer." And I remember just kind of feeling numb a little bit there and [00:06:30] kind of processing those results and then going into a state [00:06:35] where, um- I was just like, "Oh my gosh," like, "I have cancer."[00:06:40] And so one of my twins ended up crying, and it was I think my son, Tayson, and [00:06:45] he ... I went in and just was rocking him and crying and, and, you know, [00:06:50] so many thoughts going through my head, like, "Am I gonna be here to see these beautiful babies grow up? Am [00:06:55] I ... Are they gonna know life without a mom?" The way our thoughts do, that it just kept [00:07:00] kind of going a little bit to worst-case scenario. And that [00:07:05] experience for me was just crazy. Um Then I tend to [00:07:10] like to get more information, so I went through every ounce of the biopsy report and was [00:07:15] finding, doing okay, like it's breast cancer. It's-- There's some that's just [00:07:20] like cells that are looking a little bit crazy, and there are some that are pretty [00:07:25] differentiated, meaning they look nothing like breast cancer or like breast tissue. Um, so [00:07:30] there's some that are pretty wild, and there's some that were doing, just kinda hanging out and maybe starting the [00:07:35] process. And I had a high grade, which means that it was quickly developing [00:07:40] and quickly dividing. And then just realizing like, okay, [00:07:45] this is like where we're at. I knew all the details about my cancer. [00:07:50] Um, that original biopsy didn't really show any [00:07:55] estrogen or progesterone feeding this, um, so we were just kind of [00:08:00] prepping, and we called and kinda let family know and let 'em know that we would, um, have a little bit more [00:08:05] information for them later after I met with the surgeon. So I went to work the next day [00:08:10] and kept my phone with me and visited with the doctor and [00:08:15] ended up meeting with him. I had canceled some patients at the end of my day so that I could go and [00:08:20] meet with him later that day, and he was so gracious and kind and went through all of the options with me. [00:08:25] Um, looking at surgeries and maybe wanting some more biopsies [00:08:30] and maybe wanting to look into things a little bit further. Um, [00:08:35] he told me that they could get me scheduled for surgery. They also really wanted to do an MRI [00:08:40] on me, uh, where I was so young, and I had dense breast tissue. I also got a [00:08:45] follow-up mammogram. I'm trying to remember the process of all of it, but one thing the surgeon told me is he [00:08:50] really took me through, like, "Okay, here's the options. Um, we're likely going to be doing chemo. We'll [00:08:55] look at radiation and surgery," and then determining what type of surgery we wanted to do, [00:09:00] whether that was a mastectomy or a lumpectomy, and also that would have some determinants [00:09:05] on what treatments we would want to do. He also wanted to get, um, a biopsy of a [00:09:10] lymph node just to see if there was, uh, any chances that this had spread.[00:09:15] So we kinda went through this process, and one of the things that he told me, he says, "Breanne, the [00:09:20] research that we have really shows that you've got six weeks without this [00:09:25] changing survivability." And that was huge for me because it gave me some comfort and time and knowing that it's [00:09:30] like, whew, I've got some time to do some research, to make some decisions, and to move [00:09:35] forward with what we choose. Although there was a sense of urgency in me that I'm like, "Something's trying to [00:09:40] kill me, and I want to get it out." So there were things there. Um, this [00:09:45] diagnosis happened on December nineteenth. So I found out on the nineteenth. [00:09:50] I talked to the physician on the twentieth, and of course, we're going into Christmas, so knowing that I had [00:09:55] that six weeks without it changing survivability in my case was hugely beneficial [00:10:00] for me. Um, we went through Christmas, we told family, we [00:10:05] did kind of all the things there, and it definitely, you [00:10:10] know, kind of puts a damper on things and it, you're like, "Okay, here we go. We've got [00:10:15] this." And I remember in this time a family member of mine, um [00:10:20] He gave me a different perspective, and I absolutely loved his perspective.[00:10:25] Um, 'cause sometimes we're stuck in the like, "Why me? Why, [00:10:30] why did this happen to me?" And he gave me the perspective of like, [00:10:35] "Of course, why not you? You have incredible family support. You have [00:10:40] young... You're young and healthy and you can fight this. You have two beautiful babies." It's like, "Why [00:10:45] not you?" And, and that was a unique perspective that he gave me, and I will forever be grateful for [00:10:50] that from, um, my uncle. So I [00:10:55] remember kinda doing some more research, um, being connected with some other breast [00:11:00] cancer survivors that have been diagnosed young. I was 28 years old at the time, [00:11:05] and, um, kind of out of my element. Everybody was... I'm like, typically [00:11:10] women are older when they get breast cancer. And so being 28 and [00:11:15] in kind of some unique situations there, it was nice to talk to some others who had been in my [00:11:20] situation. After Christmas, we were really waiting for a certain point in my menstrual cycle because breast [00:11:25] tissue changes with the menstrual cycle. So I had to wait until I was at a certain point in my menstrual cycle to get [00:11:30] my MRI. And I remember getting that at the beginning of January, and just a few [00:11:35] days later, I was able to get in with the Huntsman Cancer Institute. The Huntsman Cancer [00:11:40] Institute was phenomenal. Um, I highly recommend it for anyone who- that's going through [00:11:45] cancer treatments. But that doesn't mean that you have to not, uh, go to your local providers as well, 'cause they are [00:11:50] getting more and more research, more and more protocols. Um, the doctors that are dealing with cancers are [00:11:55] very interconnected, and they have things called tumor boards where they can, if they're not [00:12:00] sure on something, that they can present your case at these tumor boards and discuss what's best for you. So [00:12:05] it's really neat. Um, but based on what they found on the MRI, there was another questionable spot in my [00:12:10] same breast. Um, mine was the right side, and it was so small that they weren't sure [00:12:15] that they could get a biopsy on it, but it was questionable. And then there was some things showing up maybe in a m- [00:12:20] one of my lymph nodes being inflamed, so they wanted to do a biopsy on the lymph node to guide [00:12:25] treatment just a little bit more. Turned out the lymph node came back clean, so it was determined that we would [00:12:30] kind of move forward with surgery first and then doing chemo following surgery. [00:12:35] I... At that time then, it was the decision of do I do a [00:12:40] lumpectomy or a mastectomy? And I had very small breasts at the time, [00:12:45] and I'd just finished, you know, pumping for twins, and they were kind of deflated [00:12:50] and small. And they were concerned about, with the extent of the size of my tumor, [00:12:55] with my breast, what a lumpectomy would look like. And then we had this other questionable spot. So I decided to [00:13:00] move forward with a mastectomy. And then the other decision there that I had to make was, do I do a [00:13:05] unilateral mastectomy or a bilateral mastectomy? So a mastectomy is they take the entire breast. [00:13:10] Um- I chose at the time to do a unilateral mastectomy because I [00:13:15] believe, uh, because I really wanted to have more children and wanted to save [00:13:20] some, a breast to be able to breast them, feed them in the future. And so they were very [00:13:25] much in support of that. My left breast didn't have anything that we were concerned about at the time, and so I [00:13:30] moved forward at the end of January with a mastectomy on my right breast.[00:13:35] Surgery was, um Challenging, [00:13:40] uh, exhausting. They have drains that they put in afterwards, and I'm going to [00:13:45] have somebody that's gonna talk about surgical options, but I'll give you a little bit, kind of my perspective. [00:13:50] Um, the drains were the worst part. So they put some drains, which has a little bulb at the [00:13:55] end connected to a tube, and they create some little bit of suction. When we create an empty [00:14:00] space in the body, uh, the body tends to want to fill that space with something, and so it'll tend to [00:14:05] do it with fluid, and if we're not getting that fluid out and letting it accumulate, then it can breed [00:14:10] some infections. So they've got these tubes that, um, are stitched. [00:14:15] They come right out of your body, and they're stitched a little bit to the side to help them not move and, [00:14:20] uh, I had the tubes in for about two weeks. Uh, I think after one week [00:14:25] I got one of them removed based on the amount that was coming out, and then I had to wait one more week to get the second one removed, [00:14:30] and it was quite the experience, and that was the most uncomfortable [00:14:35] part for me. I remember looking down after surgery. They were able to save my nipple. They were able to test the [00:14:40] tissue underneath the nipple, and it was clear for cancer, and they'd gotten pretty [00:14:45] clean margins, and they didn't find any, so they were able to save my nipple. And I remember looking down and being [00:14:50] like, "My nipple is still here." Like, it still looked like me. It was a little deflated, but it [00:14:55] still looked like me. And then they place what they call a tissue expander inside, and the tissue [00:15:00] expander is... The way I think of it is like the really old-school, um, [00:15:05] ice packs. Do you know- that have kind of the hard top and then they've got kind of a bag underneath? That was [00:15:10] similar to what was inside of me. And the hard tip, they would, um, poke [00:15:15] saline needles into, and they would fill up or pump up the expander [00:15:20] to allow for my breast to maintain the size that it needed to maintain for an implant [00:15:25] later on. Now, there's many surgical options that people can undergo for, [00:15:30] um, reconstruction afterwards if they choose to, and I chose to [00:15:35] just do a silicone implant. I did not want to deal with healing from other parts of [00:15:40] my body, nor did I need to. I had really healthy tissue and, um, [00:15:45] didn't really need to worry about things there. But sometimes they can take a flap from your [00:15:50] belly or from your back. Sometimes they'll pull muscle with it, depending on what your tissue quality is like, [00:15:55] and, um, I was lucky enough or chose, in my case, to [00:16:00] just do a silicone implant. So I had this tissue expander. Um, they gave my body about a month [00:16:05] to heal. In this timeframe, another decision that I had to make is where [00:16:10] we wanted more children. Uh, we'd had fertility issues to begin with. The type of chemo [00:16:15] they were going to recommend for me was one that [00:16:20] would likely result in some infertility and damage eggs and do [00:16:25] things that way, so they would not be able to ensure that we could have kiddos, um, [00:16:30] future kiddos. Um, so that was another decision that I had to make along with my [00:16:35] husband as we were talking and- they can go [00:16:40] through the first steps of, like, the IVF process to get to frozen embryos in order [00:16:45] to save some things for people. I, at that time, I was like, "Mentally, I'm not in a place [00:16:50] where I can put my body full of hormones." So they wanted me to have surgery to get the cancer out, [00:16:55] and then in that month timeframe where my body's trying to heal, we would go through the IVF [00:17:00] process. We would have kind of one shot at it, um, to where they would [00:17:05] stimulate things with hormones to produce more eggs. We would fertilize those eggs with my husband's sperm into [00:17:10] embryos, and then freeze the embryos for future use. That was something, after a lot of [00:17:15] consideration, that I chose not to do, and for me, it was a good choice. I was [00:17:20] just like, "I don't think I can put my body through that process in this healing [00:17:25] timeframe," nor did I think I could mentally handle it at the time, just because of everything that I was going [00:17:30] through. Um, but they gave me one month in between surgery and starting chemo. [00:17:35] Um, about a week before chemo, I had another surgery to place what's called a Port-a-Cath, [00:17:40] and it went in right under my left collarbone, and they [00:17:45] thread it, it directly into a vein so that it gives them good access, um, [00:17:50] to be able to administer the chemo that's in a safe way. And so [00:17:55] we did that, and then the week later, I started chemotherapy. So my [00:18:00] cocktail that they called it was called ACMT. [00:18:05] Um, it was Adriamycin, which is also known as the Red Devil, and I would get that independently on [00:18:10] its own, and then I would have Cytoxan and Taxol together. I believe [00:18:15] I had six treatments, and I had three of Adriamycin, and then I had three of, uh, [00:18:20] Cytoxan and Taxol. And I don't wish chemo on my [00:18:25] worst enemy. It was the most awful thing I've ever done in my life. But you go [00:18:30] in, and I remember my first treatment, and they [00:18:35] kind of take some-- they take a blood draw, like a quick blood draw, in order to make [00:18:40] sure that you have good enough cells that they could do the treatment, that your body could withstand [00:18:45] the amount of damage that they were about to do. 'Cause if you, if your [00:18:50] blood cells and things haven't recovered well enough, they will delay the treatment by a week and [00:18:55] then try again. But there's... Your body has to be, have enough recovery [00:19:00] that it can handle another beating. And so they took a blood draw, get your base levels, and [00:19:05] then I went in, and they hooked me up to the Adriamycin, and it was like a six to [00:19:10] eight-hour drip that they put in. And so they also give you a lot of [00:19:15] medicines to help with allergic reactions, with nausea, with different things there. And, uh, [00:19:20] I just remember it's like, okay, you came in, you watched a movie, you took a nap, I journaled, I would [00:19:25] blog, I would do different things. And it was an interesting [00:19:30] experience to kind of watch. And then felt pretty decent other than tired [00:19:35] during the actual infusion. And then when I got home, it was about an [00:19:40] hour later that the nausea and the, like, absolute feeling so crappy hit me. [00:19:45] Um It was awful. I [00:19:50] was not sure I could keep anything down. I did throw up. Um, I was lucky [00:19:55] enough to have family and friends that would come and stay with me and help take care of our kiddos. I [00:20:00] was still at a point where I had lifting restrictions. Um, and somewhere in this [00:20:05] timeframe, I would feel pretty crappy for about five to seven days. It was usually [00:20:10] about five days. Um, I would have chemo on a Wednesday. I would take Thursday, Friday off of work, [00:20:15] and then I would end up going back to a light day at work, kind of a modified day, a little light day at work on [00:20:20] Monday, and then I would continue through, uh, the week, and then I would go Monday, [00:20:25] Tuesday, and then again on Wednesday, I would have another chemo. So my chemos were happening every other [00:20:30] week. And so I would have a decent week where I could eat and [00:20:35] sustain myself, and I would have a week of pretty much survival based on energy levels. [00:20:40] So at this point, this was my life. We would go back in. Uh, the next [00:20:45] day, they would give me a shot that would encourage my body now to produce more [00:20:50] blood cells, even though that we were, like, trying to kill them, and that shot would make me so [00:20:55] achy all over my body. I remember, uh, knowing where [00:21:00] every single bone was in my body because each and every one of them ached. There were days that I would spend [00:21:05] almost all the time in the tub because it was the only place I could find some relief. I would be just in a [00:21:10] bathrobe and lay in bed for the first several days. It was, it was rough. And [00:21:15] then GI upset. Um, if it wasn't nausea, it was definitely coming out the other [00:21:20] end, um, just like a fire in the rectum. It was awful. [00:21:25] Um, I do not wish chemo on my worst enemy. And then it comes down and I'm like... [00:21:30] I had kinda recovered that first time, and then the second treatment [00:21:35] that day, I got my second treatment, um, and it's day 14, your [00:21:40] hair will start to fall out with my r- with my, um, cocktail. [00:21:45] So day 14, my hair started falling out. I remember showering, uh, the day after [00:21:50] chemo And, uh, just like tugging on your hair and the whole thing would come [00:21:55] out. I took a shower and it was like all just clogging up [00:22:00] the, the drain. Um, I tried to blow-dry my hair and it would just like... Hair [00:22:05] would just, like the amount of hair I cleaned up off the floor was crazy. And I remember that night being like, [00:22:10] "Okay, I need to shave my head because I can't keep watching it fall out like [00:22:15] this." Um, so I- we had a head shaving party. We shaved my head that night. [00:22:20] And, um, several of my husband, like my husband and several of his friends [00:22:25] also shaved their heads with me. I had a dear friend that she ended up chopping her hair [00:22:30] and getting a pixie cut so that she... That was her way of [00:22:35] supporting. She's like, "I always wanted to try one and you gave me a great excuse to kind of do that." And we grew our hair out [00:22:40] together when it came to that point. Um, but that was a hard day when I shaved [00:22:45] my head. And people showed up for me in amazing ways with food, [00:22:50] or would keep track of my chemo schedule and bring an Italian ice 'cause that would sit [00:22:55] well, or stop by with Rumbies or apples 'cause those were things that I could stomach. [00:23:00] Um, it was one of those things where it was like, okay, people are amazing and our community showed up [00:23:05] and I have never felt so much love before in my life. So we went through this kind of every other [00:23:10] week feeling crappy. About halfway through we switched my treatments to the other rounds which my body [00:23:15] tolerated a lot better and would rebound better, so I was actually able [00:23:20] to try not getting the shot the day after, and that helped my system so [00:23:25] much. I wasn't as achy. I could kind of function a little bit better. And then they make [00:23:30] you, after chemo, they make you wait about three months before you head to reconstruction. And [00:23:35] reconstruction has lots of considerations as well, where I was only... [00:23:40] And along this timeframe I was having follow-ups with my surgeon and I was-- we were talking about [00:23:45] expansion into the breast tissue with that expander that they would see, okay, how [00:23:50] big do we need to go? Um, do we overstretch just a little bit and then allow it to tighten [00:23:55] back down? So there were a lot of discussions happening there. I was really aiming to [00:24:00] just match my opposite breast at the time, and we went through that process [00:24:05] and I remember in, um, it was in August, I was able to have [00:24:10] my final reconstruction where we swapped out my tissue expander and they put the, [00:24:15] um, they put the silicone implant in and it was such a [00:24:20] great day for me and it went amazing. And by that point forward, we went [00:24:25] forward and, and, you know, then you start living life as a survivor which is [00:24:30] unique in and of itself. Like there's a lot of mental games that take place. There's a lot [00:24:35] of, um- Whenever anything goes wrong, you have a headache that lasts longer than a day or [00:24:40] two, all of a sudden it's like, "Wait a minute, is there cancer?" Um, anytime you get sick and you don't [00:24:45] rebound as quickly, "Wait a minute, is there cancer?" Like, it's always there in the back of your mind. The [00:24:50] further I've been out from my diagnosis, the better I've done, and, um, I only give [00:24:55] myself permission to worry when I go in for a yearly check still with my oncologist. [00:25:00] And it's been a unique thing that's taught me so much. Um, I have so much more empathy. [00:25:05] I gained strength I didn't know I had, and things that don't kill us make us [00:25:10] stronger. They really do. And it was an incredible experience to go [00:25:15] through and one I hope I never have to do again. Right before I opened Aylara [00:25:20] I chose to have a prophylactic mastectomy on my other side. So I was [00:25:25] about, uh, 12 years in to my [00:25:30] survivorship journey and was ready for, um, [00:25:35] a kind of swap on my, on my right breast, [00:25:40] and at this point I'd gained some weight. I actually-- So I was able to have two more babies. [00:25:45] Um, one thing I didn't mention is that I've, I've been lucky enough to go through menopause once [00:25:50] already and get to go through it again. I'm pretty sure I'm in perimenopause right now, [00:25:55] and I am the lucky one that gets to go through menopause twice because chemo shut down all [00:26:00] function in my body, and I was in menopause for about a year and a half after [00:26:05] my chemo treatments. And then we were lucky enough and very blessed enough to be able to have [00:26:10] more children afterwards. I did so very closely watched [00:26:15] by my oncologist, and we were making sure that my breast tissue wasn't [00:26:20] changing too much on my remaining breast, and we went through and I was able to breastfeed, um, both of [00:26:25] my subsequent babies. So we had two more babies and actually had no fertility issues, [00:26:30] interestingly enough. I almost kinda felt like my body went through a reboot with the menopause and when things started [00:26:35] back up, um, and we didn't have any fertility issues afterwards and that was such a [00:26:40] blessing to us. I know that's not everyone's story, but it was our, our blessing and our story. [00:26:45] And, um, my remaining breast served its purpose for me and [00:26:50] I had decided that it was like, okay, I'd gained some weight. I had one breast that changed with weight, one breast [00:26:55] that didn't. I had about a cup size difference between the two, and I decided I was ready to go in for a [00:27:00] symmetry surgery and decided that it was like, okay, if I'm gonna do something with my left breast, [00:27:05] that I wanted to actually get to where, um, my right breast and my left [00:27:10] breast were the same and that I was going to do a prophylactic mastectomy on the left [00:27:15] in order to just decrease any breast cancer risks that I had. My left breast did come [00:27:20] back free of cancer, which it was incredible and it was so [00:27:25] interesting and so neat, um, to have that experience to be like, "Okay, I've taken care of my [00:27:30] belli- body. I've watched my health. I've changed my diet in order to [00:27:35] kind of help with cancer prevention of recurrence," and it made a huge difference for [00:27:40] me. My second experience with the mastectomy is now more fresh. Again, it was [00:27:45] clear, um- which was really neat to hear and went [00:27:50] through, I did actually a reduction on my left breast and asymmetry surgery on [00:27:55] the right to then even it up. So we did some expansion again on my right [00:28:00] and a reduction on my left. Had expanders in both again. I had to expand the right breast, [00:28:05] um, and just maintain space in the left one while we were evening things up and [00:28:10] allowing things to heal. And I will take you a little bit through, um, my healing [00:28:15] process, uh, later on in a different episode where we'll talk about what rehab can look [00:28:20] like and maybe show you some pictures of my journey along through this podcast if you're choosing [00:28:25] to watch on YouTube. I am a breast cancer survivor. It no longer defines me, [00:28:30] although it is still a big portion of who I am from what it taught me and what I've learned. [00:28:35] And I hope that as you follow along, we're gonna talk through some episodes and maybe walk you [00:28:40] through a little bit of what people go through through a breast cancer experience, and [00:28:45] maybe helping someone as with a new diagnosis be able to make some decisions. I [00:28:50] hope this episode of Healing At Your Core was informative, that you will enjoy this kind of [00:28:55] month-long series on breast cancer as we are in Breast Cancer Awareness Month. [00:29:00] And thanks for listening and also for following and we hope that you find this helpful ​[00:29:05] [00:29:10] [00:29:15] [00:29:20] [00:29:25] [00:29:30]

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