Emotional aftermath following breast cancer treatment

Posted by rhongirl @rhongirl, Aug 23, 2022

While I was diagnosed in Dec. 2019, chemo, cancer surgery, and four more surgeries took place over the next 2 1/2 years (one of which was a second cancer surgery). I'm 6 weeks out from my last surgery, feeling somewhat normal physically, but wading through the emotional aftermath. "What just happened to me?" I told my husband that I've spent the past 2 1/2 years trying to stay alive - and I'm exhausted. Exaggerated emotions with up-and-down mood swings. . . I find myself yearning for that sense of emotional equilibrium I had before this all began. I'm doing my best to give myself time for this part of the healing - but I find myself weary. Family and friends look at me like I'm fine now, and the trauma has passed - but the truth is, I am not fine on the inside. It's as if my body is trying to reboot emotionally, and its short-circuiting a bit. I am so goal-oriented. . . if I just had that "magic" date of when everything would be normal again, I could focus on that; but it doesn't work that way. I have to be patient with this portion of the healing - and I'm finding that hard. What are others' experiences with this? How long does it take for your emotions to settle from the trauma of breast cancer?

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Profile picture for Chris, Volunteer Mentor @auntieoakley

We kind of are getting together for coffee, right here on connect. I kind of wander from table to table (conversations), but this feels like when I used to go to the tea parties. We all sat around sharing all the things we have in common and things we don’t, other people join our table then wander off to another table to join a different conversation. So brew a cup and get comfy, we are all here to be that girlfriend across the table.
I am 20 years from my original diagnosis and I can’t say I have ever really just moved past it, I have a “new normal” and life never just returned to the way it was.
How can we make this new life stable, for me it is gratitude, for life, for all of you, for my home, and my remaining abilities.
Please share ways that help you move forward each day, can you share your resilience tips?

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@ auntieaokley. I found myself wandering over the posts again with this topic. This is such an up-and-down business of dealing with the aftermath of breast cancer. I get to a place where I am so engaged with life, that the emotional leftovers are tucked away for the time being, yet truly not going away. I didn't notice, or perhaps it didn't sink in enough the first time I read your reply here, "I am 20 years from my original diagnosis and I can't say I have every really just moved past it. . " It's like these leftovers almost threaten to chip away at the progress we can make (emotionally) after breast cancer.

I was finding myself more easily hurt and/or irritated by things others would say (or not say), and recognizing that subtle depressed mood underneath, so I took inventory again. On the outside, I still look normal to others (I am so highly functional with life). But on the inside - things still remain a different story. Before my breast cancer diagnosis, I had had a stretch of medical challenges that had gone on for a number of years prior. A couple major accidents, one leaving me with a surgery and a lot of recovery time. . . a 6-month illness . . . and then I rolled into breast cancer, followed by endometrial cancer. Though I'm approaching my 4-year cancer-free appt, things have felt relentless for almost ten years. So, it's normal to feel so tired underneath it all! But I don't like this emotional limping I'm still doing. The limping has been noticeably affecting my physical being (disrupted sleep, lower energy, lack of regular exercise, weight gain [and isn't that a guilt and shame factor for a cancer survivor], irritability). One morning, I told myself that I needed to address this more fully.

I made the call to start seeing a psychologist for regular therapy. Though I find these sessions to be hard work (having to bring-to-the-front these pieces of emotional aftermath), the asking myself to talk about how I feel about everything has been good for me. I'm in a safe space with a professional who is genuinely trying to help me process what's leftover, and work to move through this stage of the breast cancer journey - into a life that is not just appears productive, wonderful, and fulfilling, but one that IS all that on the inside. It surely is a process of learning.

Thanks, Chris, for reminding me (and us all) that this is an ongoing thing - that we can continue to move forward in healthy ways as we live our new normal. One foot in front of the other. :).

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Being sick or diseased or incapacitated by trauma certainly is source of what we now term PTSD. At least, we acknowledge our distress and know we have special coping to do. No pretending otherwise. But in fact, a huge percentage of us humans live with these traumas. It’s almost more normal than to be whole and well! We help each other in our own new normal. Sending hugs to all.

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Hi
I totally relate to what you are saying and I'm only in the beginning stages of this. 2 years ago I had a fracture in my spine and my sleep had no idea I had osteopenia so was having treatments for that then had my follow-up mammogram last October where they found a thickening long story short I have my first surgery December 15th lumpectomy pathology showed some invasive cancer had my second surgery two weeks ago they had to take out some glands only one thank God but my body is just reeling from two surgeries emotionally I'm having a difficult time relating to the fact I have cancer and I also have fibromyalgia so it's like my body's been in two car accidents in 2 months. People look at you and think you're okay but they have no idea like you said of the trauma and emotional roller coaster we ride going through this. Thank you for sharing your feelings

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For me, I think it is something you just have to live with. I equate it to someone having a horrible experience and never being able to forget it. I have had BC twice and all that goes with it. Just the thought it can happen again is horrible. People who have never had breast cancer do not understand. Or people that have had any kind of cancer or even a bad disease probably would understand. I think you could call it breast cancer PTSD. It’s always there. The positive thing of all this is that you made it and you can do it again if needed. Just be thankful for the good days and good times to come.

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Profile picture for rhongirl @rhongirl

@sharon35981 Hi Sharon, Your post resonated with me. . . "I grieve for my life the way it was before BC." I am almost 4 years cancer-free, and once-in-a-while, I still find myself aching a bit on the inside with those thoughts. . . though, it's not so much grieving, but a deep ache when I give my mind license to think on it. Sometimes, it has been helpful to give myself that time, ache for a bit, and then, move on. Other times, I have just told my heart, "Not now", and continue on. I think it's important to do both. In reality, our lives are never the same from day to day. . . we've lived the day we're presently in, and changes are happening all the time. I think having BC just brings that into view in a very real way. We are forced to see the changes, not glossing over them and moving on quickly to the next thing.

In that regard, in the not "glossing over", I've learned to be more perceptive - of emotions, of others, of myself, of my purpose, how I spend my time, and so on. It doesn't mean I never waste a day anymore (drat! that human nature still plagues us all), but I count my days differently, I think, than I did before. So, in that light, there have been good things that were born out of my BC, yet, there are still residuals. Sometimes just a good "sigh" is what's needed for those residuals (those things I can do nothing about). and helps me keep moving forward.

Before BC, we wonder if we'll ever get the disease. After BC, we wonder if it will come back. I'm trying to tell myself to live in the day, and refrain so much from thinking about the what-ifs. Doing so takes away from my today. God tells us in His Word, "So, do not worry about tomorrow, for tomorrow will worry about itself. Each day has enough trouble of its own." (Matthew 6:34). So very hard to do, but surely, a healthier way to live in body, mind, and spirit.

Life is such a balance. And BC interrupts that balance a lot. Finding a new balance, takes time. And you will get it. :). PS. Love the image you shared

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Thank you for your post. I found it inspiring.

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Profile picture for myoga @myoga

I'm happy that your condition is stable! Just take one day at a time and keep that beautiful smile. You have lots of sisters here to listen and cheer for you. My MRI result came back clear. Thank God! We might not find the new us, but I'm glad I found this website. We're are here for one another and it gives me some sense of normalcy. Knowing that I'm not the only who feel this way is like finding the calmness in the chaos. Wish you all the best. Hugs.

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Thank you, prayers for us all.

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Profile picture for mssewest @mssewest

Still trying to find the new me again. Since I have been stable since my last Enhertu treatment in July 2023, my Oncologist and Oncology Cardiologist think I should hold off on taking Lapatinib and Xeloda. My tumor markers ca 27.29 ca 13.5 are very low and CT & NBM scan show no progression.

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I'm happy that your condition is stable! Just take one day at a time and keep that beautiful smile. You have lots of sisters here to listen and cheer for you. My MRI result came back clear. Thank God! We might not find the new us, but I'm glad I found this website. We're are here for one another and it gives me some sense of normalcy. Knowing that I'm not the only who feel this way is like finding the calmness in the chaos. Wish you all the best. Hugs.

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Profile picture for myoga @myoga

My heart goes out to you! I pray God will give you strength to get through this tough time. Sometimes I wish we could all get together for a cup of coffee, share our feelings, and support one another in person. Most people don't know what it feels like to get the cancer dx. They wonder why we still are not emotionally over it when all the treatments are done. Hugs.

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Still trying to find the new me again. Since I have been stable since my last Enhertu treatment in July 2023, my Oncologist and Oncology Cardiologist think I should hold off on taking Lapatinib and Xeloda. My tumor markers ca 27.29 ca 13.5 are very low and CT & NBM scan show no progression.

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Profile picture for rhongirl @rhongirl

@sharon35981 I grieved my former life, too - and at times, still do, but it's more of that ache now, and not so debilitating and cloudy as grief can sometimes be. And I began to say my thankful list out loud. It helped me to hear the truth of those words, in my own voice. Believing it began slowly, and then my mind followed suit and accepted those words as facts. 🙂

I love that you are playing the piano. I did that, too. And dogs? Hooray for you. I have a host of them. 🙂 Big hugs.

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Thank you for your response. Yes, good idea speaking gratitudes out loud. There is a lot to be grateful for; so easy to forget. I’m grateful for your letter. Kisses to your doggos. ❤️

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Profile picture for sharon35981 @sharon35981

Thank you so much for your heartfelt letter. I nodded “yes” all throughout your thoughts. I find that forgiveness—letting go—that I got BC (February 2021) is a practice; a moment to moment thing. Hard for me to do.

And then there’s gratitude. Sigh . . . I’m a work in progress. My last three Signatera blood tests were negative.

One of my joys before BC (in 2020) was playing the piano. Yesterday I started again.

Had my knee replaced in September 21 and hip in December 23. The dog is my service dog. Something else to be grateful for. I’m grateful for you and your wisdom. ❤️

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@sharon35981 I grieved my former life, too - and at times, still do, but it's more of that ache now, and not so debilitating and cloudy as grief can sometimes be. And I began to say my thankful list out loud. It helped me to hear the truth of those words, in my own voice. Believing it began slowly, and then my mind followed suit and accepted those words as facts. 🙂

I love that you are playing the piano. I did that, too. And dogs? Hooray for you. I have a host of them. 🙂 Big hugs.

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