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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@mir123

This is so helpful, Chris. I feel the same way. I think people distance themselves from illness and death by saying a sick person "did" something wrong. But every person on earth falls ill, and will die. It is our mutual fate, and should engender friendly compassion rather than blame! (For ourselves too). I recently had coffeee with an acquaintance--we both do some writing about breast cancer. She started fretting about how she could have gotten it. I said--it's just because we have human bodies. She surprised me by bursting into tears! I was just trying to be sensible but it turns out this lifted some burden of self-blame. Maybe our job is not to discover causes but to be kind to ourselves and others.

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Reposting this graphic illustrating that unless a person has a strong genetic predisposition, one will probably never know the cause.

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@sharon35981

Diagnosed in February 2021. (Stage1B) Tried Verzenio, and I could only stand it for four months before I would wake up in the middle of the night suffocating. I’m on Anastrozole. Dr. said he wants me to take it for ten. I told him I wouldn’t live that long. I have had two spinal fractures and then a rib fracture getting a breast MRI. I refuse to get any more mammograms. I’ve threatened to stop my AI several times. I get the come-to-Jesus lecture. I grieve for my life the way it was before BC. I get a Signatera test every three months to check for cancer DNA in my blood. So far three negative test results. Wouldn’t it be wonderful to be done with even thinking about the possibility of BC recurrence.

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Were they concerned with your rib fracture as far as it getting into the bones? I just had a xray that showed fractures on rib 5 and 6.

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@val97

Hi friends. I'm not quite a year past diagnosis. July 31st will be one year anniversary of finding out "something" was wrong. I'll never forget it. About two and a half weeks later, I was a breast cancer patient. I had a double mastectomy in Oct. '23, redo surgery for clear margins in Nov., and reconstruction in March. I didn't have to go through chemo and chose not to do radiation, so that's a whole other set of traumas I didn't experience. I feel for those who did, my mother being one of them. It was hard to watch let alone go through, I imagine. However, post my last surgery, I was pretty far down the depression rabbit hole.

Medication might be an issue for some? Tamoxifen, I've read, has major side effects. I've read many on this site think their medications are affecting their moods. Some even started taking anti-depressants to combat it. However, there is also the fact we've all experienced this crazy trauma that changed our minds, bodies, and souls forever and became members of a club we never wanted to join...and that's a lot to process.

I found exercise and writing in a journal have helped me. Accepting who I am NOW has helped. Coming to this site has helped me immensely - being able to connect with people who truly understand this experience has been HUGE. And I'm focusing on getting good sleep. The meds cause hot flashes, so I sleep terribly some nights, but I'm trying different strategies to combat that. I find when I don't sleep well, I'm more of a mess.

One thing I'm giving myself some grace on -- getting cancer wasn't my fault. I actually needed to understand that, accept that and let it go. It happened to me. It totally sucks. I have to deal with it, probably, for the rest of my life. But I don't need to let it continue to take me down emotionally.

The day I got my diagnosis, I felt like my life got immediately shorter. And it may be true. It filled me with fear and sadness, so much so I started to shut down. I can't pinpoint what snapped me out of it, but one day I decided...I'm going to go live my life. I need to keep moving forward for me. (And should anyone here need a cheerleader along your path...I'm your girl.)

"Yesterday is gone. Tomorrow has not come. We only have today. Let us begin." -- Mother Teresa

Holding you in my heart, BC sisters.

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What an elegant, perfect assessment of this experience we're all sharing. Please keep posting. your words are so helpful!

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@sirene

Were they concerned with your rib fracture as far as it getting into the bones? I just had a xray that showed fractures on rib 5 and 6.

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Well stated! 🌸

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Be patient with yourself. This will take time .
Join a club or find a new hobby to get your mind off cancer,which has run your life .
You are not alone we survivors understand.

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Hi
Wow I finished treatment this apr. Struggling with fatigue and the same emotional turmoil. Mood swings, depression. Also had 4 deaths happen during my treatment and putting my mom in a nursing home. In therapy and getting on meds. I have never felt this kind of mental exhaustion. I was told it's a form of ptsd

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@sandyjr

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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I completely agree with the cancer PTSD. I had IDC in 2021. I was told it was caught very early and that my chance of recurrence was very, very low. I was told to be thankful, and I tried. Fast forward to 2024 and I was diagnosed with bone mets. Stage IV cancer is rough, its lonely and treatment has become a full time job. Although I grieve the life I no longer have, I am thankful for every additional day I am given.

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I am going through similar circumstances with stage four breast cancer metastasized in the bones. I was at stage two and had a three-year remission period that ended with a broken arm. Also have been diagnosed with PTSD. Not sure how to micromanage that. Or anything sometimes…I cannot get the support that I need from my family and my partner is absolutely nonresponsive and when he is, he’s ugly and insensitive. I am not ok but am expected to be absolutely fine.
I found that recovering from all the medication I went through and all of the surgeries at stage 2 was very difficult and it did take a couple of years. Remind yourself that you are not crazy. You went through a traumatic situation and your body is offkilter trying to survive and find balance, which is natural. Medicine is hard on our bodies. Just give yourself a little time and things will start to feel better and I do pray you are cancer free forever. Make sure you receive annual follow up scans!

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I just posted a new note that included some of what you are saying. My surgery was 2/2024. Last chemo was the end of May 2024. Am on Exemestane, AI drug. Will be 85 soon. I am not myself either. Very tearful, irritable and so very tired. I was just told by a Dr., not cancer Dr., that I needed to talk to someone, that I was holding in the emotions too much. I did release some of it in a small church group. I want to talk to a counselor. I know from past trauma that it takes a long time to find that normal or new normal again. Speaking with a good counselor can help. Did you say you are on an Al drug? I didn't have a rough menopause but think this must be what some women feel at menopause. Hormones are changing with the drug. I encourage talking to someone. Hang in there. We are members of a very large"club" of men and women going through much the same thing. Make sure your vit D and B12 lab work has been done.

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@sue417

Hi
Wow I finished treatment this apr. Struggling with fatigue and the same emotional turmoil. Mood swings, depression. Also had 4 deaths happen during my treatment and putting my mom in a nursing home. In therapy and getting on meds. I have never felt this kind of mental exhaustion. I was told it's a form of ptsd

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I didn't think about PTSD but it sure fits. We have been through a lot. I too have had deaths to deal with along with everything else. I am a widow and family not nearby. Friends were wonderful and helpful, just not the same as family.

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