Not doing well - PTSD?
I really need to get this out, and I'm sorry if it turns out to be long.
The last 5 months I have been emotionally hurting. Tired, drained, anxious and scared. I'm almost 3 yrs out from diagnosis and I thought "things" were suppose to get easier. They are not.
I was doing really well.....untill I took that cyp2d6 test and came out as a poor metabolizer. Since then, I have sunken into depression. Even though my onc explained the whole controversy regarding this test. He even printed out the latest news regarding this test, hoping to make me feel better. I don't. My ooph is booked for June 3rd. And although I should be relieved to have the surgery date quickly.....I'm terrified what they will find at pathology.
I had a scare last month that turned out to be a B9 cyst in my foob. I feel traumatized from that whole ordeal. The otherday, I was lying on the couch watching tv and had some stomach flutters on my right side. I built it all up in my head that my BC has returned in my liver. I kept pressing down on my stomach to see if I could feel anything, causing myself pain......and that made me convinced I was right. That brought me in to my GP today. My GP did a breast exam, felt my stomach and said she did not feel anything and everything feels and looks normal. She reviewed my last set of tumor markers and said they are well within the normal range. I know from the boards, that tumor markers are not too reliable....but, anyways.
My GP thinks I should go back on the Effexor, and I hate to admitt...but I think/know she is right. She said that she hates to see me hurting, and seemed concerned. I hate having to take another pill. But I'm suffering. My daughter does not deserve to have her mom emotionally not available and my husband.... can not wake up in the middle of the night, to find his wife crying in the bathroom. I'll be starting back on Effexor next week once I stop my Tamox for my ooph.
I see my onc on Thursday just to go over the ooph procedure and ask questions. I don't want to go there and sit down and be crying all over him. I have done that enough times. Thats why I'm writing everything out here.
Comments
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I rarely post here anymore but I do check in - I just wanted to stop and give you a hug.
This is not easy stuff - I agree that going back to the Effexor is a good plan. Why suffer if you dont have to.
I dont have much to add other than you are in my thoughts and I hope you get some relief soon.
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I so understand....
Your mind looks at all the logical things that the onc has to say but your heart is overwhelmed by news that things weren't what you thought. There's times when all the postive comments in the world just aren't enough. We need to let our heart hurt and then it can start mending.
I had a pretty down day today also. But I'm so glad I'm taking wellbutrin because I think I would have gone even lower. I think going back on Effexor is a good idea and would be a good pill to take. We get hit with such hard stuff. And like you've implied, it would be good for you and for your family. They want you back to feeling strong also.
I hope writing your post helps and you can find solace in the responses.
Hugs.
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Yes, Effexor does sound like a good plan. Thinking of you and hoping you feel better very soon.
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I'm so sorry you are having a tough time.
In coping with this stupid disease I think we rebuild ourselves a fragile little world, and one thing can send us tumbling to the bottom again.
I would try the Effexor again, if it works it is worth taking another pill every day.
You don't deserve to be miserable.
BTW - I was terrified by what they would find after my ooph too. Hang in there, I am sure it will be fine.
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Oh, sweetie, I am so sorry that you are going through this. I know how hard you have worked to get where you are emotionally, and all that's happened is that you have tripped over an ugly tree branch.
I made it through treatment ok, but any additional illness or threat completely destroys me. I have been known to drive to a doctor's appointment (like a primary care physician, for a parathyroid check) weeping all the way.
I truly believe that you are entitled to not feel the way you do, and would encourage you to use something to take the edge off.
Incidentally, if you had any issues with Effexor, don't forget that you can now take any pills you want! You aren't limited to things that interfere with tamox metabolism!
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I totally understand where you are coming from. I'm still doing Herceptin and won't be done until July. Even though I am excited for that part of treatment to be over, I am scared. Scared to the point of crying all the time, waking in the middle of the night and my thoughts were wondering to places that it shouldn't. I talked to my doctor and she put me on Effexor. I feel so much better about everything. Try it - it will be temporary - just to get you through this hurdle.
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Lexi
just wanted to let you know i am thinking of your; all of this stuff....is just so hard. returning to the effexor is a good idea. remember; depression and PTSD is a physical issue; not all emotional. we think it is emotional...but the reason why we respond to anitdepressants is because it is medicine...which helps us physically//emotionallty. depression, trauma...all the treatments...all the tweeking of our hormones...affects our bodies..which affects our feelings about life...ourselves.. my wish for you is that once you restart the effexor..you will begin to feel better.
keep writing to us. it really helps to put it all out there....and know you are not alone.
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i am the same way! two years out this month. I just had to start taking lexapro again. I hate taking it, but my depression was affecting my kids and my husband!!! Cant live like that! You can pm me if you like, but my daughters callling me sso cant type anymore.
Laura
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I feel bad that I had to let everything out like this. Almost guilty because I am almost 3 yrs out....I don't want to worry the new girls about "post treatment issues."
I went to bed early last night, and managed to have a good sleep. I don't get that very often. I forgot to also mention that I fell really...really down because of the lymphodema that I have developed. It makes me feel very self consious. I start Monday for treatment with that.
I was on 37.5mg of Effexor for 6 months. It did wonders. I didn't need a lot, but went off it because I wanted to see how I was off it. I was great for 5 months....then that cy2pd6 test happened.
I think I have read somewhere that Effexor can inhibit Tamox. Is this right?
I have about 20 pills left from my perscription 6 months ago. My GP gave me 2 samples of Cipralex 10mg.Does this interfere with Tamox?
I will be on Tamox likely till the 20th of this month, then stopping for my ooph surgery. I don't know if I should wait the 3 weeks before starting anything.....I need some relief sooner.
Thank you all for your responses and thoughts. Like I said, I usually don't put things out there like this, but I really don't want to bring anymore stress on my family. BTW...I've decided to book myself a massage today. A looooooong one!
xo...xo
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Hi Lexislove, I don't post often but I feel we have something in common. I am having my ooph on June 2nd and I know how you feel. I also am a poor metabolizer and so I have been on Arimidex for almost a year. The side effects are tough. I'm glad to stop the Lupron after my ooph. I also am on 37.5 Effexor. I was hoping to stop it after my ooph but after hearing you I may want to stay on it.....
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Gosh, Lexislove, I understand 110% of where you are coming from! I know what you are saying about every little ache you feel you think that something is wrong. It is completely normal to feel that too because look at what the 3 years that you have been through.
Who would have ever thought that they would have cancer? It is a blow and after you know your body didn't do it's job to purge all bad cells, you automatically think it is happening again..you have been through it once and it influences how you see EVERYTHING.
All I can really say, is that I understand. I am having to deal with an ovarian cyst and the Dr. wanted to do a hysterectomy...well, knowing I would never have HRT, I said 'no'...but I didn't know that it was a COMPLEX cyst...So I am sitting here freaking out that every little pain is the cyst growing. Enough to drive you nuts.
I understand about not wanting another pill on top of everything that you are already taking...what we have lived through is a hard path to walk.
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I am having my oomph June 11th and I am scared as well. I asked my oncologist and she told me mets to ovarys are very very rare. Also, I asked my obgyn to do an ultrasound of my ovarys so I can go into the surgery knowing everything is ok.
I am sorry your struggling. It sounds like an anti depressant might work well for you. I work out a lot and that is how I cope. On the really bad days I take xanax.
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It's a tough road for everyone here, and don't ever worry about the newbies. I actually think posts like yours help us understand that the end of treatment (chemo/rads) doesn't mean we're dancing through daisies. It requires an incredible amount of emotional energy to deal with the unknown and I think that you are right to be proactive and think about using an antidepressant. From what I understand, a prolonged depression can actually change the chemistry of your brain. It's best to treat it soon and then if warranted, you can wean yourself off.
Sorry about the lymphodema. Another area, like the psychological effects of living with this type of dx ,that could use more research.
Enjoy your massage.
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Just a question about the Tamox - why are you stopping it for your Surgery? I took it all the way through until I started Arimidex 2 or 3 weeks after my ooph. They gave me a shot of blood thinner during my pre-op, but I took it the night before and the night of my surgery without an issue.
And Effexor is one of the safe antidepresants to take with tamoxifen, Paxil i think isn't.
Glad you are feeling a bit better today.
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Dear Sweet lexislove, my heart so goes out to you. PTSD is a "natural response to an unnatural traumatic event" God knows this BC bitch is so foreign and unatural to what we as women are, and is so traumatizing. Just even from the beginning it is sooooo traumatizing from the very moment we are told we have breast cancer. Then with everything that follows is another nightmare. Lexislove, I too have PTSD. Was diagnosed and treated for it in 1999. Went thru a lot of therapy for PTSD. Panic attacks are also part of this condition. I was in treatment for it for several years, and was put on Effexor full doses. I was told I will probably always have to take it, although I only take 75 mgs a day now. But I think it's an excellent drug for depression and maybe your doc can also give you something for anxiety also. I was given Ativan along with the Effexor. I had gone thru an extremely traumatic event that brought on the PTSD that had been in me from childhood trauma,and came on full blown during the severe traumatic event in 1999. I actually went into the hospital for treatment at a specific center for treating PTSD. Although I was able to finally become successful in overcoming it and all I had gone thru, I do notice that since I've gone thru this BC thing, I do get a little isolating, and have my dark periods and become extremely anxious. I know that I need to stay on the Effexor and take the anti anxieties if needed also because I know PTSD can rear its ugly head with new traumatic events. I have not seen a therapist in years, and sometims wonder if sometimes I should, but I guess because I've already been thru so much therapy during those years learning how to manage and control my tirggers that bring on the depression and panic, I just feel a therapist is only going to say things I already know and have learned. Besides, this board is my therapy now. So take care sweat heart and don't feel down over PTSD. Again, it's a Natural reaction to Unatural traumatic events.
Barb
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I am so sorry for all that you're going through. (((HUGS))).
All of the medications we take for this disease affect us not just physcially, but emotionally as well. Although I am not quite at one year out - I found it helpful to read posts from everyone at different times. It helped me to feel that I wasn't alone in my symptoms, SE's or feelings. Putting it out there helps not only you, but others along the way.
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Kerry,
I'm thinking they want to stop the Tamox incase of blood clots? I stopped it as well when I had my exchange surgery.Those were the best 2-3 weeks I've had in a long time...I have seen on the boards womans onc saying yes to stop or no.
Pure,
Thanks for reasuring me that BC mets to the ovaries is rare. I've read that as well, but the mind still thinks up crazy scenarios...right?
Had my massage it was really good. I'm going to try to have one at least once a month.
I'm going to start the Effexor tonight. I remember for the first couple of days having a sick feeling....not looking forward to that, but I am looking forward to feeling better again.
Thank you all for listening/being there......
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Very honestly hon, and i can only speak for myself-I needed a full bio-psycho-social eval. Two weeks ago (four months out of a bad chemo reaction and surgery) my PCP found out that the chemo had destroyed my thyroid-i head no thyroid functiona nd my mood swings were beyond awful. I was not produsing Vit D and am now on 50000 units of Vit D a week: i had pernicious anemia and am now on iron meds: i have heart damage-now on BP meds bec my BP would not stabilize and i was protein difficient-my brain could not function-result for me....DEPRESSION!! I have been stable on my antidepressants for years and stable, but the chemo trashed my ability to have my antidepressants work at a theraputic level. And BARB could not be MORE RIGHT!!! I suffer from PTSD from childhood trauma-I have been sober for 22 years and thought I had worked thru all of my issues-I had but the BC triggered all of the PTSD in me (there is not that is cannot!!). I think this one of the huge errors that BC specialists overlook-with cancer, I was being appsed to so many specialists that noone could look at the whole picture and how it affected my PTSD and how it triggered my childhood issues!! i am working hard in therapry, but there is no quick fix and it is such drudgery. i cancelled a mammogram today because i cannot be touched in that way right now (i am four months out of chemo and surgery). I will rescedule and did make an appt to talk to my BS to review some of my PTSD issues and how they affect my cancer recovery-and it does have a huge impact on many women's recovery. But I needed to pull in all of my professional resources to deal with BC, not just with the cancer, but with the treatment and all of the 'undignified' ways in which my body was handled during all of the ID of the tumor; the biopsy, the surgery-everything!!! Get help gal and best of luck-you can do this but you need an organized and effective treatment plan!!! Blessings, SV
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Hi Lexi,
I am so sorry your feeling this way. I have admired you as you have always been so upbeat and reach out to so many women here on the boards. I had not heard of Effexor and will be asking my Onc about it. I too need something to help me out as I am constantly consumed with this damn disease and wake up in the middle of the night with panic attacks. I am thinking about you and sending positive thoughts your way! I am hoping that surgery goes smooth for you and you have a quick recovery.
Hugs
Frankie
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Hi, I am new to this site,but I have learned so much from you wonderful women as I read your post everyday. I also have been out two years and still live in fear. I had tumor markers done in the last six months and they have been up slightly ca29-27, 39-43-47-43 bone scan clear ct scan and pet scan clear so whats going on? Will have them repeated june14, How can I relax. My family just don't get it. Sorry we all have to be in the same boat.
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Dear Lexilove: I am sorry your feeling this way and I get it. I am almost three years out and I have been hypervigilant about my cancer returning. I do have swollen underarms and my groin hurts and swell after walking about two blocks and I am waiting on my tests for this. I hate feeling like this, it's all I think about I am reading Oncoblast info, but it is so out of hand. I think it is PTSD as well. I just finishe reading Wally Lambs book, the hour I furst believed. And it was about his wife and PTSD and everything she went through and put her family through and I got to thinking that boy oho boy it sounds like me. I also had the Cpy2d6 test, but no one has given me an answer the test was on Nov 9th 2007 my last chemo, (before herceptin) but I don't know what the results are, when I called the clinical trial number it was disconnected. I wish with all my heart I could bounce back to my old self, go to work, not be in pain every single day. But I think I will do the same as you and see about some strong antidepressants. What is really weird is that I have had suicidal ideation, and my sister called a week ago and she mentioned to me that she was thinking that way as well. I would never act on it and that is what she said, but it scared me. It felt so good to be able to share my ideation with my sister, made it go away. But not for long. I wouldn't ever do it, it would traumatize my children way to much, But I am tired of waking up sick waking up tired, or not being able to sleep. I have never used Effexor, but if it's working for others I will ask for it, how long does it take to kick in. Oh and Lexilove, it's Paxil that infterfere's with tamoxifen and that is the only antidepressant I have read about so far, I even posted the artical on bc.or. Didn't talk to anyone just posted it. The fear of this cancer return has taken over my life, with every bump, bruise, pain I seem to think it's cancer why am I doing this. I watched the documentary Sexycancer (I think that was the name) and I remember thinking about the one women who continued to feel pain and couldn't believe her cancer was gone, I remember thnking it wa so sad, and now I'm doing it. I will call tomorrow about getting some help for this, Thank you Lexilove for writing your so very honest words, I would never have writtien this without them, I need help!
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sweetie, I just wanted to chime in. There was a study back when I was dxed that gave stats on how many women w and post BC tx were on anti-anxiety meds. I don't remember the %, but do remember it was suprisingly high.
Well, not really if you think about the trauma and fear of it all.
Anyway, before BC I never took anything. A very wise woman told mewhen I was dxed that stress is far worse on the body( immune system, inflammatory processes, et)c then taking a med. I have to agree.
Please know that it does get easier . Really.
God Bless.
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Thank you Ikc: Stress is the worst thing and it does cause so many physical problems I could kick myself for being in denial for so long. Thank you for the your reply and I really can't wait to see if there will be a real diffeence. Jeeesh, if this pain was caused from stress alone and I did nothing for so long , I will be relieved but I certainly will feel stupid, because I know better, How is that when it comes to myself I can't or won't give myself a break, I have wasted almost a year tottally isolating and blaming the whole sheebang on cancer. I aml lucky that lately I've been lurking (and found Lexilove's post). I couldn't seem to talk much, denial again, I am so good at that and I hate that I do it. I know better I even taught action plans to avoid depression, panic attacks the whold shebang. But of course I didn't want to admit where I really was with my emotions. I am so very happy that I found Lexilove's post or I never would have opened up. I wante to start an advocates group up here in my small town and boy that would have been a huge mistake, I have to fix myself emotionally before I ever think of helping another cancer patient. When I first moved by up North I went to three funerals all good friends and all passed from cancer. And I still missed it. Live and hopefully learn, And you are right it will get easier, i can't wait until I can send a post feeling human again. Thank you Ikc and Lexilove good night and good luck.
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ah yes... we are forever in the waiting room... shudder.
I certainly am not free from the stress of worry... just a day and I could simply 'go away'.
it is unfair we have to deal with fear. good luck Lexi
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(((((((Lexi))))))) and (((((((SnowyDay)))))))), we're all in this together. I hope you wake up today feeling healthier and stronger....I hope you find the right meds to help you feel better.
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My thoughts are with you. I so know how you feel. I've been on Lexapro since I was diagnosed and I've been on it ever since. I believe its helping me cope because I have felt and done some of the same things you;ve describe, but I tend not to get down for too long. I jump right back to my normal self. I believe its the Lexapro that is helping me not remain down, because being a breast cancer survivor, I personally feel like I have a black cloud called cancer, is following behind me at all times.
((((hugs))))
Deb
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Dear sweet sisters,
I can relate so much to what you have all eloquently stated. We are real people, dealing with a horrible thing. When I was going through chemo my brain was so fried I wanted to die. I was so depressed. My family and my faith and my sisters here got me through it. I am a psychologist by profession--I "know" all the things to do to help ourselves. It was just so overwhelming. I am in a good place now, and I pray and send love to all my sisters who are suffering. I am proud of the honesty in this group--we are who we are, we feel what we feel, and it is ok to say that we are scared, hurting, sad, depressed, anxious, etc. That is our truth. Please don't be afraid to reach out to professional therapists--and keep searching till you find the one for you. In sisterhood. xo
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If you spend time every day on a breast cancer forum, it's difficult to move beyond the fear and obsession stage.
Honestly, for your own good, stay away.
I had to for months just to clear my mind of the constant focus on bc.
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Lexi,
Just wanted to drop in and say hi. I am thinking of you! Hope you had a better day today!
Hugs
Frankie
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Hi Lexi,
I so get what you are saying. During chemo although I felt like sh%# I didn't stress too much about a recurrence. Everyone thought I'd be thrilled to be done, and couldn't understand why I didn't feel like celebrating. And now during rads I've been having lots of misc pains that of course I am thinking are a recurrence. It IS like PTSD! We have been through a war and we will never be the same. And definitely if the Effexor works for you by all means take it! If you had diabetes you'd take the insulin wouldn't you? You need to think of it like that.
Hope things look up soon.
Love,
Sharon
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