it's been quite a year
Tomorrow to the day will be exactly a year since my UMX. A lot's gone on in the year since, and much of it has been been good stuff, and not cancer related... like my first marathon this past January... but I still can't help thinking about where I was last year this time and where I am now. And it's not even like I have much to say about it all. I was lucky, had no chemo or rads, just three surgeries. But still, I find I want to bring attention to it, talk about it... I know I'm starting to bore and turn off my friends and family, and I'm trying so hard to block it from my attention, but I know better than that.
So here I am, one year later, back to running, feeling strong and almost like myself again. But still, something's different and I don't know how to really get past that.
Comments
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It's funny, isn't it? You feel different... but look just the same and because you look just like you used to, everybody thinks you should be "over it". I still feel the need to analyse what happened and why, but find myself writing about it instead of talking because I can see my family/friends growing uncomfortable/bored.
I think the only way to really get past that feeling of "otherness" is time... -
Thanks Selena. Patience has never been my strong suit.
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Monday is two years since my bmx. I hear ya.
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orangemat- I'm 2 years out from BMX and still feeling the same way. (Maybe I'm a slow learner?) My friends and family's eyes glazed over long ago at the mention of BC. But still feeling a need to talk about it and analyze the heck out of it I still post here. I guess I look at it as therapy. I remember someone once said that your body doesn't know the difference between a MX and being on the losing end of a mugging and knife fight. Guess if that had happened to me 2 years ago I might still be processing it, huh? lol! I did read that it takes about 2 years for a cancer patient (any cancer not just BC) to process things and start moving forward. Guess my time is up and I better get on it!
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Uh oh, I guess me too Kate! (c:
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Thanks Adey, Kate. I was chatting last night at the track workout with a running GF who is about two years out from her lumpectomy. As much as I feel the need to discuss, rehash, whatever, I think I'm sick to death of the topic already myself. I don't want to be "that cancer girl", but I find it so difficult not to be aware of it so strongly. Maybe because I'm a runner and my physicality is so important to me? Well, technically I just started to be a "real" runner a couple months before my DX last year, even though I'd been running on and off for about 18 years before that. And here I was, just starting to make some real progress, doing races and signing up for marathons, and I literally got derailed for a year. I think I'm more pissed off about that than anything else.
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Like you, my only treatment has been surgery. I think because you could never tell that I was sick( actually I look better now than before) people did not realize the extent of the anguish that I went through and how I am still feeling. Like how many times I think about cancer and worry about it comiong back. How every little ache makes me wonder if it has. How I feel sometimes when I see myself naked in the mirror or cannot feel any sensation when I hug my kids. Part of it is my fault though because my answer has always bee "great" when asked how I feel. I have learned telling the truth makes for an awkward conversation.
I also sense that people do not want to talk about it anymore and want to move on with me. Which is fine because I do too. It would be nice though if people close to me would ask how I am really feeling once in a while. I would love to talk about it a little bit but would never open the subject. I have been thinking about a bit of therapy to help with this. What I wish that I could find is somebody in my situation to get together with to discuss this. Thank goodness for these boards as they are the only check that I have for myself to realize what I am feeling is normal.
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People don't get it even if you have had the visible signs. I did radiation and chemo too. Still don't get it. They care but don't understand. Hopefully they never will! (c:
A lot of people on the boards that are in the same area get together. The Illinois gals do so often, probably monthly. I think NJ-ites do as well. I don't know where you are Mallory but if there are no get togethers yet you could arrange one. I am so happy to see my "cancer chicks" whenever I can.
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Mallory- Sometimes if you put your location in your profile (like Adey has Chicago) you find yourself connecting with others in your area. I've had a few get togethers from others seeing I'm close by. You could also start a thread asking "Anyone in the ___________ area?" I think BCO is great but sometimes you need that face to face, too.
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I just went to a NJ get together, a first for me. I'm not sure if that made more of these feelings come up or not. There's so much unknown I'm dealing with, and I second guess myself all the time. When you're in active treatment and recovery, there's less of that, I think. You're told you can't do this, you have to do that, so there's guidance and support, in a way. Now, I have no restrictions at all. Then why am I still feeling bound?
I'm also still in physicaly therapy. That's a reminder. I think I want to stop, just because of that. Maybe then I'll finally feel free and clear?
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I think we all have that feeling sometime or more often than we want.Sometimes when people ask me how are u--I really want to tell them--but as usual we say fine. Mentally I have come to terms with how I feel, but I think no one else has cuz I kid about it alot so it doesn't sound like anything really bothers me anymore. I honestly don't think about more cancer creeping in but I just feel like crap and I'm sure no one wants to hear about it anymore so I don't say anythin about it. But I do come here and vent and it sure helps.
But this year has had changes for me--I've moved--after 25 yrs. in my condo--it was foreclosed so now I live with my dgtr and her family---I'm glad they like me LOL so far????? The problem is they see me on a daily basis so they see more of how I feel and I really don't like that. Oh well it is what it is.
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I feel like I just cannot be the person I was before BC, but I do not know who I am yet. The uncertainty is very uncomfortable especially when family and friend expect the old me to still be there.
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Orange and Elizabeth I have no idea how long all his takes not to be concerned about it---I'm sure in time it has to get better, but the question to all is it is different for all of us--so no answers thereLOL
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orangemat, in 3 days...May 26th...it will be my 6 year cancerversary. It doesn't haunt me everyday anymore, it doesn't pry on my brain anymore but it will always be with me. That is why bco is so successful. We can always come here to vent, to talk about it, to get advice, to just be with people who truly understand. Here we don't have to worry about bringing attention to it...because we all truly understand. Here we don't have to worry that we are talking about it too much...because we all truly understand. So go ahead and talk my friend, we are all here to listen, to comment, to hug, to support, like no where in the world! There are so many different threads here also. Fun ones, spiritual ones, serious ones, supportive ones, artistic ones. We all truly understand!
hugs
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Hi all,
Oh I get it. I'm living in the parallel universe of cancer still too and my heart goes out to others in the same place.
It's been about 6 months since my intensive treatment finished (surgery, chemo, rads) and I'm on the "less-intensive" tamoxifen treatment, which I'm not finding fun. I thought I'd start off this year feeling much better physically (I have a lot of body pain), cognitively (post-chemo brain problems), and mentally (gamut of emotions). It didn't help that I had symptoms in other parts of my body beginning on New Year's Day, so I was investigated for bladder cancer and uterine cancer. Also, my breast scans came back with issues of concerns so they need to be repeated. And I've had worse neck pain since radiation (having to have my neck tilted back for 6 weeks) so I had a brain and neck MRI yesterday and it seems I have a spinal cord problem. The fun never stops.
I went to a session of equine (horse) facilitated therapy to try to address some of my cancer-related fears and help me live each day more fully whether or not I'm in pain. It was very worthwhile and a great feeling to be beside a gentle giant of an animal. The only drawback was that I happened to tell the counsellor that cancer trumped all the violence and health problems and other crap in my past. That derailed the process for me, as she started asking me about the past violence. When we debriefed afterwards, I think she finally understood that I don't feel the need to go back there and don't want to waste my time on that.
I'm trying to live in the moment as much as possible. Hope you all have many good moments!
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Elizabeth- "I feel like I just cannot be the person I was before BC, but I do not know who I am yet."
You summed it up perfectly.
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Yep.
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And for me at least, it takes so much energy trying to figure out who that person is now. I'm so tired, ya know?
OK, one thing I've decided is it time for PT to end. Enough with the twice weekly reminders of the past year's surgeries. My arm/shoulder/chest are fine enough. In fact, with all the weight work I've been doing there, I think I've actually sprained my other shoulder. Figures...
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Esther- your post and the comments following it really sum up how I' ve been feeling too. I am just past my 1 year anniversary of diagnosis. I had 4 surgeries in the past year and lived through lots of pain. I have a frozen shoulder, lymphedema, episcleritis and severe sleep apnea and all that came on in the last year.
I feel like a gerbil in one of those wheels and I want to get off! I go to appts almost every day after work. But when people ask me how I am I say fine because no one wants to hear it and I am sick of it all. I think it takes time to process all the experiences and emotions we have had. BCO is my way of coping and I am thankful everyday for the courageous sisters who bare their souls here showing us we are not alone! -
Ginger- Though I'm farther out I feel like we're living some what parallel lives. I've been dealing with a recent dx of LE after a screw up by my PS who did my revision. LE PT twice a week for the past 6 weeks and she's recommending 2 more after that. When I'm all done with that I start my regular PT for a frozen shoulder. (Had to wait to start until I got my compression sleeves.) That should be another 2 days a week. I don't think anyone (other than us) has any idea what a long process this is.
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So it's normal to be feeling so not-normal. Huh. Hardly something to take comfort in, but I guess it'll have to do.
Thank you, everyone, so much! I haven't really felt like I belonged at BCO, since I didn't actually have ongoing issues, treatment, etc... just a bunch of scars around my Franken-boobs that no one would ever know about unless I specifically told them (or showed them). And I'm usually not one to go around complaining about things (really, I'm not!), so I guess this need to talk has just overpowered me. As I mentioned in my opening post, my running GF suggested I go to a support group. That really didn't appeal to me. And then I remembered I had this group HERE. So here I am. Hugs to you all!
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Esther- I like this support group better. I can show up in my p.j.'s (like I am now)!
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Same here, Kate!
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Me too!
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I often come here in my robe and slippers.
Kate and everyone, Thanks for understanding my words. It helps so much.
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It's a pajama party!
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I'm feeling MUCH better today, just wanted to say.
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Yes, Kate, we seem to be following similar paths! I am hoping to detour off and resume my relatively uneventful life one of these days...
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On May 31st, 2011 at 9:34 p.m., I found my lump. And, thank the goddess I did, because my most recent mammogram did not. Although I won't be celebrating that in a few days time, I will be remembering- and counting my blessings that I did. And thinking about how strong- and well, and hopeful that I feel now.
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I would love to join this "support group" --- pj's and all ---
I am so not me .... I have put on weight because I allowed myself bad behaviours when I was diagnosed and then have not stopped. I know what to do and how to do it but I cannot get motivated ....
Sometimes I feel like I am in a daze. My friends and family see the "up" me ... rarely do they see the real me. I know that they have over the period of 6 months but my treatment is over and I am physically healing after radiation and life is to return to NORMAL. What is that.
Thanks for this thread -- it is obvious we need it.
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