MBC is Not a "Journey"

13

Comments

  • journey61
    journey61 Member Posts: 32
    edited February 2014

    Funny, I don't think I'm courageous either, even when people say I am. I just think, if people were in my situation they'd do the same thing. I look at women on this board who are dealing with so many issues and still get up each day to deal with them and reach out to each other. Within this board, I term them courageous. Maybe we are more terrified, but it takes alot to hear bad news time and again and just keep going.

    The first time I was diagnosed I felt like I'd been hit by the bus that everyone talks about and eventually got up. Then I was given Tamoxifen without Herceptin and walked down the wrong road. I hadn't even gotten up to dust myself off and find that I've actually crawled over to the train tracks. That train is bearing down, but is it going slow or at full speed, and my healthcare team is driving it. I'm trying to use a communicator but its processing is slow, the team is talking to each other but not seeing me and the train appears to be hurtling. Yet, I also have events that have helped me through divine intervention and that's the only way I can describe the situation, because I would not be here if those events hadn't happened. 

    I like the terms that have been brought up on this thread-we are sure dealing with alot of dreck combined with more shizzle and it certainly is terrid.

  • Iwillwinthisbattle
    Iwillwinthisbattle Member Posts: 1,076
    edited February 2014

    I see my life as a journey, some parts great and some parts not so great. The not so great parts require me to fight my way through them. The really "not so great" parts require me to really fight, so I do see it as a battle. I intend on fighting this crappy disease until I decide the I am ready to rest. The battle is mine  to fight and mine to surrender to.

  • Springlakegirl
    Springlakegirl Member Posts: 216
    edited February 2014

    Iwillwinthisbattle,

    I love your post!  That is exactly how I feel!

    deniseneish.com

  • Heidihill
    Heidihill Member Posts: 5,476
    edited February 2014

    I don't think journey trivializes our disease as to me the word conjures images from Dante's nine circles of hell.  I also believe we can be fighters, survivors, warriors, whatever gets us through the day. Maybe we are just battling with our own fears, that's justification enough. i think it's best though to just avoid metaphors as people have different reactions to them.

  • carpe_diem
    carpe_diem Member Posts: 1,256
    edited February 2014

    Metaphors can be helpful in describing your own reactions to breast cancer.  For me the problem comes from others, particularly cancer organizations, who want to impose their metaphor on me.  Since I see cancer as random and chaotic, I think of my breast cancer as a bad hand I've been dealt. As the saying goes, "ya gotta know when to hold 'em, know when to fold 'em."  Right now I'm holding on for dear life, but when the time comes I hope I'll "know when to fold 'em."

  • Brendatrue
    Brendatrue Member Posts: 1,830
    edited March 2014



    IF I were to consider my cancer experience a “journey,”
    I would have to say the following:

    I thought my tickets were for stage I only.

    My travel agent must have been a con artist.

    My itinerary has been changed repeatedly, without my
    permission.

    Too many detours have been taken by every one of those
    cheerful tour guides.

    I no longer resemble my passport photo.

    I keep throwing stuff away, but my baggage seems to be
    getting heavier and heavier.

    My travel clothes are now threadbare, and my “sexy
    clothes” have been tossed.

    None of the other people visiting the same places want to
    be there either.

    My souvenirs suck.

    The only food I trust is dark chocolate.

    My lodging too often consists of fluorescent lighting, green
    walls, and strange odors.

    I’ve spent way beyond what my budget allows.

    I should have read the fine print on my travel insurance:
    my unforeseen circumstances are not covered!


  • Moiralf
    Moiralf Member Posts: 1,056
    edited March 2014

    Oh Yes, Brendatrue,

    That is so true. But I have meet some amazing tourists on this journey too.

    Love your humour on this journey.

    Moira

  • Brendatrue
    Brendatrue Member Posts: 1,830
    edited March 2014

    Moira, I agree with you. Some of the kindest, funniest, and most interesting people I've ever met also have been visiting some of the places I'd rather not have on my itinerary!

  • surfdreams
    surfdreams Member Posts: 1,132
    edited March 2014

     Brendatrue - You make it sound like one of the Hangover movies. 

  • carpe_diem
    carpe_diem Member Posts: 1,256
    edited March 2014

    Brendatrue,

    I'm with you on the dark chocolate. Right now I'm into Ghirardelli squares in Sea Salt Soiree and Raspberry Filling.

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited March 2014

    Yes,Yes,Yes! It is obvious to so many of us that chocolate, while not curative, can greatly add to QOL. We must have clinical trials, immediately. I will volunteer as long as I'm not getting a placebo (and believe me, I would know!)

    Caryn

  • Bestbird
    Bestbird Member Posts: 2,818
    edited March 2014

    Brendatrue, your post eloquently sums up the situation. 

    An additional thought, "I got on the wrong train and I can't get off!"

    Thank you for sharing your original and poignant summary!


  • Brendatrue
    Brendatrue Member Posts: 1,830
    edited March 2014

    Oh, I forgot: "Almost all of the relics and artifacts are PINK!"

  • sandilee
    sandilee Member Posts: 1,843
    edited March 2014

    Brendatrue-I love your "journey" post.  Especially clever because we can all relate!  Really gave me a good laugh.  :-D

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited March 2014

    Brenda,

    Well, you know I adore travel. Just never thought I'd go to such an "exotic" destination! Why couldn't we have all won trips to Bali instead?

    Caryn

  • naturelover
    naturelover Member Posts: 91
    edited March 2014

    To all on this thread: is there a forum for being able to express your true feelings without the fear of being offensive to anyone. I think we all need a place to vent our true feelings whether anyone or everyone agrees with us or not.

    Will any of you agree or disagree with me, please?? One thing I literally despise is once a lady in my church was headed my way and I knew what she was going to say so I tried to avoid her in a discreet way. Well, she comes anyway and she said: "I am so glad that I don't have what you have going on right now. I had colon cancer eight years ago and it hasn't come back!!" Well, I just wanted to get out of there. You can't tell by looking at me that I am Stage IV MBC with bone and lung mets but I hate pity more than the disease itself! I would Never, Ever do that to anybody!!!!

    Thanks for letting me vent!

    Judy 

  • curveball
    curveball Member Posts: 3,040
    edited March 2014

    vent away, naturelover! It does no good to bottle those feelings up inside. It's safe to let them out here.

  • Jill49
    Jill49 Member Posts: 494
    edited March 2014

    Brenda - I love your description of the "journey with cancer".  Gave me a good laugh.

    I do see my life as a journey, though.  And even though we will all end up in the same place eventually, some of us will have some pretty rough roads to travel along the way.  As Ebru once said - "life is not a five star hotel"  I love that, Ebru!

    Saying that, I am reminded that on a scale of 1 - 10 I couldn't possibly claim a 10 when there are so many in this world who are suffering unimaginable circumstances.

    The journey for me is an inner one to, hopefully, greater insight, compassion, acceptance and joy.

  • naturelover
    naturelover Member Posts: 91
    edited March 2014

    Thanks, curveball!! I plan to do a little of that! It's a wonderful release to let out our frustrations especially when people unknowingly can be so crude!! I just try and avoid them when possible! I think since my DX and especially the mets, I have my radar on all the time and can see them coming! I think that's a good thing and there are plenty more of them since my DX!

    Have a great night all!

    Judy

  • Kjones13
    Kjones13 Member Posts: 1,520
    edited March 2014

    first, Brenda, love the train analogy. The word I cringe at is "survivor". I just have to tell myself I'm surviving day by day. I feel like life is a journey. I don't like thinking of it as a battle. I don't like to lose. This is just the hand I was dealt. I think of all the stories I've heard from the kids at school that I counseled...I have to say that I would choose this hand over some of their hands. It all sucks, but I am just so grateful for the life (parents, family, friends, husband, kids) that I have had...near perfect in my eyes. I am not brave, just doing what I have to do to live! And in the end, I feel like I win because I know where I am headed. Just my thoughts.

  • LizLemon
    LizLemon Member Posts: 540
    edited August 2014

    Bump

    Beautiful words and concepts, Ladies, to consider for our own obits and such. 

    Thank you,

    LL

  • raro
    raro Member Posts: 1,092
    edited August 2014

    Awhile back I remember reading someone's obituary (unfortunately I can't remember whose) that began, "On such-and-such a day, [this person] finally won her battle with breast cancer." I thought that was a great way of putting it. No "giving up," no "lost her battle," no "ended her journey," etc. Because really, by the time we go, we will have achieved something. We will have been stronger, more compassionate, more knowledgeable, and more understanding (hopefully). So when the time comes, I think I'll have that in my obit, as well. Although I don't much like the "fighting" analogy, if we're "warriors," then we're all winners. 

  • LizLemon
    LizLemon Member Posts: 540
    edited August 2014

    Interesting, Raro. I'm not sure I'd say that for myself, but I see what that obit is conveying. Very different way to put it.

  • Vadre
    Vadre Member Posts: 225
    edited August 2014

    Naturelover,

    I don't mean to edit or correct you, but I have one observation to share relating to the story you shared about the woman at Church. You said that you didn't want her pity. Well, you see, I don't think you had her pity. In order to pity someone you have to care about what is going on in their life. Clearly this Churchlady doesn't have the ability to pity because she is so busy thinking of herself! "I am so glad... I don't have... I had colon cancer..." See, she didn't really need you there for that conversation! I pity her because she thinks about herself so much that she doesn't see how much good in people she is missing! All of that aside....she was an ass to say those things to you. I hope that you vented and stomped your feet until you were ready for some ice cream!

    PS. There is a thread that I really like. I think you might like it too!

    Topic: Lets do a Sh*t People say to Metastatic BC Patients

    https://community.breastcancer.org/forum/8/topic/7...

    Lots of venting, no judging!

  • diana50
    diana50 Member Posts: 2,134
    edited August 2014

    As an athlete ( basketball, running , road bike, plus coaching for 20 years) my thinking and emotional self seems to be competition, suffering, breaking through huge bumps; understanding winning and losing. Training. I actually look at cancer as my opponent. That seems to fuel my outlook and every day I am "training" to defeat my opponent. There have been some setbacks and very scary moments. But I have been " doing breast cancer" since 2002. Mets 2012. 

    I just got a new port yesterday. My one from July 14 broke. I have dodged kidney stents. Today is number 4 taxol. Cancer is wrapped around my ureters. My kidneys are swollen. It all sucks. 

    This is my life along with so many other aspects to me. I am not a survivor. Not a warrior. Journey ?  I don't know and I don't care what I call it or what anyone else calls it. I just want quality , joy and grateful feelings to surround me. On a very bad day I am still grateful to be alive. At least now. And that is all I have. Today. 

  • skylotus
    skylotus Member Posts: 304
    edited August 2014

    @ Brenda....funny.... ;-)

    @ Raro, speaking of obits and last words, if I were to have a headstone, it could simply read:  "That was weird".

    Life is a journey for certain, and mbc becomes a part of that journey, because it becomes a part of our life.

    I don't think anyone needs to have this be a part of our life to become (insert any number of code pink words here, ie, stronger, resilient, fighter, spiritual, more compassionate, etc.).

    But, since no one asked us, and this is part of our journey now, I think we all just do what we have it in us to do, and carry on. And who is anyone to stand in judgement of that journey of our life?

  • Vadre
    Vadre Member Posts: 225
    edited August 2014

    Beautifully put, Diana50. I know that words like "battle," and "journey" don't work for some. I hope I use the right lingo when I speak to each of you. I personally don't care for "battle" and "war" but I grew up in the military and those words just meant that my Dad was away for a long time and we were all scared and sad. I think it's all about your perspective. I, too, don't care what we call it. I just want it not to make my life difficult to live. As long as I am enjoying my family & friends and laughing every day AND the world is taking MBC seriously, well, then I'm OK. Just let me know what you are comfortable with when we speak and I'll do my best to be sensitive. 

    Pax, Virginia

  • Longtermsurvivor
    Longtermsurvivor Member Posts: 1,438
    edited June 2016

    Yesterday, this topic/thread came to mind when I was writing at bco about Kelly A. Turner's book, Radical Remission

    https://community.breastcancer.org/forum/79/topics/845005

    For over 25 years now, I've been mulling over how to refer to my life in breast cancer land. Like everyone else here, I don't like having descriptors put on me by others - whether they "know" or "don't know" me and what it's like to live with serious illness.

    A purely medical telling of my story with times and dates of diagnoses & treatments reduces me to medical materialism and that's not how I experience my life.

    As a lifelong pacifist, I don't engage in wars or battles.

    Unlike Diana, I'm not an athlete, so sports analogies make no sense to me. I seldom use the term "team" (that's just for hospice), but am happy to use healing allies.

    Survivor makes me shudder, because I've got a good case of survivor guilt, having outlived many beloved ones.

    Breast cancer clearly isn't a holiday or tourist activity - though that's what we modern, Western humans consider journey...something you pay for, control and enjoy. Yes, there are many joys, but also many sorrows.

    Journey or quest works for me. I'm an avid reader, story and metaphor person. To be called forth on a journey begins a fairytale or quest narrative. I was literally pulled into worlds, tasks, meetings that I would never have sought in my previous state. It's not what I would have consciously chosen, but I recognize that my entire life has been transformed...not just my body.

    Maybe I'm comfortable with journey, because I've had many adventures outside the medical-industrial complex, as well as within it. I've also had the "gift" of a very long time with advanced breast cancer (now 60 and began in mid-30s)...so my perspective is a slow, rather than rapid one. Yes, I've been tossed around quite a bit, but have the opportunity to reflect on my experience and choose my response...at least sometimes.

    One author whose work I admire immensely is Arthur Frank, whose book The Wounded Storyteller: Body, Illness and Ethics describes three types of illness narratives - restitution, chaos and quest.

    Here is a short synopsis of the three different types of illness narratives ~

    https://abetternhs.wordpress.com/2013/02/16/forgiv...

    It's fascinating to me that Frank chose to profile Audre Lorde, the breast cancer poet and guiding light to many of us, as his example of the quest narrative. I identify most closely with this type of narrative, though I've a more refined and detailed personal experience.

    Bestbird and I have had offline conversations about cancer as a journey and have respectfully agreed to disagree on this one.

    Thanks for reading and listening, I appreciate the opportunity to clarify my thinking on this important topic!

    warmest healing wishes for all, whatever you choose to call yourselves, Stephanie

  • Bestbird
    Bestbird Member Posts: 2,818
    edited June 2016

    Dearest Stephanie, thank you s]for sharing your insightful perspective. Your thoughts are always appreciated, as is your wisdom!

    Sending you hugs and very beautiful wishes, today and always.

  • pwilmarth
    pwilmarth Member Posts: 235
    edited June 2016

    Stephanie

    Thanks for the link. One of the things that struck me about the OP's POV - and that is what she was expressing - is the anger she was feeling about the disease and coming to terms with it. So she hated the idea of journey. I'm not particularly fond of the War On Cancer metaphor and using The Battle perspective. I've never found fighting something that is part of me (and make no mistake, cancer is as much a part of me as my fingers and toes) as very useful for my overall mental health. I prefer to live in hope, love, forgiveness and positive thinking.

    I cringe whenever someone says "You're so brave". That's also a war mentality, but there's also nothing Brave about it. I have no choice.

    Cancer, chronic disease, old age, and death are part of what it means to be human. All of our ancestors experienced what it means to progress through these phases of life that make us human. So I choose not to comment on someone else's expression of what being human means to them. Each of us are at different places. If someone is at the anger, denial, and resistance stage, I let it be and let them express what is their reality. Over the course of time, as people adjust to their new reality, these words soften. But in the beginning, people want to think that having a diagnosis of metastatic breast cancer marks them as different or special from other human beings who are dealing with difficult realities of being human.

    We had a reminder just two weeks ago about how suddenly the "journey" can end in Orlando. From what we know, those were young, healthy people out celebrating at a local nightclub. They had no idea that their journey was about to end. Those who died had no chance to contemplate what it means to die. Those who survived are now on that path in their lives when they get to learn what survivorship means. And some of them will be sure to tell us their stories.

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