The Pressure to Be "Okay"

Becs511
Becs511 Member Posts: 303

I came across this op-ed from the LA times and really resonated with me, and thought I would share. Between, work, friends, family, docs, and everything else, I often feel the need to put on a show for people; stylish outfit, well-applied make-up, perfectly brushed-out and placed wig, and a big sunny smile. I try and fit in with society, and for somebody walking down the street to never even guess what is going on behind the scenes. For everybody in my life to see me as being ok- whatever that means.

http://www.latimes.com/opinion/op-ed/la-oe-1209-baer-sickness-upbeat-notes-20151209-story.html

Comments

  • 50sgirl
    50sgirl Member Posts: 2,527
    edited May 2016

    Becs,

    This article really hits home. I have told only my family (DH and sons) and three close friends about my diagnosis because it is too hard to answer questions, too difficult to face "that look", too painful to feel the pity. I know that I am projecting a happy face to everyone. I don't want my disease to make others feel sad, scared, or uncomfortable. My DH accompanies me to many of my appointments, and we have had frank discussions about reality, so he knows all the ugly details. Why, then, do I still sometimes shield him from my aches and pain and fears? I don't want him to worry. I know it is already hard for him to live through this with me.

    I think that I am drawn to these boards because I can let my guard down here. People here understand me. You all know how I feel. I can rant, complain, seek sympathy, or express my fears, and no one will be hurt. Instead, I receive support and advice and hugs.

    So I will continue to live my life with a smile. Now that I think of it, that smile actually helps me feel better.

    Lynne

  • Becs511
    Becs511 Member Posts: 303
    edited May 2016

    Lynne,

    Everybody has their own way of dealing with things and it is interesting to see how others handle our shared reality.

    I have taken the opposite path of you. I am very open with my friends, family, co-workers, and on social media about my diagnosis, treatments, and current physical health status (I rarely share my emotional status). It helps me to have others know what is going on and provide prospective on how their everyday stresses are nothing in the scheme of things.

    I also feel without sharing my experiences, people don't have a true understanding about the seriousness of breast cancer and the short-term and long-term impact it has. It gives me a chance to educate, advocate, and potentially help others, especially among younger women whose only knowledge of breast cancer has been "pink-washed".

    -Rebecca

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited May 2016

    Although people knew I'd been diagnosed with bc, for almost five years only my family knew about the stage iv diagnosis. I preferred not to deal with trying to make others feel "okay" about it.

    Becs, I think part of your feeling the societal pressure is your age. I am in my mid 50s, but when I was your age, I was still in the people pleasing mode. At age 40, my parents both passed away within a short time of each other causing me to rethink many things and I weeded out much unnecessary stuff from my life. In my early 50s, the bc dx brought more changes and more simplifying, and less pressure to take care of everyone else before me.

    Another thing: when I worked (as a teacher's aide) there was much pressure to appear normal. Some of the women there liked to flash the right hair, clothes, jewelry, shoes and handbags. I quit working 1 1/2 years ago, so that pressure is gone.

    The article talks about being authentic. That's a good way to describe the life I try to lead now. Of course I get off track, sometimes too easily, but I try to be true to myself. If someone tells a joke that's not funny to me, I don't laugh. I turn down social activities I'm not interested in. I don't give false compliments. When I find that I'm over extending myself, I dial back. It's all stuff I've had to learn, and it's a process.

  • car2tenn
    car2tenn Member Posts: 515
    edited May 2016

    Becs,

    Thank you for the link to the simply wonderful article from LA. I so enjoyed reading it. The other side of the coin for me was I revealed appropriate amounts of information to all my family and contacts. A. I am an extrovert and find it hard to hide that big an issue in my life. B. I am a nurse practitioner still working. I have patients who have cancer and there is value for them to see me face cancer. C. Being open about my condition has netted me hugs, prayers and pats on my back. I think we all win. Nevertheless, I respect everyone's method of getting through this diagnosis. Regardless of who you are, the Stage 4 diagnosis is an enormous blow. Blessings to all - Carolyn from Music City

  • Tina2
    Tina2 Member Posts: 2,943
    edited May 2016

    I've told only close friends and family members.I don't want friends and acquaintances to treat me any differently. I know I couldn't deal with the "How are you?" delivered with furrowed brow, or the "She's sick" whispers at parties or meetings, or the falling away of people in my life who just don't want to face my or their own mortality.

    I'm pleased with this decision. It gives me some control. In Cancerland, that's something to treasure and protect.

    As far as my appearance is concerned, I've slowed down physically, I've put on weight from meds and inactivity, I'm letting my grey hair grow out to see how I like it, and I smile and joke as much as ever.

    "Fake it 'til you make it" is good mantra for me right now. I am able to be pleasant, energetic and somewhat productive. Perhaps a day will come when I can't be, but for now putting on my metaphoric slap (Laurie!) to face the world works well for me.

    Tina


  • Shutterbug73
    Shutterbug73 Member Posts: 791
    edited May 2016

    I too have been very open about my diagnosis, but I keep most of the emotional stuff for a close friend who also has cancer and "gets it" and the Stage IV groups to which I belong. Sometimes my husband will catch me in a moment when I am mourning over someone we have lost. He is very loving and understanding and I know he wants to be there for me, but I hate burdening him with more than I have to. Physically I feel great right now, so it is largely the emotional aspects that I struggle with.

    I sometimes feel like I have one foot in each world. I have the "cancer" world and the "real" world. In the cancer world I can be honest when I am frightened or angry. In the "real" world I mostly appear ok. I wouldn't say it is an act...I just pick and choose who to share the deep stuff with.

    Now that I've been at this for over a year and a half and am doing relatively well, I think what I struggle with the most is survivor's guilt, especially when we lose someone much younger or with children. It isn't that I think my life is worth less than theirs, it is just so hard to watch it happen over and over again. I've decided the best way to honor them is to live my life with kindness and generosity and to be truly thankful for every bit of it.

  • Lynnwood1960
    Lynnwood1960 Member Posts: 1,284
    edited May 2016

    I have also been very open about my diagnosis. I am also working full time as a nurse, and use my illness as a way to educate people about MBC. My patients do not know but my coworkers do. I need their support, especially on days that I struggle physically. There are still some people who continue to tell me that I can "beat" this despite the education I have provided them. DivineMrsM took the words right out of my mouth! At 56, I have no need or desire to be anything but authentic.

  • cive
    cive Member Posts: 709
    edited May 2016

    I do tell people. For one thing I live in a senior apartment with 250 units. So.... there is a rumor mill and I'd rather them have it from the horse's mouth than what ever goes around. I am one of the most physically active folks here, so I just smile when they ask me how I feel, and say Great!. Which I do, my diagnosis meant my symptoms went away. Finally.

  • stagefree
    stagefree Member Posts: 2,780
    edited May 2016

    and my answer definitely is..


    :)))

    Hugs

    Ebru

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited May 2016

    If someone with cancer is spending excessive amounts of energy trying to come across as "okay", it is time to evaluate why. I feel it may be an insecurity if the need is always there, as tho the person feels their true self will not be accepted. It is a falseness and really should be addressed.

    When it comes to appearance, everyone is different. I feel best when my hair looks nice. I will spend time on it even when I just stay home. I could care less about a manicure as I am a gardener; don't wear fancy jewelry, mostly just simple earrings. Bad feet due to side effects of meds dictate that I often wear sneakers with insoles, the feminine high heels are far in the past. I have gained weight.

    There's a lot of acceptance about where my life is at this point. Some healthy people have so many more things going for them than I do and yet are miserable and have out of sync priorities. Again, my philosophy may be easier because of my age. I just don't care as much about the rat race and keeping up with the Joneses. And I wish I'd been this way a long time ago.

  • Becs511
    Becs511 Member Posts: 303
    edited May 2016

    I don't think it is insecurity or age at all, I think has more to do with what current disease status, prior life experiences and what stage you are in life(for example all 4 of my parents (mom, dad, and step-parents) are all at least 6 years older than you are still work full-time).

    I am currently on weekly chemo (current disease status) and live by myself (what stage I am on life, because most people my age are married or at least living with someone). So if I don't pull myself together and go out and see friends on the weekend, despite not being "okay", I will spend the entire weekend by myself on my apartment. So for me, sometimes it is easier to be okay and be out with people, than being totally alone while everyone else around me is doing normal weekend things.

    To go along with that, I also work full-time, and the reality of working for a decent sized company is if I am not okay, there is always going to be someone younger and less experienced willing to take on more tasks. So if for one second management doesn't think I am "okay", I am going to lose out on assignments and responsibilities that somebody at my career level and experience should be getting. That is not an insecurity, that is a truth. For example (and back to where you are in treatment), I was in the hospital for a few days after numerous seizures, and answered work e-mails and joined in on conference calls to show the company that I could still keep up.

    And one of the biggest reasons I feel this pressure, is due to my life experiences as a teenage cancer survivor. I was totally bald, bloated from steroids, and pale as a ghost due to lack of blood. I never wore a wig because at that time they were totally itchy. I clearly stood out in the crowd. From those who understood what the situation was, I always got the look of pity or overheard conversations from adults saying what a shame it was, or how they felt badly, etc. But what was worse was from the people who didn't understood my looks where due to cancer. This was the late 90's when the goth look started to be a thing and often people thought my appearance was a choice. I remember one specific time that my mom and I went to the movies and two ladies were talking loudly in a passive aggressive manner about how they couldn't understand how a mother would let her daughter out of the house looking like that. After about 5 minutes, my mother went up tot them, told them the truth and shut them up really fast.

    So as of now, I have lost my hair 3 times (once as a kid, once as taxol, and once due to radiation after brain mets), so it is very important to me to wear my wig, put on my make-up, and blend in so I dont ever have to get those looks or comments again. As a 14-16 year old, things like that are very traumtaizing and def. influenced who I am today.

  • Tina2
    Tina2 Member Posts: 2,943
    edited May 2016

    I'm with you, Becs. To each her own! Whatever gets us through this is good.

    I'm not insecure or false. I'm a fairly private person whose public persona is not a mask, but rather putting my best face forward for my own sake. This deprives me of nothing except perhaps victimhood. For my entire adult life, it has given me equal standing and self-confidence in a world in which people are only too willing to judge, stereotype, pity or dismiss others.

    Tina

  • Heidihill
    Heidihill Member Posts: 5,476
    edited May 2016

    Oh boy, that sounds like a lot of pressure, Becs. I'm with Tina, whatever gets us through this. In my case I wanted my daughter to get through it as unscathed as possible and this meant being "OK" to her friends, teachers, family.

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited May 2016

    Becs, it just sucks that you, a young woman, have to deal with breast cancer. I have always said, especially with stage iv, that it is the most unfair to young women such as yourself and my heart really goes out to you and all those in the 20-30-40 age bracket. I really do think that in many ways, the diagnosis it is harder for youthan on older women.

    Then, for you to have had to deal with cancer as a teenager, I cannot even imagine how life changing that is, and to deal with cancer twice is doubly unfair. All of that, certainly, alters your perspective on life.

    Imo, age often equals stage in life. As a woman in my mid 50s, my life is different from that of a woman in her 30s. I am married with grown children, young grandchildren and an empty nester. All of these things influence my life and how I deal with bc and how I interact with the world around me.

    It sounds like you benefit from putting your best self forward, especially when you want to maintain friendships, so I don't see that as a falseness or insecurity. If you have a friend or relative or two with whom you are able to be with when you are down, then that lessens the pressure to always be okay. It's when a person doesn't have anyone or any kind of retreat but feels always that they must be "on" that comes across to me as insecure. For the record, I know a number of physically healthy people who think they must always be "up".

  • JFL
    JFL Member Posts: 1,947
    edited May 2016

    I am also with Becs and Tina - I am not insecure or false but chose to keep the Stage 4 dx private. We are all in different life stages which plays a part in how we want to live out our remaining days. I am still continuing with my career as long as I can and moving up the ladder. This gives me great mental and emotional satisfaction and helps me to deal with this horrible diagnosis. Feeling "normal", spending a lot of my day thinking about things other than cancer and staying away from the judgment of others about my dx is what keeps me positive and happy day to day despite the nightmare that is my life. Disclosing my diagnosis with everyone at work would cause people to consciously or subconsciously write me off, wait for me to die and preclude any chance of future promotion. It would also cause people to attribute every action as due to my "condition", such as coming in late to work or leaving early when I want to (which, as a senior professional, I have the autonomy to do now without judgment). I learned that after my original early stage dx (even though I kept that secret at work until I finished treatment and only became open about it afterward).

    Aside from work, I don't want anyone to write me off, feel sorry for me or assume I am going to die before they see me again. When I was first dx'd, and baby was born and in the NICU, the head nurse (who knew from the hospital about my dx) would look at me like a poor soul, about to die and talk to me that way. I hated being in that position, as if I am a helpless victim. I handle this whole dx pretty well by treating my cancer aggressively, living a healthy, active lifestyle and otherwise living as normal a life as possible. This empowers me. I don't want anyone else but me to decide how I live out the rest of my shortened life. And inviting others in to judge me and make decisions about what I can and can't do would do just that.

  • 3-16-2011
    3-16-2011 Member Posts: 559
    edited May 2016

    wow Becs

    I loved the article and loved your willingness to share your story here. I think context is everything. The way I can be authentic in sharing my story is to be careful where I share it. I have people in my life who are awesome. These friends and family can hold me together emotionally and do practicle things when needed. I also have truely nice people in my life who don't get it. Overtime, I have learned who gets what kind of info.

    I am facinated by the variety of who we are and how we get through. I do think we all find our own unique path. For me reading and sharing on bco is an important part of what gets me through.

    Thanks again Becs

    Mary

  • 3-16-2011
    3-16-2011 Member Posts: 559
    edited May 2016

    wow Becs

    I loved the article and loved your willingness to share your story here. I think context is everything. The way I can be authentic in sharing my story is to be careful where I share it. I have people in my life who are awesome. These friends and family can hold me together emotionally and do practicle things when needed. I also have truely nice people in my life who don't get it. Overtime, I have learned who gets what kind of info.

    I am facinated by the variety of who we are and how we get through. I do think we all find our own unique path. For me reading and sharing on bco is an important part of what gets me through.

    Thanks again Becs

    Mary

    Ps ebru I love alter bridge and the song is beautiful. Thank you

  • artistatheart
    artistatheart Member Posts: 2,176
    edited May 2016

    I think we all deal with it in our own unique ways and adjust as new situations arise. I too shared the informational aspects in the beginning as sort of regretted it. Although living in a small town makes it hard to hide such news. I do feel pressure to "be OK" just so people will stop withdrawing from me. I do not mind sharing info as long as people ask with respect and concern, but emotionally I am a somewhat private person and am limited in who I can share with. Like JFL, I do not want to be written of. It is a lonely enough disease as is. I don't want to dwell on it 24/7. I try to spare my DH from too much right now, although sometimes I just have a meltdown and he is directly in the line of fire. I do not want him seeing me as his "sick wife" every day until he has to.

  • Shutterbug73
    Shutterbug73 Member Posts: 791
    edited May 2016

    Artist- when you said "I do not want him seeing me as his "sick wife" every day until he has to" it really resonated with me. I remember in the very beginning when I was first diagnosed and crying all the time I said to my husband "I don't want you to remember me this way". I think that is part of what got me over the hump of depression in the beginning. I forced myself to get back to living my "normal" life, or as close to normal as I could. Sometimes in the beginning it did feel like an act, but now I can truely say I am mostly happy. In fact sometimes I feel I am happier than I was before my diagnoses because I don't take an average day for granted anymore. That is not to say I don't have moments of sadness, fear, anger...especially when we lose someone or it is scan time.

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited May 2016

    I always give credit to this forum for helping me move forward after the diagnosis. (This...and anti anxiety meds!) At first, I literally did not know what to do, what to think, how to approach the rest of my life, whatever remained of it. Then I would read first hand accounts here of women who continued hiking, camping, traveling, shopping, having birthday parties for family members, playing the piano for church services, ect. Their lives weren't always one big hoopla; they were intentionally choosing how to spend time and energy, whatever that meant for each individual, in meaningful ways. And I learned.

    Many of us have heard how all matter has a vibration to it, including people. I feel like my vibration has gotten lower since dx, not necessarily in a bad way, but to maintain more of an even keel to conserve energy and be able to go the distance. Lower vibration, but more deliberate. It is easier to edit out things that don't matter as much and follow my heart more often, something I know I wasn't doing as well before bc when I apparently didn't feel I was worth as much or felt I always had to do for others, ignoring my needs and even feeling guilty in going for what I wanted and succeeding.

  • JFL
    JFL Member Posts: 1,947
    edited May 2016

    Artist and Shutterbug, I hear you on the not wanting to be the sick wife until I have to be issue. I know how draining and hard this is on our spouses and I don't want to further increase the drain if I can avoid it. I don't want him to suffer from emotional burnout while I am still alive.

    Divine, lowering the vibrations is a good way to explain it. I need to lower mine a bit more than I have already done!


  • artistatheart
    artistatheart Member Posts: 2,176
    edited May 2016

    Divine, I have read several of your posts about how you now live more authentically and feel more free to say no to situations/people who do not add value to your day. Not laughing at crummy jokes, no false flattering people. I love it and I totally agree with you. That is one way my life has changed for the better! I wish I had had the courage to be more authentic way long ago too! JFL, that is the perfect way to describe my feelings. I do not want him to suffer from emotional burnout. I swear this disease robs us of so many things it is indescribable.

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