Dealing with Upset Family after Diagnosis

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Chevy226
Chevy226 Member Posts: 2

I'm 32 years old, married,with no children. Last year I was diagnosed with Stage III IDC and after battling for a year we just got the news on Wednesday that it has spread to my liver.

I'm doing as well as can be expected, but to say my family is devastated would be an understatement. My mom can't even look at me without bursting into tears. As this new information has spread, I've received many calls from family and friends that are understandably upset. I'm repeatedly telling them everything is going to be alright, but I can tell all they can think about is that I'm dying. It's extremely depressing at a time when I'm trying to be as optimistic as possible.

I've started to avoid them because I'm finding it very emotionally exhausting, but that (obviously) just upsets them more. Does anyone have any advice on what I can do to ease their anxiety? I know that they all mean well are not in any way trying to upset me, but that knowledge doesn't seem to make it any easier to deal with.

Thanks

Comments

  • Sue2009
    Sue2009 Member Posts: 228
    edited August 2018

    my dear sister, I wish I knew your name. I know your pain too well. I was Dx at age 47. After the grueling year of chemo, bilateral mastectomy, followed by radiation, I was told I had one spot of mets in my right intermammary lymph node , original Ca in left breast only. My mom told most of my relatives I was dying. I have now battled w/bone mets since 2013, fractured pelvis 3 times last year in 3 different spots, more radiation. Last summer a tumor was growing behind my eyeball, more radiation. This past June I was told I have liver mets. My husband & I decided to only tell a few very close friends & a couple of my children. My mom must suspect , but hasn’t said anything. Everyone deserves time to grieve , I call it my pity party. I have only gotten worse, but I am trying to stay positive. I had severe liver pain 2 weeks ago, but it is now minimal. I screen my calls, do not answer anyone who may bring me down or who I am not in the mood to talk to. Those who can’t handle your Dx should be brought in to talk to family. 10 years, I have been fighting, I refuse to give up yet. Reading these boards helps a lot. Stay positive & remind loved ones how important it is for them to do the same. Parents, children & spouses are tough, sometimes u have to just cry w/them. 😪 Sue

  • JFL
    JFL Member Posts: 1,947
    edited August 2018

    I don't have any tips but can relate. It can be a second job having to comfort others about your cancer. Exhausting. I don't really tell anyone about my BC - very few family know and only a few friends, outside my BC friends. I don't want to deal with people's pity stares and emotional breakdowns and most of all, don't want to be written off, with people assuming I don't matter because I will be gone pretty soon anyway. If you have one family member or friend that can speak on your behalf and communicate with people about your updates (and ideally, communicate that you are going to be okay and are doing well right now), it can take a huge weight off your back. For those who do know, they see that I look healthy and am pretty active in life and take their cues from that. They assume I am fine now because I look fine and have been keeping up, for the most part. I am currently wearing a wig but no one knows. I put in effort to "fake it" because it helps me feel better emotionally to be treated like a normal person, talking about normal subjects, not just cancer. I think over the last 3.5 years, some people have forgotten I have Stage 4. I would never have thought that possible but do know a woman through work whom I met when she had just been diagnosed with Stage 4 colon cancer, with very, very swollen ascites belly - 9 month pregnant look. I saw her lose her hair and expected she would only have a year or two left. However, over time, I completely forgot about the her cancer. I have known her about 8 years and forgot completely after a year. I only remembered later on after my own diagnosis.

  • Moderators
    Moderators Member Posts: 25,912
    edited August 2018

    Chevy226-

    We just want to welcome you here to our community. You're in the right place for support. We know how hard it is to deal with a diagnosis while also trying to help your family process it all, and we're all here for you.

    The Mods

  • vampeyes
    vampeyes Member Posts: 1,227
    edited August 2018

    Chevy - I am so very sorry for your new diagnosis of mets. People can live a very long life with mets as I have seen here on BCO. My thoughts on your family is tell them straight out what their anxiety is doing to you and if need be tell them they should find a support group to go to. (I think there may be a forum on here for family). You don't need the added stress they are causing you and they won't know they are causing you any until someone (you) tells them. Sometimes though, our emotions can't be controlled, most of the time I was good around my step dad while he was fighting his battle, but once I broke down and cried telling him I didn't want him to die. I realized afterwards how I must have made him feel. For my step dad we knew he had a year at most to live, unfortunately we got a lot less than that, but a lot of people don't realize that stage 4 does not mean your dieing. HUGS Chevy, we are here for you always.

  • Chevy226
    Chevy226 Member Posts: 2
    edited August 2018

    Thank you all so much for sharing your stories and your encouraging words, and also for the great advice! I can't tell you how good it feels to be able to talk with people who are sharing similar experiences. As sad as I am that some of you have been struggling with cancer for years, it's also heartening to know that there are still treatment options available to me and this isn't by any means over. My oncologist told me that I will probably be fighting cancer the rest of my life. But that doesn't necessarily mean I'm going to die this year, or next year, or even within a decade. She has a "terminal" patient with a very similar story to mine that has been dealing with her diagnosis for 24 years!

    I'm definitely going to form my own "pity party", and my mom has agreed to be my go between to field all questions and take the burden off of me. I have a bone scan and biopsy scheduled this week and I plan on only letting a very select few know the results. Unfortunately the cat is already out of the bag about my liver mets and change to stage IV, but I'm going to start taking control from now on and ask those few people not to spread any news until my husband and I are ready to deal with the inevitable questions.

    I spoke to my mom to let her know how my family's reactions have been weighing on me, and I asked her to spread the word. I sort of expected her to be upset, but she understood completely and has told my brothers, dad, and other relatives (aunts/uncles and cousins). Now, when any of us in my immediate family are feeling overwhelmed with emotion we have a "safe word" and all talk of cancer stops. We tell jokes, play music, dance like idiots, whatever we can do to lighten the mood. It doesn't change my illness or prognosis, but if I only have a small amount of time left, I want to spend it having as much fun as possible with the people I love the most :)

    Also, side note, I totally agree with people correlating how someone looks to how they're doing. As a result of my last chemo I lost 35 lbs (I was slightly overweight before so no complaints there), and my hair also grew back so I have a short pixie style. I constantly get compliments that I look so great now, that I look healthier than ever, etc., and that feels like it couldn't be further from the truth. My husband recently posted a picture of us on Facebook and there were several comments of how great we both look and how life must be "treating us well". We both had a good chuckle at lol

    Thanks again everyone for your help and support <3

  • mara51506
    mara51506 Member Posts: 5,088
    edited August 2018

    I am so sorry you had to join us in Stage IV. The first time you are told that it is a punch in the gut and scary. First thing to know, your family is in shock as much as you are. You will find ways of dealing with emotions. I am glad you found us here. This is a great place to ask questions and also talk with like minded people going through something similar. It will allow you to get out any of your darkest thoughts that might scare your family.

    I found a social worker helpful in framing my thinking about how some of my family handled things. I used to get upset at my younger brothers family as I did not think they cared. We do not see each other much BUT after the social worker explained some people cannot deal with it, it is better to allow them space. Less stress for you and easier to come together later. Time will also blunt the fear.

    The other thing is to tell your family what you need from them to help you. You also can be a help to your family by letting them know you are still here and interested in their lives too. I found that I lived in cancerland and constantly talked about it, not giving much thought to other people's lives. I actually found it less stressful listening to what was happening. I listen to meditation music in my earbuds at night while I sleep. Keeps me calm and not having to wake up about cancer.

    If you still feel healthy, tell your family you are living with cancer. Don't frame it as I am dying from cancer as this will make treatment feel even more difficult for you. It can also be something that is helpful to them as well. If they say they want to help, give them things that can help you like help housecleaning, organizing bills or something. They will appreciate you allowing them to help.

    A lot of what I am saying comes with time, the online support here is great and if you need it, I am sure your cancer center can give you locations of support groups. I have been dealing with cancer a long time and a lot of this took a couple of years.

    Cry if you need to whenever you need to and lose stress, don't allow a doctor to say too much about prognosis and don't bother with the survival stats. Let your family know that for now, you are still here and carry on as normally as possible. Stay active if you can as well, great stress buster and helps make any side effects of ongoing treatment smaller. Good luck, you can message me anytime. I may not be triple negative but I am still living with cancer and having a good life.

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