Diagnosis this morning

Options
maybish
maybish Member Posts: 13
edited June 2020 in Just Diagnosed

So I just came over from the waiting group. If you'd like to read my long indroductory post I think you can find it by just clicking on my name or something. No?

Anyway Had biopsy Tuesday. This morning (Thursday) I received a cancer diagnosis. The doctor said invasive ductal carcinoma. Said it's the most common. It's small and still early and very treatable. Not much else is known. Still waiting for the rest of the results to come in. Probably tomorrow. So since I've been crying my eyeballs out all day. What should I do next? Besides wait for the doc to tell me to come in.

«1

Comments

  • Dani444
    Dani444 Member Posts: 522
    edited March 2019

    Maybish- As you already know the waiting stages are the worse. I am sorry you are going through this it really does suck. It will feel a bit better if you can imagine when you get more of a detailed picture of your pathology and come up with a plan. I took the advice I read on here and put together a binder. I included calendar pages to track all of my appointments, blank pages for questions I would think of to take to my appointments. I also included pockets for copies of my medical records, insurance statements, and reciepts. It was something that I could busy myself with that felt like I was doing something, that and deep cleaning my house multiple times :) Here are a couple of sites that might help with what questions to ask.

    https://www.breastcancer.org/symptoms/diagnosis/dr_questions

    https://www.mybreastcancercoach.org/Prepare-for-Your-Appointment

    Please do not hesitate to ask any questions you need to here. For your first appointment with your surgeon you will get so much information. If you have someone you could take with you to listen along and take notes it would be helpful. I have also heard of some people recording their visit on their phone. It is hard to keep all of it straight during that first visit, so it helps to have someone there. Best wishes to you.


  • cleokeep70
    cleokeep70 Member Posts: 13
    edited March 2019

    Hi Maybish- I just read through your original postings. Am I understanding correctly that they biopsied the suspicious lymph node too? Did you get a pathology report for that one yet or just the breast mass? I'm sorry you find yourself in this club nobody wants to join. The advice and support in this community is amazing. I can understand needing to take a day off work, especially as stressful as being an emergency dispatcher must be! Be gentle with yourself, and take this one day at a time. We're all here for you!

  • Frog-on-the-lilypad
    Frog-on-the-lilypad Member Posts: 190
    edited March 2019

    Hi Maybish,

    I am so sorry thay you are here, I am exactly a year apart from where you are today. I found my lump on 9th of March 2018. Its been quite a ride since. But that comes later. For now, breathe. Waiting is one of the worst parts.

    Breathe, and frankly do what you feel like. Its okay to be emotional, sad, angry and all at the same time. Remove yourself from situations that aggravate you. Distract yourself. And please do NOT google.

    Come over here to chat, watch netflix, pinterest whatever, do NOT google.

  • maybish
    maybish Member Posts: 13
    edited March 2019

    To dani444 thank you! I will head to Michaels tomorrow and grab something. I'm pretty terrible at keeping organized so hopefully that will help! I'm definitely going to print out the questions!

    @cleokeep70 yes they found the abnormal lymph node right before doing the breast biopsy. So they did a biopsy of the lymph node as well. He didn't say anything about it this morning. Got my appointment for Thursday next week. I hope I'll get all the answers then!

    @frogonthelilipad too late. I had the longest 3 weeks of waiting. Google was my best friend. 😑 I took today to cry it out and Feel sorry for myself. Because I know in a week I'm going to have to be the strongest I've ever been. Everyone told me to be strong. Why can't I just cry right now? How are you doing?



  • edwards750
    edwards750 Member Posts: 3,761
    edited March 2019

    Google is for information purposes only. People recommend not going there because it’s easy to take the information to heart. While the diagnosis doesn’t necessarily apply to you it is helpful for research.Just remember BC is not one size, fits all.

    Diane

  • rachelcarter35
    rachelcarter35 Member Posts: 368
    edited March 2019

    Staying off google helped me when I was doing all the initial waiting. It gets easier. You get a game plan and you weirdly get used to the idea that you have cancer. I'm a year out (almost to the day) from DX and have had surgery, chemo and reconstruction. I'm not the toughest person in the world and I got through it and am back at work and wiser for it. Some day you will be looking back at this time and you will have gotten through this hard part.

  • beep7bop
    beep7bop Member Posts: 130
    edited March 2019

    Get your favorite candy, a box full of popcorn , favorite drink, your snuggle, dog, cat, husband , mom or sister. Don't forget favorite sad movie !! Have pity me night, because that's OK. Tomorrow is another day you'll deal with this tomorrow! Prayer and Love all around..

  • voraciousreader
    voraciousreader Member Posts: 7,496
    edited March 2019

    Register at the NCCN’s website and read the breast cancer treatment guidelines that are specific to your tumor’s characteristics.


    The brginning of the journey is always the hardest. Once you have a treatment plan, you will begin to feel better....


    Good luck

  • Salamandra
    Salamandra Member Posts: 1,444
    edited March 2019

    The message to 'be strong' where they mean 'act like nothing is going on' is a bunch of bs. Being strong means showing up for the tests, showing up for the appointments, showing up for the treatments, even when it's scary and nerve wracking and has unknowns and side effects. It means doing what you have to do to survive, keep a roof over your head, keep your health insurance. It shouldn't mean putting on an Oscar-worthy performance so other people can pretend the cancer doesn't exist. It shouldn't mean not crying when you feel like crying.

    Sending supportive thoughts and repeating the mantra that it does get better.

  • PurpleCat
    PurpleCat Member Posts: 358
    edited March 2019

    Salamandra, just spotted your post about staying strong and couldn't leave the thread without saying YES, ABSOLUTELY, EXACTLY THAT to what you said about staying strong.

  • Dani444
    Dani444 Member Posts: 522
    edited March 2019

    Maybish- just want to add that of course it's ok if you cry it out, feel sorry for yourself and even get pissed off if that's what you are feeling. You have no obligation to “just be strong." There were ( and still are) days I felt pretty empowered and proud of getting through this, and days I just cried, and curled up on the couch and ate comfort food. It is ok to gently remind your friends and family that right now you just need them to meet you where you are emotionally and not place an expectation of how you should respond to this diagnosis. I have learned that sometimes people just don't know what to say. Gentle hugs to you and sending restful healing thoughts.

    Edited to add, YES to everything Salamandra said so well!

  • maybish
    maybish Member Posts: 13
    edited March 2019

    Wow you ladies are amazing! Thank you salamandra! I always respected the women that went through breast cancer. The strength the poise the determination. Now here I am. A place I never thought I would be. I'm 44. Never had any risk factors for bc. 2 daughters that I breast fed never smoked. I never even had a mammogram before this started. This day has been incredibly hard. Had to show a happy face after picking my daughter up from school. I'm glad I found this place you ladies seem so supportive!

  • readytorock
    readytorock Member Posts: 199
    edited March 2019

    Hi, Maybish -

    I was 43 when diagnosed and this September will reach 5 years cancer free! I can't believe I've come this far. In ways, I still feel like a cancer patient as I still have so many appointments and testing (and I just found out I am on the 10 year follow-up plan rather than 5 years), but otherwise life is bak to normal. Good luck!


  • AliceBastable
    AliceBastable Member Posts: 3,461
    edited March 2019

    Allow yourself some fun during this whole ordeal! Cry for now if it helps, but I found that keeping some emotional balance really helped. I went to a concert the day after my biopsy, and Hubby and I would take (inexpensive) day trips and short vacations between appointments, tests, surgeries, and treatments. Even going to hang out at a park and hike was great. And looking back to last year, I remember the fun days more than the cancer-related ones.

  • DATNY
    DATNY Member Posts: 358
    edited March 2019

    I've read your first post...there are many similarities between our situations..noticing the indent first, 44 years old, kids 15 and 11, breastfed. This was two years ago, and now I have days when I completely forget about it. You'll get to this stage before you know it. There are millions of women who've been through this. It is hard, but you'll make it and soon will put it behind you.


  • blah333
    blah333 Member Posts: 270
    edited March 2019

    Unfortunately you just kind of have to hang tight until your next appointment and they tell you more about the stage of it etc. Usually this will mean mastectomy or lumpectomy + radiation and possibly chemo or hormonal drugs. You won't know until there is more information and your doctors give you recommendations. It's stressful.... biopsies/waiting/results are the worse. I didn't really feel better until my surgery and when I was on the other side. I spent the 2 months between my diagnosis and surgery spending more time with friends... There's really not much ACTION you can take at the moment.

  • Sin28
    Sin28 Member Posts: 2
    edited March 2019

    hello I am in the same situation as you last week. I am 43. 3 kids that is 8, 5, and 2. And I cried my heart out and many sleepless night after the diagnosed. It’s very stressful. The waiting game having a plan is nerve-wrecking for me. But today I finally met my surgeon. It gives you some kind of relief. It’s ok to let it all out. I did for sure. It’s hard to think positive but once a plan in place, we can be strong and fight this demon



  • maybish
    maybish Member Posts: 13
    edited March 2019

    @sin28 im glad you have your plan. and of course sorry about what youre going through. what did you get diagnosed with?

    @blah333 i definitely dont feel as anxious as i was while waiting for the biopsy. just hard getting the news ya know!

    thank you everyone! i think i feel a little better having cried the last couple days and starting to tell family and close friends. knowing that everyone is behind me and supporting me definitely helps. good luck to you all, ill keep posting and looking foward to making new friends here.

  • Salamandra
    Salamandra Member Posts: 1,444
    edited March 2019

    to maybish and Sin28!

    It is a haul but we support each other through,

  • CherylFl
    CherylFl Member Posts: 11
    edited March 2019

    After my experience please GET A SECOND OPINION ON YOUR PATHOLOGY SLIDE before doing

    any surgery. You can do this yourself or have a surgeon or oncologist do it.

    Johns Hopkins, Moffitt , MD Anderson all do this and can tell you how to get it done go to there web sites.

    Pathologist make mistakes and can report you have cancer when you don't!!!!!

  • maybish
    maybish Member Posts: 13
    edited March 2019

    Is a second opinion really necessary? I'm pretty sure the US, mammogram and biopsy results are pretty definitive. No way all three are going to be false positives.

  • rachelcarter35
    rachelcarter35 Member Posts: 368
    edited March 2019

    I personally thing if you are confident with your medical team you don't necessarily need a second opinion. I had a second opinion because I initially wasn't completely confident with my medical team and ended up changing my plastic surgeon. Follow your gut.

  • maybish
    maybish Member Posts: 13
    edited March 2019

    @rachel why weren't you confident in your team? Was it something they said? Did you feel like they weren't caring? Did you not like them? I'm still waiting for my appointment for the rest of the results. I guess what comes next staging and a treatment plan.

  • Sin28
    Sin28 Member Posts: 2
    edited March 2019

    @maybish I was diagnosed with stage 2 idc, 3cm. This is all I know from the pathology. I am getting MRI coming this Friday before surgery. Surgeon want to do lumpectomy, but I’m concern what if?? I don’t know what else I can go to since I am on Obamacare. Reading everyone’s comments from surgery to rad to chemo and the aftermath is overwhelming. Tearing up and sleepless night. I’m lost even though I felt a little comfort after seeing the surgeon last week.

  • Salamandra
    Salamandra Member Posts: 1,444
    edited March 2019

    Hey Sin28,

    It's ok not to fully inform inform yourself all at once. You have time, and you don't need to be an expert at all if you don't want to be. If it's less stressful for you, it's really really ok to just trust your medical team and stick to the Cats topics or games topics here. When this board is stressing you out, take a break. Sending you big hugs from across the aether. You WILL find your way through this.

    Whatever works for you for stress, do it. If it's playing silly phone games or exercising or eating cake or rewatching old movies, now is the time to treat yourself and not judge yourself. You can also ask your doctor for anti anxiety meds. I know Ativan was helpful for me around diagnosis and for a lot of other people. It can help with sleep too.

    The 'what if' game is a killer! You still have time to decide. In fact, even if you go forward with the lumpectomy and decide six months later that you want a mastectomy, that's a possibility.

    I bet that you still have options with Obamacare. Can you call a healthcare navigator or ask a friend who's good with paperwork to sit down and try to figure out some options? Does your cancer center have a social worker who might be able to help you? Many insurance companies *want* to pay for you to get a second opinion, since the course of cancer treatment is expensive for them, they'd rather pay a little more up front to make sure it's right the first time.

  • beep7bop
    beep7bop Member Posts: 130
    edited March 2019

    I got my diagnosis today invasive ductal carcinoma don't have all of stats yet. But surgeon said bring family or support person. My husband is going with   me  

  • beep7bop
    beep7bop Member Posts: 130
    edited March 2019

    So sorry we are going thru this, You think you want results and then we get them and it's so unreal, So much to take in. But we will get over this HUMP!! I still can't believe what I heard on the phone a few hours ago.

  • blah333
    blah333 Member Posts: 270
    edited March 2019

    My mom wanted me to get a second opinion (months later, she said she wished her own surgeon had looked at my results) but it seemed so unnecessary to me. I know I had a lump, they showed me my mammogram images, I could see the constellation of microcalcifications, I read everything I could about it, I highly doubt they were "wrong." If you can see the imaging and read the reports, it's highly unlikely they accidentally report cancer. Cancer cells look a lot different from healthy ones. I know the fact they hvaen't found a cure and that cancer is so "profitable" and expensive makes us skeptical but it seems like in most cases reports are accurate. If anything they'd be more likely to accidentally not find cancer than to accidentally diagnose someone with it.

  • Irishlove
    Irishlove Member Posts: 82
    edited March 2019

    Oh I'm so sorry to hear this.beep7bop, I was looking for you in the MS and BC site. Thinking of you and all that have had to face this diagnosis.

  • rachelcarter35
    rachelcarter35 Member Posts: 368
    edited March 2019

    maybish My surgeon and oncologist were respectful and clear in explaining things. I also felt heard by them. My first plastic surgeon however was horrible. He made me feel like my questions were ridiculous and was not clear about what to expect. He placed my expanders during my mastectomies but I changed plastic surgeons for my exchange. When I went for a consult with my current plastic surgeon I realized that my discomfort with my first PS was reasonable. All of the sudden I felt heard and safe. We've got to follow our gut and feel confident in our doctors. This is hard enough.

Categories