I have breast cancer in my EAR!

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TwinkleCat
TwinkleCat Member Posts: 85

Hello everyone -- I was diagnosed with mixed IDC/ILC on 7/23, and I just learned today that I have bone metastases (upper right arm, left clavicle, and left lower back and hip) and a small brain met. I am so overwhelmed! I am sure I will be up all night reading through posts in this forum and all the helpful resources on this site -- but I just wanted to reach out and introduce myself, and share my story (so far).

I am 41 -- will be 42 in 2 weeks. Married, but no children. Strong family history of cancer on both sides -- but as yet, no one has been tested for genetic mutations. (I had blood drawn last week -- expecting results in another week or 2).

I had my usual screening mammogram last November, and all was clear. I also had a clinical breast exam in January, and it was unremarkable. At the end of June I noticed that my right breast appeared to be very full and firm. My breasts are on the smallish side -- 34B and not very full -- so it was quite noticeable. I waited a week to see if it would go away. When it did not, I scheduled an appointment with breast care. I got in for a diagnostic mammogram (bilateral) and ultrasound (right breast only) on 7/5. The mammogram did not show anything on the left, but there were new calcifications on the right that corresponded with an ill-defined 2cm mass that was observed on ultrasound. I had a biopsy of the mass on 7/16, and received the results of IDC/ILC (ER+/PR+/HER2-) on 7/23. Because my breasts are extremely dense, I had an MRI on 7/30, which showed diffuse disease throughout the right breast (explaining why it was so big!), and probable lymph node involvement, as well as an additional mass in the left breast. I met with the breast surgeon, medical oncologist, and radiation oncologist on 8/1 to discuss a probable treatment plan. They ordered a PET scan to assess for distant mets, an ultrasound of the left breast, and drew blood for genetic testing. At that point, the probable treatment was mastectomy on the right (and possible bilateral, depending on genetic test results and further assessment of left breast), followed by radiation and endocrine therapy. Decisions about chemo pending results of PET scan. The PET scan was yesterday (8/8), and the ultrasound was this afternoon (8/9). Ultrasound showed a solid 1cm mass that was suspicious (BIRADS 4), and biopsy was recommended. I am supposed to get a call about that tomorrow.

Around the same time I noticed the changes in my breast, I started experiencing extreme dizziness. I made my husband take me to urgent care on 7/4. They did a basic neuro exam and a CT, but didn't find anything. They gave me an urgent referral to neuro. Again, I had a brief neruo exam that was unremarkable -- she thought it was likely an inner ear issue (either Meniere's disease or vestibular neuritis), and gave me a referral to ENT with audiology and a short course of steriods. The earliest appointment I could get was 8/6. But the dizziness got better with the steriods, and was totally gone by the time I got my diagnosis on 7/23, so I didn't think anything of it. I kept my ENT/audiology appointment, though, and I'm glad I did! The dizziness returned on 7/27, with a feeling of fullness in my left ear and noticeable hearing loss. Audiometry confirmed that I have sensorineural hearing loss on the left, and MRI was recommened. The ENT (8/6) also recommended MRI, did a ton of blood work, and prescribed me a longer course of steroids at a higher dose. I mentioned to him that I had recently been diagnosed with breast cancer, and that I was concerned I might have it in my ear (as silly as that sounds). He acknowledged that was possible, but thought it was unlikely, due to my specific symptoms. Thus far, the steroids have helped tremendously, and I had the MRI this morning.

This afternoon, I got a call from the medical oncologist, and I immediately knew the news was bad. First -- because it was after 5:30 when she called. And second -- because they told me I wouldn't need chemo unless I had distant metastases. She then confirmed that I did, in fact, have distant metastases -- including in my ear (well... brain... but next to my ear!).

SERIOUSLY!? I HAVE BREAST CANCER IN MY EAR.

Anyway, she told me that the scheduler will call me tomorrow to set up appointments with the radiation oncologist to address the brain (EAR!) met, and the medical oncologist to address everything else.

Comments

  • Meow13
    Meow13 Member Posts: 4,859
    edited August 2018

    Twinkle when they found these spots in the bone and brain did they determine them to be cancer with an actual biopsy or just from MRI? I am asking because I didn't think they could draw that conclusion without an actual biopsy.

    I am sure others will be here soon to help you.

  • bigbhome
    bigbhome Member Posts: 840
    edited August 2018

    Twinkle - I'm so sorry that you have been diagnosed with this horrid disease. Im sure you are reeling! We have all been there and for what it's worth, you will find more information and support here than you can imagine!

    This is the worst time but once you have all the facts and a comprehensive plan in place, you will feel better! If you feel like the anxiety is getting out of control, please ask your Mo for some anxiety meds. I know that a lot of us had too. They help!

    In your ear...crazy huh! They found mine in my face, wrapped around my main masseter (sp) muscle! Crazy!! Take heart that that was six years ago. Please don't Google! Dr Google is so out of date, it will scare you to death! They are making huge strides in the treatment of this disease!

    The people here will support you during the best of times, and the worst of times! You will also find lots of information about treatments and dealing with side effects.

    I have you in my thoughts and prayers and before you know it, others will respond.

    Claudia

  • illimae
    illimae Member Posts: 5,710
    edited August 2018

    wow, twinklecat, that is totally crazy and yet, it makes complete sense to me. I was diagnosed stage IV de novo at 41 (43 now), married, no kids, met to bone and brain as of last October. I’m sorry you’re dealing with all this but it’s true that having a plan gives you some needed control.

  • Meow13
    Meow13 Member Posts: 4,859
    edited August 2018

    Bigbhome, was your masseter muscle met found with pet scan image? I am curious I have some issues like twinkle but it seems like the major nerve. I had a root canal done 2 days ago. They saw infection and verified it on the tooth roots but I am having further issues like intense sinus pain coming and going strange throbbing impossible to ignore, ringing in my ears ongoing. I just call my oncologist but they are gone for the day. I think I need a sinus MRI. The root canal lady said my infection might be more extensive in the sinus cavity. She said my bones and teeth looked fine on the pet scan. Thirty years ago a had upper and lower jaw surgery so I have hardware embedded in the bone.

    I will keep track of you guys. Hope twinkle get those spots cleared and bigbhome you continue to stay NED

  • bigbhome
    bigbhome Member Posts: 840
    edited August 2018

    Oh meow, I wish I was Ned! I am not.

    They found mine because I had been having jaw issues and the tumor got so big it pushed my cheekbone out. Of course, I waited until that happened before I said anything! I could not decide if I should see a dentist or a doctor, so I just waited until my next visit to my Mo! Crazy, I know! Of course, when she saw it, everything went into warp drive and things happened quickly! That was six years ago. I am on my third treatment and living my life!

    Hugs and prayers,

    Claudia

  • TwinkleCat
    TwinkleCat Member Posts: 85
    edited August 2018

    Thanks! This is just so wild... thankfully, a couple of girlfriends came right over and we had a nice 2 hours of distraction and wine. I am so grateful to have a good support system.

    Meow -- this diagnosis is based on the PET scan.

  • illimae
    illimae Member Posts: 5,710
    edited August 2018

    Wine certainly works and Happy Birthday 🎂

    image

  • TwinkleCat
    TwinkleCat Member Posts: 85
    edited August 2018

    LOL!!!!!!!!!!!!!!!!! (I wish this forum had better emojis!)

  • illimae
    illimae Member Posts: 5,710
    edited August 2018

    twinklecat, Here’s cancer 101 using Bitmoji, lol

    image

  • Meow13
    Meow13 Member Posts: 4,859
    edited August 2018

    oh Bigbhome, I was hoping it was only an unpleasant memory.

  • Grannax2
    Grannax2 Member Posts: 2,551
    edited August 2018

    I've been having what I thought was a sinus infection, SE of IL for me, so my MO ordered a zpac. It really helped but a day after I finished it came back. Saw MO she said go to dentist. There is some jaw pain, ear pain and tooth pain, upper back right tooth. So, like you bigb, I really don't know what this is. I go Monday to the dentist, I know I will walk out w much less money in my pocket. They will do xray, I'm sure. Maybe I will just have an infection in my jaw bone, not cancer. I did not even know that could be a real thing.

  • TwinkleCat
    TwinkleCat Member Posts: 85
    edited August 2018

    Hi everyone! Just wanted to give you all an update, now that I've had my RO and MO consultations and have an actual treatment plan in place!

    1) Technically.... I don't have breast cancer in my ear. But still! It's what's causing my ear symptoms! Turns out there are a couple of things going on that are impacting my balance and hearing... first, I have a 1.2cm lesion on my cerebellum, which is probably the biggest culprit in making me dizzy. I also have a skull met near the affected ear, with associated inflammation of the dura -- this is probably also contributing to the dizziness, and is likely what is causing the ear pain, tinnitus, and hearing loss. Good news is that all of these symptoms have improved a lot with the steroids, and I'll be starting radiation therapy (3 weeks) this coming Tuesday, which should address the brain and skull mets. They think the inflammation is just reactive -- but said that if there is also cancer in the dura, the radiation will address it.

    2) I got my first injection of Faslodex this past Thursday, and I'll be starting Ibrance after I complete my radiation therapy, once I get back from my trip to Italy. I will also start Zometa after I get back to strengthen my bones.

    I know this sounds weird, but I am actually excited to finally get moving on treatment! It feels like I've been waiting and waiting and waiting.... although, when I think about it, it really hasn't been that long. My initial diagnosis was 7/23, and my first faslodex injection was 8/16 -- so less than a month! Even though it feels like it has taken forever!

    Anyway -- I'm in good spirits.... maybe it's just the prednisone talking, but I'm feeling pretty good.

  • illimae
    illimae Member Posts: 5,710
    edited August 2018

    Great news twinklecat, it really helps our outlook and motivation to have a clear plan in place. Please keep us posted on the brain rads over on the brain mets sisters thread, if you don’t mind. It’s so helpful for us brainiacs to know what/how others are doing 🙂

  • Runrcrb
    Runrcrb Member Posts: 577
    edited August 2018

    thanks for the update Twinklecat. My favorite part was "after my trip to Italy" - great job of not letting cancer stop you.

  • Georgia1
    Georgia1 Member Posts: 1,321
    edited August 2018

    So glad you have a plan Twinklecat. And enjoy Italy! It is such a wonderful country and an opportunity to eat, drink and see amazing things.


  • Meow13
    Meow13 Member Posts: 4,859
    edited August 2018

    Twinkle have a wonderful trip, excited that things are improving and you will be getting Ibrance. Thank goodness they found the lesions now they need to zap them.

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