Infiltrating ductal carcinoma, grade 3
I just received the call that I have infiltrating ductal carcinoma, grade 3. According to my radiologist, this type responds well to chemotherapy along with surgery. The rest of the pathology results should be in tomorrow.
I have an appointment with the surgeon tomorrow at 11. The MRI is scheduled for Monday at 2:15.
Everything is moving extremely fast, which I am grateful for. I want this out of my body!
I'm feeling confident that my outcome will be amazing, but I know that I have a tough journey ahead of me.
I will continue to update my journey as it progresses.
Comments
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Hi HappyAnyway,
Good luck with the meeting and next steps!
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Hi HappyAnyway,
I am glad appointments are set up already for you. I remember they wanted me to wait for an MRI for a month because that hospital was all booked up. I told them I can get an MRI in a different hospital only a few miles away. They wanted all the procedures be done in the same hospital for financial reasons. I refused and went to the other facility for an MRI. Can you take someone with you tomorrow to the appointment who can take notes? Also the result of the MRI is important to decide what type of procedure you need to do as far as mastectomy or lumpectomy. Good luck with your appointment tomorrow.
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Thank you both for responding.
My husband is going with me to meet with the surgeon. I'll probably be the one to take notes. I think his head is spinning more than mine. I'm going to listen with an open mind.
New2bc, I'm glad that you were able to get your MRI at the other facility. The insurance and financial aspects of this process are more difficult for me than the diagnosis at this point.
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So sorry you had to join this club. So nice that your center had your appointment set up so quickly. Mine had done the same and I was grateful. Here are a couple of links if you would want to check them out. It is just some ideas of questions you may want to ask at your appointment. Wishing you the best
https://www.breastcancer.org/symptoms/diagnosis/dr_questions
https://www.mybreastcancercoach.org/en-US/Prepare-for-Your-Appointment
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Thank you, Danni444!
My family doc called me today to check on me. So blessed to have good doctors and to have found this community.
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HappyAnyway- it's wonderful you're getting your MRI done so quickly. The waiting is the worst part. I love your attitude.
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HappyAnyway, what a great doctor to call and check on you! And you're right, you have found a great community that understands the road you didn't choose but have found yourself journeying on. I have not been one to comment much but wow, during my early diagnosis, I literally clung to the stories where women with Grade 3 tumors that were huge just disappeared while on chemo! It gave me such hope and I pray you find the same hope here!
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Beesy, thank you so much for your kind words and prayers! The more prayers that I have, the stronger and more positive I feel.
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Hello happyanyway, My gosh, wish I could have experienced such optimism after my diagnosis. I was a walking zombie all of February. You are a strong woman, and with your positive attitude I just know you will do great. I also have a meeting with my surgeon tomorrow. I had a lumpectomy on march 20th. Unfortunately, my margins came back positive, so had a reexcision surgery last week. I should get additional pathology reports as well. Original biopsy said I had IDC grade 2, but after surgery it changed to a grade 3. Not sure why that was. Also pathology had to retest my er/pr and her2 status. Wish me luck. I will pray for you as well. You just have to take things one step at a time. I know it is easier said.....
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UpstateNYer, I'm sorry for all that you have gone through. I absolutely will keep you in my prayers.
I broke down for the first time today when I went to the surgeons website to print out the paperwork for tomorrow. It plainly states that, if the bill isn't paid within 30 days, 18% will be added on to it.If it goes to collections, add 30% more. I called the office immediately, nearly in tears, afraid that we can't afford my treatment. I couldn't even get my first sentence out without completely losing it. She was comforting, explained that they are good about working with people and told me to come in tomorrow and let them take care of me. Again, I am surrounded by angels.
My sister reminded me that my treatment is more important than our out of pocket expenses. Being a stay at home mom with three girls and a husband, that is difficult for me.
Prayers for everyone. We got this!
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Good morning everyone!
I'm struggling a bit this morning. For the last several nights I've only been able to sleep for 4 or 5 hours a night. That's never been a problem before. Feeling a little run down.
My spirit is calm, but my mind and body are full of nervous energy. I'm not sure exactly how that works, but that is where I am.
My 8 year old walked out to the truck with her shoes on the wrong feet this morning. That made me giggle. It's a beautiful morning, though. The sun is shining, the birds are chirping.
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Hi HappyAnyway: hang in there, once you are through with your appointments and have a treatment plan, you will feel a lot better. I was so stressed at first: it would take me hours to get to sleep every night and then I would wake up every hour or so while I waited for my surgery date. I felt that the cancer had to be getting worse and that something had to be done immediately; once all the test results were in and the surgery date set up, I felt so much better because finally something was being done to get rid of the cancer. Sending you hugs and prayers.
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Thank you, Elephant.
I've been praying off and on all morning. Not just for me, but also everyone on here, all of our friends and family, our doctors and medical professionals. Praying for clarity and informed choices.
I'm nervous about the rest of the pathology results. I'm trying to tell myself that the results are simply a key to my treatment. Nothing more, nothing less.
I will update everyone as soon as I get back. Just posting and putting myself out there, so to speak, is therapeutic.
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In the waiting room. Ugh!
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Hi Happyanyway. I am breathing prayers for you, sweetie. As far as not sleeping, I went through the same. My primary doctor prescribed Xanax and it really helped me regarding getting a good night's sleep. I never had to rely on any kind of drugs, but this was truly a God- send. I hope your husband with you in waiting room. As far as paying for treatment, the doctor/facility should work with you. I know that if you financially qualify (with one income and 3 kids you might), you may even be forgiven of copays and out of pocket expenses that are hospital affiliated. I have been treated since February, and have only received one bill so far. We in a high deductible plan, so we are facing quite a lot, however I know deductible has been met now, so everything will be covered in full going forward this calendar year. Keep the faith. Feel free to personally message me as well if you need to talk or vent. Prayers and many ((((hugs))) Pat and remember... What you are feeling now is completely NORMAL. We are all human, and it is natural to have our good and bad days.
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I just stopped to say a prayer for you! I so remember those sleepless nights. Please don’t hesitate to talk to your doctor about that. I hope you have gotten an idea of a treatment plan. It really does feel a bit better when you get a plan, however sometimes you need to wait for additional testing. I found it to be up and down emotionally, especially in the beginning. Some days I felt empowered and strong, and some days I parked my butt on the couch and binge watched Netflix because that’s all I could muster. Be gentle with yourself, and let others take care of you. Sending gentle hugs.
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Thank you both.
I am triple negative. Ki-67 75%. Not really surprised and not worried. Does it suck? Of course. I refuse to be negative.
On the bright side, my surgeon and I got along really well. His nurse is great, too.
My MRI is Monday. I am getting my chemo port on Wednesday. I meet my oncologist on April 23. I should have a bone scan sometime, but it isn't scheduled yet.
That's it for now. Maybe I can sneak in a quick nap before I get little bit from school.
May you all be well! I will be.
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Sending a prayer for you. Refusing to be negative is an awesome thing, some days harder than others. A lot of wonderful people here to come and talk to on any day. I had the MRI, hope they let you listen to music, so you don't have to listen to the MRI, it will tell your story well. I had the chemo port, not a bad deal at all. I had the bone scan, not bad. My little bits are all grown up and I have a grand little-bit. We are here for you - stay strong! Lisa
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Thank you, MissouriCat.
I'm not looking forward to the MRI. My doctor said it shouldn't be too bad as I will be laying on my stomach. I'm a little concerned because my mass is high up on the 12:00 position and hurts. Hopefully the technician can help me find a comfortable way to situate myself.
Thank you for your input on the port. The thought of something inserted into my jugular freaks me out! Lol
Prayers right back to you!
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HappyAnyway: don't worry about the MRI, it is not so bad. I had music, I was able to choose the music I wanted; unfortunately it was not up loud enough so all I heard was the MRI banging. At first lying there face down without being able to move was hard, but then I just told myself to complaining about everything and that it would soon be over which it was. The hardest part was waiting for the results as the technician who had to analyze the results got sick and I had to wait two weeks. My tumor was also at 12:00. Hugs.
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HappyAnyway - I had to use a specialist for my blood clot in NYC. He did not accept any insurance. I received a huge bill. I wrote a nice letter, asking if they did receive insurance coverage, what amount would be acceptable to them and if they could lower my bill... I received a very nice letter instead of paying $6,000. I only had to pay $600...stating this amount will be a payment in full...
Maybe you can do the same... Doctors receive a much lower amount agreed upon through the ins co. Hopefully your Dr will be kind to work with you.... Good Luck.
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I will definitely keep that in mind. Any advice that I receive, whether financially or medically oriented, is very helpful.
The hospital called me today to register for the MRI. She was very nice. At the end of the conversation she said that I had met my deductible, my part was $482.20. I said I was sorry, but our HSA account was nearly depleted. I asked if she would take a partial payment. I offered $42.20. She paused. I was thinking great, here we go again. She accepted the payment stating that the procedure was urgent. Of course I said thank you. She wished me well.
I forked out $300 yesterday so I may have my chemo port installed next week. This is the same office that assured me that my treatment was important and they would set up a payment plan. The fact that payment is required before an imperative medical procedure is performed is absolutely appalling to me. It's all about the almighty dollar.
Again, thank you all.
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I'm sorry that you are going through this. I hope that the MRI will given you good news and no surprises. My right shoulder had really been hurting, too,but it was not an issue for the Oncologist -- just from lifting and gardening.
I don't know when your insurance policy could be changed, everyone is in a different sItuation. I had the surgery under one policy, and then the year ended. I had to research and research! I bought the most expensive policy I could afford and did the rest of it. Family is still helping out. Chemotherapy is expensive.
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Thank you, MexicoHeather. I have around $5,000 left to spend until I have met my maximum out of pocket expenses. Then the insurance will be completely responsible for my bills. I'm going to ask my doctors to throw whatever treatments they believe will benefit me, from a to z.
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Happy - we have a large deductible too like $5k. We have BC/BS. We met the deductible in 3 months. Thankfully by the time I had to have radiation we were at 100%. I can’t imagine how we could have paid for those treatments given we had already exhausted our flex plan.
We did make payments on one bill. I agree ask because all they can say is no. I had a friend who has worked for doctors for years tell me the best way to get a bill lowered, etc is to be persistent. Another friend’s husband appealed a bill that was denied by their insurance company 3 times before they got it approved. The bill was $5k. Not chump change.
It’s a shame we have to deal with financial worries on top of everything else but it is what it is unfortunately.
Good luck!
Diane
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sweetheart you have the Hope and Positive outlook that got me to today 25yr Survivor this yr Praise God. Keep it up Hope and Positive thinking. Like "i Will beat this". msphil idc stage2 0/3 nodes 3 mo chemo before and after Lmast got married was planning our wedding then 7wks rads and 5yrs on Tamoxifen.
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HappyAnyway, I'm sorry that you find yourself here, but am sure that you'll find the forum a great resource for information and emotional support. As your doctor said, being high grade in this case can surprisingly be advantageous because the rapidly growing cells are generally more responsive to chemo. You may want to look for a group with a subject line, "Starting Chemo in April 2019" or something similar. It can be helpful to interact with others going through the experience.
Lyn
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Thank you, everyone, for your insight and support.
I'm running into the pharmacy now to get the Xanax filled that my BS ordered for me to take before my MRI this afternoon. No shame in my game! 😂
Feeling pretty optimistic this morning. May you all have a great day!
Much love.
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happyanyway- within a week after receiving my diagnosis I took the advice of women here and ask for a prescription for Valium. I took half the amount ordered for 8 days. I just needed a little help over the hump.
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Jo6359, I will take that into consideration. My PCP is very supportive. I think she would prescribe that for me.
The MRI went well. I made sure that my body was in a comfy (under the circumstances) position. I was covered with a blanket and snug as a bug. They also placed a pillow under my feet. The pillow for my head was horseshoe shaped. I was face down with my forehead resting on it. My only slight discomfort was my cheekbones of all things! They were resting strangely on the end of the pillow. Overall, 1 being easy, 10 being difficult, I would rate it a 1. That's including the IV that I received prior. No music was offered, but the noises, although a little loud, didn't bother me.
Next step, MO at 9 tomorrow morning. I'm spending the night with my sister tonight. She's going with me tomorrow. She'll help me with questions and processing information. Hope this doc has a good sense of humor. We tend to find humor in even serious situations.
My faith and humor serve me well.
Have a good evening everyone.
I'll update tomorrow.
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