long story short....i'm 34, have a family history of BC.
i went for my very first mammo and ultrasound on tuesday and mentioned that about 2-3 weeks ago i felt a lump (mind you had made this appointment back in April). I assumed it was due to being pre-menstrual.
they did mammo and ultrasound and a doc looked at ny utrasoud and said "i'm concerned it may be early breat cancer, you need a needle biopsy". So here on my 1st experience i ended up having a needle biopsy and i'm terrified of needles.
today the doc who did the needle biopsy called me at 2:02pm and said it was benign but still looked suspicious but that "they can look odd but still be benign and this is how you are"
At 2:51pm she called me back and said that the lab was looking at the wrong papers and that my lump is malignant. she called it invasive ductal carcinoma.
she told me to call my primary doc who referred me for the tests and get a hold of a breast surgeon.
i'm livid now and pissed and scared.
i called my doc's office and was told that she never should have called me with any results, good or bad, that when a lab sees cancer they call the patients doctor and send everything to the doctor who then calls the patient. my doc's office had not recieved any info from them at that time. I am going tomorrow to see what's up.
i'm praying and staying positive that the first result of benign is still right but if its not, i'm scared to death to go through treatment. i have no idea what goes on, i've never been hospitalized for anything.
someone told me to go prepared with questions and a note pad.
can anyone tell me what to ask, anything...i have no real question for you guys...i just want to hear back from anyone with advice, suggestions, knowledge, wisdom...all of the above. :)
Thanks a lot
Kendall
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fmakj Joined: Jul 2009 Posts: 100 |
Aug 20, 2009 09:52 pm
fmakj wrote:
Try to keep calm and positive. Try to bring someone with you tomorrow when to go to the Dr. so there are 2 pairs of ears hearing everything. You should ask for a copy of your pathology report so that you can do some research. Don't get too far ahead of yourself... this is the worst part.... waiting.... waiting.... waiting! Just know that you are not alone. Treatment IS do-able! I'll be thinking about you tomorrow... try to get a good nights sleep! ML
Dx 6/1/2009, IDC, <1cm, Stage I, Grade 3, 0/1 nodes, ER-/PR-, HER2- |
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bettysgirl Joined: Jul 2008 Posts: 557 |
Aug 20, 2009 10:06 pm
bettysgirl wrote:
i'm sorry you are having to go through this. I can't imagine being told it was benign then reversed. You do need to take someone with you to be a second set of ears and hear what you don't. (there will be stuff you just don't hear) The beginning IS the worst part because there is so much unknown and so much waiting. I don't know how things will be for you but once I went back for the actual DX things moved quickly with lots of other tests. I know that it is a difficult thing to swallow and it is a scary time for you. For me once we were "doing" something I felt a little better but those first two weeks were pure agony. DO get a copy of the path results so you can see it for yourself AND research it. Come here to question, rant or rave or scream if you'd like and know that while we always hate to see a new member there is lots of love and support here. Dx 6/20/2008, IDC, 5cm, Stage IIIa, Grade 3, 2/13 nodes, ER+/PR+, HER2- |
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one-L Joined: Jul 2009 Posts: 327 |
Aug 20, 2009 10:10 pm
one-L wrote:
Kendall, sooo sorry you are having to go through this. It is hard enough to get the dx, but to go though what you have been through is just wrong. The first step is not easy, in fact non of it is easy, but you will make it through it, one step at a time. I know first hand how hard it is when you hear the dx for the first time, I was there last month and now I am post op, waiting to see the rad oc. I am hoping I will not need more surgery, but if needed, it will be done. You are not alone, there are many women on this forum that have gone through it all and we are here to help you. Please let us know what the doctor says and keep a positive attitude, it helps in many many ways. Hugs Juannelle Dx 7/21/2009, IDC, <1cm, Stage , Grade 2, 0/3 nodes |
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swest Joined: Dec 2008 Posts: 631 |
Aug 20, 2009 10:42 pm
swest wrote:
Kendall - After you meet with the doctor go by the book store and purchase "The Breast Book" by Susan Love. It is loaded with information. It will help you gather your thoughts and questions. I cannot tell you how helpful this book was to me. Ask your doctor to refer you to a breast surgeon, then you can ask the majority of your questions. Based on the pathology of the cancer your breast surgeon can give you your options. He/She will give you all of your options. What I did is ask "if this were your mother, wife or sister what would you recommend" Please let us know how you are doing. Hugs to you!!! Sonia Dx 10/22/2008, IDC, 2cm, Stage Ib, Grade 3, 0/3 nodes, ER-/PR-, HER2- |
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marlie67 Joined: Jul 2009 Posts: 10 |
Aug 21, 2009 09:02 am
marlie67 wrote:
Kendall, I am so sorry you are going through this. I am new to this too. I hope for you the first news was true and that it is B9. I totally relate to you about being afraid of treatment. I have never had any surgeries or broken bones, and have rarely been sick. But, here I am with bc and getting ready to go through treatment. I am going to do whatever I need to do to make sure this thing is gone. If it comes to it, you will find your inner strength. We all have it; and it will get you through. Keep us posted. Hugs and prayers to you! |
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swest Joined: Dec 2008 Posts: 631 |
Aug 21, 2009 03:52 pm
swest wrote:
Kendall - How are you doing? How did your apt. with the Dr. go? Thinking about you! Hugs! Sonia Dx 10/22/2008, IDC, 2cm, Stage Ib, Grade 3, 0/3 nodes, ER-/PR-, HER2- |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Aug 21, 2009 05:54 pm
Klawless9 wrote:
Hello everyone! First of all i want to thank each and every one of you for your words of support and your love! I just came in from my doctor and I have the copy of what i guess is the report. Its 4 pages. this is what each page says: page 1- at the top it says "Benign-fibrocytic changes of breast and cysts with apocrine metaplasia. pathology findings are not felt to be consistent witht eh suspicious imaging findings. excision is advised". At the bottom is the correction and that says "the pathologist phoned to indicate that there was an error in the original report. correct diagnosis is invasive ductal carcinoma, mri is recommended as well as excision" Page 2-this is regarding the ultrasound guided large core needle biopsy and this says a whole lot of crap including, "an Inrad clip was placed" page 3-is the bilateral mammo with CAD: says that the breast tissue is very dense, there is a grouping of 3-4 microcalcifications...no skin thickening or nipple retraction... page 4-bilateral ultrasound:there is a 12x13 mm irregular solid nodule. no other cysts or solid lesions are identified. small benign appearing lymph nodes are seen in both axillary regions" so there you go....i was given the name of a breast surgeon to go to. i called but they are closed until monday so i left a message to make an appointment. ideally i would like to get an appt. for monday or tuesday to get the ball rolling because months ago i planned a trip to Los Angeles for aug 26-30. what is the consensus about my trip? i live in NY on Long Island any of you ladies from there? Hugs! Kendall i must post a picture of myself...wait until you see me...i look 10! LOL |
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swest Joined: Dec 2008 Posts: 631 |
Aug 21, 2009 09:11 pm
swest wrote:
Kendall - I'm glad you got your report. However, I'm not quite sure what it is saying. Is it b9 or IDC? Are they telling you that you will need an excisional biopsy to be sure? Have your Dr. help you get in to a breast surgeon this week. He can make it happen. You do look 10! You are so precious!!! Dx 10/22/2008, IDC, 2cm, Stage Ib, Grade 3, 0/3 nodes, ER-/PR-, HER2- |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Aug 21, 2009 09:28 pm
Klawless9 wrote:
thank you! well my doctor explained that what could have happened is that the pathologist saw good cells and then a bad one. we're not sure on the report it first says b9 and then invasive ductal C. my doctor's feeling is that she wants it out whatever it is and wants me to get in to the breast surgeon soon. i googled him and he has a website that says if there is availability he takes same day or next day appointments so hopefully he can see me monday or tuesday. my doc informed me that it does not necessarily mean that the whole lump is cancer, it could be a few cells but that they find that out when they take it out. my thing is that whatever it is, i don't want chemo! that scares the hell out of me! plus i'm so damn petite (between us gals...i'm not even 90 pounds) i'm afraid that stuff will take everything outta me or something. i printed out the questions to ask the surgeon just now as well as the what to expect with surgery article. i will be going to barnes and noble tomorrow to get the susan love book recommended.
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fmakj Joined: Jul 2009 Posts: 100 |
Aug 21, 2009 11:27 pm
fmakj wrote:
Hi Kendall, You really do look young! You have been in my thoughts today. You have to get that out, then you know what you will need to do. Keep positive and try to keep to your regular schedule. The "clip being placed" I believe, is to let them know exactly where the site is. This makes it much easier for the surgeon to know what and how much to take out to get good margins. Don't worry too much. Hopefully you will be able to get in to see the surgeon and still make your trip. Keep us posted! Be Well. ML
Dx 6/1/2009, IDC, <1cm, Stage I, Grade 3, 0/1 nodes, ER-/PR-, HER2- |
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yellowfarmh
Joined: Feb 2005 Posts: 853 |
Aug 22, 2009 11:00 am
yellowfarmhouse wrote:
Dear Kendall, wow, you've been through a lot already. it's so frustrating waiting for appointments and waiting for info to trickle in. I was blessed to have a grandfatherly surgeon who went to bat for me and made calls... I overheard him saying.... " just get us a surgery date for tomorrow." It scared the crap out of me because it made me feel like I was really in bad shape but at least he shortened the time I had to wait. He told me that his own daughter had breast cancer at age 33 ( she's fine now) . I was 39 at diagnosis. It was a scary time... I'm praying that all this is caught really early for ya ... in my case... they didn't want to do mammo earlier than 40 as I had no family history... if I had it done at maybe 35 or 36 would have been much earlier stage... but that's water under the bridge.... I pray you have awesome docs and great care and good support... speedy surgery and recovery.... and hopefully no chemo... I had to do that and rads... not fun but doable. prayers and blessings, Wendy blessings and love to all my sisters here!
Dx IDC, 3cm, Stage IIIa, Grade 3, 4/9 nodes, ER+/PR+, HER2+ |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Aug 25, 2009 10:10 pm, edited Aug 25, 2009 10:12 PM
by Klawless9
Klawless9 wrote:
This Post was deleted by Klawless9.
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Klawless9 Joined: Aug 2009 Posts: 70 |
Aug 25, 2009 10:11 pm
Klawless9 wrote:
Hi everyone
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swest Joined: Dec 2008 Posts: 631 |
Aug 30, 2009 03:37 pm
swest wrote:
Kendall - Keep in touch! I'll be looking on Wednesday! Dx 10/22/2008, IDC, 2cm, Stage Ib, Grade 3, 0/3 nodes, ER-/PR-, HER2- |
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swest Joined: Dec 2008 Posts: 631 |
Sep 2, 2009 01:35 pm
swest wrote:
Thinking about you Kendall!! Dx 10/22/2008, IDC, 2cm, Stage Ib, Grade 3, 0/3 nodes, ER-/PR-, HER2- |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 2, 2009 06:07 pm, edited Sep 2, 2009 06:07 PM
by Klawless9
Klawless9 wrote:
This Post was deleted by Klawless9.
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 2, 2009 06:10 pm
Klawless9 wrote:
Hi there! I didn't forget about you! I just came back from the doctor. Not the doctor i had an appt. with because when i got there they told me they didn't take my type of insurance. So they gave me the name of another doc who does take it and his office was in the same building. mom and i went up to make an appt and luckily he saw me right then. He looked over papers and examined me. I liked him because he was funny. Sense of humor is wonderful for lifting the spirits. anyway, next steps are that he will send for the pathology samples and have Winthrop University Hospital's lab look at them. After that, he will call me to set up the lumpectomy. He said he's gonna make a small incision over the areola because the lump is above my nipple which is weird because when i first felt it it seemed like to was more to the right of my nipple. he said it will be a go home the same day procedure. after that is taken out then we will see what the pathology of that is and go from there. i liked him cuz he was like "don't put no thoughts into it and don't take nothing from it....just be cool...and take it easy". so stay tuned...and keep praying... love you all
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Faith316 Joined: Jul 2009 Posts: 154 |
Sep 2, 2009 06:35 pm
Faith316 wrote:
Glad you liked the doctor. That is important. Let us know what they find out and what treatment they recommend. Just one other comment --- you said you are scared to death to do chemo. I have been taking various chemo treatments from June 2008 through now. It is nowhere near as bad as all the stories you hear. Not fun, of course, but certainly not as bad as I envisioned it would be. I have never thrown up one time in all the time (17 months) I have had treatments. Don't be too afraid of it should you need it. You CAN do it and you will get through it just fine. |
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swest Joined: Dec 2008 Posts: 631 |
Sep 2, 2009 09:24 pm
swest wrote:
Kendall - Thanks for checking back in. I'm glad you like your new doctor. It is very important that you feel comfortable with your team of doctors. When will you be having the lumpectomy? After they look at the biopsy slides? Please feel free to contact me with any questions or if you just need to vent. Take care! Sonia Dx 10/22/2008, IDC, 2cm, Stage Ib, Grade 3, 0/3 nodes, ER-/PR-, HER2- |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 2, 2009 09:36 pm
Klawless9 wrote:
Thanks sonia!
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fmakj Joined: Jul 2009 Posts: 100 |
Sep 2, 2009 10:12 pm
fmakj wrote:
Hi Kendall, I had a lumpectomy and a Sentinel Node Biopsy. It is considered a day surgery. I was put out for the surgery and it really wasn't bad. Even the recovery was quite easy. You should ask about the need for a SNB prior to surgery so that it could be done all at once (the less surgeries the better!) Hope you had a great trip and that you are able to remain as positive as possible. Thinking and praying for you. Mary Louise ML
Dx 6/1/2009, IDC, <1cm, Stage I, Grade 3, 0/1 nodes, ER-/PR-, HER2- |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 2, 2009 10:42 pm
Klawless9 wrote:
Hi mary louise!
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 2, 2009 10:43 pm, edited Sep 2, 2009 10:44 PM
by Klawless9
Klawless9 wrote:
This Post was deleted by Klawless9.
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Faith316 Joined: Jul 2009 Posts: 154 |
Sep 2, 2009 10:49 pm
Faith316 wrote:
I had a lumpectomy and axillary node dissection in May 2008 after my first breast cancer diagnosis (invasive ductal carcinoma). Yes, they did intubate me, but it was in after I was under anesthesia and out before I came to so I never knew it. My recovery after the surgery was very easy. Really not much pain at all. I never used the prescription pain pills my surgeon prescribed for me. The biggest pain was from the drains and they were only in a week. Very uncomfortable but not really painful. Not a bad surgery to recover from in my opinion. |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 2, 2009 10:54 pm
Klawless9 wrote:
Thanks for the info! |
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awb Joined: Aug 2005 Posts: 2,764 |
Sep 2, 2009 11:14 pm
awb wrote:
klawlass---I had conscious sedation for my lumpectomy--no intubation, just meds thru the IV-- didn't feel a thing or remember anything. I was wrapped in a snug chest binder which I had to keep on for 2 days, then was allowed to remove it and shower with just the steri strips on. I had very little pain. I was back to normal activities in less thana week. Anne "I don't know what the future holds, but I know who holds the future"
Dx 9/5/2003, LCIS, Stage 0, 0/0 nodes |
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fmakj Joined: Jul 2009 Posts: 100 |
Sep 3, 2009 08:16 am
fmakj wrote:
Hi Kendall, Yes I was "tubed", but it was all done after I was out and removed before I came to! I did not have any drains (but I did only have the 1 node removed) and I also took only 1 dose of the pain med (tylenol 3) which made me sick, so I took just regular tylenol. I actually went to visit my mother the next morning! Keep positive! ML
Dx 6/1/2009, IDC, <1cm, Stage I, Grade 3, 0/1 nodes, ER-/PR-, HER2- |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 8, 2009 12:00 pm
Klawless9 wrote:
Hi ladies! Question...should i make an appointment to see an oncologist now before the surgery? reason i ask is because my primary doctor called me this morning because she just recieved the letter from the surgeon i saw last week stating that he saw me. when all of this transpired, she was on vacation so this morning she called me in total shock as she was reading everything. she said that i should make an appointment with an oncologist and gave me 2 names just because of my having a family history of bc. But i'm wondering if i should do that now or wait? what has everyone else done? also i called the surgeons office this morning to see if he got whatever he needed from the lab that did my pathology stuff (he was requesting the samples so that his hospitals pathologists could look at them) . Anyway the receptionist said she didn't see any new info in my file. how long does it typically take to set up surgery and what are the steps? i don't want to be sitting here waiting when i should be doing something else, ya know? let me know... kendall |
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cbm Joined: Jun 2009 Posts: 131 |
Sep 8, 2009 01:47 pm, edited Oct 23, 2009 07:05 AM
by cbm
cbm wrote:
Hi, Kendall. I think you should do what your primary care doctor recommends and make an appointment with one of the oncologists. It really helped me to talk to the oncologist before deciding on surgical options; I also had brca testing before surgery, at the direction of the oncologist. I also had a PET scan and MRI to stage the cancer, and we had discussion about the cancer's characterisitics--i.e. hormone receptors and Her2 status, grade and stage, all of which helped me decide what to do first and what to do down the road. Your path report recommends an mri also. That's an important step. Before I had surgery the mri showed I might have at least one other spot in my breast where changes had occured--if it was more cancer, it might change the surgical plan. As It was I had decided on a mastectomy. If I had decided on a lumpectomy, we would have had to have more tests. It is only my opinion, but I think you should have more info before being asked to make some of these decisions, and it sounds like your primary care doctor is suggesting that the oncologist is the doctor who should guide that process. Warmest; so much information to digest, and so many details. It gets easier. Good thoughts go with you. Cathy |
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Klawless9 Joined: Aug 2009 Posts: 70 |
Sep 8, 2009 02:08 pm
Klawless9 wrote:
so if i make an appt with an oncologist, the only thing i have is a copy of the pathology report after the mammo, ulta and needle biopsy. I had to give my films to the folks at the hospital. i'm so confused now! i thought the breast surgeon tells me the steps to take. PLUS this is my period week so i'm waiting on that and feeling moody! Kendall |
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