Diagnosed with BC yesterday, scared!!

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Mary59G
Mary59G Member Posts: 139
edited December 2014 in Just Diagnosed
Diagnosed with BC yesterday, scared!!

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  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014
    • Had a ultrasound and needle biopsy on Monday, I was told my doctor will contact me in 3 days. Well she did, she asked me to come to the office and so I knew it would not be good. My son insisted on going with me (wasn't sure about having him go with me as it hurts me more to see my kids hurt). My doctor came in the room and said Mary you have Breast Cancer!! Nothing else was said but the tears were rolling. She said with the holidays and all (plus my husband just passed away 4 weeks ago) she said they will set me up with an appt with a cancer doctor in a few weeks. I have no idea how bad or anything so I called the office back and asked them to get me in as soon as possible to the cancer doctor.......so we shall see??? So many questions, should I have received the paper results or something??? Any help would be appreciated, I feel lost......
  • Luvmydobies
    Luvmydobies Member Posts: 766
    edited December 2014

    Mary I'm so sorry about your news and the passing of your husband. This is a great forum and we may not be able to answer everything but we will be here for you. You can ask for a copy of your pathology report and they should give it to you. Don't hesitate to ask for anxiety medication. Many folks need it, especially in the beginning! We all know how lost you feel but once you meet with an Oncology team and get a plan you won't feel so lost. Again I'm so sorry you have to deal with so much! HUGS!!!

  • MarcelaBR
    MarcelaBR Member Posts: 34
    edited December 2014

    Mary I am so sorry that you have to be here and about your husband. But you've come to the right place, there is so much support on these boards. I think that you are on track for the best course of action. Meeting with the oncologist is the best thing you can do, maybe it is even a good thing that you have no details and no test results with you, otherwise you would be googling everything and that is DEF not a good idea. Keep in mind that as scary as it might be there are a LOT of treatments that can make you better and this is just a phase in your life. The disease sucks, but it is not as scary and terrible as we think, and chances are you're gonna be just fine!!!

    Sending you good thoughts on these difficult days! :)

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    Thank you for the news, any news would be great at this point. How do you know if you have the right doctor or do you have to search for one?

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    Thanks for responding, I have never joined anything like this so I'm very confused. Thanks for the information, it means alot to me at this time

  • MarcelaBR
    MarcelaBR Member Posts: 34
    edited December 2014

    I believe the first thing you should do is make an appt with an Oncologist and a Breast Specialist. In my case I found the breast specialist first and he referred me the oncologist of his trust. Both of them work at the same hospital which is where I have surgery and treatments. Also I had two opinions in everything, it just made me feel safer...

  • Moderators
    Moderators Member Posts: 25,912
    edited December 2014

    We are sorry to hear about all you are going through in terms of your diagnosis and loss of your husband. As the others have said, you have found a very supportive group who can help guide you along the way, understand your pathoylog report and steps you need to a take.

    Sending you gentle hugs,

    The Mods

  • Beezmets
    Beezmets Member Posts: 2
    edited December 2014

    I am sorry to hear about your diagnosis and your loss of your husband. I was shocked when I was told that my fine needle biopsy showed something, even more shocked when my sugical biopsy showed more serious findings, and beyond belief when my lumpectomy revealed invasive breast cnacer and would require a masectomy. Yes  the tears flowed, and sometimes today they still do. ALong with my family and friends, my wonderful plastic surgeon was a great source of comfort.As other people mentioned in their posts, the diagnosis is not as dire as it may seem. I am fortunate in that I did not need radiation or chemo. There is alot of information on the Internet. Read but try not to get caught up in too much negativity that you may find there. I have a very kind oncologist. Finding the right supportive doctors has been a big help.This website and its forum have been a tremendous asset..As you can see--there are many breast cancer survivors out there today. Take deep breaths, stay strong, and take it all one day--one step forward -at a time. I wish you good luck!

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    Thanks for your words of encouragement, doctors office called and I have am appointment with the surgeon on Tuesday. Trying to handle this day by day but hopefully on Tuesday he will be able to tell me something other than just the word 'breast cancer.

  • Ariom
    Ariom Member Posts: 6,197
    edited December 2014

    Hello Mary, I am so terribly sorry you are dealing with this now, so soon after your terrible loss.

    Please know that we all understand the fear you are feeling. You won't be alone here, there are women here, who will support you and answer your questions, ask anything, but please stay away from Dr Google, there is a lot of outdated irrelevant information, which can confuse and frighten you. The information on this site is up to date and is checked before it is added to this forum.

    The waiting is the worst part, but once you have more information and a plan in place, it does get easier, because you'll feel more in control. In the meantime, while you wait, try to take some deep breaths and keep yourself busy, with things you enjoy. It will be Tuesday before you know it, try to have someone go with you, or record the appointment to make sure you remember everything. Also, ask for a copy of your results so far. It is important to have copies of all your results for your own records.

    Big hug to you, you'll get through this.

    Let us know how you get on.


  • Rosiesride
    Rosiesride Member Posts: 513
    edited December 2014

    Mary...so very sorry about the recent loss of your husband and now this diagnosis... I was also diagnosed around this time last year and reliving those days...the hardest part for me was telling my kids...twin girls 20 and 26 year old son...right at the holidays...but for you and having just lost your husband, my heart aches for you....

    Happy you will see a surgeon and get the ball rolling...truly, once you begin to have a plan in place, you feel more in control. I did learn to get paper copies of all pathologies and test results and always bring someone with you to appointments to take notes for you. If you have friends in the area who could recommend an oncologist, that helps, or if you know and like your surgeon, she/he may have a recommendation ...it's a whirlwind and it all happens so fast...I learned that it's ok to wait and get second opinions and research options given to me. My bc was stage 2 invasive lobular carcinoma with lymph node involvement...although my surgeon suggested bilateral mastectomy with reconstruction ( a week after I was diagnosed) I just wasn't ready to make that decision...lots of percentages to examine and options...I kept my lumpectomy because it was right for me at the time...I know I can always revisit...when I am past this year and the emotional well being and physical strength returns....I also got 2 other opinions that helped me with my decision...and the tumor board met with my case. I never knew they even had that until I read about it on this forum.

    I did not go to the internet about having cancer...one surgeon suggested national cancer institute website, American cancer society and I sometimes looked at Johns Hopkins website...I only researched my type of cancer and did not do too much of that...I only came on this board in the middle of chemo, 4 months after diagnosis...didn't want too much info. I guess but bco is a great support!

    Good luck and strength to you and your family during this hard time. Rosie

    Ps...I lived by this quote:

    image

  • Chloesmom
    Chloesmom Member Posts: 1,053
    edited December 2014

    Mary so sorry to hear of your diagnosis. Mine was 2 weeks ago and now that I have my surgery date I feel so much better. I agree with the ladies here. The info is more up to date on this site than goggle as well one of the doctors I consulted. This is the hardest part. Getting another opinion and waiting to get the plan in place. I also found it helpful to talk to a counselor for an hour to make a list of the pros and cons of each option and what it meant to me. Got side tracked for a while on what the doctors gave me as other options, what I thought would be easiest on my family, etc. I had to make a choice that I was at peace about

    Also I didn't want to tell friends and family. It was hard to see their sad puppy dog faces. But joe they are rallying around and I'm lad I did. Am being surrounded by love. Everyone is different. This has just been my journey these 2 weeks

    Wishing you peace!

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014
    • Thank you so much, Chloesmom! I too am very blessed with 2 sons and a daughter and 6 wonderful grandchildren. I don't know what I would do without them during this time. My question to you is this.....I have a appointment scheduled for Tuesday afternoon with a surgeon...do they come as a package deal or something with the onocologist and all? I'm so confused but this discussion board has truly answered many questions I didn't even know to ask. So I thank you all..
    After I see this surgeon do I need to call around and get a second opinion? I would like to but is there time? I have a very dear friend that will be going with me to this appointment which I am grateful for.
  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    Thank you Rosiesride so much for all the advise. I went back to my doctors office and I now have a copy of the report from the biopsy (although truthfully I do not understand it all. Scary part is and I need to stop doing this is looking up the words on the internet then I really get scared. I am terrible with surprises. My husband never had a heart condition and when I took him to the hospital with shortness of breath they said he was having a small heart attack, they put a stint in and he would be home the next day..... 30 minutes after they put the stint in he had a massive heart attack as I was sitting there with him..........Trying to keep my mind straight but it is truly hard. Between all the death stuff and now this.....I so appreciate all the kind words and I LOVE YOUR QUOTE, I'd like to use it myself

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    Ariom, thank you for your kind words....is there time to get 2nd opinions? Guess I will know more on Tuesday thank goodness for this discussion board.

  • kris1114
    kris1114 Member Posts: 82
    edited December 2014

    I was just diagnosed on Wednesday afternoon. Mine was a phone call. She said expect a mastectomy, chemo and radiation and I was by myself, yikes! You will know more after your surgery appointment (mine is Monday) and you will know even more when the final pathology report is in. I was told sometimes you meet with your oncologist before surgery, sometimes after for a game plan. The surgeon will tell you. My hospital gave me an informative book to read before my appointment.

    The waiting is grueling. It is miserable. Last night was the 1st time I have slept since Wednesday and that was only because of the Xanax my doctor gave me yesterday.

    You never know much at 1st and that is just aweful. Stay off the internet except here is what I learned. I am sure they will move things along fast for you and if you need to talk PM me.

  • kris1114
    kris1114 Member Posts: 82
    edited December 2014

    Also, what I have learned so far. Find the courage for the day you are facing only. Courage today. If you start snowballing into the future, you spiral out of control.

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    kris1114, gosh I'm so sorry how they delivered your message too. good luck on Monday and I hope you get all the answers you need. Yes it sounds like getting a plan will be helpful. and Yes, I did look on the internet and that was absolutely terrible. I will stay on this site as I feel very comfortable getting information from people who have been there and continue doing and fighting this. I have figured out that no 2 are the same. Just hope when its decision time I make the right one. Please post and let me know how you do on Monday as I go Tuesday and any insite would be great. Hopefully you have someone going with you and I have started my file of results, etc....

    And yes I have had to live off these Xanax for a somewhat peaceful sleep, Altho I think my sleep only lasts about 5 hours a night.

  • tgtg
    tgtg Member Posts: 266
    edited December 2014

    Mary--First, my condolences on the death of your husband. Now, to you, who have entered a whole new realm of experiences and lingo to deal with. I understand your emotions, especially at this season, since I got my biopsy results 4 days before Christmas. My best advice to you is to use the information from the professionals on this site, beginning with "Breast Cancer 101" and moving on to specific areas where you need/want more details. The information at BCO is accurate and not alarmist (and is unlike most info on almost any website with a ".com" address, as opposed to ".gov" and ".org").

    Now to your question, "I have a appointment scheduled for Tuesday afternoon with a surgeon...do they come as a package deal or something with the onocologist and all?" They don't have to be a "package deal," and you can seek a second opinion if you wish (be sure to first find out your insurance protocols for coverage on this, though, and then follow them--very important these days). Before I met the surgeon to whom the breast health center at our hospital referred me, I checked out his stats--especially how many breast surgeries he does yearly--and I also called a physician friend (associated with the same hospital) and asked him, "To whose hands would you entrust your wife if she were in my situation?" The recommended surgeon was on his short list of 2, so I was relieved. But he also reminded me that I was free to change to another surgeon if "the fit" with the first one didn't feel right. Long story short, I felt really good about him, especially since he anticipated and answered all but one of the questions on my lengthy list before I ever asked them and since he is a caring, gentle-person.

    Radiation was a different story, though. The natural place for it would have been the cancer center at this hospital, but I nevertheless researched rad oncologists in the other 2 hospitals in the same health system as ours. When I met with the local hospital rad onc, I simply had NO confidence in his experience (or lack thereof) and couldn't trust him using as powerful a tool as a linear accelerator on my body,. So I walked away, and went to a really competent and highly regarded rad onc in a partner hospital of my local one. She inspired confidence, and being treated by her and her team was worth the added driving time (30 minutes one way instead of 15). Being able to stay in the same health system, though, made the arrangement really simple, since both she and the surgeon have access to all my medical info in the system--no paperwork hassles or endless forms to sign for me. (I liked the med oncologist at our local hospital cancer center, but only saw her once, since I declined hormonal treatment.)

    Before Tuesday, write down all your questions and ask any of them that he/she hasn't already anticipated. Try to take someone with you to take notes (or record the visit, with the surgeon's permission of course). Good luck to you on Tuesday--you'll do fine. TG

  • kris1114
    kris1114 Member Posts: 82
    edited December 2014

    I will post on Monday for sure. I will do it both for support and also to help ease the apprehensions and fears of others.

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014
    • Well my son just stopped by, bless his heart! He says Mom call U of M tomorrow and make an appt. with them. They are the best and I will take the time off work to go with you. I am so happy and after looking up the surgeon the my doctor is sending me to seems a bit off, I think they just put me in for any surgeon as it doesn't look like this is his specialty. After looking up U of M, it has made me slow down and breathe and knowing that everything I will or may need is right there. Wish me luck, I will call them in the morning and get that ball rolling with some answers other than you have BC!!

    • From reading all the posts here which are so helpful, all have said you need to feel comfortable with your doctors. Well I hope I can do this at U of M. Sounds silly but I already feel better just looking at their website. Thanks to all who continue to post your thoughts on the doctors and getting 2nd opinions!!
  • Obxflygirl1
    Obxflygirl1 Member Posts: 377
    edited December 2014

    I've heard great things about U of M from this board. You could start a forum asking who has been to U. Of M., their experience and recommendations. So sorry you are dealing with this and the passing of your husband in less than 4 weeks. Ask any question here as these ladies saved my sanity. I learned so much and knew what questions to ask the doctors because of this site. Let us know how things are going. We are here for you.

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    Obxflygirl1… thanks for your concern and response so quickly!! I am not sure how to start a forum but that would be a great idea. This site has been so helpful in calming me down and realizing that I need to take care of 1 day at a time and breathe. I am so thankful I found this site and all the kind women on here that share their experiences.


  • jillann
    jillann Member Posts: 3
    edited December 2014

    Mary, I am where you are.....diagnosed and now ready for surgery on Dec. 17th. I am also scared and anxious and I feel like my old life has floated away. I know it must be especially hard since you just lost your husband. I have a good breast specialist surgeon in Dallas. If you would like to start a special group of newly diagnosed, I could really use some support too.

  • Mary59G
    Mary59G Member Posts: 139
    edited December 2014

    jillann, wow you are way ahead of me. Although I do have an appt at U of M on Monday. I'm just hoping they diagnose the same as that would ease my mind that it is what it is. Thanks for the condolences and I'm so glad you are confortable with your surgeon I think that is huge!! Please feel free to PM me anytime. My daughter moved back here to Michigan about 6 months ago from Houston. Sometimes I think God works in mysterious ways and I do believe that everything happens for a reason.......still looking for that with the cancer, but so far it has made me more knowledgeable and have yet another new meaning on life. Stay strong!


    Hugs,

    Mary

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