Overwhelmed... (newly diagnosed)

Kathysuej
Kathysuej Member Posts: 16

I am 38 yrs old and was just diagnosed with Multifocal Invasive Ductal Carcinoma (clinical stage 2). I found out on the 2nd of December. I have met with my oncologist and a couple surgeons. I have met with a plastic surgeon and am waiting to hear back from another. My insurance is not the greateset, so that doesn't make anything easier. I just feel so overwhelmed right now. I'm trying to take it step by step. I have to have surgery first, I know that. They cannot save any part of my left breast, as there is too much cancer in there. I am opting to have a double masectomy, even tho there is no cancer that we know of in the right. I'm a natural worrier and I couldn't bear not to.
I think the hardest thing so far was telling my children. I have 3 kids. My daughter is my youngest, she just turned 10 a few months ago. Then I have 2 boys ages 14 & 16. They have been so great. Constantly showing support, telling me I got this. And not to worry, it'll all be okay. I thought I was the one that should be reassuring them, lol. And I have. But they are just that great!
This is what I know so far, if anyone has any advice or anything, please let me know. I'd love to get some input from people who have been thru this. See what types of reconstruction you chose (or not). And hear some of your stories. 
I know the area of cancer that is just behind the nipple is the largest, it is also quite painful. It is grade 2, Estrogen-Pos 100% and Progesterone-Pos 95% Her2 Neg. And the other one they biopsied is 8cm away from that (there are other areas in between the 2 but they only biopsied the 2 farthest apart areas). that one is almost the same, but it's only grade 1. One thing that really worries me is that these are hormone sensitive cancers, and I have the Mirena IUD. My oncologist doesn't want me to rush and get it removed because I also have endometriosis and adenomyosis, and it may cause me to bleed a lot and have a lot of discomfort. But I don't think I want it in.
The holidays have made things take a bit longer than expected, with my surgeon & oncologist both leaving town for a couple weeks. But I am supposed to get a date for surgery this week. Although I have just come down with a cold and I doubt they will be able to do anything until I am better. IDK?
If anyone has any thoughts or advice or anything, please let me know.

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Comments

  • RozHopkins
    RozHopkins Member Posts: 578 Member
    Hi.  Lots of ladies will be

    Hi.  Lots of ladies will be in touch on here soon with good, solid advice and support.  I am not an into details kind of person just did as I was told kind of thing when I was diagnosed.  But would say your children's support is brilliant and will help them and you through your treatment.  You would be surprised at some family and friends bad handling of cancer news.  And your comment of taking things one step at a time is again the best way to deal with everything going on now and over the next months.

    Sorry you haven't good insurance cover but hope you can afford the treatment you choose.

    Reconstruction is your choice, everything is your choice come to that and we all realize that fact here first.  Go with your gut feeling.  Ask every question you can think of and make sure you like your oncologist and plastic surgeon.  One side was reconstructed straight after surgery the other was inflated over several weeks (long story).  But reconstruction can be done both sides after surgery it depends on what the surgeon recommends, plus the plastic surgeon and if they work well together.  Mine were a very good team.

    I did have a double mastectomy, basic four chemos, no radiation.  Lots of ladies have much more than I had and in my opinion deserve medals.  Honestly the surgery is you go in and come out with something taken away, but afterwards can be a challenge.  The worst part for me was the drains, a nuisance and one was very, very sore.  But two weeks average they are gone.  A port is helpful but not absolutely necessary for chemo if required, up to you and what you want to spend available funds on.  Note if you are getting chemo the port can be put in while you have mastectomies hence one procedure not two.  Reconstruction....... some don't bother some do.  I personally did, it rarely is perfect and you may need a tweek but I look absolutely fine and no one would know 'they weren't mine'.  Plastic surgeon was way off matching the second breast size and did it again and did a darn good job.  I didn't get nipple tattoos and was reduced in breast size.  Originally 38 DDD so now can wear lovely tops with a smaller, pert bust, much more comfortable.  I never wear bras as get too hot but have the ones that are very soft and fit where they touch and pull over your head for things like doctor appointments and going to the gym.

    After surgery you need to be careful, no ironing or lifting anything for a while.  There will be pain, please take the painkillers, won't be for long THEY WORK.  No stretching, rest as much as you can and let people help.  Bring things like frequently used kitchen ware down to an easy height.  May be easier to sleep in a chair at first, recliners are good or in bed on your back (a problem for many).  Wear PJs that button up the front (very important at first) they must be comfortable, then other clothing that buttons up front for a while.  The drains can be placed in PJ pockets or pinned on so they don't pull as you move.

    You will feel much better after a few weeks I promise you, and low waterline baths feels like heaven when allowed.  I wrapped the drains around my neck during a bath.  Get some one to wash your hair which also makes you feel better as you can't get the chest wet for a while.

    I think this is enough info as you say one step at a time, later hormone treatment, chemo if required etc. more advice will come your way.  Try not to worry too much........ I know easier said.

    We are all here to help. XX 

  • button2
    button2 Member Posts: 421
    Welcome to a wonderful support site

    Roz gave you a great reply. Everything seems so difficult and confusing at first, but just focus on the surgery for now. I got a right sided mastectomy and it was a bit painful for a few days, but honestly much easier than childbirth. I chose not to get reconstruction for many reasons, but if you do chose to get it, the ladies on this site are extremely helpful. Make sure the decision is your own, sometimes the doctors get carried away with their expertise and expect you to go along with all their ideas. Your children sound wonderful, mine helped me get through the whole cancer ordeal and became very mature and thoughful people along the way. Keep us posted with your progress! Hugs, Anna

  • Apaugh
    Apaugh Member Posts: 850 Member
    edited December 2016 #4
    New Diagnosis

    Hang on and fight like a girl!  Go through every topic on this breast cancer site.  The pink ladies know their stuff and it will help you to make your own choices.  It takes time and thought.  It's your life your fighting for. 

    Mine was left breast/middle.  Stage I, HR 2 +, no lymph node.  Because of the family history of breast, lung, throat, lymph node, liver, colon cancers, and the area it was in, I chose double mastectomy, no reconstruction at all.  I am 54 and post M and just was over it mentally and I had a great fear of it going to the other and could not bear to be cut on again.  I got so sick, I had to quit working.   4 high dose chemos, no radiation, now on a year of targeted therapy (Herceptin)  Port was installed (best choice I made for chemo since I still have it until Aug. 2017).  Plus they started me on Anastrozole that I have to take for 5 years.  HOT FLASH heaven.  The healing is tough, you will need help around the house.  The high dose chemo is hard, you will need help.  Fatigue is huge, you will have to listen to your body and rest as needed.  Please please read all these post on here and they will help you.    I took the time and made mine and have no regrets.  I am alive and will fight fight fight!  Everyones bodies are different and handles it differently, but your not alone hon, we are all here for you.

    Hugs and prayers going up for you.

  • Kathysuej
    Kathysuej Member Posts: 16
    edited December 2016 #5

    Hi.  Lots of ladies will be

    Hi.  Lots of ladies will be in touch on here soon with good, solid advice and support.  I am not an into details kind of person just did as I was told kind of thing when I was diagnosed.  But would say your children's support is brilliant and will help them and you through your treatment.  You would be surprised at some family and friends bad handling of cancer news.  And your comment of taking things one step at a time is again the best way to deal with everything going on now and over the next months.

    Sorry you haven't good insurance cover but hope you can afford the treatment you choose.

    Reconstruction is your choice, everything is your choice come to that and we all realize that fact here first.  Go with your gut feeling.  Ask every question you can think of and make sure you like your oncologist and plastic surgeon.  One side was reconstructed straight after surgery the other was inflated over several weeks (long story).  But reconstruction can be done both sides after surgery it depends on what the surgeon recommends, plus the plastic surgeon and if they work well together.  Mine were a very good team.

    I did have a double mastectomy, basic four chemos, no radiation.  Lots of ladies have much more than I had and in my opinion deserve medals.  Honestly the surgery is you go in and come out with something taken away, but afterwards can be a challenge.  The worst part for me was the drains, a nuisance and one was very, very sore.  But two weeks average they are gone.  A port is helpful but not absolutely necessary for chemo if required, up to you and what you want to spend available funds on.  Note if you are getting chemo the port can be put in while you have mastectomies hence one procedure not two.  Reconstruction....... some don't bother some do.  I personally did, it rarely is perfect and you may need a tweek but I look absolutely fine and no one would know 'they weren't mine'.  Plastic surgeon was way off matching the second breast size and did it again and did a darn good job.  I didn't get nipple tattoos and was reduced in breast size.  Originally 38 DDD so now can wear lovely tops with a smaller, pert bust, much more comfortable.  I never wear bras as get too hot but have the ones that are very soft and fit where they touch and pull over your head for things like doctor appointments and going to the gym.

    After surgery you need to be careful, no ironing or lifting anything for a while.  There will be pain, please take the painkillers, won't be for long THEY WORK.  No stretching, rest as much as you can and let people help.  Bring things like frequently used kitchen ware down to an easy height.  May be easier to sleep in a chair at first, recliners are good or in bed on your back (a problem for many).  Wear PJs that button up the front (very important at first) they must be comfortable, then other clothing that buttons up front for a while.  The drains can be placed in PJ pockets or pinned on so they don't pull as you move.

    You will feel much better after a few weeks I promise you, and low waterline baths feels like heaven when allowed.  I wrapped the drains around my neck during a bath.  Get some one to wash your hair which also makes you feel better as you can't get the chest wet for a while.

    I think this is enough info as you say one step at a time, later hormone treatment, chemo if required etc. more advice will come your way.  Try not to worry too much........ I know easier said.

    We are all here to help. XX 

    Thank you!

    Thank you Roz! I actually have chronic back pain. I have degenerative disc disease and also a few bulging discs and sciatica. So I have been on a pain regimen for quite some time. That adds another concern as to how hard it may be to get my pain under control after surgery, since my body is already tolerant of the meds. But this is something I am talking with my doctors about. They have reassured me it should be fine, but I still worry a little, lol. As I stated above, I'm a natural worrier.
    I think the whole "losing a part of myself" thing won't really hit me fully until after surgery, and I'm not really looking forward to that. I have tried to come to terms with it now, but it's just unimaginable at this point. So I know it's going to be tough when the reality hits me.
    As far as the financial things, being able to afford certain treatments...we are a single income family and live paycheck to paycheck. I do some work from home, but it's more of an added bonus from time to time. Now my fiance has had to take time off work to take me to appts and stuff, and I know there will be much more of that to come, so yeah, if my insurance doesn't cover something I'm kinda screwed. I have to just do whatever they will cover when it comes to treatments. Although, I do have some really wonderful authors who have put together an online book auction to try and help raise money for me and my family. They are so amazing and sweet. I have been doing things on social media for my authors for a few years now (promoting releases, sales, PA work, cover/graphic design & proofing/editing), it doesn't pay much, just a little here and there, I do a lot of it for free (just to help) cuz it's something I really enjoy. I'm hoping I can continue some of this through everything I am going through.
    From what I've read about others, there are some really strong courageous women on here....I hope I can be one too! #FightLikeAGirl Right?!

  • Kathysuej
    Kathysuej Member Posts: 16
    Thank you all!

    It does seem difficult and confusing. For sure! It's a lot to take in and a lot of choices that have to be made fast, without a whole lot of time to really process everything. Personally, I have to do reconstruction. For myself. I have been told that it's possible with having the double masectomy, that I may not need chemo or radiation if they get it all. They will be testing the lymph nodes during surgery though. I do have a lump in my underarm, but they have said it appears to be superficial, like an infected hair folicle or something. We'll see.
    Also, I can't help feeling like the cancer is spreading through my body. As I sit here and wait for surgery dates and all that. Did anyone else have this worry? Do you know if they do like a full body scan or anything? I guess that's probably dependant on each situation and the doctors you have, but I sure hope they check me thouroughly. 
    Is this a natural worry, or am I being overly worrisome? 

  • msgreen1958
    msgreen1958 Member Posts: 3
    Kathysuej said:

    Thank you all!

    It does seem difficult and confusing. For sure! It's a lot to take in and a lot of choices that have to be made fast, without a whole lot of time to really process everything. Personally, I have to do reconstruction. For myself. I have been told that it's possible with having the double masectomy, that I may not need chemo or radiation if they get it all. They will be testing the lymph nodes during surgery though. I do have a lump in my underarm, but they have said it appears to be superficial, like an infected hair folicle or something. We'll see.
    Also, I can't help feeling like the cancer is spreading through my body. As I sit here and wait for surgery dates and all that. Did anyone else have this worry? Do you know if they do like a full body scan or anything? I guess that's probably dependant on each situation and the doctors you have, but I sure hope they check me thouroughly. 
    Is this a natural worry, or am I being overly worrisome? 

    I was diagnosis with BC April

    I was diagnosis with BC April 2012, left breast...I had the tumor remove surgical. I considered at that time to have both breast removed, but my sister who works in the medical field talk me out of it. I just wanted to get rid of cancer and didn't want it to come back.. Every 6 months I went back for my mammogram. It came back clear..COOL!!! Last year, Labor day I woke up in could barely walk...I was taking baby steps.. Of course I went to the emergency room. Made them aware that I had breast cancer...So they did a CT Scan...they walked back in the room in looked like someone had shot their mother...I was told that my cancer has spread. It spread to the liver and my spine. .All I could say was O.K... heck what else could I say...I found an oncologist and started chemo Oct2, 2016...I am only telling you this to make you aware. During those 4 years, no one did a  CT scan, MRI, or a PET scan...During those 4 years when I got the "It's OK" after the mammograms, I thought I was good, but that darn cancer was slowly growing in other spots... Right now I am doing pretty good. My tumor markers are decreasing...I got a good and caring doctor. So, I feel good. Let me know how things are going. I pray for a speedy and successful surgery…Just take care of yourself. Thank God for your support team too!!!

     

  • Very similar to my own

    I was diagnosed last year age 47 have 3 kids. Multifocal IDC and lots of DCIS. Had 2 x 8mm tumours in left breast and 9mm spread to a lymph node. ER+/PR+ HER-. Had double mastectomy (my choice) after many operations to try and remove what they thought in beginning was 1 lump. Had initially Grade 1 Stage 1 then went to Stage 2. Have had rebuild done in August and had my expanders exchanged for implants. My life is getting back to as normal as it can ever be now. Be positive and read my notes about me for more information about what happened to me, it may just help you. It is like an emotional rollercoaster, and just when you think you are making headway, you crash down and depression sets in. But as time goes by it starts to happen less and hopefully it will get to a stage when i don't think about it every day . At the beginning it was every 5 minutes and thats no lie. I'm sure others can agree they felt the same. Message me with any questions if you need. xx

  • I was diagnosis with BC April

    I was diagnosis with BC April 2012, left breast...I had the tumor remove surgical. I considered at that time to have both breast removed, but my sister who works in the medical field talk me out of it. I just wanted to get rid of cancer and didn't want it to come back.. Every 6 months I went back for my mammogram. It came back clear..COOL!!! Last year, Labor day I woke up in could barely walk...I was taking baby steps.. Of course I went to the emergency room. Made them aware that I had breast cancer...So they did a CT Scan...they walked back in the room in looked like someone had shot their mother...I was told that my cancer has spread. It spread to the liver and my spine. .All I could say was O.K... heck what else could I say...I found an oncologist and started chemo Oct2, 2016...I am only telling you this to make you aware. During those 4 years, no one did a  CT scan, MRI, or a PET scan...During those 4 years when I got the "It's OK" after the mammograms, I thought I was good, but that darn cancer was slowly growing in other spots... Right now I am doing pretty good. My tumor markers are decreasing...I got a good and caring doctor. So, I feel good. Let me know how things are going. I pray for a speedy and successful surgery…Just take care of yourself. Thank God for your support team too!!!

     

    scans?

    after all the surgery i had which eventually ended in double mastectomy my health professionals told me that they dont do routine scans after . That they couldnt do mammograms any more as i dont have any of my own tissue left and that they dont do routine bone. PEt or MRIs. It was my main worry for a while and when pushed i was told it is like this....... if you get it back you will have signs, then we deal with it. If you DID have scans and it showed you had something then we would then deal with it. My problem is this, one way is earlier than the other and you could live longer. They told me the outcome would still be the same. And sometimes scans dont show everything they are not 100% also they sometimes show things that are not cancer. The problem is the feeling of lack of a safety net and also some people in some areas do get scans, which worry those that dont. I personally would feel better if i had 6 months/ 1 year scans but it isnt going to happen. Do you think it would have made a difference if they had done other scans to you earlier? msgreen1958?

  • Kathysuej
    Kathysuej Member Posts: 16
    edited December 2016 #10

    I was diagnosis with BC April

    I was diagnosis with BC April 2012, left breast...I had the tumor remove surgical. I considered at that time to have both breast removed, but my sister who works in the medical field talk me out of it. I just wanted to get rid of cancer and didn't want it to come back.. Every 6 months I went back for my mammogram. It came back clear..COOL!!! Last year, Labor day I woke up in could barely walk...I was taking baby steps.. Of course I went to the emergency room. Made them aware that I had breast cancer...So they did a CT Scan...they walked back in the room in looked like someone had shot their mother...I was told that my cancer has spread. It spread to the liver and my spine. .All I could say was O.K... heck what else could I say...I found an oncologist and started chemo Oct2, 2016...I am only telling you this to make you aware. During those 4 years, no one did a  CT scan, MRI, or a PET scan...During those 4 years when I got the "It's OK" after the mammograms, I thought I was good, but that darn cancer was slowly growing in other spots... Right now I am doing pretty good. My tumor markers are decreasing...I got a good and caring doctor. So, I feel good. Let me know how things are going. I pray for a speedy and successful surgery…Just take care of yourself. Thank God for your support team too!!!

     

    That is what worries me!

    Thank you for sharing with me. That is exactly what worries me most! I am hoping I can talk them into doing some sort of other imaging or something, to make sure I don't have this growing elsewhere. I have heard so many stories like yours, some who didn't find out till it was too late. I just won't be able to really feel comfortable after all this unless I know FOR SURE that they have checked elsewhere and that nothing is present. I'd still probably worry even then, just as time goes by I'll wonder. But at least I'd have the peace of mind that we did all we could at the time.
    I hope you continue to succeed in your battles. I'll be praying for you too! Thank you so much <3

  • Kathysuej
    Kathysuej Member Posts: 16
    edited December 2016 #11
    Thank you! Yes, that is how I

    Thank you! Yes, that is how I'm feeling. Like it just never leaves my mind. I did successfully make it thru most of Christmas Eve and most of Christmas day without dwelling or thinking about it much. It was nice. I kinda felt "normal" again, if even for a day or 2, lol. Even when the pains would come it was still a distant thought. So that was a very nice break. But now it's back to reality....
    Just had my genetics test done today. Calling my surgeon to (hopefully) schedule surgery. I have a cold, so they may make me wait.
    And yes, my emotions are all out of whack! One minute I'm fine, then I'm crying.... I'll be laughing, then cry again just out of the blue...I feel like a nutcase, lol.

  • Kathysuej said:

    That is what worries me!

    Thank you for sharing with me. That is exactly what worries me most! I am hoping I can talk them into doing some sort of other imaging or something, to make sure I don't have this growing elsewhere. I have heard so many stories like yours, some who didn't find out till it was too late. I just won't be able to really feel comfortable after all this unless I know FOR SURE that they have checked elsewhere and that nothing is present. I'd still probably worry even then, just as time goes by I'll wonder. But at least I'd have the peace of mind that we did all we could at the time.
    I hope you continue to succeed in your battles. I'll be praying for you too! Thank you so much <3

    lessons learnt

    Hi there, what i have learnt throughout this awful process is that you or the professionals can never really be sure that you wont get it back. That is the awful raw truth. And because someone has had it before you think that you are more likely to get it back than someone who hasnt had it. I found it most diificult when all my treatment had finished. While having treatment you have things to focus on, emotions are mixed up, life isn't normal. When that all stops you are left with trying to live your life again. The truth is your life will never be the same again. You can make the best of it but it will never be the same as it was. I am getting better each month at dealing with it. It is a case of accepting what happened and trying to live your life again without it controlling your every thought and action. I still have worries every time i have a niggle somewhere and i think thats what it will always be like. I am sure others will agree. I have to accept that i wont be routinely tested unless i get a problem, that is just how it works here. I maybe could pay privately but would cost numerous thousands of pounds every year and even then i am not sure they would do it as i was constantly being told alot of tests give you radiation that we want to avoid. I cant change what has happened and i cant ever guarantee my future health,so i can only adjust to my new life. Take care of yourself and remember there are alot of survivors too xxxxx

  • Kathysuej said:

    Thank you! Yes, that is how I

    Thank you! Yes, that is how I'm feeling. Like it just never leaves my mind. I did successfully make it thru most of Christmas Eve and most of Christmas day without dwelling or thinking about it much. It was nice. I kinda felt "normal" again, if even for a day or 2, lol. Even when the pains would come it was still a distant thought. So that was a very nice break. But now it's back to reality....
    Just had my genetics test done today. Calling my surgeon to (hopefully) schedule surgery. I have a cold, so they may make me wait.
    And yes, my emotions are all out of whack! One minute I'm fine, then I'm crying.... I'll be laughing, then cry again just out of the blue...I feel like a nutcase, lol.

    Bless you

    Hello you are far from a nutcase. That is really normal to feel like that. I still after 1 year after mastectomy feel down and cry sometimes. I will be honest i dont think a day has gone by without thinking about it yet, But this is an improvement from August which was still about every 10 minutes. I am hoping that as time progresses this will improve. I havent been to express or help anybody until yesterday as i tried to keep it within. I tried to make my family think i was strong by not really disgussing it and not getting upset. I didnt want visitors as i have always been the sort that wanted everything to stay the same, if everyone flocked on me i think i would have broke. What i didnt realise was that my mother and sisters felt pushed away. My 3 grown up children actually didnt want to talk about it, because in their eyes it made it real. My husband....well he got it all from me. Crying, tempers, drunk, obscure requests. He was my rock and saw me at my lowest. So if i can give you any advise, play it how you need to play it. I think you need at least 1 person that you can turn to. I have always been quite strong so was happy to think that people thought i was strong still(little did they know that i was a mess inside, but hey ho, they will never know that). Good luck and message me if you want to ask me or tell me anything. xxx

  • Sasu
    Sasu Member Posts: 39
    edited December 2016 #14
    Help available

    there is a lot of good advice from the people on this board.  Keep us posted as you go through this journey.  Most cancer treatment locations have patient resources available. Please use them.  There are people to talk to, they will help you with information requests, they will guide you through financial programs available to cancer patients, and most have counseling and classes to help people deal with the emotional aspect of this disease.  There are also people for your family to talk to, and personally, I think this should be a required meeting for family and caretakers. Yes, it is a nightmare at times, but you can do this and you are not alone.

  • aisling8
    aisling8 Member Posts: 1,627 Member
    edited January 2017 #15
    Three months

    I waited three months between diagnosis and surgery and thought I'd go insane with worrying about the delay. I pictured it spreading up and down my spine, all over my body. That was six years ago. I completely understand your fears.

    xo

    Victoria

     

  • Double Whammy
    Double Whammy Member Posts: 2,832 Member
    I waited about 3 weeks for lumpectomy

    and then I had to wait 6 more weeks for my hysterectomy before I could start any adjuvunct treatments!  (I had both breast and endometrial cancers).  Then I waited 3 weeks after hysterectomy before starting chemo for the breast cancer.  I could just feel it growing here and there and everywhere and I was sure that my endometrial cancer had grown just about everywhere - it hadn't, was Stage 1.  In hindsight, I can say all was well and that was in 2010.  No recurrence.  Nothing even scarey (except my thoughts).  My breast cancer was Grade 2 but Stage 1 (node negative), only one 9 mm tumor but lots of DCIS.  Margins around tumor were not clear but because I was also getting/having a mini-breast reduction on that side (it was much larger than the other one), the margins for the entire chunk were clear.   I had chemo because of high oncotype score.  The waiting was the absolute worst!  I feel very thankful and lucky.  I hope all goes well for you and you get that surgery date tomorrow!  While holidays seem to drag things out, if your cancer needed surgery sooner, it would have happened.  So, I'm thinking this is good news. . .

    Keep bringing the IUD to their attention.  I really don't know about those things, but I do know that estrogen is not a good thing for ER+ cancers and PR, too?  It will give you peace of mind to have that removed and that part of you paid some attention to as well.  I have loved being a woman, but the older I get, the more I recognize that stuff happens because of being a woman.  Both my breast and uterine cancers were estrogen related.  But it was sure good to have estrogen back in the day . .

     Hugs, Suzanne

  • Kathysuej
    Kathysuej Member Posts: 16
    Thank you all...

    Thank you all so much for sharing with me, it really helps just knowing so many have gone through or are going through the same thing (thought, feelings & worries too). I do have one question that has been on my mind a lot recently....About how long after diagnosis did you have surgery? I know this varies for everyone, and depends on how aggressive your cancers are, but I am really starting to worry as I was diagnosed on Dec 2, and now it is almost Jan 2nd...one whole month later. And I still have no surgery date set! Although, they are working on getting a date for me and I may find that out tomorrow.
    I was told my cancers are growing at a rate of 17%. They said it isn't a super fast growing kind, but it isn't the slow kind either. Being a clinical stage 2, with grades 1 & 2 tumors (at least 3 areas that we know of. One is 11mm, one is 8mm and the 3rd is 4mm. In the beginning I was told I would have surgery within the first couple weeks, that it would all go super fast. But with the holiday and everything it's taking a bit longer. My Oncologist & surgeon both were out of town for a couple weeks. But now they are back and we're moving forward. I just feel like it's gotten bigger. My left breast has definitely grown and the pain has gotten worse. It used to only hurt around the nipple, now that pain has moved towards my armpit. So yeah, it scares me.
    Did any of you have to wait this long for surgery?

  • Kathysuej
    Kathysuej Member Posts: 16
    edited January 2017 #18
    aisling8 said:

    Three months

    I waited three months between diagnosis and surgery and thought I'd go insane with worrying about the delay. I pictured it spreading up and down my spine, all over my body. That was six years ago. I completely understand your fears.

    xo

    Victoria

     

    Wow! That makes me feel a lot

    Wow! That makes me feel a lot better! I still can't help but feel that way, like it's spreading all over. And the pain I have been having in my breast was localized just around the nipple area. It's like an electrical jolting feeling, combined with an internal ache. But now it has started happening over more too, like towards my underarm/side. That, in addition to the breast getting larger, really makes me think it's growing/spreading.
    I was hoping I'd find out my surgery date today, but didn't realize the clinics are closed. I guess they reserve New Year's on Monday if it falls on a Sunday. My bad, lol. So hopefully I'll know tomorrow!

  • Kathysuej
    Kathysuej Member Posts: 16
    edited January 2017 #19

    I waited about 3 weeks for lumpectomy

    and then I had to wait 6 more weeks for my hysterectomy before I could start any adjuvunct treatments!  (I had both breast and endometrial cancers).  Then I waited 3 weeks after hysterectomy before starting chemo for the breast cancer.  I could just feel it growing here and there and everywhere and I was sure that my endometrial cancer had grown just about everywhere - it hadn't, was Stage 1.  In hindsight, I can say all was well and that was in 2010.  No recurrence.  Nothing even scarey (except my thoughts).  My breast cancer was Grade 2 but Stage 1 (node negative), only one 9 mm tumor but lots of DCIS.  Margins around tumor were not clear but because I was also getting/having a mini-breast reduction on that side (it was much larger than the other one), the margins for the entire chunk were clear.   I had chemo because of high oncotype score.  The waiting was the absolute worst!  I feel very thankful and lucky.  I hope all goes well for you and you get that surgery date tomorrow!  While holidays seem to drag things out, if your cancer needed surgery sooner, it would have happened.  So, I'm thinking this is good news. . .

    Keep bringing the IUD to their attention.  I really don't know about those things, but I do know that estrogen is not a good thing for ER+ cancers and PR, too?  It will give you peace of mind to have that removed and that part of you paid some attention to as well.  I have loved being a woman, but the older I get, the more I recognize that stuff happens because of being a woman.  Both my breast and uterine cancers were estrogen related.  But it was sure good to have estrogen back in the day . .

     Hugs, Suzanne

    Thanks! That does help me

    Thanks! That does help me feel a little better knowing I am not out of the "norm," per se. And yes, the IUD does worry me, but since I have Endometriosis and Adenomyosis, they want to keep it in for now. The doctor's reassure me the IUD is supposed to only release the hormones in that lower region of the body (the pelvic area), they said if I were taking the pill or shot that they would have me stop immediately. But it does still worry me. I am debating having a hysterectomy in the future, just to get rid of all the trouble the uterus and ovaries have caused me. I have 3 children, and while I do wish I could have more (I just LOVE babies!), financially and physically I am unable. So why not get that all out of there so I have one less thing to worry about? Is it rough? After the hysterectomy? Going into menopause and all?
    Oh, and I didn't realize that the doctor offices reserve New Year's on Monday when New Year's day falls on a Sunday....the clinics were closed today! But hopefully I'll find out the date tomorrow!

  • Kathysuej
    Kathysuej Member Posts: 16
    edited January 2017 #20
    Another question...unrelated...

    Does anyone know if there is a discussion board for Cervical Cancer? I can't find one. My sister is pre-cancerous, and I referred her to this site, but we cannot find anything on cervical?

  • aisling8
    aisling8 Member Posts: 1,627 Member
    edited January 2017 #21
    Try gynecological cancer

    I think you might find cervical cancer there.