not convinced about chemo and all the other drugs?

Options

i was diagnosed in july with invasive breast cancer stage 2 grade 3. it is her2 positive. I have had surgery and had 5 lymph nodes removed and margins all clear. I have had 2 scans showing no other cancer so it is not metastic. Since all this began i have not felt ill at all and i have kept it tomyself/family and employer. I am a teacher of 4/5 year olds and love my job! i also have 3 girls 14yrs 10 yrs and14months  2 rabbits 2 guninea pigs and a dog(mad i know but fantastic). I live an extremely busy but happy life with my hubby. I am scared stiff that if i have chemo etc that we will not be able to maintain this and life will crumble around us. My husband is wonderful however not superman! My children are fantatic too but just children! I feel with every bone in my body that chemo will make me ill and that i will be changed for ever. My sister is just finishing 6months of chemo and she is knackered and has some side effects. She lives on her own and only has herself to think about!

Should i enter into the world of drugs and chemo, sickness and side effects?

Should i wait and see what happens with the cancer?

 How i am goin to cope with all that goes on in life?

I wish  to keep working, is this possibe?

Why would i make myself so ill and damged when i feel fine with no guarantees? 

Comments

  • ladyboss1997
    ladyboss1997 Member Posts: 202
    edited October 2012

    I am one year out from my chemo, and I am so glad I did it. I just refused to let it interfere with my life. I had my slow and tired days, but I kept on moving. What does your doctor recommend? - Diana  

  • Noranelly
    Noranelly Member Posts: 30
    edited October 2012

    seeing him this Monday! 

  • Denise-G
    Denise-G Member Posts: 1,777
    edited October 2012

    You have an aggressive cancer.  I had an aggressive cancer.  I always felt good.  I feel good again.

    I didn't want to do chemo, but knew I would die if I did not do it.  My Oncologist told me so, and I believed him.  And I watched my friend die who decided against chemo with a similar diagnosis as yours because she "didn't want to feel bad."

    Chemo will make you feel bad.  There is no way around it.  And you will want to quit while you are doing it.  Most of us do.  But we continue because we want to live.  And most of us do. 

    I have a Blog that I began when I was diagnosed a year ago.  I get many, many emails from women who don't want to start Chemo or they want to quit Chemo.  From most of them I get thank you letters telling me they are so thankful they endured chemotherapy, they made it and are cancer free.  That is the best reward.

    One woman told me she told her Oncologist she wasn't going to do chemo.  He pulled a piece of paper out from his desk, then asked her the name of who was going to take care of her 2 year old.  She did Chemo and never regretted it. 

    The decision is yours, however. 

  • Momine
    Momine Member Posts: 7,859
    edited October 2012

    I did the chemo, 8 rounds. It was tough at times, but my life did not crumble. I am a year out from surgery and feeling good.

  • CoolBreeze
    CoolBreeze Member Posts: 4,668
    edited October 2012

    Nobody wants to do chemo.  Nobody.  But, nearly everybody who does it says that it wasn't nearly as bad as they had expected.  It's not like the movies.  I don't know what your sister is going through, but I worked as a school secretary during my first rounds of TCH, had my dogs, my sons, my family life, and I just got a bit tired at the end of it.

    I am HER2+ too, had no nodes.  And, even with doing my six rounds of TCH and my year of herceptin, my cancer came back.   Who knows why?  None of the woman I started with have had it return.  

    But, I am still alive today because of chemo and now I live on chemo forever.  If I had made the choice not to do chemo, I would be dead already.  HER2 cancer grows very fast and very aggressively and without treatment, you are not likely to be around to enjoy all the things in your life you are worried about missing.  Without treatment,   I wouldn't have seen my son turn 15, become a junior in high school, I wouldn't have seen my older son's 25th birthday, i wouldn't have had my new puppy.  All of this would have happened without me.

    So yeah, I now have a terminal disease and cancer will kill me.  But, I really love life, as you seem to.  And, I want to live it as best and as long as I can.  So, I have been on chemo for three years now.  I still enjoy my family and I enjoy my life.  Things have slowed down for me but they aren't over.

    I think you should give yourself the best chance you possibly can.  Don't look backwards, look ahead.  FYI:  I worked up until this July, 2012.  I started chemo December 2009.  The ONLY reason I'm not still working is my job began at 7:00 a.m. and I could no longer get up that early.  I need more sleep.  But, if I had a job that started later in the day, I could have done it.  I worked as a high school secretary so there was no chance of switching my hours.  You will be able to work on your therapy.

  • greenfrog
    greenfrog Member Posts: 269
    edited October 2012

    There is no such thing as "waiting to see" what happens with cancer Noranelly. It doesn't give second chances.

    Please make sure you have a full honest frank conversation with your oncologist. Your cancer has already spread to 5 nodes and is ER neg and HER2 pos. Chemo and Herceptin are not the enemy - they could be the things that ensure you are around long enough to enjoy your grandchildren.

    My life was very busy and bubbling along when I was diagnosed with cancer. Timing was awful. But I just had to accept that it would mess up a year of my life and then I could get back to business - and that is what I have done but secure in the knowledge that I have done everything medically possible to try and remain cancer free.

    My son was 1 month younger than your youngest child when I was diagnosed. And I am a single mum. I did it for him - and you will do it for your kids.

    Good luck and keep posting.

  • Beesie
    Beesie Member Posts: 12,240
    edited October 2012

    Noranelly, 

    You said "I have had 2 scans showing no other cancer so it is not metastic."   Actually, you don't know that.  What you know from the scans is only that you don't have metastatic cancer that is large enough to be detected.  And that's a very good thing.

    I recall reading in Dr. Susan Love's Breast Book that 20% to 30% of node-negative women with no signs of mets in fact already have breast cancer cells that have moved out of the breast to somewhere else in their body.  These cancer cells left the breast either through the bloodstream or through the nodes, but there were too few of them to be detected.

    It's because this happens that you find women who seem to be fully cured who discover, some years later, they have have mets to the bones or liver or some other organ.  Most women who are Stage IV did not start out as Stage IV.  They started out as Stage I or II or III, with no visible sign of mets.  But by the time they had their surgery, just a few cancer cells had already escaped into their bodies and over time those cells took hold and developed into mets. 

    It's because this happens that chemo is often prescribed to women who are node negative and who show no visible signs of mets, if they have what's considered to be a high risk diagnosis.  The role of chemo is to track down breast cancer cells wherever they might be in your body, and kill them off.  When it's just a few rogue cells that have not yet taken hold and started to develop into a metastatic recurrence, chemo can be effective at killing off these cells. Chemo can get rid of these cells and as a result, the patient never develops mets.  But if you wait until you have mets that is detectable on a scan, it's too late. At that point chemo may be effective at stalling the continuing development of mets, but it will not be able to stop it permanently.  

    With your cancer being HER2+, you have an extremely aggressive, high risk cancer.  Even though mets is not visible on your scans, there is a significant risk that some cancer cells may have already moved into your body.  Right now, while you have no signs of mets, the combination of chemo and Herceptin can kill off these cells and help you avoid mets. But once mets is detected, chemo can at best extend your life.

    I am unclear about your nodal status.  You say had 5 nodes removed, but your signature line indicates that you had 5 positive nodes out of 15 nodes removed.   Your signature line also says that your diagnosis is Stage IIA, and that would not be the case if you had 5 positive nodes.  So I'm guessing that you don't have any positive nodes and the "5/15" on your signature line is incorrect.  Did I guess right?

    Have you seen LifeMath?  This doesn't substitute for your discussion with the oncologist, but it will give you some insight into the risks you face with your diagnosis. You can input your diagnosis and other data, and look at the charts both if you decide to forgo any further treatment, or if you have treatment. That will give you an idea of how much benefit you will get from treatment, in terms of improving your long-term odds of survival.  This is the type of information you need to decide if treatment is worth it to you.  Your oncologist should also be able to provide this information. 

    Here's the link to LifeMath:  Breast Cancer Treatment Outcome Calculator   You can display the data in many different ways. I find the "pictogram" to be the easiest graph to understand.  

    Is it an oncologist that you are seeing on Monday?  

  • Rockym
    Rockym Member Posts: 1,261
    edited October 2012

    Noranelly,  you ask:

    Should i enter into the world of drugs and chemo, sickness and side effects?

         As others have said, with Her2, I believe you will have to.

    Should i wait and see what happens with the cancer?

         The only thing that happens with cancer is it typically grows.

    How i am going to cope with all that goes on in life?

         I carried on with my regular life as did many other ladies.  If you are fortunate, you'll only be down and out a few days after each treatment.

    I wish to keep working, is this possible?

         You may have to adjust, but work is possible.

    Why would i make myself so ill and damaged when i feel fine with no guarantees?

         That's the strange part about cancer is that lots of us feel fine.  It seems to be the invisible disease.  Lastly, as you know there are no

         guarantees in life.

    I also have a 14 year old and 10 year old and they were great.  They watched me go through a lot over the last year plus and both have grown and matured.  I was also able to "let go" a bit more with them because of my health and I'm very proud of both of them.  I know you will be proud of yours too.

  • markat
    markat Member Posts: 909
    edited October 2012

    I've never met anyone that wants to have chemo, but with Her2+, you pretty much have to.



    I have two young girls and I would do anything the docs told me to do to get to spend more time with them. This year has been tough, but definitely doable.



    I wish you the best!

  • Jennt28
    Jennt28 Member Posts: 2,021
    edited October 2012

    Chemo is not something doctors do TO you, it is something they do FOR you...



    Her2+ and estrogen negative cancer means your best option for long term survival is going to be chemo and Herceptin.



    I did FEC x 3 cycles then 10 weeks of Taxol/herceptin and am now just doing 3 weekly Herceptin until March 2013. Chemo was surreal and not an experience I would wish on anyone - but it was necessary and despite some side effects I got through still functioning at home and at work.



    Herceptin makes me tired for a day and gives me a runny nose, but that is all.



    Jenn

  • Racy
    Racy Member Posts: 2,651
    edited October 2012

    Noranelly, as a newly diagnosed patient, you would still be learning about the complexities of bc. This site is the place to learn. It may take a while to understand. The ladies who have posted here have been living with bc and on this site long enough to give you credible advice.



    Keep posting and feel free to ask anything that is on your mind.

  • lovetodance
    lovetodance Member Posts: 9
    edited October 2012

    IM 2 YEARS OUT, DID TCH,TOUGH BUT DOABLE, SO FAR SO GOOD, 4 PET SCANS IN 2 YEARS ALL CLEAR(TOO MANY PETS), IM RUNNING, DANCING, WORKING. I HAD NO NODES AND NOT LVI(LYMPHOVASCULAR INVASION) CHECK YOUR PATH REPORT FOR THAT. DO NOT FOOL WITH HER2, WE HAVE MUCH BETTER PROGNOSIS THAN HER2NEGATIVE(SOME ONCOLOGIST SAY) BECAUSE HERCEPTIN IS ANOTHER WEAPON THAT ATTACKS BC CELLS WHETER THEY ARE DIVIDING OR NOT AND HELPS TAG BC CELLS TO BE HIT BY IMMUNE SYSTEM..PLEASE DO NOT UNDERESTIMATE BC AND HER2..IF YOU DO NOT DO IT FOR YOURSELF,DO IT FOR YOUR FAMILY IT IS ALSO TOUGH ON THEM

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited October 2012

    I'm sorry to learn of your diagnosis.  

    It almost sounds like you're in denial.  It's not the treatment that will change you.  You are already in the process of changing just because of your diagnosis.

    I'm a paraprofessional (instructional aide) at an elementary school.  Several years before my diagnosis, a 32-year-old teacher at work had a bc diagnosis.  She had three children under the age of 4.  Over the next year or so, she had chemo, surgery-a double mastectomy, radiation, as well as reconstructive surgery.  She just recently had a hysterectomy.  She took needed time off, and her chemo was done during the summer, but for the most part, she still showed up for work much of the time.  She has the support of the whole community (about 5,000 people) as we all knew what she was dealing with.

    Even if you have to take big chunks of work off for your treatment, you need to do it.  It will be a hellish year, but you will get through it. 

  • Noranelly
    Noranelly Member Posts: 30
    edited October 2012

    thank you  everyone for all your advice and i hear what you are saying, you all sound so brave and knowledgeable. You made me cry as i have not really talked to anyone outside my family about this! I think i am in denail however am slowly coming to accept it and how it will effect my life. We have had i devastating last 2 years with the death of my 15 year old niece to hodgekinsons L, plus the loss of my step father to stoamch cancer, the diagnosis of my mum with bowel cancer ( however all clear with her now, hooray) diagnosis of my sister with breast cancer and now me! What just happened?/?/??????? We are all trying hard to be positive and move forward and my diagnosis is another mountain to climb. We are being assessed for a genetic link as it looks like my cancer was in the family in the past as well. Life  feels very uncertain at the moment and that i would be happy to run away however i know i wont. 

    thanks Noranelly 

  • Racy
    Racy Member Posts: 2,651
    edited October 2012

    Noranelly, I am very sorry for all that your family has gone through. Everyone here will support you as you deal with your own cancer, including if you decide to do chemo.



    Please stay in touch. This is a remarkable community.

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited October 2012

    noranelly, I'm so sorry for all you are experiencing.  My family has had some difficulties in the last year and a half, and I felt like someone just shot dozens of poison arrows at us.  So I really feel for you, that is a lot that you are dealing with.

    With any major crisis I've gone through, I learn to weed out a lot of crap that I didn't realize I put up with.  Even tho I've felt blessed in many ways (tho certainly NOT with bc), during hard times I re-evaluate my life and get rid of what doesn't work anymore for me.  It's like being pruned. Getting rid of the garbage gave me more resources to deal with new challenges. 

    kayb is so right, a well written post. We're all learning as we go. It sucks that we are here.  But you will find that you still have lots of life, lots of living to do.  The beginning of the journey is rough, but it does get better.

  • vlnrph
    vlnrph Member Posts: 1,632
    edited October 2012

    Everyone gives very good advice. I am worried for your girls, with their mother & aunt both having BC (and grandma w/ bowel). Have either of you thought about BRCA gene testing?

  • 1Athena1
    1Athena1 Member Posts: 6,696
    edited October 2012

    Noranelly:

    You ask good questions that no one can answer for you. I was not Her2. With that caveat (and the other salient caveat, which is that only about 50 percent of those with Her-pos get a positive response from Herceptin) I did not do chemo because I was not convinced by the science, I believe I am alive BECAUSE I did not do chemo (but of course there is no knowing for sure) and I will never regret my decision - even if I am diagnosed with mets tomorrow.

    The people who die of or have debilitating SEs from chemo generally do not post or go elsewhere. There is no knowing what the effects will be on you - no two people are identical.

    There is a way to make a separate decision about Herceptin - although most of the studies and treatment protocols for Herceptin deliver the drug with chemo, some oncs will consider it alone.

    I wouldn't use others' experiences as guides for what will happen to you. The variety of experiences here show how maddeningly uncertain living with ad treating cancer may be.

    Also, don't be too taken in by statistics, as you own medical profile may suggest different odds.

    My final piece of advice: make no decision out of peer pressure or fear. After all, you have only yourself to answer to.

    And I am so sorry to hear about your recent loss. It has to be hard to disentangle that from this.

  • Noranelly
    Noranelly Member Posts: 30
    edited October 2012

    Thank you for all you support. I saw my oncologist yesterday. I was told chemo was a must have and that continuing my job as a teacher thro the 6 months was not a good idea. I cried until 3am and feel completely flat and out of control. I think if it was just me and I had no children I would so no to chemo but I have others to think of. I am a mother, wife and daughter and all these people want the best chance of life for me. I feel pressured although they say they would support my decision. I feel really sick and flat and almost in a bubble. I saw my niece die and she didn't have any quality of life before passing away due to all the side effects of chemo etc I always said I wouldn't put myself thro what she went thro and here I am about to. I keep thinking I,m entering something that is completely out of my control. Noranelly

  • 1Athena1
    1Athena1 Member Posts: 6,696
    edited October 2012

    ((((Noranelly))))

  • stride
    stride Member Posts: 470
    edited October 2012

    Noranelly, no wonder you are worried about chemo, based on what you saw happen to your niece. That sounds like it must have been awful, and I'm so sorry for her and for your loss of her. But remember, you are not her. Undoubtedly your diagnosis is different, and your chemo regimen probably will be, too. For most of us chemo is unpleasant, but we go on to live high-quality lives. It is an interruption in your life, but it may save your life.

  • Momine
    Momine Member Posts: 7,859
    edited October 2012

    Your niece was most likely stage IV, if she died. You are NOT stage IV. The idea is that if you do the chemo, you may end up with a ton of good, healthy years before keeling over from old age.

    Also, not all chemos are the same, and docs are getting better and better at helping with the SEs.

  • Noranelly
    Noranelly Member Posts: 30
    edited October 2012

    Thank you so much for all your advice and support. It helps to hear others stories. I look forward and hope to feel the person I was before. Noranelly

  • DivineMrsM
    DivineMrsM Member Posts: 9,620
    edited October 2012

    noranelly, there are wonderful threads on this website for women going through chemo.  I joined the "March 2011 Chemo Lounge" thread last year.  All of us on that thread began our chemo during that month and supported one another as each of us went thru this new experience. My chemo was once every three weeks for six treatments. So I went from March till June.  I had one week of crappy and two weeks of not too bad.  It was my son's senior year in high school, and I still made it to all those end of school banquets plus had a large graduation party for him in my back yard 10 days after my last chemo that June (with lots of family help).  I also had two surgeries and radiation.  Since then, I've taken a trip to New York City for the first time (LOVED it), gone to Las Vegas, seen the Grand Canyon for the first time, held a big Thanksgiving dinner at my house, seen Van Halen in concert, ect. ect. ect.  And I'm not the only one continuing to live a full life despite the diagnosis.  You are going through a lot, but you will come out on the other end and keep going.

    I encourage you to check out the chemo forum; so much knowledge is shared there.  There will be others just beginning chemo the same month as you so join or start a thread for you and those women.  God bless.

  • Jennt28
    Jennt28 Member Posts: 2,021
    edited October 2012

    Someone put this up on one of the other message groups and I thought this might be good for here...





    "Your relationships are about to change. All of them. Some will get stronger. They will probably not be with the people you would expect. The people you want to handle this well might not be able to for a variety of reasons. Some of the reasons will be selfish. Some of them will be entirely innocent and circumstantial. All of them will be forgivable because no one plans for cancer. Carrying bitterness or anger won't help your recovery. Fighting for anyone to stick with you won't cure you. Those who can, will.



    You will be determined to have more energy than you do. You will convince yourself that you are thinking straight, are able to handle all of this and do not need anyone. You will run out fuel. Your body will change first and your mind will follow. You won't lose your mind, memories or sensibility. It will all come back. But, you will be different. You will never have the same sense of self. You should embrace this. Your old self was probably really great. Your transformed self will be even better. Give into what is happening and trust it.



    You are going to feel fear. Even if you are normally stubborn, confident and seemingly invincible you will finally find yourself admitting that you are scared of something. Cancer is scary and incredibly confusing. The unknowing will eat at you worse than the disease itself. You'll need distractions. Music and sleep will probably be the ones you resort to most. Reading will become difficult. So will watching TV or movies, having conversations, writing and basically everything else. They call it "chemo brain" for a reason. You will feel normal eventually. Just a new kind of normal. When you feel afraid let yourself lean on those around you. Cry. Be vulnerable. You are vulnerable. There will be time for strength, but never admitting weakness will cause anxiety to mount and your condition to worsen. Let it all out. Yell if you need to. Sing when you feel up to it. Sob uncontrollably. Apologize for your mood swings. Treatments and prescriptions will often be the cause of them. The people that love you will understand.



    The people that love you will be just as scared as you are. Probably more. They will be worrying even when they are smiling. They will assume you are in more pain than you are. They will be thinking about you dying and preparing for life without you. They will go through a process that you will never understand just like they will never understand the process you are going through. Let them process. Forgive them when they don't understand. Exercise patience when you can. Know that those that were built for this will be there when you get to the other side and you will all be able to laugh together again. You'll cry together too. Then you'll get to a place where you will just live in the world again together and that is when you know that you have beaten this.



    The sooner you recognize that you are mortal, the sooner you can create the mentality for survival. There is a chance you might not make it. Just like there is a chance that you will. Don't look at statistics. You are unique and what is happening inside you is unique. Your fight is yours alone and there are too many factors to compare yourself to others that have had your condition. No one will want you to think about death, but you won't have a choice. You will think about it from the moment you are given your diagnosis. Come to terms with it. Calmly accept it. Then, shift every thought you have into believing that you won't die. You are going to beat this. Your mental focus on that fact will be more powerful than any treatment you receive.



    Your doctors and nurses will become your source of comfort. You will feel safe with them. If you do not feel safe with them you need to change your care provider immediately. There is no time to waste. This shouldn't be a game played on anyone's terms but yours. When you find the right caretakers you will know immediately. Do not let insurance, money or red tape prevent you from getting the treatment you deserve. This is your only shot. There is always a way. Find those hands that you trust your life in and willingly give it to them. They will quickly bring you a sense of calm. They will spend time answering your questions. There will be no stupid questions to them. They won't do anything besides make you feel like you are the most important life that exists. They will never make you feel like they don't have things in control. They will be honest and accessible at all times. They might even become your friends. You might celebrate with them over drinks months or years after they have cured you. They deserve your gratitude, respect and appreciation daily. If you get upset at them during treatment know that they'll forgive you. They get that you're going through something they can't imagine- but they understand better than anyone. They see it every day and they choose to be there because they want to make the worst experience of your life more tolerable.



    You will need to find balance after treatment. Start by seeking balance during treatment. Eat well. Sleep well. Listen to your body. Explore meditation. Experiment with new forms of exercise that aren't so demanding. Embrace massage and other body therapies. Go to therapy. A therapist will be able to guide you through your journey in ways you could never fathom. Do not be too proud to speak to someone. You cannot afford to store up the intensity of the emotion that comes with fighting a life-threatening illness. Let it out for yourself. You will begin to hear your voice changing. That voice is who you are becoming in the face of mortality. Listen to that voice. It will be the purest, most authentic version of you that you have ever known. Bring that person into the world -- strengths and vulnerabilities and everything between. Be that person forever.



    You will inspire others. It will feel weird. People you haven't spoken to since grade school will be in touch. Ex-girlfriends, former colleagues... even people you felt never wanted to talk to you again. The influx of interest in your seemingly fading life will be greater than any living moment you have ever experienced. That support is what will shift a fading life into a surviving one. Be grateful for every message. Be appreciative of each gift and each visit. There will be moments where all of this attention will make you feel lonelier than you have ever felt in your life. In a hospital room full of people with messages stuffing your inbox, voicemail and mailbox you will find yourself feeling completely alone. This is when you will realize that you could afford to have a stronger relationship with yourself. That only you walk this earth with 100% investment in you. Make the investment and use this as an opportunity to reexamine your self-worth. Love yourself more than ever and recognize how much love there is for you in the world. Then start sharing that love. You will come to see that even when you are the neediest person you know you can still be giving. Giving will make you feel better than taking.



    When you get to the other side you won't believe it. They will tell you the disease is gone. Everyone you know will rejoice and return back to their lives. You'll constantly wonder if it is coming back. Slowly this feeling will fade, but cancer will always be a part of you. It will define how you see the world moving forward. You're going to feel like the future is a funny thing to think about because the present is going to suddenly seem incredibly important. Keep moving. You'll be more productive. You'll understand who truly loves you because they will still be there. You'll want to meet new people that connect to the newly evolved version of your old self. You'll want to let go of those that don't "get" who you are now. You'll feel a little guilty doing it. Then, you'll move on. You don't have time to waste. The greatest gift you've been given is that you now understand that and you're going to make the most of every second. You're going to be the most passionate person you know going forward. Translate that passion to a greater purpose. Be fearless again.



    I was diagnosed with leukemia at the age of 27. Now 28, I have been told I have no trace of the disease in my body.



    Jeff Tomczek is a freelance writer and the founder of C2Bseen, offering consulting services to niche brands and entrepreneurs.



    Follow Jeff Tomczek on Twitter: www.twitter.com/C2Bseen"

  • RachelM11
    RachelM11 Member Posts: 9
    edited November 2012

    Hi,

    I felt the same way you did. I had a BMX and was told I had a 50/50 shot if I didn't do the treatment they were asking me to do after surgery. The long term side effects scared me too much to even consider facing them if I didn't have to and I couldn't accept that I was still sick when they couldn't show it to me on a scan and I felt fine. To me it wasn't logical to fight something I couldn't see anymore.

    I watched people around me die miserable deaths from results of chemo or live on to struggle with side effects that never went away after treatment. So, I told the doctors that I hoped I never had to see them again, bought a convertible and went on vacation to Mexico Laughing I completed reconstruction, had more clean scans and just started to live my live like the "old me" when the cancer came back (not even 6 months later).

    Despite the "I told you so's" in my life, I don't regret my decision at all. I made the choice I felt was right for me at the time. I obviously had no choice but to do treatment this time around but I continue to be my own advocate.  My cancer did a personality change this time so we realized that Tamoxifen would have been unecessary. Perjata got approved in the 6 months I wasn't in treatment giving me an option I didn't have to choose from before. So, there were some small benefits to what I did in the past. I didn't stop challenging treatment options until we came to one that I could wrap my head around.

    I got second opinions again. I saw a doctor that said there were 40 different chemo options and we could pick one that I felt comfortable with. I decided to keep seeing someone that actually listened to my fears and didn't force "standard of care" on me. Only you know what is right for you. None of us would wish these decisions on our worst enemy, but you will decide what's best for you and you'll make it through!  Discuss all the options and don't let anyone tell you what you can't do--I work everyday during treatment!

    Best Wishes,

    Rachel

  • crying
    crying Member Posts: 4
    edited December 2012

    thank u jennt28 your post is makining me rethink my decision not to have any tx. 

  • Jennt28
    Jennt28 Member Posts: 2,021
    edited December 2012

    crying - I'm glad to be of help... I didn't say yes to everything (I actually quit rads and said no to an axillary clearance) but I have said yes to the most beneficial treatments. For me those are: surgery, chemo with herceptin, and Tamoxifen.



    Jenn

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