November 2009-Starting Chemo

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  • Cafelovr
    Cafelovr Member Posts: 1,534
    edited August 2014

    Pam, Congratulations! I am so thrilled this part of your life will be over. Life is very sweet!

    I see several Pam Rosenberg's, one in Ft. Wayne IN. Can you friend me? Linda Randolph-Justice.

  • RedheadPam
    RedheadPam Member Posts: 98
    edited August 2014

    Linda - I'm in Indianapolis...

  • doronet
    doronet Member Posts: 342
    edited September 2014

    Just "popped in" to share some info I got from my oncologist during my annual check-up this past week. I mentioned that May will make 5 years of being on the Femara maintenance medication (the equivalent of Tamoxifen for post-menopausal women) and I asked her if I would stop taking it then. She said that recent studies of indicated that staying on the Femara for 5 more years extends its benefits. She said this goes for Tamoxifen as well.  I found this on-line, which further explains what she said: Women with ER-positive breast cancer who underwent 10 years of adjuvant treatment with tamoxifen were at reduced risk for late recurrence and breast cancer-related mortality compared with those who underwent 5 years of treatment, according to results of the phase 3 aTTom study presented at the ASCO Annual Meeting.

    The longer duration of tamoxifen treatment was associated with increased adverse effects, but the overall benefits outweigh any potential risks of extended therapy, researchers said. 

    I hadn't heard anything like this and wanted to pass it on.

    I hope everyone is doing well.  I know this was a hard month for those of us diagnosed around this time 5 years ago; however, that's why I choose to focus on the date when I finished treatments instead of when I was diagnosed. At least now, I can almost get through Sept. 1st without thinking about it.

    Take care, All!!!

    Nette  :)

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited September 2014

    Hi Nette - I'm going to continue on Aromasin. I don't see my onc anymore but I'm just going to do it - the GP agrees.

    I'm recovering from a knee replacement - I finally got up the courage to have surgery after the whole BC experience - it took a while. I must say I was pretty miserable in hospital and screemed the place down, but 6 weeks on I'm starting to feel normal and am appreciating being able to straighten my leg and walk properly.

    When I had the surgery I woke up in ICU - we found out a week before the surgery I have atrial fibrillation (irregular heartbeat). Wondering if Herceptin has anything to do with it. I'm now on heart meds and all is good.

    Went out clothes shopping yesterday - I've lost about 17 lbs and none of my work clothes fit. It was my first shopping trip on my own - I took a crutch but didn't really need to use it.

    Saw the knee surgeon on Friday and he was pleased with my progress - I've got 125 degree bend which is good - aiming for 130. I go back in 6 weeks. I'm not going back to work for another couple of weeks as I have back trouble that needs fixing first.

    I'm aware of the 5 year mark coming up too my birthday is a constant reminder - the day I had the mammo - not looking forward to screening in October - would love to skip it, but they found a benign thing last year, so I'll have to keep going.

    So good to hear from you - I really miss all of our Nov09 chemo friends.

  • doronet
    doronet Member Posts: 342
    edited September 2014

    Hi back, Sue!

    Sorry to read that you needed the knee replacement, but it sounds like you had no choice and that you are progressing nicely!!  I expect it will all be worth it once you are fully recovered.

     I hadn't heard of Hercep. causing A. Fib, but who knows what medication that strong can cause! I am blessed not to have to be on that one, but I remember that several other Warrior Ladies are. I've been told recently that my glucose levels are too high, so I need to watch the bad carbs and sweets and this is very unfortunate since I have a terrible sweet tooth!  However, as much as I hate having to take pills and watch my diet and do all the things I have to do to stay healthy, it beats the hell out of not being here at all.  :P

    I still keep up with the facebook ladies, you included, but I never post or comment.  Decided to give up doing everything except reading due to a disgusting video that popped up on my newsfeed. Is better that I just observe anyway.  :)

    Take care of yourself.  Continue to get that knee stronger!  Nette  :)

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited September 2014

    Nette - I don't know for sure that the Herceptin caused it. Apparently AFib is very common but it would be interesting to compare my last echo from back then to the one they took in hospital. My GP hasn't recommended seeing a cardiologist at this stage seeing my heartbeat has stabilised on the meds.

    I'd needed a knee replacement for years and was waiting until I was old enough - it's so great to be able to straighten my leg properly now. I'd been limping for a few months and had taken to working from home because of it and my back kept going out because of the limp. So something had to be done.

  • Cafelovr
    Cafelovr Member Posts: 1,534
    edited September 2014

    I have been on Herceptin for almost 5 years (January 2015). It can cause all sorts of damage to the heart. This far out, and I still have my echoes to check my ejection fraction (must be over 55%) and make sure my left ventricle is up to speed. Luckily it is!

    Another thing that can screw the heart up is if you had radiation on the left breast/chest wall. I did, and my cardiologist says that more than likely, I will have congestive heart failure when I'm older because it's almost a given that your heart and lung is hit during the rads.

    But on the merry-go-round I will stay. Still rocking the NED! Love to you all!!

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited September 2014

    Linda - great to hear from you. I did have rads on both sides. They say they avoid the heart, but who knows. The left side is slightly enlarged. It can also be caused by thyroid problems and I have a large goitre which we've decided to leave alone until it causes problems. I'll discuss with the bs when I see her next month.

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited October 2014

    Hi Lady Warriors, 

    Well pinktober is here again 5 years later.

    What a ride these years have been to say the least. 

    I'd recently been laid off from my job, which sucks at 61 years of age, let alone the smal, town that I live in.No jobs to be had here, except cashiers and labor jobs. I tried cooking for a say and was too weak. Everyone says everything happens for a reason. Be patient.  It's been 3 months.

    Anyways, got my yearly mammo this Tuesday.  They took several x-rays this go around. More than usual.  The tech said all the pictures where very clear for the radiologists to read. Then I got a call yesterday and I was asked to come in, they needed more pictures,, USUALLY, I get a letter a week or so later saying everything is good.  So, this call has me a bit anxious.  OMG!!! This may be that reason. I don't think I could work like I did the last go around with mt treatments. I just have a feeling ,,,,,,,,,,,,,,,    ;*( 

    I'll post back once I have more to tell. March of 2015 would be when I'd of been 5 years clean, after completion of all treatments, chemo and rads. If  I have to deal with this again,  I know I canbe strong and make Iit through.  I just wonder what kind of treatment I will receive.  I'm pretty sure that they don't repeat the same treatment. 

    ((((( Hugs)))))

  • BrendaSharon
    BrendaSharon Member Posts: 506
    edited October 2014

    isn'tHi Lady Warriors, 

    Well pinktober is here again 5 years later.

    What a ride these years have been to say the least. 

    I'd recently been laid off from my job, which sucks at 61 years of age, let alone the sml, town that I live in.No jobs to be had here, except cashiers and labor jobs. I tried cooking for a day and was too weak. Everyone says everything happens for a reason and to be patient. But, It's been 3 months already that I haven't worked. Just been hard work looking for a job!!.  Trying to collect unemployment first time andis that a callange in itself.  In 3 months I've only received 2 small checks.

    Anyways, got my yearly mammo this Tuesday.  They took several x-rays this go around. More than usual.  The tech said all the pictures where very clear for the radiologists to read. Then I got a call yesterday and I was asked to come in, they needed more pictures,, USUALLY, I get a letter a week or so later saying everything is good.  So, this call has me a bit anxious.  OMG!!! This may be that reason. I don't think I could work like I did the last go around with my treatments. I just have a feeling ,,,,,,,,,,,,,,,    ;*( 

    I'll post back once I have more to tell. March of 2015 would be when I'd of been 5 years clean, after completion of all treatments, chemo and rads. IF, I have to deal with this again,  I know I can be strong and make it through.  I just wonder what kind of treatment I will receive.  I'm pretty sure that they don't repeat the same treatment. 

    ((((( Hugs)))))

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited October 2014

    Hi Brenda - I've missed you SO much!!

    Sorry about your job - that sucks. Why don't you get decent unemployment? Shouldn't the payment be regular? Typical of the US. People here get really good unemployment and it never stops unless they find a job.

    Don't panic about them wanting more scans. I had a biopsy last October - turned out to be nothing. Had a follow up Ultrasound 6 months later and it was OK. You are right they can't radiate the breast twice. I've had both done, so if anything new pops up a mastectomy is the only treatment.

    I'm booked in for my screening next Thursday. I called knowing they usually are very booked up and thought I would have to wait weeks - well - oh we've had a cancellation next Thursday - so that's when I'm going.

    How are the peeps? I often think of your lovely chicks and think about how nice it must be to have fresh eggs.

    (((((((((((((((((Big Hugs)))))))))))))))) - sending good vibes for your scans.

    Sue

  • doronet
    doronet Member Posts: 342
    edited October 2014

    OMGosh, Brenda!  So sorry you are having to go back in, but try not to think the worst.  As Sue said, it might not be anything and is best to double check than let something go. Let us know when your appt. is so we can send prayers and good vibes!  Prayers and good vibes next Thursday to you, too, Sue!

    Is so hard to believe that we are all looking at 5 years since diagnosis. Sometimes it seems like yesterday and sometimes it seems like an eternity ago.  Heaven forbid we get through an October without having to relive it with all the pink hype!!! :P  And major Props to all of you who can put the pics of your bald heads on facebook.  I could never stand to look at any pics of me that way, but that's just me. The main thing is that we all made it through!!  Am totally looking forward to April's 5 year survivorsary!!!!   Nette  :)

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited October 2014

    Thankyou Nette - I hate going but one must do as one's told.

     

  • Cafelovr
    Cafelovr Member Posts: 1,534
    edited October 2014

    I've lost count, but I've had around 70 Herceptin treatments and about 60 Zometa treatments. It never ends, it never gets easier, but it does get mundane. I'm still going strong. October 19 is my cancerversary for being diagnosed. My, how time flies. Not to be a downer, but I didn't think I'd be here 5 years out. I'm here...kicking Cancer's A$$ and taking names.

    I love you all so much. I don't know if I could have done this without my fearless warrior sisters!

    Brenda, our fearless fearless leader, you are always in my prayers. Everything will be good...

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited October 2014

    Linda - you are a miracle - I am so glad you are here all these years later.

    (((((((((((((HUGS))))))))))

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited October 2014

    HI girls ~ just popping in to say HI in the midst of PINKTOBER.  Our 5 year mark for so many.  Brenda any word on your mammography results???  Praying so hard it was just a false alarm.  

    Sue ~ sorry to hear about your knee but glad you are doing well

    Linda ~ you are a warrior !  So happy for you ~ you keep kicking cancers ass.

    Nettie ~ Pam !  Glad all is good.

    Hang tough girls, keep fighting the fight !!!

    :)

    All good here lots of medical testing and dr visits constantly.  But I'm still here cancer free as far as we can tell.

  • JustmeAlicia
    JustmeAlicia Member Posts: 1,529
    edited December 2014

    How is everyone doing? Thinking of you all as the holiday season is upon us. Wishing you all good health, love and peace xoxo

  • livelife
    livelife Member Posts: 38
    edited December 2014

    Hello form the UK.

    I disappeared off this fantastic link about 2 years ago when I was given an amazing opportunity to set up an Institute for Dementia, whilst having chemo etc for spread to my skin. Talk about if you want something doing ask a busy person.

    It is great to see you all on here.

    I get scan results tomorrow- so fortuitous that a link to Alicia's post popped into my inbox.  Something showed up on a rib a bone scan a couple of weeks ago. So now I have had a ct scan. I did fall skiing in February- maybe I broke a rib then???

    It's always a worry isn't it Brenda...

    Natalie xx

  • livelife
    livelife Member Posts: 38
    edited December 2014

    I got my CT scan results and all that was on there was the broken rib ( well there was a body there too.... but nothing else was wrong). Even the Dr was relieved- he was so keen to tell me he didn't even wait to sit down to tell me the news. He just came into the room and blurted out 'Your scan is fine !!!!!'

    Seems that three courses of radiotherapy plus three courses of chemo have made my right sided rib bones prone to fracture, even though I am on biphosphonates- I think they will always be weak. Must remember to fall on my left hand side in future.

    Wishing good health to you all at this Christmas time and for 2015. Always good to take it a year at a time


    Natalie x

  • Cafelovr
    Cafelovr Member Posts: 1,534
    edited January 2015


    Natalie, that is WONDERFUL news!!

  • livelife
    livelife Member Posts: 38
    edited January 2015

    Thanks Linda.


    I joined a committee of senior Doctors as the patient representative at my hospital this week. The project that they are working on is to set up a data base in England of women who had radiotherapy before they were 30 years old and therefore at risk of breast cancer (which is what happened to me). Is great to be able to make a difference, the plan is to make sure these women get access to screening so if they do start with breast cancer it will be detected earlier. Unlike me !!


    Is amazing to think that this special group of women are still in touch after 4 and a half years.

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