Calling all TNs

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  • rdeesides
    rdeesides Member Posts: 459
    edited April 2018

    I’m so sorry. It sucks to not be done when you thought you would be. It’s a shock to the system. It’s great that your doctor is being so proactive though! That can give you some measure of confidence in your care at least. Hugs. Once your mind is able to wrap itself around this news you will hunker down and get it done, just like you did with chemo.

    Rebekah

  • PaulaAtlantaGA
    PaulaAtlantaGA Member Posts: 99
    edited April 2018

    Thank you, Rebekah.

    I'm fortunate to be able to talk to friends who have helped me, including you!

  • Hats2
    Hats2 Member Posts: 7
    edited April 2018

    Thank you aterry for the advice. I finally have the planning session scheduled and my radiation onc has assured  me that 90% of their patients receive 3-D and not IMRT. The denial was an insurance error. I thought perhaps the aggressive nature of TN was a reason for the more precise radiation. My team has been wonderful in coordinating my treatment. They reassured me that starting radiation within 12 weeks of surgery is meeting the standards.

    PaulaAtlanta I'm sorry you received disappointing news. I didn't have a pCR either and completely understand the let down when it seemed the tumor responded. I have heard of a genome study that uses the tumor genes to match to known chemo agents. It may still be enrolling. The bummer is exactly as you said, months of more chemo. Wishing sunshine to come your way.

  • Beckham2
    Beckham2 Member Posts: 17
    edited April 2018

    Hello, all! I was diagnosed in December 2017. I've mostly lurked here but I did reach out to others with multifocal. I'm currently doing weekly Taxol with Carboplatin every third week. My last Taxol was delayed due to low counts. MO says now we will do Carbo weekly so it's more tolerable. This scares me a little. I just want to get my treatments on time. I did fine with AC and mammogram and MRI showed significant decrease. You ladies have been such a wealth of information and source of hope. Thank you all for sharing your experiences.

  • ALHusband
    ALHusband Member Posts: 344
    edited April 2018

    Hello Ladies and A Gentleman Or Two,

    I am proud to announce that this coming Sunday, April 8, 2018 my absolutely amazing rockstar of a beautiful wife will celebrate her 5 years from diagnosis milestone! I am so proud of her, as this was her second battle with the monster. The first was an unrelated lymphoma 17 years prior to her TNBC. Thanks to God, this forum, this website and everyone, new and "experienced", that has been so supportive, informative and inspirational over the past 5 years! What a blessing breastcancer.org has been.

    That said, all of you newly diagnosed ladies, there IS a light at the end of the tunnel! It DOES get better and you WILL see this milestone as well! Keep the faith!

    Love to all,

    Mike

  • rdeesides
    rdeesides Member Posts: 459
    edited April 2018

    Beckham2, I had weekly Carboplatin and it was no big deal. Hopefully it will be the same for you.

    Mike, I’m so happy for you and your wife and this gives me hope too. Congratulations!


  • AgathaNYC
    AgathaNYC Member Posts: 473
    edited April 2018

    Mike,

    Thank you for sharing your wife's anniversary with us. It's so encouraging. Enjoy the 8th - hope you both do something memorable.

    I'm not sure when to start counting towards my anniversary: my diagnosis, end of chemo or when I got my pCR result after surgery. Or maybe when I finish radiation?

  • rdeesides
    rdeesides Member Posts: 459
    edited April 2018

    AgathaNYC - I think the most common way is to count from date of diagnosis

  • anotherNYCGirl
    anotherNYCGirl Member Posts: 1,033
    edited April 2018

    Mike, - Thank you for posting! All best wishes and hugs to you and your wife!!

    Welcome Beckham! You have joined a wonderful group. This board of friends has been my comfort/ support group since I was lucky enough to find it!

    As always, I send hugs and BE WELL wishes to all here!

  • VLH
    VLH Member Posts: 1,258
    edited April 2018

    Hi, Charmell,

    I know you're scared. I'm sorry that you find yourself here, but am glad you've found a group that understands what you're going through. My Ki-67 was 90% and my tumor 2.2 cm so larger than yours. I initially found my lump nearly two years ago and, fortunately, have no evidence of disease so far. I hope you'll be sharing a similar report two years from now. 🙂

    Mike, fabulous news about your wife!

    Lyn

  • JAN69
    JAN69 Member Posts: 947
    edited April 2018

    Mike, Hugs to you and wife. So wonderful. Jan

  • Valstim52
    Valstim52 Member Posts: 1,324
    edited April 2018

    Mike hugs to you and your wife. Thanks for being a source of hope. To all in treatment, newbies, lurkers there is hope. Stay close and vent as needed. As you can see from my signature I am 2.5 years from a nasty IBC/IDC dx.

    I’ve had my challenges post treatment. Especially lymph edema, and radiation issues. The forums have been such a source of help.

    Most don’t achieve PCR, and still are here many years later. Same with treatments. 2.5 years ago MD Anderson told me Xeloda was a stage 4 line of defense. Only extreme cases would a lesser stage get it. Now it is given after surgery. Hopefully more good things will come. MD was my second opion


    This is a club no one wants to join, but once in you never leave.


    Val

  • ALHusband
    ALHusband Member Posts: 344
    edited April 2018

    AgathaNYC. Who cares? Celebrations are fun! Celebrate ALL OF THEM!

  • AgathaNYC
    AgathaNYC Member Posts: 473
    edited April 2018

    Mike - I so appreciate your attitude!

    I'm not going to pick my diagnosis. It was Sept. 11 of last year whenI got "the" call while I was at work in the (new) World Trade Center. Needless to say it was a crappy day all around. I'll celebrate all the others with pleasure.

  • LoveMyVizsla
    LoveMyVizsla Member Posts: 813
    edited April 2018

    Where’s that “Like” button, Mike? Congrats to you and your wife.

    Had PT again today for my breast lymphedema. She has been using a steel tool and a cold laser on my scars, and a physio-touch suction machine and manual lymphatic drainage her hands). It has gotten much better, but it takes a while. She also taped me with kinesio tape, 7 ways to Sunday.

    Welcome, and sorry to the new members.

  • VL22
    VL22 Member Posts: 851
    edited April 2018

    Just checking in - at exactly 100 days post chemo I really started to feel like myself. Because of also having an Er+ tumor I am on Tamoxifen, but so far so good.

    So now it’s just living - no appointments until June. It is strange and scary and exciting all together. I’m thankful and fearful all at once. Most of the time I’m calm and happy. But I won’t deny that I can let my mind wander and worry, which is a waste of time. Key for me is not to read anything about TN - most information is still presented in such a dismal fashion.

    So I’ve planned 2 great summer vacations, Busch Gardens/Williamsburg in the RV and Glacier National Park, and we’ve started college visits with our older son, who will be a senior next year.

    Life is sweet and I’m thankful.

    Please give updates!!

    Congrats to all who are staying healthy


  • helenlouise
    helenlouise Member Posts: 420
    edited April 2018

    Congratulations VL22.

    I am surprised by the tamoxifen considering your last dx was TN but anything that can help beat this is something we should do. I have heard the tamoxifen can play havoc but being able to continue with precautionary measures is good.

    I'm still doing the chemotherapy, so a long way to go. if the response is positive the plan is mastectomy then radiation. I can't imagine being at the end of treatment just yet. Still trying to get my head around the rest of the chemo, surgery, stay positive and realistic.

    I too plan to holiday as soon as possible. Very pleased to hear you are battling the negative thoughts and life is sweet. Travel safely and enjoy. It is good to get updates from the other side. Thank you.
  • VL22
    VL22 Member Posts: 851
    edited April 2018

    I was surprised about the Tamoxifen too. But I had three tumors - 2 of which were strongly ER+. I had micromet in an intramammary node right next to one of the ER+ tumors, so the thought was take the hormonal as a precaution. I truly hesitated, but I figured I should take it and see how I handle it.

    Redeesides - any word on Xeloda?



  • DiV
    DiV Member Posts: 231
    edited April 2018

    Hi all! So sorry I haven't posted lately. I've been posting on another thread. I've also taken time off the site. I wanted to forget about cancer for awhile. Now for the bad news. I wound up in the ER a week ago Saturday with severe pains on right side. They took x-rays and found a walnut sized mass in right lung. Saw oncologist and had ct scan. Mass undetermined. Saw pulmonologist yesterday. He believes it is breast cancer that metastasized to lung. I go for biopsy tomorrow at 10am. It just never ends for me.

  • jenjenl
    jenjenl Member Posts: 948
    edited April 2018

    Over the last few weeks I've observed an increase in pain on the right side. Below the ribs and to the right of the belly button. I have this pain/pull feeling, sometimes sharp. It's inconsistent but present. It's heighted when I bend down (ie to tie a shoe it hurts) but doesn't hurt if I push on it sitting or standing.


    I have an appt with onc on Monday but coming here to learn more about what the pain feels like if it has metastasized to the liver.

    This is a very different pain then I've experienced in the past. I had a scan January last year and it said:

    Gallbladder, Pancreas, bladder, Liver and spleen unremarkable. Lung bases are clear. Clips are seen in abdomen. Small umbilical hernia is seen containing only fat, with no inflammation.

  • jenjenl
    jenjenl Member Posts: 948
    edited April 2018

    DiV. Damn it 😠. Happy you went to get it checked and are proactive. Hate you need to do a biopsy and really hope it's not cancer. Ugh. Keep us posted!!

  • Whirlaway
    Whirlaway Member Posts: 64
    edited April 2018

    Div, I followed your 'journey' last year. I was so impressed with your courage and strong will to beat this shitty disease and now this is happening:(  Can't you ever catch a break?! I am so sorry you have to go through this again!!  I am so hoping that doc. are wrong and biopsy will be benign against all odds. What a horrible card you have been dealt! You will be in my thoughts! You have an amazing spirit to fight!! 

  • anotherNYCGirl
    anotherNYCGirl Member Posts: 1,033
    edited April 2018

    Div, - Hoping you get B9 results!!

    Jen, - Maybe it is a gas pocket??

  • rdeesides
    rdeesides Member Posts: 459
    edited April 2018

    Div - This sucks. God, I hate cancer.

    Jen - Hoping this is something else. Please let us know.

    VL22 - Xeloda is a GO. Just got my pills today, but don't start for a few weeks. I'm still doing radiation until the end of this week and then I will take a few weeks off before starting Madame X. I also have a 3rd opinion with a research doctor. Hoping to get some insight as to whether an immunology trial would be worthwhile. I don't 'think' it would as I am PD1/PDL1 negative, but I have been reading some things that make me think there may be a small chance it's still worth it. So I will talk with this guy and let you know what I find out!

    For everyone that is battling this every day, I pray that researchers come up with something soon. I feel like they are getting so close to some major breakthroughs. I pray that they have clarity and speed to help all of us.

    Rebekah

  • Valstim52
    Valstim52 Member Posts: 1,324
    edited April 2018

    Div you are in my thoughts and prayers. Sending virtual support however you need it. Please keep us posted

    Va

  • LoveMyVizsla
    LoveMyVizsla Member Posts: 813
    edited April 2018

    ((DiV)). I hope that doc is wrong. Please let us know as soon as you know.

    Jen, what kind of surgery did you have where the abdominal clips are, and how long ago?

  • helenlouise
    helenlouise Member Posts: 420
    edited April 2018

    Hoping the best for those of you, Div and Jen, waiting results!

    Has anyone doing neo adjuvant chemotherapy 'felt' any change in the size of their tumour/s? Mine is definitely still there. I will have a restaging scan prior to starting Docetaxel on 30/04.

    Very interested in the Xeloda and any info on the immunotherapy Rebeka, please.
  • jenjenl
    jenjenl Member Posts: 948
    edited April 2018

    DIEP flap 4 yrs ago

  • VL22
    VL22 Member Posts: 851
    edited April 2018

    Div - you are in my thoughts.

    Jenjenl - it could be a strained muscle. I’ve gotten that in that area. Good luck Monday.

    R - so glad you’re getting started. Yes, keep us updated about the trial

  • Batesburg
    Batesburg Member Posts: 199
    edited April 2018

    Div, I am so sorry to hear of more challenges for you. We have GOT to get at the bottom of this cancer epidemic. There is so much money being thrown at it- I know its complicated stuff- but, come on......

    Jenjeni- I had pain in that similar area after treatment was over. It eventually went away when I stopped thinking about it. I think we can guard ourselves and make ourselves sore in areas that we focus on......there are many layers of muscle in our abdomens and easy to strain/pull than we sometimes think. Have you done any different kinds of exercise/other?

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