No chemo for me.

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Comments

  • MomoB
    MomoB Member Posts: 68
    edited October 2009

    Thanks, Nan and Sunris.  I'll check it out!

  • MsBliss
    MsBliss Member Posts: 536
    edited October 2009

    Hi Sunris!

    Back at 'cha!

    Good to see you too!

  • MsBliss
    MsBliss Member Posts: 536
    edited October 2009

    Nan,

    Absolutely count on me to go to TNBC daily if I can....I learn so much at TNBC.

    Hugs and more,

    MsBliss

  • gardenbeetle
    gardenbeetle Member Posts: 12
    edited November 2009

    Returning to the original 'no chemo' topic, I found an interesting piece of research. It's main objective was to determine the minimum % benefits that patients need to find chemotherapy acceptable, and to explore potential preference determinants.

    The most interesting thing for me was the finding that almost 40% of the participants undergoing chemotherapy said that they would have accepted chemotherapy even if it had NO clinical benefit, ie 0% benefit! Have to say this doesn't really surprise - I've seen many conversations on forums where a patient's oncologist has not recommended chemo, but the patient argues for it. 

    You can download the full paper here: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363690/

     

  • margarita88683
    margarita88683 Member Posts: 3
    edited November 2009

    Hi,

    My name is rita i was diagnosed in April of this year . I have been doing alternative treatments i am triple negative too. Just found malignant lump under my armpit which is only 1/3 malignant having surgery monday the 16th to remove it. Right and Left breast ok through MRI but it said metastatic adenopathy for the armpit. I am stage 2, grade 3 what else are you doing as far as alternative medicine maybe i need more. I was looking into IPT chemo but very pricey with less side effects may need it now since it says metastatic not sure. seeing oncologist in 2 wks to see what he recommends i really only been following with a MD where i go for my IV's. I had 2 opinions back in april and they both said chemo but i chose not to do it. Now i am scared because of this lump hope i made right decision help.

    ritapmc1@verizon.net

    ER PR- Her - stage 2 grade 3

  • Titan
    Titan Member Posts: 2,956
    edited November 2009

    Hey Rita...it's sooo hard to make the "right" decision..you just never know and have to do what is right for YOU..however, please listen to your doctors..PLEASE!  I did dd chemo...and I'm OK..for now...there is no way I would not have done it..but that was my decision..only....

    I don't know how old you are, or if you have any other health issues...but chemo was not that bad...wasn't fun..but definitely doable..maybe consider giving it a try....?

    Hugs to you...everything is so darn scary....continue with the holiistic treatments too...

    Let's us know..we are here for you..no matter what you choose...

  • MsBliss
    MsBliss Member Posts: 536
    edited November 2009

    What kind of IV's have you been getting?

  • MsBliss
    MsBliss Member Posts: 536
    edited November 2009

    As far as alternative med, what therapies have you been doing? 

    Have you been doing any of the following:

    curcumin  coq10  loxin 5  mega vitamin D  vitamin A  modified citrus pectin  avemar   coriolus

    LDN indole 3 high plant/green/colorful foods  flax and fish oil

  • Titan
    Titan Member Posts: 2,956
    edited November 2009

    MsBliss..did chemo/rads..but still take the vitamins..Vitamin D 3...Vit. D., calcium, fish oil, drink green tea, eat lots of veggies, limit the meat   I like combining the foods./vitamins with the chemo/rads...I figure..the best of both worlds...at least I hope!

  • cookiegal
    cookiegal Member Posts: 3,296
    edited November 2009

    Hey I'm not a tripple neg, but I appreciate what all of you are saying. I always thought I would not do chemo given a choice, but now I am wavering. I wish all of you the very best of luck and health!!!

  • clicrowley
    clicrowley Member Posts: 1
    edited December 2009

    For the time being I decided no chemo only radiation. I believe this was the best decision for me and feel great about it.                                                                                                            I never believed cancer would strick me but it did, at 32. I excersiced 4-6 days a week, eat  healthy, and just make green choice for my family and home

     I  found my own lump, I was told the lump was likely a cyst because of my dense fibro cystic breast tissue, until pathology report came back. Now I tell everybody to check there breast and to follow there gut, doctors can be wrong.

  • JenXX
    JenXX Member Posts: 32
    edited December 2009

    I'm glad I found this threat - it gives me hope.

    I had a miserable response to my first TC, so the onco reduced the taxotere by 25%.  2nd and 3rd tx were okay, but the 4th one I had last week was worse than death.  I have bleeding sores, 1 week + of extreme nausea, I have blood clots, am anemic with low potassium, my chest port hurts, and it goes on and on.  I am worried also about the long term implications on my health from the chemo.  I have only 2 treatments left but think it might be best to just consider it "done" now - that 67% completion, which I think is enough.

    I am interested in focusing on the healthy lifestyle protocols going forward, that people have mentioned in this thread.  I truly believe that me gaining 70 pounds led to a cycle of unhealthiness in my body in which cancer flourished.

  • worldwatcher
    worldwatcher Member Posts: 205
    edited July 2010

    Hi dsgirl.

    I'm new to the forum and happened across your earlier post regarding "I happened to have a reaction to the blue dye, lots of hive bumps at the injection site, over and over, they come and they go, even now 7 months later, ugh, Later I found out there is sulfa in the solution which I have an allergy to."

    I just wanted to thank you for posting this. I have surgery scheduled for July 16, lump and SNB and have a severe sulfa allergy. This gives me a chance to alert all the medical team concerned with the SNB.  I have found that sulfa is a sneaky little bugger, hiding out in the compounding of quite a few drugs including diuretics.

    I have pretty severe SE problems with just about everything especially sulfa and am  leaning towards no chemo, and leery of the rads and the Herceptin. Waiting until the post-lump path results come back to decide what if anything further to do.

    I know that my allergy is probably in my records, but mistakes happen. This will enable me to pester everyone concerned with the dye about this situation.

    Thanks for the warning.

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