Questions for all, PLEASE help
1.) Is there any of you who did or considered any natural treatments (ex:ozone treatments)??
2.) What have been the worst side effects of chemo and rads?
3.) I've heard that organs can shut down or be damaged and then you have to deal with more health problems. How true is this?
Thanks again Ladies for all your help!!
Comments
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Hi there
I did chemo, no radiation. I dont think my side effects have been to horrible. I would have to say the worst for me is the sinus issues I have right now.
I had adriamycin which can cause issues with your hear....but the really important word is "could" not would but could.
I looked at it this way, the odds of having no treatment and my cancer returning was huge. The odds of me having long term damage or problems due to chemo is low. It could happen but I want to live and for me the risk was without a doubt worth it.
Teresa
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Hi tooandrea
I was diagnosed with breast cancer earlier this year. I was given 5 doses of radiation and have had no chemo.
But what I have done is IV Vitamin C, High dose Melatonin, Curcumin, Biotin, Quercetin, Calcium and Esther C. All these things are natural products, at my last scan in July there showed no new cancer and I had signs of healing at the tumor site.
So in my opinion I think that the natural products are helping my body fight this damm thing by helping my immune system.
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I choose not to do chemo and so far (one year later) I am doing just fine. You will find that the majority of people with triple negative do have chemo and it is very difficult to find support for this decision. I feel like I am all alone so anytime I read about a person not having chemo and coming out AOK, I copy it and read it whenever I feel down in the dumps. Whatever your decision, go for it, accept it and I wish you all the best and good luck.
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Malady, WOW really right-on ! I didn't think that I would find someone that decided to not have chemo with such a similar Dx as I. It looks like everyone just goes with the flow. Can I ask you some more questions? If they are too personal for here and you will still answer them you can email me at tooandrea@aol.com, thanks.
May I ask how old are you?
Have you had children, if so did you breast feed?
Did you change your life style at all (ex: eat better, take vitamins, etc..)?
What made you decide not to do chemo?
Did you do rads?
What tests do you do regularly to keep an eye on it?
Have you ever done PET scan?
I think that's it, for now.
Thanks, Angel
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Beastybabe,
Is that treatment I can do here in the USA too? I was going to go get a second opinion from a doctor that uses natural and western medicine together soon. I am just trying to cover all bases if I decide to give in and do chemo and/or rads. What side effects did you have from rads? Will you answer any of the questions that I asked Malady (above)? My doctor just told me my insurance wont cover the PET scan I wanted because I only have Stage 1 Cancer. Trying to get a big picture here.
Thanks, Angel
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I chose to go lumpectomy, chemo and rads. The reason I chose this route is that I wanted them to kick butt on this dang cancer thing. The grade 3 and triple negative are strikes against us -- it is an aggressive cancer. But, I am stage 2a .... and you are stage 1 .... it may make the difference for you that I did not have .... we all have to live with our decisions .... make them and then don't look back on the maybes.
My chemo was Cytoxan/Taxotere, 4 rounds and then 33 rads .... for me the chemo was hard but I made it through and so were the rads. I feel good overall now that it is 5 months later ... the only problems that I am having now is tennis elbow, pain in my boob ... I have a cyst/seroma and a mass. Next week I will have an MRI that will tell the doc if this mass is cancer again or just scar tissue (it is really, really big) and she has some tricks in her bag to help heal the breat tissue that has a cyst/seroma. I am praying that this mass is not a malignancy.
I am 54, breast one child 4 months,
I applaud your thinking out your options!! I will keep you in my prayers tooandrea.
Blessings,
K
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Hi tooandrea
I would assume that because we have it here in New Zealand that you guys in the States would have it, (Vitamin C IV), you will just need to find a clinic that offers it.
As for the rads, unfortunately I did have a reaction to the rads, although I only had 5 doses, I had an almost instant reaction, nausea, vomiting when I tried to eat, headaches and really tired alot of the time.
Im 38, I have one son that I breast feed until he was 8months old. As you know I take a range of vitamins to help keep my body strong to fight this dam thing, I also try to eat fresh veges and fruit. I would like to eat only organic food but it is quite expensive here so I get organic milk, butter and cereal.
I see my oncologist every three months and have a CT scan every 4 months, and Im sure that once this last one is shown to be clear that my check ups will go to every 6 months.
I dont think Ive ever had a PET scan, unless they call it something different here. When I was first diagnosed with it in my spine, I had a range of X-rays, like, normal xrays, bone scan, mri and CT scan.
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Hi Andrea.
I just sent you an e-mail and if you don't get it, let me know.
I am 67 and turned the chemo down as I did my own research (my Oncologist at the time) did not explain anything to me. I decided to not take the chance of having chemo kill off all the good cells and possibly do nothing for me if there were no cancer cells to begin with. I have very little support for this decision but feel I am a strong person and happy to live with my decision. I am very positive and have gone one year so far. Make your own decision and then live with it. All the best.
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The idea of doing chemo freaked me out more than actually having it. I am also TN and felt that my risks of reoccurrence were just to high to not have it. I was so anxious but I do not regret having the chemo at all. I had a really difficult time with chemo because I had allergic reactions to the drugs and had really low blood pressure, but it was treatable. The hardest part was losing my hair and temporarily going into menopause. I was able to do egg harvesting prior to starting chemo as I have not met Mr. Right yet and was in my late thirties. The best part for me was knowing that I did everything I could possibly do to prevent this from coming back. I am about 7 months post and the only problem I still have is some joint pain but it is manageable. It started about 1-2 months after and has seemed to moved around different joints. I did not have radiation as I made the choice to have a mastectomy post chemo (I started with a lumpectomy). I have friends that had the same chemo as me without any problems at all. Everyone is different.You have to do what you feel is best for you. Gather as much information you can get and make an informed decision. Have you thought about asking for an MRI? I was not able to get a PET scan either but my breast surgeon did order the MRI for me. I would encourage you to ask for a second opinion and ask for the oncologist to go through the Adjuvant online with you to give your risk percentages, if you do and do not do chemo. I found it was really helpful. My oncologist also talked about chemo as an insurance policy. I am happy to answer anymore specific questions, just PM me anytime.
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I chose to have a mastectomy and chemo, the other option was lumpectomy, chemo, and rads. The worst side effect was nausea, tiredness, and for me diarrhea, most have consipation. Have not regretted my decision. They give you a muga test to see if your heart is strong enough. To save your life it is doable. I hope for the best for you. Please keep in touch with the women here who can guide you through the process. gentle hugs sherry
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I am so sorry ladies for not replying to the questions you answered for me.Thank you very much they were helpful. My mom has been in and out of the hospital for the past month and I was trying to work while dealing with that then I had jury duty and now I will have training for work, and applying for a (promotion) job with a lot of questions to answer and some doctors appts. The information I get from the drs, I would love to get all of your opinions on it.
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