Triple Negative Breast Cancer
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Sorry to hear of your diagnosis. I was also diagnosed with triple neg breast cancer in July. I had two mass in my right breast . My oncologist started me on chemo in Sept and discussed my options with surgery. I decided to have a double mastectomy , which I had at the end of April. I am now cancer free. I pray all goes well for you and you can get this over with and move on with life
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I have been diagnosed with triple neg breast cancer. The dr told me I will have to undergo 6 months of chemo. It was not brought up about the genetic tests. Does the Oncologist order those and are those blood tests? The dr has not talked about using Keytruda, will the Oncologist make that determination?
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My Dr sent me for genetic testing. She was also the one who decided what different types of chemo for me. I had 3 months of 3 mixtures of chemo and then another 3 months of a different mixture of chemo. I was on keytruda but had problems with it and had to stop it. Prayers and best of luck to you. Stay strong
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Hello Lettie,
Thank you for you response. How are you doing now? Did you get a port put in for the chemo? I pray you are getting close to being cancer free.
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Oh I am so happy to hear you are cancer free!!! Thank you for your story, it gives me hop that all will go well with me.❤️
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Yay, RPStumpf! It's a good feeling to have only 3 left. I had those same side effects with my legs. It seemed like it got worse as time went on, with the final treatment being the most painful. I wore knee-high compression socks while I slept, and they helped a little bit. I also had some of the fatigue. And yes, your doctor is totally right. The leg pain goes away. Mine did after about a month. Fatigue can last a bit longer, but it's hard to tell if it's from the Keytruda or just the general trauma of aaaalll of this long process. I started feeling more normal about 3 months out. So you have plenty to look forward to! Here's to kicking cancer to the curb!
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When the dr first told me my diagnosis and I started reading of the prognosis, I was very afraid. But, since being in this forum you ladies have given me the courage to expect a life after cancer.❤️
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I will be posting my progress with the forum. I go Thursday to get my port.
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Thank you for that encouragement!! I so appreciate hearing that my experience is not unique, and that there is a light at the end of the tunnel! This forum has been really helpful. We need to have reminders that there can be life after cancer, and shared experiences are a little easier to bear. Blessings to you all!
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The port has been wonderful for me. I have a hard time with blood draws normally. Several pokes, fishing around, etc. You get the idea! But with the port, I can go in and have them access it, draw blood for labs, and then do the infusion. Accessing it is not very painful at all, although I have them give me a lidocaine shot just in case. :-) It's a little unsettling to have it in, this odd thing, poking up out of your skin a little bit, but oh boy, it is worth it.
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I had triple negative as well. I agree with everyone. Positive energy and people will definitely help you through the process. Also if you have a daughter tell her so that she can get tested when it is time. I didn't have the gene but my biological mom had it as well. I am here for any thoughts you might have about this journey.
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