Hi, I’ve recently been diagnosed with tnbc and had ct scan and full body bone scan which shows no spread. Then I had to have a pet scan. Has anyone else had to have this after other scans were clear.
thank you.
I’ve just read your thread. Sorry to butt in. But your humour is great and that’s how I was when I was diagnosed June 2023 with a 3cm and two positive nodes. I didn’t lose my hair as I used the cold cap. I had the same treatment. Pembro, carbo and paclitaxol then EC. It’s a journey but honestly I kept going and kept my humour so kept positive. You will get there.
Brilliant thread!! Good luck you amazing girls!! You’ll be through it soon
What a lovely thing to say ️ Thanks so much c22 xx
I did. I had a lumpectomy and then radiation. Now on capecitabine. It’s a long road. Now back at work. I took ten months off work. I had neuropathy quite bad but now that has gone away and I feel ok. Not fully back to normal. It’s kinda harder when it’s over as you feel you are on your own a bit. When you are in the middle of chemo you just zone in on that. Week by week you get through it. A t almost feel surreal at times.
You're a soldier!! Give yourself a minute... You are doing ridiculously well. ️You've gone through all of that (successfully!) gone back to work and shook off neuropathy (which I can imagine is a bloomin nightmare, lots of people struggle with that) you will get there with the other bits, this is still pretty new for you! What a legend! You keep going girl and be kind to yourself you are absolutely crushing it, even if sometimes the little demon in your head tells you otherwise ️ xx
Capecitabine is ok. Feel tired on it but nothing like IV chemo. But when I was on chemo I carried on as normal. I have four kids and just kept going. Got the tube to Guys hospital in London and back every week.
In the beginning I was like a rabbit in the headlights! I didn’t even come onot these forums. Now I want to help others if I can. I would say to stay off the internet. You end up going mad.
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