Trodelvy - any info to share?
Hi, I am reaching out to see if anyone else has commenced Trodelvy chemotherapy and if yes, what are your side effects experiences. I am only in 1st cycle, 2 weeks on/1 week off. Main reaction has been some insomnia and bad fatigue. Wondering about hair loss and at what stage, if anyone has experienced this? Does fatigue get worse? Any other lurking side effects to be aware of?
New member - Question re oral chemotherapy capecitabine
Original post created by member @Brondocs - moved to Metastatic breast cancer discussions Hello, I am a new member and appreciate so much hearing everyone’s stories. In May 2018, I was at work and as I brushed some fluff off my shirt I felt a golf ball sized lump on my chest. This turned out to be triple negative breast cancer and the lump had literally popped up overnight. I know this because I am small breasted and would have noticed if it had been there before. Within two weeks I was in surgery for a lumpectomy which was the easiest part of the whole process. The cancer had not spread to my lymph glands so I felt lucky. I then started 6 months of chemo. For the first four months of the heavy going chemo I was sicker than I ever imagined from the side effects. I ended up staying in hospital each time. But after that, when I went to once a week lighter chemo, I was managing pretty well. I was also part of an exercise physio research program which really helped me feel as If I had one thing to help me through. Then I had a month of radiotherapy – which was fine. THEN I had two years of great health until February this year when I developed a recurrent cough. I thought it was some sort of asthma, so I went to my GP who send me for a chest Xray. I was completely shocked to find out I had metastatic cancer all through my lungs, in my brain and in my neck. I had a week’s radiotherapy on my brain which had horrible side effects ( nausea, headaches, hair loss) combined with starting the heavy going chemo for the next 6 months. Again, I had terrible side effects – mainly trouble breathing, dizziness, exhaustion and clotting in my arms for the first four months, so spend more time back in hospital. My oncologist has moved me now onto an oral chemotherapy- capecitabine. I was wondering if anyone else was taking this and if the exhaustion from the 6 months of strong chemo infusions will dissipate or persist ? I haven’t had any additional side effects so far. My insomnia is also persisting and quite a few of the other side effects from the infusions. Any advice or info much appreciated !
Mum's first chemo session
Hi, my mum will be having her first ever chemo session early next week. The oncologist will treat her with Paclitaxel and treatment will be once a week for 4 weeks followed by 1 week break each cycle. I would appreciate any tips on how to prepare mum before treatment and what do do after treatment to minimise side effects as much as possible. Mum is 82yo and it worries me how she will cope. Thank you.
