Hello everyone.
I had BC with spread to lymph nodes 20 years ago. All been well until now and have secondaries in my lung and skin.
My memories of chemotherapy IV 20 years ago are not fond, and have been told this time I will have chemo tablets, and oestrogen surpressents.
How have your experiences been with chemo tablets? Are they given daily, weekly? monthly? I keep being advised that chemo tablets are a bit kinder than IV.
I'm seeing the oncologist next week again, but would like your real life experiences.
Many thanks x
Hiya, I have experienced both tablets and IV over the last 18 months and is ongoing. I had the tablets first, Taken twice a day and a lot of them, When they stopped working, I have since moved onto IV. For me, the side effects on tablets and IV were minimal as such, although with both, they do get worse as you go on. I try and put things in perspective, ie the side effects against the benefits and feel it is well worth the cost. I was told that IV has progressed a lot in the last few years and also told that it gives you a stronger dose of Chemo, as my cancer is very aggressive, this is what I needed, it may be different for you. Tiredness, dry skin, sicky stomach were common for me but I did find a little exercise each day, a short walk etc, helped loads. Sometimes I get a rash and bone ache, and I have lost quite a lot of sensation in both hands and feet. Different chemo, you have to remember, has different side effects too. Trust your Oncologist and wishing you the best
Hi @surrey lady
Similar to Vapeman - I've had both recently. I started with capecitabine oral chemo. Daily twice a day, 6 tablets twice a day. Fir some reason second cycle I kept forgetting the evening tablets straight after dinner.
Oral chemo fir me was a walk in the park. Could carry on WFH, no side effects to speak of. The capecitabine didnt work for me so I am now on IV chemo which has more side effects for me.
Good luck - I hope the tablets go well for you x
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