Hi, I am new to this site. Just seen this thread. I am 6 weeks post TCHP chemo. I had 6 cycles. Yes I found it tough - I struggled eating as my tastebuds went to the point that even sometimes water tasted bad. Also struggled with diahorrhea and fatigue. I lost 2 stone during my treatment and have put 1/2 stone back on now as I am eating relatively normally. As each cycle went on I found my down time grew. I did use the cold cap and had good results with it. I did have very thick hair to begin with and still have a full head of hair just thinner. You cannot tell to look at me that I have been through the treatment. I have sparce eyebrows and my eye lashes were ok but I have lost a few on the top row towards the end. Having said that its 6 weeks this week since I finished my chemo, taste buds came back pretty quick and I would say I am near as dam it back to normal. Eyebrows are growing as well. I have recently had my mastectomy on my right side and am due to have my 2nd of 12 herceptin injection next week. Good luck to everyone with their treatment. Looking back on mine, I found it very heard but you learn to cope. It doesn't last forever and it helped me to focus on that.
Hi
I'm just coming to the end of six sessions of TCHP (with Zoledronic Acid) .... we seem to be in the minority, don't we ..... and yes, I was also warned it is the pits in terms of chemo (by the oncologist). The layman thinks that all chemo is the same and I haven't found it helpful hearing about people living normally through their chemo, working, exercising .... different regimes do different things and TCHP is a toughie. My chemo nurse tells me this every time. I have felt daunted from time to time and not wanted to go on with chemo but I think we all feel that at times ..... it IS brutal. Loss of hair, dignity, sense of yourself, it asks a lot of us and our loved ones.
I am mid fifties and previously very fit and active and have found it hardest dealing with tiredness and chemo brain fog and being totally unable to concentrate on anything..... I had to stop work which was heatbreaking for me (I love my job) and it has felt like a long haul .... but I have been relentless in taking all the medication prescribed prior to and after each chemo cycle and I think this has helped with nausea and etc though some ladies have a rough ride. I have had a regular bout of ghastly diarrhoea for a day or two a week post chemo but this has been controllable by great drugs which were prescribed with the treatment. I had a very sore mouth which I was given mouthwash for - ask for it! Also lots of acid stomach which for I was prescribed Omaprazole which was fantastic - made a complete difference to painful swallowing (pain in gullet). I had an itchy sore skin/acne type reaction after the second cycle (very uncomfy) so the onco dialled down the Taxotere which really helped. One of the worst things is your taste buds go on strike so for a period everything tastes like soggy cardboard, it is foul! So it's hard to eat ..... I found crumpets with marmalade worked when I couldn't stomach anything else. It is really really odd when your favourite foods and things you crave taste utterly vile when you try them and it's a case of trial and error .... I love a good cup of tea but even that tasted funky which was upsetting as it is my comfort a big mug of strong tea..... but it does come back to normal after a week or so, I promise. I have only just developed a little bit of peripheral neuropathy (needles in feet and hands) but will tell onco before the final chemo so may have carboplatin or taxotere dialled down a bit again. I have sometimes been a bit breathless and always feel cold (lots of hotwater bottles)..... I am told often that effects are so individual ... I felt really pathetic as so many ladies seemed so capable through their chemo but different chemos also do different things. My nails are sore (finger and toes) and I have black big toenails which will come off and which I took care to keep clean so no infections. The hardest was the tiredness and not being able to do things, just flop in bed and around the house which I found mentally really difficult and has meant I have lost a lot of (my usual) confidence .... but ALL these things I am told are normal ... chemo messes with everything not just our bodies. Lots of people told me to binge watch TV and just enjoy the downtime but I really havent been able to do that; being at home without energy is hard for me but I am conscious that I have had an easy ride compared to some. Losing my hair and now my eyelashes has been very very hard - I didn't think I was a vain person but my long, thick hair and long black lashes were my sort of signature (I'm a 'natural' look lady, no make up as my hair and lashes I felt were enough to carry me through really) and was always told I looked young for my age .... I feel aged but am told it is only temporary (we are being poisoned after all) .. but I also have two wigs and lots of bandanas and have learnt to use eyeliner for the odd times I have to face the world and feel I need to feel more normal
......Hoping my honesty is okay ..... TCHP IS OKAY. Like my haematologist nephew says ..... chemo is horrid but cancer is horrider. And you are not alone .... we are all here doing this thing with you and holding your hand. I'm nearly there and I'm a wimp .... so you can do it 🙂 xxxx
I had TCH so your minus the perjeta. I was told that because the Herceptin can damage your heart they don't give you another drug known to damage your heart unless you are young - breast cancer needs harsher treatment the younger you are.
The "tax" side of the chemo is very tiring but it does not make you sick (as in throwing up). It is tough because all of your chemo is that rather than half of one type and then switching to another. You tend to cope better with that because the side effects are different - not better, not worse just different. Is it better to be tired but not feel sick? Or is it better to feel not too bad but you constantly have your head down the loo?
Make sure that you take claritin hay fever tablets everyday - if not you will get aches and pains from the g-csf injections and possibly the Herceptin.
Hi Cathysid - I'm from the May 2017 starters - I believe we have a lady in our group who is on your combo. May be worth puting your question on there. J
Hi Cath
I had TC chemo ( not the other 2) and I think compared to other ladies on here, it was abit easier, especially in terms of sickness. I only felt slight nausea at the start and was never sick. I did struggle with the fatigue, but I think that was partly me! Also, I had chemo every 3 weeks, but I think some are every 4. So you get through it quicker, but obviously there is less time to recover.
Best of luck!
Sue xx