Palbociclib-anti cancer drug effects
Hi Ladies Just wondering if anyone is on both Letrozole and Palbociclib, I am about to start the Palbo and hope I can tolerate it so I can go back to work. I am 61 and have stage 2 inoperable cancer at the moment and the oncologist wants to try and shrink it over the next 6 months. I am worried about the nausea and fatiique and as I work in primary schools walking and talking a lot, feel stressed just thinking about it, but really need the income to fund all these private treatments and meds.
Post chemo / zoladex & letrazole side effects (hoping for some hope - please!)
Hello ladies, I finished 6 months of chemo (doxy then paclitaxcel) recently and then started on zoladex and letrazole last week. I am feeling VERY anxious all the time, very tired and flat - not like "myself" at all and really pretty non-functional. I can barely make a cup of tea and seem to just stare at walls when I'm home alone (often). I managed surgery and 6 months of chemo basically alone and unsupported and I coped. Now that I'm closer to family I seem to have really mentally crashed. Motivation is zero and the smallest things are an effort. I was more functional than this DURING chemo... Is this normal post chemo? A crash? Or is it the new hormone suppressants? Will it pass? Can anyone PLEASE offer me any words of wisdom or hope around recovering from chemo and the adjustment times to the hormone suppressants? Wishing you all so well. SDM.
Chronic fatigue on Tamoxifen
Hi all, l am a year out from finishing chemo and almost a year after a double mastectomy. I am still experiencing chronic fatigue and am now certain it's from Tamoxifen, as l have changed the time of day, l am taking it and the fatigue has moved from the afternoon to morning. I am considering changing it to the morning and maybe the fatigue will be while l am sleeping. Has anyone experienced this and have any advice? I would really appreciate it, l want to improve my quality of life!!!
Pain after breast cancer
I am almost 2 years post breast cancer diagnosis and omg the bone pain is horrendous. I’m currently on Letrozole, Gabapentine, vitamin D and calcium my pain is 24/7 from my feet to my head and I’ve had a continuous pain in the middle of my back. I have an appointment to see a rheumatologist this week… but omg I just need some relief from it….I have looked in to medicinal cannabis what are everyone’s thoughts pleasefatigue will it ever end
I have completed my Doxorubicin and Cyclophasphamide (8 weeks of fortnightly treatment) and after the last "top up" i was super fatigued, could only last 2 hrs before eyesight goes and i have to lye down. They said this was normal after the last one and it will go away .... it has been 4 weeks now and no change. I have Hashimotos ( underactive thyroid ) so i was wondering if anyone else has not recovered with their fatigue or has anyone else also got hashimotos and what effect did the chemo have on your medds ThanksMemory
For some as a result of diagnosis and treatment the effect on our memory can be distressing - fatigue or chemo induced or anything else in between, stress, anxiety, menopause! I have a sister who has early onset Dementia and on the road to diagnosis she was seen by a health professional, Neuro Psychologist. She has written a book and there's a precis of it here that some may find interesting or useful to someone you know Memory-wise - Dr Anne Unkenstein -- Allen & Unwin - 9781760296384 - Allen & Unwin - Australia (allenandunwin.com) Best wishes to allanother delay, sad and mad and very disappointed
Hi, I've had a disappointing week and I thought I would drop in with all you wonderful people and unload (sorry it feels like going down not up lately) I'm about 4 weeks into my 2nd time round, I had the lumpectomy in 2020 and now I'm ready for double mastectomy and not considering reconstruction. Had surgery booked for Friday 1st and I had a recent UTI but Thursday afternoon had the details and what was required then an hour later it was cancelled , I was so broken about that for a couple of days and just started to settle and now I am covid positive. When the test showed positive I just shut down don't really feel anything. I'm lost at the moment wondering what's next.. thank you all for being here, for your time and thoughts!!Tired after Paclitaxel Chemo completed. ( EC prior)
After getting through all of my Chemo quite well. I find myself more tired than during most of the Chemo. The tiredness started during a last two weeks of Chemo. I was told it could be an accumulative effect of the Chemo. Has anyone else become more tired at the end? I probably need to get fit. But my thighs don't have much strength, and my knees are weak too. Has anyone done rehabilitation after Chemo?
Last ac cancelled
What a journey so far !!!! I have had 3 ac and I am so terribly sick. Just about passed out in oncologist's surgery, he is quite worried about me. my body cannot handle any more of this ac so hoping the 3 I have had will do the job !!!!!!Have to see him again this week to see when I am going to start the 12 x weekly palax ones. Has anybody else had this happen. I am sooooo exhausted and sick lucky for me I have a great husband who is doing everything for me. Even to have a shower is awful. Hoping things do improve.
Struggling with fatigue
Hello all I was diagnosed in March with Stage 2 invasive carcinoma, mastectomy in April with 2 lymph nodes positive. Hormone and Her-2 positive. I completed my 4 rounds of A/C and now have started on Pacliaxel and Herceptin. My reason for posting is the extreme fatigue. I’m battling guilt watching my husband trying to cope with work and looking after everything. Is this normal experiencing fatigue on Paclitaxel? Will it ease when I’ve finished the 12 doses? Has anyone found help going to speak to a councillor? Thanks for any advice
