Pain meds post mastectomy
Hi everyone, I’m 2 weeks post mastectomy and wondering how long you needed your pain meds for? I’m still taking 2 Panadol & 1 Neurofen every 8 hours & still getting pain/tightness in arm/chest is this normal or should the pain be easing off now? I have my follow up appointment with surgeon tomorrow
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 please
Tamoxifen side effects
I've been taking Tamoxifen (exemestane) for 3 weeks now. The hot flushes are manageable but the pain in my joints and muscles has been pretty bad. I was told it usually peaks at 4 to 6 weeks? Does it get easier then or just plato? Circulation seems to help but by the end of the day I'm sore and tired and the last thing I feel like is exercise. Nights are the worst, I'm not sleeping well and after a while laying in bed because pretty painful too. Does it get better or do you get used to it? It started mostly in my legs (feet, ankles, knees then into my calfs) and then my groin. Now my chest, elbows and wrists have started? My journey has happened quickly, 8 months since diagnosis, chemo, surgery and radiation. Stage 3. They said this is my best shot so I want to make it work. Does anything make it easier? Hemp oil? Vitamins? Anything?
Ongoing issues
Greetings all from Adelaide. Just wanted to ask you all quick question about any ongoing issues any of you might have after going through your BC journey. I was diagnosed in 2015 and had a mastectomy (with lymph node removal) and reconstruction. I have been luckily been given the all clear by my breast surgeon every year since. My concern today is that yesterday i started having this aching pain underneath the left arm. This was the arm that had the lymph nodes removed back in 2015. It feels like there is a bruise (there isn't - i checked) or that I have strained the muscle. It is still ongoing as of this morning. I did have a recent check up a couple of weeks ago where the breast surgeon gave the ok - noticed a little fat necrosis in the reconstructed boob, but otherwise ok. Is this something I should be concerned about? I understand that I will have these occasional 'twangs" ongoing - but this is different. It feels "raw" under there/side boob area. I dont have a breast cancer nurse (I got my BC early and went the surgery route) and had no chemotherapy/radiotherapy. I am thinking about ringing my breast surgeon and at least speaking to the nurse. Thanks all for your assistance/suggestions. Cheers Rachel H
Docetaxel pain
Hi All, I'm about halfway through my chemo. I've finished 3 cycles of FEC and have just started on Docetaxel. I thought the Docetaxel was better at first, since I didn't seem to get any nausea (a relief after the FEC which made me feel very ill). But now I've started getting strong all over body aches and pains. Even my finger nails hurt. I'm taking panadol and ibuprofen and going swimming whenever I can (which seems to take the pressure off). But has anyone else had this? Any tips on managing the pain? Will it go away or am I just going to feel like this for the rest of my treatment time?another 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!!
Medicinal Cannabis Oil & reduction of pain, improvement in well being
Hi guys I've also put this link in the 'Early Days of Letrozole' thread - as so many are having extremely painful side effects and watching this video (shown last Dec) that follows the life & death of Dan Hallam (a young Aussie with Bowel Cancer) may help ..... The use of Cannabis Oil as a pain killer can make the difference in quality of life in MANY cancer sufferers (and other nasty conditions which can otherwise be debilitating to the extreme) ...... as this video shows as it follows the story of many (particularly kids.) Please watch the entire video before commenting ...... it takes a while, but it is well worth the watch, as it is Australian made & relates to our own health system. Share the link with family & friends. We NEED this to be freely available to those in chronic pain - especially those with Mets BC or extreme pain side effects from AIs https://www.youtube.com/watch?v=cmEjlMdLi5wMore nose sores
It was July 2020 when I had little sores up my nose from constant runny nose after chemo. Like others I still have a runny nose from time to time. I've got these little sores back. It feels like my whole nose is swollen and it is incredibly painful to touch. I've tried all sorts of creams to help them. If I sneeze I feel my head will explode. Has anyone else had these little sores. I was only at gp the other day. Looks like I'm going back to gp for help. In the scheme of things it is only sores up my nose but it's so damn painful.
Achy hips
I have been on the AI drug Anastrozole for 3 years. And since I can’t get to a pool for therapeutic walking in water at the moment, I’ve noticed that my hips are aching a lot. The doc got me to have an MRI which showed all was good, so we are assuming it’s the AI drug. I’m 64, ten years past menopause. I walk a lot. I exercise fairly consistently. Does anyone have any advice on how to cope with this unrelenting ache? Is it an inflammation issue? Does anybody actually know what the chemical/mechanical process is that’s causing it? In my case there is no bone loss, arthritis, etc. Just aching pain.
Tamoxifen side effects
Hi, I'm new at all this so I hope I get it right, new to the group discussion process, 5 months since diagnosis, surgery treatment etc and now I have started on Tamoxifen. Can anyone give me hope the side effects will settle. Chronic nausea, insomnia, burning skin, dizziness, I can manage all that but it is the pain in my joints and bones that I'm really struggling with. I'm not usually an overly teary person but the pain has caused me floods of tears. I'm trying to find remedies to help manage the pain, and wonder if anyone else doing this journey has come across anything that works... I have spoken with my oncologist who tells me many women can't complete the treatment for this reason and I can stop whenever I want too... but then he tells me that if the cancer comes back a 2nd time it could affect brain, lungs or liver and would be stage 4 terminal... which kinda terrifies me that I don't want to stop taking the tamoxifen, regardless of pain factor. I've done heat packs, cold packs, magnesium, over the counter painkillers... unfortunately I can't do prescription painkillers due to allergies. Would absolutely welcome any advice. 😊
