Pain on my pelvis and lower back is g... - SHARE Metastatic ...

SHARE Metastatic Breast Cancer

6,808 members8,425 posts

Pain on my pelvis and lower back is getting worse

PLASEM profile image
14 Replies

Tonight I can not sleep my pain on my lower back and pelvis is worse I am on Ibrance and Faslodex for thre months with this combination and one year with Ibrance and Letrozole, my last bone scan on last October and act scans were ok, my oncologist told me that maybe is arthritis what are your recommendations thanks

Written by
PLASEM profile image
PLASEM
To view profiles and participate in discussions please or .
Read more about...
14 Replies
Barbteeth profile image
Barbteeth

I really can sympathise..I’m the same but my pain is during the day so it doesn’t keep me awake..the hot sweats do though!!

Do you have a good mattress?.. I invested in a water bed a long time ago as have had back pain for years..it’s amazing..the only thing I miss when on holiday

I’ve also succumbed to taking the heavy duty painkillers..rode my horse this morning..not for long but there’s no way I could do it without the medication

You really shouldn’t have to suffer like this..it’s bad enough having this disease without the misery of pain..do get some good medication so you can feel happy and get a good nights sleep

I’m on Ibrance and letrazole and I’m sure they’re responsible for some of the pain

All the best

Barb xx

PLASEM profile image
PLASEM in reply toBarbteeth

Thanks my mattress is good I recently bought it God bless you

youngfarm profile image
youngfarm in reply toPLASEM

Receiving same treatment for MBC and MRI revealed cancer cell attacks on lumbar vertebrae which seems to have caused same pain you are describing. Have you had vertebrae examined recently or has this area been eliminated for the cause?

PLASEM profile image
PLASEM in reply toyoungfarm

Thanks

PLASEM profile image
PLASEM in reply toPLASEM

I just had done an MRI waiting for results

Snowcone16 profile image
Snowcone16 in reply toBarbteeth

Hey there, when is your scan scheduled? I just recall mine was for 6 months. At 3 months, my rib was achy. It wasn’t severe but suspicious. I had my scan moved to 4 months. The meds didn’t work...onc said they might have worked 2 months then stopped. I don’t want to worry you — it could actually help ease if the scan comes back neutral. 🤗

PJBinMI profile image
PJBinMI

I have heard two things that might be relevant to you. Healing bone mets can hurt. The pain from bone mets tends to be constant, so wouldn't just show up at bedtime, though I guess we might notice it more then. Also Letrozole can cause bone pain. When I went off it after almost five years, I was surprised by how much better my bones felt! If your onc is not a bc specialist onc, you might benefit from getting a second opinion from one who sees only patients with bc. I recommend that to anybody with mets. And some oncs communicate with patients better than others.

PLASEM profile image
PLASEM in reply toPJBinMI

My pain is all the time but at night is worse

Tomorrow I will have an MRI please pray for me thanks

Sandig1948 profile image
Sandig1948 in reply toPJBinMI

I had bone pain for the 12 years I was on Aramidex but thought it was caused by my life style. Came off it and within 3 months free of discomfort. I do believe i remained cancer free because of it. Letrozole now and discomfort but worth putting up with. I am very sorry for those it has such an impact on your lives and wish I had an answer.

Gigixxx

Bailey3266 profile image
Bailey3266

Try alternating heat pack and/or ice pack or bath with Epsom salts. The letraziole contributes to weird pains for me—intermittent in upper right quadrant of abdome-tho my nets are in pliers, lungs & Lymph. Yoga for cancer (gentle warm water pool group exercise combined with speakers & get-together for survivors @ no cost YWCA Encore program is “free”! Go figure! I’m anti-Med and anti-therapy; but since on Ibrance convo x13 mos I’ve tried it all therapy, yoga, Encore, walking my doggie (best outcome); if you don’t want a dog fulltime; a cat is alternative. Somethings help; others don’t touch it; especially an occasional meltdown. I even tried but hated acupuncture/massage and mani-pedis are also gd medice=pampering (self-proclaimed quite bliss)!

PLASEM profile image
PLASEM in reply toBailey3266

Thank you for your good advice

Purple60 profile image
Purple60

Pain is worse at night for any condition- not just cancer or bone mets. Our tissues swell at the end of the day and can compress nerves that may cause pain. When I lay down at night the pain increases very much so. My doctors have explained that by laying down and increased pressure on areas of bone mets they may compress nerves even more and results in pain. This explanation makes a lot of sense to me and so I take pain meds or acetaminophen or anti-inflammatory drug like ibuprofen before I get in bed so I can get ahead of it. Good luck!

Snowcone16 profile image
Snowcone16 in reply toPurple60

Yes...feels like I age 15 years after 8 pm!

PLASEM profile image
PLASEM

Thanks the bone cancer pain has that characteristic of being worse at nights

Not what you're looking for?

You may also like...

Ibrance, and back pain

I am on my last week of my second round of ibrance. The last week or so I have been experiencing...

Back on Ibrance and can’t sleep

When I go back on my Ibrance after a week off I just cannot sleep for a couple of nights. So, I’m...

Is anyone on affinitor and aromasin?

Just came from M D Anderson with Dr wanting to change meds after progression . I was on Ibrance and...

Knee, foot and joint pain on Ibrance, Faslodex and Xgeva

So, I'm on 75 mg. of Ibrance, monthly Faslodex and every 8 weeks on Xgeva for about 6 months now....
lynnhbtb profile image

Anyone had an increase in bone/joint pain after being on Ibrance and Letrozole for a few years?

I was diagnosed Metastatic BC with a lot of bone mets back in June 2022. The Letrozole and Ibrance...
lovnmycat profile image

Moderation team

See all
Jslanovich profile image
JslanovichAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.