Ladies...
I know this has been covered before...over and over....but I was wondering how many of you experience "aches" or tenderness ? I have noticed that the last couple of weeks my lower back has been tender.
It has not changed, and Im thinking its all the sitting I was doing with hours of driving and a 12 hour plane flight last week.
The last few days I have been running around like crazy doing errands ect...and my ankles hurt and still this lower back thing.
I visited my onc today and he didn't seem to concerned. Just asked the basic questions. Is it getting worse? When you sit or lie down does it continue? No...and no. My blood work was good.
My onc is thinking its the lack of estrogen being on Tamox and Lupron...<blah>
Sigh....I hate when my mind goes to the worst case scenario....
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kk69Z Joined: Aug 2008 Posts: 77 |
Oct 15, 2009 08:44 pm
kk69Z wrote:
lexis: I've been on tamoxifen for 14 months and have never had aches, pains or sore joints. Did have hot flashes in the beginning, but they went. It could be what you said. Who knows with side effects. |
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lexislove Joined: Sep 2007 Posts: 1,942 |
Oct 15, 2009 08:52 pm
lexislove wrote:
My pain is mainly hip / lower back and ankles...I found an older thread just now so Im hoping some woman can respond now. I have a magic bag on it right now... KK...your very lucky..I hope it doesnt change!! Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
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JacquelineG
Joined: Jan 2009 Posts: 96 |
Oct 15, 2009 09:20 pm
JacquelineG wrote:
I have some hip pain and also a bit of pain in the ankles (joint stiffness, mainly). I've been on Tamoxifen since January and really hope that is the cause of the hip pain! I did find a thread on hip pain and tamoxifen so it made me feel like I wasn't crazy... I definitely get achy sometimes and have a good friend on Tamoxifen who has experienced joint and muscle aches since she's been on it as well... Jackie Diagnosis: 6/2/2008, IDC, 2cm, Stage IIIc, Grade 3, 6/40 nodes, ER+/PR-, HER2- |
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lexislove Joined: Sep 2007 Posts: 1,942 |
Oct 15, 2009 09:31 pm
lexislove wrote:
Thanks Jackie! I googles se's of tamox and that thread popped up for me. It made me feel a wee better. Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
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Member_of_t
Joined: Sep 2004 Posts: 5,555 |
Oct 15, 2009 10:13 pm
Member_of_the_Club wrote:
I thought everyone on tamoxifen had hip pain. I'm sure I was in that earlier thread. I am finding a lot more aches and pains that I think are from the aging process. I am on tamoxifen so maybe that has something to do with it, but for me it started even before bc. I;m sure its nothing serious, but if it continue you might want to go back to your doctor. Diagnosis: 9/30/2004, IDC, 3cm, Stage IIb, Grade 2, 1/17 nodes, ER+/PR+, HER2- |
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Susantc Joined: Jul 2009 Posts: 17 |
Oct 16, 2009 06:48 am
Susantc wrote:
I've been on tamoxifen since August. About a week after I started, I began to ache in my neck and between my shoulders. Sometimes my heels hurt too. It was so bad at first, that I had to turn over in bed in stages because it was just too uncomfortable. I think it's receding, but I am definitely stiff. I do accupuncture, two yoga classes a week and walk each day after work. I just keep moving. The other phenomenon that has been annoying has been nausea which starts about an hour after I take my pill and continues for a good chunk of the day. I seem to have solved that one by taking my pill at night and now feel much better. |
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chelev Joined: Feb 2009 Posts: 917 |
Oct 16, 2009 11:33 am
chelev wrote:
I have been on tamox since August also and have just started noticing my lower back and hips aching. It's not debilitating like on femara, but I've noticed it. I have not decreased my workouts, and am powering through them, but I find myself more sore in the hip and low back afterward. My neck/shoulders ache a little too - mostly in the shoulder joints. Guess that means it's working? chelev - Life is what you make of it - keep what works and get rid of what doesn't. TC - 2 rounds, Radiation - 33 rounds. Oncotype score - 27 (18%). Tamoxifen. "What that does not kill you will make you stronger."
Diagnosis: 2/14/2009, IDC, 3cm, Stage II, Grade 2, 0/4 nodes, ER+/PR+, HER2- |
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lexislove Joined: Sep 2007 Posts: 1,942 |
Oct 16, 2009 11:39 am
lexislove wrote:
Thank you all. I so appreciate it. It is my lower back and hips. I have just noticed maybe the last 3 months or so. It was probably there longer but I thought it was a se of the Taxol I did....sigh.. I think I have read that woman take Glucosamine(sp?) to help...does it work? Im desperate now. I sure hope it means its working...Ive been on it for 16 months .. Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
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pinkedx1inp
Joined: Oct 2009 Posts: 3 |
Oct 17, 2009 10:54 pm
pinkedx1inpennellville wrote:
Hi Ladies.... This is my first post and I have a Tamox question. I have been on Tamox for 1 year, and my feet have been very sore the past couple of weeks. I asked my gyn.,but he was not sure if it was the Tamox or not. I have had arthritis in my r ankle even pre-diagnosis; but both my feet hurting has been discouraging as I need my feet! Just wondered if anyone out there has had sore feet, and this site has been a saving grace for me since I was diagnosed in 2008. Dx.Feb.2008, IDC 1.7 cm,lumpectomy,7/13 nodes, ACT chemo,radiation, now on Tamoxifen |
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AmyJ Joined: Oct 2009 Posts: 3 |
Oct 26, 2009 05:37 pm, edited Oct 26, 2009 05:37 PM
by AmyJ
AmyJ wrote:
Hi I too am nauseated from the Tamox. I take it at night now but still have nausea on and off throughout the day ok in eve. Any other suggestions? I do have to take Gravol for nausea fairly frequently. And this makes me tired Diagnosis: 2/6/2009, IDC, 1cm, Stage I, Grade 3, 0/3 nodes, ER+/PR+, HER2- |
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lexislove Joined: Sep 2007 Posts: 1,942 |
Oct 26, 2009 07:42 pm
lexislove wrote:
Hi Athena, Interesting about the Lupron....I have been on Tamox with Lupron for 16 months. I started taking my D3 again, Oct-April, I do not take it in the warmer months since Im outside everyday with my 4 year old. Since my complaints I have been working out and stretching. My back and hip pain? almost gone! I think the culprit was the 12 hour flight I had a few days before. So thats good news. But I think the combo of Lupron and Tamox has added extra weight wich causes stress on me. Im only 5'3 , small framed but I have about 50 lbs to loose. I do have ankle aches but I think its all weight related. I've started to fix that problem......onward!!! Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
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robyn33 Joined: May 2008 Posts: 82 |
Oct 30, 2009 03:20 pm
robyn33 wrote:
Lexislove-- I am stiff and achy from time to time. I feel it especially when I've been sitting in a chair for a long period of time, or when I get up in the AM. My back/hips kinda hurt, but it goes away after a little movement. I also have sore feet when I get up in the AM. That goes away, too, afer the first 10 steps or so. I'm thinking that your doc is right: Low estrogen, and tamoxifen are to blame. That's my story, and I'm stickin' to it! Diagnosis: 5/13/2008, IDC, 2cm, Stage IIIa, Grade 2, 5/15 nodes, ER+/PR-, HER2+ |
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Kleenex Joined: Jul 2008 Posts: 422 |
Oct 30, 2009 09:31 pm
Kleenex wrote:
I have had issues in the last month or so (11 months on Tamoxifen, 46, premenopausal) with my knees being a bit uncomfortable. Also my fingers. I haven't seen anything specific about Tamoxifen causing joint pain on the lists of side effects, but there's been anecdotal evidence on these threads. My question: WHAT is the source of this sort of pain? Is it just some sort of sensitivity/achiness thing, or is some sort of damage happening to my joints with less estrogen circulating in my system, or??? If it's just a sensory thing, it's annoying but I can deal with it, but if I'm damaging them in some way, that would be a bummer... Diagnosis: 6/19/2008, ILC, 2cm, Grade 1, 0/2 nodes, ER+/PR+, HER2- |
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lexislove Joined: Sep 2007 Posts: 1,942 |
Oct 30, 2009 09:34 pm
lexislove wrote:
Thanks for the responses ladies.....Im glad Im not alone in all of this. I still have just under 4 years of taking Tamoxifen....oh joy. Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
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kpthfaith2 Joined: Jan 2008 Posts: 53 |
Oct 30, 2009 10:43 pm
kpthfaith2 wrote:
Hi, I have been on Tamoxefin for 2 yrs and have found I have aching in my knees especially if I have been sitting awhile. And yes I felt as if 5yrs was going to be a long one but actually time has flown by very quickly. I think everyone is different with side affects so I don't believe when someone never has had a certain symptom doesn't mean that isn't a side affect for YOU. For me I have gained alot of weight while on Tamoxefin, along with being menopausal for about 6yrs. Proverbs 3:5 Trust in the Lord with all your heart and lean not on your own understanding but in all your ways acknowledge Him and He will direct your path.
Diagnosis: 5/2007, DCIS, 1cm, Stage 0, Grade 2, 0/0 nodes, ER+/PR+, HER2- |
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Jane108 Joined: Feb 2009 Posts: 16 |
Nov 2, 2009 02:06 pm
Jane108 wrote:
My doc would give the same answers because he doesn't have a clue. May I suggest going online and doing research on side effects. I've been doing that for my chemo and rads and will soon be doing it when I go on Tamoxifen in Dec. I get a sampling from JohnsHopkins site, WebMD, and Amer. Cancer Society. Sometimes the worst effects are quite normal and will go away. At least with a little research, you can go to your doc with what you found. Diagnosis: 12/29/2008, IDC, 2cm, Stage IIa, 3/6 nodes, ER+, HER2- |
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Jane108 Joined: Feb 2009 Posts: 16 |
Nov 2, 2009 02:12 pm, edited Nov 2, 2009 02:12 PM
by Jane108
Jane108 wrote:
When I was on chemo, a friend gave me Orbit gum. Whenever I feel a little queasy, I chew the gum and I was never a gum chewer! This has really worked for me and I take it everywhere I go. Sometimes our precious nerves can bring on a sour stomach but chewing gum takes my mind off my troubles. Diagnosis: 12/29/2008, IDC, 2cm, Stage IIa, 3/6 nodes, ER+, HER2- |
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LT1203 Joined: Oct 2009 Posts: 6 |
Nov 3, 2009 05:42 pm
LT1203 wrote:
Robyn33, I have the exact same symptoms and have been on Tamoxifen since 7/1/09. I don't know if it is leftover symptoms from chemo (which I finished in April) or Tamoxifen related, but I'm thinking the latter. Linda Diagnosis: 10/31/2008, IDC, 3cm, Stage IIb, Grade 2, 3/20 nodes, ER+/PR-, HER2- |
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LT1203 Joined: Oct 2009 Posts: 6 |
Nov 3, 2009 05:55 pm
LT1203 wrote:
All, I too have had painful feet (mostly in the morning, but also after sitting for a long period of time) and the hip pain/stiffness. I swear that it is related to the tamoxifen. I was running regularly throughout my chemo (Jan - April 2009) and have been pretty active since. I had the foot pain during chemo and for a while thereafter, but attributed it to neuropathy. I started tamoxifen 7/1/09 and have since had the hip stiffness/pain, so much so that I have mentioned it to doctors and been to a physical therapist. I am getting Zometa 1x every 6 months, but have only had one (in July 2009). Something has caused the foot pain & hip stiffness/pain -- either tamoxifen, chemo, or the menopause caused by the tamoxifen. Like others, it is not debilitating so I power through, but it certainly is annoying. Linda P.S. I guess I'm lucky ... at least tamoxifen doesn't make me nauseous like some. Diagnosis: 10/31/2008, IDC, 3cm, Stage IIb, Grade 2, 3/20 nodes, ER+/PR-, HER2- |
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pinkedx1inp
Joined: Oct 2009 Posts: 3 |
Nov 3, 2009 11:27 pm, edited Nov 3, 2009 11:31 PM
by pinkedx1inpennellville
pinkedx1inpennellville wrote:
Hi LT1203, I am sorry to hear that your feet hurt too. Some days are o.k., but some days I can hardly walk unless I put my sneakers on. I think that it is the Tamoxifen; I finished chemo in July of 2008, and I started having difficulty with both feet in September 09, close to my year anniversary on Tamoxifen. What do you do for your foot pain? I find that warm baths help. 2/2008 IDC 1.7c.m./lumpectomy,7/13 nodes,chemo,rads,tamoxifen |
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keno41 Joined: Aug 2009 Posts: 34 |
Nov 10, 2009 02:32 pm
keno41 wrote:
I have been on Tamoxifen for a month now and am having bad foot pain at night. (just one foot) I have not done chemo, so it must be the Tamox. The night sweats and hot flashes are tough, but this pain in the foot is a pain in the butt. I've been taking Tylenol PM and using the heating pad, but it hasn't helped that much. I'm hoping this will subside. Diagnosis: 7/2/2009, ILC, 3cm, Stage IIa, Grade 2, 0/3 nodes, ER+/PR+, HER2- |
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marlenet Joined: Jan 2009 Posts: 195 |
Nov 20, 2009 01:11 pm
marlenet wrote:
wow I feel better after this site! I have developed hip pain and at times get really scared! For the past couple of weeks or so it had bother me on and off. Today it feels much better. I thought the tamoxifen caused it but had that scary cancer flash through my head. I meet with my Dr ( oncologist ) next month. I will have to ask. I am 1 year since dx . onco score of 25 ( 16 % ) but after chemo it went down to between 4 or 6 % Still get that scared feelings. My heal also started to bother me, but I think that was from the new high heal shoes i started to wear. I don't normally wear heals! Bought them pads for my tennies and that pain is almost gone. Diagnosis: 11/14/2008, IDC, <1cm, Stage I, Grade 2, 0/1 nodes, ER+/PR+, HER2- |
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sherridl Joined: Apr 2004 Posts: 101 |
11 hours ago
sherridl wrote:
I had horrible muscle/bone (or joint) pain during Tamoxifen. Have any of you had any muscle cramps? I had those, too. One thing that helped was 400 mg of magnesium oxide. Most magnesium vitamins you find are 250 - the 400 is much better. I used Mag-Ox and this now comes in generic form. |
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lexislove Joined: Sep 2007 Posts: 1,942 |
11 hours ago
lexislove wrote:
I get muscle cramps alllllll the time. The ones in your calf, that wake you up in the middle of the night?..*OUCH!!!* Dx: Sep 2007, IDC 8cm, 0/6 nodes, ACT Chemo, R Mastectomy, 1 yr Herceptin, 28 Rads,Currently on Lupron, Tamox & Zometa. Exchange Sx Fall 2009, BRCA -
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wallycat Joined: Apr 2007 Posts: 908 |
10 hours ago, edited 10 hours ago
by wallycat
wallycat wrote:
If I don't take my potassium/magnesium supplement, I will die from night leg cramps. My achilles heel/tendon KILLS me and my foot bones kill me...I get some pain in may hands as well. My worst is between my shoulder blades and this just started...I think it may be nerve endings regenerating from my bilateral mx and it is intermittent, but that is what I am telling my brain...who knows Because tamoxifen is still making me ovulate, I occasionally have lower back pain and groin pain, as if I were having a period...but no period. Best to you. Dx 4/07 1 month before turning 50; ILC 1.8cm, ER+/PR+, HER2 neg., Stage 1, Grade 2, 0/5 nodes. Onco score 20, Bilateral Mast., tamoxifen
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CatbirdC Joined: Sep 2009 Posts: 59 |
10 hours ago
CatbirdC wrote:
Just for any one that wonders if their chemo or Tamoxifen is the cause of foot cramps..... I never took chemo, just on Tamoxifen, and I had terrible foot cramps daily for about a month and a half and now it's just once every so often. Bonnie CatbirdC
Diagnosis: 5/19/2009, DCIS, Stage 0, 0/3 nodes, ER+/PR+, HER2- |
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