PAIN PAIN PAIN!
I'm so sick of feeling pain all the time, and living on ibuprofen or excedrin. I'm noticing it much more in the last few weeks since starting Arimidex, and I don't know if it's from that or post rads since November, or just everything in my surgery areas tightening up. I still have under armpit pain almost as bad as when the drains were in, pain in my back shoulderblade extending into my front shouder (deltoid) and all down my arm and numbness in fingers. I don't want to call my onc and ask for pain meds because I hate taking anything stronger than what I'm taking. I can't even do my upper body arm weights because I'm afraid it will only aggravate it more. I was doing my 5 lb wts every day since treatment but had to stop a few weeks ago because of the pain. It also is iin my clavicle , and my new breast mound from Tram surgery. I was wondering if this is more healing and tightening at the mastectomy site underneath, but I'm so weary of wondering why I am in pain everywear, including knees and ankles. Whats going on with me anyway??
Comments
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Hi Shana
I can relate & sympathize. Saw my PS yesterday for 10-week follow-up after DIEP; she indicates that the pain I am experiencing is normal, especially the stabbing ones in the breast areas and stomach. Plus, I have constant pain in my shoulder and underarm and arm, and intermittant numbness and tingling in my "bad" arm. It makes me want to hunch over, which then causes me pain in my trapezoid and lower back. I don't take any painkillers not even OTC, but it REALLY puts me in a bad mood. Some of the pain I have is from my original mast (shoulder blade and armpit), some is from lymphedema I developed later (armpit and arm), and some is from healing from the bilat DIEP (breastbone, breasts, abdomen). I also apparently have a small seroma between my breast & clavicle on my cancer side. If it doesn't resolve, I'm going to ask to have it aspirated.
I am sick of all the pain too. I am tired of feeling like crap all the time. Thank goodness we can vent here.
Have you been evaluated for lymphedema?
Gayle
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I'm almost 4 weeks PFC and still have a lot of pain. Most of it has to do with neuropathy, but then there are the other pains. I am still very tender to the touch around my shoulders and upper back, like my nerves are hypersensitive and I get sharp pains in my thighs. When someone hugs me - its painful. I'm guessing between the surgeries and toxins put into our bodies it causes these crazy pains. Wish I had something good to offer, but I don't so I'll send a ((HUG)) instead.
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Shana....knee and ankle pain are probably from the Arimidex....not sure about the other pain as I had expander/implant recon and its not as invasive as your TRAM recon. Gapabentin helps with joint pain (ibuprofen never worked for my joint pain). I can't take any of the narcotic pain meds as they make me queasy, sick to my stomach and constipate beyond belief.....numbness in hands could also be from Arimidex (CTS is a side effect of Arimidex)...I have some numbness at times in my hands and also Reynauds since chemo and AI's. My BC side also pulls when I reach too far....I just figure that its the way its going to be. I second what you and jenn3 and gayle said....I just want to feel good most of the time.....Shana....congrats on your one year yesterday....you have been through a lot in the past year and your body is still healing....maybe call your onc, or PS and find out what they think of the pain....it may put your mind at ease....(((((((((HUGS))))))))
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karen1956 ~ Thanks Karen, yeah I just can't believe it already been a year. One year cancerversary. It's been the worst year of my life, and I think I am going to call my onc tomorrow. I went for an hour walk with the dogs today on the beach, hoping it would loosen me up but, I'm still sitting here with my shoulder pain and numbness. I can't stand this bullsh@t, it really sucks.
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Gentle hugs Shana......May I suggest a physical therapist?......I too had all tose pains and my wonderful onc sent me to a place called Turning Point in my neighborhood.....It ia PT treatment center solely for breast cancer survivors and fighters.......They treat only women who are experiencing pain due to surgery and cording...Did you know you can have cording along your back and sides, too?....Well I didn't know, but I soon found out I had it there too!.......I can honestly say those wonderful ladies straightened me out very well and gently too.......Hopefully you can find a PT center that takes only BC patients and knows their special needs....Good luck to you...By the way ti has been almost a year since my last visit to them and it has been 3 years Feb 2 since my surgery of bilat mast with immediate TRAM flap recons.....I had cording all down my left arm and could not move it above my hip ......I also had numbness and tingling in both hands due to the trauma of cut nerves and pulled muscles from the surgery....I also had pain from the Arimidex but after a couple of months this subsided......I wish you Godspeed and a quick recovery from all this pain.....
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Hollyanne ~ I also had a 'free Tram flap". I do have the numbness and pain from the armpit, shoulder front and back, clavicle and down arm to fingers. The numbness feels like I got hit in the funny bone. I'm not sure what cording is. Do you think it could be lymphedem? There's no swelling. I'm pretty good with range of motion and stretching. I'm gonna call my onc tomorrow. Is "cording" really common?
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Shana,
First, big...big congrats on your one year. Second, like the others, the ankle/feet,joint pains are likely from the Arimedex. Look up the se's.
You can try uping your VitaminD, or taking Glucosamine(sp) I saw some woman on the AI threads talking about this and it seems to work.
Im starting up with Femara in 4 weeks after my surgery, so Im hoping my se's are not severe. I already have joint pains and stifness but thats likely from all the Lupron shots Ive been doing for the last 18 months. No estrogen, no quality of life...or less quality of life...hopefully.
If your are still having bad se's, you can always switch AI's and find one that is more tolerable.
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My experience with arimidex was that i had a lot of pain; my body ached most of the time. i stayed on it because i wasn't thinking that switching to femara might be a good idea. my friend was on arimidex...had the same kind of pain...and switched to femara and has done much much better on the femara. way less pain. it seems that femara is more tolerable then the arimidex from what i have read on the boards..and heard from other women. remember, these AI's stop the production of estrogen; which really does have a big influence on your body. also, you are only a year out....all that chemo and rads really plays havoc on our body...and i think it takes awhile to heal. since i have been off the arimidex after 5 and half years...my body feels better then it has since being diagnosed. hope you feel better....HUGS. hang in there
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I'm bumping this again because I am just miserable with the bone and joint pain today. I hate taking the Arimidex and wish I could stop it. I want to talk to my onc about how much pain I feel in my spine, hip and clavicle areas. I keep worrying about bone mets but also know the Arimidex does this. It gets' me so depressed about my quality of life. I am even walking 2 1/2 miles a day to keep moving but that doesn't help much.
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A girl in my Chemo group had loads of pain with Arimidex and her Onc switched her to Aromasin. Apparently Arimidex gives you more pain, Aromasin more mood swings. But it might be worth switching. My Onc said sometimes you need to switch until you find the lesser of the evils!
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Kerry, I'm going to talk to my onc about it. The only thing that really concerns me if I switch to another one, is the possible weight gain. I've gained 30 lbs since chemo, and have really totally been trying to do everything to get it off. I'm started walking 1 1/2 miles a day and now since last week i'm going 2 1/2 miles a day. Cardio sculpting 3x week, and have changed to almost meatless diet, no sugar or white flour and low glycemic. Drinking 64 oz water every day, and I still am not losing anything. I'm blaming it on the Arimidex. I'm so frustrated not only about the pain but now the extra lbs too
Barb
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I would try switching. It can't hurt to try.
I haven't had a problem with weight gain, but I do know it is a problem for lots of people.
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Bumpin this again for faithfulheart
Barb
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Shanagirl,
Love you girl! thank you, so glad to know I am not alone. I know arimidex can cause a lot of bone pain, I did not think tamox did the same though?
How do you feel now and did you every have a bone scan for the pain?
Thanks sweeti!
stephanie
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