radiation and fibromyalgia
Hello everyone,
I am wondering if there are any ladies out there who have done radiation and have fibromyalgia. I am 14 days into my rads and my fibro is acting up bad. My muscles in my chest and the muscles in my shoulder are twitching, tightening, and hurting very bad. I am afraid to continue with the rads because of what it is doing to my muscles. Is it temporary or permanent. I know rads changes tissues, so I am afraid it is just distroying my muscles. Anyone with fibro knows the pain we deal with this stuff!!. I know I need to be concerned about making sure the cancer doesn't come back and believe me I am. I am also concerned about the quality of life I will have after all this is done. Anyone out there that can help me? Unfortunatly my rads doc is out of town until Thursday, so the office just said to stay home until I can see her. Any info on this would sure be appreciated!!
Susan
Comments
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Susan,
You are not alone! I've had fibro since the mid 80's and went through radiation last summer. I had a lot of zinging random pain in the breast during rads and afterwards that was quite uncomfortable. The treatment center recommended anti-inflammatory meds, which did nothing to treat the pain. When it started waking me up at night, I contacted my Dr who gave me a script for Darvocet, which helped alot. I still have some pain in the breast and affected arm, probably related to lymphedema and continue to take an anti-imflammatory. Staying on schedule with rads is very important, so I hope your Dr is able to adequately address your pain this week. You might try gentle stretching exercises to maintain the range of motion in your shoulder. Many people, myself included, also take anti-anxiety or anti-depression meds during treatment. Don't hesitate to do whatever you need to to get through treatment, and be sure to get as much rest as possible.
My QOL has been greatly affected by fibro, and was impacted by the pain & discomfort of rads and the 4 hour round trip each day. I'm happy to report though that the pain is subsiding and I'm able to get back to walking which helps me to manage my fibro.
I wish you the very best during this journey!
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Hi:
Also have fibromyalgia and it did act up during rads. I continued on and finished today. I do water exercises which help and I hope I will get better. I used the anti-anxiety meds that they gave me during chemo to help me sleep. I also have bad tendonitis and use Motrin and/or hydrocodone.
Peeps
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I had posted a thread a couple months ago asking if anyone else had fibro and no one answered! It made me feel very alone...
Lyrica is amazing but I gained weight and had to stop. Apparently Neurontin is good too, but I haven't tried it yet. NO ONE understands the pain. Absolutely no one. That is the reason I am not getting reconstruction. I am amazed I didn't fall into a flare with the mastectomies!
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Barbe1958,
I'm so sorry you didn't get a response to your posting. Fibro is tough enough to deal with, let alone a cancer diagnosis. Balancing treatment, side effects & fibro is a challenge, but I do think it gets a little easier with time. FYI, I take neurontin for nerve pain that flared during rads and found that it helps. I think it is very similar to Lyrica, but much less expensive.
Hope your recovery goes well and that your fibro is managable.
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Ladies thank you for your responses. It helps to know I am not the only one dealing with the radiation/fibro stuff. I finally got to see my rads oncologist, but all he said was he doesn't know how the rads will affect my fibro long term, but you have to keep going. He did give me a presciption for some pain meds, although they don't seem to help much.
Sister I am glad to hear you are starting to feel better. I took your advice and put myself back on my xanex today and it does seem to help. As I am sure you know well, rest is a big factor when it comes to fibro and that is something I have not had much of since I started rads. Just can't seem to sleep. They even gave me a prescription sleep aid, which does not putt to me sleep. What time I do sllep it is not restful. I am sure that is not helping my problems.
Barb I am also sorry your questions did not get answered. If I would have seen it I would have. You are so right how noone understands the pain. I have had this since I was a little girl and had test after test run. Noone could figure out what was wrong and finally said it was all in my head. It wasn't until I was 30 yrs old that I was finally diagnosed. I got so tired of being told I was not really hurting. I KNEW how I felt..and it hurt! I did have a flare with my mastectomies and had a very long hard recovery. I was just starting to feel somewhat better when rads started and it started all over again.
peeps congratulations on finishing those rads! I know you are excited!
I wish you all the best of luck!
Susan
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Susan,
So glad that you were able to get a script for pain meds. Hope it helps! I totally agree that QUALITY sleep is critical with fibro. If you are not feeling refreshed after sleeping, you might give some thought to anti-depression meds, which can help you to get REM sleep. I've been on a low dose for years and for me it's made all the difference in the world.
Sending healing thoughts your way!
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I had radiation last year and I went to rheumatologist when ALL aches, pain, etc. Dr. said I do not have fibro. Now after getting the permanent implant I'm hurting again. I don't know if I should go to another rheumatologist or see a nuerologist? I'm so confuse I could think of MS, fibro, arthritis, post mastectomy pain syndrome and go crazy.
Any advice?
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I've had "fibro" for over 30 years .... before they called it that or understood very much about it. I had been doing very well for about the last 10 years after prolo-therapy treatment (www.prolotherapy.com) and I swear by it. I combined occasional chiro with exercise, prayer, meditation, occasional muscle relaxers or pain meds, and a positive attitude. I've been in treatment for breast cancer for 1 year now including 10 mos of chemo, bilateral mastectomies, pneumonia, lung clot and wound healing issues. Despite all this have done well until this week and after my THIRD radiation treatment I already feel pain and stiffness. I have 5 1/2 weeks to go. I just googled fibro + radiation and go directly to this site. I'm glad to know there is a link and that I need to address it in treatment and not just suffer through the symptoms. Thanks for all your posts.
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I have fibromyalgia and had breast cancer surgery for stage 1 Sept 2011, followed by radiation. Chemo was not nec as field was negative and nodes were negative. I was suppose to have 21 rounds of radiation. The last 4 radiation appts are called boost appts. I had one boost and it stopped me completely form functioning. I consulted with the Dr. who wanted me to continue but I knew I could not so I opted out of the last 3 appts. Prior to the cancer surgery, I had reduced my full time work to 30 hrs / wk. Since the surgery and radiation, my bad days are increasing. I've just gone though a physical therapy appt because the fascia around my left breast is so tight, I have limited range of motion. The PT appt has hit me like a brick wall. I have only been out of the house 1 day since. AM continuing to rest and do mild stretching and marching in place because they say mild exercise helps. Let me know how your treatment progresses.
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Hello, I would like to hear from women who have fibromyalgia and did well with the radiation. Seems like there are more stories of people who had difficulty with the rads. I am trying to make the decision about doing radiation or getting a larger margin with a second lumpectomy and avoiding the radiation. My DCIS was small 5 mm, but grade 3. I've had fibro for 30 years, managed well with exercise, etc.
Thank you.
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I was just dx with stage 1 idc and am facing 5 weeks of radiation treatment. I am concerned with being able to work (I'm a 2nd grade teacher) while receiving rads. Wish there were more posts here for input.
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