I have taken this med several times before in my life with no problem, but this time it gave me awful pain in my shoulder and arm. I had to give it a try and within 3 days I felt immediately relief. Feel free to e-mail me at [email protected]'m a 31 yr old guy, finished 12 months of treatment for Hodgkins disease about 9 months ago, had radiation to the abdomen and chemo called frontal hybrid - think it's a more aggressive version of ABVD.Within about 3 months of finishing my treatment I was getting fit again. From the posts that I've read it sounds like these aches and pains don't go away, but maybe can be decreased by exercising, walking. I have been very active all my life and now I feel crippled when I get out of bed to walk.

This at the same time my WBC, hit rock bottom. Dennis. I was also convinced at the time that the cancer had come back but I was fine. But from reading the board its nothing Dr's can do. Neurontin numbs the nerve endings. Thank you for taking the time to read this and I pray for help and feedback. After that, I give up. But at age 54, I feel like I'm 90. I finished chemo in oct 2000 and developed neuropathy in my feet and legs.

I have had the same reactions from doctors. I feel that chemo and radiation gave me a second chance and taught me to slow down and live each day as if it were my last. All this was due to fracturing my hip and back in somolia when I was in the army 11 years prior to that. The aching, throbbing pain would have me in bed for days on end..It has now been six years and the side effects are still here. I'm so tired and ache so badly it's all I can do some days to get out of bed. Whether from taxol or endocrine therapy is ruining my life. I take at least 800-1600 mg of Motrin each day (which my stomach doesn't like) but it doesn't take all the pain away. My shoulders and hands are also sore and my right thumb, index and middle fingers are swollen. One of my many docs finally tried prednisone which wiped it out, so we know it's inflammatory, and my rheumy workup (which was very thorough - the blood labs required 12 tubes of blood!!) We are now in May 2014 and I am still suffering from severe pain in my back at my bra line, my legs, my shoulders, you name it... anywhere there is a joint.

I often talk way to much, I am a bit to clingy at times but I am working on that , I am argumentitive but I am learning to pick my battles wisely these days. The doctor says it is most likely due to the prednisone (steroids). However, I have started to have increasing joint stiffness and pain in hands, knees and hips.

where I was born and raised. !I regret choosing to pursue chemo and am considering ending endocrine therapy despite knowing the … chemo and joint pain 21 Nov 2008 17:51 i was diagnosed with breast cancer a year ago and stated treatment soon as i had surgery, radio and chemo.

I started gabapentin two months ago but it doent work yet. They made it perfectly clear that they aren't interested in the after effects of treatment and that I should be happy to be alive.Would be interested in hearing from anyone who has suffered from similar problems and especially anyone who has managed to find an answer to these problems.Hi my name is noelle.my last chemo was feb 04 my chemo were taxol/carboplatn . If I had known the pain and suffering I have been experiencing since taking that chemotheraphy, I can assure you I would have opted out of the plan and left it in God's hands. I give thanks to God for those of you that have shared the joint/bone pain I have been suffering with for almost five years. I use a brace and sometimes a cane.

I feel the doctor is creating an addict because now if I don't take the 60 mg in the morning, by mid day, I am having withdrawal pains.Breaking out in cold sweats and barely able to do anything but lie in bed or on the couch.

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