NeuroTalk Support Groups - Chemo Neuropathy

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tomboy mel

04-15-2013 09:39 AM

Chemo Neuropathy

I have peripheral neuropathy due to taxotere and an aromatase inhibitor according to my oncologist. I have been embarrassed about the constant pain since my doc poo pood the situation at first. It took a year before I saw a neurologist who confirmed the small nerve pain.
After surviving breast cancer and all that that entails, I cannot understand why I felt ashamed to admit that my hands and feet buzz with pain constantly. I am taking Lyrica. I also juice green vegetables.
Any other suggestions?

mrsD	04-15-2013 09:47 AM

Welcome to NeuroTalk:

If you come and visit our PN forum (peripheral neuropathy) we have discussions on what may help chemo induced PN.

Just type in "chemo" to our search there and the posts discussing it will be listed.

http://neurotalk.psychcentral.com/forum20.html

Darlene

04-16-2013 01:15 AM

Nice to meet you!!

http://dl8.glitter-graphics.net/pub/...hfu88kseah.gif

tomboy mel,

:Wave-Hello: It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray:

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