Neuropathy

CathyHorner

I'm over 4 months done with chemo/rad. From time to time and today ALL day my feet will tingle. It doesn't hurt and I can walk just feel weird like they are falling asleep. I remember being warned about neuropathy. We were mostly worried about my hands because I play guitar. ANy experience with this and does it eventually go away?

KB56

Neuropathy

Cathy, I've experienced similar feeling in my left leg and foot (all my cancer/treatments were on my right side) And told my wife it felt like my leg and foot were asleep.   it happens randomly and seems to be less frequent now than it was  a few weeks ago. I'm seven months out of treatment tomorrow.   

my right vocal cord was/is paralyzed and I'm dealing with a long thoracic nerve issue now and have "frozen shoulder" that I'm doing some exercises to help free it up.  All of the other issues are my right side where the cancer was but it's definitely my left leg and foot that seem asleep at times which just seems wierd.  But the vocal cord paralysis, long thoracic never and the leg issue all seem to be nerve related. 

It will be interesting to see what others say.  

 

Keith

dunedintech

Stretching

Sorry to hear about the tingling. Not sure if this will help but I have found Pilates very helpful in reducing the tingling. So much so I now have none and I am 8 months post treatment. Failing that, running / walking or any exercise to stimulate the nerves may help. Good luck. 

CPC

fishmanpa

Learning to live with it

Hi Cathy,

I too was worried with getting Cisplatin. Being a musicain (guitar, vocals) neuropathy and hearing loss concrned me. I had no issues with hearing and my voice, while a bit different due to the surgeries, is Ok and getting stronger. I do have neuropathy in my feet but fortunately not my hands. I also developed RLS. My feet are basically numb with stabbing pains added for good measure. It feels as if I'm walking on buched up socks all the time. I was put back on Gabapentin (300x3) and it has alleviated the stabbing pain and RLS. I was told it's permanent. 

Positive thoughts and prayers

"T"

 

phrannie51

I have it...

hands and feet....but no pain.  Like T said, in my feet it just feels like my socks are wrinkled (they never are, and I seem to always check)....my hands are more of a pain in the bootie.....they have basically no feeling except for tingles to the first knuckle, and then it lessens further down into my hands....my thumbs are numb almost the whole way.  I think I'm getting used to it pretty much, tho it's still hard to tie my shoes if I'm not watching exactly what I'm doing....and changing the bed is a real time consumer because I can't get a real hold of the sheets or feel the difference between a blanket and a sheet.

Oh....my husband says my dish washing skills have gone downhill, but I don't see him asking to take over the job .  I think imy neuropathy is here forever.

p

osmotar

phrannie51 said:

I have it...

hands and feet....but no pain.  Like T said, in my feet it just feels like my socks are wrinkled (they never are, and I seem to always check)....my hands are more of a pain in the bootie.....they have basically no feeling except for tingles to the first knuckle, and then it lessens further down into my hands....my thumbs are numb almost the whole way.  I think I'm getting used to it pretty much, tho it's still hard to tie my shoes if I'm not watching exactly what I'm doing....and changing the bed is a real time consumer because I can't get a real hold of the sheets or feel the difference between a blanket and a sheet.

Oh....my husband says my dish washing skills have gone downhill, but I don't see him asking to take over the job .  I think imy neuropathy is here forever.

p

Same here

Same here, except not in the hands .. only place on right foot under the 2nd toe..not bad but your discription of wrinkled sock is exactly how I told foot doc, he has me on a low dose of gabapentin which I take before bed...and yes I think it's here to stay 

Roar

I have it in my feet

It has gotten much better- I am 13 months past treatment- it was very bad first 6 months- since I began working out seriously it subsided substantially but is still there. When I get into those zones where I don't work out at all it definitely gets worse again- moral of the story- " I think exercise helps"