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Tingling in feet

Posts: 6
Joined: Jan 2004

I am 37 yo male HD 2A NS patient and I finished ABVD in August 2003 and completed mantle field radiation in October 2003. To date, I have had no tingling of my peripheral nerves except for occasionally waking up at night with my hands "asleep". Within the last week I am experiencing tingling in my legs and feet, usually during/after physical activity. I also have noticed that if I lower my chin to my chest I get an immediate tingling in my legs/feet. Has anyone experienced this, is it associated with Vinblastine?
Thnaks for your help!

Posts: 47
Joined: Jul 2003

I've only had short term loss of feeling in my fingertips when I was taking vinblastine in December 2000 and January 2001. I had an allogeneic bone marrow transplant in May and afterwards I was taking a drug called cyclosporine (up until a couple months ago). Whenever I put my chin to my chest I get a mild tingling sensation down my lower half. That's supposed to go away over time. Talk to your Doc.

Posts: 3
Joined: Jan 2004

yes.....the drug i had was vincristine(or something like that) I'm sure its just a different brand name. I had had trouble walking, my knees felt like they were going to give out.....my DR. cut the med in half....i felt better after that

Posts: 6
Joined: Jan 2004


Did you have these symptoms after chemo? I had chemo back in Aug '03, but the tingling just recently started


truejoy8's picture
Posts: 41
Joined: Jan 2004

I've finished my ABVD but half way through it I too had a numb tingling in just my big toe. But it went away as soon as I stopped chemo. With all the people who posted here before me I'd say there's a good chance it was the Vinblastine or the "V" in ABVD.

Posts: 27
Joined: Feb 2004

I am 31 now, but was diagnosed at 29 with Stage 2A Hodgkins. I finished Chemo (ABVD) 16 months ago and radiation 14 months ago. While I was having Chemo, I had horrible leg cramps that no pain killers or muscle relaxers could help. About 6 months after I had finished Chemo treatment, I started having numbness and tingling in my feet when I would look down or touch my chin to my chest. I told my Oncoligist about it, and she did not seem concerned, she did not know what could be causing it. It went away after about 4 months. I still get really back cramps in my feet at night, but I hear that it is a small price to pay. So, I am not sure what causes it, but at least in my case, it went away.

Posts: 4
Joined: Feb 2004

I thought I was the only one. After a few cycles of chemo, my feet were not even responsive to pain because they tingled so much. My hands were the same way, for days I couldn't feel the tips. I of course thought I was going to lose some fingers and toes because of this, but I read up a little on it, and I think it's normal. I had 8 cycles of ABVD and after the treatments, it seemed as though it was a figment of my mind. I think you can tell your doctor, however, they informed me that there were a certain number of things that are associated w/ this type of chemo that are just routine, and can't be medicated. You will live :-) Hey, we are all survivors here, and this is just a bump in the road. Take care

Posts: 2
Joined: Feb 2004

I too have experienced the same sensations after ABVD and mantle field radiation therapy for HD. My radiologist said that I was experiencing "L'hermitte's Sign" and it is most prominent when I bend my head down or exercise. There is some information out there on it, and people report it lasting from 6 months to 6 years or longer. Mine started about 3 months after radiation and has lasted 18 months now.

I also have some numbness (peripheral neuropathy) in my extremities from the chemo.

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