Peripheral neuropathy : My CIPN started... - SHARE Ovarian Can...

SHARE Ovarian Cancer Support

2,800 members994 posts

Peripheral neuropathy

kdffol profile image
7 Replies

My CIPN started a year ago right after my last chemo treatment. It seems to be getting a bit worse now. Any hope for it improving at this point?

Written by
kdffol profile image
kdffol
To view profiles and participate in discussions please or .
Read more about...
7 Replies
Teal810 profile image
Teal810

Acupuncture helped me. I also saw an occupational therapist for my hands which was a major help.

kdffol profile image
kdffol in reply toTeal810

How long after your neuropathy started did you have the acupuncture? I'm almost a year out and have been told it won't help at this point. Thank you for responding.

Archeveritas profile image
Archeveritas

My hands recovered but my feet got worse as time passed. I have learned to live with it. No tight shoes. Comfort is the name of the game. I tried acupuncture, medication, and vitamins but nothing worked for me. Everyone responds differently. I just look at it as a small price to pay to still be here. I would say to try acupuncture and Gabapentin (spelling?) and see if they work for you.

Here2Day profile image
Here2Day

I had neuropathy almost immediately after I finished chemo. It was milder than what I heard others suffer. But it did get increasingly worse, so I asked my doctor to send me for Physical Therapy. There is a PT place near me that uses a machine that stimulates the nerve endings (I forget the name of it, but it's like a TENS unit, only different). That, in combination with actual physical therapy exercises, Vitamin B-6, and also CBD creams have been tremendously helpful. It's keeping it at bay for now, thank goodness. Maybe you can ask your doctors about these options.

Greytmom profile image
Greytmom

I have been on chemo and had neuropathy for the past 5 years. Acupuncture helps immensely as does massage. Hopefully you can find an acupuncturist who deals with cancer treatment. Mine is through the Roy and Patricia Disney Cancer Center. I really notice how much it helps when for one reason or another and I am unable to make my appointment. Ideally I try to get it twice a week. Hang in there.

kdffol profile image
kdffol in reply toGreytmom

Thank you for your reply. Totally off topic I'm guessing you have greyhounds. Had two several years ago...best dogs ever!

Greytmom profile image
Greytmom in reply tokdffol

Yes I have rescues. I love them and they bring such joy to me.

Not what you're looking for?

You may also like...

Chemo induced peripheral neuropathy with Ovarian Cancer

Does anyone have a successful treatment to at least alleviate CIPN? I do NOT have pain, but rather...
Kilorpt profile image

Neuropathy. No taste.

Hi all I just finished six rounds of carbo/taxol and I’m done. I’m experiencing neuropathy in my...

Neuropathy - how did you deal with it?

Many of us experience neuropathy especially during our first line treatment of carboplatin and...
GwenHP profile image

Stage 3c low grade serous cancer tumor pressing against my colon

I am 46 years old diagnosed with stage 3c serous low grade cancer in 2015. I had a debulking...
LDBottoms profile image

Got my CT results today

I previously posted "Possible Recurrence - Beyond Scared. Well, I got my CT results yesterday. I...
SDlady profile image

Moderation team

See all
Jslanovich profile image
JslanovichAdministrator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.