Neuropathy treatments
What is there in the medical pipeline for treatment of neuropathy after all present medicines
have lost their punch???
Comments
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I think there should probably be another forum on the topic of neuropathy and how to treat it..
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I am currently on Neurotin for it. They might give me Lycria. B12and co-enzyme Q10 is supposed to help, but I did not notice a difference. The co-enzyme Q-10 is expensive. This is all I know about.
Hopefullt someone else knows more, good luck.
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I, too, am really concerned about neuropathy. Haven't started chemo yet, & oncol. has recommended agressive Dose Dense, even though my b.c. is Stage 1 & 2 (have in both breasts), Grade 2A, & I had bi-lateral mast. 6/29. I have been on neurontin for over 10 years for other, non-chemo/cancer related neuropathy, so am really afraid of exaccerbation of this problem. I am hoping someone can tell me their experience with Dose Dense chemo & its side effects. BTW, Trader Joe's sells COQ10, as does COSTCO, at fairly reasonable prices. Hang in there ...and God Bless Us Everyone!
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SOCAL and others, I have peripheral neuropathy in hands and feet from chemo, it was just your generic ACT, with the Taxol giving it to me. But it's supposed to go away within a couple months. Numbness really doesn't bother me much, I drop things more. The swelling is more annoying. I massage my hands and feet to perhaps keep the nerves "alive" since swelling locks them off, I presume. Coolish water helps with discomfort. Could be an online peripheral neuropathy organization might have some tips on drugs for it and so forth.
MA I think you will like Lyrica, I have taken both Neurontin and Lyrica, and like L much better, I also take it for other nerve pain issues from a busted-up back. I don't know if it helps or not, haven't paid attention, it's on board all the time so... post-chemo leg bone pain is driving me up a wall more than anything else, takes a lot of opiates to kill it, but it's not related to the ever-present neuropathy. GG
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Thyanks for the comments about Lycria, gives me hope.
I thought that it was the Taxenes like Taxotere and Taxol that did the neuropathy, not the Dose dense AC. I'm I wrong? I had the Taxotere/Carboplatin 1st round and am on Taxotere again. In between it improved to only my right foot tripping me every now and than.
cydsong, did you find the Q-10 helpful? I didn't notice a difference after 1 month. They also say B12 is helpful.
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I too thought it was caused by Taxotere (what isn't) - I've had my neuropathy for three years now and mostly it's out of my mind but there are days when it flares up and I get pretty ticked off - it can make walking fast difficult on those days - it affects my hands somewhat too and I do drop more things in the kitchen and of course the swelling is in my hands (I need all my rings re-sized but with gold at an all time high don't know when that's going to happen). I tried neurontin - way too powerful a drug for me I slept for 20 hours, onc agreed not a good idea, then tried B-12 - nothing happened - I haven't tried anything else - I seem to metabolize drugs too well so I'm waiting to see if something comes on the market unless anyone has any more good ideas - I wish I'd been told before treatment - I sure would have rather had Taxol.
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I took amytrptoline, neurtontin and have been, on Lyrica now for five years, but it is either not working as well, or my neuropathy is getting worse..
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socalllisa, If your is getting worse and you are not on a Taxene, than go to your family doc. There are other causes of neuropathy like diabetics, etc.
208sandy, It is very frustrating when walking and the feet fail to move and you almost fall flat on your face.
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Oh mine is from paraneoplastic syndrome set off by my T cells attacking my nerves
instead of the breast cancer tumors...
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Sorry to hear that socall lisa, that sucks.
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It would be nice to find something that helps. I've been on neurotin for 2.5 years. It helped for awhile but now it is slowly getting worse. I haven't tried Lyrica. I'm sure it cost more & I am stretched to my limit now on meds. NJ
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NJ,
try going to the Lycria web site and see if they would help with the cost. Most drug companies will.
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Norma June, I'm on Medicare, I have AARP drug program as part of Medicare, and they are one of the few groups who pays for Lyrica, gotta love those AARP folks. I forget the exact cost, but it's one of those $10, $20, $50 co-pay numbers. On the bottle, it says "Pregabalin," the generic name, so for all I know, I'm now getting generic, altho I thought Lyrica was Lyrica and didn't have generic, so at one time it was SO expensive for me. But I bit the bullet until I was finally eligible and put on Medicare. But in the meantime, they can always up the dose on Neurontin for you, might make a difference. I never could stick with it, upset my tummy something fierce and I have Irritable Bowel to begin with. But you know what, this whole "Drug War" thing is preventing me from getting the REAL pain relief I need, docs are so reluctant to goof up their legal lists of opiate drugs they hand out. I'm seeing my neurologist in September for my biyearly checkup, and I'm gonna keep Lyrica, but BEG him to give me a drug that will wipe me out and wipe out the pain, sometimes I feel like I might throw up from the constant discomfort. Oh, dear, I've gone on too long. Well, just wanted to share with you all that I know. GG
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I have neuropathies from my MX and injuries. VA has case studies about elavil for nerve pain. You can start at really small doses and get pain meds with it, it has taken 8 months but my family doc and ONC think we have the right mix. I have been able to decrease my pain meds and take ibuprofen in between...my pain meds are down to twice a day from 6 times a day.
I take most of my meds at bedtime, docs are so afraid to order stronger meds, but sometimes one needs that to get relief and figure out what works. There are things that can be prescribed to help the pain meds work better like a low dose sedative/ tranquilizer.
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