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NeuroTalk Support Groups (https://www.neurotalk.org/)
-   Peripheral Neuropathy (https://www.neurotalk.org/peripheral-neuropathy/)
-   -   Vicks Vapor Rub and Neuropathy (https://www.neurotalk.org/peripheral-neuropathy/24143-vicks-vapor-rub-neuropathy.html)

glenntaj 05-05-2009 06:01 AM
Cyano--
 
--refers to the cynadie chemical radical that is attached to the cobalamin portion of the B12 molecule in most commercial B12 preparations.

This is the cheapest way to supplement cobalamin (which, by the way, is so named because it has a cobalt atom in its chemical structure), and while cyanocobalamin supplementation does work for many people with B12 deficiency, there are some who have trouble chemicaly removing the cyanide radical and then methylating the cobalamin portion in order to make it usable by the body. Such people should always take methylcobalamin or other activated B12 form.

And, since methylcobalamin is now readily available and not really expensive, there's no reason those of us who need supplementation, or merely want it, to not get it--who wants a cyanide radical running around the body anyway? :D

MelodyL 05-05-2009 09:05 AM
Glenn:

thank you SO much for explaining the cyano thing. I read her post and when she said she used Milk Thistle (I know what that is), to get the cyano out of her liver, I said to myself "There's cyano in my liver, but I take Methyl B-12".

So is it safe to assume that because I take straight Methyl B, that I don't get cyano in my liver and I don't have to take milk thistle?

Thanks much Glenn.

Melody

mrsD 05-05-2009 09:29 AM
I have a long explanation on cyano and other forms of
B12 on the new B12 thread in the stickies above.

Most of the general info on this subject is there now.
http://neurotalk.psychcentral.com/thread85103.html

Tell me if there is something else I should add.

Stephen Comency 03-05-2015 12:52 PM
Vaporub & Neuropathy in Feet
 
Hi everyone,
I've dealt with severe peripheral neuropathy pain for 10 years. Lyrica works somewhat but its side-effects are annoying. In 5 years on Lyrica I have gained 40 lbs. Anyway, at night I would usually resort to Icy-Hot, Ben-Gay or some other ointment to try and alleviate my pain. For the most part the didn't work and I experienced countless sleepless nights of severe foot pain/twitching. Last week I ran out of ointment and tried Vicks Vaporub on my feet for the first time. I slathered both feet and put on loose socks and had the most restful night of sleep in years. Every day since I apply Vicks after my morning shower and before bed, I've been virtually pain free and sleeping like a baby since. I know there are several different kinds of neuropathy and this may not work for all but it worked for me. Try it, but don't be stingy, lay it on thick and wear loose socks. I hope you have as much luck with it as I did. All the best, Stephen

MelodyL 03-05-2015 01:09 PM
Quote:
Originally Posted by Stephen Comency (Post 1127653)
Hi everyone,
I've dealt with severe peripheral neuropathy pain for 10 years. Lyrica works somewhat but its side-effects are annoying. In 5 years on Lyrica I have gained 40 lbs. Anyway, at night I would usually resort to Icy-Hot, Ben-Gay or some other ointment to try and alleviate my pain. For the most part the didn't work and I experienced countless sleepless nights of severe foot pain/twitching. Last week I ran out of ointment and tried Vicks Vaporub on my feet for the first time. I slathered both feet and put on loose socks and had the most restful night of sleep in years. Every day since I apply Vicks after my morning shower and before bed, I've been virtually pain free and sleeping like a baby since. I know there are several different kinds of neuropathy and this may not work for all but it worked for me. Try it, but don't be stingy, lay it on thick and wear loose socks. I hope you have as much luck with it as I did. All the best, Stephen
Hi.

I just read your post and showed it to my husband who announed "Son of a B", I'm trying that tonight.

Will update. lol

And thanks much

Melody

Enna70 03-05-2015 01:23 PM
My two cents
 
I had to stop using noxema YEARS ago, guessing it was the menthol. It was horrible both for my skin (having to give it up), but worse on my nerves...so I had to do it....

Kitt 03-05-2015 01:51 PM
Welcome Stephen Comency. :Wave-Hello:

MelodyL 03-05-2015 04:11 PM
Quote:
Originally Posted by Kitt (Post 1127669)
Welcome Stephen Comency. :Wave-Hello:
Isn't it amazing how all these lotions, potions and meds affect people SO differently!!!!

Melody

zkrp01 03-06-2015 12:44 PM
Mortons Epsom Salts Lotion
 
Quote:
Originally Posted by rfinney (Post 126372)
Lot so folks have made good points here. I also have a severe small-fiber neuropathy. I can't allow anything at all to touch the top of my feet. And of course it is nonsense that Vick's or anything like it can "cure" neuropathy. However, there are many shades in between "cure" and no relief whatsoever. As Glenn indicates, Vick's has menthol in it. And I find that menthol does provide a small measure of relief - many times it won't last very long - but it can help just to break up unremitting pain for even a little bit.

I have searched extensively to find as many little things like that. I have assembled a bag of tricks, as I call it, that I use as needed to help manage my overall situation. Does it eliminate the need for medications? - unfortunately not. But in addition to whatever actual relief I get, I also get a feeling, even if it's just an illusion, of increased control over my life. And I do mean life, not control over the pain. I don't want to fight that battle - can't win . . . it does feel like I am least not losing when it comes to life and usually much better than that.

rafi
is perhaps the only thing I have found that is not illusionary for the tops of my feet that scream at bedtime. Good Luck, Ken in Texas.

caroline2 08-25-2015 06:38 PM
I just posted about Vicks that I use for my Osteoarthritis feet and then thought about the neuropathy and looked and found this NT thread. Guess some have tried it and then I read about the statin drugs and thought of one of my non-computer friends, she has been taking statins for 30 yrs and deals with horrific "ideopathic" neuropathy. I just called her and said "you know what has caused your neuropathy, the statins"...so it's not unknown as your doctors have told you. She says that about 4-5 yrs ago her daughter printed out info on statins and neuropathy and she took it to her doctor and he denied the statins are the cause!!!! Soooo many people just don't question their doctors or the drugs, etc. Well, off my soapbox..had to vent a bit.


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