Anyone here dealing with peripheral neuropathy?

Posted by rabbit10 @rabbit10, Apr 9, 2016

Anyone here dealing with peripheral neuropathy?

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I WAS "SHOCKED"? TO SEE SO MANY ON THE DIGEST ASKING ABOUT,AND,OR,TAKING MARIJUANA.! WHY??

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@ujeeniack

I WAS "SHOCKED"? TO SEE SO MANY ON THE DIGEST ASKING ABOUT,AND,OR,TAKING MARIJUANA.! WHY??

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I believe it was Dr. Sanjay Gupta that did a 3-part special on marijuana for TV. Most interesting - evidently, there is a lot of research going on in its use medically - especially in UK. I think (just my opinion) that use of anything has to be geared to many things - the individual's ability to tolerate pain, tolerate the drug prescribed to provide less pain,, etc. I think what we all want is to identify a cure and while the treatment of symptoms seems to be the trend, the CURE is still a mystery.t

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Apparently you do NOT have much pain. Please do not be shocked that we do and want to have less pain in our lives.

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@medic7054

I have had Idiopathic Peripheral Neuropathy for about 10 years (am currently 70). It started shortly after I suffered a neck injury and subsequent 3 level cervical fusion. It started with unbearable burning/tingling in both feet progressing to severe pain/numbness in both feet. I also get severe shooting pains emanating from both feet. I currently take Lyrica (300 mg 3-4 times daily (a lot), and Cymbalta 25 mg daily as well as Tylenol and Advil as needed. I also took Morphine 25mg daily and Tramadol (can't remember dose) for 8 years until going thru Mayo's Pain Rehab program a year ago. They got me off the Opioids and taught me alternative ways to manage/cope with my pain. Coping with pain sounds easy until you are the one having it. I do pretty well with that, but my pain limits my activity level a lot. My primary physician has recommended medical marijuana and I have been referred to a center. Have ANY of you tried Marijuana for your pain? If so, I would love to get your opinions on it.

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I do, primarily in my feet and ankles. Responding to the question asking if anyone deals with peripheral neuropathyu.

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I'm still wondering why the RLS discontinued in my legs and moved to my arms. I don't really understand it. Does anybody else have it in their arms?

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@medic7054

Apparently you do NOT have much pain. Please do not be shocked that we do and want to have less pain in our lives.

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why do you say that?

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@jimhd

I do, primarily in my feet and ankles. Responding to the question asking if anyone deals with peripheral neuropathyu.

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Welcome to the group. I have had it since a neck injury 10+ years ago. What do you take for it? Have you ever considered Medical Marijuana?

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@mfelton

ginny, I take a multi vitamin B called Nerve Renew that helps some, however I have found a pain pill (hydrocodone) to be the best treatment for me. The Nerve Renew was recommended by the Neurologist and I order it from Neurophy Treatment Group in Indiana over the Internet.

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I know Hydrocodone helps your pain as do all Opioids. I took it for quite awhile as well, BUT.......it's a slippery slope. Soon, the original dose needs to be increased, increased again, and again. Mayo has an excellent Pain Rehab Center that helped me a lot. If you live near one of their clinics, I heartily recommend it. .

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All the time with my MS. I have to wear Prisms in my glasses.

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