Anyone here dealing with peripheral neuropathy?
Anyone here dealing with peripheral neuropathy?
Interested in more discussions like this? Go to the Neuropathy Support Group.
Anyone here dealing with peripheral neuropathy?
Interested in more discussions like this? Go to the Neuropathy Support Group.
I WAS "SHOCKED"? TO SEE SO MANY ON THE DIGEST ASKING ABOUT,AND,OR,TAKING MARIJUANA.! WHY??
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
Apparently you do NOT have much pain. Please do not be shocked that we do and want to have less pain in our lives.
@medic7054, you may be interested in these discussions:
https://connect.mayoclinic.org/discussion/cbd/
https://connect.mayoclinic.org/discussion/chronic-pain-2bd75e/
I do, primarily in my feet and ankles. Responding to the question asking if anyone deals with peripheral neuropathyu.
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?
why do you say that?
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?
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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2 ReactionsAll the time with my MS. I have to wear Prisms in my glasses.