← Return to Dose anyone else feel like neuropathy is taking over their life?

Discussion

Dose anyone else feel like neuropathy is taking over their life?

Neuropathy | Last Active: Aug 2, 2023 | Replies (82)
Comment receiving replies
@nanuk2386

I do use marijuana. That is the only way for me to get real relief. It's really odd because for an hour or so, my joints and that type of issue hurts worse. BUT!!! the relief I get where my feet stop sweating and freezing while in pain, get red and warm and in pain. ha ha. That is the best it gets. By Counselor, are you meaning like psychiatrist? My PCP just said that she cannot work on anxiety due to the other meds for pain. It sounds like that is a route I may have to go.
Thank you for all of your help and support!!!
Thank you,
T

Jump to this post

Replies to "I do use marijuana. That is the only way for me to get real relief. It's..."
gvkmnj | @gvkmnj | Apr 18, 2023

I wonder if my waking up in total bodywide sweats is akin to your feet. I get hot/cold almost within the same 60 seconds. I have that burning all the way up from my feet to my waist. I also have tingling and the weird almost electrical shock feeling, worse in my right hip.

I don’t say a psychiatrist , but a knowledgeable counselor who can help you sort out the steps. You need to establish a way to get disability; talk with people who know the way to make it happen. There are things we never hear that are well known to those people on the inside

I am not sure I understand about MJ, I really need to learn about it and what it will do. Also, my lungs are shot, so I cannot smoke, need chewies.

Gen

VIEW AND REPLY