Ive looked at previous posts from the past here and on facebook groups and it always made me wander why there doesnt seem to be much interest in Winsantors drug? But if you post about some kind of frankinscense essential oil cream you get hundreds of replies. This is a serious disease and sorry essential oils …come on! Meanwhile Winsantor has peer reviewed studies you can read online and an article in the lancet….their claim seems to be backed up and no interest from Neuropathy patients. It makes me wonder, I dont understand? No I am not a shill for WinSanTor as previously mentioned I also wonder about them as well. Out of everything I have read or looked into their product is the only thing that gives me some hope. False hope? Possibly but I hope not. I received the email that is in the original post today so I came back to this forum. I can see that their are people here who have had neuropathy for a long time and are aware of WinSanTor. I mean they are pushing a product that claims to regenerate nerves and all I see is dust blowing in the wind. I’m not even fifty years old….my life is ruined because of this disease. Im losing my mobility more each day and am terrified of whatever my future is. I dont know I just dont get it. So I wander is it a carrot being dangled but on the other hand they have data to back up their claims. Perhaps I dont understand the data enough as I am not a medical professional but it darn seems to make more sense then essential oils or apple cider vinegar or what not. Sorry for the rant but there it is and sort of want to get this thread back to the original topic.