Living with Neuropathy - Welcome to the group
Welcome to the Neuropathy group.
This is a welcoming, safe place where you can meet other people who are dealing with neuropathy. Let’s learn from each other and share stories about living well with neuropathy, coping with the challenges and offering tips.
I’m Colleen, and I’m the moderator of this group, and Community Director of Connect. Chances are you’ll to be greeted by volunteer patient Mentor John (@johnbishop) and fellow members when you post to this group. Learn more about Moderators and Mentors on Connect.
We look forward to welcoming you and introducing you to other members. Feel free to browse the topics or start a new one.
Let’s chat. Why not start by introducing yourself? What concerns would you like to talk about?
Interested in more discussions like this? Go to the Neuropathy Support Group.
Bruce Kelso. I have and are suffering pain from Neuropathy.
I'm taking vitamin B and other supplements. Exercising every day, seemed to help for a long time.
but not as much now. Pain is getting worse.
Welcome @p9n8, I'm sorry to hear your neuropathy pain is getting worse. I also taking supplements to help my small fiber peripheral neuropathy. I shared my story in the Member Neuropathy Journey Stories: What's Yours? discussion here - https://connect.mayoclinic.org/comment/310341/
Do you mind sharing a little more about your neuropathy diagnosis and how long you've had neuropathy?
thanks and yes!
Hello, Bombas does have well made cushion socks. Although, I typically wear the gripper socks as the grippers offer padding and I like the way the sort of massage my feet.
I understand. I have found that they last very well. I wear them daily and have had my pair for over two years.
And for you !
So far that has been a big help for sleeping. I completely agree!
I have had this for 3 years now and it’s getting worse with a lot of pain in my feet. Are they any experimental treatments that show any promise?
Welcome @davelobb12, Sorry to hear your neuropathy pain is getting much worse now after 3 years. The only fairly new one I'm aware of that shows some promise is the clinical trial for WST-057 (4% pirenzepine free base monohydrate) from WinSanTor.
"Treating Peripheral Neuropathy
The hope is that these new findings support the potential for select anti-muscarinic drugs already on the market, like pirenzepine, to be repurposed as a possible preventative, and even treatment, for the clinical effects of peripheral neuropathy, which, for patients, has been largely been a matter of pain relief, and associated with significant health care costs." — Blocking Anti-Muscarinic Drugs May Reverse PN: https://winsantor.com/anti-muscarinic-drugs-may-reverse-peripheral-neuropathy/
WinSanTor’s lead compound, "Treating Peripheral Neuropathy
The hope is that these new findings support the potential for select anti-muscarinic drugs already on the market, like pirenzepine, to be repurposed as a possible preventative, and even treatment, for the clinical effects of peripheral neuropathy, which, for patients, has been largely been a matter of pain relief, and associated with significant health care costs." — Blocking Anti-Muscarinic Drugs May Reverse PN: https://winsantor.com/anti-muscarinic-drugs-may-reverse-peripheral-neuropathy/
WinSanTor’s lead compound, WST-057 is the topical containing pirenzepene – https://winsantor.com/pipeline/
More info on the Phase 2 clinical trial page – https://clinicaltrials.gov/ct2/show/NCT04005287 is the topical containing pirenzepene – https://winsantor.com/pipeline/
More info on the Phase 2 clinical trial page – https://clinicaltrials.gov/ct2/show/NCT04005287
Have you made any lifestyle or diet related changes to see if they might provide a little relief?
Yes all the usual suspects like Vit B and Alpha Lipoic Acid…I swim to get some exercise but getting harder to walk as time goes on. THC helps me sleep at night but I need relief during the day. Very discouraging!