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.
Thank you. I’m seeing the doctor on the 30th so I’ll mention it. The worst is at nighttime so my new wake up time is 4 am because I can’t sleep. I take so
Many showers a day because that’s the. Only place I get relief.
Hi, Please hang in there and know in time it will get better. Have you connected with a pain clinic? Also, maybe a place like the Mayo Clinic? I don’t think you have adequate pain relief. I’ve been there many times and I’ve felt desperate. I have nerve pain throughout my body and it is horrible. I took gabapentin and low dose tramadol and ibuprofen for 17 years without ever going over the prescribed amount of tramadol, always under the prescribed amount. I had flares of horrible pain but I could keep it under control. It recently spread throughout my body and I was referred to a major pain clinic. They recommended switching from gabapentin to Lyrica and they also recommended other medications like Cymbalta. I was prescribed an anti-depressant when the nerve pain began 20 years ago. I stayed on it for a year and it really helped me feel like I could deal with the pain.
@mistic -- Have you tried any complementary or integrative therapies? The Foundation for Peripheral Neuropathy has some listed here that may provide some relief - https://www.foundationforpn.org/living-well/integrative-therapies/
Thank you, I will look I to it.
I will check
Into pain clinics. I actually recently stopped taking an antidepressant and I’m doing really well without it so I’d like that to continue. I’m hoping that my neuropathy is reversible but only time will tell.
Be careful with the gabapentin. I too was on 3600 mg which is the top of the recommended dosage. Drink the recommended amount of water. Make sure your doctor (and you) are watching your kidney function via blood work. I now have stage 3 chronic kidney disease probably from pain meds. I had a spinal cord stimulator placed two years ago and it cut my gabapentin in half. I’m sorry you’re suffering from so much pain. I also get that you don’t care about anything else when you’re consumed by pain. Good luck.
My post was lost. Dang. I spilled my guts. Anyway, bottom line is that I’m at my daughters cottage for the summer. My son-in-law is an excellent cook. I eat what I see. Not walking much until after foot surgery next month. Tons of medical diagnoses. So yes, I’ll get back to healthy eating after Labor Day.
Has anyone heard of albation for neuropathy? Does it work? Is there any REAL help out there?
@mjf - I've heard of ablation for neuropathy but haven't read much about it. Here is a discussion from 2017 that discusses the topic and may answer some questions you have:
-- Experience with Radio Frequency Ablation procedures?: https://connect.mayoclinic.org/discussion/experience-with-radio-frequency-ablation-procedures/
Mayo Clinic has some information here - Radiofrequency neurotomy: https://www.mayoclinic.org/tests-procedures/radiofrequency-neurotomy/about/pac-20394931
Have you discussed it with your doctor or care team? Wondering if they had any thoughts on if it would help.
When my husband with Parkinson's had terrible pain in his gut he would take a cold shower and it shocked him out of it.