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.

My 79 year old mother is dealing with neuropathy. I see commercials daily about clinics for neuropathy. Are these legit or snake oil?

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@soonerchris

My 79 year old mother is dealing with neuropathy. I see commercials daily about clinics for neuropathy. Are these legit or snake oil?

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Hi @soonerchris, Welcome to Connect. My vote leans toward snake oil but then I'm no medical expert. It's good that your mother has you to help her navigate this condition. There is another discussion on neuropathy clinics that you might find helpful here:

-- Neuropathy Clinics: https://connect.mayoclinic.org/discussion/neuropathy-17/

A couple of legitimate sites to learn more about neuropathy and treatments:
-- Neuropathy Commons: https://neuropathycommons.org/neuropathy/neuropathy-overview
-- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/

Has your mother been diagnosed with neuropathy and on any treatments?

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Hi Everyone,
so glad to find a place to learn about this awful condition.
Elder gal just wondering how I'm going live with this.
Look forward to meeting you.
Recently diagnosed with P
Neuropathy.
MMK

.

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@mmksf

Hi Everyone,
so glad to find a place to learn about this awful condition.
Elder gal just wondering how I'm going live with this.
Look forward to meeting you.
Recently diagnosed with P
Neuropathy.
MMK

.

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Hi MMK @mmksf, Welcome to Connect. I'm sure you have a lot of questions and you've found a nice safe place to meet others that share your symptoms and concerns. You are definitely not alone. There is another discussion that you might want to read through where members have shared their neuropathy journey.

-- Member Neuropathy Journey Stories: What's Yours?
https://connect.mayoclinic.org/discussion/member-neuoropathy-journey-stories-whats-yours/.

There are also some good sites to learn more about neuropathy that you might want to get familiar with:
-- Foundation for Peripheral Neuropathy - https://www.foundationforpn.org/living-well/
-- Neuropathy Commons: https://neuropathycommons.org/neuropathy/neuropathy-overview

What is your most difficult neuropathy symptom to manage?

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@johnbishop

Hi @soonerchris, Welcome to Connect. My vote leans toward snake oil but then I'm no medical expert. It's good that your mother has you to help her navigate this condition. There is another discussion on neuropathy clinics that you might find helpful here:

-- Neuropathy Clinics: https://connect.mayoclinic.org/discussion/neuropathy-17/

A couple of legitimate sites to learn more about neuropathy and treatments:
-- Neuropathy Commons: https://neuropathycommons.org/neuropathy/neuropathy-overview
-- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/

Has your mother been diagnosed with neuropathy and on any treatments?

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@johnbishop see's seeing a neurologist and is currently on Lyrica but still having pain and numbness. I've done some reading about The Protocal 525 and some of the other mineral and vitamin products. We ordered one of these but not The Protocol as I just read about it after ordering the other.

I'll do some more research and steer her away from a clinic.

Thanks for the info.

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@mmksf

Hi Everyone,
so glad to find a place to learn about this awful condition.
Elder gal just wondering how I'm going live with this.
Look forward to meeting you.
Recently diagnosed with P
Neuropathy.
MMK

.

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My name is Gary and I am 77 years old. I was diagnosed with idiopathic peripheral neuropathy 12 years ago and was told if it begins in a mild form it generally stays that way. Conversely if it begins aggressively it gets progressively worse. Is this true. My tingling and burning in the toes has progressed to mild electric shocks in the lower legs with stiffness and mild weakness in the quads. I have been taking Metanx for the entire time. Embarrassed to say I am not sure it works. A herniated lumbar disc with stenosis and radiation down the leg has come and gone a few times. Walking a few miles everyday no matter what has made the difference. Not sure what future holds

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@gbrodnan1945

My name is Gary and I am 77 years old. I was diagnosed with idiopathic peripheral neuropathy 12 years ago and was told if it begins in a mild form it generally stays that way. Conversely if it begins aggressively it gets progressively worse. Is this true. My tingling and burning in the toes has progressed to mild electric shocks in the lower legs with stiffness and mild weakness in the quads. I have been taking Metanx for the entire time. Embarrassed to say I am not sure it works. A herniated lumbar disc with stenosis and radiation down the leg has come and gone a few times. Walking a few miles everyday no matter what has made the difference. Not sure what future holds

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My diagnosis is PNS.
I understand the tingling and burning that you are experiencing. To start, I am sorry to here of your condition. I was unable to walk. My neurologist prescribed low doses of Lamictal and increased milligram slowly. 15 years after the onset of this condition rarely do my feet burn. I continued my care with the Neurologist that first started my case.
Wishing you the best.

@Hopefully53

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@gbrodnan1945

My name is Gary and I am 77 years old. I was diagnosed with idiopathic peripheral neuropathy 12 years ago and was told if it begins in a mild form it generally stays that way. Conversely if it begins aggressively it gets progressively worse. Is this true. My tingling and burning in the toes has progressed to mild electric shocks in the lower legs with stiffness and mild weakness in the quads. I have been taking Metanx for the entire time. Embarrassed to say I am not sure it works. A herniated lumbar disc with stenosis and radiation down the leg has come and gone a few times. Walking a few miles everyday no matter what has made the difference. Not sure what future holds

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HELLO GARY,
I WISH I COULD OFFER YOU INFO, WITH REGARD TO.NEUROPATH
BUTI HAVE ONLY RECENTLY BEEN DIAGNOSED WITH NEUROPATHY
AND I AM SQUEAKY BRAND NEW TO THIS CONDITION. I DO HOPE OTBERS ON THIS SITE WILL BE ABLE TO ASSIST YOU.
MY BEST WISHES TO YOU THAT YOUR PAIN IS BROUGJTNTO.AN END.SOON!
BEST OF LUCK GARY,
MMKSF

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@ottosnanny

Nothing specific to the psoriatic arthritis has been brought up. I had a virtual appointment during covid with a dermatologist and the report was sent to my primary care doctor.
That included a diagnosis of psoriatic arthritis.Withh topical meds I managed the psoriasis on scalp, ears and body and have maintained good results until about a week ago. The flare up is psoriatic arthritis primarily. I just don't want to have to start a new diagnosis and treatment. It just feels overwhelming. I want to thank you for the sites you recommend. I'm going to read them. You see I'm 81. Im diagnosed with PTSD, ADHD, major depressive disorder and anxiety. To add psoriasis and psoriatic arthritis and new regimens is overwhelming.
Many thanks, Otto's nanny

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I am 64 post head and neck cancer. 8.5 weeks of chemo/radiation has triggered plaque psoriasis (entire body) resulting in PA. I have a lot of collateral damage. I too have PTSD/Anxiety. If you are a veteran, the VA might be able to help. The VA has a few different studies ranging from HBOT (Hyperbaric Oxygen Therapy), microdosing MDMA, microdosing psilocybin with very promising results. The AMA and insurance makes HBOT almost impossible to get treatment or out of pocket is about $1000 per treatment and the total treatments are about 30. I feel for you brother, you are in my prayers.

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@gbrodnan1945

My name is Gary and I am 77 years old. I was diagnosed with idiopathic peripheral neuropathy 12 years ago and was told if it begins in a mild form it generally stays that way. Conversely if it begins aggressively it gets progressively worse. Is this true. My tingling and burning in the toes has progressed to mild electric shocks in the lower legs with stiffness and mild weakness in the quads. I have been taking Metanx for the entire time. Embarrassed to say I am not sure it works. A herniated lumbar disc with stenosis and radiation down the leg has come and gone a few times. Walking a few miles everyday no matter what has made the difference. Not sure what future holds

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This neuropathy affects us all so differently, and some have accompanying spine issues, others like me do not. My idiopathic PN slapped me very quickly; one day my legs felt weak, then 10 days later I was in a wheelchair, with minimal hand function as well. I lived in the wheelchair for 6 months, before aggressive PT helped me build muscle strength and regain balance. I use my walker when out, but today can walk unassisted short distances and even drive. I still have bad neuropathy and take Gabapentin to help make it tolerable, but hands down, I got better from where I started, not worse, and have been at this plateau for a few years.Like many others here, what I’m trying to do is maintain strength and energy to do anything we might be able to control to maintain our current state and not get worse. Think positive, and borrow from the tips from this group to see what you might be able to do to help stop the slide!

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