Red light therapy idiopathic neuropathy numbness tingling

Posted by lindamaegirl @lindamaegirl, Aug 8 11:20am

I have idiopathic neuropathy and the neurologist have pretty much shrugged there shoulders and are doing nothing. I want to try EVERYTHING to get rid of numbness tingling and burning feet. Who out there has what I have and has had success with red light therapy and or compression boots?

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Profile picture for lindamaegirl @lindamaegirl

@cwloeffler thank u for your input. I found one on the top of neurology teams at mass General in Boston and they have done. absolutely nothing for me ?They tell me this will be progressive overtime and we can give you medication for pain. I could not be more disappointed, even though it is idiopathic, which we know means they don’t know the cause I feel that nobody is even trying to discover the cause…it almost feels like they’re shrugging their shoulders. They even said doing the EMG and they would do it if I want it, but it would probably not change the protocol! Why would I put myself through that discomfort for no reason at all ?people in this kind of discomfort are absolutely desperate, I am just looking for some hope …unfortunately the scammers know that and take cash only for what they tell you is a cure. I wish there was somebody out there I could trust who actually had some interest in finding out what the issue was.

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@lindamaegirl I have tried many test to see what caused my neuropathy. Finally figured it out that I have Amyloidosis. Get tested for Amyloidosis from your doctor.

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Profile picture for toejam @toejam

@cwloeffler
I had neuropathy of both legs I'm a diabetic the my provider told me I had neuropathy so I did everything I could to help it the whole thing everything you could think of come find out I had a CT scan on my legs and it wasn't neuropathy at all it was I wasn't getting any blood in my legs which was causing cramping the hold on yards pain and I started taking blood flow and it all stopped so a lot of people think they have neuropathy come and find out it's just you're not getting any blood in your lower part of your body I could get blood fine up at the top but you couldn't even find a pulse in my toe had to reach clean up to the groin to find a pulse so that isn't neuropathy that's no blood going to your things I hope this helps somebody God bless you all

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@toejam
I completely understand your complaint. I too have poor circulation in my legs and feet, but the doctors just dismiss that off-hand as having anything to do with my neuropathy.

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Profile picture for cwloeffler @cwloeffler

I have idiopathic neuropathy in my feet. In addition to a couple of oral supplements and topicals, I've used red light therapy (double boot) for the past 4 months. I try do it three times a week for 15-20 minutes, but have missed a few sessions. So far, I can't say that it has helped much, if at all. Might my neuropathy be a little worse without the red light therapy? Who knows?

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@cwloeffler I have been very successful in treating my PN for years with encapsulated berries from Juice Plus. I take for a day. It takes about 6 weeks to notice the improvement in the circulation. It also improves the circulation in our entire body, it heals on the cellular level. Recently, I added Dynamic Nerve from Stonehenge. It keeps the pain away. When I missed taking it for a few days the pain came back. If you message me I can refer you to someone who understands the healing of the berries. Doctors often prescribe Gabapentin for the pain but it's not healing it's an attempt to stop the pain and it's addictive and the dosage has to be increased as it progresses. Best wishes.

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Profile picture for toejam @toejam

@cwloeffler
I had neuropathy of both legs I'm a diabetic the my provider told me I had neuropathy so I did everything I could to help it the whole thing everything you could think of come find out I had a CT scan on my legs and it wasn't neuropathy at all it was I wasn't getting any blood in my legs which was causing cramping the hold on yards pain and I started taking blood flow and it all stopped so a lot of people think they have neuropathy come and find out it's just you're not getting any blood in your lower part of your body I could get blood fine up at the top but you couldn't even find a pulse in my toe had to reach clean up to the groin to find a pulse so that isn't neuropathy that's no blood going to your things I hope this helps somebody God bless you all

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@toejam low circulation is the cause of the numb feet and legs. Doctors are not trained to do healing but to prescribe meds. Read my journey with my PN and how I am using more healthy treatments. I'm not associated with any product that is mentioned. I'm a retired nurse. The medical profession has a lot to learn and they are slow to see the connections to continued healing. Best wishes.

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Profile picture for lindamaegirl @lindamaegirl

@cwloeffler thank u for your input. I found one on the top of neurology teams at mass General in Boston and they have done. absolutely nothing for me ?They tell me this will be progressive overtime and we can give you medication for pain. I could not be more disappointed, even though it is idiopathic, which we know means they don’t know the cause I feel that nobody is even trying to discover the cause…it almost feels like they’re shrugging their shoulders. They even said doing the EMG and they would do it if I want it, but it would probably not change the protocol! Why would I put myself through that discomfort for no reason at all ?people in this kind of discomfort are absolutely desperate, I am just looking for some hope …unfortunately the scammers know that and take cash only for what they tell you is a cure. I wish there was somebody out there I could trust who actually had some interest in finding out what the issue was.

Jump to this post

@lindamaegirl
I feel as though I could have written your post Linda. I have been trying to find the root cause of my neuropathy symptoms for over 3 years. I have been sent to every specialist imaginable and multiple EMGs that say my pain, numbness and tingling is not neuropathy. The only treatment option offered is gabapentin (docs) or Tumeric (ai) Meanwhile, my symptoms continue to progress and my quality of life deteriorates. So frustrating and sad. Five years ago I walked five miles a day - today I can barely make it around the block. No hope in sight

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Hi all

Regardless of whether the diadnosis is neuropathy. Increasing blood flow to your feet is a good thing. I use redlight therapy daily, I have had it professionally twice it worked for me. I also try to eat the best foods for my health (well at least I try), I exercise ( youtube foot yoga with Sally McNally), I massage my feet with lotion everynight, and I have a positive attitude. I put effort and time into my feet feeling somewhat normal and for the most part it works. The numbness in my hand from typing ...( i do know the cause- i just do not like the solution).

JFN

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Profile picture for lindamaegirl @lindamaegirl

@cwloeffler thank u for your input. I found one on the top of neurology teams at mass General in Boston and they have done. absolutely nothing for me ?They tell me this will be progressive overtime and we can give you medication for pain. I could not be more disappointed, even though it is idiopathic, which we know means they don’t know the cause I feel that nobody is even trying to discover the cause…it almost feels like they’re shrugging their shoulders. They even said doing the EMG and they would do it if I want it, but it would probably not change the protocol! Why would I put myself through that discomfort for no reason at all ?people in this kind of discomfort are absolutely desperate, I am just looking for some hope …unfortunately the scammers know that and take cash only for what they tell you is a cure. I wish there was somebody out there I could trust who actually had some interest in finding out what the issue was.

Jump to this post

@lindamaegirl I feel your frustration. I have been trying to find resources and doctors to help me control this horrible disease with no luck. They just want to test again and then tell me “yes, you have idiopathic neuropathy “. 😡
Sometimes I put on one of those compression socks and it offers some relief. I also have a red light therapy shoe I bought on Amazon that I use every morning and night. Some days are better than others. 🤷‍♀️

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Profile picture for snarky101 @snarky101

@lindamaegirl
I feel as though I could have written your post Linda. I have been trying to find the root cause of my neuropathy symptoms for over 3 years. I have been sent to every specialist imaginable and multiple EMGs that say my pain, numbness and tingling is not neuropathy. The only treatment option offered is gabapentin (docs) or Tumeric (ai) Meanwhile, my symptoms continue to progress and my quality of life deteriorates. So frustrating and sad. Five years ago I walked five miles a day - today I can barely make it around the block. No hope in sight

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@snarky101 Be careful with the gabapentin. I heard and read that it can cause dementia. Google it for more info.

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Profile picture for snarky101 @snarky101

@lindamaegirl
I feel as though I could have written your post Linda. I have been trying to find the root cause of my neuropathy symptoms for over 3 years. I have been sent to every specialist imaginable and multiple EMGs that say my pain, numbness and tingling is not neuropathy. The only treatment option offered is gabapentin (docs) or Tumeric (ai) Meanwhile, my symptoms continue to progress and my quality of life deteriorates. So frustrating and sad. Five years ago I walked five miles a day - today I can barely make it around the block. No hope in sight

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@snarky101
have you had genetic testing. I have had lots of tests and they couldn’t identify what cause my neuropathy. I asked my dr for a genetic evaluation. Which is scheduled for next week. I have been researching the different types and I think that my problem.

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Profile picture for mistymom @mistymom

@snarky101
have you had genetic testing. I have had lots of tests and they couldn’t identify what cause my neuropathy. I asked my dr for a genetic evaluation. Which is scheduled for next week. I have been researching the different types and I think that my problem.

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@mistymom please keep me posted. No i never thought of genetic testing

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