Has anyone tried infrared or red light therapy to relieve neuropathy p

Posted by bryce49 @bryce49, Sep 25, 2024

I was recently told that a friend's parent used infrared or red light therapy to successfully relieve neuropathy. Is anyone using it? Or is that another bogus claim?

Interested in more discussions like this? Go to the Neuropathy Support Group.

Profile picture for esthersue @esthersue

@debbo66
Hello, no, I only have nerve pain and tingling in my legs. From reading the Mayo Clinic blog, I can see that neuropathy can be a very confusing condition. There are numerous causes, symptoms, and therapies. From the best of my understanding, the light therapies are all very different. The only Healthcare professionals that offer this are chiropractors and functional medicine clinics; at least in my experience. From reading this blog, it seems that sometimes the light therapies help (but do not cure) and sometimes they don't. I have been on a trial and error journey for a long time. I'm not sure what kind of red light therapy you are using, but maybe a professional opinion would help? My Anodyne system uses thermal light energy and I had a referral from a chiropractor for it (after going for appointments for 3 months). I bought my home cold laser 5 years ago for $4000 after using a similar system at a chiropractor's office. I am assuming that you've been to a neurologist and have had all the available tests for causes for your neuropathy. I hope that your red light system works!

Jump to this post

@esthersue
So have you noticed any improvements in your neuropathy symptoms using your US$4000 Anodyne Cold Laser System? Please.

REPLY
Profile picture for seadog @seadog

@esthersue
So have you noticed any improvements in your neuropathy symptoms using your US$4000 Anodyne Cold Laser System? Please.

Jump to this post

@seadog
Hello, the light therapies reduced my pain and allowed me to be more active. The latest skin biopsy showed that my small fiber density had improved. But I am not sure if this was because of the therapies. I also went gluten free and take a lot of expensive supplements from the functional medicine doctor. I think that you definitely have to try the light therapies first before purchasing. For me, without the light therapies I would be back to a "couch potato ". But again, this is not a cure. From all of my doctor appointments, I know that diet is extremely important. Gluten and other protein foods caused severe inflammation and pain for me. But even control of the diet is not a cure. Until I find the cause, I will always be trying to control the pain. (You can Google Anodyne red light therapy and Avant hand held cold laser for more information on the characteristics of each type of therapy....and how circulation is improved, etc)

REPLY
Profile picture for debbo66 @debbo66

@esthersue hi I never met anyone else that has small fiber neuropathy. Mine is idiopathic also. I don’t feel pain but I feel a crawling sensation over my whole body especially feet. Did you ever feel that. I have a red light I just bought for my home. Praying it works

Jump to this post

@debbo66
Oh gosh, mine is as you describe! No pain but like my whole body including my face is filled with static, buzzing. Nothing makes it stop.
If your red light has helped over the months since you posted, please share what you bought, I’m desperate.

REPLY

I too have tried red-light nred light therapy, class IV laser. I have small fiber neuropathy and experience tightness or glove sock feeling around ball of feet, toes and ankles and hypersensitivity to sheets and sometimes cramping of toes through legs. I was told its idiopathic, had the EMG twice and large fiber nerves are healthy. I have not had the skin puncture to determine amount of small fiber nerves for clinical diagnosis but doc believes it is small fiber. I noticed first sensations of numbness in 2019. I was also told I have vascular deficiency disease in my legs as well as I had Hypetitus undetected for years and treated 2 years ago, after also having been treated for cancer with chemo radiation a year after neuropathy began. With that said, I do believe the nred light therapy helps but I agree you have to continue using it to continue seeing results. I use a full body bed called ARRC at a wellness center using the neuropathy and/or nerve setting. I also noticed that when I ate mostly vegan my symptoms improved. Recently I returned to eating meat for the protein needs in growing bone after suffering late term spontaneous sacral fractures as a result of my radiation in 2020. Someone here mentioned gluten and protein potentially worsening neuroapthy. I'd like to hear more about that, as I perceived my neuropathy worsening some after returning to eating meat.
I have not purchased one but was recommended by one chiropractor knowledgeable in neuropathy to use the LZR ultrabright handheld on one's feet. It is very expensive and someone needs to train you on its use, but the doctor is very expensive to be followed. I will follow this group to learn more.

REPLY
Profile picture for esthersue @esthersue

@seadog
Hello, the light therapies reduced my pain and allowed me to be more active. The latest skin biopsy showed that my small fiber density had improved. But I am not sure if this was because of the therapies. I also went gluten free and take a lot of expensive supplements from the functional medicine doctor. I think that you definitely have to try the light therapies first before purchasing. For me, without the light therapies I would be back to a "couch potato ". But again, this is not a cure. From all of my doctor appointments, I know that diet is extremely important. Gluten and other protein foods caused severe inflammation and pain for me. But even control of the diet is not a cure. Until I find the cause, I will always be trying to control the pain. (You can Google Anodyne red light therapy and Avant hand held cold laser for more information on the characteristics of each type of therapy....and how circulation is improved, etc)

Jump to this post

@esthersue
Hello, I would like to hear more of your experience or knowledge on gluten and "other proteins" affect on neuropathy. What "other proteins" are you referring to.
Thank you.

REPLY

Hello
I'm afraid that I am not an expert on protein recommendations. I can tell you what I have experienced.
A long time ago I had blood tests for food allergies. Wheat and eggs caused an inflammation response. These tests were done by a chiropractor neurologist, and unfortunately we're quite expensive. Since I was basically unable to sleep or walk because of the pain, I had to resort to services not covered by my insurance.
I've been told that Gluten has a protein substance in it.
Many years later I am still searching for new therapies, as I still have considerable pain without the red light therapies.
This led me to a therapy at Loma Linda University in California called Intraneural Facilitation. This is a new physical therapy which unfortunately is expensive.
In this therapy, food tests are done by using an ultrasound to measure blood flow in the body before and after consuming a particular food. I was told that protein foods are most likely the source of inflammation in the body for people with neuropathy. The inflammation will slow blood circulation. And for me, the blood flow to my legs is reduced. Through the testing I found several protein sources causing significant inflammation (and pain). At this point my diet is very restrictive, and I do the therapy every day ( a long with the red light). Unfortunately this is a long process for me, but as I'm not willing to stop trying yet, I just do what I can . I'm not saying that everyone can or should go to this therapy, but you can Google the website and call for information. Hope that this helps in some way.

REPLY
Please sign in or register to post a reply.