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Red light therapy idiopathic neuropathy numbness tingling
Neuropathy | Last Active: 3 days ago | Replies (23)Comment receiving replies
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?
Replies to "I have idiopathic neuropathy in my feet. In addition to a couple of oral supplements and..."
@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
@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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@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.