Does anybody have experience with SANEXAS for neuropathy?

Posted by knucklehead4352 @knucklehead4352, Jan 6, 2021

Does anybody have experience with SANEXAS. It is touted as Electric Cell Signaling Treatment especially for peripheral neuropathy.

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

Profile picture for beardog @beardog

Yes I have,I had 14 treatments and it really helped me a lot.

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@beardog If you had stinging and burning type pain - did it resolve/help it?

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I went twice a week for eight weeks. Worked wonders

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Profile picture for Reg @metwo

@duquer How amazing for you! It sounds like the model of the machine was key - so do you think that now, years later, they are still around or are the new ones smaller and just as effective?

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@metwo I am not privy to the model of the machine. I do know the ones that were available at that time worked wonders for me.

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Profile picture for duquer @duquer

I went twice a week for eight weeks. Worked wonders

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@duquer Where did you go for the Sanexas treatments?

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Profile picture for jchet @jchet

@duquer Where did you go for the Sanexas treatments?

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@jchet there Is a wellness center about 45 miles from my home in Falmouth Maine. They had three machines there and they were all busy with patients getting Sanexas treatment treatments. You can call the company direct in Nevada and they will share with you the nearest Sanexas treatment center near you.

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Profile picture for duquer @duquer

@jchet there Is a wellness center about 45 miles from my home in Falmouth Maine. They had three machines there and they were all busy with patients getting Sanexas treatment treatments. You can call the company direct in Nevada and they will share with you the nearest Sanexas treatment center near you.

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@duquer Thank you for your reply. Hope you continue to do well.🙂🤞

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Last year I was diagnosed with Axonal neuropathy due to Sjogren's. My neurologist did not explain the difference between Axonal and demyelinating. I am doing all that I can to keep it from progressing further up my leg. Reading about other's journey inspires me to keep trying to find a better treatment than gabapentin. Acupuncture has helped but it requires regular treatment.

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Profile picture for sashi10 @sashi10

Last year I was diagnosed with Axonal neuropathy due to Sjogren's. My neurologist did not explain the difference between Axonal and demyelinating. I am doing all that I can to keep it from progressing further up my leg. Reading about other's journey inspires me to keep trying to find a better treatment than gabapentin. Acupuncture has helped but it requires regular treatment.

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Hello @sashi10, Welcome to Connect. Learning more about your condition and what treatments are available is one of the best things you can do to help yourself. You are not alone worrying about your neuropathy progressing. Many, if not all of us, worry about the neuropathy getting worse. I thought I would share a few links others, including myself, have used to learn more about neuropathy.

-- Foundation for Peripheral Neuropathy: https://www.foundationforpn.org/
-- Neuropathy Commons: https://neuropathycommons.org/
-- Neuropathy Resource: https://neuropathyresource.com/

There are many different discussions here on Connect that you might find helpful. Here is a search of Connect using "neuropathy what helps" if you want to scan through them - https://connect.mayoclinic.org/search/discussions/. Have you tried the search function to find others with similar questions?

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Thank you for the links, I will be checking them out.
I did find PT for neuropathy on you tube and have started the recommended exercises.

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