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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.

thistooshallpass1 | @thistooshallpass1 | Jun 22, 2022
In reply to @bevely "There is lots of information out there, you will just have to let your fingers do..." + (show)
@bevely

There is lots of information out there, you will just have to let your fingers do the typing (researh) LOL That's how I found out about Sanexas. I wasn't going to live with "nothing can be done" attitude and also, places where helping others but WON'T have anything to do with you because of your insurance! Crap.....
So, I got my feathers in a knot & went on a hunt to do something that is natural & fairly easy on my body. It is working & I am so thankful I didn't give up. I even went back to yoga, (basics ) for now to help the process along to strengthen my muscles. Again, I didn't give up. I am 75 yrs young & want to live a good life without pain.
I hope you can look more into the Sanexas treatment for yourself. Good luck

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What did you do that is natural along with yoga please?

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bevely | @bevely | Jun 22, 2022

Before I got the courage to go back to yoga, I did squats against the wall & rubber band around both legs just above ankles & squatted & walked a line, right foot not moving, lifted up the left foot and pulling the band tight, then put the left foot down (still tight band) ... Start again, bring right foot to meet left food, then right foot stays planted & move left foot to exand band , then place left foot on floor . At that point, both feet are on the floor, band is pulled tight with legs apart. Repeat 10 times, rest & 10 more 2 X daily. Keep the muscle active.
I also found supplements to help with inflamation, I found Alpha Lipoic Aid to stop the pins & needle feeling that was driving me crazier in feet & hands. lol Also finally ended up with Aloe that has lidocaine mixed in for the HOT BURNING feet, Hands happend once in awhile. I keep it in the fridge, as it feels so good when applied on the fire (feet) & works for a long time. (sometimes days)
I finally went back to my neurologist (after 2 years) as the numbing was going up the outside of my ankles & legs, my balance was starting to be unstable & I notice when I was walking, when I put my foot down, it would wabble..He suggested the Sanexas, & it's working for me in a lot of ways. I am very pleased..
I also changed up my diet & eat less bread (starchs) berrie fruit for fiber & more veggies. There is noice-cream, cheese or milk now in house. ( I really miss) no chips, snack, eat apples or green tip banana instead. Watch anything that has sugar in it. I've have applied all this thru research. Something is working..
It tooks years to get my body in this mess & it's not going to be an instead cure. It will take time with out drugs.
I hope this answers your question on the natural way I'm handling Peripheral Neuropathy.
Good luck

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Angie P. | @ancopau1998 | Jun 23, 2022
In reply to @bb0753 "Yes I am certainly not giving up. Except for this numbness in feet that has progressed..." + (show)
@bb0753

Yes I am certainly not giving up. Except for this numbness in feet that has progressed over 5-6 years to ankles and shins but no pain I feel great at 69. I had to visit nursing home recently and seeing all those struggling to walk has made me even more determine to find answer. Sadly this treatment is not available anywhere within 4-6 hours of me and can't see how I could get that many treatments that far away. Also this is first treatment I have heard of that medicare may actually cover. I take no medication and not interested in any. Can't understand why this is not more widely available if medicare covers that cost.

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Hi bbb0753 I read your post about the numbness is your feet. I also have that and no pain in mine too. I have diabetes well controlled and was Dx with Multiple Myeloma 3 years ago. I had slight numbness but after taking chemo pills now for 3 years the numbness is worse. What are you doing for this? Also the treatment you found what is it called? Thanks so much and Good Luck!!

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1 reply
bb0753 | @bb0753 | Jun 23, 2022
In reply to @ancopau1998 "Hi bbb0753 I read your post about the numbness is your feet. I also have that..." + (show)
@ancopau1998

Hi bbb0753 I read your post about the numbness is your feet. I also have that and no pain in mine too. I have diabetes well controlled and was Dx with Multiple Myeloma 3 years ago. I had slight numbness but after taking chemo pills now for 3 years the numbness is worse. What are you doing for this? Also the treatment you found what is it called? Thanks so much and Good Luck!!

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AngiePP. Sadly I have so far found no treatment to help numbness. I checked to see if the Sanexas mentioned above was near me but is not. I have tried several things and the only slighty effective treatment I found was acupunture . However I have idiopathic PN i.e. I know of know cause except at a blood test did show toxic levels of b6 which was caused by EmergenC and melatonin which also contained b6. I took these over 3 years. I recently learned that b6 toxicity can continue long after excess b6 is out of your blood especially with high b6 diet and I was eating high protein low carb diet thinking it would help numbness. I am now eating low b6 diet to see if that will help. Am told it could take months/years to remove b6 stored in muscles and nerves andcrequires exercise and good hydration. Very frustrating!! Hope you find solution to your numbness.

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2 replies
duquer | @duquer | Jun 24, 2022
In reply to @bb0753 "AngiePP. Sadly I have so far found no treatment to help numbness. I checked to see..." + (show)
@bb0753

AngiePP. Sadly I have so far found no treatment to help numbness. I checked to see if the Sanexas mentioned above was near me but is not. I have tried several things and the only slighty effective treatment I found was acupunture . However I have idiopathic PN i.e. I know of know cause except at a blood test did show toxic levels of b6 which was caused by EmergenC and melatonin which also contained b6. I took these over 3 years. I recently learned that b6 toxicity can continue long after excess b6 is out of your blood especially with high b6 diet and I was eating high protein low carb diet thinking it would help numbness. I am now eating low b6 diet to see if that will help. Am told it could take months/years to remove b6 stored in muscles and nerves andcrequires exercise and good hydration. Very frustrating!! Hope you find solution to your numbness.

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Hi there, please use this link to look for the nearest Sanexas treatment center near you. Hope this helps
https://www.rstsanexas.com/contact-us
It did for me. If you’re interested I can share my story with you

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2 replies
Angie P. | @ancopau1998 | Jun 24, 2022
In reply to @bb0753 "AngiePP. Sadly I have so far found no treatment to help numbness. I checked to see..." + (show)
@bb0753

AngiePP. Sadly I have so far found no treatment to help numbness. I checked to see if the Sanexas mentioned above was near me but is not. I have tried several things and the only slighty effective treatment I found was acupunture . However I have idiopathic PN i.e. I know of know cause except at a blood test did show toxic levels of b6 which was caused by EmergenC and melatonin which also contained b6. I took these over 3 years. I recently learned that b6 toxicity can continue long after excess b6 is out of your blood especially with high b6 diet and I was eating high protein low carb diet thinking it would help numbness. I am now eating low b6 diet to see if that will help. Am told it could take months/years to remove b6 stored in muscles and nerves andcrequires exercise and good hydration. Very frustrating!! Hope you find solution to your numbness.

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Thanks for your response bb0753. I have never heard of Sanexas. I live in Ohio will have to check on that. It is very frustrating for sure. My sister said check on a Chiropractor which I have not done yet. Well good luck to you too, and thanks again!!

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1 reply
thistooshallpass1 | @thistooshallpass1 | Jun 24, 2022
In reply to @duquer "Hi there, please use this link to look for the nearest Sanexas treatment center near you...." + (show)
@duquer

Hi there, please use this link to look for the nearest Sanexas treatment center near you. Hope this helps
https://www.rstsanexas.com/contact-us
It did for me. If you’re interested I can share my story with you

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Please share your story I would love to hear it. Thank you

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1 reply
duquer | @duquer | Jun 24, 2022
In reply to @daschicago "I too have severe, chronic pn in both legs from knees down, esp the feet. So..." + (show)
@daschicago

I too have severe, chronic pn in both legs from knees down, esp the feet.
So much so that I cannot walk any longer.
I’m desperate to learn if this is a legitimate treatment modality, as there are lots of folks that prey on this pt population with $ scams because we are so desperate.
So please, anyone, is there any objective outcome data on this treatment? Any pt reviews after having the treatments?

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Here is hoping that this might help you. My name is Ralph
https://www.rstsanexas.com/patient-resources/

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duquer | @duquer | Jun 24, 2022
In reply to @thistooshallpass1 "Please share your story I would love to hear it. Thank you" + (show)
@thistooshallpass1

Please share your story I would love to hear it. Thank you

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I have already posted it here. Please check this link out
https://connect.mayoclinic.org/comment/645606/

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duquer | @duquer | Jun 24, 2022
In reply to @martyk "Thank you for sharing your story. You have been through so much .Your very resilient. Hopefully..." + (show)
@martyk

Thank you for sharing your story. You have been through so much .Your very resilient. Hopefully you will continue to improve the quality of your life.

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You’re welcome. I do hope you find the correct treatment that you are seeking.

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