Does anybody have experience with SANEXAS for neuropathy?
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.
Do you know if people that have a pacemaker could take the injections?
Good evening @kp6350, I am out of my element here a bit. And yet I noticed that you have flat feet which appear to be a factor in the successfulness or unsuccessfulness of treatments. My life partner has a pronated and flat left foot. He is hobbling around right now in a boot after spraining that ankle when he fell off our little bridge down by the river. His visit with a podiatrist today revealed some realities and offered some suggestions for dealing with the flat pronated foot. Included were new orthotics and a special brace that keeps the pronation straight. Might that be worth looking into for your debilitating situation?
May you be safe, free and protected from inner and outer harm.
Chris
Thank you so much. Have a podiatrist appt next week will mention it. Thank you.
That's timely isn't it? Would you please fill. me in on the pronation/flat foot issue after your appointment.
Thanks,
Chris
Yes
I am so glad I found you used Sanexas. I had an appointment with a local doctor who does these treatments. They suggested 3 times a week to start out. I have been putting it off and trying to find information from others' experiences, so hearing of your success is wonderful to hear. I am over my feet hurting all the time and the tingling and numb feeling up my legs. I have also developed arthritis in my back and 2 doctors have told me it may also be playing into the issues with the neuropathy.
My neurologist offered drugs but this was not my first choice and at that time told me within 10 years I would be using a cane. I have taken Gabapentin and Lyrica for nerve issues in the past and both cause my feet and hands to swell.
Hi I to am going to be starting Sanexas treatments next week. They will be testing on this Friday 5/27. I'm not sure if I can fit in 3 X wk but will try. I've have had Peripheral Neuropathy for many years & went to have it checked out & at the time, the only thing that was bothering me was the tingling or prickling feeling in hands & feet. I did & do have numbness. The Dr suggested I take a suppelment called Alpha Lopoic Acid. It does work very well. I started with 400mgs a day & I'm now taking 600 mgs twice a day, going on 2 yrs now but then the burning in the feet started ( I use Aloe with Lidocaine to stop the burning )& I noticed I was tripping on things, my right leg was wabbley as I stepped down on it. I am not much for drugs & will always do natural before anything. I am looking forward (in a way) (needles-I don't like) in trying this. I'm like you, I do not want a cane or a walker but I'm still going to continue in doing yoga to help strengthen what they are trying to do. Let's keep in touch about what we are doing & how we are feeling. Thank you for posting. I live in the Phx, AZ area
Just started with a chiropractor who is recommending Sanexas for my back issues. The only thing that has helped in the past has been decompression. I have a herniated disk L5 and 4 along with arthritis and scoliosis.
Yes, it's very expensive and am unsure if I want to spend the money with no guarantees. Can anyone with back issues that has had the treatment, please respond!!!
Thanks
Sanexas is covered by Medicare.
I was told that it is not.