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.
I am really glad that you were able to find Sanexas and that You have found a treatment that works well for you. It was very kind of you to share this with me I hope that you will continue to let me know how well you’re progressing. Wishing you the very best, Ralph
Welcome @susan1542, It's really great news to hear that the Sanexas treatments are helping you after treatment number 6. It's also good to hear that Medicare is paying for it. Can you come back and give us another update after a few months to let us know how you are doing with the treatments?
I shared your comment with Sanexas, and this was their reply
That’s terrific. Do you think this patient would allow us to share their testimonial? I would need to get permission in order to comply with HIPAA guidelines. Let me know and if so how I can follow up directly with him/her.
Thanks
They would need to contact you directly
I did 19 treatments, did nothing for me.?
You do not need HIPPA clearance for this to happen. This is a common excuse for being lazy or not actually knowing what HIPPA is actually about
Will you share what your symptoms are/were>
That's great. Where are you going?
@susan1542 Thank you for sharing your positive results. It would be very helpful to know what your symptoms are or were and what type of neuropathy you had (pain, numbness, etc.)
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?
Hello @daschicago, Welcome to Connect. @duquer shared his experience with SANEXAS earlier in this discussion here https://connect.mayoclinic.org/comment/645606/. You might find my reply to his post interesting if not helpful.
You are wise to do your own research. There are many less than honest treatment providers when it comes to neuropathy pain and suffering. The Foundation for Peripheral Neuropathy has some complementary and integrative treatments for PN on their site here - https://www.foundationforpn.org/treatments/
Are you able to share any treatments you have tried or ones that helped a little?