Neuropathy Relief Centers: Is the price worth it?
I've been suffering from peripheral neuropathy for the past 5 years. Started in the toes of my right foot and has been steadily rising up to my thigh. The numbness, tingling and burning sensations have been driving me crazy. And now my balance is getting so bad I'm careful not to fall over. Even driving is becoming difficult as I can barely feel the foot pedals. All doctors have told me that there is no cure and that it will just get worse with age. They prescribed Gabapentin and my neurologist suggested spinal injections which I do not wish to pursue. 1'll soon be 75.
Now I've recently come across a Neuropathy and Chronic Pain Center in Connecticut which claims an 80% success rate with their patients. They use SANEXAS and other electrical stimulation devices. However they do not accept insurance and patients have to pay in advance out of pocket. The price tag is hefty: over $6,000 for 16 sessions. Does this sound outrageous or reasonable? Any opinions would be welcomed!
Interested in more discussions like this? Go to the Neuropathy Support Group.
I believe Medicare covers SANEXAS treatments only if neuropathy is the result of diabetes, which is not my case. There are no specific injections with this treatment here.
Hi @gm123 and others, I thought I would share a couple of links to these related discussions which might also be helpful.
--- Does anybody have experience with SANEXAS for neuropathy?: https://connect.mayoclinic.org/discussion/sanexas/
--- Neuropathy Clinics: https://connect.mayoclinic.org/discussion/neuropathy-17/
I don't have diabetes. Medicare covered the treatments.
Since stopping the treatments I have found that some clinics don't use the injections.
Drtypaws are you in California? Tell us more about the treatment please? Was it beneficial? Long lasting?
Medicare does cover these treatments. I’m living proof
Thank you so much for sharing, and yes so would I as I have already. I am 56 and Progressive Peripheral Neuropathy attacked me at age 54 unfortunately and it began at it worst stages for me from the waist down and it was servers with no warning. There are no clinics near that are able to be of any assistance I could continue to say unfortunately but I won’t. I don’t really have a good balance , it’s hard for me to walk , stand for long periods of time , and my stability is not there at all , but I am still able to push my way through and for that I am beyond grateful. So as for me I won’t complain I continue trusting God each and every day, and that along with my beautiful Daughter has been what has helped me through this ailment. I would encourage any and every one that can afford it or have a clinic nearby to look them up if that’s what you decide, but what has helped me press forward and keep my sanity is staying in constant prayer and the love of my Daughter. I pray that something was said that blessed your heart. Have an amazing weekend.
I totally agree, and these are reasons why I need this group because there are always helpful perspectives from others that open my eyes and for that I truly that you so much. Have an amazing weekend and thank you again for sharing.
Are there any clinics in Lehigfh Valley Pennsylvania?
My experience with Sanexus for my feet after 30 treatments was that it was a complete waste of time and money.
I had had my neuropath for about 10 years. Perhaps it works better for someone whose neuropathy symptoms are more recent. I also tried Calmare treatments. Same outcome. I would consult studies from reliable sources to see what they reveal in terms of positive outcomes.
Yes, I'm in Northern California. It was helping me. My PN was mainly bad in my right foot. The treatment calmed it down so I didn't have any sharp pain esp. in my big toe. I'm sure it would have helped even more if I was able to continue the treatments without the injections.
My PN has progressed now but I'm on an IV infusion of Orencia for my arthritis. I wonder if that has anything to do with it.