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Neuropathy Relief Centers: Is the price worth it?
Neuropathy | Last Active: Jun 14, 2023 | Replies (41)Comment receiving replies
Claims of high success rates coupled with high uninsured costs would cause me to do a deep internet dive into the organization. Before jumping in, be sure to read as much as possible about it. How long have they been around,,, who are the people in charge... who are the medical people... is only 16 sessions,,, is it only $6000,,, are there any actual patients' comments... have they had any legal or regulatory proceedings... etc...? It may be great breakthrough. But if it sounds like it's too good to be true, it probably is.
Replies to "Claims of high success rates coupled with high uninsured costs would cause me to do a..."
The full price for 16 sessions was quoted to me a month ago at $6,989.00. I was told I would get a discounted price of $6,290.10 if I signed up within 30 days which ends tomorrow, June 2. I've read many patient testimonials which praise this center (The Hartford Neuropathy & Chronic Pain Center, located in Plainville, Ct). They utilize electrical cell signaling treatment (EcST) with the SANEXAS machine and a LED device and they pride themselves on being honest and translucent, claiming 80% success rates.
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.
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I would add that you should do as much medical research as you can. Try to read articles about the specific therapies they offer. Even if you can't completely understand the technical literature, you can read the "conclusion" or "summary: sections, which will give you an idea of the content. You can also discuss these treatments with your neurologist, or, if you don't have one, show the articles you found to your family physician, and ask them what they think.
I agree that this therapy sounds too good to be true, and is very expensive, and probably unproven. However, these are just guesses, as I haven't researched this particular treatment.
Often, people will establish specialized "clinics" to treat difficult diseases that have no good standard medical treatment because the patients are frustrated and suffering, and often lose faith in their doctors. The clinics are sometimes even staffed by actual medical people, but this doesn't prove anything. Even some doctors and nurses are not immune to trying to make a quick buck off people's suffering.
I too have PN, and have tried some unproven therapies and gadgets in the past, so I understand your desperation. The only thing I have found to be very helpful is an adjustment in my attitude. Try to eliminate the fear, anger, and anticipation of it getting worse in the future. I know, a tall order.