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Anyone tried the Rejuvacare Neuropathy Machine for Feet??
Neuropathy | Last Active: Oct 30 3:15pm | Replies (46)Comment receiving replies
I must have seen the same infomercial as I , too, am always looking for help. I am a 20+ sufferer and so exasperated by all my medical professionals, I am about to “reset” and work on this myself again. The cost for these foot wraps won’t break the bank, and guarantee 100% refund, which is tempting for me… My pain is 24/7 , more in left foot/calve and , and worsening in right. And as I age, it’s only getting more difficult to walk. I have a home routine PT/stretching routine , eat healthy (no processed foods) and just recently added occasional dessert, glass of wine and bread. I was depriving myself for so long and there was no change in my pain level. I recently was weaned off of duloxetine because it caused intestinal issues. I was off it three days, and my intestinal issues quit, however, the withdrawal symptoms are horrendous, and my chronic pain level is back to normal”8”…. I am convinced taking drugs to mask the pain is not the answer, nor is eating right/healthy. Curiosty of knowing why - I will probably die not knowing and I think that is sad that someone can’t figure out nerve problems.
Replies to "I must have seen the same infomercial as I , too, am always looking for help...."
@patriciaschulz1950 So sorry you are dealing with this monster, also. IF you decide to try the Rejuvanator, please let us know. And though they say it is not on Amazon, I believe I DID find it there, as well.... and it would be easier to return through them.
I tried going without any beer or wine for several months, and I noticed NO difference in my problems.... so I now have a glass of wine with my meals, as was my custom before. This is MY experience, of course, and I can't recommend that others would have the same lack of effects. I take Prozac.... never tried duloxatene.... I believe they are similar? But it sounds like the duloxatene really helped your symptoms. I will ask my PCP about it when I see him in November.
An added issue for me is that I have a slight touch of AFib, so the cardio put me on Eliquis. And there were a couple of episodes of brief tachycardia, so he put me on Flecainide. Since I take those TWO meds, I can take NOTHING for pain except Tylenol. And sometimes I could use something stronger for the Arthritis pains I have.
I am considering...... and thinking about a spinal cord stimulator..... Some people say it helps.... others say it made no difference.... but we are all unique in how we respond. A fried got one a couple of weeks ago, and she has ZERO back and leg pain now.
I wish you the best!! Mike
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@patriciaschulz1950 I'm not sure if you have seen the Foundation for Peripheral Neuropathy's YouTube channel but they have a lot of great webinars for learning about the different therapies people have found helpful for neuropathy pain. We had a discussion started by Barry @user_che214927 that you might want to scan through to see if that might be an option that doesn't cost much other than time to learn about it.
-- Neuropathy and Brain Neuroplasticity: https://connect.mayoclinic.org/discussion/barry-sheales-australia/
I did a search of the Foundation for Peripheral Neuropathy's YouTube channel for "brain training" and was surprised at the number of webinars on the topic. Not sure they are all relevant but a few looked interesting for folks battling with the neuropathy pain. Here's a list of the webinars - https://www.youtube.com/@foundationforperipheralneu4122/search