Quote:
Originally Posted by MelodyL
Hi Mrs. D.
This morning (and I forget how I came to find this site), I stumbled upon this website.
http://www.neccp.com/chemotherapy-in...uropathy-cipn/
They are located in Stamford Conn. The doctor is a chiropractor and I phoned them. Spoke to a very kind nurse.
I asked her "what's the difference between this and using a tens or a rebuilder?" and she explained they put the electrodes "not on the place of pain" but higher up. And it affect neurons in a special way.
Insurance doesn't cover it and it's a course of 5 or so visits, and it's about $2000. So I did ask the pertinent questions.
I also asked if they treated anyone who had NON chemo induced neuropathy and she said 'oh yes"
So if anyone is interested they should check out the website.
Melody |
Hi Melody. I have been researching PN for many years. I have never read where if the found there cause of PN there was anything they could do about it. Thirteen years ago i took ZOCOR. Unknowingly it said PN was a side effect.
Within 3 months of taking it i had PN.
Why spend millions of dollars trying to find the cause when their is nothing anyone can do about it. I look for ways to lessen my pain so i can have a better life.
Less pain to all. GEORGE