← Return to Has anyone been prescribed EB-N5?

Discussion
Ray Kemble avatar

Has anyone been prescribed EB-N5?

Neuropathy | Last Active: Sep 18 4:23pm | Replies (109)

Comment receiving replies
Profile picture for NJ Ed @njed

@ray666 Ray - it has been two years (hard to believe!) since you posted this question. Since we have very similar symptoms, could you please provide, in your opinion, the pros and cons of this product. If you're no longer taking it, why? Thanks - Ed

Jump to this post


Replies to "@ray666 Ray - it has been two years (hard to believe!) since you posted this question...."

Hi, Ed,

Geez, has it reallybeen TWO years? How flies when you're having fun –– or at least doing everything we can to have fun. 🙂 Regarding EB-N5, I've been asked many times if it was doing to me any good (or any harm) –– asked by the neurologist who suggested I give EB-N5 a try. My answer has always been the same: I can't be sure, either way (good, or harm). All I can really say is my PN (chronic idiopathic large-fibre axonal polyneuropathy –– a mouthful!) has, in all these years, not grown measurably worse. Can I attribute that to EB-N5? I can't say, not for sure.

But now that same neurologist (whom I really like and trust) has asked me to switch to EB-M8, a somewhat different "medicinal food." I've been taking EB-M8 for only a little over a week, so the jury's still out on that one; "still out"? actually, they're still leaving the courtroom. I'll keep everyone posted, though, as I continue to monitor my one Big Bad PN Symptom (poor balance).

My super best to you, Ed, and to everyone!
Ray (@ray666)