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Has anyone been prescribed EB-N5?

Neuropathy | Last Active: 21 hours ago | Replies (93)

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@tcgunn

Yes, I've beenon it for about a year and half now. It was prescribed by my Endocrinologist for my PN. The PN flare ups that I used to get were quite painful, severe, deblitating, and frequent (once every 4-6 weeks; over 4-5). Mainly in my feet and sometimes my hands. After taking EB-N5 about a month or so noticed the attacks weren't as severe and didn't last as long. Fast forward a a little over a year now. I may go 2-3 months and experience some minor tingling that is absolutely tolerable compared to what I was experiencing before starting on EB-N5. This is phenomenal considering that I used to take Lyrica 100mg three times a day with minimal, brief relief. I use a little cold therapy (ice pack) now to help with the minor flare ups and that gets me through with ease. I pray this is helpful and you have a great outcome as well. All the best to you!

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Replies to "Yes, I've beenon it for about a year and half now. It was prescribed by my..."

Hello, @tcgunn

I'm glad to hear that EB-N5 appears to be working for you. I believe it is for me, too, although I've been fighting a sepsis infection for the past nine months. Sepsis has made my balance much worse, and my sepsis symptoms seem to be waning, it has been impossible for me to report with any authority on the effectiveness of EB-N5 in halting or at least slowing any worsening of my PN balance difficulties. That said, I've no reason to think that EB-N5 has done me any harm; therefore, I'm continuing to take it.

All the very best to you!
Ray (@ray666)