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Pudendal Nerve Entrapment/Neuropathy/Damage

Chronic Pain | Last Active: 3 days ago | Replies (555)
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@jesfactsmon

@qball2019

Thanks for the link to the article about PEA (Palmitoylethanolamide). I will look at it.

My wife Linda, who has severe PN burning in her feet, started taking PEA a few weeks ago. So far she tells me that she thinks it is giving her energy. I'm not sure about what it is doing for her pain, but it seems like (and I know this is too early to come to any conclusions whatsoever) she is in less pain overall. Just my impression, not her statement, although she and I have not discussed it in depth yet. She did stop it for 2-3 days because she thought it was making her tinnitus worse. But I think she is back on it again. She takes four 400 mg pills per day. In case anyone wants to try it, here is the link to the kind she is currently taking:
https://smile.amazon.com/gp/product/B01HFN5R9I/ref=ppx_yo_dt_b_search_asin_title?ie=UTF8&psc=1

Best, Hank

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Replies to "@qball2019 Thanks for the link to the article about PEA (Palmitoylethanolamide). I will look at it...."
qball2019 | @qball2019 | Sep 29, 2020

@jesfactsmon

So glad to hear that your wife is already taking PEA! Not sure what she is taking for inflammation but she may want to start Tumeric and maybe take some info. in to her doctor. There is some very interesting reading about pain and inflammation on both websites I listed. Please urge your wife to check them out. Best wishes to both of you!!

Here is the PEA (Palmitoylethanolamide) that I'm taking. I take one in the morning and one at night. https://www.amazon.com/gp/product/B084T9BFHT/ref=ppx_yo_dt_b_asin_title_o00_s00?ie=UTF8&psc=1

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