Author Topic: Has anyone tried palmitoylethanolamide (PEA)?  (Read 1611 times)

swell

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Has anyone tried palmitoylethanolamide (PEA)?
« on: April 27, 2020, 01:33:51 PM »
Has anyone tried palmitoylethanolamide (PEA)?
How does it feel?
How would you compare it to CBD?
POIS Free, 2+ yrs (occasional/predictive lapses)
Pois symptoms: Peripheral (Skin: Urticaria, dryness, pale blotchy skin), Exasperation of: [Nerve weakness, Muscle weakness + Mental (CNS: Brain Fog, Irritation, Isolation, Speech lethargy, Anxiety)].
Other conditions: ASD, ADD, GA

millstone

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Re: Has anyone tried palmitoylethanolamide (PEA)?
« Reply #1 on: April 28, 2020, 03:22:42 PM »
Yes. I've actually been taking it for the past 30 days or so. My mix also includes Curcumin.

This was prescribed from my functional doc to focus on reduction of inflammation throughout the body.

Nothing feels different other than I feel more like my old self. I've also been abstinent since early March for my own personal recovery protocol, so your milage may vary.

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From my visit notes:

Anti-inflammatory protocol for prostate/overall inflammatory burden:

* Myomend: 2 capsules three times per day for 14 days. Then, move to daily thereafter. May finish bottle and then stop. Would cycle off and on every few months.
* Pea+:2 capsules three times per day for 14 days. Then, move to daily thereafter. May finish bottle and then stop. Would cycle off and on every few months.

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Here are the products:

* https://enzyscience.com/products/myomend
* https://enzyscience.com/products/pea

swell

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Re: Has anyone tried palmitoylethanolamide (PEA)?
« Reply #2 on: April 30, 2020, 03:43:18 PM »
Nice, so I presume you are saying, PEA has made you feel very good in general, though you cant comment its effect on POIS, since you are practicing abstinence?
POIS Free, 2+ yrs (occasional/predictive lapses)
Pois symptoms: Peripheral (Skin: Urticaria, dryness, pale blotchy skin), Exasperation of: [Nerve weakness, Muscle weakness + Mental (CNS: Brain Fog, Irritation, Isolation, Speech lethargy, Anxiety)].
Other conditions: ASD, ADD, GA

millstone

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Re: Has anyone tried palmitoylethanolamide (PEA)?
« Reply #3 on: May 05, 2020, 12:56:21 PM »
That is a fair way to put it  :)

I do not believe that this supplementation, by itself, will cure POIS, but I do believe it is a strong element to add to any anti-inflammatory healing protocol plan.

swell

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Re: Has anyone tried palmitoylethanolamide (PEA)?
« Reply #4 on: May 05, 2020, 03:05:52 PM »
Cool, I have been taking Palmitoethanolamide (low-dose, 100mg) and I have been taking Hemp oil (since CBD is beyond my purchasing power) for 5 days now.  And a disclaimer: I have been also taking low-dose amphetamines since few years.  Interesting effects of PEA and Hemp, which I really like, but they are subtle.   Most important (to me) effect has been on my facial nerve tingling, it has disappeared ..... yay!.  I cant comment on POIS, since my protocol had already eliminated POIS effects. 


That is a fair way to put it  :)

I do not believe that this supplementation, by itself, will cure POIS, but I do believe it is a strong element to add to any anti-inflammatory healing protocol plan.
POIS Free, 2+ yrs (occasional/predictive lapses)
Pois symptoms: Peripheral (Skin: Urticaria, dryness, pale blotchy skin), Exasperation of: [Nerve weakness, Muscle weakness + Mental (CNS: Brain Fog, Irritation, Isolation, Speech lethargy, Anxiety)].
Other conditions: ASD, ADD, GA