neuroinflammation

[soulution121]

Hi friends. New to the board. Thanks for all your work.

I stumbled across this the other day and thought of what I go through.

I definitely believe that my whole body and brain goes through serious inflammation especially the brain.

This article pretty good in what happens to the brain. It almost like my brain reacts like I have some sort of degenerative brain disease when going through a POIS episode.

https://thefnc.com/research/do-you-have-brain-inflammation/

I'm experimenting with a supplement that may have a soulution.

Stay strong friends

[Quantum]

Welcome to the forum, soulution

I totally agree with you, about part of the POIS symptoms looking like symptoms of brain inflammation (encephalitis). I have proposed that opinion a while ago, on the forum, like here : https://poiscenter.com/forums/index.php?topic=2078.msg16432#msg16432 .

At the end of the article you linked too, they mention a list of supplements that can be used to help with brain inflammation.  I used many of those through the years.  I am still using curcumin quite often. and catechin through green tea, one of the first allies I found against POIS.  I also used chamomile tea for the apigenin in it.
Curcumin is still part of my pre-pack to avoid POIS symptoms.

[soulution121]

Hi Quantam.

Cheers for your reply.

I've just taken something which has changed the game for me in regards to synapses activity.

Its called Cognitex Elite by life extensions. It allows me to think clearly after an ejaculation and mental recovery is retained days after.

https://www.lifeextension.com/search#q=cognitex%20elite&t=coveo4A2453FD

I'm also looking in to Mast Cell Activation Syndrome. Due to the nature that my entire body feels under attack, sore joints, chronic fatigue, mental, breathing issues this also might be an issue to address.

https://www.geneticlifehacks.com/mast-cells/

https://hoffmancentre.com/natural-treatments-for-mcas/

I'm a divorcee and also a widow. People don't understand how this disease affects my life. The symptoms last for 7 to 21 days! I have to find a cure and we will.

For the time being though I've found a way to manage the symptoms and recovery rates and the greatest victory is reclaiming my mind!

[Quantum]

I am glad for you that you are slowly finding ways to lessen the intensity and duration of your symptoms. 


On the topic of Mast cell activation syndrome, there is a discussion going on on the forum about it, for quite a few years now.  You can find this thread at https://poiscenter.com/forums/index.php?topic=2301.msg18956#msg18956 .  Using the search function on the home page, you can also find other posts on MCAS on the forum.