Phosphatidylcholine Is Working for Me

Im 33 yo. Yesterday i buyed 2 bottles of Phosphatidylcholine 420mg by Newton-Everett, they send me from eeuu to spain and im waiting that arrive. For sure i take 2 pills for day, is recomended dose.

 

@Albertus hopefully you will update your results on this thread!

 

U can take the nac yourself

 

Maybe this is the reason that you improve with PCT:

It is now known the cause for the destruction of the myelin in the lesions is overactivation of the microglia in the region of the myelin. An enzyme that converts glutamine to glutamate called glutaminase increases tremendously, thereby greatly increasing excitotoxicity. Mercury also activates microglia, even in subtoxic doses.

Any dietary excitotoxin can activate the microglia, thereby greatly aggravating the injury. This includes the aspartate in aspartame. The methanol adds to this toxicity as well. Now, the secret to treatment appears to be shutting down, or at least calming down, the microglia. It has been found that the antibiotic minocycline powerfully shuts down the microglia. I tried this treatment on a friend of mine who just came down with fulmanant MS. He was confined to a wheelchair. I had him placed on minocycline and now, just a few weeks later, he is walking.

The good news is that other things also calm the microglia-the most potent are: silymarin, curcumin and ibuprophen. Phosphatidylcholine helps re-myelinate the nerve sheaths that are damaged, as does B12, B6, B1, vitamin D, folate, vitamin C, natural vitamin E (mixed tocopherols) and L-carnitine. DHA plays a major role in repairing the myelin sheath. Vitamin D may even prevent MS, but it acts as an immune modulator, preventing further damage – the dose is 2000 IU a day. Magnesium, as magnesium malate, is needed in a dose of 500 mg 2X a day. They must avoid all excitotoxins, even natural ones in foods-such as soy, red meats, nuts, mushrooms and tomatoes. Avoid all fluoride and especially all vaccinations since these either inhibit antioxidant enzymes or triggers harmful immune reactions.

Phosphatidylcholine helps re-myelinate the nerve sheaths. What is this stuff and how can I get me some?

Phosphatidylcholine is a phospholipid that is a major constituent of cell membranes. Phosphatidylcholine is also known as 1, 2-diacyl-:ussn:ue-glycero-3-phosphocholine, PtdCho and lecithin.

So Phosphatidylcholine, is a fancy name for lecithin. Perfect! I already have some. Interestingly enough, three of the main supplements that are required for rebuilding the myelin sheath, the iridologist told me I didn’t need them:

Magnesium, Vitamin D and DHA from Omega 3.

Our auditory nerves was damaged by excitotoxicity by Ad's. An T is the result. We can try repair myelin seath.

 

That's interesting because in addition to the phosphatidylcholine i'm taking Magnesium and Calcium, Vitamin D and getting DHA from Fish oil. Good find. So maybe added the phosphatidylcholine to the mix after I was already taken the other stuff made things really work.

 

Thanks for sharing this! I've been using phosphatidylcholine and phosphatidyl serine for a few days and I have to admit, I've stopped taking trobalt (for 4 days, cold turkey) and switched to this and it does seem to work! Thank the lord!

These are the brands I've been using-

http://www.amazon.com/Solgar-Phosphatidyl-Choline-Complex-Softgels/dp/B00FYBARNK/

http://www.amazon.co.uk/BULK-POWDERS-100mg-Phosphatidyl-Serine/dp/B00IZD3KOC/

 

This is awesome!! Same effect than RTG and no secondary effects. Maybe PTC rebuild mielyn seath and this create a permanet effect with time.

 

Well, trobalt just made me really happy, as of GABA...But this does seem to help and I don't want to be on trobalt. So it's all good for now. Are you taking it yet?

 

From what I understood this whatever it is called comes from eggs too so eating eggs will do the same so does it really work?

 

This morning i take my first capsule, how many capsules of serine and coline take you at day?

 

You must eat ten eggs TID so it maybe work. Is better take two pills of PTC (SOY).

 

is that its relieves H ?

 

Danny hi! Forgive me for asking this but you stopped taking Trobalt for one week some months ago when you were in hospital for a nasty kidney infection which was thankfully sorted out. Anyhow during that time your T did not go back up but in fact went back up later on for some unknown reason and when you were back on Trobalt.
So guess my question is how do you know that the Solgar Phosphatidyl Choline Complex with Phosphatidyl Serine is acting the same as the Trobalt after using it for four days?
Dont get me wrong please - if it does work then I would jump to take this rather than Trobalt of course......just dont want to throw money away on something that just doesnt make any difference....but if it helps then fantastic.......did you feel any side effects since stopping trobalt cold turkey some 5 days ago now?
How is your general health now? after being on Trobalt for a year? thanks

 

Just loads of insomnia. Anyway, yeah, I started to use them both and it works and no, it doesn't work in the way as trobalt, as that's impossible. However, my tinnitus is low after using these supplements, not much I can really add. It does seem to be working, thankfully. But I will say, I will update over the coming weeks, to see if these supplements continues to work or not.

 

But your T was low from using Trobalt so how do you know that it is low from using these supplements - I mean you say your T is low from everything you take - the latest thing i think was moringa? thanks

 

Moringa? No I never said that. I've never really took moringa. The latest thing I tried was that CBD oil before these supplements and it never worked. Additionally, this is not my thread, I never started it. Dafodeu started it and thankfully he did! Otherwise, I wouldn't have never came across it. Cheers, Dafodeu. Also, will keep everyone updated on my progress.

 

Apparently, there has been some interest in using phosphatidylcholine for neuro-degenerative diseases like Alzheimer's. I could find not legitimate research that it works for these disorders or for tinnitus. But might be worth a try.

I do agree, though, that it can be hard to tell exactly what is working for you if you keep jumping rapidly from one thing to another.

 

Is very dificult that a natural suplement have effect in only four days. Often three weeks is a normal time for feel any improve.

 

Well I'll give phosphatidyylcholine a try. I'll keep you posted on its affect if any? I certainly wouldn't win a spelling contest if that was one of the words to spell.

 

Here in Belgium we had a doctor called Herman Lecompte, he believed we could live to at least 150 years old just by taking the correct vitamins and supplements, he passed away at 78 due to a hearth attack, so take this live longer stuff with a grain of salt.

That being said, I might give this supplement a go and see if it works for my tinnitus, thanks for sharing, I never even heard of this stuff.

 

Here are some other options... they also talk about Melatolin with Sulpiride
http://www.lifeextension.com/protocols/eye-ear/tinnitus/page-07

 

I've been taking this for a couple weeks; no big differences noted.

 

PTC or Sulpiride + melatonin???
I try sulpiride two months and i dont feel any changes in my T.

 

sorry; I meant phosphatidylcholine.

melatonin seems to make me incredibly depressed the day afterwards, and so I don't take it anymore.

 

Did you get man-boobs? Cause that's a common side effect
Seriously though, sulpiride is one nasty dopaminergic drug and I dont understand why the relevant study (this one, fairly recent too) was not conducted using one of the (relatively) safer ones like Quetiapine.

As De Ridder has mentioned, you just need the dopamine blocking component to decrease the brain's reaction to internal and external stimuli so I would do the sulpiride-melatonin trial using some other dopamine blocker.

 

I think Phosphatidilcolina would assist people suffering neurological tinnitus, trying to repair the damaged auditory nerve (myelin sheath). For those who suffer from acoustic trauma and have the dead hair cells do not believe that works. In this case I think it would be much more effective RTG. Like a pulsatile tinnitus is treated with vasodilators, there are many types of causes and therefore many types of possible solutions, it is my opinion.

P.D. Its a cheap supplement, why dont try?.

 

I take a 4-5 a day...Of each.

 

On Friday last week, i had a hard time of T a spike. On Saturday i forced myself hard to go out and socialize instead of staying at home and depressing while listening to my T. It helped a lot and when i returned home in the evening i found Phosphatidyl Choline and 5-HTP waiting for me at my door step. Had the dinner and got these pills afterwards along with a VitaminD tablet and useless Betaserc. I was already feeling fine prior to that. I had an easy sleep and next day (Sunday) i was feeling very good with a very mild T.

Monday was fine, Tuesday as well. Only from Wednesday, i started feeling a slight increase in my T, which was bearable still.

So not sure this improvement is related to the drugs i started having or not. Maybe yes maybe no, but probably in between which is a partly yes. I just feel better than last week, less T and as a result of that better mood.

If my T stays this way, i feel like i can endure it until we have SF0034 in ~4-5 years which is supposed to provide a significant relief.

Thanks to Dafedou who pointed out this.

 

Liquefact,

Glad your t has settled down

Which phosphatidylcholine brand did you take and dose before you noticed a difference in your t annoyance?

 

These are what i'm using;
Phosphatidyl Choline: http://www.amazon.com/gp/product/B00020I7VC
5-HTP: http://www.amazon.com/gp/product/B001IS1K16

2 tablets/day of each, one after breakfast, one after dinner.