Day 15 of taking TTFD: *** I ended up with... - Cure Parkinson's

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Day 15 of taking TTFD

Gcf51 profile image
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*** I ended up with High Blood Pressure taking TTFD. I no longer take TTFD. Based on my experience, I would not recommend TTFD. ***

I am posting here in fear HU will change link address, if I change Tittle and I don't want to have to change my Facebook link again either.

I have not received enough Likes or Comments on my Post to make it Popular. If you like Please, Like and Comment at the Link (I am Editing the Link):

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Gcf51 profile image
Gcf51
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6 Replies
Boscoejean profile image
Boscoejean

I hope this continues to work for you

Gcf51 profile image
Gcf51 in reply to Boscoejean

Promising. but still tp early to rule out Placebo.

HekateMoon profile image
HekateMoon

Hi. Im also taking TTFD. 4 days so far. More energy, less brain fog...lets see how it goes. Ill follow you.

Gcf51 profile image
Gcf51

Check.... beware i have thoughts running through my head like balls in a lotto machine,,, and took a day off, I am now at (50mg TTDF every other day). I am investigating making by own smaller dose caps. I am not a doctor don't rely on my advice!!!

Gcf51 profile image
Gcf51

Because External Links are going to page “Not Found” I am adding up dates to: healthunlocked.com/cure-par...

Gcf51 profile image
Gcf51

A comment I made on my lost data post:

@Gioc TTDF has been shown to be 100% absorbed by analysis of human urine and readily crosses the BBB. My blood test from 3rd day showed 260 (B1) normal range of 8 -30. A major side effect for me was worsened of cotton mouth that I notice after my full dose Botox injections for drooling a mouth before trying TTDF (first time was half dose). I do have a funky taste in my mouth (probably worsened by cotton mouth) that is not unlike the awful taste of a little of the contents of a TTDF cap. I have stopped my med that is suppose to help me hold my pee because one of listed side effects is dry mouth. Hopefully, I won't need taking TTDF by the time the Botox wears off (next schedule Botox 7/14 at appointment with MS). I have reduced in 2 steps my C/L from 2-1/2 twice daily to 1-1/2 twice daily. as of today (6/7). I feel Great with little to none symptoms of PD. I have a little tremor when I am nervous which has been normal for me all my life. I am going to copy/paste as a comment on another post.

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