500 MG of thiamine joy: My First day was... - Cure Parkinson's

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500 MG of thiamine joy

tarverusmc profile image
37 Replies

My First day was amazing with my dose of 500 MG of Thiamine.

Still taking my PD meds, I felt totally normal with no tremors, having normal thoughts and communication, and my foot started to work again.

Today, with med's, I am at a state where I can type again, walk normal again, without any tremor's or any PD symptoms..

Wish me luck in the next coming days and just maybe, No More PD Meds....

PD meds list

25/100 Carbadopa Levadopa x10 daily

Encatapone X 3

.5 mg of cenamete x daily

Donald Tarver

2695680512

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tarverusmc profile image
tarverusmc
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37 Replies
AmyLindy profile image
AmyLindy

Here’s to ya! And Q: Oral or injection of 500mg?

tarverusmc profile image
tarverusmc in reply toAmyLindy

thank you and semper fi navy girl.

tablets is what I started. my wife found and article and we have started a test of thiamine and now are searching for answer's.

100 p&t va

and currently in line for va surgery dbs.

may put a hold on that.

thanks again for your service

AmyLindy profile image
AmyLindy

& Semper Fi,

Navy Girl

cshamb profile image
cshamb

WONDERFUL NEWS. DO TAKE A CAPSULE OR IS THAT AN INJECTION. DR. C INSTRUCTED ME TO TAKE 4 GRAMS A DAY WHICH WOULD BE 8 CAPSULES. I JUST STARTED ABOUT 4 DAYS AGO.

THANK YOU

tarverusmc profile image
tarverusmc in reply tocshamb

great, we both are newbie's. I just email dr c. hopefully he will respond

I take 500 mg pill orally

Mjm012649 profile image
Mjm012649 in reply totarverusmc

What brand do you take?

tarverusmc profile image
tarverusmc in reply toMjm012649

brand from vitamin store. nothing specific. now looking for cheaper alternative

tarverusmc profile image
tarverusmc in reply tocshamb

how r u doing

JANVAN profile image
JANVAN

Is that correct ??

10 times Carbidopa/ Levodopa a day ??

tarverusmc profile image
tarverusmc in reply toJANVAN

one tablet 10 times yes

tarverusmc profile image
tarverusmc in reply totarverusmc

I thought that was crazy amount. dr from u of m was looking for me to dekanezy (spelling)

in reply totarverusmc

See Doctor Fahn, healthunlocked.com/parkinso...

MBAnderson profile image
MBAnderson in reply totarverusmc

Do you mean U of Minnesota?

tarverusmc profile image
tarverusmc in reply toMBAnderson

michigan

alaynedellow profile image
alaynedellow

Well done- never give in theres always hope

AmyLindy profile image
AmyLindy

Are u 100% VA - SDV? Not sure what that line meant. I’m at 90% rated. Toxic water at Camp Lejeune back in the day could have been a contributor. I fall under that umbrella for

“Presumed service connection” on the disability scale... how about you (and any others reading this post)?

MBAnderson profile image
MBAnderson in reply toAmyLindy

I'm rated only 70% by the VA (and I was 50% before I had PD.) I think I got shortchanged. Next month I'm filing a "Decision Ready Claim" for 100%.

tarverusmc profile image
tarverusmc in reply toMBAnderson

rigidity, painful extremity, swallowing, curling of toes, multiple left right upper lower extremities, just a few of symptoms pd.

sleepless, depression, can individual adds up to 100%

MBAnderson profile image
MBAnderson in reply totarverusmc

Then I definitely got shortchanged. I have found the VA healthcare to be excellent, but the claims processing side is terrible.

tarverusmc profile image
tarverusmc in reply toMBAnderson

severe....conic....debilitating....range of motion....ect

tarverusmc profile image
tarverusmc in reply totarverusmc

honesty is the best policy. especially on your worst day

tarverusmc profile image
tarverusmc in reply toAmyLindy

sorry that drinking water was so dangerous. I was at cherry point and visiting weekends camp lejune drinking that water as well. on that list as well. my pd symptoms dates back to about 2006.

AmyLindy profile image
AmyLindy

SF, Amy

Erniediaz1018 profile image
Erniediaz1018

Excellent I'm very happy for you. Thank you for sharing. Please let us know how it goes 😊

tarverusmc,

If possible, could you please copy your post to the following thread where I am trying to get all of the results that people are getting using Dr. Costantini's thiamine protocol into one place so members can get a good idea of what results or lack of results people are getting with thiamine.

healthunlocked.com/parkinso...

Thank you!

Art

Grumpy77 profile image
Grumpy77 in reply to

You could also ask admin to pin that thread to top, so it will easy to add relevant post to it. At the moment that thread is lost deep among others

in reply toGrumpy77

Yes, the information flow through this forum is very fast and things move along quickly and sometimes get lost in that high speed flow of information. Not sure how to get in touch with an administrator. I contacted HU before about another issue related to that post, but the person I contacted only worked on technical issues and they referred me somewhere else, but I was not able to figure out how or who to contact from that point.

Art

M1tz1 profile image
M1tz1

You're in my thoughts and my prayers.

tarverusmc profile image
tarverusmc

thank you

AmyLindy profile image
AmyLindy

Wow!!!

Hiroko profile image
Hiroko

Semper Fidelis Devil Dog and best of luck.

delboy381 profile image
delboy381

I wish you good luck I hope you can reverse yours symptoms .

tarverusmc profile image
tarverusmc in reply todelboy381

today is my fith day.

reduce 1/2 mirapex. and 8 pills not 10 pills of sinemet. daily

I did up bumped up my b1 thiamine to 2000mg.

recap

I'm doing well. stronger and able to run with my left side being very mobile. before disability.

I hope for the next 4 days to recover and reduce more PD meds

Rujack profile image
Rujack

How’s the thiamine working out?

tarverusmc profile image
tarverusmc

really well.

update is 1000mg breakfast

1000mg lunch

PD med regular.

no left leg pain

no left side tremors

mind and body is clear

relax and not anxious

no rigidity

no pd symptoms that I had before the thiamine protocol

two weeks with this dosage and i will try to reduce pd meds slowly

in reply totarverusmc

I copy and pasted your post to the following thread so that others can get a broad idea of the effects of short term thiamine dosing in PWPs.

healthunlocked.com/parkinso...

Please update that post with your progress when you can! Thank you for sharing your progress!

Art

jimcaster profile image
jimcaster

Hi! I'm curious to learn whether thiamine is still helping you. I've been taking thiamine for a month and am very encouraged. Less stiffness and slowness on right side, more energy, slightly better handwriting. How about you?

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