What is the percent of people with PD tha... - Cure Parkinson's

Cure Parkinson's

26,583 members27,899 posts

What is the percent of people with PD that B1 has helped?

parkie13 profile image
34 Replies

Would any one know of a study or anecdotal evidence of people with PD that B1 has helped?

If it has not helped how many times was it tried and for how long and what dosage?

Thank you

Written by
parkie13 profile image
parkie13
To view profiles and participate in discussions please or .
34 Replies
Gcf51 profile image
Gcf51

"TTFD, could significantly improve physical activities" I question the dose recommended.

ncbi.nlm.nih.gov/pmc/articl...

RedJY5 profile image
RedJY5

Started taking vitamin B1 about 6 weeks ago gradually increasing dose to 500gm and 500gm x 2 alternate days, my writing has just returned to its larger cursive nature and I’m told by my husband that I appear to be more myself and that I am now lifting my feet when I walk instead of the Parkinson’s shuffle! It’s early days but things are moving in the right direction. I recommend reading Daphne Bryan’s book on this subject.

parkie13 profile image
parkie13 in reply toRedJY5

Definitely, if it wasn't for vitamin B1,I would be bed-bound.

Gcf51 profile image
Gcf51 in reply toparkie13

Most B1ers use high dose B1 as hcl, but how about the under researched B1 in TTFD, I feel results at 16.65mg B1 as in TTFD.

Dap1948 profile image
Dap1948

In my book “Parkinson’s and the B1 therapy” available from all amazons, I include 30 stories from people having success on B1. On the Facebook group there are many morefacebook.com/groups/parkins...

Often if people report they haven’t been helped, it’s because of some rectifiable reason. I’ve addressed this in my book.

I know this doesn’t exactly answer your question but I hope it helps.

Gcf51 profile image
Gcf51 in reply toDap1948

Most B1ers use high dose B1 as hcl, but how about the under researched B1 in TTFD, I feel results at 16.65mg B1 as in TTFD.

kevowpd profile image
kevowpd

Multiple estimates put the success rate (and by success i mean some perceived benefit) at 10 to 20%. This would include people who are enjoying a non-placebo therapeutic benefit and those enjoying a placebo benefit. My completely finger in the air assessment is that this range (10 to 20) seems about right.

Gioc profile image
Gioc in reply tokevowpd

I didn't know that the same substance could give a placebo effect for some and a therapeutic effect for others. LoL. Here we are really at the top.

Kia17 profile image
Kia17 in reply tokevowpd

Do you mind to tell us where you have found these numbers?

HekateMoon profile image
HekateMoon

There is a fb group with about 6000 members. Im sure you can have responses there...

ForViolet profile image
ForViolet

It helped with my husband's ability to swallow pills almost immediately after his first 500mg dose of thiamine. Happy to hear of the many numbers on the fb group.

Springbreak profile image
Springbreak in reply toForViolet

hello good to know that his swallowing improved. How often does he take the 500mg of b1

Hikoi profile image
Hikoi

parkie13

I find questions like this can't and don't prove anything because you do not ask about other drugs specifically levadopa, mucuna and agonists. All will improve symptoms so if you don't know if they have been adjusted or started you have an incomplete picture of the effects of thiamine. Also helpful would be disease duration so you can at least measure reported success against one marker.

parkie13 profile image
parkie13 in reply toHikoi

I was and am taking sinemet c/r

Hikoi profile image
Hikoi in reply toparkie13

Parkie have you adjusted your pill regime since starting thiamine, increased or decreased? Are you only taking sinemet CR, no other drugs? Your bio says you have been diagnosed 3 years, correct?

Juliegrace profile image
Juliegrace

I have written about this in the past but I don’t have the energy to go through my history to find it. I was one of the early ones to use B1 and I was in touch with Dr. C. I took injections for almost a year, adjusting doses and timing with no discernible response. I also tried oral HCL and the sublingual version with no success. Initially I had some jitteriness so I know I was having some response to it. Long term I believe it exacerbated my dyskinesia. It certainly did nothing to alleviate it. I went into it with high hopes and an open mind. However, I recall many people here who reported no response or improvement, but it seems that that is glossed over regularly. I have become quite skeptical (and cynical) about it. I have never been comfortable with the claim that it “stops progression.” Maybe for some people it slows progression, especially if it is taken early on. I have no patience with claims that it is a panacea and that it will work if ‘you just get the dosage right.’ I believe that there are more people who don’t respond than people who do.

parkie13 profile image
parkie13 in reply toJuliegrace

I am so very sorry that it is not working for you. My PA wrote to doctor C. and got an email reply. My question was how come my blood pressure was going high? After a while it's stopped and my blood pressure is still not low but it did go down. My blood pressure was always higher. Then my other concern was that injectable B1 h a d aluminum added to it as a preservative. It even had a warning on the leaflet saying that if you are taking a lot you might want to look into it. Dr. C said that in Italy their injectable B1 did not have aluminum in it. So I started on the capsule form of vitamin B1 and another capsule of magnesium. Almost right away I noticed things where better. My balance was so bad I would have to take a step back so I would not fall. I also had the droopy Parkinson's face, my writing was starting to get small, I could not pull my pants up. Once I got into bed I would not be able to move. Vitamin B1 for for me was like a miracle. Thank you to all of you for your shared knowledge. Mary

ssrs profile image
ssrs in reply toparkie13

So do the injections in the US still have the aluminum in them? If so, that can’t be good, at least I don’t think it would.

Turnipbarrow profile image
Turnipbarrow in reply tossrs

The b1 injectable from Canada does not have aluminum in it

ForViolet profile image
ForViolet in reply toTurnipbarrow

Thanks. Good to know this. Do you know the brand on that? I'm buying capsules but would like to note that in case we switch to injections. Maybe it's all the brands in Canada. Will note. thanks

parkie13 profile image
parkie13 in reply tossrs

I'm using Vitacost capsules, however I'm sure they still have it.

Gcf51 profile image
Gcf51 in reply toJuliegrace

Have you tried B1 as in TTDF?

Juliegrace profile image
Juliegrace in reply toGcf51

TTFD, yes.

Gcf51 profile image
Gcf51 in reply toJuliegrace

How did it work for you? Did you pop a few thinking it was B1 as in hcl?

ion_ion profile image
ion_ion

75%!?

Gcf51 profile image
Gcf51 in reply toion_ion

75%!? in reference to what.....

Juliegrace profile image
Juliegrace

I’m glad it helped you. There was no aluminum in the B1 i was injecting. I had a prescription from my naturopath to a reputable compounding pharmacy.

parkie13 profile image
parkie13 in reply toJuliegrace

I went to my Pharmacy and supposedly they did research and could not find one with no aluminum. I don't think that they are a compounding pharmacy.

HekateMoon profile image
HekateMoon

I started b1 Hcl with the solgar 500mg. At the time my balance was terrible. My kitchen is small an i was stumbling from side to side. I also had lost rotation of my left foot that was dragging and my left shoulder was in pain. I couldnt turn without taking a few steps. I was depressed. It was the beginning of the pandemia and the neuro had sent me home saying it was nothing.. I knew it was Pd. My mother had it. Within a couple of weeks of taking B1 Hcl my balance was restored i kept increasing. At 2000mg i was able to turn, balance was improved with some exercises my shoulder got better and my brain fog was clearing. My foot started to rotate. It was unsustainable for me to continue with the solgar as i would have had to take 5 enormous pills a day and it was expensive on welfare. I found powder. The taste is bitter. I kept at it for as long as i could. Tremor and central pain were still there. Im still exploring. At the moment taking TTFD but not sure it is the same. Have to find a financially sustainable source or continue with the powder...but defo i got better.

parkie13 profile image
parkie13 in reply toHekateMoon

Vitacost has a fairly inexpensive thiamine hcl. You can get a big bottle of capsules. The bottle contains 300 capsules of 500 mg B1. I think this last time I paid something like $29. I hope that helps. This inflation is awful. Mary

HekateMoon profile image
HekateMoon in reply toparkie13

Thank you Mary. I tried. They didnt send to Ireland. And most of the time they were out of it.

Turnipbarrow profile image
Turnipbarrow in reply toHekateMoon

Have you tried dr Clark store to see if they send to Ireland.?

HekateMoon profile image
HekateMoon in reply toTurnipbarrow

Hi Turnip. Finally i got through to vitacost!!! Happy i got my supply sorted. Thanks

Turnipbarrow profile image
Turnipbarrow in reply toHekateMoon

👍

Not what you're looking for?

You may also like...

Motegrity helped me with the off time

I got prescription for Motegrity (2 mg) to help me with the constipation. It is effective and it...
felixned profile image

PD research: What is the problem?

In a well written letter posted on...
fwes profile image

IS THERE PEOPLE WITH MILD PD SYMPTOMS

hello friends, is there people who never progress to severe symptoms of PD? i saw a lady at my Dr...
RS313 profile image

Do other people feel that PD is misunderstood?

I mentioned this earlier and my opinion was reinforced a couple of days ago when talking to a lady...
Court profile image

What PD has given me.

I always thought I could do it all, work harder, push myself more, some day I would be rewarded....
Sedona profile image

Moderation team

See all
CPT_Aleksandra profile image
CPT_AleksandraAdministrator
CPT_Anaya profile image
CPT_AnayaAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.