Send your testimony, thiamin HCI

Help our Italian friends that have done so much for us for such little reward.

Send letters and posts.

To:

PwP and caregivers; Friends and relatives of PwP; Researchers and Research hospitals; Michael J. Fox; Famous people with Parkinson's

Example below:

Dear sir,

B1 Thiamine therapy stops progression, suppress motor and non-motor symptoms:

(Thiamin HCI is oral substitute to IV B1) 2 x day (morning 2g and at lunch 2g)

Doctor Costantini strategy that I find helpful "thiamine hcl stops the progression forever...".

.

I have gone from slow motion to normal motor action since joining the growing number of PwP that have started B1 regimen/protocol. –

Doctor Costantini - “Why is this? Because there is no medicine or drug that is able to affect all of the organs, whereas all of the organs function thanks to Thiamine. An important detail”, adds doctor Costantini, “the Thiamine therapy brings no collateral damage with time”.

High-Dose Thiamine: A Novel Promising Therapy for Parkinson's Disease.

blogtalkradio.com/parkinson...

Dr. Marco Colangeli and Dr. Antonio Costantini

healthunlocked.com/user/sur...

healthunlocked.com/parkinso...

Dr. Costantini's email address : [e-mail]

My name is Marco Colangeli, I am Dr. Costantini's research assistant, co-author, and when needed, also translator. Thank you very much for listening to this show, it was a remarkable opportunity to share the findings of our research with more patients.

From our point of view there are a few aspects that should be highlighted and possibly further mainstreamed:

1) It is important from our point of view that also your own practitioners and MD are involved with this novel therapy. Therefore we do call upon your contribution to this research by informing your Doctors about this therapy and the beneficial effects you are experiencing. We have experienced an unspeakable amount of skepticism and lack of trust towards this simple yet incredibly effective therapy. If on the one hand we can see why this may happen, on the other hand we do consider that regardless the personal skepticism or any less-than-professional form of competition among doctors, it is fundamental for the well-being of the patients that your doctors are asked to contribute actively. This is particularly relevant in light of the fact that we have limited time and resources to follow a continuously increasing number of patients worldwide.

2) It is paramount that out clinical findings are taken to the next level by partnering with research institutes and pharmaceutical companies to fully understand and fully exploit the potential of this therapy. Our resources are too limited (since 2011 we have worked on this 100% without any form of external funding sometimes even purchasing from third parties the thiamine to provide our patients with) and we cannot mainstream the results of this research alone. The exact mechanisms of action of Thiamine on PD patients (as well as on a number of other conditions we have studied and documented at case-study level) must be researched and fully comprehended. Moreover, in the context of a proper double blind label type of research, this therapy can be A) improved even further and B) recognized by the scientific community. The most direct consequence of this is that millions of patients worldwide will experience the same if not better results that those who have tried the therapy because already in direct contact with us have.

Thank you for your attention

Best regards

Dr. Marco Colangeli and Dr. Antonio Costantini

[e-mail]

[KERRINGTON]

Watch, once Thiamine is recognized they will say it'a drug, and pull it off the shelves !

[tbirchf in reply to KERRINGTON]

Yikes! Start stocking up!

[Gioc in reply to tbirchf]

Well in case I'll give a bucket to the brewery in front of my house.

(as it is also used in the production of beer and wine)

[tbirchf]

Today my husband finished up his first bottle of thiamine Solgar brand, four 500mg tablets before breakfast and four 500 mg tablets before lunch. I thought we should give the Vitacost brand a try...it has less additives and costs less. My husband started Vitacost today, choked on a capsule til he kinda puked it up (he has Parkinsons swallowing problems), and has felt bad all day after taking the four 500mg capsules. He says he feels jittery inside is how he explains it and his left arm is a bit shaky. So do you think the Vitacost is more potent and we need to cut back to maybe 3 capsules instead of 4? Do you know of anyone who has had this problem (feeling jittery after taking thiamine)? An order for the powder form of thiamine is on its way from Amazon, but now I am afraid the will make him feel bad! The Solgar did not make him feel bad but it also was not really giving any relief from Parkinsons symptoms. Do you think I should email all this to Dr. Constantini? I hate to bother him, he must be swamped with emails!

[Hidden in reply to tbirchf]

I have no answer