Not many people have a chance to say they have as great of a doctor as I do. Thank you for everything you’ve done for me and I’m so happy I’ve found a doctor like you.
You’re such a wonderful doctor and you always make me feel so safe. Thank you for being the best doctor for me.More than a good doctor, I value the fact that you were a good listener. More than being just professionals, I value the fact that your attitude was exceptional.Thanks for teaching me the difference between Fact and Faith: Fact is when any ordinary doctor diagnoses illness in a report. Faith is when good doctors like you give their patients the strength to recover.
Kia
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Kia17
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There are not words to adequately thank a great human being like Dr. Costantini, who everyday of his life gives his all to help others to get better from these dreaded neurological disorders! Just look how many people he has already helped on this forum alone and he has patients around the world who he helps too and this does not even take into consideration his office patients (over 2,500) or other neurologists that consult with him in order to learn about his HDT protocol. I wish only the very best for Dr. C because he certainly deserves the very best! Just imagine how many more will ultimately be helped by what Dr. C is doing!
We talk about many things on this forum and much of it suggests hope and promise for the future of PWPs, but Dr. Costantini's HDT protocol is in a class by itself and it is already delivering on the promise of an improved quality of life for many who are already using it or testing it. By all appearances so far, it looks like his protocol is going to, at an absolute minimum, let many PWPs be able to be around to try many of these other promising treatments that we read about everyday on this forum!
God must be very proud of this man and I wish there were many more like him in the world to make it an even better place!!!
Dr. C doesn't have to spend all of his weekends, evenings, early mornings and free time answering these emails, but he does because he deeply cares about his patients. Some doctors put in their nine to five and that's it. They can only give you 15 minute visits and then they have to move on to their next patient, whether they want to or not. It is clear from the members who have gone to see Dr. Costantini, that time limits on visits to his office is one of his last considerations. With him, the patient comes first!
Thank you, Dr. Costantini for being so caring of others!
You too Art, you're like Dr C's favorite cousin, or like a cousin of Dr C who's our favorite. Thank you so much for being an integral part of this family.
Je viens de lire votre message (datant d'il y a 2 ans!) ou vous rendez hommage au Dr Costantini... . Vous dites que le Dr Costantini vous a dit "Prenez rendez vous à mon bureau et nous trouverons la solution à tout"... vous répondez il en a été ainsi... Pourriez vous me dire quelles ont été les améliorations après votre visite auprès du Dr Costantini.. Je suis tellement heureuse de lire des messages comme celui ci... merci d'avance pour votre réponse
Merci de m'avoir rappelé ses paroles. Après je me suis sentie très bien, tellement bien que je suis allée nager à la plage en sautant ma dose de l'après-midi. Effet placebo? ou est-ce peut-être le pouvoir des saints? Le docteur Costantini n'est plus parmi nous, mais son travail ne sera jamais oublié. Je ne sais pas si cela fonctionnera pour vous aussi, mais cela a très bien fonctionné avec moi.
Vous pouvez trouver ce que vous recherchez en tapant HDT dans la barre de recherche. HDT signifie Hight Dose Thiamine.
Merci beaucoup d'avoir pris le temps de me répondre.. Je souhaite également que le protocole du Dr Costantini (qui nous a malheureusement quitté il y a peu) fonctionne sur mon mari... Je vous souhaite de bien vous porter
Je vous souhaite le meilleur. Si vous rencontrez des difficultés, posez une ton question sur ce forum sans hésitation et vous recevrez toute l'aide dont vous avez besoin. La maladie de Parkinson ne court pas vite et le temps est peut-être de notre côté.
Encore Merci pour votre bienveillance,, je sais que les malades de Parkinson forment une grande famille d'entraide dans le monde entier... une chose est sure, je ferai tout pour que mes petits enfants puissent profiter de leur papy le plus longtemps possible...
Vous êtes au bon endroit. Nous ne donnons pas de compassion mais des réponses efficaces si possible, il y a beaucoup à apprendre pour cela, êtes-vous prêt?
Depuis l'annonce de la maladie de mon mari, j'ai fouillé, fouillé sur le net pour en savoir plus sur cette maladie en allant sur les groupes, c'est comme celà que j'ai trouvé les articles sur le protocole du Dr Costantini. (mon mari n'aime pas vraiment internet),, les vidéos de l'avant et après des patients du Dr Costantini m'ont redonné de l'espérance, ainsi qu'à mon mari... Ensemble on est prêt à déplacer des montagnes pour arrêter la progression de cette maladie.,, Pour répondre à votre question, je suis prête à apprendre et à faire ce qu'il faut pour transmettre à mon mari les bons conseils de ce site...
Brava! bien! Tout d'abord, je vous suggère d'ouvrir un de vos post où vous décrivez brièvement où se trouve la maladie, quels médicaments il utilise et quel type d'informations vous souhaitez recevoir du forum et je les traduirai en anglais si vous le souhaitez, donc les membres du forum ils peuvent mieux comprendre le cas et donner des conseils appropriés pas seulement sur la thiamine.
I wish not only to tell everyone I come in contact with (the world) about this honorable Dr., but I sincerely pray they would listen. My Parkinson's treatment story has become intimately interwoven with B1 (Dr.COSTANTINI’S HIGH DOSE THIAMINE). Every time I tell anyone about my Parkinson's treatment, I'm most excited about telling the part of high those thiamine being prescribed to me by a Dr in Italy and he's real 😃. I'm fascinated not only by the fact that he's a real Dr., but by his actions. How he's promptly responded to me via email for FREE. I feel this post should be considered our reasonable service. So please join me in saying GRAZIE MEDICO CON MOLTO AFFETTO. I'm in the Dom. Rep. on vacation and there's a neighbor here who I know dearly as a church brother who's had Parkinson's for approximately the same amount of time I've had and seeing the state he's in, has allowed me to witness in a more vivid manner how B1 has reversed my symptoms. I am going to get him started on the B1 protocol with the Solgar tablets I bought because I also brought some powder for myself on the trip, which I've been using all along, I also think we should spread the word as much as possible. I have contacted Gary Null (Google him) via email haven't heard back, but will eventually contact again.
If you think that Dr C. answers your emails for who knows what fate, moreover in English, a language unknown to him, you are wrong. His presence and disposition has been searched, taken care of and strongly desired by Art Easilly with his work, here for you, available to anyone who wants to try and if you want my personal opinion do it.
He, Art has done it, because he loves to help others like all of us.
This is an easy way to at least say thank you to Dr. Costantini. Thank you Kia for initiating this movement of gratitude. I can't say it enough thank you Dr.
I have just recently heard of him, and his remarkable protocol! My husband was diagnosed with PD in December 2018. Still no meds, but exercise and CBD oil. I have watch Dr C’s videos and read about him! God bless him. I want to talk to my husbands neuro about the therapy.we live in US.
Predictably your Neuro will be a sceptic. Ignore him.
Diagnosed 2012
My regimen:
The positives: no bradykinesia, I cut my food with a knife, no button difficulties, brush my teeth now w/o needing elect brush, more strength. Getting in and out of bed, turning over is easier. No more constipation. Parkinson's progression stopped. Suppressed all motor and non-motor symptoms...
Entering my 7th year post diagnosis and have not fallen, not once, to the surprise of my neuro. Was seeing neuro every 6th month, last visit he set app one year. He said if needed we could do some changes earlier. He said my condition can change in as little time as one week.
New schedule, now I follow this regimen:
3 x day C/L 50-200 ER : 8 am, 2 pm, 8 pm. Because it is ER, I take with or w/o food.
2 x day (8 am 2g, and 2 pm 2g) Vitacost vitamin B1 (as thiamine HCL) 500mg, easy swallow capsules
B1 Thiamine therapy reference / stop progression, suppress motor and non-motor symptoms:
(Thiamine HCL is oral substitute to injecting B1) 2 x day (morning 2g and at lunch 2g)
Doctor Costantini strategy that I find helpful "thiamine hcl stops the progression forever...".
Parky people say the first five years is your honeymoon stage with Parkinson's. After that, progression more rapid.
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”.
Thank you, Roy!!! Sounds awesome. I am wondering if my husband should start taking the therapy now or wait? I really appreciate your detailed response.
53. Recently I asked Dr. Costantini if some PWPs can take B-1 by itself without prescription meds or other supplements because the question has come up multiple times on the forum. He sent his reply today and here it is. Importantly, please keep in mind that there is a very broad range of symptoms in PD and to a similar extent, a very broad range of PWPs at various stages of disease progression and though you may feel your symptoms are severe, Dr Costantini, in his broad experience may not feel the same because he is taking into account the fact that there are some very advanced stages of PD that he has seen in over 3,000 patients on his B-1 protocol.
A. When the patient has been diagnosed by us for a few months with a mild symptomatology and without any therapy in place, or we diagnose him at a very early stage, we treat him only with thiamine and often with lower doses than patients who are at a more advanced stage. The patient improves considerably and remains at a standstill. It is difficult, however, given the previous damage, that the symptoms, especially the motor ones, all have a total regression. The surviving cells, even if healed, are not able to do all the work that the system did when it was healthy. At this point either the patient is content to have some slight symptoms or get the complete abolition by adding to the treatment small doses of levodopa. We only have three patients who use only thiamine because they have had a complete regression of symptoms.
Furthermore, suppose that for any reason the patient cannot or does not want to take any kind of classical treatment for Parkinson's disease, the right dose of thiamine can give him, at any stage of the disease, an improvement that can range from 30 to 70%, while at the same time abolishing the progression of the disease!
Apparently Dr. Costantini wants to be very clear on this subject because he has responded to it in 3 separate emails! This is his third addition on this subject :
To be clearer: all Parkinsonian patients, at any stage of the disease have benefit on symptoms and stopping the progression of the disease, whether or not they are being treated with other drugs. We do not have any patients who do not respond to treatment with thiamine.
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What do you think about this: Dr Gundry: One harmful food?
Thiamine as per Dr. Constantini
Dr. Jonathan Sackner-Bernstein & Dopamine 
What unusual or bizarre things have you discovered about Parkinson’s?
If you want to know the future for Parkinson Disease Dr Roger Barker’s Edinburgh Lecture is superb.
