In short
Parkinson's research studies continued. This month's update focused mainly on topics outside Parkinson's research.
Most of the December 2025 update covered other topics. The items about the Parkinson's research are summarized here.
Vika Montano wrote that Zhittya had by then dosed more than 240 people with Parkinson's, five who had had a stroke, two with dementia and two with autism. She said FGF-1 is given as a spray into the nose.
One participant's journey
The update told the story of one participant. When the Parkinson's studies began, it said, the company was reluctant to accept people at more advanced stages. Its priority was people with clear signs of Parkinson's who were not so far along that the body might be unable to respond to FGF-1.
In May 2023 it made an exception for a participant in the later stages. The update shared his own later reports about walking and hand-eye coordination, and linked to a video.
Other participant reports
The update shared further comments from participants and family members. Topics included saliva control, balance, coordination and falls. One came from a participant with progressive supranuclear palsy (PSP), another brain condition, who reported fewer falls and said he still had a long way to go. The update also repeated a family's long account from the month before.
Looking ahead
The brain imaging studies at Washington University in St. Louis were continuing.
In his closing section, Dan Montano, the chief executive, wrote that over the years he had met with participants with stroke, Parkinson's disease and other conditions, and that seeing people do better was what gave the work its meaning for him.
This summary covers the Parkinson's research in the December 2025 update. The complete update, including the other topics it covered, is below.
Read the complete December 2025 update as published
The text of the update Zhittya sent, word for word. Pictures, charts and layout are in the PDF. Open the PDF.
December 17, 2025, Monthly Update Freedom to Try Medical Innovations for Life-Altering Diseases or Conditions
Zhittya is sponsoring the Nevada Freedom to Try: a constitutional amendment to the Nevada Constitution that allows people to try medical innovations and allows providers to try advanced new medical breakthroughs without the barriers of the FDA.
Zhittya Genesis Medicine is sponsoring an initiative to amend the Constitution of the State of Nevada to protect the freedom of people suffering from life-altering diseases or conditions, and allow them to seek medical innovations to enhance their health and extend their lives. The Freedom to Try, which Zhittya is sponsoring, is very different from The Right to Try, which has been a proven failure! According to the FDA’s official Right to Try Reporting Summary Page, from 2018 to 2025, the Right to Try has been used 21 times in 7 years in a nation of 340 million people, with tens of millions of sick people. Patients suffering from late- stage cancer, ALS, no-option heart disease, and more do not qualify to try because the Right to Try was written by FDA bureaucrats, Washington DC healthcare lobbyists, and lawyers. Is it any surprise that desperately sick people do not qualify to try to save their own lives? I have complained many times in this Monthly Update that the FDA barrier to medical innovation is suffocating. I have written, based upon my analysis of the biotech discoveries made since 1985, only a few classes of novel biological medicines have made it through the FDA. I have seen medical breakthroughs, which eradicated 100% of cancer tumors in pet dogs with naturally occurring cancers, sitting on the shelf for 19 years. Would that medicine eradicate cancers that have spread throughout the human body? In theory, yes. Will it work on humans? I do not know. What I do know is we have a duty and an obligation to find out. According to the Tufts School of Medicine, it takes the average drug over 20 years and a cost of $2.6 billion USD to be approved by the USA FDA. I have spent $100 million myself on our heart medicine to treat the #1 cause of death in the world, “small vessel heart disease.” We have great human data for a terminal disease that kills around 15 million people per year (~650,000 Americans per year), and we are trapped in a Catch-22 with the FDA. The worst part of those $100 million USD that I spent was the ~$50 million that did not go to medical research. That ~$50 million went to FDA consultants, lawyers, and lobbyists whose sole goal was to guide us through the FDA, not to pursue any medical research. They did guide me somewhere: “The Hole of Perpetual Pain, the Land of Continued Delays, and the Universe of Unlimited Demand for my Money!”. I believe Zhittya’s FGF-1 injected into a diseased heart could extend the lives of ~500,000 Americans per year. Here is a look at this ABC News broadcast: our medicine works in saving lives. https://www.youtube.com/watch?v=IPtv_0LWK4k
The Nevada Freedom To Try allows companies, like Zhittya, to be able to bypass this major barrier that is the USA FDA. Rather than waiting for bureaucrats in Washington, DC, to take years to respond to appeals, requests, and documents, a coalition of companies, doctors, and consenting patients can conduct actual medical research to impact patients suffering from nearly any disease. Moreover, the Nevada Freedom to Try opens the gates for patients suffering from any disease which alters their quality of life, NOT only the diseases that have been subjectively deemed as “terminally-ill” by a nameless bureaucrat at the FDA. Our Nevada Freedom to Try Amendment will give companies the opportunity to offer advanced medicines to consenting patients, under doctors’ supervision, and with IRB oversight to ensure that patients are getting cutting-edge and safe treatment, all while navigating around the 20 years and $2.6B cost at the FDA. The Nevada Freedom to Try allows Zhittya Genesis Medicine to conduct medical research studies in Nevada to treat no-option heart disease, strokes, Parkinson’s disease, dementia, type 2 diabetes, and more. This allows for Zhittya to rapidly advance what we believe is safe and what we believe works. I believe this Freedom to Try will also allow Zhittya to be cash flow positive and self-funding. It is reported that about 90% of biotechnology companies fail, not because their medical idea is bad, but because they run out of money in the expensive pursuit of FDA approval. Everyone knows: when you run out of money, it is bad! When the goalpost to victory is 20 years away, and you need $2.6B USD to get there, many things can break a company: the Great Financial Recession, COVID-19, supplier failures, competitors, and more. We cannot have medical innovation in an economic environment where everyone knows you have a 90% failure rate, because you cannot access cash to survive.
I believe the Nevada Freedom to Try will create a medical innovation boom that will change the world. Please keep in mind two things:
(1) Sick people: There are tens of millions of sick people with heart disease, strokes, diabetes, respiratory issues, kidney issues, and more and more. Plenty of people want better health and longer lives.
(2) Tens of thousands of medical research papers generated from trillions of dollars spent on medical research sit on the shelf; some of them, with amazing possibilities, have not advanced to help sick people.
Freedom to Try and improve one's own health and extend one’s life is a RIGHT, not a privilege granted by a bureaucrat in Washington, DC.
You will see throughout this update that the Nevada Freedom to Try not only helps to bring research out of the United States and into the hands of patients that most desperately need it but also helps to bring research stuck in limbo in other nations around the world to the United States. 1. United States Biotech Companies:
This December 17, 2025, Update serves as Zhittya’s first public announcement of the Nevada Freedom to Try. Despite our efforts to keep this project a secret, word of mouth has already brought us 5 US biotechnology companies wanting to participate in the Nevada Freedom to Try. One is a fellow Nevadan biotechnology company that reports they have a revolutionary breakthrough treatment for cancer. I have listened to them and have never heard anything so unconventional for treating cancer. Is it real? Again, I do not know. What I do know is that they have the right to have the freedom to try and treat cancer, to maybe save lives.
The definition of insanity is doing the same thing over and over again that has always failed, but doing it again expecting different results. For the last 40 years, medical institutions, Big Pharma, and governments around the world have spent trillions of dollars on a system that has failed to yield results for patients 99% of the time and has led to countless possible medical treatments being shelved, ignored, or discarded.
I am an optimist. I believe that with the Nevada Freedom to Try, rather than the 20 years to achieve the FDA’s rubber stamp, companies can know within 7-8 years if their medicines are safe, efficacious, and proving beneficial to patients. The pent-up demand by medical innovators to be Free to Try is overwhelming.
As the current system is, companies that have developed a treatment for diabetes, cancer, or whatever it might be are not stopped because of medical science but because of consultants, lobbyists, and no-name bureaucrats in a clandestine building in Washington, DC. That is why the cost to get a drug approved is $2.6 billion and takes 20 years, not because medical innovation is slow, but because the gears of bureaucracy grind every penny out of you over decades.
From December 8, 2025, to December 11, 2025, Vika and I attended the Family Offices Super Summit in Fort Lauderdale, Florida, with over 600 wealthy investors who have personal family offices to manage their wealth. My presentation was on: Breakthrough Biotech Medicine: Treating the Cause of Death of 65% of All Adults. We had a great response since many of them were interested in their own life and health. As part of that presentation, I mentioned the Nevada Freedom to Try in one slide of my presentation, and the response was overwhelmingly positive. We received at least 6 inquiries from individuals stating that their family offices had invested millions in a biotechnology project to treat a specific disease affecting their family. They have expended many millions of dollars to advance that medicine, and oftentimes that medicine was trapped at the FDA. All of them asked if they could move their project to Nevada to advance their research. They are frustrated that they want to spend their money and hopefully improve the outcomes of a disease that has ravaged their family. They have sat in their chair for years, sending money to a project they believe in, only to see it rot for years at the desk and in the darkness of the FDA.
They are coming to Nevada to see the clear skies of Freedom to Try and to do good. Instead of paying the swamp to stop their hopes and dreams, they will be free to provide their treatments and ideas in Nevada to make people’s lives better.
- Other Nations’ Biotechnology Companies:
It is important to note that the FDA serves as a barrier not only for American research and development but also for international research to make its way into the United States. There have been countless medicines that have been approved and in use in Canada, the European Union, the United Kingdom, Japan, South Korea, Australia, and more, which have not been able to make it through the barrier that is the FDA. Admit it: 20 years and $2.6 billion dollars and no assurance of getting approved is a real barrier.
The same applies to research that is not yet approved. In the 1990s, I was hired by the Ukrainian government to help their nation switch from a communist economy to a free market economy. As a Californian investment banker with experience in high-tech, I had asked the Ukrainian government to show me all the discoveries that their research institutions had developed. To my surprise, they took me to the headquarters of the KGB in Kyiv. We walk out of the car, and I ask, “Why are we here?” They respond, “Because all the valuable discoveries from the Soviet Union are state secrets and must be protected so no one steals them. Secrets to be kept from development are no good for humans.” I found two amazing biotechniques in Ukraine, moved them to California, and the world is a better place for it. So, what if a cure for cancer is discovered if it sits on the shelf forever oceans away, while people are suffering and dying?
South Korea:
We have had an excellent relationship with the South Korean government for the last 27 years. We are especially close to the Korean Institute of Start-ups and Entrepreneurship Development (KISED). KISED has organized about 80 Korean companies to come to the Consumer Electronics Show (CES) in Las Vegas, Nevada, from January 6, 2026, to January 9, 2026. Some of the companies in attendance are biotechnology companies that have developed cutting-edge medical devices and medical research. Since informing Korean biotech and pharmaceutical companies about the Nevada Freedom to Try, the response has been amazing, with 8 CEOs from some of Korea’s most cutting-edge companies, signing-up to attend in less than 24 hours. Korean companies with already approved medicines and devices in South Korea and Europe that cannot spend 20 years and $2 billion dollars to attempt to get their medicine approved in the United States want to know more about the Nevada Freedom to Try.
For example, let’s say a Korean company has developed a niche treatment for liver cancer. In the United States, this market would be too small for a big-pharma company to risk billions of dollars to develop a better treatment. A Korean company with an enhanced treatment would have to risk all of its capital and profits for the next 20 years to try and bring their medicine to the United States. If the potential profit of their drug in the United States is $50 million USD per year after spending 20 years and $2.6 billion USD to maybe get their drug approved by the FDA, they would simply never come to the United States.
To support bringing international medicines to American patients through Nevada, Zhittya is hosting a Korea-USA Biotech Innovation Investing and Partnering Event on January 8, 2026, at the Wynn Hotel in Las Vegas, Nevada.
For those of you who are entrepreneurs and are interested in attending, please email me directly at: Dan333@aol.com
Seating is already tight. In the 1997-1998 Asia Financial Crisis, I advised the government and companies on how to assist companies to restructure, while also helping to set up the “Seoul Angels Investment Fund”, where we raised over $200 million USD to invest. South Korea has always been good for me!
Summation of the beginning to the effort to protect the Freedom to Try Medical Innovations for Life-Altering Disease or Condition.
Click here to link to read the” Initiative Petition for the Constitutional Amendment: https://www.nvsos.gov/sos/home/showpublisheddocument/17296/6389959493 37730000 Zhittya’s willingness to sponsor a Constitutional Amendment in the State of Nevada to advance the Freedom to Try Medical Innovations, and I believe unleashes the creative genius of Free Markets to solve life and death issues is a good thing. I am betting ten years from now people will look back and see that 90% of the medical innovations that are saving lives in 2036 will have come through Nevada where they had the Freedom to Try and not through the USA FDA where they die in the swamp of darkness. Let the competition between Nevada and the FDA experiment begin!
We are reminded of the words of our hero Milton Friedman: 'The FDA has already done enormous harm to the health of the American public by greatly increasing the costs of pharmaceutical research, thereby reducing the supply of new and effective drugs, and by delaying the approval of such drugs as to survive the tortuous FDA process.'
Please wish Zhittya good luck with what needs to be done to free medical innovation from the FDA's bureaucracy! Background and Type 2 Diabetes Medical Research December Glance Report by Vika & Sergiy Montano
We need 80 volunteers for January 2026, February 2026, & March 2026 who are willing to travel to Las Vegas, Nevada, for the Type-2 Diabetes Medical Research Studies. As a note:
While the medical services and medicine that patients receive during this study come at no cost to the patient, we do not pay to treat people in the study, and everyone who is accepted into this study must pay for their own travel and commit to staying in Las Vegas for at least 3 days.
Patients enrolled in this study cannot be currently using GLP-1 medications, have the presence of other neurological conditions, or use certain anxiolytics or antidepressants.
If you are interested in participating in these studies, please reach out to vika@zhittyamedicine.com or reply to this email. Vika’s Patients’ comments:
Zhittya has now dosed over 240 Parkinson’s disease patients, 5 stroke patients, 2 dementia patients, 2 autism patients, and more. We have not seen any adverse events, and there is zero pain, as the medicine is sprayed up the nose without breaking the skin. I provide these comments to make you aware of what I believe is an amazing success: Type 2 Diabetes Patient Comment:
From Rock, a patient in our Type-2 Diabetes Study: https://youtube.com/shorts/FpCLpk_OuAw?si=bhQG_rYI-R1XUEW9 Vika Parkinson’s Patients emails
#1) When Zhittya Genesis Medicine first began its medical research studies for Parkinson’s disease, Zhittya Genesis Medicine was reluctant to take on patients who had more advanced stages of Parkinson’s disease. Our priority was focusing on patients who had clear onsets of Parkinson’s disease but were not so far gone that the body would be unable to respond to the FGF-1.
In May 2023, Zhittya made an exception to the rule and took on a patient who had already advanced into the later stages of Parkinson’s disease, arriving at the study being wheelchair-bound and nearly unable to walk.
In April 2025, we shared with you his story, where this patient had regained the ability to walk after 2 years of intensive work with Zhittya Genesis Medicine.
One week ago, in December 2025, this patient shared with Zhittya that his journey towards progress continues as he has regained his hand-eye coordination to get back to throwing a ball with his physical therapist.
Watch his journey here: https://youtu.be/UCaHvglxGQc
#2) Vika another change Nick has had such excessive saliva he had trouble not drooling to the point he got some medication from his Neurologist for that, but he has used it for just a short time because that has quit!!! We are so excited for these changes and so very grateful for you and Dan!!! And the work you are doing…
I cannot believe the blessings that you and Dan are is so many people and the possibility of so many more! \<3
#3) Hi Vika, This is a short note to keep you and Dan in the loop regarding the progress of my husband. He was in your BVI Cohort last May’24 for Parkinson’s. Immediately there was obvious progress after one week of BVI FGF-1 treatments and then for the next eight months it was 2 steps forward and one step back from those BVI improvements.
One year ago in Fall ‘24 He officially retired from his business only because of Parkinson’s.
September ’24: RV trip to Yellowstone Nat’l Park with our kids and grandkids.
Then a camping / hunting trip. He realized he was not able to hike and fish and hunt. Parkinson’s took away his hobbies. He still was able to take walks on the beach with me and the dog. Then the first Sunday morning of February’25. I awoke and found him on the bathroom floor, cold and unresponsive. Fire dept. and Ambulance arrived and he was transported to the Hospital. He had fallen and hit his head then strokes and seizures followed. All stemming from undiagnosed UTI on top of Parkinson’s. After 4 weeks of hospitalization Drs recommended we take him home or to a facility on hospice care. Now I had to consider planning his funeral. I called Vika and she counseled me to get him home as soon as possible and begin the FGF-1 protocol again. At that time the protocol was FGF1 every three months. Vika advised me of the new protocol to use. I brought him home where he had full time caregiver in the beginning. Drs sent him home on stroke and seizure Rxmeds. Also needed Ambien for sleep. He learned to walk with a walker and a wheel chair was needed for a while. He couldn’t get on his hands and knees to get a dose of FGF1. We had to get our son and son-in-law to do the dosing in the beginning before new applicators were sent. So he could then be dosed sitting upright. The following Parkinson’s symptoms he has struggled with for a year prior to the fall. But everything was exasperated by the results of the brain injury from the fall.
He was unable to dress himself, (could not figure out how to lay out a t-shirt and get his hands in the right holes) or a button up shirt. His food had to cut into bitesize pieces. Swallowing issues. Feeding himself, even a sandwich was very messy. He was unable to grip and hold the sandwich together. Drinking only from a straw or he would wear it. Morning cup of Coffee was a big challenge even with a Yeti. Evening glass of wine… yes, more challenging. He sat in a recliner chair most of the day and napped. Watched a lot of same channel tv because he “forgot” how to use a tv remote control. He was unable to get himself ready for bed (thank goodness for electric toothbrush, bathing, pjs.)
Over the next three months, March, April, May
I titrated off stroke & seizure meds and added many supplements and detoxing Traded RX Ambien for WYLD Sleep GUMMIES plus extra CBN10 for sleep. Also some Melatonin 20mg. This combination seems to do the trick and adjust dosing as needed. This took some getting accustomed to as he had never tried cannabis before. He is sleeping mostly uninterrupted 7-9 hrs each night. Not feeling drugged up in morning.
By Summertime we were in the swimming pool and he started working out, walking and balance exercises and stationary bike and shooting hoops indoors and the AirHockey table. He daily used Platinum Red Light therapy, weekly acupuncture and a few crazy diet changes. Always looking I found on the internet more physical therapies/activities for Parkinson’s patients.
My husband does not recognize a lot of his improvements over this past year and is disappointed with slow progress. His memories of February March and April are sketchy at best.
Fast forward fifteen months from the beginning FGF-1 treatments in BVI to September’25 during an appt with the acupuncturist, she reminded him of when he began acupuncture treatments before 2024 BVI - FGF-1 and the progress he has made since BVI – FGF-1 treatments.
He and his caregiver are walking with his dog one mile every day around here then back home to ride a stationary bike for 45 - 60 min. He does balancing exercises and then puzzles and memory games. Grandkids come here every day after school to play. He laughs with the grandkids and his face doesn’t look so scary now, without his mask (Parkinson’s not Halloween). His cognitive skills have dramatically improved over the past year.
He now gets up each morning and bathes and dresses himself before he comes out for morning coffee (drinks from his old favorite mug.)
He includes himself in our family conversations around the dinner table every Sunday evening. His voice is heard and he is relevant and keeps up with the conversation. His memory is wonderful and shows off every day.
His caregiver said her past 4 patients all had Parkinson’s Disease and have passed away. She has never seen improvements like he is experiencing. She had never heard of ZHITTYA or FGF-1. Recently, she took on another Parkinson’s patient and works for us only a few mornings now during the week for physical therapy, organizing schedules, pills, and his companion while I am gone.
I have scolded him about taking risks and falling, worried he can’t get up and I am unable to get him up off the floor without help.
The first week of August, he challenged me to sit on the floor and then stand up without using my hands to push myself up. Or for support. Go ahead - try it yourself! I was not able to stand up without using my arms to push myself up. Then he abruptly sat down and proceeded to do ‘sit to stand‘. He did it three times from the floor without using his hands.
Granted this is not the retirement I planned for us. He said he did not plan it this way either. He continues to use the nebulizer with FGF-1. He still has tremors and rigidity. He also wants to consider supplement therapies to FGF1. BUT Tomorrow I am driving him to buy a new iPhone ProMax17 (the one biggest screen).
He believes he will be able to use it now. Thank you FGF-1 ! He is ready to try it again. And I guess I am the one who lost it.
We recognize improvements big and small made since he started FGF-1 a year ago. He has suffered with Parkinson’s Disease and was diagnosed over 9 years ago. Parkinson’s did not show up overnight. We are both grateful. Thank you ZHITTYA and Dan and Vika for your commitment and support in changing lives. We believe!
#4) Hey Miss Vika, Everything is going great. I reduced my intake of carbidopa from five times a day to twice a day. I am taking amantadine for dyskinesia twice a day as well, but doing so much better I cannot thank you all enough. Balance coordination across the board. Everything has been better and continues to get better with each dosage.
So Thankful Cody
#5 from PSP patient: hey there Dan i thought that i would give you a update on my condition. anyway i just came off of the month long protocol that you all establish on a couple in your British island and a second month on it two weeks ago and i’m on my two week pause. I hope that you can forward this to your wife vika. and like i said at the beginning of this letter. i went from 3 to 5 falls day to 1 fall in 3 weeks and in saying that i still have a long way to go to be fully prepared to be able to walk w out a walker? thank u j xxxxxxxx Zhittya’s Medical Research Studies Funding
Type-2 Diabetes:
We have about 90% committed of the $5 million to fund the first 100-person study in Las Vegas. I believe we will be able to close that funding for the Type 2 diabetes study within 30 days. This will be the only opportunity to be part of the Type 2 Diabetes Medical Research Studies funding. Now that we have data that shows it appears to be successful in reversing type 2 diabetes, it reduces the risk. Don’t miss out on the possible 10 times return on your money with a backup guarantee from Zhittya of doubling your money in four years if you are not happy. I believe that all the investors will be happy.
Also, some of the investors are excited that they might directly be involved in a cure for diabetes. As one investor told me, he would like to tell his grandchildren they will not have diabetes in their lives when they grow up, because he directly contributed to the discovery to eradicate diabetes. He told me in 1955 his father collected dimes for the March of Dimes to find a cure for polio. His father told him, “Son, you will not have polio, because your daddy helped to defeat it.” He told me, “Dan, I have given a lot of money to charities, and all I have ever gotten back were more letters asking for more money. Dan, I read the Zhittya diabetes updates as if it were my own personal medical discovery project. I may know within 12 months that I helped to cure diabetes. Making ten times my money back does not excite me; I have plenty of money. What I want, Dan, is a wall plaque that says, “John XXXXX was a partner in finding a cure for diabetes.” I said he would get the plaque, and then he clarified that he still wants ten times his money back.
No Option Heart Disease:
Zhittya will begin treating No-Option Heart Disease Patients in the Bahamas in January 2026. In my opinion, small vessel heart disease is the biggest unmet medical need in the world. The World Health Organization (WHO) reports that about 18 million people die from heart disease every year. I believe about 85% of those deaths are from small vessel disease, which your doctor may call congestive heart failure, so he does have to explain small vessel disease. FGF-1 has been utilized in two heart studies in Germany, showing FGF-1 is safe and triggers the growth of new blood vessels, thereby re-establishing critical blood supply to the heart muscle. We did a USA FDA-cleared Phase I to show it was safe, and it grew new blood vessels, thereby extending the lives of no-option heart patients by over ten years. See with your own eyes: https://www.youtube.com/watch?v=IPtv_0LWK4k
I believe 85% of the annual deaths due to small vessel disease are around 15 million people per year. People with small vessel disease or congestive heart failure are generally in pain from their heart condition and therefore know they have a life-ending medical situation. I believe people who know they have a life- or-death situation are within two years of death, so that would be 2 times 15 million, or 30 million people who know they have a life-ending heart condition. Out of those 30 million people, the richest 1% would be 300,000 people, who have several pains in their hearts and know they are at risk of dying and have a net worth estimated at more than $31 million USD a person. The richest 5% of that 30 million would be 1.5 million people with an estimated net worth over $3.5 million. I do not believe a person worth $30 million USD with severe heart disease, with less than two years to live, is not seeking Zhittya’s heart treatment to extend his life maybe 10 or 15 or 20 years because he wants to have a nicer funeral for himself. I believe that the cardio medical establishment is not telling those patients about Zhittya’s treatment because (1) they do not know about it, (2) it is not approved by the FDA, and (3) it is not within what they can offer as a treatment, so they do not offer it.
Dr. Conville S. Brown, cardiologist and principal of The Bahamas Heart Centre, Nassau, Bahamas, has obtained clearance from “The National Medical Ethics Committee of The Bahamas (NMEC) to conduct a Medical Research Study to treat no-option heart disease patients in the Bahamas. The Zhittya team has visited Dr. Brown’s facilities in the Bahamas to perform heart procedures, and they are first- class with expert medical doctors.
I believe the wealthiest 1% no option patients (net worth over $31 million USD each); for example, a man in Hamburg, Germany, has not decided to accept pain and death from his heart condition and rationally chosen not to seek Zhittya’s medicine to save his life. I believe he has not sought out the Zhittya heart treatment because his medical doctors have told him he is getting the best medical treatment in the world for his heart, and there is nothing else to do but die. I believe Zhittya needs to raise global awareness that we can treat these millions of people and extend their lives. Towards that, Zhittya with Dr. Brown's Bahamas Heart Centre, is conducting a 100-person Medical Research Study to treat no- option heart patients with FGF-1, like we have in three other 100% successful heart studies. Zhittya will be trying to raise $10 million USD to fund this Medical Research Study for no-option heart patients, starting January 2026. I believe since we have had 100% success and zero adverse events regarding the heart when confronted with certain death, many of those 1.5 million people (wealthiest 5% net worth $3.5 million) will travel to the Bahamas to save their lives.
I believe that as Zhittya treats thousands of patients who are suffering from no- option heart disease, it becomes more difficult for the FDA to ignore our treatment. Equally, Medicare is the largest payer of healthcare benefits in the world. From my sources, Medicare spends around $250,000 on a no option heart patient in the last three years of their life. I believe Medicare should make Zhittya’s medicine “Standard of Care” for no-option heart patients available to all its coverage, save themselves tens of billions of dollars, and enhance the lives of millions of retirees.
If this Medical Research Study breaks the FDA’s Catch-22 trap mindset and Common Sense is used, I believe in the USA and then, followed by the rest of the world, we can save millions of lives.
Medical Research Studies Funding Investment Opportunity.
If you are interested in learning more about the Medical Research Study Funding investment opportunity (minimum investment of $25,000), please email me at Dan333@aol.com or call me at 702-802-8373. Besides making money, you can advance medical innovation to benefit millions of people.
Cross Border Medical Tourism
Cross Border Medical Tourism services are for those people who want to be considered for Zhittya’s future clinical trials or its current Medical Research
Studies. Cross Border’s is now arranging Medical Tourism to treat Parkinson’s disease and enhance stroke recovery in Las Vegas, starting January 2026
Cross Border is working on filling the Las Vegas Medical Research Studies (intranasal FGF-1 for Parkinson’s disease) on the following dates:
Cohort #43: January 26, 2026 – January 29, 2026
Cohort #44: February 23, 2026 – February 26, 2026
Cohort #45: March 23, 2026 – March 26, 2026
Please get in touch with Sam Cross at Cross Border Medical if you wish to be considered for the BVI cohorts. Sam’s email address is:
In addition, if you are interested in participating in a functional MRI brain scan study, which will take place at Washington University in St. Louis, please let Sam know. There is a finite number of slots for the imaging studies. These studies will look at brain blood flow before and after treatment with FGF-1.
Events:
Las Vegas: January 8, 2026
Korea-USA Biotech Innovation Investing & Partnering Event at the Wynn Hotel.
Zhittya will be presenting on the Nevada “Freedom to Try: Advancing Lifesaving Korean Innovations & Regulatory Path to the United States Market for Success for Patients and Providers.” If you are interested in attending this event, please email: dan333@aol.com Conclusion by Dan Montano
The Freedom to Try Constitutional Initiative in Nevada is my 2nd most important task on my list to accomplish. I will introduce the most important thing to you; I hope in January 2026.
For those of you who think I am crazy, I provide you with one more piece of evidence that you might be right. I have been on this project for 27 years. I have put my entire fortune in and work 14 hours a day, 7 days a week. My simple goal was to prove to myself that my existence, my life, mattered. I have met with the No Option Heart patients who received FGF-1 in Germany in 1995, another heart study in 1998, and the USA FDA cleared study in 2004/06. I have seen it work to save lives and lessen suffering. I have met with patients with stroke, Parkinson’s disease, autism, PSP, dementia, type-2 diabetes, and more. Always seeing that the medicine is safe and the people are better. Here is a link to Mark, in a wheelchair, two years later walking on his own, and recently catching and throwing a ball: https://youtu.be/UCaHvglxGQc
This is real wealth, knowing your life has done good.
When we started the Freedom to Try, it was to give Zhittya a chance to treat millions of people who are being denied modern medical discoveries that could make their lives better. I know the Washington, DC, FDA swamp: it ate tens of millions of dollars of my money and decades of my life in frustration. As other medical innovators have come out to join us in seeking FREEDOM to Try and provide what is needed, it has reinforced my belief that the Nevada Freedom to Try will change the medical innovation of the world. Already, we have been contacted by a Czech pharmaceutical company with great medical products they have developed, but they cannot afford to enter the United States, because the cost of $2 billion per product and 20 years is impossible. Homeopathic medicine is 30% of the medical treatments in Europe. Europe has half the chronic disease of the United States, a longer life expectancy, and 1/3rd the cost of medical care, and yet the FDA has effectively banned homeopathic medicine, even though there is proof in many cases it is better and costs much less. France is a leader in homeopathic medicines; several French companies want to know more about Nevada’s Freedom to Try. Being able to treat sick people better at 1/3rd the cost, I think, is good.
I have traveled all over the world as an advocate of free market economics. Where nations are free, the people are better off and wealthier. Where government (communist, socialist, central planning, Keynesian) is practiced, people are poorer and suffer. Why?
A PhD in business can develop a great central plan for a society. An entrepreneur has no grand plan to control and direct society. What everyone forgets, especially the PhD with no common sense, is: something will always go wrong. If it can go wrong, it will. In economies planned by PhDs, when something goes wrong, no one takes responsibility for fixing the problem; they can hide from it. The poor, stupid businessperson (entrepreneur) has to address the problems that come their way, or they will lose their business and their livelihood. Not being able to hide from your problems is the secret sauce of entrepreneurship and free market GENIUS! It is dealing with problems and fixing them so you can move forward that is the genius of free markets. I hate being wrong, but in the world of free market competition, I have to deal with it, or I fail. It is amazing how many people who have never done anything in their lives talk about businesspeople wanting to get rich. You’re not an entrepreneur until you wake up at 2 AM in the middle of the night with a pounding heart, a dry mouth, and terror in your soul about how you're going to make payroll next month? What someone should tell those people that have never accomplished anything, the fear of failure is strong motivation. In free markets, you succeed or you fail. You provide something people want, or you lose. We need this fear of failure in the health care world, where do not rock the boat is the mantra of the establishment. I want to live long and healthy, and if someone does that for me, I want them to be happy.
Communism did not work in the Soviet Union, China, Cuba, or Venezuela. It does not work in our public schools, where kids get lower math scores now than at any time in our nation’s history. Why do we think that centrally planned medical research will do better than Free Market Genius?
Medical Freedom is a Right!
May you all be Blessed with Grace.
Remember: Fortune favors the bold.
You have to grant that Zhittya is bold; we are trying to change the constitution of a state to allow Freedom to Try. We have a duty, an obligation, to save lives and end suffering if we can! Join us!
Thank you!
Dan Montano, CEO Zhittya Genesis Medicine 8683 W. Sahara Ave., Suite 280 Las Vegas, NV 89117 USA 702-802-8373 zgm.care
<https://www.youtube.com/watch?v=IPtv_0LWK4k>
[mailto:Dan333@aol.com](mailto:Dan333@aol.com)
<https://www.nvsos.gov/sos/home/showpublisheddocument/17296/638995949337730000>
<https://www.nvsos.gov/sos/home/showpublisheddocument/17296/638995949337730000>
<https://unleashprosperity.us19.list-manage.com/track/click?u=dc8d30edd7976d2ddf9c2bf96&id=06757da8a6&e=3d59d5ccd9>
[mailto:vika@zhittyamedicine.com](mailto:vika@zhittyamedicine.com)
<https://youtube.com/shorts/FpCLpk_OuAw?si=bhQG_rYI-R1XUEW9>
<https://youtu.be/UCaHvglxGQc>
<https://www.youtube.com/watch?v=IPtv_0LWK4k>
[mailto:Dan333@aol.com](mailto:Dan333@aol.com)
[mailto:dan333@aol.com](mailto:dan333@aol.com)
<https://youtu.be/UCaHvglxGQc>
<https://www.zgm.care/>
