My Brain Restore™ can be accurately described as all three, depending on the context:

✅ Nutraceutical

This is the most accurate scientific and regulatory term. A nutraceutical is a food-derived product that provides medical or health benefits, including the prevention or treatment of disease.
My Brain Restore™ fits this category because:

• It uses a natural compound (Ziziphus seed) APDI, Inc. uses a breakthrough process called Ultra Chill Milled™ for maximum potency.
• It’s based on Japanese university research showing 100%  neurological recovery in mouse models of Parkinson’s, Alzheimer’s, and dementia.
• It is intended to support neurological health beyond basic nutrition.

• The study behind My Brain Restore™ was conducted by an independent, highly respected university in Japan — ensuring its integrity and objectivity. While the key ingredient originates from a 2,000‑year‑old Chinese medicinal fruit, it has been uniquely refined and advanced through our proprietary Ultra Chill Milled™ process. The result is a formulation unlike any other, making this ancient remedy palatable and easy to use in modern life. It blends seamlessly into yogurt, shakes, or smoothies, just like a protein powder,  making it simple to incorporate into your patience daily routine.

✅ Nootropic

A nootropic refers to any substance that enhances cognitive function, especially memory, focus, or executive function.
My Brain Restore™ fits here too because:

• It’s designed to support brain health.
• The Japanese study showed even healthy mice performed 20% better on maze tests, implying cognitive enhancement potential. Therefore making it useful for those people predisposed to genetic neurological diseases.

✅ Supplement

A supplement is the broadest term. It’s used for any product taken orally that contains a priority blend “dietary seed, <99% Ziziphus and seaweed >1% Ecklonia Cava ingredient” intended to supplement the diet.
My Brain Restore™ qualifies as a supplement legally and by industry standards.

🧠 Bottom Line:

My Brain Restore™ is a nutraceutical with nootropic properties, sold as a dietary supplement.

It offers neurological support, cognitive enhancement, and is backed by scientific research—making it stand out from typical supplements.

Here is the pure Science behind the experiments and why MY BRAIN RESTORE™ (MBR) works.  It’s extremely scientific and drawn directly from The Japanese university research. 

Different mouse models were used that had neurodegenerative diseases,

APP23 (19), Mice that Produce Alzheimer’s symptoms and are used to study Alzheimer’s (AD)

Tau784 (21) Mice are used as a model for frontotemporal dementia (FTD, DLB)

Huα-Syn(A53T) Mice Produce Parkinson’s disease (PD)

G2-3 line (24)  Mice are used for studying Parkinson’s disease and other synucleinopathies associated with motor neuron loss and ubiquitinated inclusions in the brain stem and the spinal cord, Lewy bodies, and synaptic plasticity.

Also, mice with no diseases whatsoever as test mice and to study MBR powder Capability to produce 20% better memory improvement in mice that were considered normal and younger.

Collectively known as transgenic mice Tg, were used. All Tg mice were maintained and used as heterozygotes. The mice were individually housed, and after reaching an age at which neuropathology and cognitive/motor deficits could be reliably observed, they were divided into several groups with equal mean body weight and equal number of males and females.

The mouse models were designed to mimic conditions such as Alzheimer’s, frontotemporal dementia, Parkinson’s, and dementia with Lewy bodies—all of which involve the aggregation of toxic proteins that impair synaptic function and motor control.  The results after dissecting the mice were mind boggling as to how well the product worked.

The study specifically focused on demonstrating MY BRAIN RESTORE™ ingredient ability to:

• Remove toxic protein buildup
• Repair damaged neurons
• Suppress cellular senescence

The treatment was found to remove Aβ, tau, and a-synuclein oligomers, restore synaptophysin levels, enhance BDNF expression, promote neurogenesis, and improve both cognitive and motor functions in mouse models of Alzheimer’s disease, frontal dementia, dementia with Lewy bodies, and Parkinson’s disease.

The study also highlighted that MY BRAIN RESTORE ^TM main ingredient significantly reduced Aβ oligomers and amyloid deposits, while synaptophysin levels in the mossy fibers of the hippocampal CA2/3 regions were significantly restored following treatment.

Some of the mice used in the experiment were mostly older, some reaching 15 months or more, which is considered old for mice. The study found that mice’s memory improved in a dose-dependent manner, with higher doses resulting in a complete recovery, which honestly got me excited about the potential of this!  In the higher dose, 100% of the mice ran mazes equal to the control mice without any affliction.

“Neurodegenerative diseases like Alzheimer’s, Parkinson’s, frontotemporal dementia (FTD), and dementia with Lewy bodies (DLB) are all marked by a buildup of toxic proteins in the brain — Aβ, tau, and α-synuclein. These proteins form harmful clusters that damage brain cells, disrupt communication, and trigger the loss of memory, movement, and thinking abilities. Alarmingly, this damage begins decades before symptoms appear”

Synaptophysin levels in the hippocampal CA2/3 regions were significantly recovered by the by “My Brain Restore Ingredient” “MBR powder” to a level higher than that in non-Tg mice littermates

MBR powder … repair damaged neurons, we examined the expression level of brain-derived neurotrophic factor (BDNF), which promotes the growth and regeneration of neurons (23). MBR powder significantly increased BDNF expression in the hippocampus to a level even higher than that in non-Tg littermates.

MBR powder significantly increased neurogenesis to levels higher than those in non-Tg littermates. These results suggest that MBR powder is effective at repairing damaged neurons. Huα-Syn(A53T) mice can be used as a model of DLB (Dementia with Lewy bodies) at 6-8 months. Thus, the Japanese university investigated the effect of MBR powder on DLB using younger mice. MBR powder was orally administered to 6-7-month-old mice for 1 month. Mouse memory was significantly improved to a level similar to or slightly less than that of non-Tg littermates

MBR powder has not only disease-preventing effects but also brain-rejuvenating effects.

MBR powder significantly enhanced aged mice’s cognition to a level similar to that of water-treated young mice. Synaptophysin levels in the hippocampal CA2/3 regions, BDNF expression in the hippocampus, and neurogenesis in the dentate gyrus were significantly increased in MBR powder treated aged mice, reaching levels similar to those in water- treated young mice. Cellular senescence is one of the hallmarks of aging and has been suggested to underlie the pathogenesis of neurodegenerative diseases. The Japanese university measured the levels of cellular senescence focusing on its intracellular markers, p16^INK4a, p21^CIP1/WAF1, and γH2AX; the former two represent cell cycle arrest and the last one reflects DNA damage. The levels of these markers in the cerebral cortex of aged mice were significantly higher than those in young mice MBR powder significantly reduced them to levels similar to or lower than those in water-treated young mice

MBR powder significantly reduced the levels of 8-OHdG and its autoantibodies to levels similar to or lower than those in water-treated young mice. MBR powder has remarkable medicinal effects on neurodegenerative diseases; It removed Aβ, tau, and α-synuclein oligomers, restored synaptophysin levels, enhanced BDNF expression and neurogenesis, and improved cognitive and motor function in mouse models of AD, FTD, DLB, and PD. Furthermore, in normal aged mice, MBR powder reduced DNA oxidation and cellular senescence, increased synaptophysin, BDNF, and neurogenesis, and enhanced cognition to levels similar to those in young mice.

The Japanese university proposed that neurodegenerative disease-prophylactic agents should have activities to remove toxic oligomers of etiologic proteins, repair damaged neurons, and suppress cellular senescence. The results show that the MBR powder meets these requirements. In addition, such prophylactic agents must be safe, inexpensive, and non-invasively available because the preventive treatment would last for a long period. Since MBR powder is safe (i.e. treated as a non-pharmaceutical in Japan and the US), cheaper than medicines, and orally available, the powder can meet these demands as well. Thus, MBR powder is a promising dietary material for aged people to avoid neurodegenerative diseases and brain aging.

The data suggests that any attempt to modify the raw material—whether by traditional tea preparation or extraction—destroys much or all its effectiveness.  This may explain why, despite thousands of years of traditional use, this plant was never recognized for neurological benefits. Historically, it was primarily used as a sleep aid, but the way I am preparing it does not induce drowsiness or make me feel sleepy at all.

Any effective solution must not only help remove these toxic protein clusters but also support the brain’s natural ability to repair and regenerate. That’s what we strive for MY BRAIN RESTORE™.

That’s how My Brain Restore™ was born.
We took the science seriously, improving the formulation with our proprietary Ultra Chill Milled™ process to preserve the neurological activity that heat destroys. We made it palatable, blendable, and easy to take, even for the elderly. We added targeted supplement support for cognitive cleanup and glymphatic support.

And most importantly, we kept it natural, because nature worked when nothing else did.

So no, I won’t be volunteering for dissection to prove what changed inside my brain.
The mice can take that one.
But I know it’s working — and so will the millions of people who finally have something real to fight back with.

Research from : Department of Translational Neuroscience, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan

The scientist who discovered the glymphatic system, the brain’s waste-clearing network active during sleep, is Dr. Maiken Nedergaard, a Danish neuroscientist. She published her key findings in 2012-2013, revealing how cerebrospinal fluid flushes toxins and metabolic waste from the brain, a transformative discovery for understanding sleep’s importance and conditions like Alzheimer’s. Other scientists, including the NIH, have also indicated that this may have the same effect on Parkinson’s and dementia, but no further studies exist. Unfortunately, most of these studies in the United States have been defunded.

Her team published research showing the glymphatic system, a plumbing system piggybacking on blood vessels, uses cerebrospinal fluid (CSF) to clear brain waste, a process vastly more efficient than previously known and most active during sleep.   Mechanism: Astrocytes (glial cells) help shuttle CSF through channels along blood vessels, flushing out byproducts like amyloid-beta, which builds up in Alzheimer’s.  The name of this old but newly discovered system is a combination of glial (cells) and Lymphatic, hence Glymphatic.

Significance: This discovery explained a fundamental function of sleep, linking sleep deprivation to neurodegenerative diseases, and opened new avenues for treating brain disorders.   This discovery was considered amazing because it revealed the brain’s active, organized cleanup process, fundamentally changing neuroscience and sleep medicine. The Japanese scientists later discovered a unique cultivator of Ziziphus that cleared the brain of all issues associated with Alzheimer’s, Parkinson’s, and dementia with Lewy bodies. 

“There is growing evidence from animal experiments that the glymphatic system dysfunction is involved in many neurological disorders, such as Alzheimer’s disease, stroke, epilepsy, traumatic brain injury, and meningitis. Increasing researches over the past decade have shown that the glymphatic system acts clearing the metabolic waste and modulating water transport in the brain, and the dysfunction of the glymphatic system is proved to be involved in various neurological diseases through animal experiments, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), epilepsy, stroke, traumatic brain injury (TBI), mood disorder and infectious or autoimmune disease.”  Department of Neurology, Neuroscience Centre, The First Hospital of Jilin University, Changchun, China and Department of Neurobiology, Care Sciences and Society, Karolinska Institute, Karolinska University Hospital, Solna, Sweden.

Although the groups worked at different time points and in different countries, this explains how the mice excreted the toxic components from the brain and that the core ingredient in My Brain Restore^TM actually Supports the Glymphatic System^TM.  The Japanese were unable to determine which component of the natural ingredient would work on its own and could be patented. That ended their scientific research because they could not make it into a drug for a large pharmaceutical company.  The scientist in the scientific journal said in one sentence that this should be a supplement because it would be inexpensive and do the same thing. 

The unique cultivator Ziziphus (over 100 varieties, including hybrids) is often used to make hot tea or an extract. The Japanese Scientists found that heat destroyed its neurological effects. This is why it was never noticed to have neurological effects, unlike the plant species from India in the 60s, which became L-DOPA and was noted to stop tremors over 100 years ago.

My brain restore uses an ultra-chill milled^TM process, keeping the temperatures well below what is known as cold milling, preserving all the oils and volatile components of the seed, and uses a resealing foam jar lid to preserve its unique components

Taking a nutraceutical like My Brain Restore™ doesn’t require a prescription, but it’s always wise to keep your doctor informed. While physicians are trained in pharmaceutical protocols, they are often not familiar with emerging supplements or nutraceuticals, especially those not yet mainstream. That’s not their fault, it’s simply a matter of time and bandwidth: the average doctor spends just seven minutes per patient. Staying current with every new discovery or product is a challenge, and unfortunately, many tend to stick with what they know.

In my case, I had to advocate for myself. When I requested the most advanced Parkinson’s diagnostic testing available, tests covered by Medicare, my doctor had never even heard of them. But I pushed for it. The results? A 100% positive diagnosis backed by advanced biomarkers, not just clinical observation. I did the same with a controversial but now FDA-approved Alzheimer’s blood test (Aβ42 ratio), again, something my doctor hadn’t yet adopted.

These kinds of tests may eventually reveal how My Brain Restore affects disease progression. But even if biomarker levels don’t shift, that doesn’t mean improvement hasn’t occurred, just as cancer in remission can still leave markers behind. What matters most is: are your patient improving?

When I told my neurologist I’d stopped taking Levodopa (L-DOPA) and replaced it with my own nutraceutical formula, my neurologist was visibly impressed by the reduction in my tremors, without any pharmaceutical support. Going from stage 3 Parkinson’s to stage 1,  My neurologist didn’t know I had also completed a Parkinson’s-focused marathon without falling once, something unthinkable months before.

Still, there’s a bigger point here. Doctors, and patients, must understand how plant-derived treatments can activate dormant biological functions. Just like Ozempic reawakens insulin-producing cells in the pancreas, I believe My Brain Restore™ reactivates dopamine-producing neurons in the brain possibly by clearing the tendrils as pointed out in the university study on the mice. This isn’t theoretical, mice in the Japanese study were cured of Parkinson’s, Alzheimer’s, and dementia with Lewy bodies. Not treated, cured. All of them. How could that happen if they didn’t take anything else and they didn’t?

In my own experience, My Brain Restore appears to work not by replacing dopamine, but by encouraging the brain to resume its own production. That’s critically important because continuing to take dopamine (like insulin with Ozempic) when your brain is producing its own insulin from your pancreas the doctor start could never return. That may risk an imbalance as the brian or insulin as the pancreas gets back to work.

Sadly, many physicians are not yet aware of this. Drug development takes 10–15 years and around $2.5 billion. And even then, the results often come with long warning labels and major side effects even death. By contrast, My Brain Restore™ is based on a 2,000-year-old natural seed extract with a clean safety history and no reported deaths over centuries of use.

Doctors should read the FAQ that says the pure science medical facts. This is the heavy duty research and its results.

We encourage patients to share this information with their physicians. Doctors can visit our website for more technical data and the underlying science behind our formulation and the published animal research. Most medicines come from plants, Tamiflu from star anise (used in Vietnamese pho soup, Levodopa from Mucuna pruriens plant ( comes from India and southeastern China). This is no different, except no one had ever processed the plant this way before.

If you’re experiencing improvement, better memory, steadier movement, fewer tremors, it’s critical your doctor knows. Not just for your safety, but because your brain may be repairing itself. And maybe creating its own self controlled L dopa. That’s what we all want. Your doctor should, too.  But your doctor needs to be aware especially if you’re getting better that your body may be producing its own L dopa and your doctor may need to adjust accordingly.

These statements have not been evaluated by the Food and Drug administration. This product is not intended to diagnose, treat, cure or prevent any disease.  Except for mice and myself

 We recommend starting with 1 teaspoon per day, included with your jar. This is an ideal preventive dose. (Genetically inclined for neurological issues or for those that want to help want to help the brain work more efficiently )

For those managing active symptoms, use: Active 2X – 2 teaspoons daily (4 scoops)

Dosage may vary depending on your condition. Because there is no official human clinical data yet on optimal dosing by severity, we suggest starting low and gradually increasing over several weeks. Monitor your progress and adjust as needed.  Gas or let’s put it plainly farting is that unusual since this is a fibrous seed so just like you would increase fiber in your diet it’s similar.  You should not take it if you have seed allergies or extreme asthma.  You should also take more in the evening or when you have no other activities the original use when heated in a tea used to be a sleep aid.  But now that we process it differently and don’t heat it it’s exactly what the mice took to cure 100% of neurological diseases.  So never put in anything hot to consume, that’s a waste of your money.  But because it has the capability of providing restful sleep until you get used to it you should only use it in the evening or afternoon.  Personally, I never found it in any way causing anything to make me sleepy nor has anyone reported that, and this is probably because we make it totally different than the 2000-year tradition of roasting it, frying it or putting it in hot water. Which in mouse studies destroyed its ability to work.

Many users report subtle improvements—less shaking, better balance, improved memory—that become more noticeable over time. I improved significantly on the 2X doses over six months but no after a year I have see even more inmpovments. Remember, neurological healing takes time.

This product is dose-dependent, as noted in Japanese research. Higher doses may lead to better outcomes, but it’s important not to rush. Let your patience’s body adapt gradually. If you experience success or find a dosage that works well, please share your results via our contact page so we can support others on this journey.

Results vary by individual, but here’s what we’ve seen:

Our company president—diagnosed with both Parkinson’s and early Alzheimer’s—noticed subtle improvements within a few months (such as his pinky no longer twitching when typing, and better balance). However, significant changes became evident after 5- 6 months of consistent use at the 2X Active dosage. Some people my require a year.  Balance and strength seem to be noticed first and with things like Alzheimer’s sharpness and more memory is noticed quickly However things like tremors can take considerable amount of time maybe over a year depending on the Erson’s severity.

Incredibly, after six months on My Brain Restore™, Mark ran and completed the Michael J. Fox Parkinson’s Foundation Marathon outside Washington, D.C., a milestone that would’ve been impossible just months earlier due to daily tripping and instability.

In the Japanese studies that inspired this formulation, mice showed full reversal of neurological diseases like Parkinson’s , dementia and Alzheimer’s, but mice have much shorter lifespans (about two years), so their timeline to improvement was faster.  Humans may take a great deal longer to improve but what we believe happens is subtle changes.  We ask our users to use a chart we have to mark all the problems they have and then in three months remark it six months and then a year.  The return to being normal is not always noticeable it wasn’t for me I hadn’t really realized I wasn’t falling down anymore or tripping over things doing weird things with my hands they went away so gradually that it took all the combinations of those to go wow this really did change me.  So we encourage health practitioners to assist with that to reevaluate each time do you feel you’ve improved in certain areas maybe prompt the questions or give them a sheet to fill out which we can provide.  Obviously my doctor noticed from clinical observations that my tremors had greatly reduced and that only took a few moments to figure out.  

Key Takeaways:

• Initial small improvements may be noticeable in 3 months.

• Major improvements tend to appear around the 5–6 month mark.

• We recommend giving it at least 6–12 months for optimal results.

• Like insulin or Ozempic for diabetes, continued use is essential. Stopping may lead to a return of symptoms.  Since My Brain Restore also was noted to help normal people with better memory I can’t see a reason to stop and I don’t wanna go back to the way I was. 

Even control mice (with no disease) improved 20% in maze tests, showing possible cognitive enhancement—suggesting benefits for prevention and brain optimization, not just treatment.

Ultimately, this isn’t a quick fix—it’s a daily commitment to long-term neurological health.

Shipping & Handling

We ship every order FREE via USPS Priority Mail (Small Flat Rate Box). Once your package arrives, please remove it from the mailbox as soon as possible—prolonged exposure to heat can degrade the product. While it can tolerate brief warmth, sitting in a hot mailbox for more than a day or two is not recommended.

If you’re a subscriber and plan to be away, just email or call us in advance. We’ll happily delay your shipment until you’re back home.

Most orders arrive within 2–3 business days after shipping, but delivery times may vary depending on your location and USPS processing.

Store My Brain Restore in a cool, dry place—ideally wherever you keep your prescription medications. Each jar contains a powder similar in texture to protein shake mix and is designed to be mixed with cold liquids.

For best results, blend it into smoothies, yogurt, pudding, applesauce, or similar cold foods. I use a product called instant breakfast which you mix in with milk that gives you plenty of vitamins and also mixes extremely well with the product.   But you can mix it around. Change it each day with different things you don’t wanna get bored eating the same thing.  Do not consume it as a dry powder.

Our formula mixes more easily than traditional protein powders, though slight graininess may occur with thicker bases like pudding—this is normal and expected.

Interested in Investing in APDI, Inc.?

In today’s volatile markets—where public stocks swing unpredictably and bonds offer little confidence—many investors are looking for something different: a high-growth opportunity grounded in real-world impact.

APDI, Inc. (Alzheimer’s, Parkinson’s, Dementia Impaired) is a private class C Delaware corporation, health-focused startup that has developed My Brain Restore™ Based on university research showing 100% recovery in mice from Parkinson’s, Alzheimer’s, and dementia, we’re targeting one of the fastest-growing medical challenges of our time.

Why Consider APDI, Inc.?

• Massive Market: Neurodegenerative conditions are rising rapidly as the “Silver Tsunami” of aging Americans grows.

• Unique Product: Our Ultra Chill Milled™  Proprietary blend in each jar of My Brain Restore^TM formulation uses a proven ingredient never before delivered in this way.

• Consumer Demand: Early results and feedback are generating significant interest from individuals, caregivers, and healthcare professionals.

We Are Currently Raising $1,500,000

This capital will fuel our product launch, production scale-up, expanded marketing, and distribution channels, including major platforms like Amazon and Walmart.

Types of Investment Opportunities:

• Equity Investment: For qualified, sophisticated investors (i.e., individuals with sufficient assets or income), we are offering stock in the private company. Please note: APDI, Inc. is not publicly traded.

• Revenue-Backed Product Lending: We also welcome small private lenders who help fund raw material purchases. These inventory-based lenders receive a fixed return on their investment, tied directly to wholesale-to-retail product conversion.

Our Exit Strategy:

As we gain traction, we expect interest from larger supplement or pharmaceutical firms for potential acquisition or strategic partnership. Any such developments would benefit our investors through increased valuation and opportunity for a profitable exit. 

Ready to Learn More?

We welcome a conversation to explore how you might be part of something that’s both meaningful and financially promising.

Call Us: 202-635-5000
Email: Mark@MyBrainRestore.com
Located near Washington, DC in Fort Washington, MD

Due to the nature of My Brain Restore™ as a supplement/nutraceutical, we do not offer refunds—whether the product is opened or unopened.

• Opened jars cannot be accepted for return under any circumstances for health and safety reasons.

• Unopened jars are also non-returnable, as we cannot guarantee proper storage conditions after they leave our facility.

Important Storage Note:
Exposure to heat and sunlight can degrade the effectiveness of the active ingredients. Do not leave the jar in a mailbox, car, or direct sunlight.
For best results, store in a cool, dark place, such as a cabinet, pantry, or nightstand.

Thank you for understanding. Our priority is your health and maintaining the quality of every jar we produce.