Brain Mind & Memory Institute

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Brain Mind & Memory Institute Adbanced brain diagnostics and neurotherapy solutions. Our institute promotes neuromarkers as precision tools for mental health and wellbeing. Welcome to BMMI!

Brain Mind & Memory Institute (BMMI)- is a foundation established as a research and development initiative of Brain Mind & Memory Centre, formerly known as Solstice-Mind Matters. Being deeply inspired by the exponentialgrowth of Neuroscience and as a result of an ongoing revolutionary transformation of mental health, we have set ourselves the goals that can take us into the future of Brain and Mind Health. Main goals of the Brain Mind & Memory Institute:
-Promote Precision Medicine in Mental Health and for brain based disorders.

-Promote and contribute to further development of Neuromarkers as precision medicine tools.

-Support Research & Development of Neurotechnology both within Australia and internationally.

-Contribute to improving Brain Diagnostics in clinical practice using qEEG (Quantitative EEG) and ERPs (Event Related Potentials) techniques.We have established an extended network of experts around Australia and overseas who are actively implementing Neuromarkers in clinical practice. to achieve our goals we closely work with our scientific adviser Prof. Yury Kropotov from the Human Brain Institute, Russia, St Petersburg, as well as our consultants and collaborators in Australia: Prof. Richard Clark and many other experts in the field.

-Contribute to the implementation of Neuromodulation and neuroplasticity based modalities into clinical practice. These include non-invasive brain training methods such as EEG-Neurofeedback or brain-computer interface, transcranial direct current stimulation, computerised cognitive training

Our current focus is to promote Electrophysiological Neuromarkers-precise measurements of brain activity using electroencephalography or EEG. EEG offers the most affordable and informative way of investigating brain health and brain disorders. More specifically we use QEEG (quantitative EEG) or brain mapping , as well as Event Related Potentials to study the information processing in the brain.

17/10/2026

What can I say?

What can I say that I have not said before?
So I’ll say it again.
The leaf has a song in it.
Stone is the face of patience.
Inside the river there is an unfinishable story
and you are somewhere in it
and it will never end until all ends.

Take your busy heart to the art museum and the
chamber of commerce
but take it also to the forest.
The song you heard singing in the leaf when you
were a child
is singing still.
I am of years lived, so far, seventy-four,
and the leaf is singing still.

~ Mary Oliver

Art: Maggie Vandewalle
Maggie Vandewalle Watercolors

17/10/2026
17/10/2026

🧠🦠 Your Gut Bacteria Might Be Talking to Your Brain's Reward Center. This might contribute to why cravings feel so hard to resist. Research suggests your gut microbiome could be part of the conversation.

Scientists at UCLA studied 63 healthy adults, looking at f***l metabolites (byproducts of gut bacteria breaking down tryptophan, yes, the same amino acid in turkey!) alongside brain scans of the reward network.

What they found:
🔹 Three gut-bacteria metabolites, indole, skatole, and indoleacetic acid, were strongly linked to connectivity in the nucleus accumbens, a key brain reward hub.
🔹 Skatole was associated with connectivity of the amygdala (emotion processing) AND correlated with higher food addiction scores.
🔹 Indole showed a link to BMI and was associated with connectivity in the anterior insula, a region tied to cravings and urges.
🔹 These three brain regions, amygdala, nucleus accumbens, and anterior insula, form a circuit thought to drive hedonic (pleasure-based, not just hunger-based) eating.

This is some of the first evidence in humans connecting specific gut bacterial metabolites to the physical wiring of brain circuits involved in food cravings and reward. It doesn't prove gut bacteria cause cravings, this was a correlational study, but it opens the door to future research on whether shifting our microbiome could influence appetite and eating behavior.

The gut-brain connection keeps getting more fascinating.

Reference: Osadchiy et al., (2018)

16/10/2026

#2!

03/10/2026
02/10/2026
24/09/2026
This is particularly interesting from an ERP perspective. With ERPs we can identify different stages of information proc...
24/09/2026

This is particularly interesting from an ERP perspective. With ERPs we can identify different stages of information processing with very high temporal precision — essentially asking not only *whether* the brain responds, but *when* the processing begins to diverge.

In an auditory oddball paradigm, for example, we can examine early sensory processing and discrimination, attentional orienting and novelty detection, and later processes involved in evaluating and updating the significance of a stimulus. Components such as N1, P2, mismatch-related responses, P3a and P3b can help us distinguish where in this processing sequence an atypical response occurs.

The important distinction is that fMRI and ERPs provide different kinds of information. fMRI is much better at identifying the network of anatomical regions recruited during novelty processing. ERPs provide millisecond-level information about the sequence and dynamics of information processing, but conventional scalp ERPs cannot tell us with the same confidence that, for example, 13 rather than 23 specific anatomical regions were activated.

Source-localisation methods can estimate the cortical generators contributing to an ERP, but this remains an inverse problem and should not be interpreted as equivalent to fMRI localisation.

So the two approaches are highly complementary: fMRI tells us more about *where* the novelty network is recruited, while ERPs can tell us much more precisely *when* processing diverges — sensory registration, novelty detection, attentional orienting, or later context updating.

For ADHD, this can be much more informative than simply saying that someone has an “attention deficit.” The processing difficulty may occur at a particular stage, and it may differ substantially between individuals.

ADHD may not simply be a problem of “not paying attention.” An fMRI study of adolescents with ADHD showed something more specific. Their brains could activate many of the same regions as healthy adolescents when they were asked to detect important target sounds.
But when an unexpected, novel sound appeared, the difference became much more noticeable.

The ADHD group activated only 13 of 31 brain regions involved in novelty processing, compared with 23 of 31 regions in the control group. These regions included areas involved in attention, working memory, and orienting toward something new.

So the interesting question may not be simply, “Can the brain pay attention?”
It may be: “How efficiently does the brain notice and shift toward something that suddenly becomes important?”

The study also found slower and more variable performance in the ADHD group, supporting the idea that attentional processing can be inconsistent rather than simply absent.

One important limitation: this was a relatively small study of boys with combined-type ADHD, so these findings should not be generalized to everyone with ADHD.

Reference: Stevens MC, Pearlson GD, Kiehl KA. An fMRI Auditory Oddball Study of Combined-Subtype Attention Deficit Hyperactivity Disorder. American Journal of Psychiatry. 2007

09/06/2026

Nature Reviews Neuroscience: Recent advances in large-scale electrophysiology now enable researchers to record from thousands of neurons distributed across the brain. This Review describes the principles underlying this technology and outlines the key considerations, challenges and opportunities associated with collecting, analysing and sharing large electrophysiological datasets.

Link to the Review in the comments.

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PO Box 935
Tweed Heads, NSW
2485

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