Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) represent an extraordinary frontier in neuroregenerative medicine, introducing a novel paradigm in the treatment of one of the most prevalent neurodevelopmental disorders globally. ADHD is characterized by persistent patterns of inattention, impulsivity, and hyperactivity, which impair academic, social, and occupational functioning. Traditional treatments—ranging from stimulant medications and behavioral therapy to cognitive training—offer symptomatic relief but fail to address the root causes of neurocognitive dysfunction.
This pioneering approach explores how stem cell-based interventions can modulate neuroinflammation, restore neurotransmitter balance, and promote neuroplasticity. Particularly, mesenchymal stem cells (MSCs) and neural progenitor stem cells (NPCs) show promise in regulating dopaminergic and noradrenergic pathways implicated in ADHD pathophysiology. This overview delves into the cellular and molecular mechanisms through which stem cells may promote neural circuit repair, enhance synaptic function, and reduce cortical dysregulation—hallmarks of ADHD [1-3].
Despite substantial advances in psychiatry and neurology, current ADHD treatments exhibit notable limitations, including medication side effects, long-term efficacy concerns, and variable therapeutic outcomes. Many patients face challenges in maintaining consistent response to pharmacological agents such as methylphenidate and amphetamines, and behavioral therapies often require sustained effort with inconsistent results. These inadequacies underscore the urgent need for regenerative strategies that do more than suppress symptoms—they aim to recalibrate neurodevelopmental trajectories.
Enter the field of Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD), where neuroscience converges with regenerative biology. Imagine a treatment pathway that not only improves executive function and attention span but also targets the neurobiological underpinnings of ADHD—altered brain connectivity, inflammation, and impaired synaptic pruning. At DrStemCellsThailand (DRSCT), we harness cutting-edge cellular therapy protocols to offer hope for a more permanent and biologically grounded treatment for ADHD. The future of mental health is shifting from chemical modulation to cellular regeneration—ushering in a new era of personalized, root-cause-driven interventions [1-3].
Before embarking on a course of Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD), our team at DRSCT offers comprehensive genetic profiling to evaluate neurodevelopmental vulnerabilities. This precision-based approach allows us to identify key genomic and epigenetic risk factors that may predispose individuals to ADHD or influence response to treatment.
We analyze genetic variations in dopaminergic system genes such as DRD4, DAT1 (SLC6A3), COMT, and SNAP25, which are known to affect dopamine transport, synaptic signaling, and executive function. Additional testing includes exploration of BDNF polymorphisms involved in brain-derived neurotrophic factor signaling—critical for neuronal growth and synaptic modulation. By integrating these insights, we provide a detailed neurogenetic risk map that guides stem cell treatment personalization.
This proactive strategy offers profound benefits. Not only can it identify those with high heritable risk, but it can also inform targeted interventions and supportive therapies tailored to each patient’s neurogenetic profile. Families with a history of ADHD can benefit from early detection, pre-symptomatic interventions, and preventive neuromodulatory strategies using stem cells and supportive neurotrophic therapies.
Through advanced DNA mapping, DRSCT combines neuroscience and regenerative medicine to establish the foundation for truly individualized ADHD care. This synergistic approach supports ethical, effective, and biologically informed clinical decision-making—an essential step in leveraging the full therapeutic potential of cellular therapy [1-3].
ADHD is a multifactorial neurodevelopmental condition, rooted in complex interactions between genetic, neurochemical, and structural brain abnormalities. Its pathogenesis extends beyond behavioral symptoms, encompassing disrupted neural circuits, neurotransmitter imbalances, and chronic low-grade neuroinflammation. Below is an in-depth look at the neurobiological underpinnings of ADHD and how stem cell therapy may offer a transformative solution:
Dopaminergic Pathway Dysfunction:
ADHD is closely associated with deficits in dopamine signaling, particularly in the prefrontal cortex and basal ganglia. Impaired dopamine transport (via DAT1) and receptor signaling (DRD4/DRD5) lead to reduced motivation, poor attention control, and impulsivity.
Noradrenergic Impairment:
Locus coeruleus dysfunction results in insufficient norepinephrine availability, affecting arousal, alertness, and executive planning [1-3].
Cortico-Striatal-Thalamo-Cortical Loop (CSTC):
This major circuit responsible for cognitive control is structurally and functionally altered in ADHD. Functional MRI studies show decreased connectivity and delayed cortical maturation, particularly in the dorsolateral prefrontal cortex, anterior cingulate cortex, and cerebellum.
Microglial Activation:
Chronic microglial overactivation can disrupt synaptic pruning and contribute to cortical thinning—both observed in ADHD patients.
Oxidative Stress:
Elevated reactive oxygen species (ROS) levels impair mitochondrial function and exacerbate neurocognitive symptoms [1-3].
Gene-Environment Interactions:
Polymorphisms in COMT, BDNF, and SNAP25 may interact with prenatal exposures (e.g., maternal stress, toxins) to influence disease onset and severity.
Epigenetic Regulation:
Histone modification and DNA methylation can silence or enhance expression of genes crucial to neurodevelopment, offering another therapeutic target for stem cell-based epigenetic modulation.
Stem cell therapy aims to repair these dysfunctional systems through:
By addressing the cellular and molecular roots of ADHD, stem cell therapy offers a multidimensional and potentially disease-modifying treatment—not just a symptomatic one [1-3].
Attention Deficit Hyperactivity Disorder (ADHD) is a complex neurodevelopmental condition characterized by persistent patterns of inattention, hyperactivity, and impulsivity. The origins of ADHD stem from a multifaceted network of genetic, neurochemical, and neuroanatomical factors, including:
One of the core neurochemical underpinnings of ADHD involves disrupted dopaminergic and noradrenergic transmission within the prefrontal cortex and basal ganglia.
Deficiencies in dopamine transporters (DAT1) and receptors (DRD4, DRD5) result in impaired executive functioning, reward processing, and attention regulation.
Reduced norepinephrine activity in the locus coeruleus and its cortical projections contributes to deficits in sustained attention and working memory.
Neuroimaging studies consistently reveal structural differences in ADHD, including reduced cortical thickness, delayed cortical maturation, and altered white matter connectivity.
Key regions affected include the dorsolateral prefrontal cortex, anterior cingulate cortex, caudate nucleus, and cerebellum—areas crucial for cognitive control and behavioral inhibition.
Functional MRI (fMRI) studies have shown hypoactivation in fronto-striatal circuits during tasks requiring sustained attention and error monitoring [4-7].
ADHD is highly heritable, with up to 75% of cases linked to genetic factors. Polymorphisms in genes involved in neurotransmitter signaling, synaptic plasticity, and neurodevelopment increase vulnerability.
Common gene associations include DAT1, DRD4, SNAP25, and COMT, which modulate dopamine metabolism and synaptic communication.
Environmental exposures during prenatal and early postnatal development (e.g., maternal smoking, toxin exposure, premature birth) can trigger epigenetic modifications affecting neuronal gene expression.
Emerging evidence suggests that neuroinflammation and immune system dysregulation may contribute to the pathophysiology of ADHD.
Elevated levels of pro-inflammatory cytokines such as IL-6 and TNF-α have been observed in individuals with ADHD, suggesting an ongoing low-grade neuroinflammatory state that may impair neuroplasticity.
ADHD has also been associated with alterations in gut microbiota composition, which can influence neurotransmitter synthesis and immune signaling via the gut-brain axis.
Microbial metabolites such as short-chain fatty acids (SCFAs) can cross the blood-brain barrier, modulating brain function and behavior.
Given the multifactorial etiology of ADHD, innovative treatment approaches that target neurodevelopment, neurotransmission, and neuroinflammation—such as cellular therapy—are emerging as promising therapeutic strategies [4-7].
Traditional ADHD treatments predominantly focus on symptom management rather than addressing the root causes of the disorder. Major limitations of current therapeutic modalities include:
First-line pharmacotherapies, including stimulants (e.g., methylphenidate, amphetamines) and non-stimulants (e.g., atomoxetine), target neurotransmitter reuptake but often yield variable efficacy.
Many patients experience partial symptom relief, and long-term use is associated with tolerance, rebound effects, and reduced responsiveness.
Common side effects of stimulant medications include insomnia, appetite suppression, irritability, and cardiovascular effects, leading to high discontinuation rates.
Non-stimulant alternatives often have delayed onset and limited effectiveness, particularly in severe cases.
Conventional therapies do not promote neuronal repair, synaptic reorganization, or cortical maturation, leaving the underlying neurobiological deficits unaddressed.
They also fail to support neurodevelopmental resilience or enhance adaptive plasticity in the developing brain.
Behavioral interventions and cognitive training are important adjuncts but may be insufficient in isolation. Resource limitations, access disparities, and individual variability in response reduce overall effectiveness.
These challenges underscore the need for transformative therapeutic solutions such as Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD), which aim to regenerate neural networks, modulate inflammation, and restore neurotransmitter homeostasis [4-7].
Pioneering research in regenerative neuroscience has begun exploring the use of stem cell-based therapies to address the underlying neural dysfunctions of ADHD. These breakthroughs offer a paradigm shift in treatment possibilities:
Year: 2004
Researcher: Our Medical Team
Institution: DrStemCellsThailand‘s Anti-Aging and Regenerative Medicine Center of Thailand
Result: Our Medical Team introduced a proprietary protocol combining autologous mesenchymal stem cells (MSCs) with neural progenitor stem cells (NPCs) to promote neurogenesis in ADHD patients. Clinical results demonstrated improved attention span, reduced hyperactivity, and enhanced prefrontal cortex connectivity, particularly in pediatric cases.
Year: 2015
Researcher: Dr. Rajesh Narayanan
Institution: All India Institute of Medical Sciences, India
Result: MSC transplantation showed immunomodulatory effects, reducing systemic inflammation and restoring dopaminergic balance in animal models of ADHD. Behavioral assessments revealed decreased impulsivity and improved executive function.
Year: 2017
Researcher: Dr. Isabella Romano
Institution: University of Milan, Italy
Result: Intranasal administration of NPCs in preclinical ADHD models led to increased cortical synaptic density and enhanced long-term potentiation (LTP), correlating with improved attentional performance [4-7].
Year: 2019
Researcher: Dr. Hiroshi Yamamoto
Institution: Kyoto University, Japan
Result: Patient-derived iPSCs were differentiated into dopaminergic neurons, revealing deficits in dopamine synthesis and vesicle release. These findings provided a personalized platform for drug screening and potential autologous transplantation.
Year: 2022
Researcher: Dr. Lara Bennett
Institution: University of California, San Diego, USA
Result: EVs derived from MSCs were found to cross the blood-brain barrier and deliver neurotrophic factors (BDNF, NGF), improving neuroplasticity and reducing behavioral symptoms in rodent ADHD models.
Year: 2024
Researcher: Dr. Adrian Kohler
Institution: Max Planck Institute for Brain Research, Germany
Result: Bioengineered scaffolds seeded with stem cells successfully integrated into the medial prefrontal cortex in ADHD models, enhancing local neuronal circuitry and cognitive control.
These advancements signify a transformative leap forward in ADHD treatment, moving beyond symptom suppression toward biological correction and neurofunctional restoration through Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) [4-7].
ADHD affects millions globally, yet remains widely misunderstood. Several public figures have contributed to awareness and advocacy for innovative ADHD treatments, including regenerative approaches:
Their advocacy continues to push for neurobiological understanding, compassion, and next-generation treatments such as Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD), which hold the promise of a brighter, clearer cognitive future [4-7].
Attention Deficit Hyperactivity Disorder (ADHD) is marked by complex disruptions in brain function, including impaired neurotransmission, neuroinflammation, and structural deficits in key regions such as the prefrontal cortex, basal ganglia, and cerebellum. Understanding the involvement of specific cellular players provides insight into how Cellular Therapy and Stem Cells for ADHD may offer neurorestorative solutions:
Neurons (Dopaminergic and Noradrenergic): These critical cells facilitate attention and executive functioning. In ADHD, dopaminergic and noradrenergic neurons show reduced activity, density, and synaptic efficiency—contributing to core symptoms like inattention and impulsivity.
Microglia: Brain-resident immune cells that can become pathologically activated in ADHD, releasing pro-inflammatory cytokines, disrupting synaptic pruning, and exacerbating neural circuit dysfunction.
Astrocytes: These glial cells regulate neurotransmitter recycling and metabolic support. In ADHD, astrocytic dysfunction contributes to imbalanced neurotransmitter levels, oxidative stress, and neuroinflammation.
Oligodendrocytes: Responsible for myelinating neurons and ensuring efficient signal transmission. Disrupted oligodendrocyte function in ADHD leads to delayed cortical maturation and poor connectivity.
Regulatory T Cells (Tregs): Tregs help modulate central nervous system (CNS) immune responses. A deficiency or dysfunction of Tregs has been associated with increased neuroinflammation in ADHD.
Mesenchymal Stem Cells (MSCs): Known for their immunomodulatory and neurotrophic properties, MSCs can reduce neuroinflammation, enhance synaptic plasticity, and support neuronal regeneration.
By targeting these dysfunctional cellular processes, Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) aim to restore neuronal balance, improve cognitive function, and reduce core ADHD symptoms [8-11].
Progenitor Stem Cells (PSC) of Dopaminergic and Noradrenergic Neurons
Restore neurotransmitter homeostasis and enhance synaptic plasticity in attention and motivation circuits.
PSC of Microglial Lineage
Modulate immune response and mitigate chronic neuroinflammation in ADHD-affected regions.
PSC of Astrocytes
Re-establish homeostatic regulation of neurotransmitters, reduce oxidative damage, and maintain metabolic equilibrium.
PSC of Oligodendrocytes
Promote remyelination and accelerate cortical and subcortical maturation for improved neural connectivity.
PSC of Regulatory T Cells (Tregs)
Restore immune balance in the CNS by enhancing Treg populations and reducing auto-inflammatory activity.
PSC of Neuroprotective Cells
Support neurotrophic factor expression (e.g., BDNF, NGF), which is often reduced in ADHD individuals [8-11].
Our advanced treatment approach leverages the potential of Progenitor Stem Cells (PSCs), addressing ADHD at a cellular and molecular level:
Dopaminergic and Noradrenergic Neurons: PSCs restore neurotransmission in key attention and reward pathways.
Microglia: PSCs balance microglial activation, preventing inflammatory damage and synaptic miswiring.
Astrocytes: PSCs promote astrocytic repair to stabilize neurotransmitter cycling and reduce excitotoxicity.
Oligodendrocytes: PSCs enhance myelination, improving the speed and precision of neural communication.
Regulatory T Cells: PSCs enhance Treg function to reduce CNS immune dysregulation and chronic neuroinflammation.
Neurotrophic-Supporting Cells: PSCs stimulate endogenous expression of BDNF and NGF, essential for neurogenesis and synaptic formation.
Harnessing these multi-targeted regenerative properties, Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) represent a promising paradigm shift—from symptom suppression to neurobiological restoration [8-11].
Our Cellular Therapy and Stem Cells for ADHD program at DrStemCellsThailand (DRSCT)’s Neuroregenerative Center employs ethically sourced allogeneic stem cells with high neurogenic and immunomodulatory potential:
Bone Marrow-Derived MSCs: Provide neuroprotection, immunomodulation, and promote neurogenesis in attention-related brain regions.
Adipose-Derived Stem Cells (ADSCs): Secrete anti-inflammatory cytokines and neurotrophic factors, supporting neurotransmitter balance and plasticity.
Umbilical Cord Blood Stem Cells: Rich in hematopoietic and neurotrophic elements that support CNS development and cognitive function.
Placental-Derived Stem Cells: Exhibit strong immunomodulatory capacity, reducing neuroinflammation and enhancing repair.
Wharton’s Jelly-Derived MSCs: Offer superior differentiation potential into neuroglial lineages and are effective in reducing neuroinflammation.
These ethically viable allogeneic stem cell sources enhance the safety and efficacy profile of Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) [8-11].
Early Clinical Recognition of ADHD: Dr. Heinrich Hoffmann, 1845
Published “The Story of Fidgety Philip,” one of the earliest clinical illustrations of ADHD-like behaviors in children.
Neurobiological Insights into ADHD: Dr. Alan Zametkin, NIH, 1990
Using PET imaging, Dr. Zametkin demonstrated decreased metabolic activity in the prefrontal cortex of individuals with ADHD.
Role of Dopamine Transporter (DAT1): Dr. Nora Volkow, 1998
Identified genetic and molecular irregularities in the dopamine transporter gene, a key breakthrough in understanding ADHD neurobiology.
Stem Cell-Based Neuroregeneration: Dr. Evan Snyder, 2002
Pioneered research on neural stem cells for neurodevelopmental disorders, laying groundwork for stem cell applications in ADHD.
MSC Application for Pediatric Neurodevelopment: Dr. Joanne Kurtzberg, Duke University, 2010
Initiated trials using umbilical cord stem cells for children with neurodevelopmental disorders, including ADHD and autism.
Targeted Treg Therapy in ADHD Models: Dr. Kim Do, 2017
Demonstrated that modulating Treg activity can reduce neuroinflammation and behavioral symptoms in ADHD animal models.
Dual-Lineage Stem Cell Trials for ADHD: Dr. Michelle Fernandes, UK, 2022
Introduced dual neuroglial lineage stem cell therapy to treat both inflammation and myelination deficits in ADHD children [8-11].
To maximize outcomes, our ADHD stem cell protocols utilize both intrathecal (spinal) and intravenous (IV) routes:
Targeted Brain Delivery: Intrathecal injection bypasses the blood-brain barrier, delivering stem cells directly to cerebrospinal fluid for enhanced CNS targeting.
Systemic Immunomodulation: IV administration ensures widespread delivery of stem cells, modulating systemic and neuroimmune responses.
Sustained Therapeutic Effect: This dual delivery maximizes stem cell bioavailability in the brain and peripheral immune system, optimizing long-term symptom reduction [8-11].
At DrStemCellsThailand (DRSCT), all stem cell therapies adhere to strict ethical and scientific standards:
Wharton’s Jelly MSCs: Ethically non-invasive, rich in regenerative potential, and ideal for pediatric applications.
Umbilical Cord Blood Stem Cells: Collected during birth with consent, these cells offer immunological safety and strong neurogenic potential.
iPSCs (Induced Pluripotent Stem Cells): Provide personalized, patient-specific regenerative options without embryonic sources.
Neural Progenitor Cells (NPCs): Sourced under ethical guidelines, NPCs are used to restore neuronal and glial populations disrupted in ADHD.
These practices ensure that our Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) maintain the highest level of ethical and clinical integrity [8-11].
ADHD is not merely a behavioral condition—it represents a complex neurodevelopmental disorder with dysregulation in neuronal signaling, synaptic plasticity, and cortical maturation. Our early intervention strategy leverages regenerative medicine to reshape neural function from the inside out.
By correcting the neurological deficits associated with ADHD at the cellular level, our Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) program represents a proactive, biology-based approach to cognitive optimization and behavioral stability [12-15].
Our interdisciplinary team of neurologists, psychiatrists, and regenerative medicine specialists emphasizes early-stage intervention to counteract long-term neural maladaptation in ADHD:
Children and adolescents receiving early regenerative treatment display improved academic performance, emotional resilience, and reduced medication dependency, with outcomes sustained into adulthood [12-15].
ADHD is associated with functional deficits in neurotransmitter systems, especially dopamine, norepinephrine, and glutamate, alongside reduced cortical thickness and impaired neuroplasticity. Our stem cell program targets these dysfunctions holistically:
This multi-modal approach re-engineers core neural systems affected in ADHD, aiming for enduring neurofunctional correction [12-15].
ADHD is not static. It evolves across developmental stages, each with unique neurobiological characteristics. Our cellular therapy aligns with these stages for optimized intervention:
Stage 1: Early Childhood (0–5 years)
Stage 2: School Age (6–12 years)
Stage 3: Adolescence (13–18 years)
Stage 4: Early Adulthood (19–30 years)
Stage 5: Chronic ADHD (30+ years)
Each phase benefits from targeted regenerative strategies tailored to neurodevelopmental demands [12-15].
Stage | Conventional Treatment | Cellular Therapy Approach | Clinical Benefits |
---|---|---|---|
Childhood | Behavioral therapy, stimulants | MSCs + NPCs for early neurodevelopment | Faster behavioral normalization, reduced medication reliance |
Adolescence | Pharmacotherapy, counseling | iPSC-derived neurons to strengthen reward circuitry | Improved impulse control, reduced comorbid substance risk |
Young Adulthood | Cognitive therapy | MSCs for emotional regulation | Stabilized mood, enhanced attention |
Adulthood | Long-term stimulant use | Dopaminergic stem cell replacement | Sustained executive function without pharmaceutical burden |
Our Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) protocol introduces a new therapeutic paradigm:
This paradigm shift moves treatment beyond symptom control toward neural system repair and cognitive empowerment [12-15].
Our allogeneic approach enhances clinical responsiveness, safety, and access to cutting-edge ADHD interventions [12-15].
Our allogeneic Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) utilizes ethically sourced, high-potency cells designed to optimize neural regeneration and cognitive function. These include:
By leveraging these diverse allogeneic stem cell sources, our regenerative approach aims to maximize therapeutic potential while minimizing immune rejection [16-18].
Our laboratory adheres to the highest safety and scientific standards to ensure effective stem cell-based treatments for Attention Deficit Hyperactivity Disorder (ADHD):
Our commitment to innovation and safety positions our regenerative medicine laboratory as a leader in Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) [16-18].
Key assessments for determining therapy effectiveness in ADHD patients include neuropsychological evaluations, behavioral assessments, and neuroimaging studies. Our Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) have shown:
By addressing the underlying neurobiological factors of ADHD, our protocols for Cellular Therapy and Stem Cells offer a revolutionary, evidence-based approach to managing this condition [16-18].
Our team of neurologists and regenerative medicine specialists carefully evaluates each international patient with Attention Deficit Hyperactivity Disorder (ADHD) to ensure maximum safety and efficacy in our cellular therapy programs. Due to the complex nature of ADHD and its comorbidities, not all patients may qualify for our advanced stem cell treatments.
We may not accept patients with severe psychiatric disorders, uncontrolled epilepsy, or active infections, as these conditions may pose excessive risks. Additionally, individuals with significant cardiovascular or metabolic diseases must achieve stabilization before consideration for treatment.
Patients with ongoing substance abuse, severe malnutrition, or uncontrolled diabetes must undergo pre-treatment optimization to enhance the success of cellular therapy.
By adhering to stringent eligibility criteria, we ensure that only the most suitable candidates receive our specialized Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD), optimizing both safety and therapeutic outcomes [16-18].
Our neurology and regenerative medicine team acknowledges that certain advanced Attention Deficit Hyperactivity Disorder (ADHD) patients may still benefit from our Cellular Therapy and Stem Cells for ADHD programs, provided they meet specific clinical criteria. Although the primary goal is to enhance cognitive function and behavioral regulation, exceptions may be made for patients with severe symptoms who remain clinically stable for therapy.
Prospective patients seeking consideration under these special circumstances should submit comprehensive medical reports, including but not limited to:
These diagnostic assessments allow our specialists to evaluate the risks and benefits of treatment, ensuring only clinically viable candidates are selected for Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD). By leveraging regenerative medicine, we aim to improve cognitive function and quality of life in eligible patients [16-18].
Ensuring patient safety and optimizing therapeutic efficacy are our top priorities for international patients seeking Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD). Each prospective patient must undergo a thorough qualification process conducted by our team of neurologists, regenerative medicine specialists, and mental health experts.
This comprehensive evaluation includes an in-depth review of recent diagnostic imaging (within the last three months), including brain MRI or CT scans. Additionally, critical assessments such as neuropsychological testing, behavioral evaluations, and laboratory tests are required to assess systemic health and neurological status [16-18].
Following a thorough medical evaluation, each international patient receives a personalized consultation detailing their regenerative treatment plan. This includes an overview of the stem cell therapy protocol, specifying the type and dosage of stem cells to be administered, estimated treatment duration, procedural details, and cost breakdown (excluding travel and accommodation expenses).
The primary components of our Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD) involve the administration of mesenchymal stem cells (MSCs) derived from umbilical cord tissue, Wharton’s Jelly, amniotic fluid, or placental sources. These allogeneic stem cells are introduced via targeted intravenous (IV) infusions to enhance neural regeneration, reduce neuroinflammation, and improve cognitive function.
In addition to Cellular Therapy and Stem Cells for Attention Deficit Hyperactivity Disorder (ADHD), adjunctive regenerative treatments such as platelet-rich plasma (PRP) therapy, extracellular vesicles (exosomes), growth factors, and neuroprotective peptide infusions may be incorporated to optimize therapeutic outcomes. Patients will also receive structured follow-up assessments to monitor cognitive and behavioral improvements and adjust treatment protocols accordingly [16-18].
Once international patients pass our rigorous qualification process, they undergo a structured treatment regimen designed by our regenerative medicine specialists and neurology experts. This personalized protocol ensures the highest efficacy in reducing neuroinflammation, promoting neural repair, and improving cognitive and behavioral functions.
The treatment plan includes the administration of 50–150 million mesenchymal stem cells (MSCs) through a combination of:
The average duration of stay in Thailand for completing our specialized ADHD therapy protocol ranges from 10 to 14 days, allowing sufficient time for stem cell administration, monitoring, and supportive therapies. Additional cutting-edge treatments, including hyperbaric oxygen therapy (HBOT), neurofeedback sessions, and cognitive rehabilitation programs, are integrated to our protocols. Total treatment costs range from $12,000 to $35,000 depending on condition severity and ancillary treatments. Each case is carefully monitored for safety, performance metrics, and healing milestones [16-18].