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  1. DATE: October 20, 2026 at 08:00AM
    SOURCE: PSYPOST.ORG

    ** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
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    TITLE: How chronic drinking masks the brain’s hidden scars from childhood trauma

    URL: psypost.org/how-chronic-drinki

    Early childhood maltreatment leaves a distinct structural footprint on the human brain, but chronic alcohol use might obscure or reshape these neurodevelopmental marks over time. A new study published in Addiction Neuroscience reports that while childhood trauma is linked to altered gray matter and brain folding in healthy adults, those specific patterns are largely absent in people with alcohol use disorder. The findings suggest that the heavy physical toll of chronic alcohol consumption may overwrite early structural changes, requiring researchers to account for active addiction severity when searching for the neural signs of childhood adversity.

    To understand how experiences alter the physical brain, researchers look at different measurements of its tissue. Gray matter is the brain tissue packed with nerve cell bodies, responsible for processing information. Researchers measure gray matter volume to gauge the overall size of specific brain structures. They also examine the outermost surface layer of this tissue, known as the cerebral cortex, by measuring its physical thickness.

    Another important metric is gyrification, or the degree of folding across the brain’s surface. Gyrification begins before birth and helps pack a larger surface area of brain tissue into the limited space of the skull. Folds form primarily during fetal development and early childhood, making them a relatively stable marker of early life events. Cortical thickness, on the other hand, can change more readily throughout adulthood due to aging or environmental toxins like alcohol.

    Adverse experiences during childhood, such as emotional neglect or physical abuse, can disrupt early neurodevelopment. These experiences often lead to lasting structural changes in brain areas that manage emotion, stress, and self-control. These same brain regions are heavily implicated in addictive behaviors later in life.

    Lead author Franca Schmid, a researcher at the Université de Reims Champagne-Ardenne in France, and corresponding author Sarah Gerhardt, a researcher at Heidelberg University in Germany, wanted to explore how trauma and alcohol interact physically in the brain. The research team set out to map how childhood maltreatment relates to brain structure in adults with and without an active addiction to alcohol.

    They focused their investigation on four specific brain regions known to be sensitive to both stress and addiction. The amygdala and hippocampus process emotions, handle stress responses, and manage memories. The orbitofrontal cortex helps the brain value rewards and make decisions. Finally, the inferior frontal gyrus acts as the brain’s braking system, managing impulse control and the regulation of emotions.

    The research team analyzed data from 84 individuals with varying severity of alcohol use disorder, many of whom were recruited from inpatient or outpatient treatment programs, and 83 adults with no history of substance use issues. Participants completed extensive surveys detailing their alcohol consumption habits. They also completed questionnaires asking if they had experienced emotional, physical, or sexual abuse, or emotional and physical neglect during childhood.

    Following the surveys, the researchers used magnetic resonance imaging, or MRI, to capture high-resolution, three-dimensional scans of each participant’s brain. Specialized computer software then mapped the volume, thickness, and folding patterns of the four targeted brain regions.

    Looking at overall brain volume, the researchers found that adults with alcohol use disorder had reduced gray matter across all the examined regions when compared to the healthy adults. This overall reduction aligns with extensive previous research detailing the neurotoxic effects of chronic, heavy alcohol exposure, which physically shrinks brain tissue over time.

    The researchers then looked for structural changes linked specifically to childhood trauma rather than alcohol. In the healthy group, individuals who reported higher levels of early life maltreatment exhibited reduced gray matter volume in the right side of the inferior frontal gyrus. At the same time, these healthy adults showed an increase in cortical folding on the left side of the exact same brain region.

    This increase in folding might represent a biological compensatory response. Because these individuals did not develop a substance use disorder, their brains might have adapted to early stress by altering their folding patterns to maintain cognitive functions. Structural changes in the inferior frontal gyrus might help resilient individuals process emotions and maintain self-control despite a history of trauma.

    These trauma-related patterns did not appear in the adults with alcohol use disorder. The addiction group showed no link between childhood trauma scores and gray matter volume or brain folding. The absence of these specific differences suggests that chronic alcohol exposure might mask the structural signatures of early childhood adversity. The severe tissue loss caused by years of heavy drinking might physically erase or overshadow the earlier, more subtle changes caused by childhood trauma.

    To test this idea, the researchers conducted an additional analysis restricted entirely to the alcohol use disorder group. When they statistically adjusted the data to account for the exact severity of each patient’s current alcohol consumption, a different pattern emerged.

    By factoring in the intensity of the addiction, the researchers peeled back a layer of alcohol-related damage. In this adjusted analysis, higher rates of childhood trauma were associated with a thinner cerebral cortex in the left inferior frontal gyrus of the patients. This suggests that the structural traces of childhood trauma are still present in these individuals, but they are hiding beneath the more prominent damage caused by active, heavy drinking.

    Because the study measured brain structure at a single point in time, the results cannot establish a direct chain of events from childhood trauma to brain changes to alcohol addiction. Researchers cannot prove causality from a cross-sectional design. They can only establish that a mathematical relationship exists between the reported trauma and the physical brain measurements.

    The study also relied on retrospective self-reports of childhood trauma. Human memory is fallible, and asking individuals to recall events from decades past can result in memory biases. Prospective studies, which follow children in real-time as they grow, often yield different rates of reported trauma than retrospective surveys.

    The analysis of cortical thickness in the alcohol use disorder group was an exploratory step conducted on a slightly smaller subset of the participants. Some patients did not have complete survey data for their recent alcohol severity, reducing the number of people included in that specific test.

    Future research requires tracking individuals over long periods of time, from childhood straight into adulthood. Researchers need to measure brain structure before alcohol use begins and monitor how the tissue changes as drinking escalates. Only by watching the brain change over time can researchers fully map the overlapping impacts of early adversity and later addiction.

    The study, “Childhood Maltreatment Related Effects on Brain Structure in Alcohol Use Disorder,” was authored by Franca Schmid, Fabien Gierski, Falk Kiefer, Cagdas Türkmen, Audrey Henry, Bernd Lenz, Farid Benzerouk, Arthur Kaladjian, Sabine Vollstädt-Klein, and Sarah Gerhardt.

    URL: psypost.org/how-chronic-drinki

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    #psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #ChildhoodTrauma #AlcoholUseDisorder #BrainStructure #GrayMatter #CorticalThickness #Gyrification #InferiorFrontalGyrus #Amgydala #Neurodevelopment #TraumaAndAddiction

  2. DATE: September 30, 2026 at 08:00AM
    SOURCE: PSYPOST.ORG

    ** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
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    TITLE: A single dose of MDMA prevents trauma-fueled drinking in genetically prone rats

    URL: psypost.org/a-single-dose-of-m

    A recent experiment in rats suggests that MDMA can prevent the increase in alcohol consumption that often follows a traumatic event, particularly in subjects genetically predisposed to drink heavily. The findings indicate that the drug alters the way fear is expressed in the moment rather than permanently strengthening the brain’s ability to unlearn fear memories. The research was published in Neuropsychopharmacology.

    Post-traumatic stress disorder, or PTSD, is a mental health condition triggered by experiencing or witnessing a terrifying event. Many individuals with PTSD also develop alcohol use disorder, drinking to cope with intrusive memories and emotional distress. This relationship is complex and mutually reinforcing, as chronic alcohol use dysregulates stress systems in the brain, often worsening trauma symptoms over time.

    To treat PTSD, therapists often rely on fear extinction. This is a learning process where an individual is repeatedly exposed to trauma-related cues in a safe environment until those cues no longer trigger a fear response. A 2015 study covered by PsyPost in 2015 indicated that administering MDMA prior to this exposure process helped accelerate fear extinction in mice.

    Building on such animal research, early human studies suggest that MDMA-assisted therapy might ease symptoms of both PTSD and addiction, including a small, uncontrolled 2021 pilot study that found the approach safe and promising for treating alcohol use disorder. At the same time, scientists recognize that the connection between fear and alcohol is strongly influenced by genetics. For example, a 2016 study provided evidence that rodents selectively bred to prefer alcohol also display exaggerated fear responses, pointing to an innate biological link between anxiety and drinking.

    Despite this progress, it was unknown whether giving MDMA specifically to treat trauma-like symptoms would also reduce a later urge to drink in subjects actively displaying both behaviors. The research, led by Kade L. Huckstep, Billi Newton, and Leigh C. Walker of the Florey Institute of Neuroscience and Mental Health and the University of Melbourne, set out to see if MDMA could curb trauma-triggered drinking in genetically prone animals.

    “One of the challenges with clinical trials of MDMA-assisted therapy is determining how much of the observed benefit is attributable to MDMA itself,” Walker, deputy lead of Mental Health Research and Group Head of the Hormone and Behaviour Laboratory at the Florey Institute, told PsyPost. “Because the subjective effects of MDMA are very noticeable, effective blinding can be difficult, and factors such as expectancy and the therapeutic setting may also influence outcomes.”

    To overcome this, the researchers aimed to mirror real-world research. “We wanted to develop a rodent model that, as closely as possible, reflected ongoing clinical trials investigating MDMA in people with co-occurring PTSD and alcohol use disorder (e.g., MPATHY),” Walker explained. “This allowed us to examine the effects of MDMA in a highly controlled setting, without expectancy or placebo effects, and determine whether MDMA itself alters fear-related behavior and alcohol consumption.”

    “Importantly, we also wanted to identify any unintended effects, e.g., whether MDMA could worsen fear-related behavior or alcohol consumption under particular conditions, an important factor relevant to our clinical collaborators conducting the corresponding human trials,” she added.

    To explore this, the team used 53 Indiana alcohol-preferring rats, a strain selectively bred to voluntarily consume high amounts of alcohol, and 64 Wistar rats, a standard outbred strain. Both male and female rats were used. The animals first underwent auditory fear conditioning, a procedure where a specific tone is repeatedly paired with a mild, one-second electrical foot shock. This teaches the animals to associate the sound with an aversive event, causing them to freeze in place whenever they hear it. A separate control group heard the tone but received no shocks.

    Following this conditioning, all the rats were given intermittent access to a solution of twenty percent alcohol and water for six weeks. This allowed them to develop a voluntary drinking habit. Afterward, the researchers removed the alcohol for three weeks to simulate a period of abstinence.

    At the end of the abstinence period, the animals received an injection of either MDMA or a simple saline solution. Thirty minutes later, they were placed into a fear extinction session where the tone was played repeatedly without any foot shocks. The following day, the rats underwent a drug-free test to see how well they remembered the extinction learning. Finally, they were given free access to alcohol again for eight sessions to measure their post-treatment drinking behavior.

    The researchers found that the initial fear conditioning modestly increased later alcohol consumption, but only in the genetically vulnerable Indiana alcohol-preferring rats. The Wistar rats learned to fear the tone just as strongly, but this distressing experience did not drive them to drink more alcohol than their unshocked counterparts. This finding suggests that trauma-like stress drives increased drinking specifically when a genetic predisposition is present.

    When the rats received MDMA before the fear extinction session, their immediate reactions to the tone changed. The drug initially reduced their freezing behavior early in the session. However, as the session went on, the two strains reacted differently. The Indiana alcohol-preferring rats ended up freezing more overall while on the drug, while the female Wistar rats froze less.

    Despite these in-the-moment changes, MDMA did not improve how well the rats remembered the safety of the tone the following day. During the drug-free recall test, the MDMA-treated rats showed no better fear extinction than those given the saline solution. However, the MDMA treatment had a modest protective effect against trauma-induced drinking. In the Indiana alcohol-preferring rats that had experienced fear conditioning, those treated with MDMA did not show the trauma-related escalation in alcohol intake that was seen in the saline group.

    “For us, the most important finding was not necessarily how large the effect was, but that it differed depending on the animals we studied,” Walker noted. “MDMA reduced drinking in rats that were particularly vulnerable to high alcohol use and more stress sensitive — and this effect persisted over 3 weeks. It will be interesting to see whether a similar pattern emerges in clinical trials, and whether particular groups of people may benefit more from MDMA-assisted therapy than others.”

    To verify whether the drug’s effects on fear depended on the animals’ six-week history with alcohol, the team tested an additional group of 25 Indiana alcohol-preferring rats. These animals went through the same conditioning, MDMA, and extinction procedures, but went straight to extinction the day after conditioning, skipping the weeks of drinking and abstinence.

    In this alcohol-naive group, MDMA still altered their immediate fear expression during the extinction session without improving their drug-free memory of it the next day. When these rats were introduced to alcohol for the first time after treatment, the MDMA-treated males showed lower initial consumption than those given saline, but this reduction was short-lived, and their overall drinking quickly matched the control group. This indicates that MDMA’s most reliable benefit in this model is blocking the long-term escalation of drinking that results from a combination of trauma and prior alcohol experience.

    This decoupling of fear and drinking behavior was an unexpected outcome for the team. “We were surprised that MDMA’s effects on alcohol consumption did not seem to be directly linked to its effects on fear,” Walker said. “We initially thought that reducing fear responses might also reduce subsequent drinking, but the two effects appeared to be separate. This suggests that MDMA may influence alcohol use through other mechanisms that we still need to understand.”

    As with all research, there are some caveats to consider. The study measured voluntary alcohol consumption under a limited-access schedule and did not measure blood alcohol concentrations, meaning the shifts in drinking might not reflect intoxication-level binges. The team also tested a single dose of MDMA given thirty minutes before extinction. Different doses or timing schedules might yield varying effects on learning and alcohol consumption.

    “The main caveat is that this was a study in rats, and our findings should not be taken to mean that MDMA will reduce alcohol use in people,” Walker cautioned. “What the study does show is that responses to MDMA can vary considerably depending on the individual, including their vulnerability to heavy drinking and their sex. Understanding these differences will be important as we learn more from ongoing clinical trials. If so, we can use this model to delve into the mechanisms that may be responsible.”

    There are a few other things to keep in mind regarding how these animal behaviors translate to humans. Animal models of fear extinction only capture a narrow aspect of trauma therapy. They cannot replicate the complex relational and emotional support that defines MDMA-assisted psychotherapy in clinical settings.

    Moving forward, the researchers hope to use this model to investigate the biological foundations of the treatment. “We would like to understand the brain and biological mechanisms that drive the effects of MDMA and MDMA-assisted therapy,” Walker said. “Ultimately, this could help identify who is most likely to benefit from treatment. Understanding how these treatments actually work may also help move the conversation beyond some of the stigma or fear associated with taking drugs such as MDMA during therapy, allowing their potential benefits and risks to be considered based on scientific evidence.”

    “One important lesson from this study is the need to better reflect human diversity in preclinical research,” she added. “By studying co-occurring conditions such as trauma and problematic alcohol use, and considering biological factors such as sex and genetic vulnerability from the outset, we can uncover differences that might otherwise be missed. Keeping these factors at the forefront may help us better understand why treatments work for some people but not others, and ultimately improve how findings from animal studies translate to the clinic.”

    The study, “MDMA alters fear extinction, and reduces alcohol consumption in inbred alcohol preferring iP rats but not outbred Wistar rats,” was authored by Kade L. Huckstep, Billi Newton, Grace Bailey, Annai Charlton, Amy J. Pearl, Xavier J. Maddern, Robyn M. Brown, Gavan P. McNally, Dan I. Lubman, Shalini Arunogiri, Kirsten C. Morley, Erin J. Campbell, Andrew J. Lawrence, and Leigh C. Walker.

    URL: psypost.org/a-single-dose-of-m

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    #psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #MDMA #FearExtinction #PTSD #AlcoholUseDisorder #TraumaAndDrinking #PreclinicalResearch #RodentStudy #GeneticVulnerability #MDMATherapy #Neuropsychopharmacology

  3. Alcohol Abstinence Linked to Brain Activity Suggesting Relapse Risk

    📰 Original title: Quitting alcohol may prime the brain for relapse

    🤖 IA: It's not clickbait ✅
    👥 Users: It's not clickbait ✅

    View full AI summary en.killbait.com/alcohol-abstin

    #neuroscience #alcoholusedisorder #brainactivity #relapserisk

  4. Alcohol Use Falls in Spain, But Alcohol Use Disorder Persists, Oasis Premium Recovery Says

    A private ensuite living room at Oasis Premium Recovery, designed to support comfort and personalized care during treatment.…
    #Spain #ES #Europe #Europa #EU #alcoholusedisorder #OasisPremiumRecovery #structuredtreatment
    europesays.com/spain/68624/

  5. Large Veterans Study Shows How GLP-1 Weight Loss Drugs Could Treat Addiction

    Credit: MotivateBootCamp. Drugs originally designed to treat diabetes and obesity are reshaping medicine in unforeseen ways. Their impact…
    #NewsBeep #News #Health #Addictionresearch #alcoholusedisorder #brainrewardsystem #CA #Canada #diabetesdrugs #dopamine #glp-1drugs #metabolichealth #Neuroscience #obesitytreatment #opioidaddiction #Semaglutide #substanceusedisorder #VAstudy
    newsbeep.com/ca/527512/

  6. Aspirin and N-acetylcysteine co-administration markedly inhibit chronic ethanol intake and block relapse binge drinking: Role of neuroinflammation-oxidative stress self-perpetuation [2019]
    pubmed.ncbi.nlm.nih.gov/317330

    link to full text:
    repositorio.udd.cl/server/api/

    ~
    Female only study ('Adult female rats, Wistar-derived, bred for over 90 generations as alcohol consumers').

    #neuroinflammation #glutamate #AlcoholUseDisorder #NAC #aspirin

  7. Maryland doctor explains how ‘dementia risk rises with every increase in alcohol intake’

    There may be no safe amount of alcohol when it comes to brain health.Dr Kunal Sood, a physician…
    #NewsBeep #News #Headlines #alcoholconsumption #alcoholdementiarisk #alcoholusedisorder #dementiarisk #heavydrinkers #Latvia #LV #moderatedrinking
    newsbeep.com/253198/

  8. Beyond Willpower in Addiction: 4 Powerful Lessons

    Originally Published on November 11th, 2025 at 08:00 am

    We often think of addiction as a private, grueling battle of willpower.

    Whether it’s a dependency on a substance, a behavior like gambling, or even an unhealthy pattern in a relationship, the prevailing narrative suggests that breaking free is a matter of pure, individual strength.

    If you just try hard enough, you can overcome it. If you fail, it’s a personal failing. 

    But what if this framework is fundamentally flawed? A recent, year-long study offers a more structured, hopeful, and evidence-based path to recovery.

    Researchers applied a specific form of therapy, Cognitive Behavioral Therapy (CBT), to individuals struggling with a range of addictions and discovered that the right tools can do more than just help people cope; they can fundamentally transform their lives.

    It’s about building a life so full and satisfying that the addiction no longer has room to thrive.

    This year-long study is particularly significant because it was conducted in Kazakhstan, a region where evidence-based psychotherapy is still emerging and social stigma can be a major barrier to recovery. 

    This article distills the four most impactful takeaways from this groundbreaking research. It reveals how a systematic therapeutic approach can lead to profound, measurable life changes, challenging the myth that recovery is simply a matter of gritting your teeth and pushing through. 

    Lesson 1: The Change to Isn’t Small, It’s Transformative

    While we might expect therapy to offer some benefit, the sheer magnitude of improvement seen in this study was extraordinary.

    Participants who received Cognitive Behavioral Therapy didn’t just get slightly better; they experienced a dramatic and measurable enhancement in their overall well-being. 

    The study used the World Health Organization’s Quality of Life scale (WHOQOL-BREF), which measures well-being across four key areas. The results were staggering.

    On average, the experimental groups saw their quality of life scores jump from the low 40s to the mid-70s on a 100-point scale. To put that in concrete terms, participants with alcohol use disorder went from an average score of 42.31 before therapy to 74.47 after one year.

    This isn’t just a number on a chart; it represents a profound shift from a life constrained by addiction to one filled with new possibilities and well-being. 

    Meanwhile, the control groups, those who did not receive CBT, saw no meaningful improvement in their quality of life, with their average scores remaining essentially unchanged.

    This powerful contrast repositions recovery as a genuine opportunity to build a measurably better and more satisfying life.

    It’s about building a life so full and satisfying that the addiction no longer has room to thrive. 

    Are you exploring your trauma? Do you feel your childhood experiences were detrimental to your current mental or physical health? Utilize this free, validated, self-report questionnaire to find out.

    Take the Adverse Childhood Experience (ACE) Questionnaire

    Beyond Willpower Lesson 2: The Same Tools Can Fix Different Problems

    One of the most compelling aspects of the study was its breadth.

    Researchers applied the same core therapeutic model, CBT, to four very different challenges:

    • Alcohol use disorder
    • Drug addiction
    • Gambling disorder
    • Codependency

    The key finding was that CBT was highly effective across the board. 

    For every single group that received therapy, there was a statistically significant reduction in the severity of their addiction. The data paints a clear picture of this versatility: 

    • For drug addiction, the experimental group’s average severity score dropped from 7.96 (signifying harmful use) down to 3.14 (representing low-risk or minimal use). 
    • For gambling disorder, the average severity score plummeted from a “severe” 39.55 to a “mild or moderate” 14.36. 

    This suggests that no matter the substance or behavior, the underlying challenge is often the same: learning to recognize triggers, challenge automatic negative thoughts, and develop new, healthier coping strategies.

    CBT provides a toolkit for rewiring these exact processes, effectively helping people move from a place of denial or ambivalence into decisive action and long-term maintenance. 

    Do you have enough hours for your LPC renewal? Are you in need of continuing education, but bored with the current offerings? Check out Dr. Weeks’ course on Cannabis Use Disorder, and other unique courses on her practice website.

    Sexual Addiction Treatment Services has been approved by NBCC as an Approved Continuing Education Provider, ACEP No. 7250. Programs that do not qualify for NBCC credit are clearly identified. Sexual Addiction Treatment Services is solely responsible for all aspects of the programs.

    Lesson 3: Codependency Isn’t Just a “Relationship Problem.” It’s Treatable.

    The study took the significant step of including codependency, an excessive emotional or psychological dependence on a partner, often linked to that partner’s addiction, alongside clinical addictions. While codependency is not formally classified as a standalone diagnosis in major manuals like the DSM-5-TR, the researchers recognized it as a clinically significant phenomenon that is actively addressed in rehabilitation. 

    The results were a powerful validation of this approach.

    The experimental group for codependency saw their average severity scores drop from a “high level” of 69.12 to a “moderate or low level” of 31.44. The control group, in stark contrast, showed no significant change.

    For anyone who has felt trapped in a dynamic of supporting someone else’s addiction at the expense of their own well-being, this finding is a beacon of hope. 

    This is a crucial takeaway.

    It frames the struggle of codependency not as a character flaw or an intractable relationship dynamic, but as a treatable condition. It offers empowerment and a clear path toward building greater independence, self-esteem, and healthier relationship dynamics. 

    Beyond Willpower Lesson 4: Recovery Isn’t Just Stopping, It’s a Total Life Upgrade

    The study’s design was brilliant in its simplicity: it measured success in two ways. It tracked the reduction of the negative (addiction severity) and the increase of the positive (overall quality of life). The results showed that these two things are deeply intertwined. 

    The “quality of life” assessment wasn’t a vague feeling of happiness; it was a concrete evaluation of four essential domains of life: 

    • Physical Health: Including energy and fatigue, quality of sleep, and even physical mobility. 
    • Psychological Health: Covering everything from positive feelings and self-esteem to the ability to concentrate and learn new things. 
    • Social Relationships: Examining the quality of personal relationships, the strength of social support networks, and even sexual activity. 
    • Environment: Looking at practical, real-world factors like financial security, physical safety, the comfort of one’s home, and access to healthcare. 

    The participants who underwent CBT saw significant improvements across all of these areas. This demonstrates that effective treatment doesn’t just happen in a therapist’s office. It radiates outward, improving every facet of a person’s existence.

    True recovery, as this study shows, is about building a life that is so robust and fulfilling that the old addictive behaviors no longer hold the same power or appeal. 

    Conclusion: A New Framework for Change

    The findings from this study in Kazakhstan provide a powerful, evidence-based roadmap for recovery that moves far beyond the limited concept of willpower.

    It shows that addiction, in its many forms, is not a moral failing but a condition that responds remarkably well to structured, compassionate, and science-backed intervention. 

    By focusing on cognitive and behavioral strategies, individuals can achieve not just abstinence, but a transformative and holistic improvement in their lives. The tools exist, the evidence is clear, and the potential for change is immense.

    This research leaves us with a vital question to consider: 

    If we can treat these complex issues so effectively, what does that change about how we should approach mental health and personal growth in our own lives? 

    Are you a professional looking to stay up-to-date with the latest information on, sex addiction, trauma, and mental health news and research? Or maybe you’re looking for continuing education courses? Then you should stay up-to-date with all of Dr. Jen’s work through her practice’s newsletter!

    Do you feel your sexual behavior, or that of someone you love, is out of control? Then you should consult with a professional.

    Are you looking for more reputable data-backed information on sexual addiction? The Mitigation Aide Research Archive is an excellent source for executive summaries of research studies.

    #addiction #addictionRecovery #addictionTreatment #alcoholAbuse #alcoholRecovery #alcoholUse #alcoholUseDisorder #cbt #cognitiveBehavioralTherapy #drugAbuse #drugAddiction #drugAddictionRecovery #drugUse #evidenceBasedTherapy #gambling #gamblingAddiction #kazakhstan #therapyOutcomes #willpower

  9. 🥂🚶‍♂️ Wow, Sherlock! Social drinking *might* lead to alcohol use disorder! Who knew? 🤔 If only there were some way to avoid this well-trodden path that everyone and their dog seems to have figured out... #MindBlown 🥳
    news.illinois.edu/review-socia #SocialDrinking #AlcoholUseDisorder #MindBlown #HealthAwareness #ResponsibleDrinking #HackerNews #ngated

  10. pubmed.ncbi.nlm.nih.gov/392143 The effect of intranasal (R,S)-ketamine on symptoms of fatigue in severe major depressive disorder or bipolar depression with and without comorbid alcohol use disorder: Results from a randomized, double-blind, placebo-controlled trial (Machado-Veira, et al, 2024) #ketamine #fatigue #depression #alcoholusedisorder #bipolardisoder #psychedelic #psychedelics #fda #mentalhealth #psychedelicmentalhealth

  11. pubmed.ncbi.nlm.nih.gov/387432 The entactogen 3,4-methylenedioxymethamphetamine (MDMA; ecstasy) as a treatment aid in psychotherapy and its safety concerns (Baldo, et al, 2024) #mdma #fda #entactogens #psychedelic #psychedelics #psychedelicresearch #psychedelicassistedpsychotherapy #mdmaassistedtherapy Note: FDA has approved trials of MDMA for: #ptsd #socialanxiety (especially related to #autism) #alcoholusedisorder #eatingdisorders #asociality related to #schizophrenia #deathanxiety

  12. lemmy.world/post/11126588 Awakn Life Sciences Completes Successful Investigative Study to Establish Dissociative Effect of a Proprietary Sublingual S-Ketamine Oral Thin Film Formulation in Harmful Drinkers #psychedelic #esketamine #alcoholusedisorder #ketamineassistedpsychotherapy

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