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This paper was originally presented on May 2, 2013, at the Verdeil Foundation (e-TEM School), Pierrefleur 21, Lausanne, with the support of the Insieme Foundation.
In « Between self-sacrifice and the sacrifice of others: Walking the tightrope of family balance », Giuliana Galli Carminati examines the tensions experienced by families caring for a person with an intellectual disability. She argues that disability is neither the result of parental fault nor failure, but rather an often unpredictable reality of life.
Drawing on several clinical cases, the author highlights the complex relationships of dependency that develop between the individual with an intellectual disability, their family, and healthcare and support professionals. When difficulties remain unspoken, emotions are concealed, or each person tries to protect the others, tensions accumulate and may lead to violent behaviours, caregiver exhaustion, and inappropriate decisions.
The author emphasizes that the continuous self-sacrifice of a parent or family member is not a sustainable solution. Assuming every responsibility out of love can lead to isolation, guilt, and even unintended forms of harm, both toward oneself and the person receiving care. The clinical examples illustrate the importance of open communication, shared responsibility, and multidisciplinary support in preventing family situations from becoming destructive.
Finally, Giuliana Galli Carminati reminds us that parents must come to terms with the loss of the idealized image of the "perfect child," a long but necessary grieving process. When guilt gives way to solidarity, the burden of adversity becomes easier to bear. Despite the many challenges involved, the author pays tribute to the resilience, wisdom, and remarkable capacity for adaptation demonstrated by the vast majority of families living with intellectual disability.
Keywords: Intellectual disability; family caregivers; family dynamics; caregiver burden; dependency; health and social care support.
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| Article 2-2026 |
In « From an autism diagnosis to self-understanding: How spoon theory and sensory processing differences can transform everyday life », Carmen Zecca-Tagan argues that an autism diagnosis should not be viewed as an endpoint, but rather as the beginning of a journey toward greater self-understanding. Through psychoeducation, autistic individuals learn to understand their neurodivergent way of functioning, identify their specific needs, and develop strategies that help them preserve their well-being instead of exhausting themselves by trying to conform to neurotypical expectations.
The author draws on spoon theory, a metaphor for energy management, to explain that every daily activity carries a different energetic cost depending on the individual. This approach helps autistic people anticipate their energy expenditure, plan recovery periods, and reduce the risk of meltdowns, shutdowns, and autistic burnout.
The article then explores the sensory processing differences associated with autism. Hyper- and hyposensitivities may affect hearing, vision, taste, smell, touch, interoception, and the vestibular system. A wide range of practical environmental adaptations — including noise reduction, adjusted lighting, appropriate clothing, structured routines, and sensory tools — can significantly reduce sensory overload and improve daily well-being.
In conclusion, Carmen Zecca-Tagan encourages a shift in perspective on autism. Rather than attempting to change autistic individuals, the goal should be to adapt their environment so they can invest their energy in their strengths instead of constantly compensating for their difficulties. Understanding one's own neurodivergent functioning promotes autonomy, self-esteem, and a better quality of life while recognizing and valuing the unique abilities of each autistic person.
| Article 3-2026 |
Artificial intelligence is profoundly transforming the way we understand human intelligence. This article offers an original reflection on the connections between philosophy, intellectual disability, autism, and AI by returning to the foundations of Platonic and Aristotelian thought. The authors demonstrate that the historical association between rationality, human value, and citizenship has had a lasting influence on the perception of individuals with intellectual disabilities or autism spectrum disorder.
Through an analysis combining ancient philosophy, ethics, and cognitive sciences, the article highlights how current debates on artificial intelligence ethics, neurodiversity, and inclusion are rooted in these ancient conceptions. The emergence of AI is now challenging traditional criteria used to define intelligence and encourages moving beyond a vision based exclusively on logical performance and reasoning abilities.
The authors also introduce the original concept of neuronism, presented as an evolution of Aristotelian hylomorphism. This approach opens new perspectives for rethinking the place of human beings in relation to intelligent technologies and for promoting a more inclusive society.
Beyond rationality alone, the article advocates for a plural conception of intelligence that incorporates emotional, relational, embodied, and spiritual dimensions. It argues that artificial intelligence should not reinforce the cognitive hierarchies inherited from the past, but should instead become a tool for inclusion, recognition of cognitive diversity, and respect for human dignity. This analysis represents a significant contribution to contemporary debates on AI, neurodiversity, philosophy, and the future of inclusive societies.
| Article 4-2026 |
The article “Shame”, offers a multidisciplinary reflection on a universal yet often unspoken emotion: shame. Drawing on the author’s therapeutic experience with people with disabilities and their families, the article demonstrates that shame, although rarely expressed, represents a major source of psychological and social suffering. Through an exploration of philosophy, literature, sociology, psychology, and disability studies, the author examines the mechanisms underlying this complex emotion and its impact on individuals and their relationships with others.
The article begins with a quotation from Mohamed Mbougar Sarr, suggesting that one can never completely escape a history that causes shame. This idea is extended through the reflections of Edgar Morin, who spoke of feeling “ashamed of his own species” when confronted with human violence and atrocities. However, this shame does not prevent commitment or hope; on the contrary, it reflects a lucid awareness of human complexity, in which individuals are capable of both the best and the worst. Shame is defined as an emotion connected to self-image and the perception of oneself through the eyes of others. Although it was long neglected by the human sciences, shame has gradually become a significant field of study, particularly through trauma studies, which have highlighted the close relationship between trauma and emotions such as fear, sadness, anger, and shame. The author distinguishes between different forms of shame — individual, familial, social, and cultural — which frequently overlap and influence one another.
Literature provides an essential perspective for understanding shame. Jean Genet transformed shame into an instrument of rebellion against bourgeois norms. In his works, what society considers shameful becomes a source of pride, provocation, and identity. Albert Camus explored shame from different perspectives: his own experience of social inequality, the absence of shame in the character of Meursault in The Stranger, and the overwhelming guilt and shame experienced by the protagonist of The Fall. Jean-Paul Sartre offered one of the most influential philosophical analyses of shame, arguing that shame always emerges in relation to another person. It appears when individuals become aware of themselves through another’s gaze and suddenly perceive an image of themselves that they cannot control. Shame is therefore fundamentally a relational experience.
Contemporary writers such as Édouard Louis, Annie Ernaux, and Sorj Chalandon further illustrate the social dimension of shame. Their works describe experiences of social mobility and the painful distance between their origins and the worlds they later entered. They experience a double form of shame: shame about their social background and shame about feeling ashamed of their own families. Writing becomes a way of transforming suffering into meaning and sometimes into symbolic repair. For Annie Ernaux, shame becomes a central element of her autobiographical work after a traumatic childhood experience. For Édouard Louis, it becomes a tool for analysing social domination and inequality. For Sorj Chalandon, shame is connected to family violence, childhood wounds, and the hidden truth about his father’s past. These examples demonstrate that shame is deeply linked to identity, belonging, and social position.
The sociological perspective further develops this analysis. Erving Goffman showed that shame emerges when an individual’s identity is discredited by a stigma — an attribute that prevents full social acceptance. People experience shame when they feel they no longer correspond to the expectations of society. Vincent de Gaulejac considers shame a “total social fact” resulting from the interaction between personal suffering, family history, and cultural context. He highlights humiliation, contempt, and social judgment as powerful sources of shame. Pierre Bourdieu describes shame as a deeply embodied emotion, expressed through blushing, hesitation, anxiety, or physical discomfort. For him, shame reveals how individuals internalize social inequalities and dominant forms of judgment.
Psychology and psychoanalysis approach shame from different perspectives. Freud considered shame mainly as a psychological barrier protecting against certain impulses, while Lacan viewed it as a sign that the subject still preserves dignity and a relationship with reality. Jung associated shame with the concept of the “shadow,” the hidden and rejected parts of personality that individuals attempt to conceal. In clinical practice, shame is rarely presented as the explicit reason for seeking therapy. Patients more often describe feelings of discomfort, humiliation, rejection, or inadequacy. The therapist must therefore identify the hidden presence of shame behind these expressions. The article also emphasizes that shame is frequently connected to family secrets and can be transmitted across generations, with descendants sometimes carrying emotional burdens whose origins remain unknown.
A central aspect of shame is its connection with the gaze of others. Individuals experiencing shame often feel exposed, judged, or “unmasked,” leading to withdrawal and a desire to hide. This judgment is not always real; it may be an internalized perception shaped by social, cultural, or family expectations. According to Serge Tisseron, shame has a paradoxical nature: it can destroy individuals, but it can also preserve social bonds because it implies the continued existence of others and the desire for recognition. Shame is also strongly associated with loneliness, as people often believe they are the only ones experiencing it, which increases their sense of isolation.
The article then focuses on disability, which represents a major clinical context for understanding shame. People with disabilities, as well as their families, may experience profound shame due to social judgment, unconscious guilt, and the loss of the idealized child they imagined before disability was identified. Unlike temporary forms of shame, shame related to disability may persist because the situation itself is often permanent. It requires a long psychological process of acceptance and reconstruction. The author also highlights the existence of an implicit hierarchy in social perceptions of disability: acquired physical disabilities are often more socially accepted than congenital disabilities, and intellectual disability remains particularly stigmatized.
Finally, the author examines society’s response to disability. Feelings of discomfort, avoidance, or rejection often reveal a deeper fear of human vulnerability. The article concludes that shame remains difficult to express because it is frequently unconscious, inherited, or hidden behind other psychological difficulties. Nevertheless, sharing experiences through support groups, therapy, and personal narratives can help break isolation by showing individuals that they are not alone in their suffering. The article opens further perspectives for research, particularly regarding the links between shame and ethnicity, gender inequalities, cultural norms, and social exclusion.
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| Article 5-2026 |
This article presents a clinical reflection on the introduction of psychostimulant treatment in a young adult with Level 1 Autism Spectrum Disorder (ASD) and suspected Attention-Deficit/Hyperactivity Disorder (ADHD), through the case of Mr. U, a 22-year-old man. Although the pharmacological intervention was intended to improve attentional and executive functioning, its introduction coincided with increased anxiety, without producing the expected functional benefits. We propose that this outcome is better explained not by a lack of pharmacological efficacy, but by an impairment of projectuality—the individual's capacity to invest in a meaningful personal future—resulting from a developmental trajectory characterized by overadaptation, camouflaging, and insufficient reciprocal adjustment between the individual and the environment. We discuss the clinical implications of this hypothesis for the interdisciplinary care of neurodivergent adults undergoing major life transitions.
| Article 6-2026 |
This article offers a clinical and institutional exploration of the conditions of hospitality that enable a person with a disability to appropriate a place without professionals defining or shaping that place on their behalf. Drawing on the experience of Antonio, who attends a day service and presents, among other characteristics, features associated with autism spectrum disorder, the author examines the tensions between the containing function of the institution, the need for predictability, educational support, and respect for the subject’s singularity.
The care setting is conceptualized as a living environment, continually shaped by the bodies, voices, movements, interactions, and investments of those who inhabit it. From this perspective, the appropriation of a place forms part of a process of subjectivation. The issue is not simply for the individual to adapt to a pre-existing environment, but to be able to establish their own mode of presence within it and, in doing so, contribute to its ongoing transformation.
Two clinical vignettes illuminate this question. The first demonstrates how a tool initially designed to enhance predictability may become increasingly rigid and ultimately function as a constraint, both for the individual and for the group. The second describes the contingent emergence of a ball as a bodily resource during a moment of heightened tension. Unlike a prescribed intervention, the object emerges spontaneously, is temporarily invested and then disappears, without being transformed into an imposed therapeutic or educational technique.
These situations invite a distinction between supportive scaffolding and educational over-intervention. “Knowing how to let things unfold” entails maintaining a presence that is sufficiently close and containing, while remaining sufficiently unobtrusive not to override the subject’s own initiatives and movements. In this respect, the institution’s mediating or third-party function helps preserve a space for play, transformation, and appropriation.
| Article 7-2026 |
This article offers a clinical and psychoanalytic exploration of psychological health, tracing a trajectory from fantasy to delusion and, ultimately, toward a dynamic conception of mental health. Drawing on her experience as a special education professional and her work supporting people experiencing psychological disorders, the author examines the boundaries between imagination, subjective reality, psychological suffering, and processes of psychological reconstruction. Fantasy is initially understood as a natural manifestation of imagination and creativity, capable of expressing both conscious and unconscious desires. Delusion, by contrast, is conceived as a psychic construction that profoundly alters an individual’s relationship to reality. The article nevertheless emphasizes that delusion cannot be reduced to a mere loss of contact with reality. From a Freudian perspective, it may also be understood as an expression of subjective reality and as an attempt to respond to a psychic wound.
Through the architectural metaphor of a castle, the author subsequently conceptualizes psychological health as an evolving construction that requires ongoing maintenance, adaptation, and reconstruction. The contributions of Freud and Jung make it possible to understand psychological health not merely as the capacity to confront reality, but also as the ability to appropriate one’s own existence, experience pleasure, develop a sense of agency, and engage in a process of individuation.
The article finally draws on Kazimierz Dąbrowski’s theory of positive disintegration, according to which certain experiences of crisis, disorganization, or suffering may become opportunities for psychological transformation and reconstruction. A psychological wound can thus be understood not only as a source of vulnerability, but also as material through which a new organization of the self may emerge, much like the Japanese art of kintsugi.
In conclusion, psychological health emerges as an ongoing quest for meaning, ownership of one’s life, and self-construction, rather than as a definitive state free from symptoms. It entails sustained attention to one’s psychological equilibrium, together with the capacity to transform adversity into resources for psychological reconstruction.
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