France, along with Latin America, is one of the regions where psychoanalysts have historically included
infantile autism in their explanations of the condition, especially after the 1970s and 1980s. Psychoanalytic practices continue to influence psychiatric approaches to autism in the country. Additionally, there has been significant opposition between parent associations and health professionals regarding the treatment of autism. In the 2010s, French parent associations, initially focused on securing institutional care and funding, began advocating for changes in the way autistic children were treated and educated. Sociologists note that these efforts were partly driven by public authorities to push forward deinstitutionalization, although this led to concerns among health professionals about the availability of resources for vulnerable families. Over the years, the classification of autism has evolved from being seen as a rare and severe disorder to a broader spectrum of related conditions, affecting around 1% of the population. Since the 1990s, autism has increasingly been viewed as a social issue, with significant legal developments, although resistance to change remains.
Before medical descriptions . Before the concept of autism was defined, individuals with the condition were often marginalized and described as "idiots", "crazy" or "wild children." One example is Victor de l'Aveyron, a child found in 1801 who exhibited behaviors now associated with autism. Dr. Jean Itard, who cared for him, also described a form of non-verbal autism in 1828, calling it intellectual mutism. Itard and Édouard Séguin were among the first to study and describe individuals who may have had autism. The first formal descriptions of autism and Asperger's syndrome appeared in the 1940s in international scientific literature. During the German occupation of France, autistic individuals were likely among those who died in psychiatric hospitals due to starvation and harsh conditions.
1950s to 1980s Until the 1980s, autism in France was primarily understood as infantile autism, or
Kanner autism, and was categorized with
psychoses or
schizophrenia. The publication of
The Empty Fortress in 1967 brought attention to autism and influenced public perception, particularly with the idea of the autistic child as a "machine child". The 1974 television program by Daniel Karlin and conferences by Bettelheim also popularized his views on autism, including the controversial "mother refrigerator" theory. In France, autism was long equated with
childhood schizophrenia, and it wasn't until the 1980s that the distinction between the two was made. neurologist Catherine Barthélémy, and
child psychiatrist Dominique Sauvage, became pioneers in autism research and support. However, autism did not receive significant attention from French public authorities until the 1990s. From the 1950s onward, inspired by practices in the United States and the United Kingdom, psychiatrists and psychoanalysts like Roger Misès and
Serge Lebovici introduced care, education, and pedagogy for autistic children in France. These efforts led to the creation of part-time institutions, day hospitals, and outpatient care to support communication and social relationships. The creation of the Santos-Dumont day hospital in Paris in 1963, by the Association Serving Misfits with Personality Disorders (ASITP), marked a significant step in this approach. By the 1970s, these methods spread throughout France. These structures, meant for children with serious personality disorders, offered a combination of psychological, educational, pedagogical, and rehabilitative care. The approaches in these institutions were sometimes deemed insufficient due to limited resources and a focus on "care" over education. In 1989, the Creton amendment allowed disabled adults over 20 to remain in medico-social institutes, typically for those with high dependency or multiple disabilities.
First implementations of behavioral therapies In the 1980s, French parents learned about
behavioral therapies for autistic children from North America and sought to introduce them in France. This interest was driven by the guilt associated with psychoanalytic theories of autism and the desire to actively engage in their children's education. In 1989, psychiatrist Catherine Milcent translated
Eric Schopler's work into French and established the first French class integrated with the TEACCH program in
Meudon. In the 1990s, dedicated units for autistic individuals were created, offering behavioral programs like
TEACCH and
ABA. However, these programs were limited in number and faced skepticism from the medico-social sector. Despite this, the introduction of these programs led to a shift in how autism was approached, with health professionals adopting a more multidisciplinary approach and becoming more open to the Anglo-Saxon model. In April 1995,
Opinion 47 of the National Ethics Advisory Committee In 1995, disagreements between health professionals and parent associations intensified. The Autisme France association appealed to the National Consultative Ethics Committee (CCNE) in 1994, On 11 December 1996, the "Chossy law" was passed, introduced by Jean-François Chossy, to ensure multidisciplinary interventions for autistic individuals and to officially recognize autism as a disability. This change was met with resistance from many French psychiatrists, who still viewed autism as a rare and severe condition. The 2002 law on user representation aimed to encourage the participation of autistic individuals in public decision-making about their care. The report called for a comprehensive plan to address early diagnosis, research, lifelong support, training for professionals, and better integration in society. It rejected the divide between "psychodynamic" and "educational" approaches, advocating for care that meets individual needs with a multi-year plan and adequate financial support. The report was strongly influenced by the positions of Autism France.
Recommendations of 2004 and first conviction In 2003, lawyer Évelyne Friedel, then president of Autism France, brought the issue of lack of education access for autistic children to the
Court of Justice of the European Union.
Disability Act of 2005 The 2005
Disability Act aimed to ensure equal rights and opportunities for people with autism, marking France's first major step toward securing the schooling of children with autism. On the other hand, Marcel Hérault, president of Sésame Autisme, supported linking autism to the field of disability, viewing it as a condition affecting individuals at a given moment, while also acknowledging the role of psychiatry in autism care.
First Autism Plan (2005–2007) , rapporteur for Opinion No.102 of the French National Consultative Ethics Committee, in 2015 As a result of the first European condemnation of France, the first Autism Plan was introduced in 2005. It led to the creation of Autism Resource Centers (CRA) in each French region and focused on improving professional training and increasing the availability of specialized care. The report highlighted the lack of support for autistic individuals and the distress faced by families. The CCNE called for earlier diagnoses, individualized education, and access to effective educational methods, such as cognitive-behavioral programs. It also recommended the use of medication for severe symptoms and psychological support for families. The CCNE report criticized the harmful impact of the "
refrigerator mothers" theory and called for more reliable, early diagnoses and better educational support for children. The report also acknowledged the emerging role of psychoanalysts in multidisciplinary care, though it emphasized the need for approaches based on educational methods.
Second Autism Plan (2008–2010) The second Autism Plan was launched in May 2008 by
Valérie Létard. Over two years, the plan aimed to create 4,100 spaces in institutions for autistic children and adults. The High Authority for Health was tasked with developing a scientific and multidisciplinary knowledge base on autism, while the National Agency for the Evaluation and Quality of Establishments and Social and Medico-Social Services (Anesm) was responsible for defining best practices. This base was published in January 2010. At the end of 2011, Valérie Létard reported that while some objectives were not fully met, 70% of the planned spaces had been created, and 25,000 autistic children were enrolled in school.
Year of Great National Cause (2012) In 2012, autism was declared an important national priority under Prime Minister
François Fillon. The year saw various awareness campaigns and media coverage, particularly following the release of the documentary
Le Mur. In March, the High Authority for Health recommended certain educational and behavioral approaches, such as the
ABA method,
Early Start Denver Model, and the
TEACCH program, noting their effectiveness in improving IQ, communication skills, and language development in about 50% of children. The report did not recommend certain methods like the
Son-Rise program, the 3i method, and others, and excluded psychoanalysis and institutional psychotherapy, citing a lack of evidence for their effectiveness. It also opposed practices like "packing" except in research contexts. The report sparked controversy, with proponents of cognitive-behavioral therapies calling for the ban of psychoanalysis, while psychoanalysts criticized the methodology and argued that the report failed to capture the complexity of autism. Some medical professionals expressed concerns about the approach used to develop the recommendations, claiming that the focus on cognitive-behavioral methods was not well-supported and did not provide enough guidance for families and healthcare providers.
Third Autism Plan (2013–2017) , initiator of the third Autism Plan, in 2012. The third Autism Plan, announced on 2 May 2013 by
Marie-Arlette Carlotti, included measures to improve early diagnosis, support for families, and the creation of 700 specialized teaching places in nursery schools to help autistic children integrate into primary schools. The plan, with a budget of 205 million euros, focused on early diagnosis, childhood support, family assistance, research, and training for professionals. An official website was launched to provide reliable information.
Political positions In February 2014, the Council of Europe concluded that the rights of autistic children to schooling and professional training were not being fully respected in France. The report also noted that specialized institutions lacked an educational focus. In 2016, Ségolène Neuville recommended educational methods for autism and opposed blaming mothers. Later that year, Daniel Fasquelle proposed a resolution to promote care based on official recommendations, but it was rejected.
Assessment of the third plan By 2014-2015, the number of autistic children in school increased to 26,347 from 23,545 the previous year. However, a report from the General Inspectorate highlighted weaknesses in epidemiology, involvement of health professionals, and regional managements. Despite progress in school integration and screening, the support available, particularly for adults, remained insufficient. Josef Schovanec was tasked with developing a plan focused on the training, integration, and professional activity of autistic adults. In 2017, a commission of international scientists was assembled to define good intervention practices. The fourth plan, called the "autism strategy," included autism within broader disability policies and emphasized better access to medical and educational services. Recommendations for adults were published by the High Authority for Health (HAS) in June 2017. The consultation was officially launched on 6 July 2017, with President
Emmanuel Macron delivering a speech. On 1 January 2019, a key measure of the plan, the early intervention package, was implemented. In February 2019, the UN released a report on disability in France, highlighting issues such as institutionalization, under-representation of autistic individuals in decision-making, and violations of their human rights. == Diagnostic ==