This description of Valentina Perniciaro's work was prepared when Valentina Perniciaro was recognized by Ashoka in 2024.
Introduction
Valentina is helping society - especially non-disabled people - reimagine inclusion and the full participation of people with disabilities. She transforms lived experience into collective advocacy, demanding dignity over pity and belonging over barriers. Her work affirms the right to live fully - with risk, joy, and autonomy, and to receive care with respect. She reframes public space as a shared, accessible environment and recognizes caregivers as key to social equity. For Valentina, accessibility is not optional, it’s a right, and she’s working to make it universal.
New Idea
Valentina envisions a world where disability is not seen as a deviation from the norm, but as an integral part of human experience. In this future, accessibility is no longer treated as a special accommodation but as a standard—a baseline expectation embedded into how we design cities, services, and relationships. Caregiving is no longer relegated to the private, invisible sphere, but understood as a shared social responsibility, with caregivers equipped, supported, and recognized as essential contributors to social cohesion and justice. Through collaborative, community-driven work across design, education, and policy, she is building a world where inclusion is not aspirational, but operational—visible in how we live, play, work, and care for one another.
Her new idea stems from years of lived experience now transformed into a replicable model for systemic change. At its core are two strategic interventions. First, the creation of a School for Caregivers—a scalable structure providing emotional, legal, and practical support for informal caregivers, who make up the majority of Italy’s care system but remain untrained and unsupported. This school reframes caregiving as a skilled, civic role and not merely a personal burden. Second, she is creating inclusive public spaces and events that enact what she calls the “right to adrenaline”—the right of people with disabilities to participate fully in play, sport, risk, and cultural life. Initiatives like the Universal Inclusive Park in Rome, inclusive archaeological treks with Joëlettes, and multi-ability sports events break down the cultural and physical barriers that frame disability as passive or separate. Unlike existing efforts that focus either on caregivers or on integrated recreation, Valentina’s model bridges both, while anchoring the work in public infrastructure that is visible, interactive, and designed for replication across contexts.
Through these approaches, Valentina is not just advocating for change—she is building the civic, educational, and urban systems that make inclusion real. Her strength lies in translating personal experience and community energy into tangible models with institutional impact. Tetrabondi’s growing network, now over 120,000 people strong, is a testament to her ability to mobilize public will, but her true innovation lies in the concrete pathways she creates for participation, equity, and dignity. As she continues to scale these efforts, her work offers a blueprint for other societies facing similar challenges—where disability, care, and inclusion are still siloed, but where the potential for transformation is ready to be unlocked.
The Problem
The core social problem addressed by the Tetrabondi Foundation is the systemic exclusion of people with disabilities and their caregivers in Italy, driven by pervasive ableism. This exclusion manifests in limited access to social, cultural, and economic participation: there are 3.2 million people with disabilities in Italy, representing 5.2% of the population. However, only 43.5% of people with disabilities have access to a wide network of relationships, and just 9.3% engage frequently in cultural, social, political, and sports activities (Understanding the world of disability - ISTAT, 2019). These statistics reflect the deep-rooted issue of ableism in Italy, which results in widespread marginalization and a lack of accessibility to basic opportunities for participation in society.
Ableism in Italy is entrenched in cultural, historical, and social narratives that often view disability either through pity or heroism, rather than recognizing people with disabilities as equals. This mindset is perpetuated by the media and public perceptions, which fail to acknowledge disability as a natural aspect of human diversity. The notion of a “healthy” norm excludes individuals who deviate from this standard, reinforcing inequality and othering. Further exacerbating the situation, Italy’s infrastructure remains largely inaccessible to people with disabilities. For instance, only one-third of schools and 37.5% of museums are accessible, and public transportation usage among people with disabilities is significantly lower than that of the general population. These infrastructural gaps severely hinder participation in both everyday life and more specialized activities, such as cultural and sports events, leading to widespread exclusion.
The economic disparities are also stark: families with disabled members experience significantly higher rates of poverty and material deprivation. In fact, 20% of families with disabled members live in poverty, compared to 12.4% of families without disabled members (2022 ISTAT Report). This inequality is compounded by the lack of support for caregivers. According to a 2015 ISTAT survey, 74% of caregivers in Italy are women, and 60% of them have had to leave their jobs to provide full-time care for a disabled family member. This sacrifice often results in financial instability and increases the risk of poverty for the family unit. Furthermore, caregivers and people with disabilities face social isolation, with more than 600,000 severely disabled individuals living in complete isolation, a situation worsened by inadequate social support systems and a lack of awareness of their rights.
The Strategy
Tetrabondi’s strategy is centered around three key initiatives: the School of Caregiving, the Universal Inclusive Park, and a communication strategy focused on changing societal perceptions of disability. The School of Caregiving provides both paid and free training for caregivers, offering them valuable tools, resources, and a supportive community. In the past two years, over 5,000 caregivers and professionals have received training, and the National Database on Caregiving Opportunities has been created to offer easy access to critical information and services for caregivers across Italy. This initiative empowers caregivers to improve their caregiving practices while advocating for more recognition of caregiving as an essential societal role.
The Universal Inclusive Park in Rome is a tangible example of Tetrabondi’s inclusive urban planning approach. Located in a high-visibility area of the city, the park is a fully accessible public space designed for people of all ages and abilities to interact, play, and explore together. It features a variety of recreational areas, including a wheelchair-accessible skate park, and offers opportunities for non-disabled visitors to experience mobility from a different perspective using specially designed wheelchairs. These experiential elements foster empathy, understanding, and shared enjoyment. The park also includes innovative archaeological walks that allow visitors to engage with Rome’s ancient heritage in inclusive and creative ways. These walks go beyond physical accessibility by incorporating tactile paths, interactive models, and multisensory storytelling. Designed by Valentina and the Tetrabondi team, they invite everyone—regardless of ability—to connect with the city’s history in a meaningful, immersive way.
Tetrabondi’s design guidelines for the park provide a practical, adaptable framework for cities looking to implement similar inclusive spaces. Tetrabondi is helping to reshape how cities think about inclusivity, ensuring that accessible spaces become a standard in urban planning, rather than an exception.
Tetrabondi’s communication strategy plays a crucial role in challenging societal attitudes toward disability. Valentina uses storytelling on her blog, social media, and public appearances to shift the narrative away from pity and heroism, advocating instead for rights, self-determination, and inclusivity. This has led to over 70,000 people participating in community events that dismantle stereotypes and promote understanding. Through these efforts, Tetrabondi is engaging individuals in advocacy, helping to create a powerful movement that sees disability as a natural part of human diversity. In 2022, Valentina published her first book, Everyone Laughs His Own Way, where she reflects on the messy, beautiful journey of her "ramshackle" family. She also took the stage for her first TEDx talk, The Happiness of Bodies in Everyone’s World, where she emphasized the necessity of inclusion and the importance of caring for everyone’s desires and needs. Today, in addition to building up and expanding Tetrabondi’s model, Valentina continues to serve as an expert on disability and diversity, bringing her voice to public TV shows and public forums, where she uses her platform to advocate for systemic change, spread support information, fight stigma, and create spaces where all bodies and identities can thrive.
These interconnected initiatives—caregiving support, inclusive urban spaces, and shifting societal narratives—are driving lasting change in how disability is perceived and addressed. Valentina is creating a more inclusive and equitable society by ensuring that accessibility and inclusivity become the norms, not exceptions.
The Person
Born and raised in Rome, Valentina’s early exposure to social issues began in her teenage years when she witnessed a protest in support of the Kurdish cause. She started volunteering by assisting hunger strikers and supporting refugees living in informal settlements. She later pursued a degree in Arabic Language and Literature, driven by an interest in understanding the broader geopolitical and cultural contexts behind the issues she had encountered. During her studies, she spent time in Syria and Palestine, where she volunteered in refugee communities and participated in projects such as women’s sports initiatives and community radio—experiences that provided insight into building inclusive, locally driven initiatives with limited resources.
Returning to Italy after graduation, Valentina entered the challenging Italian job market. She worked a series of temporary roles before joining the national postal service. In 2015, a change in labor legislation increased job insecurity, particularly for younger employees. Valentina participated in collective efforts to advocate for basic employment protections such as severance pay. This period further developed her understanding of organizational dynamics and policy impact and exposed her to the challenges of mobilizing and sustaining collective action.
In the following years, personal circumstances significantly influenced the direction of her work. Her second son, Sirio, was born prematurely and experienced a cardiac arrest shortly after returning home from the hospital. He was later diagnosed with spastic tetraparesis and cerebral palsy. Valentina took on the responsibilities of full-time caregiving, navigating complex healthcare systems and social services.
In 2018, she began sharing her family’s story online as a way to document and reflect on their experience. This gradually evolved into Tetrabondi, a platform created with the input of her older son, Nilo. It combined storytelling with broader questions about representation, accessibility, and the role of caregivers in society. In 2021, following a successful crowdfunding campaign, she formally established the Tetrabondi Foundation ONLUS furthering her mission to challenge existing societal norms and fight for the empowerment of caregivers and those with disabilities.