About YASJC

Empowering young adults with chronic skin and joint conditions through advocacy, education, and community

black blue and yellow textile

Young Advocates with Chronic Skin and Joint Conditions (YASJC) was formed by young patients located throughout Europe who are working together to enhance and improve the quality of life for adolescents and young adults living with chronic skin and joint conditions.

To improve the quality of life for young adults living with chronic skin and joint conditions by advocating for better healthcare, raising awareness, building a supportive community across Europe, and ensuring that every patient has access to comprehensive, patient-centered care that addresses their unique needs.

Our Mission
Our Vision

A future where every young person with chronic skin and joint conditions has access to comprehensive care, feels empowered to advocate for themselves, lives without stigma or barriers to treatment, and is supported by a strong community that understands their journey.

Our Reach

Help us expand!

Our Strategic Pillars

Four interconnected areas of focus that drive our advocacy work

Raise Awareness

Amplifying patient voices through campaigns, media engagement, and public education initiatives.

Key Impact Areas:

  • Social media campaigns reaching thousands

  • Educational materials for healthcare providers

  • Public speaking at medical conferences

  • Collaboration with patient organizations

Integrated Care

Comprehensive Support

Inclusive Policies

Promoting holistic healthcare approached that address physical, mental, and social well-being.

Key Impact Areas:

  • Advocacy for multidisciplinary care

  • Mental health support integration

  • Patient-centered treatment protocols

  • Transition care programs for young adults

Building networks and resources to support patients throughout their healthcare journey.

Key Impact Areas:

  • Peer support

  • Educational workshops and webinars

  • Resource libraries and toolkits

  • Mentorship opportunities

Working with policymakers to ensure equitable access to care and treatment.

Key Impact Areas:

  • Policy recommendations to EU institutions

  • Healthcare accessibility advocacy

  • Insurance coverage improvements

  • Patient rights protection

Our Organizational History

The journey from a corporate initiative to an independent, patient-led advocacy organization.

2022

Foundation Phase

Initiated by UCB in collaboration with Patvocates to address the unmet needs of young patients.

  • Partnership established between UCB and Patvocates

  • Focus on empowering young adults with chronic skin and joint conditions

2022

Needs Assessment

Comprehensive research phase to understand the real-world challenges faced by young patients.

  • In-depth interviews conducted with 15 young patients across Europe

  • Identification of key advocacy gaps and training needs

2023

Structured Training

European Patient Advocacy Initiative (EPAI) to support:

  • Delivery of comprehensive training

  • First Face-to-Face (F2F) meeting held in Brussels

  • Focus on building core advocacy skills and network creation

2024

Expansion & Independence

A pivotal year marking the transition from a corporate initiative to a patient-led organisation.

  • Second F2F meeting in Brussels

  • Unanimous decision by members to create an independent organisation

  • Transition of leadership to patient advocates

2024-2025

Informal Organisation

Building the foundational structure of YASJC

  • Defining core mission, vision, and strategic pillars

  • Establishment of specialized working groups

  • Development of internal governance and operational frameworks

2026

Public Launch

Official introduction of YASJC to the global advocacy community

  • Launch of the official YASJC website

  • Rollout of comprehensive social media presence

  • Initiation of public awareness campaigns

2026

Path Toward Formal Hosting

Securing long-term sustainability and institutional support

  • Integration into formal hosting structures within EPAI (European Patient Advocacy Institute)

  • Expansion of European advocacy network