IFPA's Consultancy Service

Access IFPA’s exclusive consultancy service with expert patient representatives

We welcome you to present project ideas for further collaboration. IFPA can support you in the planning and operational phases of a project, or take an equal part in a project where the patient view needs to be secured.

With our strong track record in patient education, advocacy, and awareness-raising, IFPA understands the complexity of psoriatic disease and shares its knowledge in patients' perspectives. Furthermore, IFPA offers access to our expertise and our global network of patients and patient associations.

All projects are conducted according to IFPA’s code of conduct and ethical rules.

We strongly encourage potential partners to engage IFPA in the early stages of project development.

Available Consultants

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    Frida Dunger

    Executive Director

    Frida is responsible for managing IFPA operations, facilitating strategic development, and building global partnerships. Frida is committed to building a more just and sustainable world. She has extensive experience working with non-profits, including Emmaus Stockholm, ActionAid, and Forum Civ. Frida holds a Master in International Development Studies and Cultural Encounters.

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    Sicily Mburu, M.D.

    Scientific Officer

    Sicily injects the patient perspective into every stage of the research cycle. Sicily is a health professional with a clinical background and over 10 years experience in the field of global health. Sicily holds a dual MSc in Epidemiology, and Health Economics & Policy.

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    Elisa Martini

    Policy and Advocacy Manager

    Elisa is responsible for development and implementation of IFPA's advocacy and policy strategies at a global level. She has a Master´s degree in pharmaceutical sciences and a Ph.D. with a focus on psoriasis. She has previous advocacy experience as a volunteer in a local level, health sector NGO.

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    Camille Lancelot

    Community Manager

    Camille runs IFPA's member services and capacity development programs. She has a background in development work and teaching as well as a Master in Cultural Projects for Development. Camille has lived and worked in the USA, Senegal, Benin, France, and Sweden.

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    Janina Kostiukaite

    Strategic Events and Projects Lead

    Janina explores new opportunities to diversify IFPA's sponsorship to support IFPA's action against psoriatic disease. Janina is a Master of Global Health, with special training in Medical Peace Work and eHealth. She has interned at the WHO and organized international youth projects in Turkey and Macedonia.

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    Josef de Guzman

    Treasurer, IFPA

    CEO, PsorPhil / Psoriasis Philippines
    Manila, Philippines

     

    Josefino "Josef" De Guzman is a dedicated advocate for psoriatic disease, NCDs, and disability inclusion with over 20 years of experience. He founded PsorPhil in 2005, creating a leading advocacy group for Filipinos with psoriatic disease. As founder of PsorAsia, he sparked a movement across Asia, mentoring nations to build patient organizations and sharing insights globally.

    Josef is committed to training non-dermatologists and primary health workers on psoriasis to improve diagnosis and treatment access. His leadership roles include CEO of Psoriasis Philippines, Treasurer of IFPA, and Chair of the World Psoriasis Day Steering Committee. His legacy as a champion for the psoriatic community is enduring and impactful.

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    Silvia Fernandez Barrio

    Board Member, IFPA

    President, AEPSO / Psoriasis Association of Argentina
    Buenos Aires, Argentina

     

    Throughout her career as a radio and TV journalist in Argentina, Silvia has gained significant recognition for her dedication to her work and her advocacy for various causes. At the age of 18, she was diagnosed with psoriasis. When a major psoriasis flare-up in 2004 left her unable to afford her new medication, Silvia took the initiative to found AEPSO – the first and only psoriasis patient organization in Argentina. Since its founding, AEPSO has assisted over 55,000 patients and families, providing them with vital resources, information, and support. Silvia’s commitment to improving the lives of people with psoriasis continues to shape the organization’s mission and outreach efforts.