United for Rare Disorders Kenya

Rare Disorders Kenya (RDK) unites patients, parents, and caregivers to advocate for better health policies and a supportive healthcare system. Join us in raising awareness and improving lives for those affected by rare diseases. Together, we are a strong voice for change in Kenya.

Our Services at Rare Disorders Kenya (RDK)

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Patient Advocacy

We provide a strong, unified voice for patients with rare disorders, advocating for better health policies and access to care.

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Educational Workshops

Providing workshops and training sessions for patients, caregivers, and healthcare professionals on rare diseases.

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Awareness Campaigns

Raising public and professional awareness about rare disorders to promote understanding and early diagnosis.

Our Mission

Provide a strong common voice to advocate for health policy and a healthcare system that works for those with rare disorders.


Join us in making a difference!

Team

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(Sample Bio) Dr. Jane Mwangi, Founder and Medical Advisor, brings over 15 years of experience in clinical genetics and patient advocacy, dedicated to improving healthcare policies for rare disease patients in Kenya.
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(Sample Bio) Michael Otieno, Outreach Coordinator, specializes in community engagement and support services, ensuring effective communication between patients, caregivers, and healthcare providers.
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Empowering Rare Disease Communities in Kenya: The Role of Rare Disorders Kenya (RDK)

Championing the Cause of Rare Disease Patients

Rare Disorders Kenya (RDK) is a pioneering patient-led organization located in Upperhill, dedicated to representing the voices of individuals diagnosed with rare diseases, alongside their parents and caregivers. Our unique position as a community-driven entity allows us to deeply understand the challenges faced by those affected by rare disorders in Kenya. By uniting patients and families, RDK creates a strong collective voice that advocates for improved health policies and a responsive healthcare system tailored to the needs of this underserved population.

Expertise in Advocacy and Support Services

RDK offers specialized advocacy services aimed at influencing healthcare policy to ensure equitable access to diagnosis, treatment, and care for rare disease patients. Our expertise extends to providing comprehensive support networks that empower patients and caregivers through education, resource sharing, and emotional support. By facilitating connections between stakeholders, healthcare providers, and policymakers, we drive initiatives that aim to enhance quality of life and healthcare outcomes for individuals living with rare disorders.

A Unique Patient-Centered Approach

What sets Rare Disorders Kenya apart is our commitment to being a truly patient-led organization. Our governance and activities are guided by those directly impacted, ensuring that our strategies and programs reflect the real needs and priorities of the rare disease community. This authentic representation fosters trust and engagement, making RDK a vital ally for patients, families, and healthcare professionals working towards a more inclusive and effective healthcare system in Kenya.

Frequently Asked Questions


You can support RDK by making donations, volunteering your time, or helping raise awareness about rare disorders. Please visit our website's support or contact page for more information on how to get involved.


Healthcare professionals can collaborate with RDK by participating in advocacy efforts, contributing to educational programs, and helping improve diagnosis and treatment pathways for rare disorders.


RDK is based in Upperhill, Nairobi, Kenya. Our office serves as a hub for support, advocacy, and community engagement.


Contact Us

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