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KARE

Kerala United Against Rare Diseases

Government of Kerala Initiative

Kerala United Against Rare Diseases

India's first state-funded comprehensive care programme for children with rare diseases. Join us in transforming lives through prevention, treatment, and compassionate care.

KARE LogoGovernment of Kerala
About KARE

Comprehensive Care for Rare Diseases

KARE (Kerala United Against Rare Diseases) is a pioneering initiative by the Government of Kerala, making it the first state in India to launch a state-funded treatment programme for rare diseases.

Our Beginning

Drawing from the successful experience of the SMA program (2022–2024), the Government of Kerala launched KARE in 2024. The programme focuses on prevention, early identification, and provision of treatment along with access to medicines, therapies, and assistive devices.

Vision

To create a sustainable model for comprehensive care and treatment access for children with rare diseases in Kerala.

Mission

To mobilize alternative funding and ensure equitable access to high-cost treatments for conditions such as SMA, Gaucher, Pompe, MPS, and others.

Uninterrupted Therapy

Ensure continuous treatment for all eligible patients

Holistic Care

Provide comprehensive care through public health infrastructure

Transparent Funding

Build an accountable ecosystem through philanthropy and CSR

Our Impact

Transforming Lives Across Kerala

Kerala's model has shown that early diagnosis, multidisciplinary care, and timely drug access can transform outcomes in rare diseases.

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Children Supported

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Crores Target

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Diseases Covered

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Years of Care

Diseases Covered

Conditions We Support

KARE provides comprehensive treatment and support for children affected by these rare diseases.

Spinal Muscular Atrophy (SMA)

A genetic disorder affecting motor neurons, leading to muscle weakness. Kerala became the first state to provide state-funded SMA treatment.

Gaucher Disease

A genetic disorder where fatty substances accumulate in organs and tissues, affecting the spleen, liver, and bone marrow.

Pompe Disease

A rare inherited disorder caused by deficiency of an enzyme that breaks down glycogen, affecting muscles throughout the body.

MPS (Mucopolysaccharidoses)

A group of metabolic disorders caused by absence or malfunction of enzymes needed to break down molecules called glycosaminoglycans.

Health Minister
“Kerala's model has shown that early diagnosis, multidisciplinary care, and timely drug access can transform outcomes in rare diseases like SMA. KARE represents our commitment to ensuring no child is left behind due to the rarity of their condition.”
Veena GeorgeMinister for Health & Family Welfare, Kerala