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Financial Assistance

Financial Support for LSD Patients

Navigating rare disease costs in India is hard. This guide covers every government scheme, NGO grant, insurance tip, and step-by-step process available to LSD families.

Where to Start

How to Access Financial Aid

Follow these steps in order — each unlocks the next.

01

Get a Confirmed Diagnosis

Ensure you have a diagnosis letter from a recognised Centre of Excellence (CoE). This is required for all government scheme applications.

02

Contact a CoE Hospital

Approach one of the government CoE hospitals listed on our Doctors page. They process NPRD 2021 fund applications on your behalf.

03

Gather Documents

Collect: diagnosis report, Aadhaar, income certificate, BPL card (if applicable), hospital bills, and doctor's prescription.

04

Apply for IGST Exemption

If your medicine is imported, apply for IGST exemption simultaneously — this can save 12–18% on drug costs immediately.

05

Reach Out to Us

Contact Taraasha Foundation for navigation support, grant identification, and help with application paperwork — completely free.

Government

Government Schemes

National Policy for Rare Diseases 2021 (NPRD)

Ministry of Health & Family Welfare

Up to ₹50 lakh per patient

ELIGIBILITY

Indian citizens diagnosed with a rare disease listed under NPRD 2021

HOW TO APPLY

Apply through a Centre of Excellence (CoE) hospital. The hospital submits to the Rare Disease Fund on your behalf.

Rashtriya Arogya Nidhi (RAN)

Ministry of Health & Family Welfare

Up to ₹15 lakh (one-time)

ELIGIBILITY

Below poverty line patients requiring treatment at Central Govt Hospitals

HOW TO APPLY

Apply through the Medical Superintendent of the treating Central Govt hospital.

State Rare Disease Funds

Respective State Governments

Varies by state (₹5L – ₹25L)

ELIGIBILITY

State resident diagnosed with a notified rare disease

HOW TO APPLY

Check your state health department website or contact your nearest Government hospital.

IGST Exemption on Rare Disease Drugs

Ministry of Finance

0% GST on imported medicines for rare diseases

ELIGIBILITY

Patients importing medicines not available in India for personal use

HOW TO APPLY

Submit IGST exemption application with doctor's certificate to the port of import or CBIC.

NGO & Non-Profit

NGO Grants & Support Programmes

Taraasha Foundation Patient Fund

Taraasha

Focus: LSD patients across India  ·  Support: Travel, diagnostics, counselling subsidies

Apply Now

IIHMR Patient Assistance Program

Focus: Rare metabolic disorders  ·  Support: Partial treatment cost support

Visit Website

NORD India (Network of Rare Disease Orgs)

Focus: All rare diseases  ·  Support: Financial counselling and grant navigation

Visit Website

Organisation for Rare Diseases India (ORDI)

Focus: All rare diseases  ·  Support: Connects patients to CSR funds and government grants

Visit Website
Insurance

Insurance Tips for LSD Patients

Rare disease patients often face unfair insurance rejections. Know your rights.

Always mention the ICD-10 or ORPHA code for your disease when filing a claim — this helps insurers classify rare diseases correctly.

Under IRDAI guidelines, no insurer can reject a claim solely because the disease is rare. Cite IRDAI Circular 2020/IRDAI/HLT/REG if rejected.

If your employer's group health insurance excludes rare diseases, you can escalate to the Insurance Ombudsman.

Critical Illness riders sometimes cover enzyme replacement therapy (ERT) — check your policy wording carefully before assuming exclusion.

Some state public sector banks offer priority loans at subsidised rates for rare disease treatment — ask your branch manager.

Need Help Navigating These Schemes?

Our team has helped over 200 families access government schemes and NGO grants. We guide you through paperwork, applications, and appeals — completely free of charge.