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INDIA · DKMS FOUNDATION INDIA

Joining a stem cell donor registry from India

For people who live in India. Live somewhere else? Find your country.

5 registries sign up people who live in India. You only need to join one. Here’s who can join, how it works and what happens after.

You can join here, through DKMS Foundation India.

Browsing from another country? See how joining works where you live.

Ways to join

5 services sign up people who live in India. You only need to join one.

  • DATRI

    Run by DATRI Blood Stem Cell Donors Registry (registered name as printed; CIN not found on pages read), a nonprofit organization.

    18–50years old to join

    Who it’s for
    People who live in India, aged 18 to 50.
    Language
    English

    Read DATRI’s own page (opens in a new tab)

  • GeneBandhu

    GeneBandhu is an organization whose legal form we haven’t confirmed.

    18–60years old to join

    Who it’s for
    People who live in India, aged 18 to 60.
    Language
    English

    Who this suits People aged 56 to 60, past DKMS Foundation India’s age limit.

  • Jeevan Stem Cell Foundation

    Run by Jeevan Stem Cell Foundation (Be The Cure registry; Jeevan public cord blood bank), a nonprofit organization.

    Who it’s for
    People who live in India.
    Language
    English

    Jeevan Stem Cell Foundation has paused new sign-ups.

Who can join

These are DKMS Foundation India’s rules, in short. Its own pages have the full list, and the registry decides.

Where you live
India.
Age to join
18 to 55
How long you stay on the registry
Until your 61st birthday, unless you ask to leave.
Your health
Most healthy adults can join. Some conditions rule it out. Read the registry’s health rules (opens in a new tab)
Joining, staying on the registry and being able to donate are different ages.

What happens after you join

From your sample to a possible call. Each registry runs its own process; these are the steps they share.

  1. Check you can join.

    DKMS Foundation India sets its own age range and health rules. Its own pages have them.

  2. Give a sample.

    The registry takes a sample to record your tissue type. Its own pages say how.

  3. You’re on the registry.

    Your tissue type is recorded, so searches for patients can find you.

  4. If you match a patient.

    The registry contacts you, checks you’re still willing and well, and arranges more tests.

  5. Donation.

    If you go ahead, you’ll donate blood stem cells or bone marrow. The registry explains what’s involved and supports you through it.

Keep your contact details up to date so the registry can reach you. What donating is like

Questions

Can I join if I’m not a citizen?

Registries usually decide by where you live, not by nationality. DKMS Foundation India’s own rules say who can join.

I’m already on another country’s registry. Do I join again?

Registries share their lists with searches around the world, so ask your registry before you join a second one.

Is giving blood the same as joining?

Giving blood helps patients who need transfusions. It doesn’t put you on a stem cell donor registry unless that registry says it does.

Who is the Jada Bascom Foundation?

We’re a US charity. We don’t run a registry, and we aren’t part of DKMS Foundation India. We help people find the official registry where they live.

Live somewhere else?

BE SOMEONE’S TORSTEN

The same search found Jada’s donor in Germany.

Jada was a baby in Spokane, Washington, when doctors found she had acute myeloid leukemia. Her match was a stranger five thousand miles away: Torsten, who had joined the DKMS registry at a donor drive in Germany the year before she was born. If you live in India, your place in that search starts with DKMS Foundation India.

CHECKED BEFORE IT WAS PUBLISHED

Sources

The registries’ own pages

  1. DKMS Foundation India. Register as a potential donor (rendered headless) + page data https://www.dkms-india.org/page-data/register-now/page-data.json (fetched 2026-10-11T16:00:31Z) (opens in a new tab). Undated.Checked
  2. DKMS Foundation India. Frequently asked questions (opens in a new tab). Undated.Checked
  3. DKMS Foundation India. Compliance & Financials (opens in a new tab). Undated.Checked

Government and official registers

  1. Jada Bascom Foundation. About us: Jada’s story. Undated.Checked

The World Marrow Donor Association

  1. World Marrow Donor Association (WMDA). WMDA statistics JSON view (opens in a new tab). Undated.Checked

Map outlines: Natural Earth. Boundaries are for orientation only and imply no position on any dispute.

Data version hub-2026.10.15-1+68cdf352

Last checked Next check due

What we do and what we don’t. The Jada Bascom Foundation is a charity in the United States. We don’t run a registry, and we aren’t part of DKMS Foundation India. We explain how joining works and link to the registry’s own site. We can’t see whether you sign up, and we never receive anything you give the registry.

Something wrong or out of date? Tell us, with this page’s title and what looks wrong. Our contact form doesn’t accept web addresses, so the title is enough. Tell us

Joining a registry is separate from giving money to JBF. Support this work