Donation After Death

How to Register as a Donor

Register as an organ donor in about two minutes. Registration means hospitals will know you want to help others through donation. Your decision is legal and stays in control of you. You can change your mind at any time. All it takes is a few minutes online or at your motor vehicle office.

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Overview

Registering as an organ donor takes just a few minutes. Your wish is recorded in your state's official registry. If something happens to you, hospitals check that registry. If your name is there, they will know you wanted to donate, and your family is spared having to make the decision for you.

You can register online, by phone, or at your motor vehicle office. You do not need a doctor's permission, medical tests, or approval from anyone else. The only thing that matters is your own choice. You can change your mind later, and the registry will be updated.

How to register as a donor

How to register as a donor

The easiest way for most people is online registration. Here's the simple process:

  • Visit your state's donor registry or OrganDonor.gov
  • Enter basic information (name, address, date of birth, driver's license number)
  • Confirm that you want to register
  • You're done—you're now officially registered

Other registration methods work just as well. Some states require in-person registration at the motor vehicle department. Others allow registration when renewing your driver's license. You can also register by phone. No matter which method you choose, the result is the same: your name is added to your state's official registry.

What happens when you register?

Registration sets official processes in motion. Your wishes are documented and become part of the medical record that hospitals can access. Your state maintains a registry of all registered donors. Hospital staff check the registry when someone dies to confirm donor status. If your name is in the registry, they know you wanted to donate and contact the organ procurement organization.

The registry is confidential and secure:

  • Your information is protected
  • Hospitals access it only upon death confirmation
  • Staff only check your donor status, not other information
  • Your data is handled with strict privacy standards

The legal term "first-person consent" means your own decision—not your family's—controls what happens. If you're registered, hospitals honor your wishes even if your family disagrees. You don't have to worry your family might refuse donation. Your registration ensures your decision stands.

Can I change my mind?

Yes, absolutely. Your decision isn't permanent—it's entirely within your control. Changing your mind takes just as little time as registering. Removing yourself is as simple as registering. You can:

  • Logging into your state's registry website and removing yourself
  • Calling your state registry to request removal
  • Visiting the motor vehicle department to request removal
  • Updating your driver's license to remove the donor designation
  • Speaking with your family and providing written documentation

Once you're removed, you're no longer a registered donor. Your state registry updates within days to weeks. Hospitals won't have documentation that you wanted to donate.

You're always in control. You might register, change your mind and remove yourself, then register again years later. Your wishes at the time of death are what matters. Many people register and never change their mind. Others later decide donation isn't right. Both choices are completely valid.

Does registration guarantee donation?

Registration is not a guarantee that your organs will be donated. It's a documented statement of your wishes. Your organs must still be medically suitable for transplant. Registration provides important protections for your wishes and your family:

  • Your wish is legally documented
  • Hospitals won't need to search for your family's permission
  • Your documented wish is sufficient authorization
  • The process streamlines and removes burden from your grieving family

If none of your organs are viable for transplant, tissues may still be recovered. If no organs or tissues are viable, your body is treated with respect and released to your family as planned.

Registration removes ambiguity. It says clearly: "If I die and my organs can help someone, use them."

What if I have health conditions?

Many people worry that health conditions prevent donation. This concern is common but often unfounded. Registration doesn't require perfect health. You only need willingness to donate if organs are suitable when death occurs. You can register even if you have common health conditions:

  • Diabetes (controlled or requiring insulin)
  • High blood pressure or hypertension
  • High cholesterol
  • Asthma or other lung diseases
  • Arthritis or joint disease
  • Cancer that is being treated or was previously treated

You can also register if you have:

  • HIV (many HIV+ individuals are now acceptable donors and can donate to HIV+ recipients)
  • Hepatitis C (certain organs can be used and transplanted to appropriate recipients)

Medical suitability is determined at death, not registration. Conditions you have now might not prevent donation later. The modern transplant field has become increasingly sophisticated about matching organs from donors with chronic conditions to recipients who can benefit.

  • Controlled diabetes doesn't automatically disqualify you
  • Managed heart disease doesn't prevent registration
  • Many donors with chronic conditions successfully donate
  • Some conditions (active sepsis, aggressive cancers, active infections) may limit options
  • But you don't need to figure this out now

If you're unsure whether your health affects donation, ask questions during or after registration. Medical staff can clarify specific conditions and explain how your situation might be handled.

You can register and let the medical team assess suitability at the time of death when your actual condition is known. There's no downside to registering even with health concerns—it documents your willingness, and medical professionals make the final determination about viability.


Additional Detailed Information

Additional Information

State registry technical infrastructure

State donor registries are maintained by individual states, often through the motor vehicle department or a designated health agency. Some states use a centralized database; others use multiple systems that communicate. The Donate Life America network provides coordination across states. If you move to a different state, your donation preferences may not transfer automatically. You may need to register in your new state to ensure your wishes are recognized, though many states have reciprocal agreements. This is an important reason to discuss your wishes with family—they can advocate for donation even if state registry coordination fails.

Legal status of first-person consent

First-person consent is based on the Revised Uniform Anatomical Gift Act (RUAGA), adopted in all 50 states. This law establishes that a donor's documented wishes supersede family objections. The legal rationale is based on bodily autonomy—your decision about what happens to your body stands. This represents a significant shift from earlier laws that required family consent. It reflects a cultural and legal recognition that individuals should have ultimate authority over donation decisions.

Registration as documentation of intent

Registration serves as one form of documentation of intent. Other legal documents—advance directives, living wills, and organ donation designation cards—also document your wishes. While registration in the state donor registry is the most official method, discussing your wishes with family and documenting them in writing also matters. Many families honor the wishes of deceased loved ones even without formal registration, but registration removes all ambiguity and ensures your wishes are discoverable by medical professionals.

Written By:
Transplants.org Staff

Transplants.org Staff

Last Reviewed: February 26, 2026
Informed By:

Transplants.org, with participation from 23 leading U.S. transplant centers, led the largest comparative analysis of patient educational materials in transplant history. We recognize the participating centers who helped inform and inspire our direction with initial patient-centered educational content:

Transplants.org is an independent nonprofit organization and participation is not an endorsement by these organizations.

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