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Contact Congress about S. 3346: Freedom to Heal Act of 2025

Some seriously ill patients could get access to certain experimental Schedule I drugs through their doctors. Doctors would need a special federal registration and would have to follow strict supply, storage, and record rules.

Modern Action explains legislation in plain English, helps you choose whether to support, oppose, or ask for changes, and drafts a message tied to the bill, your stance, and the elected officials who can act on it.

Freedom to Heal Act of 2025 is a Senate bill in committee. The latest recorded action: Read twice and referred to the Committee on the Judiciary.

Latest action on S. 3346: Read twice and referred to the Committee on the Judiciary.

Who this affects: This bill mainly affects seriously ill patients, their doctors, and companies developing experimental Schedule I drugs. Patients could have a clearer way to seek certain experimental treatments outside a clinical trial. Doctors would face a new registration process and strict handling rules. Drug makers or sponsors would still decide whether to provide the drug and instructions for its use.

Why this matters: This bill matters because some experimental treatments are hard to use when they are also Schedule I controlled substances. It would give doctors a clearer federal route to treat eligible Right to Try patients with those drugs. It could help some patients who have few other options. But access would still depend on drug makers, state law, federal rules, and safeguards against misuse.

Key provisions in S. 3346

  • Doctors could get a new special federal registration to give certain experimental Schedule I drugs to eligible patients. The treatment must fit the federal Right to Try law.
  • The bill keeps the current Right to Try meanings for “eligible investigational drug” and “eligible patient.” Those terms come from the Food, Drug, and Cosmetic Act.
  • Doctors must already be registered to give or dispense Schedule II through V controlled substances. Without that existing registration, they cannot qualify.
  • The drug maker or sponsor must put key facts in writing. They must confirm the drug qualifies, agree to supply it, and explain how it should be given.
  • State law must allow the doctor to use these drugs with eligible patients. The doctor must also show relevant training, credentials, or experience.

How Modern Action helps you take action on S. 3346

You do not have to start with a blank letter. Modern Action turns the bill, your position, and the relevant congressional context into a message you can edit and send. The goal is to make contacting Congress clear, specific, and useful without forcing you to parse bill text or figure out the right office on your own.

Questions people ask about S. 3346

What is S. 3346?
Some seriously ill patients could get access to certain experimental Schedule I drugs through their doctors. Doctors would need a special federal registration and would have to follow strict supply, storage, and record rules.
How do I support or oppose S. 3346?
Choose support, oppose, or ask for changes on Modern Action. The action flow drafts the message for you and keeps the wording tied to this bill.
Who should I contact about S. 3346?
Modern Action uses your location to route the action to the congressional offices relevant to the bill and your representation.
Can Modern Action explain S. 3346 before I act?
Yes. Modern Action gives you a plain-English summary, current status, and action context before you send anything.

Keep acting on Modern Action

More ways to act on this issue

Compare the broader issue and related bills without leaving Modern Action.

Related issues

  • Contact your reps on Handling, storage, quantity, and site safeguardsWhether physicians and treatment sites using investigational Schedule I drugs should face detailed federal rules for storage, security, records, delivery, drug quantities, registration renewal, and treatment-location disclosure.
  • Contact your reps on Right to Try and expanded access before FDA approvalWhether seriously ill or treatment-resistant patients should be able to receive investigational Schedule I psychedelic drugs before final FDA approval through Right to Try, expanded access, or similar supervised pathways.

Related bills

  • Take action on H.R. 6434: Freedom to Heal Act of 2025
  • Take action on H.R. 9547: Veterans and Servicemembers PTSD Emerging Treatment Review Act of 2026