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MEDVETS
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Advocacy & Patient Rights

Join the Fight

Access to medicine. An end to opioid dependency. Cancer patients supported. Patient rights enforced, not just written down.

Our Advocacy Mission

Decisions about patients get made in rooms patients are not in.

MEDVETS puts them in the room. We testify at state and federal hearings, file comment on rules that affect access, organise members around live legislation, and help individual patients fight denials that should never have been issued.

Our advocacy agenda is not written by a policy team. It is set by members — veterans managing chronic pain, cancer patients navigating cost and coverage, caregivers who have spent years on hold with an insurer. If it is on this page, someone we serve put it there.

We bring the same discipline to this that we bring to a build day: turn up prepared, say what is true, and stay after the hearing ends.

Know your rights

  • The right to informed consent before any treatment
  • The right to your complete medical records
  • The right to a second opinion
  • The right to appeal a denial of coverage
  • The right to adequate pain management
  • The right to refuse treatment
  • The right to an interpreter and accessible communication
  • The right to file a complaint without retaliation
Request the full rights guide

Current Initiatives

What we are fighting for right now

Six active fronts. Each one has a live bill, a hearing date or a campaign behind it.

Access to Medicine

Removing prior-authorisation barriers and formulary exclusions that delay treatment for months on end.

Ending Opioid Dependency

Funding and coverage parity for non-opioid pain management, and safe tapering support for veterans already dependent.

Cancer Patient Support

Price transparency, out-of-pocket caps and navigation funding for patients in active treatment.

Patient Rights Enforcement

Real consequences when providers and insurers ignore rights patients already legally hold.

Statehouse Testimony

Putting veterans and patients in front of the committees that decide what care they can reach.

Caregiver Recognition

Formal standing, respite funding and training for the families holding the line at home.

Ways to Participate

Five minutes or five years — both help.

You do not need policy experience. You need a name, an address and a willingness to say what happened to you.

Add My Name

Take an action alert

We send the target, the script and the deadline. You send the email or make the call.

Share your case

Lived testimony moves legislation faster than any statistic. We help you write it and place it.

Testify at a hearing

We handle registration, travel and preparation. You tell the committee what happened.

Join a rally or town hall

Turn up in person where the decision is being made. Numbers in the room are not decoration.

Advocacy Roster

Join the Fight

Add your name and we will send you action alerts for the issues you select — targeted to your state and never more than a couple of times a month.

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Fund the fight

Travel to hearings, case advocacy hours and campaign materials are the least glamorous line items we have — and the ones that move bills.

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