A “Right to Try” bill is currently being discussed by Congress. Advocates on both sides of the story present valid points to either pass or stop the bill. That’s why groups like Rare Disease Legislative Advocates (RDLA) are hosting conversations on the topic. Keeping reading to learn more, or follow RDLA at their site for more information.

On Wednesday, March 21st, RDLA hosts its monthly webinar. The informational meeting begins at 12:00pm and runs until 1:00pm Eastern Time. The meeting takes place over the phone, and registration is open now.

Click here to register.

RDLA describes the webinar as discussion of the issues at hand without endorsement of any specific view. The agenda for the March 21st Webinar includes discussion of the Rare Disease Advancement, Research, and Education Act, The Advancing Access to Precision Medicine Act, and Right to Try. There will also be time to discuss nominations for the RareVoice Awards.

RDLA also describes the agenda as remaining open. The group invites those wishing to speak to contact [email protected].

Who: Rare Disease Legislative Advocates
What: Monthly Webinar (including discussion of Right to Try legislation)
When: March 21st 12:00pm-1:00pm EST
Where: Conducted via phone. Registration required.

What are your thoughts about the Right to Try? Share your opinions and insights with the Patient Worthy community!