The Power of Our Voice: FDA Listening Session for Adult Dermatomyositis

A look behind the scenes with patient and caregiver speakers and MSU reps

Watch the recording of our Fireside Chat, The Power of Our Voice: FDA Listening Session for Adult Dermatomyositis, where we invited the patient and caregiver speakers and the representatives from MSU who were involved.

In this, we go behind the scenes with the team and we share what we learned, what it was like, and more, all about the power of our voices.

While FDA Listening Sessions are closed meetings, we have developed a comprehensive summary that you can view below.

The power of our voice can impact the direction of research and clinical trials. Join us in a virtual Fireside Chat on the lessons learned from our FDA Listening Session for Adult Dermatomyositis.

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Myositis Support and Understanding Association (MSU) is a patient-centered, all-volunteer 501(c)(3) nonprofit organization Empowering the Myositis Community. Founded by Myositis patients, for Myositis patients, MSU provides education, support, advocacy, access to research and clinical trial matching, and need-based financial assistance.

View more information: Myositis Support

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