Attended a Champions for Change Summit previously.
Registered for the next Champions for Change Summit.
Submit your story or experience by clicking the link below.
Ask your one of the MoMMA's Voices Organizations for access
This program is supported by funding from Merck, through Merck for Mothers, the company’s $500 million initiative to help create a world where no woman has to die while giving life. The content of these publications is solely the responsibility of the authors and does not represent the official views of Merck. Merck for Mothers is known as MSD for Mothers outside the United States and Canada.
Special thanks to the review committee for their thoughtful review and editing of this content: Alexis Carena of the National Accreta Foundation, Diana Masulli of Amniotic Fluid Embolism Foundation, Jacqueline McLeeland of The Push Partners, and Meghan Viers of the Amniotic Fluid Embolism Foundation.
Patient Family Partner Training
This course is designed to give those with a lived experience an understanding of patient family partnership and learn more about patient engagement.
2020 Summit Patient Track
Content from the Patient Track at the 2020 Champions for Change Summit. Available to patient family partners and professionals with All Access Passes for free.
2020 Summit Provider Track
Content from 2020 Champions for Change Summit Provider Track.
What if I am a family member or friend?
Family members and friends have a unique perspective that we value. We might refer to "sharing your story" as a default
What if I am not a "near-miss" survivor but had a traumatic pregnancy experience for other reasons?
Our training is designed to be universal to cause or condition. So long as you are wanting to make an impact as a patient family partner, then you will find our training useful.
What if I am a professional?
We have special training specifically for professional to learn how to be effective at patient engagement. If you would like to also have access to the patient family partner training, please contact Nicole.Purnell@preeclampsia.org to discuss.
What if I don't live in the US?
The training is meant to be universal to cause or condition. While some of the training may not be applicable, our hope is that there will be plenty to learn or repurposed to your situation.
I would love to get this training available in my system or state. How do I go about that?
Please contact Nicole.Purnell@preeclampsia.org to discuss your needs and general licensing availability.
Where can I learn more about MoMMA's Voices?
If you would like to learn what we do for patient family partners, professionals or patient advocacy organizations, please check out our website at www.mommasvoices.org