Virtual Accreta Meetups
Live virtual get-togethers can provide a much-needed connection when patients and survivors have questions about accreta or are looking for emotional support. National Accreta Foundation hosts ongoing meetups within our closed Facebook support groups. Please join our online support groups and look for our virtual meetups.
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PLACENTA ACCRETA PATIENT & FAMILY RESOURCES
National Accreta Foundation helps connect placenta accreta, increta and percreta patients & families with resources and content of value.
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National Accreta Foundation is a non-profit 501(c)(3) organization dedicated to placenta accreta advocacy. Content on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own physician or other medical professional. Please see our medical disclaimer here.