PAS Postpartum, Breastfeeding & Bonding survey

This study is now closed, although National Accreta Foundation gets calls for survivor input like this often. If you’d like to be invited to future opportunities like this, please add your story to our story bank via the button below.

who is hosting this survey?

Researchers at Beth Israel Deaconess Medical Center (BIDMC)/Harvard Medical School in Boston, MA are gathering information on postpartum, breastfeeding, and bonding experiences of women who had pregnancies affected by placenta accreta spectrum (PAS) disorders. This research is led by Dr.  Scott Shainker and Dr. Uma Deshmukh who each have special interest and expertise caring for patients with PAS.

what is the intention?

To better understand the postpartum breastfeeding and newborn bonding experiences of those who are diagnosed with Placenta Accreta Spectrum (PAS). Women who are survivors of placenta accreta, increta, or percreta are invited to participate.

HOW CAN I PARTICIPATE?

National Accreta Foundation is proud to provide opportunities to the patient community to advance placenta accreta research. If you are a survivor of placenta accreta, please access the survey via the button below. It will take around 20 minutes to complete and can be done in multiple intervals. Thank you for sharing your experience to help future moms.

HOW CAN I get involved in more initiatives like this?

National Accreta Foundation receives requests by media, researchers and health care quality improvement organizations for patient stories, speakers, and representation. If you’d like to be notified for future calls like this, please add your story to our story bank.

National Accreta Foundation is an entirely volunteer staffed and donation funded 501(c)(3) non-profit organization dedicated to placenta accreta advocacy. If you find our content of value, please consider making a tax-deductible donation to help us continue this work.