Preemie Parent Alliance is a network of organizations offering support to families of premature infants. To ensure best outcomes for preemie families, the Preemie Parent Alliance is dedicated to representing the needs and best interests of preemie families in all facets of healthcare policy, care guidelines, advocacy, education and family support. As a national network we are establishing a unified parent voice to advocate for infants, who cannot speak for themselves, and their families. Together, we represent more than 250,000 NICU and bereaved families across the country.
In 2014, we introduced our PPA Speakers Bureau. Made up exclusively of preemie parent leaders, the Preemie Parent Alliance carefully hand selects speakers who are professional, personable & knowledgable. This year, after careful consideration, we are excited to welcome new members of our Bureau. We look forward to focusing all of our efforts on you - the client. We strive to select the speaker who is right for your event; one who compliments your goals and objectives, as well as your audience.
Download your copy of the presentation topics we offer
PPA proudly unveiled the NICU Parent's Bill of Rights at the 2013 National Association of Neonatal Nurse's conference in Nashville, TN. We received wonderful feedback from the nurses, parents, and advocates in attendance and encourage you to view it, download it, print it, and share it with the hospitals you support!
Enjoy collaborating with other member organizations and gain national and international exposure for your programs! Read on to learn about all the benefits of joining the Preemie Parent Alliance.
Our amazing members include:
Thank you to our Corporate Members