Prenatal Partners for Life

Prenatal Partners for Life Prenatal Partners for Life
www.PRENATALPARTNERSforLIFE.org This support can be provided in person, over the phone, by email or in written correspondence.

Prenatal Partners for Life is dedicated to providing families, either expecting, or those who have just had, a special needs child, the support, information, and encouragement they need to make informed decisions involving their preborn or newborn child's care. We believe these children are unique gifts from God and have a special purpose in life that only they can fulfill. Our goal is to provide

honest, practical information about parenting a special needs child by linking expectant parents or new parents of a special needs child with other parents who have had the same diagnosis.

Pray that all life will be valued and respected from conception until God calls us home.
05/07/2026

Pray that all life will be valued and respected from conception until God calls us home.

Please say a prayer for all the mothers whose hearts are hurting!
05/03/2026

Please say a prayer for all the mothers whose hearts are hurting!

04/29/2026

Clear, accurate, information, delivered in an unbiased compassionate way is what every family deserves. Every life is a gift!

04/27/2026
https://nrlc.org/nrlnewstoday/2026/04/five-year-old-abandoned-for-heart-surgery-his-doctor-adopted-him/?utm_source=Activ...
04/17/2026

https://nrlc.org/nrlnewstoday/2026/04/five-year-old-abandoned-for-heart-surgery-his-doctor-adopted-him/?utm_source=ActiveCampaign&utm_medium=email&utm_content=NRL%20News%20Today%20for%20April%2017%2C%202026&utm_campaign=NRL%20News%20Today%20for%20Tuesday%2C%204-16-2026%20%28Copy%29&vgo_ee=GTRV9HaiSgqhtBpKIGwTAYveWbdLhgiHp6R%2FNpRX7wpOcmUGGZXiRbYBI2D2tqDL%3AUkK6L%2BZrDjy5203sjVuV0tvCzplM9fno

By Ashlynn Lemos Texas Right to Life At just five years old, True was dropped off to get a major heart surgery at a children’s hospital in Omaha, completely alone. Born with a serious congenital heart defect called hypoplastic right heart syndrome, his life depended on a complex surgery. In 2022, ...

04/16/2026

Camden was diagnosed in utero with agenesis of the corpus callosum and two rare genetic deletions. After these diagnoses, doctors recommended termination. His parents chose a different path.

Now 8 years old, Camden requires 24/7 care and is nonverbal. But he is also full of life, often smiling, and deeply loved by his family. Through sharing Camden’s story, his family hopes others see that there are many different ways to exist in this world and that those differences are okay. This full interview is in the comments below.

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Maple Grove, MN
55311

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