We are a group of concerned parents, medical professionals, legal professionals and clergy whose aim is to support, inform and encourage expectant or new parents with a special needs child.

2024 Annual Benefit

 

Prenatal Partners for Life

cordially invites you to the
17th Annual Benefit Dinner

Thursday, June 13, 2024

The Saint Paul Hotel
350 N. Market St., St Paul, MN 55102

We are so excited to have back the amazing Matt Birk as our Master of Ceremony and the phenomenal musician, songwriter, author, performer, producer, podcaster, and philanthropist, Mick Sterling, along with his beautiful and talented wife, Cate Fierro and awesome pianist, Rick Carlson.

For over forty years Mick has been sharing his musical talents and helping others with his wonderful charity, The Thirty Days Foundation. I first heard Mick sing at the Chanhassen Dinner Theater, Andy and Bing Christmas. Mick, Cate and Rick are wonderful entertainers and very well-known throughout MN and the US. This promises to be a fantastic evening!

Purchase Tickets for the June 2024 Annual Benefit

Help Support Prenatal Partners for Life!

Mick Sterling

Cate Fierro

Matt Birk

Rick Carlson

How We Can Help

Support, information & encouragement for carrying to term with an adverse prenatal diagnosis and support for raising your child with special needs after birth.

If you have come to this site because you or someone you know has received an adverse or negative prenatal diagnosis, you have come to the right place. We are parents who have gone through similar circumstances and we want to offer support.

Most of the stories on this site are of families who have carried to term after receiving an adverse diagnosis. We are here to help you.

You are not alone!

Down the Road of Bittersweet

by Karl Kohlhase | Down the Road of Bittersweet

NEW Spanish & English Brochures
are available here.

There are few things more frightening in life than finding out your baby may not be healthy. The fear of the unknown and the pressure to terminate can be intense. Many of us who were faced with similar diagnosis have had moments where we wished we were no longer pregnant or thought that we were incapable of continuing with the pregnancy. However, after time we fell deeper and deeper in love with our child. We have yet to hear from a parent who regrets carrying their child to term. We believe that each life is a precious gift from God and that each child has a special purpose.

If you are a parent needing to contact us because of a negative or adverse prenatal diagnosis, please visit our Contact Us page. Someone will contact you as soon as possible.

If you are looking to volunteer or make a donation follow the Donate/Volunteer link to the left.

If you are a doctor or an organization that would like to be listed on our site please go to the Contact Us page and we will contact you as soon as we can.

If you are a parent who would like to share your story and be a mentor to help others, please Contact Us.

News & Updates

Prenatal Partners for Life continues to serve families who find out their child may have special needs or health issues and families raising children who face these challenges. Through our new program Lumen Caeli, which means Light of Heaven, our outreach and support now includes families who have experienced miscarriage and stillbirth. Our support has now reached into 50 countries around the world. Through our support for families, conferences, talks and publications,

Prenatal Partners for Life continues to promote the message of the gift and value of all life, no matter how long or short, healthy or sick.

 

Stories of Hope

Support information and encouragement for carrying to term with an adverse prenatal diagnosis and support for raising your child with special needs after birth.

If you have come to this site because you or someone you know has received an adverse or negative prenatal diagnosis, you have come to the right place. We are parents who have gone through similar circumstances and we want to offer support.

Most of the stories on this site are of families who have carried to term after receiving an adverse diagnosis. We are here to help you. You are not alone!

Resources

We have many resources available to help guide parents on their journey.
Lumen Caeli is our newest resource to support families. Learn more

Donate

We are a 501(c)(3) not-for-profit organization and as such all donations are tax deductable.

We are currently raising money to cover the costs of: translating (Spanish), printing, and mailing our brochure.

Financial donations are welcomed and greatly appreciated. 

 

The support, information and encouragement provided by the PPFL parents is not meant to take the place of medical advice by a medical professional. Any specific questions about care should be directed to a health care professional familiar with the situation.

 

Phone: 763-772-3868

Fax: 866-870-9175

Prenatal Partners for Life
PO Box 2225
Maple Grove, MN 55311

Email: mary@prenatalpartnersforlife.org