WE ARE HERE TO HELP

Whether your child is in the womb or celebrating their first, fifth, or twentieth birthday, we are here to support you and to celebrate the precious and perfect life of your child. At The Stella Effect, we know that our kiddos have ever changing needs. We are here for you every step of the way - from financially supporting your move for fair care, to showing the world what our babies can do by upligting them, telling their stories, and celebrating them. We can't wait to see your baby's effect on the world.

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How we can help…

01. Let's Celebrate!

Hooray! We are honored to help you celebrate your baby. Birthdays are more than balloons and cake. To children with Trisomy 18 or 13, birthdays are symbolic of everything every statistic said a child would never do. This birthday is the only thing you’ve ever dreamed/hoped/prayed for. You made it. Your baby made it. These memories will last a lifetime and we want you to know we fully understand the weight behind this day. Your baby deserves the best and there’s nothing more in the world that brings us joy than to throw the party of a lifetime for your miracle.

Whether you want a huge Moana themed birthday bash or an intimate and elegant gathering with family and beautiful decorations, we are here to coordinate, personalize your day, and make your celebration come to life. This celebration is for YOU and your child and we are here to make it everything you hoped for with love in every detail.

  • After you contact us to celebrate your child, we will reach out and first confirm whether we have availability and funds to celebrate your baby. We will then coordinate a time to hop on a call to understand your vision - depending on what you're wanting, we might go through a creative process using a shared pinterest board and create a vision board for you. We will set a budget and expectations and then get to planning with local vendors in your area as well as items being shipped to your home for the big day.

    Our services cost you nothing. If you want to spend more money outside of what we will be covering to celebrate your baby, then that's wonderful.

02. Finding Fair Care

If you're reading this, it's likely you are facing what we've faced. You've heard "your baby will only live a couple hours or days at most" or "we've never treated a baby with Trisomy 18/13" or "you need to reconsider termination" and the list goes on and on. If this is you, I first want to say, you're not alone and I'm sorry for the pain you've endured. If you're reading this, it's likely you've chosen to continue your pregnancy at a hospital that doesn't respect your wishes or views this as cruel. We've been there and we are here to help you find the respectful and loving care your child deserves, regardless of the outcome. Moving for fair care is one of the hardest endeavors we faced. After spending weeks talking to other moms, talking to cardiologists across the country, and deciding on a hospital where we knew our daughter would receive fair care, we were then left putting the pieces together of how to pack up our lives to make this happen.

When families move for fair care they often face the impossible task of losing incomes, paying for a short term apartment or hotel to live for weeks or months, juggling kiddos back home, splitting duties with a spouse or partner, and traveling back and forth as needed. We are here to make this part easier for you. The Stella Effect helps families who are traveling for fair care by helping financially with housing, food, and travel.

  • Fill out a contact form to find out if we have the resources and availabilty to help. We will reach back out, set up a time to talk and help in any way we can. We will help connect you to the closest Trisomy friendly hospital as well as connecting you to other parents in that area. After you've made plans to move, we will coordiante on what's your biggest need and help financially as much as we can, whether that's booking a week(s) of hotel rooms, sending you gift cards for food, or booking your flight across the country. We are here to make your life easier and for this transition to be the tiniest bit smoother so you can focus on what matters - the beautiful life you are bringing into this world.

    ***Our services cost you nothing...

03. Connection

We are here to connect you to our wonderful Trisomy community of parents across the country. One mama completely changed the course of ours and Stella's life when she reached out to me with love and support and told me there is hope and that there were other parents out there we could lean on. This is us reaching out to you and saying you are not alone. There's a community waiting to take you in and support you no matter what. The moms and dads of our babies have been told over and over again by Trisomy friendly doctors that we are the experts of our kiddos and this is so true. If you are seeking answers, help, empathy, support, we're here for you. We will do our best to connect you to other parents and Trisomy friendly hospitals and doctors in your area as well as online support groups. If we aren't able to find this in your area, we will help you every step of the way whether you travel to find fair care or choose to stay. We are here and you are never alone.

  • Fill out a contact form and tell us about yourself and your baby. We meet people where they are, discuss what your needs are, and help in the ways we can to connect you to resources.

    ***Our services cost you nothing...***