In this week’s episode, Ashley and Aisha sit down for a cozy end-of-year conversation to close out the 2025 podcast season. Together, they reflect on the stories, experts, and full-circle moments that shaped this year’s episodes, and share how the Dear NICU Mama sisterhood continues to impact their own healing journeys.

They also introduce something brand new to the community: our Right On Time Holiday Book Drive. After receiving more than 130 nominations from NICU moms across the country, six hospitals were selected to receive donated copies of Right On Time. This is a meaningful way for NICU families to give back to the places that cared for their babies so well!

During the episode, Ashley and Aisha walk through how the book drive works, why it matters, and how every donation helps sustain the mission of Dear NICU Mama—from this podcast, to our support groups, to the resources that meet NICU moms right where they are. $25 donates one book, and listeners can choose to gift a book to a specific selected NICU or to the general campaign.

As we wrap up another year of stories and connection, we hope this conversation reminds you that you are not alone. Thank you, mamas, for being part of this sisterhood. We can’t wait to be back in 2026 with more stories of hope!

To donate to the Holiday Book Drive, head to: https://givebutter.com/dnmholidaybookdrive

To get connected with DNM:

Website | Private Facebook Group | Instagram

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In this week’s episode, Ashley and Aisha sit down with two very special guests: Allie, a PA who cared for Ashley’s son during his NICU stay, and her husband, Troy—the illustrator of Right On Time, Dear NICU Mama’s first children’s board book. Together they share the full-circle story of how their NICU connection led to creating a book that honors and represents the diverse journeys of NICU families!

Ali reflects on her years in the NICU and her work in pediatric rehab, and Troy shares what it was like to illustrate a project so close to his family’s heart. You’ll also hear exciting updates on the book’s arrival, our successful pre-order campaign, and the upcoming Holiday Book Drive.

We hope this episode reminds you of the power of connection, storytelling, and the extraordinary milestones our NICU babies achieve, each one right on time.

Order the Right On Time book here!

To get connected with DNM: Website | Private Facebook Group | Instagram

Connect with Troy: Website | Instagram | X | Email: ttbecker@gmail.com

About Troy: It starts in New York Mills, MN where Troy was born and raised. After an affinity for drawing, comics and art - he graduated from Concordia College in Moorhead, MN with a B.A. in Art and Communications. After a few stints in Minneapolis, Connecticut and Wisconsin he found himself back in the F-M area. Troy has been an illustrator, cartoonist and graphic artist for Forum Communications for nearly 18 years. Troy also served as an adjunct professor at MSUM from 2015-2020. The art continues in his home studio where he enjoys creating screen prints, comics and graphic novels. You can find his art in local exhibits and commissions across the upper Midwest.

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On this week’s episode, we welcome Dr. KC from Milestones & Motherhood — a pediatric physical therapist, early intervention specialist, and trusted guide for parents navigating developmental milestones. KC shares her own experience with late-preterm babies and how it shaped the compassionate, parent-centered approach she brings to her work.

We talk about what early intervention really is, why adjusted age matters, how to navigate comparison, and the power of celebrating the “mini-stones” along the way. KC offers gentle reassurance for NICU parents navigating developmental milestones post NICU.

Most of all, she reminds every parent listening that you are doing enough. Your presence and love matter, and it’s okay to take breaks, enjoy your baby, and lean on the support around you. You’re not alone in this journey!

Use code DNM10 for 10% off all courses at Milestones & Motherhood! Head here to find the courses.

Resources:
1. The Milestones & Motherhood Ministones Guide
2. Prematurity, NICU Stays & A Heart to Heart on Our Journey

Dr. KC Rickerd, PT, DPT, is a licensed pediatric physical therapist and founder of Milestones & Motherhood and Journey Through Milestones Physical Therapy. With over a decade of experience working with children from birth through age 21, she specializes in motor development, functional mobility and family education. KC’s mission is to make evidence-based developmental guidance accessible, empowering parents and caregivers to confidently support their child’s growth and reach their full potential.

Connect with KC: Instagram | Website

Pre-order Right On Time, our very first children’s board book, here!

To get connected with DNM: Website | Private Facebook Group | Instagram

This podcast episode is not an attempt to practice medicine or provide medical advice. All information, content, and material on this website is for informational purposes only and is not intended to be a substitute for professional medical or mental health advice, diagnosis or treatment.

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In this week’s podcast episode, Ashley and Aisha sit down with Dear NICU Mama co-founder Martha for a vulnerable and joy-filled conversation about the early days of the sisterhood and how it all began! From the first coffee date and color-coded binder to the launch of the podcast and the years of growth that followed, Ashley and Martha reflect on what it was like to build something so meaningful together.

They share openly about the pivots, challenges, and sacred moments that shaped Dear NICU Mama, from its local beginnings in Fargo to the national community it is today. Through laughter, nostalgia, and a few tears, they revisit the “Right On Time” moments that reminded them that even in the hardest seasons, healing and connection always unfold exactly when they’re meant to.

As you listen to this episode, may you be reminded that your own story, your milestones, your friendships, and your healing are all unfolding right on time!

Pre-order Right On Time, our very first children’s board book, here!

To get connected with DNM:

Website | Private Facebook Group | Instagram

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In this week’s podcast episode, Ashley and Aisha sit down with their husbands, Ryan and Andy, for an intentional conversation about their experiences as NICU dads!

Ryan and Andy share vulnerably about the moments that shaped their journeys, from emergency deliveries and hospital stays to navigating grief, helplessness, and healing years later. They reflect on what it was like to support their partners through trauma, learn to surrender control, and find small ways to show up when so much felt out of their hands.

Together, they remind us that the NICU journey isn’t only lived by moms, and that every dad, partner, and support person plays an irreplaceable role in this story. This episode is a beautiful reminder that even when it feels like you can’t fix or control what’s happening, your presence matters more than you know.

Pre-order Right On Time, our very first children’s board book, here!

To get connected with DNM:

Website | Private Facebook Group | Instagram

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In this week’s podcast episode, Ashley and Aisha sit down with NICU mamas Vilma and Sam for a vulnerable roundtable conversation about feeding journeys after the NICU, and what it’s like when a G-tube becomes part of your story.

They share vulnerably about the emotions that come with this transition, from the relief of finally going home, to the surrender that often follows. Together, they share about the realities of adjusting expectations, redefining milestones, and learning that every feeding journey looks different–and that’s okay.

This conversation is a reminder that whether your child eats by mouth, by tube, or both, you are doing an incredible job. Your baby’s journey is unique, and no matter what that timeline looks like, it’s is always right on time.

Pre-order Right On Time, our very first children’s board book, here!

This podcast episode is not an attempt to practice medicine or provide medical advice. All information, content, and material on this website is for informational purposes only and is not intended to be a substitute for professional medical or mental health advice, diagnosis or treatment.

To get connected with DNM:

Website | Private Facebook Group | Instagram

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In this week’s podcast episode, we share the audio from our recent Walking Letter of Hope Day virtual event featuring licensed therapist and birth trauma survivor Kayleigh Summers, known as The Birth Trauma Mama!

Kayleigh joins us to talk about the lasting impact of birth and NICU trauma, what healing can look like, and the hope that comes from sharing our stories in community. She offers gentle, trauma-informed insight into understanding trauma as a neurobiological response, navigating feelings of hyper-vigilance and grief after the NICU, and finding ways to honor your healing while caring for your child.

Kayleigh reminds us that trauma is treatable, healing takes time, and that hope can often be held by community until we’re ready to hold it ourselves.

As you listen, we hope you feel seen, validated, and reminded that your story — and your healing — are deeply significant. You are never alone in this sisterhood!

Kayleigh Summers is a licensed therapist, writer, and content expert in perinatal trauma. She uses her training as a licensed therapist and her lived experience as an Amniotic Fluid Embolism survivor to support families experiencing perinatal trauma. Kayleigh has also created thriving support communities through Instagram and Tik Tok, as well as her podcast, where she provides connection, story sharing, and resources to support those experiencing birth and other trauma. You can find her @thebirthtrauma_mama.

To get connected with Kayleigh:
Website | Instagram | TikTok

This podcast episode is not an attempt to practice medicine or provide medical advice. All information, content, and material on this website is for informational purposes only and is not intended to be a substitute for professional medical or mental health advice, diagnosis or treatment.

To get connected with DNM:

Website | Private Facebook Group | Instagram

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In this week’s podcast episode, Ashley and former and beloved podcast co-host Martha revisit an important conversation for our NICU sisterhood: understanding IEPs and how to advocate for your child in school.

This replay episode features special education expert Catherine Whitcher, founder of Master IEP Coach, who shares practical guidance on navigating the Individualized Education Program (IEP) process, partnering with your child’s school, and finding hope and empowerment in every step.

Catherine reminds us that while the paperwork and terminology can feel overwhelming, an IEP is not a label: it’s a tool to help your child learn, grow, and thrive in the ways that fit them best. She also offers reassurance for the emotional side of this journey, especially for NICU families who have already walked through so many labels, diagnoses, and milestones.

As you listen, we hope you feel encouraged, informed, and reminded that you are the expert on your child, and that you and your little one are always, always right on time.

About Catherine Whitcher M.Ed and Master IEP Coach

Catherine Whitcher, MEd, founder and CEO of Master IEP Coach®, experienced the struggles of the Special Education system both as a certified teacher and as a sister to a wonderful man with Down syndrome. For the past 25 years, she has been creating nationwide change in special education by assisting parents and teachers in developing IEPs that work in the real world. Catherine currently leads the largest independent organization nationwide of parents and teachers working together to build better special education outcomes for the real world. She’s an expert in conflict resolution and leadership at the IEP table while always keeping the focus on preparing every child for further education, employment, and independent living.

** This podcast episode is not an attempt to practice medicine or provide medical advice. All information, content, and material on this website is for informational purposes only and is not intended to be a substitute for professional medical or mental health advice, diagnosis or treatment.

To get connected with DNM:
Website | Private Facebook Group | Instagram

Support the show