On this episode, I sat down with Lindsay Bachman - a true medical mama who advocates for her daughter with a rare disease every single day. She never imagined her life being in and out of the hospital, but she does so with grace and humor.

If you are parent to a child with a rare disease, or want to know what it is like, you will definitely want to listen to this.

Follow her journey on Instagram @happygolandry.

This episode is sponsored by Hello Love Nails - not your ordinary press on nails that last 2-3 weeks with 2-3 wears. Shop here.

Boy mom. Autism mom. Homeschool mom. Foster mom.

Listen to her journey and follow along by visiting her blog: Mission Mommy Journey

This episode is brought to you by Hello Love, not your ordinary press on nails! These $15 nails last 2-3 weeks and can be worn 2-3 times! Shop the nail design here.

Madison is a mental health coach for moms - specifically moms to children with disabilities. Her mission is to improve caregivers' mental health and help them be less overwhelmed & stop feeling alone.

If you are someone you know is struggling with mental health issues, seek help.

TW: ED

In this special Father's Day episode, I sat down with Mike (my husband) to hear how fatherhood has been for him.

From having a medically complex child to becoming the sole income for our family because of this, the pressure on him is never-ending. Hear his take and how he gets through it all.

Brittany Dodson is building the childhood of her dreams for her children and giving them something she always wanted.

She and her husband work hard to travel with their kids, specifically to Disney, and break the gender roles that have defined generations to fit the needs of their family!

What is it is like being a mama to a child with a rare disease? Michelle has an incredible story filled with hope, determination, and advocacy.

She is raising awareness on disease and disabilities while building up advocacy through "hope and laughter".

Follow her journey on Instagram @mamabearforrare

In this episode, I had the privilege of speaking to Sivan Hong, a former professor at New York University's Stern School of Business and now a talented author and illustrator of a best-selling children's book series, "The Super Fun Day Books."

She was inspired by her son, who is neurodivergent, to write stories for him. She gathered the courage to share these stories with the world and is inspiring children (and parents) around the globe.

When it comes to being the mom to a child with a rare disease, Heather Mooneyham is an expert. Through the many emotions that came with finding a diagnosis for her daughter, managing to raise two children through the testing phase, and trying to convince her family of her reality, this mama is not afraid of a little advocating. And by little, I mean a lot.

Her story is inspiring, and for me, extremely relatable. Take a listen to her powerful story and how she continues to fight for all three of her children. "Motherhood. Not for the weak."

Follow her on TikTok @raremamaheather