loudly

grieving

living

boldly

Welcome to ‘Her Grief, Her Strength’
Here, you’ll find honest stories of grief, strength, and everything in between, as we navigate the journey of healing together.

Two women smiling and posing with microphones against a white background, wearing casual outfits of jeans and tops.

we are

We know the weight of grief and the power of resilience. Together, we’ve built a community where parents navigating loss, complex medical journeys, or simply feeling unseen can find understanding, empowerment, and hope. Through shared stories, advocacy, and connection, we’re here to remind you: you are not alone.

her grief, her strength podcast

HGHS Podcast
episode 02
episode 02
Episode 01
Episode 01
Episode 00
Episode 00

on the blog

Blog
the little joys that carry us
the little joys that carry us

Sometimes it’s not the big milestones that keep us going.
It’s the tiniest flickers of grace. The ordinary glimmers of magic. The quiet proof that we’re not alone in this.

Denial. Anger. Bargaining. Depression. Acceptance.
Denial. Anger. Bargaining. Depression. Acceptance.

Grief isn’t linear. It’s not a tidy list of stages you check off and move past. It’s a storm—chaotic, relentless, and impossible to predict…

Cracks in the Foundation
Cracks in the Foundation

A crack in the foundation lets light pierce the darkness that consumes her mind, a fragile reminder of resilience amid chaos…

Welcome letter
Welcome letter

Welcome to Her Grief, Her Strength, where two complex medical moms share their journeys of grief, resilience, and advocacy.

community voices

  • “Her Grief, Her Strength has been a light in the darkness”

    - anonymous

  • “This community has meant the entire world to me. I would not he able to process what im going through without the love and support these women bring. It’s a safe place where I know whatever I say there is no judgement, and im met with love.”

    - sidney prescott

  • “We are early in our journey and don't have a definitive diagnosis, just symptoms. Because of that, I was nervous we wouldn't "fit in," but it has been quite the opposite. This community has so much knowledge and love to share. Truly grateful to have found it.”

    - anonymous

  • “HGHS connected me with a support system but also gives me the opportunity to support others. Being a mom to a medically complex child is isolating and friends from my pre-diagnosis life just can't relate to my new day-to-day life. It's great to have a place where talking about g-tubes, O2 says, or just really hard days isn't met with uncomfortable silence or "you're so strong" or "you'll figure it out." The women here see your strength and your struggles because they carry them, too.”

    - jj knight

  • “The HGHS community accepted me with open arms after my daughter was diagnosed with pcd, a progressive, genetic mucociliary disease. They listened without judgement and just having an ear and a space to talk was so helpful and comforting.”

    - shar