About Us

Our Mission

At The Wildflower Alliance, we empower and support families of children with disabilities through dedicated advocacy, comprehensive resources, and a robust community network. Our mission is to enhance the quality of life for these families by offering education, outreach, and compassionate assistance, ensuring every child can thrive and reach their fullest potential.

Our Vision

Our vision is a world where every family, regardless of their children's abilities, has access to the resources, support, and opportunities they need to thrive. We strive to build an inclusive community that celebrates diversity, fosters understanding, and empowers all children to achieve their fullest potential.

Programs

At The Wildflower Alliance (TWA), we offer a range of programs designed to support families of children with disabilities. Our initiatives provide guidance, resources, and a strong sense of community to help families navigate their journeys.

Coffee & Convos

A relaxed gathering for parents to connect over coffee.
Provides an opportunity to build a support system.
Features guest speakers, including mental health specialists.

School/Resource Class Adoptions

Supports resource classrooms with additional supplies and materials.
Helps supplement classroom budgets that often fall short of meeting student needs.
Encourages community members and organizations to “adopt” a classroom.

Resource Library

A comprehensive guide for parents navigating a new disability diagnosis.
Provides information on available programs, key deadlines, and essential resources.
Connects families with providers who can assist with medical, educational, and therapeutic needs.

TWA Talks

A live virtual series offering real conversations on topics that matter to families.
Features parents, professionals, and advocates sharing insights and experiences.
Provides practical advice, emotional support, and community engagement opportunities.

AWEAR

A clothing brand created to promote awareness, inclusion, and pride.
Offers apparel for children with disabilities, their families, and supporters.
Each piece helps spread a message of strength, resilience, and community.

At TWA, our goal is to empower, educate, and uplift families so they can confidently advocate for their children’s success.

Together, we grow. Together, we thrive.

TWA Talks

Denial of Your Child's Diagnosis

In this episode, we’re diving into a crucial yet often unspoken emotion many parents face when receiving their child’s diagnosis—denial. For some, denial is a natural part of the journey. It can be overwhelming, confusing, and isolating. But you’re not alone.

Join our Executive Director, LaToya Mims, as she shares her personal experience and insights on navigating denial, processing emotions, and finding a path forward. Whether you’re a parent, caregiver, or someone supporting a loved one, this conversation is here to provide understanding, encouragement, and hope.

Let’s talk about it—because every journey deserves to be heard.

Matters of the Heart

February was American Heart Month, and we brought an important conversation to the table. We sat down with Kristy Broderick, a mother, advocate, and voice for families navigating heart health challenges in children with disabilities.

💬 We talked about:

• The connection between disabilities and heart health

• Kristy’s personal journey with her son, Thomas

• How families can advocate for specialized care

• The power of community and shared experiences

This is a conversation filled with real stories, real support, and real impact.

Cerebral Palsy Awareness

Cerebral palsy is one of the most common childhood motor disabilities. It is different for every child, but one thing remains the same—every child deserves access, opportunity, and understanding.

On Cerebral Palsy Awareness Day (March 25), we created space for real conversations with two moms, our Executive Director LaToya Mims and Tiara Bozman, who are raising children with CP.

They shared their lived-experiences, the realities behind the diagnosis, what they want more people to understand about CP and even discussed some of the disparaging comments that were said to them and about their children.