Category: You Are Not Alone

This category highlights personal stories, reflections, and shared experiences from survivors, caregivers, and those impacted by trauma. Focusing on connection, understanding, and the power of shared journeys, it offers guidance, encouragement, and the reminder that no one has to navigate recovery or grief in isolation.
Post-Trauma LifeResource ConversationsSupport and CaregivingYou Are Not Alone

Personalized Recovery Support After Trauma

Resource Conversation with Matt Kalina from TandemStride

Recovery doesn’t end at discharge.

For many survivors and caregivers, that moment—leaving the hospital—is where a new kind of uncertainty begins. There’s often relief, but also hesitation, fear, and a very real question: what happens now?

This resource conversation with Matt Kalina from TandemStride focuses on that exact transition point, and how personalized, trauma-informed support can help people feel less alone in it.

These conversations are designed to give motor vehicle incident survivors and their caregivers practical tools, guidance, and support as they move through recovery—especially in the spaces where systems often fall short.

A Personal Beginning to the Work

Matt’s connection to this work is deeply personal.

His brother was involved in a pedestrian train accident 14 years ago and became a bilateral amputee at age 23. That experience shaped Matt’s understanding of what recovery can feel like when there is no roadmap—when you are trying to rebuild your life while also trying to understand what that life will even look like.

Later, after a decade of building healthcare technology, Matt kept seeing the same gap repeat itself: even with advances in medicine and systems, trauma survivors were still often left feeling alone after discharge, without clear guidance or connection.

TandemStride was built from that gap.

The Space After the Hospital

One of the most consistent challenges in trauma recovery is the transition from acute care to home.

Hospital discharge is often treated as an endpoint, but for survivors and caregivers, it can feel like the beginning of the hardest part. There is often hesitation, resistance, and uncertainty about what recovery actually looks like day to day.

TandemStride was designed to support that exact transition—helping people move from structured hospital care back into everyday life with more guidance, connection, and support.

The platform is used primarily by survivors with physical traumatic injuries such as spinal cord injuries, amputations, polytrauma, major fractures, burns, gunshot wounds, and violent crimes. Most users join within 7–14 days of discharge, though support is available at any point in recovery.

A Different Kind of Recovery Support

At the core of TandemStride is a simple idea: recovery shouldn’t be something you navigate alone.

The platform uses insights from thousands of trauma survivor journeys to better understand when challenges typically arise—such as mental health changes, substance use risk, or other barriers that can show up later in recovery.

Instead of waiting for those challenges to become crises, TandemStride works to identify patterns early and offer support proactively.

That includes:

  • Connecting survivors with peer mentors (often matched by injury type or age at injury)
  • Helping users find local resources through guided navigation
  • Offering caregiver and survivor-facing tools inside a single platform
  • Supporting both passive and active engagement, depending on what feels manageable

Get the App

TandemStride is available on the App Store and Google Play.

It is free to download and use, with some features varying depending on regional partnerships or programs (such as certain state-based initiatives).

Meeting People Where They Are

When users first open the TandemStride app, they are met with a simple question: What is your biggest challenge right now?

From there, the experience is personalized. The app guides users toward resources based on what they need most in that moment, rather than forcing them through a one-size-fits-all system.

This “choose your own adventure” approach allows survivors to engage in a way that feels right for them—whether that’s actively exploring resources or simply having support available in the background.

Community, Connection, and Not Feeling Alone

A major focus of TandemStride is building connections between survivors who understand what each other is going through.

On May 20th, 2026 – the platform is launching a new Communities feature designed specifically for trauma survivors.

Inside these communities, users can:

  • Check in daily or share updates and milestones
  • Connect with others going through similar experiences
  • Engage through likes, comments, or quiet observation
  • Use AI-supported tools to find local resources
  • Complete optional mental health screeners with guidance

Importantly, users can choose how they engage—there is no pressure to share more than they want to.

Trauma-Informed by Design

A key part of TandemStride’s approach is making sure the platform is safe and adaptable for people in different stages of recovery.

That includes features such as:

  • Content moderation to reduce exposure to triggering material
  • Options to label posts as “high intensity,” with user-controlled viewing
  • The ability to share without receiving advice or feedback
  • Topic filtering so users can control what they see

This design acknowledges something important: recovery is not just physical. Emotional safety matters too.

Small Steps Forward

TandemStride also includes a milestones feature that visually reflects progress over time.

As users engage, their milestone image gradually fills in—starting blank and slowly becoming more complete. It’s a simple but meaningful way to reflect growth, effort, and consistency in recovery.

It also serves as a reminder that progress is often made in small, quiet steps—not just big moments.

A Platform Built by Survivors, for Survivors

At its core, TandemStride is built around lived experience.

It is not just a technology platform—it is an attempt to create something that understands what it feels like to go through a life-altering injury and try to rebuild from there.

The intention is not to replace care teams or support systems, but to extend them—especially into the space where people often feel the most alone.

Why Social Support is Important in Trauma Recovery

A Closing Note

This conversation highlights something that is often overlooked in trauma recovery: the space between hospital and home matters just as much as what happens inside the hospital.

We are grateful to Matt Kalina and the TandemStride team for the work they are doing to bring more structure, connection, and humanity into that space.

A sincere thank you to TandemStride for sponsoring this episode and supporting efforts to make recovery more accessible and less isolating for survivors and caregivers.

Watch our full resource conversation with Matt Kalina from TandemStride about navigating recovery after traumatic injury, finding support after hospital discharge, and building connection through survivor-centered care.

Patient Advocacy 2
You Are Not Alone

Patient Advocacy in Action

Partnering to Strengthen Voices in Research and Care

Patient advocacy is not a concept—it is a lived necessity.

It is what happens when someone in the middle of a medical crisis tries to understand complex decisions. It is what happens when families are navigating hospital systems they never expected to enter. And it is what happens when lived experience is finally brought into the spaces where health care decisions are made.

At Sandal Blue Foundation, we believe patient advocacy is strongest when it is shared, structured, and community-driven. That is why our partnership with the University of Maryland School of Pharmacy’s PATIENTS Program has been such an important part of our work.

A Shared Mission: Centering the Patient Voice

The PATIENTS Program is a nationally recognized community-academic partnership that works to ensure patients, caregivers, and communities are not just participants in research—but co-creators of it. Their work focuses on building trust, improving communication, and strengthening the way research reflects real lived experience.

At its core, their mission aligns deeply with ours:

  • People closest to the problem should help shape the solution
  • Lived experience is essential data
  • Trust is built through consistency and collaboration
  • Health equity requires intentional engagement

This is patient advocacy in action—not as a service provided, but as a system built together.

Expanding Impact: PATIENTS Going National

One of the most powerful expansions of this work is the PATIENTS Going National initiative, which extends their community-engaged research model beyond Baltimore to communities across the United States.

This initiative is designed to bring patient and community voices into research at a national scale by partnering with groups connected through shared experiences such as chronic illness, disability, mental health, aging, and more.

Rather than treating communities as passive recipients of research, this model recognizes something critical:

Communities are experts in their own lived experience.

Through PATIENTS Going National, those lived experiences are being actively integrated into how research questions are formed, how studies are designed, and how health solutions are developed.

You can learn more about the initiative here: The PATIENTS Program and their national expansion effort.

Why This Matters for Patient Advocacy

Patient advocacy is often thought of as something that happens at the bedside or in a hospital hallway.

But true advocacy also happens upstream—in research design, policy development, and system planning.

When patients are included early in the process, everything changes:

  • Research becomes more relevant to real-life needs
  • Communication becomes clearer and more respectful
  • Barriers to care are identified sooner
  • Solutions are shaped by lived experience, not assumptions

This shift is what makes partnerships like ours with the PATIENTS Program so meaningful. It moves advocacy from reaction to co-creation.

What We See in Practice

Through this collaboration, we see a consistent truth:

When people are given space to share their lived experience—and when that experience is taken seriously—systems begin to change.

We see:

  • Caregivers who finally feel heard in clinical conversations
  • Survivors whose experiences help shape research priorities
  • Communities contributing insight that improves how care is delivered
  • A growing culture of trust between institutions and the people they serve

This is what it looks like when advocacy is not an afterthought, but a foundation.

Moving Forward: Building a More Inclusive Future in Health Care

Patient advocacy is not static. It grows as systems listen more deeply and include more voices.

The PATIENTS Program’s expansion through PATIENTS Going National represents a shift toward a more inclusive model of research and health care—one where patients are not just subjects of study, but active partners in shaping the future of health.

At Sandal Blue Foundation, we are proud to stand alongside work that reflects this belief:

Health care is strongest when it is built with the people it serves—not just for them.

Closing Thought

Advocacy begins with listening.

But it becomes powerful when listening turns into action—and action turns into shared ownership of change.

This partnership reminds us that when patient voices are centered, health care becomes more human, more accurate, and more just.

And that is the direction we are committed to moving in—together.