What is Walk and Roll Live all about?

"Walk and Roll Live - Disability Stories" is a podcast dedicated to amplifying the voices and experiences of individuals within the disabled community. It aims to foster unity, promote healing and camaraderie, and serve as a trusted source of information from disabled service providers. The podcast's overarching mission is to promote empowerment, awareness, and inclusivity, embodying the motto "Life, Limitless."

Hosts:

The podcast is primarily hosted by Doug Vincent and Addie Rich. Doug Vincent, a polio survivor himself, brings a deep understanding and empathetic style to the conversations. Addie Rich, who also experienced a medical journey that required her to re-learn walking, shares a passion for helping people blossom and reimagining what disability means. Their personal experiences contribute significantly to the authenticity and relatability of the discussions.

Summary and Analysis:

Focus on Personal Narratives: The core of "Walk and Roll Live" lies in sharing "real, raw, and inspiring stories" of resilience, advocacy, and independence from individuals with disabilities. This human-centric approach allows listeners to connect with the challenges and triumphs of diverse journeys.

Diverse Range of Guests and Topics: The podcast features a wide array of guests, including athletes, artists, advocates, and individuals who have overcome significant physical challenges. Topics covered include:

Recovery journeys from spinal cord injuries and other traumas (e.g., Alexis Mazon's story of recovering from a five-story fall).

Adaptive sports and recreation (e.g., discussions with the United States Adaptive Recreation Center, or USARC).

Advocacy and breaking barriers in various fields (e.g., Atif Moon's journey as a top wheelchair tennis player and CEO).

The role of therapy and community support in rehabilitation (e.g., interviews with physical therapists from "The Perfect Step").

Stories of finding renewed purpose and thriving despite life-altering events (e.g., Shane Martinell's comeback after a spinal cord injury).

Highlighting organizations that support families and individuals with special needs (e.g., Special Angels Foundation).

Empowerment and Inclusivity: The podcast consistently emphasizes empowerment and inclusivity. It strives to educate listeners, challenge misconceptions about disability, and celebrate the diverse ways in which people "walk, roll, and thrive." The hosts create a comfortable space for guests to share their experiences openly and honestly, fostering a sense of understanding and connection.

Informative and Motivational: Beyond personal stories, the podcast also provides valuable information from service providers and organizations within the disability community. It aims to be a resource for listeners seeking support, knowledge, and inspiration. Reviews often highlight the "valuable information" and the "positivity" listeners gain from each episode.

Empathetic and Engaging Hosting: Reviews consistently praise Doug Vincent's (and presumably Addie Rich's) empathetic and engaging hosting style. They are noted for their ability to create a comfortable environment for guests, allowing for authentic and impactful conversations.

In essence, "Walk and Roll Live - Disability Stories" serves as a vital platform for the disability community, offering a blend of personal inspiration, practical information, and a powerful message of resilience and inclusion.

 

Understanding Post-Polio Syndrome: What You Need to Know

 

By Doug Vincent

For those of us who lived through and survived polio, a chapter we thought closed may unexpectedly reopen. Post-Polio Syndrome (PPS) is a condition that affects polio survivors years—even decades—after the initial infection. Though often misunderstood or misdiagnosed, PPS is real, impactful, and deserving of greater awareness.

What is Post-Polio Syndrome?

Post-Polio Syndrome is a neurological disorder that typically appears 10 to 40 years after recovering from the acute poliovirus. It is not a resurgence of the virus itself, but rather a late effect caused by the slow degeneration of motor neurons that were damaged during the original infection.

When we recovered from polio, our bodies adapted by sprouting new nerve endings to compensate for those lost. Over time, those nerve endings can weaken or fail under the strain, leading to new symptoms.

Symptoms to Watch For

PPS often creeps in gradually. Symptoms can vary in severity and may include:

• New or worsening muscle weakness

• Severe fatigue or exhaustion after minimal activity

• Muscle atrophy or shrinking

• Joint pain or difficulty with mobility

• Breathing or swallowing problems

• Sleep disorders such as sleep apnea

• Increased sensitivity to cold temperatures

These symptoms often fluctuate, with some days feeling relatively normal and others presenting significant physical challenges.

How is PPS Diagnosed?

There is no definitive test for PPS. Diagnosis is largely based on:

• A detailed medical history and physical exam

• Electromyography (EMG) to assess nerve and muscle function

• Imaging tests like MRI or CT scans to rule out other conditions

• Muscle biopsy in rare cases

In essence, PPS is diagnosed by exclusion—your doctor will rule out other potential causes before confirming the condition.

Treatment and Management

While there's no cure for PPS, managing it effectively can make a huge difference. The key lies in conserving energy, avoiding overexertion, and adapting daily routines to current abilities. Here are some strategies:

• Energy Conservation: Use assistive devices like canes, scooters, or wheelchairs. Break tasks into smaller steps and schedule rest periods.

• Physical Therapy: Gentle, low-impact activities like swimming or stretching can help maintain function without straining weakened muscles.

• Occupational Therapy: Learn techniques to modify daily activities and use adaptive tools for greater independence.

• Speech and Respiratory Therapy: Address swallowing or breathing issues with professional guidance.

• Pain Management: Over-the-counter medications like ibuprofen or acetaminophen can provide relief.

• Emotional Support: Counseling or support groups can offer comfort and community.

Living with PPS

The progression of PPS is usually slow and unpredictable. Some people may remain stable for years, while others experience gradual declines in function. But with proper care and awareness, many can maintain a high quality of life.

Final Thoughts

Post-Polio Syndrome is a reality for many of us in the polio survivor community. It’s not just a medical condition—it's a reminder of a journey we’ve already come so far in. By listening to our bodies, seeking appropriate care, and sharing our experiences, we can continue to live full, meaningful lives.

If you or someone you know is experiencing new muscle weakness, fatigue, or other unexplained symptoms years after recovering from polio, don’t dismiss it—reach out to a healthcare provider familiar with PPS. Awareness is the first step to advocacy.