In this engaging conversation, Kijuan Amey shares his journey from a challenging upbringing in Durham, North Carolina, to becoming a highly motivated individual with a diverse range of interests and experiences. He discusses his passion for fitness, sports, and music, as well as his time in the military, particularly in the Air Force as a KC-135 Stratotanker operator. Kijuan emphasizes the importance of perseverance, personal growth, and the lessons learned throughout his life, including the challenges faced in both fitness and military training. In this conversation, Kijuan Amey shares his life-altering experience of a motorcycle accident that left him blind and how he transformed his adversity into a motivational journey. He discusses the importance of respecting life, the challenges of recovery, and the philosophy of focusing on abilities rather than disabilities. Kijuan emphasizes the significance of support systems, personal growth, and the will to overcome life's challenges, inspiring others to find their strength and purpose.

takeaways

• Kijuan emphasizes the importance of energy and motivation in daily life.
• He shares insights on how pushing through challenges can lead to growth.
• Kijuan's upbringing shaped his resilience and determination.
• Music has been a lifelong passion for Kijuan, starting at a young age.
• He was a competitive bowler, showcasing his drive for excellence.
• Sports provided structure and discipline in Kijuan's life.
• His decision to join the Air Force was influenced by family and personal goals.
• Kijuan's experience in the military taught him valuable life lessons.
• He highlights the significance of finding one's passion and pursuing it.
• Kijuan's journey reflects the power of perseverance and adaptability. Respect for the motorcycle grew after the accident.
• The accident marked a new life journey for Kijuan.
• Recovery is an ongoing process, still being navigated.
• Kijuan emphasizes the importance of mindset in overcoming adversity.
• He believes in focusing on abilities rather than disabilities.
• Support from family and friends was crucial during recovery.
• Kijuan's faith played a significant role in his healing process.
• He encourages others to find their own path to recovery.
• Kijuan's story is a testament to resilience and strength.
• He aims to inspire others through his motivational speaking.

titles

• From Struggles to Strength: Kijuan Amey's Journey
• The Power of Perseverance with Kijuan Amey

Sound Bites

• "That's how most people get hurt."
• "I wanted to create my own footprint."
• "I respected it even more."

Chapters

00:00

Introduction and Technical Difficulties

00:52

Physical Fitness and Personal Challenges

03:36

Early Life and Family Dynamics

05:56

Musical Passion and Creative Outlets

08:37

Sports Journey and Competitive Spirit

09:36

Basketball Experiences and Personal Strengths

10:06

Football and Track Background

10:56

Rivalries and School Spirit

11:10

The Impact of Football on Personal Development

12:07

Transitioning to the Air Force: A Personal Journey

14:54

Navigating Military Recruitment and Choices

21:11

Experiences in Active Duty and Transitioning to Reserves

23:52

Understanding the Role of a KC-135 Stratotanker Pilot

24:28

The Flying Gas Station

25:37

Beyond Refueling: The Multifaceted Role of Airmen

26:21

A Passion for Engines: From Dirt Bikes to Motorcycles

28:34

The Journey to Motorcycle Endorsement

31:55

The Day That Changed Everything: The Accident

41:04

Recovery and Resilience: A New Life Journey

46:56

Embracing Life After Adversity

49:10

The Power of Support Systems

52:23

Transforming Pain into Purpose

54:01

The Will to Overcome

58:32

Connecting with Others Through Storytelling

01:00:28

Advocating for Ability Over Disability

01:02:29

The Importance of Mentorship

https://ameymotivation.com/

In this conversation, Sarah Ingledue shares her profound journey as a nurse and caregiver for her sister, Rachel, who has Cornelia de Lange syndrome. Sarah discusses her early passion for nursing, her unique relationship with Rachel, and the challenges and joys of caring for someone with special needs. The conversation delves into the importance of love and support in their lives, the daily responsibilities Sarah manages, and her aspirations to create a respite care service for families in similar situations. Throughout, Sarah emphasizes the significance of happiness, quality of life, and the need for better support systems for families with special needs individuals.

takeaways

• Sarah's nursing background has equipped her to care for Rachel effectively.
• The bond between Sarah and Rachel is deep and rooted in love.
• Caring for a special needs sibling can be both challenging and rewarding.
• Respite care is crucial for families with special needs individuals.
• Sarah's husband is supportive and is pursuing nursing to help care for Rachel.
• Daily life with Rachel involves extensive care and attention.
• Sarah's daughters are learning valuable lessons about kindness and acceptance through their relationship with Rachel.
• Healthcare funding and support for special needs individuals is a significant challenge.
• Sarah is passionate about creating a respite care service for families in need.
• The importance of advocating for proper care and understanding in healthcare settings.

titles

• A Sister's Love: Caring for Rachel
• Navigating Life with Cornelia de Lange Syndrome

Sound Bites

• "Love is medicine."
• "Rachel grows on you."
• "It's just fair."

Chapters

00:00

Childhood Experiences with Rachel

07:18

Understanding Cornelia de Lange Syndrome

09:07

The Importance of Love and Support

09:32

Finding a Partner Who Understands

11:38

Family Dynamics and Support

13:08

Daily Life and Responsibilities with Rachel

15:58

Raising Daughters with a Special Needs Sister

17:21

Communication and Education for Rachel

20:16

Navigating Healthcare and Funding Challenges

25:24

Advocacy in Healthcare: A Caregiver's Role

27:20

The Birth of Raise RespaCare: A Vision for Change

29:37

Building a Community: The Need for Respite Care

32:03

Connecting with Support: Legislative and Community Efforts

34:10

Healing Through Care: The Role of Veterans

38:51

Quality of Life: Ensuring Happiness for Ray

42:07

Creating Memorable Experiences: Travel and Adventures

43:51

Raising Awareness: Fundraising and Community Engagement

https://www.raysrespitecare.org/

https://www.instagram.com/rays.respite.care/

On May 16, 2025, a groundbreaking documentary titled "Deaf President Now!" will be released, chronicling the historic 1988 student-led protest at Gallaudet University—the world’s only liberal arts university for Deaf and hard-of-hearing students. But this episode is more than a retelling. It’s a personal reflection on what that moment meant then, how it shaped Deaf education, and the cultural revolution that followed.

In this episode, I share my own journey from a curious outsider to someone deeply embedded in the Deaf community. I revisit the DPN movement not just as a pivotal civil rights event, but as the spark that lit a fire of change in Deaf education, culture, and self-representation. We explore:

• Why the appointment of a Deaf president finally mattered
• 
  
• The rise of bilingual-bicultural (Bi-Bi) education and what it really means
• 
  
• How the cultural renaissance post-DPN transformed Deaf schools and inspired students
• 
  
• The impact of cochlear implants on Deaf identity and language access
• 
  
• The continuing relevance of DPN in today’s shifting educational and cultural landscapes
• 
  

Whether you’re familiar with Deaf culture or discovering this history for the first time, this is a powerful reminder that inclusion isn’t just about access—it’s about representation, respect, and identity.

💬 As Nyle DiMarco said, “Deaf history is American history.” Let’s make sure it's remembered, celebrated, and passed on.

• [00:02:00] The Gallaudet Protest: Why It Happened
• 
  
• [00:07:30] My First Encounter with Deaf Culture
• 
  
• [00:14:45] Deaf Schools and the Bi-Bi Shift
• 
  
• [00:22:10] The Cultural Renaissance of the 1990s
• 
  
• [00:28:00] Cochlear Implants and Language Deprivation
• 
  
• [00:34:00] Why DPN Still Matters Today
• 
  

• Deaf President Now! Documentary – Releasing May 16, 2025
• Disability Scoop article on the film: [Link if available] https://www.disabilityscoop.com/2025/05/09/appletv-documentary-spotlights-pivotal-disability-protest/31447/
• National Association of the Deaf (NAD) – www.nad.org
• “A Journey Into the Deaf World” by Harlan Lane, Robert Hoffmeister, and Ben Bahan
• https://gallaudet.edu/museum/history/the-deaf-president-now-dpn-protest/the-impact-of-the-deaf-president-now-protest/#:~:text=The%20Americans%20with%20Disabilities%20Act%20(ADA)%20protects%20deaf%20people%20and,and%20the%20speed%20of%20introduction.

Have you experienced Deaf education before or after DPN? Are you a teacher, student, or parent navigating Bi-Bi vs. oral approaches today? Share your story with us on social or email!

#DeafPresidentNow

#DPN1988

#DeafHistory

#DeafEducation

#BiBiEducation

#SignLanguageMatters

#ASL

#DeafCulture

#CochlearImplants

#DisabilityRights

#NyleDiMarco

#Gallaudet

#RepresentationMatters

#DeafIdentity

#InclusionWithIntention

#LanguageAccess

#DeafAndProud

#DeafVoices

#CelebrateDeafCulture

In this heartfelt and urgent episode, I reflect on a long-standing goal I've held since the launch of this podcast: to speak with a gun violence prevention advocate about the devastating impact of mass shootings, particularly in schools. As a classroom teacher, this issue is deeply personal. The statistics are staggering—but behind them are real people, real families, and far too many children lost.

That goal led me to Moms Demand Action, a grassroots movement founded by Shannon Watts in the wake of the Sandy Hook tragedy. What began as a Facebook group created by one mother has evolved into a nationwide force advocating for stronger gun laws and safer communities.

In 2024, I attended my first meeting. But it wasn’t until I got on an "action bus" to Albany, New York—a place where I earned my undergraduate education—that I truly felt the power of community activism. I joined fellow advocates to meet with lawmakers and push for three essential bills that address:

• The ban of semi-automatic handguns that can be converted into machine guns using illegal Glock switches,
• The codification and expansion of New York’s Office of Gun Violence Prevention,
• A simplified and strengthened firearm storage law.

These aren't radical ideas—they're common-sense measures to save lives.

This episode isn't just about one person's journey into advocacy—it's about what happens when we move from storytelling to action. I found inspiration, purpose, and a network of passionate people who believe we can and must do better.

If you’ve ever asked yourself, “What can I do?”—this episode is your invitation to find out.

• Moms Demand Action: https://momsdemandaction.org
• Everytown for Gun Safety: https://everytown.org
• Shannon Watts on Twitter: @shannonrwatts
• “In the Battle Against Gun Violence, Shannon Watts Fights Like a Mother” – Glamour Article

Attend a local Moms Demand Action meeting. Speak up. Vote smart. And when the “action bus” rolls into your town—get on.

https://momsdemandaction.org/

🎧 Subscribe, share, and stay tuned for my upcoming interview with a gun prevention advocate.

In this conversation, Kristie Raymond discusses her revolutionary approach to modeling and casting, focusing on inclusivity and representation for individuals with disabilities. She emphasizes the importance of building a talent pool of adaptive talent to ensure authentic representation in media. Kristie shares her journey in founding Humankind Casting, her experiences in the industry, and the impact of inclusive casting on individuals and society. The conversation highlights the need for education, awareness, and collaboration to create opportunities for underrepresented communities in the modeling world.

takeaways

• Creating a talent pool of adaptive talent is essential for inclusive casting.
• Representation matters in advertising and media.
• Building confidence in individuals with disabilities can change their lives.
• The modeling industry needs to evolve to include diverse talent.
• Education and awareness are crucial for industry professionals.
• Inclusive casting can lead to authentic representation in media.
• The journey of Humankind Casting is about empowering individuals.
• Collaboration with organizations can enhance opportunities for talent.
• The impact of advertising on the disability community is significant.
• Creating a supportive environment fosters growth and confidence.

titles

• Revolutionizing Representation in Modeling
• Building a Talent Pool for Inclusive Casting

Sound Bites

• "It's about the human connection."
• "Representation matters, right?"
• "It's okay to go for inclusive casting."

Chapters

00:00

Technical Difficulties and Introduction

02:50

The Importance of Inclusive Casting

05:56

Authenticity in Representation

09:12

Building Confidence Through Modeling

11:57

The Journey of Kristie Raymond

15:54

Founding Humankind Casting

19:04

Challenges in the Industry

21:55

Creating a Talent Pool

25:09

The Future of Inclusive Casting

31:15

Scaling Opportunities in Secondary Markets

34:40

Building a Diverse Talent Pool

37:18

The Importance of Representation

39:12

Authenticity in Advertising

42:04

Impact of DEI Policies

44:42

The Casting Process Explained

46:18

Expanding Clinics and Opportunities

51:14

Educating the Industry

55:12

Empowering Creatives

58:14

Navigating the Hiring Process

https://www.youarehumankind.com/

https://www.linkedin.com/in/kristieraymond/

In this conversation, Erica shares her journey as a late diagnosed autistic ADHD female and the insights gained from parenting her neurodivergent child. She discusses the emotional challenges faced due to societal norms and the importance of self-acceptance. The dialogue emphasizes the value of different perspectives, the significance of asking for help, and the need to challenge societal expectations regarding disability and worth. In this conversation, Erica and Mark explore the themes of compassion, acceptance, and the interconnectedness of social justice issues, particularly focusing on autism and animal rights. Erica shares her personal journey, the importance of communication in relationships, and how her experiences shape her advocacy work. They discuss the need for understanding and validating diverse experiences, the significance of amplifying marginalized voices, and the privilege of being able to express oneself freely. The conversation emphasizes the importance of collective liberation and the responsibility to advocate for all living beings.

takeaways

• Erica's journey began as a late diagnosed autistic ADHD female.
• Understanding her child's perspective helped Erica appreciate her own neurodivergence.
• Receiving a professional diagnosis was validating for Erica.
• Emotional wounds stemmed from societal narratives about autism.
• Erica felt alienated despite being socially active.
• The concept of 'normal' is problematic and often harmful.
• Society often overlooks the value of neurodivergent individuals.
• Asking for help is a sign of strength, not weakness.
• Elders in society are often marginalized and undervalued.
• Parenting a neurodivergent child can lead to profound self-discovery. Compassion allows individuals to navigate their experiences authentically.
• Communication and trust are essential in relationships, especially in understanding diverse perspectives.
• Erica's journey highlights the importance of finding supportive environments for personal growth.
• Advocacy for animals and social justice is interconnected and essential for collective liberation.
• Understanding autism requires recognizing the unique experiences of each individual.
• The narrative around autism and disability needs to shift towards acceptance and validation.
• Amplifying marginalized voices is crucial in the fight for social justice.
• Privilege plays a significant role in how individuals navigate their identities and experiences.
• Education should come from lived experiences to foster understanding and empathy.
• Collective care is necessary for the well-being of all living beings.

Sound Bites

• "I began to see myself through that same lens."
• "I felt like I was constantly comparing myself."
• "Our worth really comes down to productivity."
• "It's not a sign of weakness to ask for help."
• "We have to give people more credit."
• "You just need to be willing to say, I believe you."
• "It's about collective care and collective liberation."
• "We can expand that to include everybody."
• "Animals are always the bottom of the rung."
• "This message needs to get out there."
• "We need to educate from lived experiences."
• "Showing up as ourselves is a privilege."
• "It's important to recognize our privilege."

Chapters00:00

Introduction and Background

02:56

Understanding Neurodivergence

06:10

Personal Experiences with Autism and ADHD

08:56

The Impact of Diagnosis

12:01

Navigating Social Norms and Expectations

15:03

The Value of Different Perspectives

17:56

Disability and Worth in Society

20:49

Asking for Help and Support

24:05

The Role of Elders in Society

27:04

Parenting a Neurodivergent Child

30:00

Shared Experiences and Understanding

34:27

Understanding Compassion and Acceptance

39:10

The Importance of Communication and Trust

44:30

Erica's Journey and Career

49:19

Advocacy for Animals and Social Justice

56:15

Intersection of Autism and Animal Rights

01:02:17

Amplifying Voices and Collective Liberation

Instagram: erica_settino

https://www.karunaforanimals.com/

In this episode, we address the dangerous and deeply offensive comments made by Robert F. Kennedy Jr. during his April 16, 2025 press conference, where he claimed autism is “preventable” and described individuals on the spectrum as incapable of working, dating, writing poetry, or living independent lives.

We confront these statements with facts, lived experience, and community response.

From debunking outdated vaccine myths to amplifying the voices of autistic adults and their families, we’re here to set the record straight.

RFK Jr.’s rhetoric isn’t just wrong—it’s harmful. And our community deserves better.

Segment 1: Breaking Down the Claims

• What RFK Jr. said and why it’s dangerous
• The truth about thimerosal and autism
• Scientific consensus from CDC, WHO, AAP, IOM, and JAMA Psychiatry

Segment 2: The Community Claps Back

• Responses from Holly Robinson Peete, Dr. Peter Hotez, and our own community
• Real-life stories of autistic individuals thriving in work, love, and creativity

Segment 3: What Families Really Need

• Support, not stigma
• Why RFK’s message misses the mark entirely

Segment 4: Moving Forward

• How to respond to misinformation
• Ways we can build inclusive, empowering spaces for all neurodivergent people

• Autism is not caused by vaccines or thimerosal.
• Genetics play a major role in autism.
• Autistic people can and do live meaningful, connected, and creative lives.
• The real barrier is not autism—it’s misinformation and underfunded systems.
• Words matter, and so does leadership rooted in truth and compassion.

• CDC on Thimerosal & Autism
• Institute of Medicine 2004 Report
• JAMA Psychiatry 2019 Heritability Study
• WHO Vaccine Safety
• Holly Robinson Peete’s Response
• Dr. Peter Hotez’s Commentary

Autism is not a tragedy. Stigma is.

We don't need cures. We need compassion.



summary

In this conversation, Gaile Valcho discusses the evolution of the Holly Springs Autism Acceptance Day, highlighting the importance of community engagement, police involvement, and the establishment of a nonprofit organization to support families with autistic children. She shares insights on training first responders, the significance of family dynamics, and the challenges of parenting a teenager with autism. The conversation emphasizes the need for awareness, support systems, and self-care strategies for parents. In this conversation, Gaile Valcho discusses the importance of guardianship for her son Brady, who has autism, and the steps they are taking to ensure his independence and well-being as he approaches adulthood. She emphasizes the need for families to understand the legal and medical implications of guardianship. Gaile also shares her role at the Hand Center for Autism, where she supports families and builds community partnerships to provide resources for children with autism. The conversation touches on the challenges of living with chronic illness while parenting, the significance of the spoon theory in understanding energy levels, and the need for better education and awareness in schools regarding autism. Gaile highlights the importance of community engagement and acceptance for individuals with autism and their families.

takeaways

• The Holly Springs Autism Acceptance Day has grown significantly over the years.
• Police involvement is crucial for building community trust and understanding.
• Training first responders on autism can prevent misunderstandings in crisis situations.
• Establishing a nonprofit allows for more structured support and fundraising efforts.
• Family dynamics play a vital role in managing the challenges of autism.
• Self-care is essential for parents to maintain their well-being.
• Involving children in decision-making fosters independence and confidence.
• ABA therapy can be beneficial for older children with autism.
• Community events can enhance awareness and support for families.
• Creative solutions are necessary for finding time for self-care. Guardianship is crucial for individuals with disabilities as they transition to adulthood.
• Families should actively pursue guardianship to ensure their loved ones' rights and needs are met.
• Community resources and partnerships are essential for supporting families with autistic children.
• Events like Autism Acceptance Day foster community engagement and awareness.
• Living with chronic illness can complicate parenting responsibilities.
• The spoon theory helps in understanding energy management for those with chronic conditions.
• Education systems often lack the necessary awareness about autism, leading to punitive measures.
• Invisible disabilities are often misunderstood by the public, leading to stigma.
• Building relationships with community organizations can enhance support for families.
• Open conversations about disabilities can lead to greater understanding and acceptance.

Sound Bites

• "You look great and I'm joking the switch"
• "They really embraced the idea"
• "It's one thing to have police involvement"
• "We became a nonprofit during COVID"
• "We need some help"
• "You need an outlet, a healthy one"
• "We find it really beneficial again for us"
• "That's the promised land."
• "It's an amazingly fun day."
• "I got diagnosed with lupus over COVID."
• "I use the spoon theory."
• "There's invisible handicaps, sir."
• "We're in a very judgy world."

Chapters

00:00

Introduction to Autism Acceptance Day

03:01

Police Involvement and Community Engagement

05:59

Training First Responders for Autism Awareness

09:09

Establishing a Nonprofit and Fundraising Efforts

11:52

Family Dynamics and Support Systems

14:59

Parenting Strategies and Self-Care

18:02

Brady's Growth and Independence

20:54

Navigating Teenage Challenges and ABA Therapy

32:45

Navigating Guardianship and Independence

36:24

Supporting Families in Autism Services

41:52

Community Engagement and Resources

42:58

Promoting Autism Acceptance

49:08

Living with Chronic Illness and Parenting

54:07

Understanding Through the Spoon Theory

57:49

Challenges in Education and Awareness

01:00:25

Invisible Disabilities and Public Perception

https://bva.foundation/

https://www.handscenter.com/

Show Notes

In this conversation, Mark interviews David Tillman, a dedicated father of a son with Fragile X syndrome. David shares his journey as a parent, the challenges and joys of raising Miles, and the importance of community support. They discuss the impact of Fragile X syndrome on Miles' life, the significance of music and arts in education, and the need for advocacy in the disability community. David emphasizes the value of patience, understanding, and connection in navigating the complexities of raising a child with special needs.

takeaways

• David Tillman emphasizes the importance of dad representation in discussions about parenting children with special needs.
• Fragile X syndrome presents unique challenges, but also opportunities for connection and joy.
• Community support is crucial for families navigating disabilities.
• Music and arts can play a significant role in the development of children with special needs.
• Patience and understanding are key in helping children with disabilities thrive in social situations.
• The Fragile X community provides invaluable resources and connections for families.
• Social media can help families connect with others facing similar challenges.
• Advocacy is essential for ensuring that the needs of children with disabilities are met.
• Preparing for the future involves teaching independence and life skills from an early age.
• Every family’s journey is unique, and it’s important to celebrate the small victories.

Sound Bites

• "I love talking about Miles."
• "We can do this, Miles."
• "It's a beautiful vision."

Chapters

00:00

Introduction to David Tillman and His Journey

02:18

Understanding Fragile X Syndrome and Its Impact

08:19

Navigating Family Dynamics and Support Systems

11:00

The Importance of Community and Connection

13:20

Music as a Bonding Tool

17:48

The Need for Arts Programs in Disability Advocacy

21:43

Advocacy and Raising Awareness

25:07

Finding Balance and Celebrating Moments

27:20

Navigating Crisis Moments

31:24

Understanding Diagnosis and Support

41:04

Building Community Connections

46:24

Advocacy and Future Planning

Instagram: @xtraordinarymiles

https://www.linkedin.com/in/david-tillman-phd/

Podcast Show Notes: Impact of Policy Changes on Special Needs Families

Episode Overview:

Welcome to today’s episode where we explore the impact of policy changes on families of individuals with disabilities. With potential cuts to Medicaid and the Department of Education, many families worry about losing access to essential services. In this episode, I break down what these changes could mean and share actionable steps you can take to protect your child's future. Please note that this information is for educational purposes and not legal advice.

Key Topics Covered:

• Understanding how Medicaid and Medicare cuts could affect individuals with disabilities
• Potential impacts of reduced federal oversight on special education
• Special Needs Trusts (SNTs) and how they safeguard government benefit eligibility
• ABLE Accounts for flexible, tax-advantaged savings
• Choosing the right trustee for your child’s Special Needs Trust

Special Needs Trusts (SNTs):

• First-Party SNTs: Funded with the beneficiary’s assets, often from settlements or inheritances. Includes a Medicaid payback provision.
• Third-Party SNTs: Created by family members or friends, with no Medicaid payback requirement.
• Benefits: Maintain eligibility for Medicaid and Supplemental Security Income (SSI) while providing supplemental support.
• Resources:
• CHOP: Special Needs Trusts Overview
• NYS Bar Association: Improved Trust Administration
• McAndrews Law Firm: Establishing a Trust
• International Bipolar Foundation: Management Models

ABLE Accounts:

• Annual contribution limit of $18,000, with additional contributions for working individuals.
• Tax-free growth for qualified expenses like education, housing, and assistive technology.
• SSI protection for accounts under $100,000.
• Complements SNTs for managing day-to-day expenses.
• Learn more at the ABLE National Resource Center.

Choosing the Right Trustee:

• Family Member Trustee: Offers personal insight and familiarity but may lack financial and legal expertise.
• Professional Trustee: Provides expertise in financial management but may have higher fees.
• Co-Trustees: Combines the strengths of a family member and a professional.
• Pooled Trusts: Managed by nonprofit organizations for cost-effective management.
• Evaluate factors like financial knowledge, understanding of benefit rules, and long-term commitment.

Next Steps:

1. Consult a Special Needs Attorney: Find one through NAELA or the Special Needs Alliance.
2. Open an ABLE Account: Compare programs using the ABLE National Resource Center.
3. Develop a Letter of Intent: Document your child’s care preferences and essential information.
4. Consider Life Insurance: Fund a third-party SNT to provide ongoing support.
5. Review Your Plan: Regularly revisit your financial plan to accommodate changes in circumstances and laws.

Resources and Support:

• The Arc of the United States
• National Disability Institute
• Family Voices
• Autism Speaks Financial Toolkit
• Parent to Parent USA
• Easterseals
• Council of Parent Attorneys and Advocates (COPAA)

If you found this episode helpful, share it with other parents and caregivers! Stay informed and empowered as we navigate these uncertain times together.

Contact:

For more resources, visit the resource page on my website. Have questions or topic suggestions? Reach out via my contact form or follow me on social media. Thanks for tuning in!

specialedrising.com