As an Autistic Dad, Autism “Awareness” Month Brings Up Mixed Feelings for Me

Photo of Kris and his daughter. Kris is a biracial man who has short black curly hair and tinted glasses. He is smiling while sitting holding his 11 month old daughter who has short black hair in two ponytails and is wearing a pink jacket on a sunny day at a park.

Autism “Awareness” Month brings up mixed feelings for me. In one sense, I have excitement because I am a proud autistic dad of an amazing almost 1-year-old and it has been such joy. But I also have frustration because of the stereotypes and discrimination I’ve experienced as an autistic person that left me feeling like I was incapable of being married, working, being an active community member, living independently, and being a dad.

During previous Autism Awareness months, the array of ads, slogans, campaigns, and images centered on things like finding a cure or portraying autism as a puzzle piece, as something missing or needing to be fixed, added to my feeling that being autistic meant something was wrong with me. This had a negative impact on my self-esteem, but therapy combined with autistic self-advocacy organizations helped me discover that being autistic doesn’t mean I am broken or incapable. It means I process the world around me in a different way.

Becoming an autistic dad has reinforced that I have many strengths and I am always learning, adapting, and growing. When I found out I was going to be a dad, I was both excited and extremely nervous, as I was unsure what it would look like to be an autistic dad with multiple disabilities and how that would impact my parenting abilities. I was worried about my sensory and cognitive overload, my emotional regulation, and my communication. I was also worried my physical disabilities, especially my mobility, and how I would perform tasks.

While I was already used to relying on tools, strategies, and different resources, I found little help from resources that I’d previously turned to when seeking information about this life transition. Books and articles I found catered to parents of autistic children. I started to panic because I needed to have time to prepare for everything but didn’t know where to get support. Now, I sit back and laugh because I prepare to the best of my ability, but even on the good days with total preparation, I must practice immense flexibility and patience (which doesn’t come easy for me) because that’s dad life with a young toddler.

Dad life has shown me the importance of self-advocacy and has helped me recognize how much I work behind the scenes communicating and preparing. I have to consider my access needs, my daughter’s access needs, my partner’s access needs, and how they all may interact with our different schedules, work, and day-to-day tasks. This gives me the best chance to show up as my authentic self, participate as fully as possible, and be fully present for my daughter and family.

I am still navigating what self-advocacy looks like across multiple dynamics of difference, as we are an interabled, interracial, intercultural, neurodiverse family. I am also trying to remember to be kind and gentle with myself, which includes realizing and accepting that I am capable of being a dad despite any previous messages that told me I wasn’t.

So, this year during Autism Awareness Month and every day after it, I am affirming that I am a proud autistic dad with multiple disabilities. I encounter challenges and joys like other parents. I have strengths and I am working on things like other parents. I adapt and use strategies like other parents. My autism and other disabilities do not make me any less of a dad or person. Every day looks different because no one day in the life of parenthood is the same. So, I am choosing to celebrate the part of my life and story that includes being a proud autistic dad with multiple disabilities to my amazing daughter.

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Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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The Power of Black Disabled Representation During Black History Month

Illustration of a row of Black and Brown fists in the air.

Each February, the United States celebrates Black History Month. It is a month that brings about many different emotions for me, ranging from excitement and pride to pain, grief, and frustration. It’s a time when school systems read books by African American authors, create special projects, and learn about the history, accomplishments, and adversities of African Americans such as Martin Luther King and Harriet Tubman. Organizations like Google add a link or section on their homepage about “Celebrating Black History Month,” highlighting moments of excellence, sharing educational resources, and spotlighting makers, pioneers, and leaders. Panels, discussions, and community activities such as screenings of Black films are scheduled. Invitations are sent to Black speakers, such as creators, writers, and professors, to fill events for each day of the month, curating a whole lineup for allies and BIPOC to honor the month.

As a person who has struggled since my youth in navigating my experiences of being Black and having multiple disabilities, it was hard for me to see authentic representations of myself during the events of Black History Month that didn’t also portray the intersections of racism, ableism, discrimination, and violence toward African Americans with disabilities. I heard messages that Black History Month was for us, but based on my experiences, it didn’t feel like it.

These experiences included being in classrooms with teachers who would read the same stories every February and give the wrong facts; racism and ableism in my community; and not being given space to participate or contribute in the way that I desired because of accessibility or other aspects of my identity including my multiple disabilities, being biracial, being transgender, and my sexuality. Often, I would find myself celebrating my Blackness and my Black heritage by myself and creating art that expressed the combination of joy, inner confliction and other feelings I had.

Leading into Black History Month 2021, I’ve found within myself the excitement of the historical election and inauguration of Kamala Harris, the first Black and South Asian female Vice President, mixed with the pain and emotions o of racism, police brutality, marginalization, violence, and other disparities that filled 2020 and continue today.

Both history and experience remind me of the power of representation and storytelling for individuals and communities. There is so much potential for connection, healing, and empowerment when the authenticity of the Black identity is represented, expressing Black joy, excellence, creativity, community, and history. I feel this connection, healing, and empowerment at my core, but with pieces of me missing. So, I always am searching for representations of Black joy, excellence, creativity, community, and history that are inclusive of intersecting identities such as sexuality, culture, disabilities, and gender identity.

The lack of whole representation of the intersections of my gender identity and disabilities as a Black and biracial person has been a source of exclusion, stigma, and isolation for me. This was especially true until I started going deeper and found that intersectionality is a part of more stories of Black history than I realized. It is embedded not only within the stigmas and maltreatment that I am already familiar with, but also embedded within successes, advancements, advocacy, creativity, and everyday life in ways that I was unfamiliar with.

I think about what it means to me, what it meant to others in my family, and what it will mean to my daughter as she grows up to see ourselves/herself in different ways. I think about the work of icons, innovators, and leaders: Diana Elizabeth Jordan, Daymond John, Stevie Wonder, Muhammad Ali, Andre Shelby, Missy Elliot, Bonnie St. John, Oprah, Tyler Perry, Haben Girma, Solange Knowles, Maya Angelou, Cicely Tyson, Forest Whitaker, Denzel Washington, Viola Davis, Zendaya, Amanda Gorman, and the late John Lewis, Martin Luther King, Malcolm X, Harriet Tubman, and Thomas Wiggins. I think about so many more Black lives across generations, with and without disabilities, whose stories are known and unknown.

Experiences of being Black, biracial, and having both visible and invisible disabilities are an integral part of Black history. Yet identities like disability are often left out of the dominant narrative during Black History Month and beyond. It’s important to see authentic representations of ourselves across all the different intersections that make up one’s identity, separately and as a whole. This holistic representation would have made a difference to me as a kid growing up, helping me to connect and see the value in myself. It would have helped me see that neither my Blackness nor my disabilities make me any less, that I have potential and talent, and that there is a future for me.

Representation matters in fighting stigma and increasing inclusivity and equity. Representation allows all people across the African diaspora within all their intersecting identities to have their experiences valued. We should all be represented in celebrations, stories, histories, dreams, and visions every day of the year.


Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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Taking Care of My Mental Health During This Pandemic Holiday Season

A shape of a person's head filled halfway with bright, colorful holiday items including a snowman, christmas tree, ornaments, and a santa hat, juxtaposed with greyed out items on the rest of the face. The background is a gray cloudy sky.

The holidays can bring about emotions ranging from happiness and excitement to stress, grief, and loneliness. Figuring out how to navigate the many different elements of the holidays can be complicated, but it’s even more so this year as the COVID-19 pandemic surges. I find myself trying to hold on to moments of joy, embracing the different kind of holiday ahead, and holding everything together during a year when everything feels full of unpredictability, loss, and chaos.

As someone with multiple disabilities, I have always started planning early for what’s needed for the holidays. This planning typically starts around mid-October as I make a list of what is most important to me and what I want to participate in, and I check in with family and friends to see what their tentative plans are that they would like me to attend. This is helpful to me because although the holiday season is one of my favorite times of the year, it is also one of the most difficult for me. I love the decorations, music, and lights of the holiday season, but I struggle with sensory overload, crowds, and the social expectations and requirements of holiday gatherings. So, I plan to shop online or do curbside pick-up during the weekday early or late store hours. This year especially, I am sensory-friendly holiday activities in my own home, while scheduling zoom holiday calls with no more than one household at a time. I also struggle with anxiety and depression as I am reminded of the sudden loss of family members and friends during past Novembers and Decembers. So, I have put some support meetings on my calendar as well.

Right now, it’s hard dealing with the guilt of not seeing family members, especially knowing how precious time is and that moments together again are not guaranteed. I feel responsible for being immunocompromised and high risk because it has impacted our family holiday decisions during this pandemic holiday season, creating more isolation. Managing my different traits related to my disabilities and participating in virtual events and social calls is difficult for me, but I only feel more isolated if I don’t participate. These feelings make it challenging for me to maintain and cope with all aspects of my recovery and health, and I feel guilty for struggling.

I am working on coming to terms with how different this holiday season will be, and I am being kind and gentle with myself. But every day seems to be filled with navigating difficult conversations and decisions, experiencing disruptions in routines, and handling conflicting wants and needs among family and myself related to mental and physical health and safety. There are constant changes with lots of unknowns and I can’t seem to shake my struggling. So, I came up with these little self-care reminder messages to help me navigate the holiday season this year, and I hope you might benefit from them, too.

  1. Every feeling I am having at this moment is valid.
  2. I choose how I navigate difficult conversations in ways that are best for me.
  3. It’s OK to struggle, and it’s OK to ask for help and seek support.
  4. When being kind and gentle to yourself is difficult, remember you are worth it. All acts of self-care, no matter how small, are a way to show yourself kindness and gentleness.
  5. It’s OK to pause, unplug, and take a break.
  6. Safety being a priority is valid, period.
  7. Having feelings doesn’t automatically mean relapse. It’s OK to feel what I am feeling.
  8. I choose to make space for my grief at every step of the grief process and that’s OK.
  9. I choose to make space for my healing at every step of the process and that’s OK.
  10. Take it one moment at a time.
  11. My best is good enough. Who I am is enough.
  12. My life, wellbeing, and safety are not dispensable.
  13. My boundaries are valid, period.

Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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Four Ways to Improve Crisis Intervention Services for the Disability Community

A red telephone receiver with a long red wire

Content note: includes discussion of mental health crises and police brutality


In 2012, my own fear of the police due to previous trauma impacted my ability to call the crisis response team for a friend who was having a mental health crisis. My trauma informed my belief that if I called them, they would send the police who wouldn’t have the skills to help, and as a result my friend would be badly hurt or lose their life. I thought I could figure out a safer option to help. Unfortunately, I received news the following morning that my friend died of suicide. I struggled with my decision, feeling like I should have done something different and that I failed to help so I was responsible for what happened. I was confused about how to use crisis intervention services when my own experiences showed that it can make situations worse. I needed to know where to turn for “safe” help.

Years later, I carry that experience alongside my other trauma. And even though I carry a wallet card to give emergency response team personnel and law enforcement which explains my disabilities, I am still worried about what could happen to me as a result of racism or stigma related to my disabilities or gender identity? Will I be able to access “safe” help? Will my wallet card really help?

As protests against police brutality grow, discussions of police reforms and mental health system reforms are ongoing. But there continues to be tragic headlines of police brutality against individuals in crisis including Linden Cameron, a young boy with Asperger’s who was severely injured, and Daniel Prude, a man with a mental health disability who was killed.

The emotional toll and the effects on mental health and overall well-being from events like these feel almost never-ending. The impacts on individuals with disabilities and families are immense.

Navigating crisis intervention services has been incredibly challenging for my friends, family, and community members, and for me—a biracial black man with multiple disabilities, including autism and complex hereditary spastic paraplegia. I wish it wasn’t so challenging, and I especially wish these services didn’t so frequently end up increasing trauma or end in individuals losing their lives instead of getting the help they need and deserve.

Undue harm and death are disproportionately the result when black and brown individuals with disabilities are experiencing a mental health crisis. These tragedies create barriers and a lack of access to supports needed for individuals and families, leading to further declines in wellbeing.

Improving Crisis Intervention Services in the Community

Crisis intervention services that serve communities need to improve in order to dismantle the barriers that inhibit individuals and families from receiving access to safe supports. First, there should be non-law enforcement options as first responders to crisis situations. And second, anti-racism, disability awareness, cultural competency, and mental health first aid are four essential areas of training that I believe should be required for crisis intervention. These trainings are centered in providing first responders and public service personnel, including law enforcement, the tools to better help the communities being served.

Anti-racism training is rooted in promoting greater racial equity by guiding participants to learn how to be aware of, challenge, and change institutional racial inequalities. Disability awareness training provides the opportunity to learn about different disabilities, misconceptions, accessible communication, and etiquette on responding based on the needs of an individual in crisis. Mental health first aid training provides an opportunity to gain tools and strategies for de-escalating and responding to mental health crisis situations in a safer manner while also decreasing stigma by focusing on expanding understanding of behaviors, challenges, and complexities of mental illness. And finally, cultural competency training helps participants develop awareness and understanding of their own culture, worldviews, values, and biases, and teaches how dynamics of difference influence interactions when providing services/responding to crisis situations.

While these areas are often viewed as separate, they intersect and inform one another, similar to how individuals have many intersecting identities that work together to make up the whole of who they are. Together, these areas of training can inform professional development and crisis response protocols and practices for everyone from law enforcement, to emergency response teams, to all professionals in helping fields (i.e. doctors, community center staff).

Holding professionals and systems accountable for their actions is also necessary. It is time for people to not be afraid of reaching out for help. It is time for people to stop being harmed and losing their lives while seeking needed help. It is time for the mental health system, crisis intervention services, and law enforcement to change so that everyone can access services in a safe, equitable way.

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Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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Navigating Virtual Employment Services During the Pandemic

An illustration of a person wearing a headset and typing on a laptop. The person is transparent and has blue connecting lines and dots inside them, indicating being online.

Navigating the dynamics of difference within the world of employment as a person with multiple disabilities has been a struggle since the moment I prepared to enter it at the age of 16 in 2001. I didn’t become aware of accommodations, self-advocacy skills, or my rights regarding employment as an individual with a disability until my late 20’s. The impact of the stress and energy trying to navigate the employment had an adverse influence on my health.

In July 2013, on the same day I was released from a three week stay at an inpatient trauma disorders program, I received a letter that I had been approved for Social Security Disability (SSDI) benefits. I was 27 years old at the time. I spent the next five years going through rehabilitative therapies. During that time, I learned more about myself, my disabilities, self-advocacy, assistive technology equipment, coping and compensatory strategies, and accommodations, all while engaging with different programs that support individuals with disabilities in independent living and vocational training.

After going through years of rehabilitative therapies, I reached a point where I wanted to try to start working again through part-time or contract work within the parameters guided by my treatment. Because I’d been out of the workforce for so long, I was confused on how to get started with the Division of Rehabilitation Services (DORS). I expended a lot of energy completing paperwork and figuring out the process during the COVID-19 pandemic.

Although the overall unemployment rate in the U.S for individuals with and without disabilities increased because of COVID-19, so did opportunities for remote work. There were also shifts in how programs that serve individuals with disabilities in independent living and vocational training/employment are offering and carrying out services.

My experiences with virtual service delivery have varied. It’s been beneficial that I have not had to navigate transportation challenges, building inaccessibility, and the impact of unpredictable medical challenges causing a need to reschedule. All rehabilitative appointments have occurred through video, and my cognitive, speech and physical therapists have connected me to apps to supplement and assist in-home therapy programming. My local independent living center offered limited services virtually including helpful demonstration sessions on video. The greatest challenge for me has been the lack of access to necessary service delivery that is performed in person, such as testing adaptive equipment and manual physical therapy. These services are either on hold until my state enters stage 3 of the COVID-19 reopening plan or not advised until further notice because I am immunocompromised.

Once I was able to participate in virtual service delivery through DORS, I discovered there would be a delay in the evaluations needed as part of my vocational training and employment plan. I was able to complete the initial phases, including intake appointments and a vocational plan, developed over the phone with accommodations and my caseworker. While I am eligible to receive services immediately, I am in the exploration phase of my vocational plan because of the in-home assessments still being on hold due to COVID-19. What in-home assessments look like during COVID-19 and remote home employment opportunities is a new area for me and DORS. It is still a learning process and I hoped I would be further along in the process, but I am looking forward to moving forward and for future vocational opportunities.

My hope has also grown through the increased access to remote mental health resources, art and writing opportunities, community connections, and support services. There has been much progress, but there is still work that needs to occur in providing equitable, accessible, inclusive employment opportunities and environments. I will continue to move forward, fighting for the chance to gain equitable employment opportunities that let me use and grow my skills and talents.


Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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Reflecting on ADA 30 While Reckoning with COVID-19 and Racism

Illustration of a pink megaphone with yellow lightning shaped soundwaves coming out of it, on a teal background.

Content note: includes mentions of COVID-19 and police brutality toward Black people


2020 brought us the COVID-19 pandemic and shed a stark light on the pandemic of racism. The impact of both these pandemics continues to grow and serve as reminders of centuries of slavery, oppression, violence, and discrimination. This year also marks the 30th anniversary of the Americans with Disabilities Act (ADA). In response, conversations at all levels about equity, diversity, and inclusion are addressing the challenges, barriers, and practices that deny civil rights protections put into place decades ago. But these conversations are still occurring separately in many ways, primarily with a focus on 1) anti-racism, diversity, and equity or 2) accessibility, inclusion, and equity. While having these conversations is extremely important and necessary, it also leaves me questioning what happens when you have someone like me who belongs to more than one marginalized group.

As a biracial black transman with multiple disabilities who has been able to serve as a human service professional and advocate for over 15 years, I have had the privilege to take part in conversations across many different platforms, tables, and organizations seeking to promote change. This especially became the case over the past 5 years with the rise in different local organizations and companies seeking to improve their diversity and inclusion programming and practices. I found myself receiving many invitations to be a part of these conversations in a guest speaker format for various Diversity, Equity, & Inclusion committees.

In the beginning, when accepting these invitations, I discovered that even as committee members shared with me how they are working to create a welcoming and affirming space, I had to navigate accessibility issues connected to physical layout, communication methods, and cognitive and sensory barriers. I also often had to navigate being the only person of color and the only person with a disability, fighting stigmas and stereotypes while answering questions on my race or disability. I was then praised about how resilient I was, told to keep pushing forward, and thanked graciously for providing a much-needed perspective. These experiences made me feel isolated and like a box on a checklist. I noticed an adverse impact on my self-image and mental health after guest speaking, so I started asking questions whenever I was approached to help determine whether I was a checkbox invite.

A shift in these conversations and advocacy opportunities happened as the two pandemics began to come to a head. First, the conversations around accessibility, inclusion, and equity rose in response to COVID-19 stay at home orders and panic around how to provide accessible distance learning, services and programs, and access to care and resources for individuals with disabilities of all ages. Second, in the wake of George Floyd’s murder, conversations, protests, and calls for action connected to diversity, anti-racism, and equity filled the air. Two pandemics were colliding.

Many people like me have been navigating both pandemics as one because of our intersecting identities. Navigating life as a multi-marginalized person during these times in a society full of ableism and racism among other forms of discrimination has provided a lens into why intersectionality must play a role in these conversations and plans all for change.

The Center for Intersectional Justice explains that one key aspect of recognizing intersectionality is “fighting discrimination within discrimination, tackling inequalities within inequalities, and protecting minorities within minorities.” If conversations about equity are not considering the intersecting identities of those involved in the planning and decision making individually and as a collective, then the question comes into play of whether equity can exist. The same holds true for conversations about accessibility and inclusion.

As these conversations continue to evolve, expanding our understanding of how ableism and racism play a role is a valuable asset. It all reminds me to reflect, to advocate, to seek growth and change into a world that will be equitable, accessible, and inclusive for all people. I envision a world that considers each part within the wholeness of an individual at all points of the lifespan. A world in which anti-racism and anti-ableism are a natural part of training, education, professionalism, and everyday interactions. We’ve come a long way in the past 30 years since the passage of the ADA and in discussions of COVID-19 and racism, but we still have a lot more work to do as we continue to fight and advocate for change, justice, equity, inclusion, accessibility, and more.

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Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

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Finding and Reclaiming Who I Am: a Biracial Black Transgender Man with Multiple Disabilities

An overhead view of a crowd gathered for a protest

Content note: includes discussion of COVID-19, police brutality toward Black people, murder of unarmed Black people, transphobia


A photo of Kris McElroy and his wife.
The author and his wife.

As I was moving my arms back and forth next to my wife in our very first protest, chanting Black Lives Matter, two beautiful strong brown-skinned African Americans in the midst of COVID-19 and racism pandemics, I was overwhelmed with thoughts and emotions. I was thankfully reflecting on the opportunity to participate in a protest that meant so much to me as an outlet to reclaim my identity as a strong, talented, biracial black transgender man with multiple disabilities. Reflecting on how much I had to fight to get to this point and how much I will continue to fight to end systemic racism, oppression, and marginalization. Reflecting on how rare and challenging it is to be able to be authentically present in the totality of who I am with all of my intersecting identities while advocating for justice and change. Each identity informing the other and each experiencing its own oppression that when combined have created a complex convergence of marginalization and oppression.

Reflecting on Who I Am

In the wake of the death of George Floyd, Ahmaud Arbery, Breonna Taylor, and Tony McDade, there are not enough words to describe the heaviness, pain, sadness, fear, anger, and more. Watching and reading the news has been another lived reminder that I and my family and other black and brown friends and communities know daily of what it means to live in a society with deeply embedded covert and overt racism. My identity as a biracial black man with multiple disabilities was formed with this understanding at a young age. I grew up attending predominantly white schools and I experienced the fall-out of family relations leading to estrangement due to my parents marrying outside of their race and having children. The racial trauma and data of what it meant to be black and brown in our society was passed down to me from my grandmother, mother, and our family. At the same time, racial slurs, maltreatment, microaggressions, and discrimination were being dished out in our neighborhood, communities, and schools. This racial trauma interacted with growing up with multiple disabilities in a community without much accessibility and full of ableism. I also experienced the slurs, maltreatment, microaggressions, and discrimination in the context of my disabilities. Then, when I got older and came out as transgender, all the same happened.

I internalized and wrestled with the consistent messages that I was an abomination just because my parents got married and decided to have a child. I internalized the consistent messages that my physical disabilities were the punishment for that and an everyday reminder of the proof for the messages of who and what others claim I am. Both my peers and adults treated me as though both the color of my skin and my physical and developmental disabilities made me less than human. When I tried to fight against those messages I was shut down in various ways, and when I expressed my voice it was unheard, filtered, and changed. Trying to advocate for myself was shut down by those that viewed me as unable and by those that meant well and thought they knew what was best for me.

Because of these experiences and more, there was not a place I felt safe in or a place where I knew I could be myself and be loved unconditionally until recently. This became a complex, deep lens through which my identity developed around my race and disabilities. I took the complex convergence of marginalization and oppression I experienced and internalized it because that was all I knew. I didn’t have anything or anyone to really counter it by offering different data or support navigating it. I wish I had that earlier in my life, but I am thankful for the therapy and work I have done, including my advocacy work, to get to know myself and merge these once very separate identities into one, while fighting for change.

A New Lease on Life Through Reclaiming My Identity

It was a surreal moment to be back in that community I grew up in that was a source of so much pain and part of so much that needed healing. To be in that community with my wife at a protest for George Floyd and the black lives lost to police and other racial-based violence against black and brown individuals. It was very emotional, still inexpressible by words, to see all the crowds, hear the speeches, march in protest and gather because the violence needs to end. It should not be a crime and death sentence to be born black in the United States. All Black Lives Matter.

It took me a long time to include myself in believing that my life also mattered when I say “All Black Lives Matter” as a brown skinned biracial black man who is also transgender with multiple disabilities. These three parts of my identity never really blended well together and rarely received messages of kindness, worth, love, and value. Rather they received the opposite which assisted in the development of self-hatred and truly believing I was an abomination and a mistake while growing up and into adulthood because of 1) being black and biracial 2) being a transgender man and 3) having multiple disabilities.

This self-hatred impacted how I interacted with myself and the world around me, including participating in advocacy work in and around my community. Often, my advocacy work itself existed in each of these identity communities without much mention of the other. It was like being seen by my race while my gender and disabilities were not acknowledged or didn’t have a place, and the same would occur when it came to interacting with groups focused on ableism and gender identity. Not feeling like I was being seen as a whole person or that anyone understood the marginalization and oppression I experienced in relation to the other parts of who I am created an isolating feeling.

Photo of a crowd at a protest, under lush green trees.
Protest photo courtesy of the author.

So, something changed that day for me rolling in my wheelchair next to my wife during our very first protest. I was reclaiming my identity, power, and value on my own terms. I was participating for George Floyd, Breonna Taylor, Ahmaud Arbery, Tony McDade, and all black and brown people including the millions of those who have lost their lives to violence including police violence and hate crimes, social injustice due to lack of equity and access to quality services, living conditions, and medical care/treatment, and more. I was participating for my family and friends. I was participating for accountability and social justice. I was participating for myself. I was fighting so that all parts of who I am may be authentically free to live fully – out and proud. Fighting so that all people may have the opportunity to live as their authentic selves safely, equally, and freely in all aspects of everyday life.

I was fighting because All Black Lives Matter. Because systemic racism needs to change. Systemic oppression needs to change. Reclaiming who I am by saying that I am not an abomination. I am not a mistake. I am not less than, not according to my race, my gender, or my disabilities. I have worth and value. I am human. I am irreplaceable. I matter. My life matters. All of who I am matters. This always has been true of me and every black and brown life. What will always remain true is that All Black Lives Matter period without any questions or conditions. This includes who I am in all its complex beauty as a biracial black transgender man with multiple disabilities.


Rooted in Rights exists to amplify the perspectives of the disability community. Blog posts and storyteller videos that we publish and content we re-share on social media do not necessarily reflect the opinions or values of Rooted in Rights nor indicate an endorsement of a program or service by Rooted in Rights. We respect and aim to reflect the diversity of opinions and experiences of the disability community. Rooted in Rights seeks to highlight discussions, not direct them. Learn more about Rooted In Rights

Click here to pitch a blog post to Rooted in Rights.