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Renegades: Brad Lomax - Watch the documentary now | American Masters | PBS
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Brad Lomax: Creating Communities of Care

Premiere: 10/29/2024 | 00:10:19 |

The story of a Black Panther Party member and founder of the East Oakland Center for Independent Living, who had multiple sclerosis and used a wheelchair. Explore Brad Lomax’s under-reported contributions to the early disability justice movement, which laid the groundwork for the 1990 Americans with Disabilities Act.

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About the Episode

Brad Lomax (1950-1984) was a civil rights and disability rights leader who had multiple sclerosis and used a wheelchair.

He was a member of the Black Panther Party and a founder of the East Oakland Center for Independent Living in the 1970s, an organization focused on assisting people with disabilities to live on their own, rather than with family or in institutions.

A room of mixed raced people, many of whom are in wheelchairs or otherwise sitting. Photo is in black and white

Brad Lomax in a wheelchair at the 504 sit-in in San Francisco in 1977.

An experienced organizer, Lomax also built a Black Panther health clinic in DC and was in charge of the first aid tent at the Black Panther Convention and at the 1972 African Liberation parade. Lomax was one of the key protesters during the historic 26-day 504 sit-in at the Federal Building in San Francisco in 1977, which demanded the government enforce regulations for Section 504 of the Rehabilitation Act, to prohibit discrimination of people with disabilities. He brought in the Black Panther Party to feed the protestors, which many credit for the success of the sit-in. The sit-in resulted in entities receiving federal funds being required to make their programs and spaces accessible, and paved the way for the 1990 Americans with Disabilities Act. Despite his pivotal role in the disability justice movement, the story of Brad Lomax is largely overlooked, and descriptions of the Black Panther Party’s alliance with the 504 demonstrators rarely mention Lomax’s previous work in civil rights and disability justice, and his coalition building efforts.

The episode features interviews with: Glenn Lomax, Lomax’s brother; Corbett O’Toole, disability rights advocate and a contemporary of Lomax who participated with him in the 504 sit-in; Cara Reedy, Director of the Disabled Journalists Association; Sami Schalk, Ph.D., Associate Professor in the Department of Gender & Women’s Studies at the University of Wisconsin-Madison, whose book Black Disability Politics provides scholarship and perspective on Brad Lomax’s life and legacy.

About Renegades

Renegades is a series of five 12-minute short films showcasing the lives of diverse, lesser-known historical figures with disabilities, exploring not only their impact on and contributions to U.S. society, but also the concept of disability culture, which honors the uniqueness of disability. Hosted and narrated by the musician and disability rights advocate Lachi, who is blind, and created and produced by a team of D/deaf and disabled filmmakers, the series is designed to increase public knowledge of disability history, and encourage cross-cultural understanding between non-disabled people and those with disabilities – who make up 1 in 4 adults in America today.

Infused with the spirit of the disability movement’s mantra, “Nothing About Us Without Us,” Renegades places a focus on authentic storytelling, with a cast and crew composed almost entirely of disabled people, and a talent incubator model of filmmaking to mentor emerging directors, producers, writers, cinematographers, and editors with disabilities.

About the filmmakers

Markus Essien is the director and producer of Renegades: Brad Lomax. With a diverse and accomplished career in filmmaking, theater, music, and education, he is a creative force driven by passion and purpose. His journey in film has seen him contribute to both feature and short films, culminating in his recent role as the writer and  director of a forthcoming film Teranga: An African Homecoming. Beyond filmmaking, he has left his mark on the stage, directing the U.S. premiere of “The Occurrence at Owl Creek Bridge” and the New York premiere of “Philomel” for Opera Works. A multifaceted artist, Essien is also the founder and bassist of the Equity and Social Justice Quartet, an ensemble dedicated to raising awareness and funds for non-profit organizations. Notably, he composed the theme for Jeffrey Robinson’s podcast, “Who We Are.” In education, Essiens brings over two decades of experience as a teacher and leader. His expertise has been sought by prominent organizations globally, including Chan Zuckerberg, Supporting Emotional Needs of the Gifted, Gifted Institute (Denmark), Kind en Beeld, and African Leadership Group. Currently, Essien is shaping the future of filmmaking through an incubator program with FWD-Doc for filmmakers with disabilities. His journey is a testament to the transformative power of creativity, education, and advocacy.

Cara Reedy is the writer and producer of Renegades: Brad Lomax. She is the founder and Director of the Disabled Journalists Association, a member organization of Storyline Partners. She is a journalist and producer who spent ten years of her career at CNN producing documentaries as well as writing for various verticals including Eatocracy and CNN Business. In 2019, she produced her most recent short doc for The Guardian entitled Dwarfism and Me, which was an exploration of the treatment of Dwarfs in American society. Reedy has spent the last three years studying disability and its coverage in the media. Along the way, she has had the opportunity to teach disability reporting in newsrooms. She also works in narrative change in the film and TV industry and is a member of the TV Academy Diversity Committee. Reedy is a mentor in the Disability Justice Project fellowship program which trains disabled disability rights advocates in the Global South how to be journalists. She is an avid fan of the St. Louis Cardinals and spends her time between NYC and St. Louis.

Original artwork for Renegades by Adriano Araújo dos Reis Botega.

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PRODUCTION CREDITS

Renegades is a production of Inspiration Films, LLC and ITVS in association with American Masters Pictures. For Inspiration Films Charlotte Mangin is executive producer, Day Al-Mohamed is senior producer, and Amanda Upson is series producer. For ITVS Carrie Lozano is executive producer and Susan Cohen is supervising producer. For American Masters Michael Kantor is executive producer.

About American Masters
Now in its 39th season on PBS, American Masters illuminates the lives and creative journeys of those who have left an indelible impression on our cultural landscape—through compelling, unvarnished stories. Setting the standard for documentary film profiles, the series has earned widespread critical acclaim: 28 Emmy Awards—including 10 for Outstanding Non-Fiction Series and five for Outstanding Non-Fiction Special—two News & Documentary Emmys, 14 Peabodys, three Grammys, two Producers Guild Awards, an Oscar, and many other honors. To further explore the lives and works of more than 250 masters past and present, the American Masters website offers full episodes, film outtakes, filmmaker interviews, the podcast American Masters: Creative Spark, educational resources, digital original series and more. The series is a production of The WNET Group.

American Masters is available for streaming concurrent with broadcast on all station-branded PBS platforms, including PBS.org and the PBS app, available on iOS, Android, Roku streaming devices, Apple TV, Android TV, Amazon Fire TV, Samsung Smart TV, Chromecast and VIZIO. PBS station members can view many series, documentaries and specials via PBS Passport. For more information about PBS Passport, visit the PBS Passport FAQ website.

About The WNET Group

The WNET Group creates inspiring media content and meaningful experiences for diverse audiences nationwide. It is the community-supported home of New York’s THIRTEEN – America’s flagship PBS station – WLIW, THIRTEEN PBS KIDS, WLIW World and Create; NJ PBS, New Jersey’s statewide public television network; Long Island’s only NPR station WLIW-FM; ALL ARTS, the arts and culture media provider; newsroom NJ Spotlight News; and FAST channel PBS Nature. Through these channels and streaming platforms, The WNET Group brings arts, culture, education, news, documentary, entertainment, and DIY programming to more than five million viewers each month. The WNET Group’s award-winning productions include signature PBS series Nature, Great Performances, American Masters, and Amanpour and Company and trusted local news programs like NJ Spotlight News with Briana Vannozzi. Inspiring curiosity and nurturing dreams, The WNET Group’s award-winning Kids’ Media and Education team produces the PBS KIDS series Cyberchase, interactive Mission US history games, and resources for families, teachers and caregivers. A leading nonprofit public media producer for more than 60 years, The WNET Group presents and distributes content that fosters lifelong learning, including initiatives addressing poverty, jobs, economic opportunity, social justice, understanding, and the environment. Through Passport, station members can stream new and archival programming anytime, anywhere. The WNET Group represents the best in public media. Join us. 

UNDERWRITING

Major funding for Renegades is provided by The Corporation for Public Broadcasting, with additional support from the Rosalind P. Walter Foundation, Anderson Family Charitable Fund, Philip & Janice Levin Foundation, Ambrose Monell Foundation, Kate W. Cassidy Foundation, The Charina Endowment Fund, Marc Haas Foundation, and Sue and Edgar Wachenheim III.

Logo for the Corporation for Public Broadcasting

ACCESSIBLE DESCRIPTIVE TRANSCRIPT

[Visual and sound descriptions: Upbeat instrumentals play over a black and white flash photo at a crowded party, Brad Lomax sits in a wheelchair looking up to the camera with a cocked head and a bright, relaxed smile. Brief commentary plays over archival photographs by individuals not yet introduced.]

– He was so intelligent and truthful. His persona projected that.

– Brad Lomax was one of those people that, as Black disabled people, we always saw his picture, but we never really knew who he was.

– Right.

– When we look at history of disability rights organizing, we see, of course, that there are a lot of white folks at the forefront. Brad Lomax was dedicated to the work and not the limelight.

[A tender piano melody begins, the Renegades theme song. Lachi walks with a white cane, wearing a tailored sky blue suit and a high ponytail. Text on screen reads: Renegades, Brad Lomax. Creating Communities of Care.]

Lachi: One in four American adults have a disability, and I’m one of them. I’m Lachi, I’m a recording artist and disability culture advocate, and I’m here to introduce you to disabled renegades.

Theme lyrics: ♪ I face each day as a renegade ♪

[Now, Lachi enters the doors of the Ed Roberts Campus, floor to ceiling windows adorn multiple levels of the tall modern building. Lachi ascends a spiral ramp pathway inside the building. Soft, groovy instrumentals begin.]

Lachi: I’m sitting here at the Ed Roberts Building, one of the most accessible buildings in the nation, and we’re going to be talking about Brad Lomax.

[Pictures and footage in black and white: A young Lomax and protest footage. Helmeted policemen walk in formation, protesters flood city streets.]

Lachi: Born in 1950, Lomax grew up in North Philadelphia during the height of the civil rights movement. Like many Black families, the Lomax family faced redlining, economic segregation, and police violence, all of which would shape his future work.

Cara Reedy, Director, Disabled Journalists Association: His mom was on the Poor People’s March with MLK, and they were just taught that we were supposed to be active in the world. We were supposed to be out making a difference.

Lachi: Right, in the family.

Reedy: When he was in high school, he went off down in the country and dug wells in impoverished communities. He was a football player, was in school plays.

Lachi: An active kid.

Reedy: Yes.

[Continued archival photographs: Lomax in a top hat, Lomax in a graduation cap. A rally poster for the Black Panthers, another poster detailing the Revolutionary Intercommunal Day of Solidarity for a list of individuals including Angela Davis. Groovy instrumentals continue.]

Lachi: In 1967, Lomax graduated from Benjamin Franklin High School and soon enrolled in Howard University, where he joined the Black Panther Party. Founded the year before, the Black Panthers were a paramilitary organization that advocated for self-defense and community empowerment, and fought against systemic discrimination. Lomax’s membership caught the attention of the FBI, whose files are one of the only written sources of information about his life. Around that time, Lomax was diagnosed with multiple sclerosis, also known as MS, a chronic immune disease of the central nervous system. MS affects both the brain and spinal column.

Reedy: In late high school, he started falling and went to the doctor and found out he had MS.

Lachi: When most people think of the Black Panthers, they think of guns and militants, but there’s a lot more to it, isn’t there?

Reedy: What we know from Brad’s FBI file, most of his days were spent building a health clinic in DC, a free health clinic for the neighborhood. He was in charge of the first aid tent at the Black Panther Convention, also at the African Liberation Parade. So he was always involved in making sure that people were healthy and had access to healthcare.

[Archival photographs and footage continue to accompany narration, slice of life footage of men walking down the street in 1970s Oakland, California.]

Lachi: In 1973, his brother Glenn convinced Lomax to move to Oakland, California, the epicenter of the Black Panther world.

Glenn Lomax, Lomax’s Brother: The Panthers, we were dealing with a lot of social issues, the breakfast program, free busing to prison, these different programs, but we had nothing for disabled people. And that’s what Brad jumped on.

Corbett Joan O’Toole, Disability Rights Advocate: I feel like there’s a history there that doesn’t typically get told. The Center for Independent Living was supposed to cover Northern Alameda County, so Berkeley and Oakland primarily, but they covered Berkeley, and they kind of stopped there.

Lachi: The Center for Independent Living in Berkeley was the very first organization focused on assisting people with disabilities to live on their own, rather than with families or in institutions.

[A superimposed graphic shows a man in a wheelchair. A protest sign reads: Civil Rights for Disabled. Typewriter font reads: Center for Independent Living, Berkeley, CA. Established by Ed Roberts, 1972. Upbeat instrumentals play.

OToole: The environment was very much focused only on white disabled people, primarily only on the issues relevant to white disabled men. So Brad came in and said, “There’s this entire population of disabled people of color that you are not serving.”

Lachi: So Lomax opened a center of his own in Oakland, with support from the Black Panthers.

[A superimposed graphic shows a photo of Brad Lomax holding a microphone. Typewriter font reads: Center for Independent Living, Oakland Satellite Office. Established by Brad Lomax 1975.]

Reedy: From 1975 to 1977, he ran a Center for Independent Living in East Oakland.

Lachi: And this was a center that was servicing a generally Black area?

Reedy: Correct.

[A black and white photograph of a young Lomax in the 1970s. Brief protest footage of protesters moving in a circle and holding signs. Then, a copy of the Rehabilitation Act of 1973. A highlighted component of the document reads: Sec. 504. No otherwise qualified handicapped individual in the United States, as defined in section 7(6), shall, solely by reason of his handicap, be excluded from the participation in, be denied the benefits of, or be subjected to discrimination under any program or activity receiving Federal financial assistance.]

Glenn Lomax: We saw the barriers and obstacles people had to deal with to get to where they needed to get to, whether it was in the hospital, in an apartment, or just going down the sidewalk. They’re going to have to accommodate, because that’s what they should do.

Lachi: In 1973, Congress had passed the Rehabilitation Act, the first major U.S. law to prohibit discrimination of people with disabilities. But few actions had been taken to implement Section 504. In response, on April 5th, 1977, hundreds of people with disabilities occupied federal buildings in major cities nationwide. However, protests were shut down one by one, as the protestors were removed from or starved out of the buildings. Lomax not only joined the sit-in at the Health Education and Welfare federal building in San Francisco, but also convinced the Black Panther Party to get involved.

[In archival footage, a group shouts “Sign 504!” in unison. Upbeat instrumentals continue. A newspaper title reads: Handicapped Rally – Sign 504 Now!]

Glenn Lomax: Because he had that smile and calm demeanor, you know, you’d have to listen to him. The love in him just came out. He was intelligent enough to convince that this needed to be done, and they couldn’t stop him even if they wanted to.

[Lachi stands outdoors.]

Lachi: This is the federal building where the sit-in took place for 26 days, where Brad made the greatest impact towards social change.

[Archival footage of the federal sit-in: A diverse group of people with varying identities and disabilities join together around a table filled with food.]

OToole: The Black Panthers came every day and fed us every day for the whole sit-in, and that’s really quite frankly how we survived. We wouldn’t have survived without food from them.

Lachi: So with this 504 sit-in, the Black Panthers brought more than just meatloaf and chicken, didn’t they?

Reedy: The Black Panther newspaper brought national coverage to the 504 sit-in. The national news wasn’t covering it, but the Black Panthers were.

[Calm, yet positive instrumentals play. Newspaper titles read: Handicapped Protest. Handicapped Win Demands – End H.E.W. Occupation. Pressure Forces Califano To Sign 504 Regulations.]

OToole: I was part of the group that was inside the building. I happened to run into them in the hall and I said, “Can I ask you a question? I don’t get why you’re doing this. It’s like a whole bunch of white people. Like, why?” And he said, “Because you’re fighting for social justice. We’re going to support people who are going to fight to change the system. And your willingness to put your lives in this building is something we want to support. And Brad is here, and the organization was supporting Brad. If the Black Panthers think that this is an important struggle, that’s what we’re going to do.”

Lachi: The sit-in convinced the government to finally implement the accessibility requirements of Section 504, and paved the way for the 1990 Americans with Disabilities Act.

Sami Schalk, Ph.D., Author, Black Disability Politics: We can clearly see with Brad Lomax and with the Panthers that there were already folks doing this expansive thinking about the relationship between all these systems of oppression and between all oppressed people, and committed to doing the work right then and there.

[A soulful melody begins of continued protest footage, including those celebrating the aftermath of the 504 sit-in.]

Schalk: They were seeing that in their alignment with women’s rights and with gay rights. And so it was really easy for them to then apply that to disabled folks.

Song lyrics: ♪ You just don’t love me the same ♪

Schalk: Labor of the coalition work really starts with making direct human connections with one another. So I think that Brad’s labor of just consistently connecting with the Center for Independent Living and making sure that the Panthers’ buildings had wheelchair access. They were doing these things that I think get really erased from the history of the Panthers.

Lachi: Do you know anything more about Brad after the sit-in?

Reedy: He continued working as a Panther in a health clinic, but at some point he was not able to work.

Lachi: Right.

Reedy: The MS had taken over.

Lachi: Mm-hmm.

Reedy: But he was still living in a Panther abode. His brother had to go get him.

Glenn Lomax: He was getting mentally incapacitated around that time, ’79, so he didn’t really know what was going on.

Lachi: In the last years of his life, Lomax’s family cared for him at home. He died in 1984 from complications of his MS. What is Brad Lomax’s legacy?

[A photograph of Lomax posing and smiling on a couch with five family members.]

Reedy: He was the beginning of disability justice, because of his work with the Black Panthers intersecting Blackness with disability. He was already there and all of the people that are working on it now, we’re all his children continuing that work.

Schalk: I think the bridge work that so many of us that are multiply marginalized and live within multiple marginalized communities, that we are often connecting these communities to save ourselves, but also to recognize the way that working together is the only way that we can save all of our communities.

[Bright instrumentals chime over a superimposed collage of protest photographs, with a smiling Lomax in the center. Credits roll over tender guitar theme song instrumentals, with Glenn Lomax featured on the right side of the screen.]

Glenn Lomax: He departed this life on August 28th, 1984. He was born in Philadelphia, Pennsylvania. He later attended Howard University in Washington DC, where he became interested in community programs. Although he was being destroyed by multiple sclerosis, a crippling disease, he remained involved in the struggle of helping others. Through his trials, he became noted for his trademark, which was his smile. Your fight is over, Brad. We loved you, but God loved you best.

[Logos for Inspiration films. ITVS. American Masters. PBS. Episode ends.]

TRANSCRIPT

[Upbeat instrumentals] - He was so intelligent and truthful.

His persona projected that.

- Brad Lomax was one of those people that, as Black disabled people, we always saw his picture, but we never really knew who he was.

- Right.

- When we look at history of disability rights organizing, we see, of course, that there are a lot of white folks at the forefront.

Brad Lomax was dedicated to the work and not the limelight.

[Tender piano] - One in four American adults have a disability, and I'm one of them.

I'm Lachi, I'm a recording artist and disability culture advocate, and I'm here to introduce you to disabled renegades.

♪♪ I face each day as a renegade ♪ I'm sitting here at the Ed Roberts Building, one of the most accessible buildings in the nation, and we're going to be talking about Brad Lomax.

[Soft groovy instrumentals] Born in 1950, Lomax grew up in North Philadelphia during the height of the civil rights movement.

Like many Black families, the Lomax family faced redlining, economic segregation, and police violence, all of which would shape his future work.

- His mom was on the Poor People's March with MLK, and they were just taught that we were supposed to be active in the world.

We were supposed to be out making a difference.

- Right, in the family.

- When he was in high school, he went off down in the country and dug wells in impoverished communities.

He was a football player, was in school plays.

- An active kid.

- Yes.

[Lachi]: In 1967, Lomax graduated from Benjamin Franklin High School and soon enrolled in Howard University, where he joined the Black Panther Party.

Founded the year before, the Black Panthers were a paramilitary organization that advocated for self-defense and community empowerment, and fought against systemic discrimination.

Lomax's membership caught the attention of the FBI, whose files are one of the only written sources of information about his life.

Around that time, Lomax was diagnosed with multiple sclerosis, also known as MS, a chronic immune disease of the central nervous system.

MS affects both the brain and spinal column.

- In late high school, he started falling and went to the doctor and found out he had MS. - When most people think of the Black Panthers, they think of guns and militants, but there's a lot more to it, isn't there?

- What we know from Brad's FBI file, most of his days were spent building a health clinic in DC, a free health clinic for the neighborhood.

He was in charge of the first aid tent at the Black Panther Convention, also at the African Liberation Parade.

So he was always involved in making sure that people were healthy and had access to healthcare.

[Groovy instrumentals continue] [Lachi]: In 1973, his brother Glenn convinced Lomax to move to Oakland, California, the epicenter of the Black Panther world.

- The Panthers, we were dealing with a lot of social issues, the breakfast program, free busing to prison, these different programs, but we had nothing for disabled people.

And that's what Brad jumped on.

- I feel like there's a history there that doesn't typically get told.

The Center for Independent Living was supposed to cover Northern Alameda County, so Berkeley and Oakland primarily, but they covered Berkeley, and they kind of stopped there.

[Lachi]: The Center for Independent Living in Berkeley was the very first organization focused on assisting people with disabilities to live on their own, rather than with families or in institutions.

- The environment was very much focused only on white disabled people, primarily only on the issues relevant to white disabled men.

So Brad came in and said, "There's this entire population of disabled people of color that you are not serving."

[Upbeat instrumentals] [Lachi]: So Lomax opened a center of his own in Oakland, with support from the Black Panthers.

- From 1975 to 1977, he ran a Center for Independent Living in East Oakland.

- And this was a center that was servicing a generally Black area?

- Correct.

- We saw the barriers and obstacles people had to deal with to get to where they needed to get to, whether it was in the hospital, in an apartment, or just going down the sidewalk.

They're going to have to accommodate, because that's what they should do.

[Lachi]: In 1973, Congress had passed the Rehabilitation Act, the first major U.S. law to prohibit discrimination of people with disabilities.

But few actions had been taken to implement Section 504.

In response, on April 5th, 1977, hundreds of people with disabilities occupied federal buildings in major cities nationwide.

However, protests were shut down one by one, as the protestors were removed from or starved out of the buildings.

Lomax not only joined the sit-in at the Health Education and Welfare federal building in San Francisco, but also convinced the Black Panther Party to get involved.

[Upbeat instrumentals] - Because he had that smile and calm demeanor, you know, you'd have to listen to him.

The love in him just came out.

He was intelligent enough to convince that this needed to be done, and they couldn't stop him even if they wanted to.

- This is the federal building where the sit-in took place for 26 days, where Brad made the greatest impact towards social change.

- The Black Panthers came every day and fed us every day for the whole sit-in, and that's really quite frankly how we survived.

We wouldn't have survived without food from them.

- So with this 504 sit-in, the Black Panthers brought more than just meatloaf and chicken, didn't they?

- The Black Panther newspaper brought national coverage to the 504 sit-in.

The national news wasn't covering it, but the Black Panthers were.

- I was part of the group that was inside the building.

I happened to run into them in the hall and I said, "Can I ask you a question?

I don't get why you're doing this.

It's like a whole bunch of white people.

Like, why?"

And he said, "Because you're fighting for social justice.

We're going to support people who are going to fight to change the system.

And your willingness to put your lives in this building is something we want to support.

And Brad is here, and the organization was supporting Brad.

If the Black Panthers think that this is an important struggle, that's what we're going to do."

[Lachi]: The sit-in convinced the government to finally implement the accessibility requirements of Section 504, and paved the way for the 1990 Americans with Disabilities Act.

- We can clearly see with Brad Lomax and with the Panthers that there were already folks doing this expansive thinking about the relationship between all these systems of oppression and between all oppressed people, and committed to doing the work right then and there.

[Soulful melody] They were seeing that in their alignment with women's rights and with gay rights.

And so it was really easy for them to then apply that to disabled folks.

♪♪ You just don't love me the same ♪ - Labor of the coalition work really starts with making direct human connections with one another.

So I think that Brad's labor of just consistently connecting with the Center for Independent Living and making sure that the Panthers' buildings had wheelchair access.

They were doing these things that I think get really erased from the history of the Panthers.

- Do you know anything more about Brad after the sit-in?

- He continued working as a Panther in a health clinic, but at some point he was not able to work.

- Right.

- The MS had taken over.

- Mm-hmm.

- But he was still living in a Panther abode.

His brother had to go get him.

- He was getting mentally incapacitated around that time, '79, so he didn't really know what was going on.

[Lachi]: In the last years of his life, Lomax's family cared for him at home.

He died in 1984 from complications of his MS. What is Brad Lomax's legacy?

- He was the beginning of disability justice, because of his work with the Black Panthers intersecting Blackness with disability.

He was already there and all of the people that are working on it now, we're all his children continuing that work.

- I think the bridge work that so many of us that are multiply marginalized and live within multiple marginalized communities, that we are often connecting these communities to save ourselves, but also to recognize the way that working together is the only way that we can save all of our communities.

[Chiming instrumentals] - He departed this life on August 28th, 1984.

He was born in Philadelphia, Pennsylvania.

He later attended Howard University in Washington DC, where he became interested in community programs.

Although he was being destroyed by multiple sclerosis, a crippling disease, he remained involved in the struggle of helping others.

Through his trials, he became noted for his trademark, which was his smile.

Your fight is over, Brad.

We loved you, but God loved you best.

[Tender guitar instrumentals] [Clap]

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