Our guest today, Philip Brubaker, notes that there’s unfortunately a real stigma around mental illness, and that needs to change. Philip is an internationally known and recognized filmmaker and videographic essayist. He also has bipolar disorder. In his most recent film, “How To Explain Your Mental Illness to Stanley Kubrick,” Philip tackles head on the often negative depictions of mental illness in Twentieth Century cinematography. In this deeply personal film, he juxtaposes his own journey with bipolar disorder with images from iconic films that show characters with mental illness as violent and suicidal. In the film, Philip challenges a manifestation of Stanley Kubrick to confront the way Kubrick portrayed mental illness and the effects those portrayals had on society.

This is not Philip’s first film on the subject of mental illness. His 2009 documentary, “Brushes With Life: Art, Artists and Mental Illness,” won multiple awards and was aired on public television. His work has been featured in the Adelio Ferrero Film Festival, the Mental Filmness Festival in Chicago, and the FILMADRID Festival in Madrid, Spain.

We’re joined today by Nicole Luongo, an advocate, author, and public speaker who has Cerebral Palsy. In 2019, Nicole started The Go Green for CP campaign to raise awareness for cerebral palsy in this country and around the world. Through her leadership, the campaign succeeded in getting at least one building or landmark in almost every state lit up in green on National Cerebral Palsy Awareness Day on March 25th and on World CP Day on October 6th. In 2021, she launched a campaign to have the White House light up in Green annually on March 25th. She also created the social media campaign What CP Looks Like.

Nicole is the author of Naked Desires, a book of poetry that chronicles her quest and challenges to find true love. She is a fitness enthusiast and has encouraged others to enjoy fitness and get moving, reshaping our notion of what fitness looks like.

Today, we are joined by two outdoor enthusiasts and avid hikers, Chris Layne and Daniel Wilson. Both Chris and Daniel are wheelchair users. They work with support teams and use specialized equipment to hike trails that are anything but wheelchair accessible. Chris has hiked up Mt. Elbert, the highest peak in the Colorado Rockies. It’s over 14,000 feet. Daniel has traversed rugged trails in the Lake District National Park in Cumbria, England, which is a UNESCO World Heritage site.

Chris acquired her disability after a fall while hiking in her home state of Colorado in 2016, when a spinal cord injury left her paralyzed from the chest down. She went on to win the Ms. Wheelchair Colorado title in 2020, and she is both an active athlete and advocate for accessibility and inclusion in the outdoors and everywhere else.

Daniel became paralyzed after complications from spinal surgery following a fall down an escalator. After recovering, he became active in the British charity organization Sportability, which supports paralyzed athletes’ participation in sports – from archery and quad biking, to tennis and flying light aircraft. Now an experienced adaptive hiker, he competed in the Race The Sun fundraiser in the Lake District National Park.

We recorded our interview with Chris and Daniel in March, as Daniel was preparing to hike the West Highland Way trail in Scotland. Just this week, Daniel successfully completed that trail, along with ten support volunteers from around the world. Daniel is the first person in a wheelchair known to have successfully completed this historic 96-mile trail. He made the trek as a fundraiser for BackUp, a UK organization supporting people with spinal cord injuries.

Hospitals don’t generally sue patients for trespassing, but that is what happened to Alexis Ratcliff. Alexis is 18 years old and has lived in a hospital in Winston-Salem, North Carolina since she was 13. Last year, the hospital sued Alexis for trespassing to try and force her to move out. Alexis wants to leave the hospital, too, just not where the hospital wanted her to go. Alexis wants to live in her own home with support from caregivers. She wants to live close to family and friends. The hospital, Atrium Health Wake Forest Baptist, wanted to transfer Alexis to a nursing home in another state. Alexis, who won a full academic scholarship to a nearby college and started classes there this fall, is saying no.

On today’s episode of Disability Rap, we speak with Alexis Ratcliff. Alexis is a quadriplegic who uses a wheelchair to get around and a ventilator to help her breathe. She acquired her disability as a result of a car accident when she was 18 months old. We are also joined by Lisa Nesbitt. Lisa is a Supervising Attorney at Disability Rights North Carolina, and she’s part of the team working on Alexis’s case.

In honor of National Cerebral Palsy Awareness Month this March, FREED Center for Independent Living partnered with the California Department of Rehabilitation to host a live recording of the Disability Rap radio show and podcast. The show featured a panel discussion focusing on the transition from youth to adulthood for people with cerebral palsy. Our panelists shared their stories of growing up with CP and the choices, obstacles, and opportunities they faced as they entered the workforce. The panel was moderated by Ana Acton, former Executive Director of FREED and Host of Disability Rap, now the Deputy Director of the Independent Living and Community Access Division at the California Department of Rehabilitation.

Click here to watch the recording of the show.

Special thanks to Ana Acton and the California Department of Rehabilitation for their partnership in hosting this event with FREED!

On this Valentine’s Day, we’re joined once again by Dan and Viola Dwyer, creators of the YouTube channel The Ginchiest, for a conversation about what makes their relationship work, how they’d like to see disability and relationships portrayed in popular culture, and what still needs to be done for greater media representation and disability marriage equality.

When Dan was nine, he acquired a traumatic brain injury caused by a hit and run accident. Dan attended Widener Memorial School in Philadelphia with other children with disabilities. He then studied at Edinboro University, where he studied Political Science and pursued a career in government.

Viola was born with Spinal Muscular Atrophy (SMA), a genetic neuromuscular disease. She also attended Widener Memorial School in Philadelphia. Viola attended Johns Hopkins University where she studied Entrepreneurship and International Relations and pursued a career in financial services. After working in different roles in the financial services industry, Viola decided to return to school and earned an MBA from Duke University.

In honor of National Cerebral Palsy Awareness Month this March, FREED Center for Independent Living is partnering with the California Department of Rehabilitation to host a live recording of the Disability Rap radio show and podcast. The show will feature a panel discussion focusing on the transition from youth to adulthood for people with cerebral palsy. Our panelists will share their stories of growing up with CP and the choices, obstacles, and opportunities they faced as they entered the workforce. The panel will be moderated by Ana Acton, former Executive Director of FREED and Host of Disability Rap, now the Deputy Director of the Independent Living and Community Access Division at the California Department of Rehabilitation.

For more information and to register, go to https://www.disabilityrap.org/disability-rap-2024-03-live.

Today, we’re joined by Dr. Michael Alexander, retired Chief of Rehabilitation Services at the A.I. duPont Hospital for Children in Wilmington, Delaware. Dr. Alexander has a long history at duPont, starting when he first set foot in the hospital as a patient at age 12 after contracting polio. As a teenager, he spent summers as an inpatient at the duPont Hospital, forming relationships and community with other children with disabilities and with the doctors and nurses working there. With encouragement from the lead physician at duPont, he decided to go to medical school at the University of Virginia and enter the emerging field of Physical Medicine and Rehabilitation. After practicing in Ohio and Pennsylvania, Dr. Alexander returned to duPont, now the Nemours Children’s Hospital, as the Chief of Rehabilitative Medicine in 1986. He retired in 2013.

Dr. Alexander is a leader in the field of pediatric rehabilitation. While at duPont Hospital, he pioneered family-centered care, bringing families of children with disabilities into the discussions and planning of their medical care and rehab. He facilitated the transition at duPont from mostly providing inpatient care to focusing on outpatients, providing children with disabilities and diseases the care and supports they need to live at home and participate fully in their community.