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Paraplegic

Prepared by Daniel Dunaief

Brooke Ellison, 45, a pioneering disabilities advocate whose abilities with words and compassion far outdid her disability, died on Sunday, February 4.

Ellison was a tenured Associate Professor in the School of Health Professions in the Department of Health Sciences at Stony Brook University.

A resident of Stony Brook, Ellison was returning home from Murphy Junior High School as an 11-year old when she was struck by a car. The accident, which paralyzed her from the neck down, didn’t deter her budding academic interest or her ambitions.

As soon as she woke from the accident, she insisted she not fall behind in school.

With her mother Jean at her side throughout her education, Ellison became the first quadriplegic to graduate in 2000 from Harvard College, where she received magna cum laude honors in cognitive neuroscience and gave the class commencement speech.

Ellison earned a Master’s in Public Policy in 2004 from Harvard’s Kennedy School of Government and received her PhD in sociology from Stony Brook University in 2012.

A passionate advocate for accessibility and opportunity for the disabled, Ellison conducted research on the ethics and policy of science and health care.

Her mission “was to turn what happened to her into a [way to] help people who are handicapped achieve independence,” said Miriam Rafailovich, Distinguished Professor in Material Science and Engineering.
Ellison wrote two books about her life. The first, called “Miracles Happen” became a movie directed by Christopher Reeve titled “The Brooke Ellison Story.” More recently, Ellison published “Look Both Ways.”

Jean Ellison said her daughter felt her recent book was one of her most important contributions. Knowing she was in failing health after surviving three bouts with sepsis over the last year and a half, Brooke Ellison felt a sense of urgency to share her experiences.

“She poured out [her life] to the universe through this book,” said Jean Ellison.

While Ellison died young, she lived for over 33 years after the accident, which is well above the seven years the medical community expected at the time for someone on a ventilator.

‘Deep sadness’

Ellison served on several committees and boards, including the Board of the Directors of the New York Civil Liberties Union and the search committee for a president of Stony Brook.

In a letter to the campus community, President Maurie McInnis, who expressed her “deep sadness” for Ellison’s passing, recounted how Ellison was one of the first people she met on campus.

“Her legacy at Stony Brook and beyond is defined by passionate advocacy for inclusive education, healthcare and disability rights,” McInnis wrote in a letter to the campus community. “She helped alert me and others to our blind spots and offered many ideas for making this campus more inclusive and welcoming.”

Ellison was recently teaming up with students using drones and artificial intelligence images to map the topography of Stony Brook.

“To go from one building to the next looks like a straight pathway, but at the end, a one-inch drop, which is not encoded anywhere” could be a huge problem for someone in a wheelchair, said Rafailovich.

Ellison’s students asked her what she would want a robot near her that she could control to do. She suggested a hand she could control that could turn the pages of a book.

Ellison was working with the Federal Emergency Management Agency to ensure that people with disabilities who need power for ventilators or other equipment receive immediate attention after power disruption.

“She noticed during Hurricane Sandy that emergency workers had no idea where people who were on life support were during two weeks,” said Rafailovich.

Ellison was working with the state to get a new system where people on life support could receive help quickly.

Ellison had planned to do a fellowship at the Harvard Kennedy Carr Center for Human Rights Policy.

Caring for everyone

In addition to her focus on helping people with disabilities achieve independence, Ellison served in many capacities at Stony Brook, including as the Director of the Center for Community Engagement and Leadership Development.

Among her many efforts, Ellison also ran for election in 2006 for the New York State Senate, where she lost to republican incumbent John Flanagan.

Ellison was a committed educator who asked students before they met her in an ethics class to describe what they thought would make a life not worth living. Students suggested this would include not being able to do things they needed, needing care from someone else, or living on life support.

At the end of the semester, she asked the same question.

“They thought if they were on life support or if they had to have someone take care of them, maybe it could be done,” Jean Ellison said. “Their whole outlook changed.”

Senior Sabah Bari, who is a Health Science student, appreciated how Ellison spent the first 15 minutes of class asking how students were doing. Describing Ellison as “one of the most influential people I’ve gotten to know,” Bari plans to dedicate her pursuit of a master’s in public health to Ellison.

Stacy Gropack, Dean of the School of Health Professions explained that the school is eager to make sure students are doing well and feeling well at all levels.

“Many of our instructors do that,” Gropack said, but “Ellison in her position took it to a different level. She was always very concerned that students were in the right place and were healthy. She made sure students had the capacity to succeed at all levels.”

A dedicated family

Ellison received considerable ongoing support from her family.

Jean Ellison served numerous roles, from getting up at 3:45 am each day to get her dressed to driving her to ensuring her slides were ready and in order for her presentation. It took six hours from the time Ellison awoke until she was ready to leave.

Jean Ellison is “probably one of the most dedicated, strongest women I know,” said Gropack. Ellison “could not have accomplished what she did without [her mother] on all fronts.”

Mathias Risse, Berthold Beitz Professor in Human rights, Global Affairs and Philosophy at the Harvard Kennedy School, recalled how he taught an ethics class that included Ellison in the fall of 2002.

Ellison was “one of the most talented students in the class,” Risse wrote in a memorial to his former student. “Jean was there with her, every time, and she was as much a member of the [class] of 2004 as [Ellison] was herself.”

When the two of them were on campus, “everyone knew who they were, mother and daughter,” Risse wrote.

Ellison’s father Ed and her siblings Kysten and Reed provided important, meaningful and ongoing care for her.

“One of us had to be with her 24 hours a day, seven days a week,” said Ed Ellison. “Jean and I feel very blessed to have had the opportunity to help her do what she wanted to do. It was a life well-lived.”

Ellison adored her family and, in particular, her five nephews, who not only returned her affection, but were also fiercely protective of her.

One of Ellison’s nephews had a cat that she almost ran over in her wheelchair. She asked her students to help her design a 360 degree camera so she could survey the perimeter when the cat was nearby.

“That’s the kind of independence she wanted,” said Rafailovich.

Ellison shared affection with her family and friends by blowing kisses frequently. Her father stroked her cheek and lifted her up out of her chair and put her arms around his neck.

“The love she had for everyone oozed out of her,” Jean Ellison said. Her daughter “constantly told people how much she loved them.”

Before the accident, Ellison had been a ballet dancer. She would sometimes dream of herself dancing.

“We both like to think that she’s dancing now,” said Jean Ellison.

Stem cell research

Ellison became a powerful voice in some of the earlier battles in 2000 over stem cell research. Stem cells are undifferentiated cells that could one day help in the treatment and care of people with neurological limitations.

Ellison, who founded the Brooke Ellison Project, helped establish the New York State stem cell research organization, which provided research funding outside of the federal level.

Ellison and the Christopher Reeve foundation “had the courage to put [state funding] in place,” said Rafailovich. “She saw stem cell research as the key if we’re ever going to regenerate nerves.”

Ellison recognized any new treatment wouldn’t happen immediately, but wanted to help people in the future who were dealing with similar challenges.

Ellison is featured in the upcoming documentary “Super/Man: The Christopher Reeve Story,” which was recently shown at the Sundance Film Festival.

Ellison served as a board member on the Empire State Stem Cell Board, which designed New York State’s stem cell policy from 2007 to 2014.

In 2017, Ellison also served on the board of directors of the New York State Civil Liberties Union and, in 2018, was chosen as a political partner for the Truman National Security Project.

“We count ourselves incredibly lucky to have known her and are extraordinarily humbled by who she was and what she accomplished in her short life,” NYCLU Executive Director Donna Lieberman wrote in an email. “I have benefited immeasurably from [Ellison’s] wisdom and friendship, and I am especially grateful or her patience and determination in helping the NYCLU to better understand and advocate for the rights of people with disabilities.”

Leaders from the Truman National Security Project, which is a diverse nationwide community of leaders united with the goal of developing smart, national security solutions that reinforce strong, equitable, effective and non-partisan American global leadership, expressed their appreciation and admiration for Ellison’s contributions.

Ellison was a “visionary, leader, teacher, and, most importantly, a true friend to us and the disability community. [Ellison’s] eloquence captured the heights and depths of the disabled experience – beauty, pain, nuances, and silver linings – while pushing society’s boundaries of a more inclusive and dynamic world. Amongst [Ellison’s] vast list of accomplishments and accolades, her kindness and strength touched everyone she met,” wrote Jessica Gottsleben and Kristin Duquette, TruDisability Experts, in a statement.

Ellison thought well outside of her wheelchair and outside of the proverbial box.

In the first day of class, Bari recalled how Ellison asked students to think about the character Thanos from the Marvel series.

Bari recalled wondering, “are we in the right class? Where is she taking us?”

Throughout the class, Bari suggested that she and her fellow students rethought numerous aspects of their lives.

In her own words

In the introduction to her book “Look Both Ways,” which people can hear Ellison read on YouTube or on her web site BrookeEllison.com, she shares her life and perspective.

Look Both Ways

 

“People living with disability are celebrated yet rejected, are the objects of both praise and of ridicule, and are heralded for their understanding of challenge, while often left to battle those challenges on their own,” she wrote.

Ellison continued, “the lens from which I view the world is not one of disability, but rather one of humanity touched by disability, which serves to heighten the lessons fundamental to our lives: those of adaptation and problem solving, leadership and growth, compassion and hope. These are the lessons of disability. These are the lessons of life.”

Funeral

Ellison is survived by her parents Ed and Jean Ellison, her sister Kysten Ellison and her husband David Martin, their sons Carter and Harrison, her brother Reed Ellison and his wife Ellen Ellison and their three sons Jamie, Oliver and Theodore.

Visitation will be held next Monday, February 12 at Bryant Funeral Home, 411 Old Town Road in Setauket  from 2 p.m. to 8 p.m. The family will hold a private burial service.
How you can help
Those interested in helping to sustain the legacy of Brooke Ellison can donate to the Brooke Ellison Legacy Scholarship through the following website: https://alumniandfriends.stonybrook.edu/site/Donation2?df_id=2660&2660.donation=form1&mfc_pref=T&designation=5701

Areatha Pickens mugshot. Photo from SCPD

By Desirée Keegan

Suffolk County Police today arrested a nurse for assaulting a paraplegic man she was caring for at his Coram home last week.

Areatha Pickens, a licensed practical nurse, was caring for an 83-year-old man and Korean War veteran who became paraplegic in a 1975 motor vehicle crash, when she assaulted the man who was confined to a stretcher June 22. Pickens punched the man several times after the victim notified Pickens’ employer that she was late for work. The victim was treated at Stony Brook University Hospital for a fractured orbital bone.

Sixth Squad detectives charged Pickens, 44, of Coram, with second-degree assault. She was scheduled to be arraigned at First District Court in Central Islip.

Putting one foot in front of the other never looked so inspiring.

A freak sledding accident in Vermont in 2009 left Greg Durso, 31, of Stony Brook unable to use his lower body from his stomach muscles down. With the help of St. Charles Hospital’s rehabilitation center, he stood and walked across a room Dec. 13 in front of his family and dozens of hospital personnel for the first time since his accident.

Greg Durso, who is paraplegic, walks at St. Charles Hospital Dec. 13 with help from an Indego exoskeleton. Photo by Alex Petroski
Greg Durso, who is paraplegic, walks at St. Charles Hospital Dec. 13 with help from an Indego exoskeleton. Photo by Alex Petroski

Durso was aided by a clinical trial product called the Indego exoskeleton, which is a wearable robotic frame. St. Charles is one of nine hospitals in the United States conducting the clinical trial, and the only one on Long Island. Durso is the first patient at the hospital to take the technology for a spin.

“It’s just an incredible feeling to be up there and be walking again — putting weight on your legs,” Durso said after his groundbreaking stroll. “Each step is kind of like a leap of faith … a month ago I probably couldn’t have told you I’d be here today, so when I heard about this, I was so happy to have the opportunity to do this.”

Indego is the second FDA-approved exoskeleton device used for lower limbs. The device weighs about 26 pounds, and requires no backpack or external wires, as other similar devices have in the past. Currently the machine is operated by Durso’s chest muscles, but future incarnations of the device will allow electrical stimulation in the muscles so that a patient’s own legs will make the machine work, according to St. Charles Physical Medicine and Rehabilitation Medical Director Jennifer Semel. The FDA gave the machine clearance in March.

“The future is really limitless,” Semel said in an interview. “It’s really exciting to see people who haven’t been able to stand up in several years not only to be at the same height as their peers, but to be able to walk. It’s really uplifting.”

Semel said Durso has been using the device for about a month, and last week required a walker in addition to the exoskeleton to get around. He progressed to crutches for his Dec. 13 walk. Semel said the plan is for Durso to continue using the device for several months to gain a better understanding of the health benefits and the impact it has on a patient’s gait.

“I think I was a little skeptical because you realize people always tell you there’s going to be advances, there’s going to be this and that in the future,” Durso said. “But when you see this — I actually get up, I actually walk, I gave my sister a hug for the first time in eight years face to face — it’s pretty emotional and empowering, and it’s just exciting to see where the future is going to go with this technology.”

It was an emotional day for the members of the Durso family in attendance. Durso’s older sister, Jessica Giovan, fought back tears trying to describe seeing her brother walk again for the first time in eight years.

‘It’s just an incredible feeling to be up there and be walking again — putting weight on your legs … each step is kind of like a leap of faith.’

— Greg Durso

“I just saw him look so proud and happy,” she said. “He works so hard at everything he does, so to see him put one foot in front of the other, literally, was just unbelievable … the person you see now is the person he has always been. He has not, for one second, wavered in his personality since the accident. In fact, he has only increased his perseverance and his humor, and he lives everyday to make everyone around him feel like it’s okay.”

His dad, Richard Durso, said he couldn’t have imagined he’d be sitting where he was, watching his son walk, when he heard the news of the accident eight years ago. He credited his son’s positive attitude for keeping him on track. His mom, Jean Durso, called what she saw “unbelievable.”

Durso has competed in Iron Man races and marathons in his life — the former both pre and post accident — and said he hopes to be able to regain some of that lifestyle in the future.

“I love to do athletic things. I mean, it could be anything. I just want to be out there, have fun and live my life the way I want to do it,” he said. “For me that’s enough.”

The Indego devices cost about $80,000 each.

John Cincar uses the eye-tracking iPad device in Stony Brook. Photo from Long Island State Veterans Home

Two eyes and an iPad is all Vietnam veteran John Cincar needs to completely transform his day-to-day life.

Cincar, a resident at Stony Brook’s Long Island State Veterans Home, lost his ability to move his arms and hands, but only needs his eyes to operate a $12,000 iPad the home helped him secure this week as part of its mission to enhance residents’ independence. With help from the device and the home, Cincar said he could open the door to a world he had not been able to access on his own for years. By looking at control keys or cells displayed on the iPad screen, Cincar said he can generate speech, activate functions such as turning on a light or television, and even surf the internet.

“It’s very easy for me to use,” he said. “It does everything. I can get in touch with the world again.”

The eye-tracking device, which the veterans home referred to as an “eye gazer,” was a by-product of a donation from Bowlers to Veterans Link Chairman John LaSpina, a Long Island native and owner of various bowling alleys across the Island. The BVL is a not-for-profit organization that works to support American veterans, raises about $1 million per year through bowlers and bowling centers nationwide, and has a working relationship with the Long Island State Veterans Home, LaSpina said.

John Cincar, center, accepts the eye-tracking iPad device in Stony Brook thanks to a donation from The Bowlers to Veterans Link. Photo from Long Island State Veterans Home
John Cincar, center, accepts the eye-tracking iPad device in Stony Brook thanks to a donation from The Bowlers to Veterans Link. Photo from Long Island State Veterans Home

“An opportunity like this just seemed so incredibly great that we couldn’t say no to it,” he said. “We’re talking about a facility totally dedicated to veterans. The place is immaculately clean. They do wonderful things.”

The BVL donation to the Long Island State Veterans Home was made possible from the proceeds of the “PBA50 Johnny Petraglia BVL Open,” which was held at the Farmingdale Lanes from Saturday, May 7 through Tuesday, May 10.

With the Vietnam era now more than four decades old, the Long Island State Veterans Home has been seeing more veterans who served in that war coming through its doors. And with each war comes a different kind of ailment that staff must combat.

“Many of these guys, their brains are fully intact, but their bodies are shot. They’re trapped,” said Jonathan Spier, deputy executive director for the Long Island State Veterans Home.

Just five years ago, Spier said, the home had only two Vietnam veterans living there. That number skyrocketed to more than 50 by 2016, he said, with former combat men suffering from specific injuries like exposure to Agent Orange and other muscle-related difficulties.

Fred Sganga, executive director of the veterans home, said the addition of the eye-tracking device only furthered his group’s mission to enhance the quality of life of more than 6,000 Long Island veterans.

“The goal is to maximize every veteran’s independence,” he said. “We want to be strategically ready for the next generation of veterans coming here, and this technology is transformational for someone who is a paraplegic.”

When asked how he planned on harnessing the power of the iPad to his benefit, Cincar said he hopes to study new languages, like Romanian — the language of the land he was born in.