John Lawson

Cincinnati Film Director Has Simple Request

Share

I have a very simple request, one that will no doubt make you smile while you are at it.

Adorable three-year-old Gia Lopez was not supposed to live due to a genetic disorder known as spinal muscular atrophy. But, today, she is flying with a dragon and starring in her very first film that my friend John Lawson has directed/produced.

By watching and sharing Gia and the Dragaon, you will be helping the film to win the Easterseals Disability Film Challenge. Judges will review the OFFICIAL YouTube and Facebook Videos for the number of overall views, shares, and likes. You have until April 29 to take action!

One of the goals of The Easterseals Disability Film Challenge is to change the way disability is viewed in media by giving filmmakers the opportunity to collaborate and tell unique stories that showcase disability in its many forms.  The Best Awareness Campaign helps to further this goal through grassroots publicity campaigns that raise the visibility of the films entered in the challenge. This visibility of film entries can also lead to jobs for everyone that is involved in the creation of a film. Whether your goal is to be an actor, director, writer, producer, or any combination of the above, the film challenge can be the door opener to the next step in establishing your entertainment career.  Remember, work leads to work!

As in any competition, there are rules. Among those in the Film Challenge – teams are given a theme and genre and four props on the morning of the commencement of film production; they are given a weekend to create the film from start to finish; and they must have both people with and without disabilities involved.

A track record for John

This is not the first entry for John, whose roots are in Cincinnati. He won Best Film in the very first year of the Challenge. Last year he entered again with Whitney’s Wedding starring well known actress Jamie Brewer, who won in the Best Actress category. That film went on to be accepted in 12 film festivals around the world, winning over six awards including three Best Film awards, three Best Actor awards for Jamie, and two Best Director awards for John.

John’s inspiration for Gia and Dragon came from reading a children’s book that featured kids with and without disabilities. “I thought it’d be a cool way to introduce my grandbaby to disabilities,” he told me.

John’s team began writing at 6 pm on a Friday night and started shooting the film Saturday morning. By Sunday they were busy in the editing bay. This marks the very first entry in the contest that include animation.

 

Cincinnati ReelAbilities Celebrates Difference

Share

These past few weeks (and months) my blog has slowed as I’ve needed to focus much of my energy on promoting the 2017 Cincinnati ReelAbilities Film Festival organized by LADD, Inc. (and a project for the Countryside YMCA and mixing in pet training). The Festival is now a week away, March 9 to 12, and I want to share information about it. I will be back after the Festival – I’ve already got some interviews lined up!

“The Cincinnati ReelAbilities Film Festival is a spectacle of human relationship in its purest form, generating an awareness of issues relative to us all. Awareness creates understanding, which in turn gives rise to perspective—and it is through perspective that we are able to truly appreciate and relate to others in our lives.”
-Richard Bernstein, Michigan State Supreme Court Justice

 

Susan Brownknight, executive director of Cincinnati nonprofit, LADD, talks about the Cincinnati ReelAbilities Film FestivalI can’t think of any words that more beautifully, more accurately explain our purpose when it comes to building a Cincinnati ReelAbilities with celebrities, parties, workshops, networking opportunities, and over 60 life changing films that showcase the art, lives and stories of people who have disabilities. Our  goal with the Film Festival is to create a Hollywood-style event where our guests will have fun, meet new and enjoy the company of old friends, be moved in some way; and leave having been uplifted with a new perception of difference, appreciation and welcoming of each other.

Susan Brownknight, executive director of Living Arrangements for the Developmentally Disabled (LADD, Inc.) – the organizing agency, has said she gets asked all the time why her nonprofit is investing such a significant amount of time and resources into building a world class film festival.

“My answer lies in the very foundation of what we do and why we do it. At LADD, we are focused and passionate about creating equal opportunities and ensuring the dignity of adulthood for all people with disabilities in our region, a community that embraces, supports and values them,” she answered, “A film festival is a powerful way for us to facilitate that and to connect with others across differences that typically lead to isolation and a hardening across arbitrary lines of thinking. Our idea with ReelAbilities is that, at the end of the day, this Film Festival is about who and what we value, and why we value it.”

Celebrations Gallore!

Thursday, March 9 at 10:00 am: Welcome to Cincinnati: Meet the Stars Q&A Event with RJ Mitte and others
Thursday, March 9 at noon:
Premiere Luncheon with keynote speaker RJ Mitte.
Thursday, March 9 at 6:30 pm: Premiere Night film reception and film screening of The Astronaut’s Secret.
Friday, March 10 at 8:00 am: Interfaith Breakfast featuring keynote speaker Richard Bernstein, the nation’s first blind Supreme Court Justice.
Friday, March 10 at 5:30: Veterans Reception with keynote speaker Michael Schlitz, retired US Army platoon sergeant, Gary Sinise Foundation ambassador and Purple Heart recipient, followed with a film screening.
Saturday, March 11 at 9:30 am: Veterans Brunch with keynote speaker Bryan Anderson, a retired US Army sergeant and Gary Sinise Foundation ambassador and Purple Heart recipient.
Saturday, March 11 at 5:00 pm: Cocktails & Zombies Party with the stars and screenwriters of Spring Break Zombie Massacre, Sam and Mattie; plus other Hollywood VIPs, and Cincinnati’s own Drew Lachey and Q102’s Jenn Jordan.
Sunday, March 12 at 7:00 pm: Local Films/Closing Night Party featuring game-changing films made by and about local people.

Workshops

Additionally, Festival guests can learn how to act, model, tell their story, see entertainment, and create films on their smart phone in workshops. Please click here for the full list. While all workshops are free, registration is required.

Celebrities Help Us Celebrate Difference

RJ Mitte, Jamie Brewer, Kurt Yaeger, and Lauren Potter are among the celebrities attending the 2017 Cincinnati ReelAbilities Film Festival

Best known for his role of Walter ‘Flynn’ White Jr. for five riveting seasons of AMC’s Emmy and Golden Globe Award-winning thriller, “Breaking Bad”, and the handsome face of GAP’s International 2014 “Lived In Summer” Campaign, RJ Mitte tops our list of Hollywood stars, dignitaries, and ReelAbilities film VIPs to join us at the Duke Energy Convention Center.

Please join us at 10:00 am on Thursday, March 9 to kick off Cincinnati ReelAbilities with a Welcome to Cincinnati: Meet the Stars Q&A Event with RJ and many of our other big name VIPs including Jamie Brewer, Lauren Potter, Kurt Yaeger, John Lawson, Nic Novicki, Bryan Anderson, Michael Schlitz, Boone Cutler, and Steve Wampler.

More VIPs will be joining us throughout the weekend’s events including Ali Stroker, Michigan Supreme Court Justice Richard Bernstein (as the keynote speaker for our Interfaith Breakfast), Sam and Mattie, Drew Lachey, Nick Clooney, and more.

Below is a list our leading VIPs and their information.

Bryan Anderson
Anderson is a retired US Army sargaent and Gary Sinise Foundation ambassador and purple heart recipient.

Richard Bernstein
A Disability Rights Attorney, he made history when he was sworn into office, becoming the nation’s first state Supreme Court Justice for the state of Michigan.

Jamie Brewer 
Known for her role of Adelaide ‘Addie” Lagdon in American Horror Story, she is also the first model with Down syndrome to walk the runway at New York Fashion Week.

Boone Cutler
Cutler is an author, columnist, music video director and Warfighter Rights leader that has become the first nationally recognized radio talkshow personality who is also a combat veteran from the current war. In 2012, Boone was diagnosed with Early-Onset Parkinson’s Disease secondary to a blast-injury in Iraq and is the national spokesperson for the Warfighter Rights’ Movement.

John Lawson
Lawson is a television, film and commercial PWD actor with past roles in the long running television crime dramas, “Law and Order,” “Law and Order: SVU and FX AMERICAN HORROR STORY: FREAK SHOW.

RJ Mitte
Known for his role in AMC’s ‘Breaking Bad’, he was also the face of the GAP’s International 2014 “Lived in Summer” Campaign.

Nic Novicki
Nic has toured around the country as a standup comedian. Included in his acting credits are tv shows: The Sopranos, Private Practice, and Austin and Ally. He is also a producer and founder/director of the Easterseals Disability Film Challenge.

Lauren Potter
As an actress, Lauren is best known for her popular role as Becky Jackson in the popular television show, Glee. However, she also devotes much time to advocating and raising awareness for disability related causes..and against bullying.

Michael Schlitz
Schlitz is a retired US Army platoon seargeant, Gary Sinise Foundation ambassador and purple Heart recipient.

Ali Stroker   
An actress known for her role in Glee, in 2015 Stroker made history by becoming the first Broadway actress in a wheelchair to appear on a Broadway stage

Sam Suchmann and Mattie Zufelt
These two best friends from Rhode Island met in Special Olympics and are filmmakers of the wildly popular, kick ass movie, Spring Break Zombie Massacre.

Kurt Yaeger
A former BMX rider turned actor, Yaeger is a below the knee amputee. His most recent TV credit s include the fan favorite character on FX’s hit show Sons Of Anarchy, the new Cinemax show Quarry and a new major recurring role on CBS’ hit NCIS: Los Angeles.

Stephen Wampler
As the world and his family watched, Steve Wampler who was born with a severe form of cerebral palsy, pulled himself with one hand 20,000 times in six days to conquer the world’s biggest rock, El Capitan in Yosemite National Park. The documentary of his journey was one of the 2015 Cincinnati ReelAbilities films.

Cincinnati ReelAbilities Film Festival
March 9 to 12, 2017
Duke Energy Center
Tickets, information, and film trailers: www.CincyRA.org

Disability Does Not Define John

Share

Through my work promoting the Cincinnati ReelAbilities Film Festival, I have gotten to know some pretty amazing people who have impacted me in very meaningful ways. Actor John Lawson is among them. I met and got to know John when I was promoting the 2015 Festival. He was a volunteer and a spokesperson with whom I spent a lot of time. Now living in the Los Angeles area for his acting, John is coming back to Cincinnati to join us next month as one of our 2017 Festival VIPs.

Actor John Lawson shares his story: disability does not define him.What I remember so much about my time with him two years ago was how John could make me laugh, but also, John is an incredible listener, an encourager and a leader. He went out of his way to let me know my work and contributions were valued, and he did that with everyone I saw him come in contact with. At our Film Festival, he spoke with eloquence and humor in spreading our message. He included people. He inspired not because he is someone who has a disability but because of who he is as a human being.

Below are two different posts John had written on his Facebook page awhile back (I am reprinting with his permission) about his story. Since they had some duplication, I cut out part of the second post. I hope that you will take a few minutes to read his words. They just may change the way you see and think about difference.

John Lawson’s Story (in his own words)

Feb 4, 2015

Wow, 28 years ago today February 4, 1987 is the day that I truly will never forget. I guess the cynical smart-ass side of me wants to write that I’ll never be able to forget for there is always someone coming up wanting to know how I lost my arms or who are very quick to remind me how “lucky” I am to be alive. I don’t know that I agree with their assessment of a measure of luck apportioned to me. I started playing the piano at age three, then began lessons at age four and studied classical piano for 17 straight years. At age 30, I had spent over half my life learning to play piano and now would spend the rest of my life without hands. That doesn’t sound very lucky.

I have been lucky to raise three wonderful, smart and somewhat “well adjusted” kids (hey I was their Dad) and had the very lucky chance to marry the love-of-my-life. Unluckily, the cancer won and I lost her too.

I spent five months of my life at the North Carolina Jaycee Burn Center in Chapel Hill North Carolina. My left hand and most of my arm below my elbow was amputated that day. My right hand was amputated above the wrist approximately one month later. As the burned skin debridement surgeries stopped and drugs wore off, I assumed a new role I never wanted to audition for as an upper extremity double amputee; a man with no hands left only to watch others play music.

While at the Burn Center, I received the best-specialized medical burn care from some of the world’s leading doctors and nurses. It was there that I decided to do my best to recover all aspects of my life. It was explained that losing limbs is similar to losing a loved one and you should experience the same emotions. While at the hospital, I never felt that I went through all the steps normally associated with a life changing experience such as my accident. If I did, I did them in my sleep, because from early on I realized I had to unconditionally accept my new role. I did find out, that since I never displayed the emotions expected, the psychiatrists that visited my room over the months noted in my chart that I was a “classic case of denial, and would suffer a catastrophic mental breakdown with in five years.”

Again, wow; twenty-eight years gone by and I’m still waiting for that mental breakdown. I think I would enjoy the time off.

Probably the most helpful wisdom I received after my amputations was by an unknown author, but passed on by my mother, “No one ever finds life worth living—you have to make it worth living.”

I am not special in the things I have done, with the conditions I have to deal with to do them. I could not control the circumstances that burned my body and resulted in the amputation of both my hands, but I can control what happens after the flesh has healed. I can control my attitude.

Early in my acting career, someone gave me a coffee mug with a saying printed on the outside, “Life is not a dress rehearsal.”

Those six words carry a powerful meaning. We only get to do this once and no matter what or where our stage, this is our one and only performance. I do not know what roles in life I will have to play in the years ahead, but I do know I will always chug along with the same attitude as the little blue engine pulling the long heavy train in the book read by my mother to me so many times as a child, “I think I can, I think I can, I think I can.”

Jan 10, 2017

I need to say I am not here to inspire you. I have lost count of strangers that approach me in public while grocery shopping or pumping gas to tell me that I am an inspiration. I guess they mean well, but to me they are just congratulating me for remembering to put on my pants before I left the house. There is nothing inspirational about pumping gas or grabbing a can of green beans off the shelf. You have been lied to about life with a disability.

Most people believe that because you have a disability that your life is worse; that being a person with a disability is a bad thing and that if you live with the disability, it makes you exceptional. Living with a disability is not a bad thing and it certainly doesn’t make you exceptional or inspirational.

Life as a person with disabilities can be difficult and we do have to overcome some things. But it’s not the things that you may think. It’s not the things to do with our bodies that we have to overcome. I believe that disability is caused by the way society is structured, rather than by a person’s impairment or difference. If society looks at ways of removing barriers that restrict life choices for people with disabilities, then disabled people can be independent and equal in society, with choice and control over their own lives. Of course I’m in a profession where the industry creates barriers that 95% of the work for characters with a disability are given to an able body actor. It’s these societal barriers of the industry that restrict the choices and control of my career.

So February 4, 2017 I will start using prosthetics for longer than I had my hands. Half of my life wearing hooks. Do they replace my hands? No, but they are a tool I’m forced to use for maintaining my independence in a society designed for able body people; a tool for me to pump gas or load my grocery cart. I’ve learned to use my prosthetics to best of my ability, so I know when people tell me “I’m an inspiration,” that they mean it as a compliment. I do understand that, but the reason it happens is because of this lie that’s been sold to the public that disability makes you exceptional and makes you inspirational. I’m sorry; but honestly, it doesn’t. I really believe that this propaganda that we’ve been sold is the greatest injustice and makes life hard for us.

Oh, and that quote about “the only disability in life is a bad attitude,” is total bullshit. It’s just not true. No amount of me smiling at a piano keyboard with a positive attitude will allow me to play as I used to touch the ivories with ten fingers.

I hope in my lifetime to live in a society where someone with a disability is not the exception, but just accepted as a norm. I hope to live in a society where a man stuffing a grocery cart is not an inspiration just because he is using prosthetics. I want to live in a society where we don’t have such low expectations of people with disabilities that we hire able body people to do jobs they are capable of performing. I hope in my lifetime to live in a society where we place value on genuine achievement by people with disabilities.

 

 

My Cincinnati ReelAbilities Film Festival Story

Share

Cincinnati ReelAbilities Film Festival posterWhen I was hired by the Cincinnati ReelAbilities Film Festival (organized by Living Arrangements for the Developmentally Disabled and presented by Macy’s)  late summer of 2014, much of Greater Cincinnati had never heard of it; and few people who I reached out to had any idea of the scope of the event or its value to our community – including me, admittedly. Even those who worked for the nonprofit host agencies did not realize the magnitude of what was to unfold.

People experiencing a disability or cognitive, genetic, physical and behavioral difference are often misunderstood. They are portrayed in photos and sometimes news stories as ‘less than’ normal or super human just by virtue of their own being. They are often not included, or at least not to the extent that they are people first with interests, hopes, dreams, talents, and even bad days, just like everybody else. Yet ‘they’ are about 20% of our population. And ‘they’ are the only minority population in which all people will be counted among them at some point in their lives.

The overarching goal of LADD and ReelAbilities in hiring me to serve as the director of public relations and communications was for me to support the unrelenting drive of determined volunteers and staff organizing the events  by being a catalyst for change – to bring the community together in support of not only an event but a cause so powerful as to have impact on each and every one of us in a direct or indirect way. I wanted to get people in this region talking to each other and realizing that inclusion and togetherness is not about ‘other people’, it is about themselves and each other. I wanted to get people excited about ReelAbilities as a world class film festival, and come out to support and learn from it. The challenge was to do all of this with a very limited budget including for my own time, but I was up for the challenge as the cause is something very important to me.

Actors Danny Woodburn, Daryl 'Chill' Mitchell, and Cincinnati Reds' Ted Kremer

Actors Danny Woodburn and Daryl ‘Chill’ Mitchell with Festival Honorary Chair Ted Kremer

For eight days beginning February 27, Greater Cincinnati was transformed into a film screening mecca with out-of-town celebrities helping Cincinnati explore our differences, and our shared humanity. Internationally acclaimed photographer Rick Guidotti; Michigan Supreme Court Justice Richard Bernstein; Project Runway fan favorite Justin LeBlanc; Cincinnati icons Ted Kremer, Drew Lachey, Nick and Nina Clooney, Dave Parker and Ken Anderson;  former snowboarding champion Kevin Pearce; and actors Danny Woodburn, Kurt Yaeger, Daryl ‘Chill’ Mitchell, John Lawson, David DeSanctis (from Where Hope Grows), Jesus Sanchez-Velez (from Stand Clear of the Closing Doors); veterans SSG Travis Mills and Michael Schlitz; and Steve Wampler, who climbed El Capitan, where just some of the big name personalities who came to Cincinnati to be part of ReelAbilities. Academy Award Winning Actress Marlee Matlin was our keynote speaker for our Kick Off Celebration Luncheon that hosted hundreds.

The films of ReelAbilities were selected from some 500 plus submitted for jurying, many of them with wide international acclaim and awards to their name. Their common thread was that they celebrated the lives and stories of people experiencing disability. Many were shown with the film actors/subjects as special guests; and all screenings included a thought provoking discussion at the end.

I saw and still do see ReelAbilities as an opportunity to open dialogue and doors about topics that, for the most part, have been barricaded from our conversations – or at least in productive ways out of discomfort or lack of interest or personal connection.

There were so many strategies that I put into place (with help from wonderful volunteers and staff) to reach out to our community and pull people in through their personal stories and connections – their differences, and their shared humanity. And, in the end, it all came together to create a community that supported the film festival beyond our wildest dreams in classrooms, board rooms, businesses, entertainment venues, stores, nonprofits, and universities. Nearly 4500 people attended our events, with numerous film screenings having sold out.

The honest questions that were asked, the open answers that were shared, and the comments afterward from film goers told all of us that others grew from it too with expanded and even new perspectives.

There were so many people whose words and actions touched me in meaningful ways that it has been difficult to find the right words to capture its impact on me.

Steve and Elizabeth Wampler at Cincinnati Children's Hospital Medical Center Seacrest Studios

Steve and Elizabeth Wampler at the Seacrest Studios

There was Kevin Pearce who took us into his life and shared his family tradition with all of us, ringing a Tibetan singing bowl to facilitate awareness of the moment – even at our formal Mingle with the Stars Gala. And, speaking of the Gala, anytime you have comedian actors in a room together and give them center stage to improvise, laughter is bound to follow. That was the genius idea (and somewhat brave too) of Festival Managing Director Susan Brownknight.

I remember the first time I met Richard Bernstein. He was so filled with genuine flattery of everyone he met. That, I came to learn quickly, is just his way. It is a gift and something I came to treasure about being around him.

We brought our VIPs to the Seacrest Studios at Cincinnati Children’s Hospital Medical Center where kids could interact with them. It is there where I saw the infectious laughter of Danny Woodburn, Daryl ‘Chill’ Mitchell and John Lawson banter between each other; and again when Steve and Elizabeth Wampler sat side-by-side. Steve shared this message with hospital patients, “Don’t let anyone tell you, no, you can’t do that. Anything is possible.”

Justin LeBlanc of Project Runway visited Ohio Valley Voices

Justin LeBlanc at Ohio Valley Voices

Justin LeBlanc promoted literacy by reading a book about inclusion to an entire gymnasium filled with school children; promoted creativity by helping students who are deaf to design and show fashions; and promoted abilities by speaking about his own personal story. Young students at Ohio Valley Voices also got to ask Justin lots of questions – like ‘When is your birthday?’, ‘What is your favorite color?’ and ‘Do you have a dog?’

While here, SSG Travis Mills , one of five surviving quadruple amputee veterans from the wars in Iraq and Afghanistan, met for the very first time a critical care doctor who provided medical care after his 2012 injury during his air care transport from Kandahar to Bagram. Together we took them to tour UC Health’s Center for Sustainment of Trauma and Readiness or C-STARS where Major Dr. Laurae Rettig was trained. I’ll always remember Travis’ wicked sense of humor…and his rotating hand that he can make go round and round and round.

I always welcome Rick Guidotti’s bear hug. The lens from which he sees the world has opened eye across the globe to see the gift of each individual and the beauty in difference.

I treasured all of the time I got to spend with my friends, Danny Woodburn, and his wife, Amy Buchwald. They are two incredible people who I look up to as examples of role models when it comes to integrity and perseverance. Equaled with their talent is their fearlessness when it comes to standing up for what they believe in.

Danny Woodburn and Amy Buchwald at Cincinnati ReelAbilities Film Festival

Amy Buchwald and Danny Woodburn

ReelAbilities gave me the opportunity to get to know and admire John Lawson, an encourager and leader, with a gift for bringing out the best in others.

Then there is the Festival Chair Kathleen Cail, Co-Chairs Sara Bitter and Kara Ayers; Managing Director Susan Brownknight; staff team – Jesse, Hannah, Molly, and Jen; and all of the committee volunteers for whom I have so much respect. They are such an awesome group of passionate, hard working, and dedicated people without whom this would not have been possible.

The Festival was about people coming together, standing up for and embracing eachother. It was about opening eyes and minds to see beyond people’s differences to what we all share – our humanity. I celebrate LADD for having the vision, foresight, courage and strength to create and organize such a community changing event. I am especially in awe of Susan Brownknight as our leader.

In her luncheon speech, Marlee Matlin looked out into the audience and shared, “We need to keep opening doors when people want them shut. We need to shine the light on ignorance when people want to keep us in the dark. And we need to make noise when they want to keep us quiet. But most of all, we need to keep on being ourselves, follow your heart and in the end accommodation will happen. We are the ones who can make it happen.”

Yes, Marlee, you are right we are. Let’s make our voices be heard!

 

#DifferentLikeYou

 

Celebrating Differences Is What ReelAbilities Is About

Share

I was reminded the other day of how great it has been knowing that my public relations career has been focused on bringing awareness and relationships to some truly impactful causes and organization.

And a client about which I was so passionate and miss the most was an organization called the Inclusion Network. For eight years I worked with them year round promoting the message that everyone has gifts and abilities, and that bringing those unique gifts together we strengthen each other. We strengthen our community.

I was one of the lead producers of the Inclusion Leadership Awards Event responsible for the strategic messaging including hiring and working with speakers to keep their speech on target, writing the script and the videos, working on all facets of the program portion, coordinating the media relations and more. And I saw that event grow to where it was hosting more than 900 people at the end.

Business and community leaders, professionals, housewives, students, volunteers, people who walk and people who use wheelchairs, people who benefit from large print programs and open captioned video screens, sign language interpreters or cups with handles instead of glassware all came together for a two and a half hour event that was designed to somehow change the world as they knew it. They heard about stories of organizations that instinctively know how to uncover talent, and of people, whose abilities are no longer obscurities. Acceptance was no longer an abstract. Inclusion, they learned, was not about THEM, but about ME.

Actor Danny Woodburn continues to stand out to me as the speaker whose message I will always remember. Danny shared his story of an actor, comedian and activist whose talents were born in the hardships of a world unaccepting of a medical condition known as dwarfism. All too well, he knows the sting of rejection and ridicule because he has lived it his entire life. But Danny told our vast audience that through his work, he has had the ability to influence attitudes. Offensive words, he has found, are generally rooted in Actor Danny Woodburn spoke at the Inclusion Leadership Awards Event in Cincinnatimisunderstanding and he openly corrects producers, directors and other actors.

At the end of Danny’s speech I remember he told us, “Even though every script is a battle to see how much I will comprise, it is worth it as long as there is dialogue.” Then he looked into the audience and added, “It is inspiring to me as I look out at all of your faces and see that there are comrades in this battlefield.”

To this day, Danny’s words and character continue to impact me. Sure, I love the fact that every time we talk he can always make me laugh but what I love even more is Danny’s true depth of humanity. He is truly one of those unique gifts and someone who I feel so blessed to be able to call a friend.

And the reason I am bringing this all up is because it is all leading up to a new client that is allowing me to continue this path of bringing communities together through the differences that make people uniquely great.

Organized by Cincinnati nonprofit LADD (Living Arrangements for the Developmentally Disabled), the Cincinnati ReelAbilities Film Festival is our region’s largest film festival that explores the world as experienced by people with disabilities. It will include a a star studded awards premiere luncheon, gala, and 30 film and speaking events throughout Greater Cincinnati. All of the film screenings benefit local nonprofit organizations that enhance the lives of people with disabilities.

The Festival will be February 27 to March 7, 2015 and next week I invite you to join us at our big red carpet unveiling party at the eloquent Obscura cocktail lounge in downtown Cincinnati from 7 to 9 pm. The films and venues will be announced before hundreds quote from Q102's Jenn Jordan about the Cincinnati ReelAbilities Film Festivalof guests by actor John Lawson and Q102’s Jenn Jordan.

Here is a link to register for the free event.

The ReelAbilities Film Festival was founded in 2007 in New York City by the Manhattan JCC and has grown to become the largest film festival in the country dedicated to sharing the stories, lives and art of people who experience disability. It is now headquartered in Cincinnati and is a division of LADD. It includes a total of 13 Festivals across the country. Cincinnati holds the second largest one.

Danny, who most recently plays the voice of Splinter in the new Teenage Mutant Ninja Turtles movie, was recently interviewed in Soapbox Media about ReelAbilities.

“Actors with disabilities are 90 percent less likely to be seen, and many characters with disabilities aren’t actually played by actors with disabilities,” he said. “It’s important for work like this to be done, and if I have the chance to speak out and be heard because I’m recognizable from being in the public eye, then I feel it’s my responsibility to do so.”

“But this isn’t just about actors getting work,” Woodburn continues. “Two-thirds of people with disabilities are unemployed; we need to raise awareness of that fact. If we want that to change, we as a society have to create an environment for change.”

Follow on Bloglovin

Don't miss hearing about Good Things! Register to receive my enewsletters.

* indicates required
Archives