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BobbyB
12-12-2006, 11:08 AM
Indestructible Newsletter #5

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ALS Film Fund Newsletter
Indestructible Update November 2006

Pre-Release Party Success!
Parenthood by Ben Byer
Support Indestructible

Greetings!

Dear Supporters and Friends,

Over the past few months, we have been working tirelessly to finish Indestructible, an extraordinary film that is certain to bring about positive change for ALS patients and those who suffer from other neurodegenerative diseases.

Indestructible is currently in the final stages of the editing process and we anticipate a 2007 festival release.





Pre-Release Party Success!



Back in July, ALS Film Fund hosted a private screening of the rough cut of Indestructible for many of our supporters who also attended the Pre-Release Party. The film was incredibly well received by all.

We would like to thank all of the generous people who contributed to the success of this event: Haymarket Properties, LLC donated the beautiful roof top venue for the sell-out crowd. Over 75 businesses donated goods or services for the auction, raising over $10,000 towards the completion of Indestructible.




Parenthood by Ben Byer



I am a single father living with a neurodegenerative disease that has a life expectancy of two to five years. This is year five.

As my body has gone through many changes over the past five years, so have my parenting methods. When my son was two and I had recently been diagnosed, the mental challenges of facing the reality of my life seemed insurmountable. I was in a fog, and the only thing that raised me out of that was my young son pulling on my toe in the morning, saying, “Up, up!” He was ready to start the day and whether I wanted to or not, I was going to be a part of that day. Simply getting out of bed and being present for my son John, was, in retrospect, a life-saving action.

One year later, we were traveling to Oregon to visit a childhood friend of mine. After three connections and nearing 11:00 PM, my three and a half year-old was exhausted. He did not want to get up from his seat on the plane. After everyone else had exited, I was still trying to convince him that walking off the plane was the best choice for both of us. But he was upset and tired and now in a full-on wail. A stewardess said, “You need to pick him up.” The degenerative disease had weakened my arms to the point that opening a can of Spaghettios was impossible. A gallon of milk weighed three hundred pounds, and my son, in a full-on temper tantrum, was impossible to carry through an airport. A woman on the cleaning crew sensed there might be something else going on and suggested we grab a wheelchair to carry him out of the terminal.

Most boys love to wrestle. When I was a kid, I wrestled with my brothers, often taking a beating, but once in a while putting in a couple of good licks of my own. John is one of the tougher kids I’ve met and relishes in the enjoyment of a good smack-down. My arms are no match for his dexterity and strength, but my feet and legs still work pretty well. This summer, while we were in Colorado, he decided to test my skills, first patting me on the head and then running around to escape my glance. The pats became gradually harder, until they were downright annoying. Using my brains to outwit a six year-old, I asked him nicely to come in front where I could see him. Then, when he was least expecting it, I took him down with a leg around the ankle and the other in the chest. This is a move that I have perfected, and within seconds he was pinned on his stomach.

I held him here for a good long time, smacking him on the butt with my foot to remind him of who is boss. My college roommate, who we were visiting, convinced him that the only way out was to call “mercy.” After an agonizing three minutes, John gave up – for the moment. He stood up, paused, and went in for another attack. In the heat of the moment, I shoved him a bit too hard with my foot. He was knocked to the floor and bumped his face on the edge of the sofa. It hurt. He ran upstairs and refused to come out for twenty minutes, angry that I had caused him so much pain. I felt horrible for my miscalculation. Unable to climb the stairs to console him, I was left listening to his despair.

I try to get other people to play baseball with my son. Reading him a story takes so much of my energy that I make him read stories to me instead. My friends, family and assistant all try to teach him the lessons that I am unable to give: how to play chess, ride a bike, work a digital camera, to tie his shoes, even some stern reprimands for inappropriate behavior. I have become more of an overseer of my son’s rearing, often watching as others get more involved in his life. The details are too depleting of my energy, so I work in broad strokes to maintain an environment that is conducive to his development and growth. Sometimes, I’m really good at this and relish my success as a manager of my son’s life. Often, I fail miserably and regret my lack of judgment.

But I must be doing something right. At 4 AM, after a thirty hour train ride home from Denver (Amtrak sucks), I was helped off the train to a wheelchair that we had just bought for this trip. (Using a wheelchair was a milestone that I never wanted to reach; no one does.) When I sat down, John, who ten minutes earlier had been woken up from a dead sleep, saw that I was struggling to put my arms on the armrests. Without being asked, he gently lifted up first one and then the other to make sure that I was comfortable, then he placed my feet on the footrests. I looked at his half-open eyes and said, “Thank you.” “You’re welcome,” he responded. John is six years old.

On a few occasions, John has asked me about death. One day, I was walking him to preschool, and he said, “Are you afraid to die?” Unsure of what the appropriate answer is for a small child, I said, “No. I’m not.” It was the truth of what I was feeling at the moment. Maybe I was overcompensating, because deep down, I probably do have a fear of death like most people. I heard my son repeat this anecdote in his own words last week. He said, “My dad is not afraid to die.” In a way, it is true. I’ve had so much time to think about my mortality that I’ve exhausted the fear out of my body.

I used to be afraid that my son would be at a loss without me, that if I left this world, he would suffer. This is true on one level. But I have also learned that through suffering comes growth, and John has grown well beyond his six years. Often, I fear, too much. But I do not worry about him. I know he will not only survive the challenges he is faced with, but use them as stepping-stones to greater achievements in his life.

Ben's Bio



Support Indestructible



Please continue your support of ALS Film Fund and Indestructible. We are currently seeking completion funds for the musical composition, final edit, legal costs and initial distribution effort.

Now is the time to get in your tax-deductible contribution before the end of the fiscal year. All contributions to ALS Film Fund over $250 are tax-deductible through our fiscal sponsor, Film Arts Foundation. Click here to make a contribution.

If you do not need the tax deduction and would like to save ALS Film Fund 10%, please click here for instructions on how you can donate.

If you would like to host a private screening of Indestructible to assist in our fundraising efforts, please contact Rebeccah Rush at alsfilm@gmail.com.

Thank you for your support of Indestructible and the fight against ALS.

We wish you and your families a happy and healthy holiday season.

Ben Byer & Rebeccah Rush



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email: alsfilm@gmail.com
phone: 312-848-5919
web: http://www.indestructiblefilm.com






ALS Film Fund | PO Box 5126 | Winston Salem | NC | 27113

BobbyB
05-21-2007, 10:44 AM
Newsletter #8
May 2007

A Mother's Celebration
Some Quotes About Indestructible
We Still Need Your Money
How Have You Been Affected By ALS?


Dear Friends and Supporters,



In honor of Mother's Day, Ben's own mother, Barbara Byer, has written this month's newsletter article. We hope you enjoy.





A Mother's Celebration



Some days. . .

Black clouds swarm above my head. The weight of ALS bears down with a force so huge it takes my breath away. I have to wrench myself free, force myself to do something, anything that will let in the fresh air. I've become difficult, I know, when I'm terrified and want only to stay in bed, under the covers and sleep forever.

But on other days. . .

I let optimism rule. I believe we will overcome these terrible circumstances. I project into the future and imagine Ben physically vibrant the way he was years ago when I drove him to the airport for his third year as a college exchange student in Paris, France. He hoisted a huge duffel over his shoulder as if it weighed a few pounds, kissed my cheek and was gone. When we visited him four months later, he'd already made dozens of friends who called out 'Binyamin' as they waved him into their lives. Ben lived in an apartment, a boat, then someone's loft, while he studied Deconstructionism, a difficult philosophy to comprehend in English, let alone, French.

He traveled throughout Europe that summer, visited friends from the states in each country, slept on the floors of their rented rooms. Ben returned in September, packed a few belongings into a pickup truck and drove to California to film, act and write. My wish for him to complete his degree at Indiana University vanished, replaced by the hope he wouldn't lose his way in the West Coast jungle. I needn't have worried.

In the early morning light, I soothe the ache with childhood memories of Ben, our independent, resilient little guy, who always found his way home without bread crumbs or pebbles in his pockets. Baseball season brought Little League tryouts. Ben practiced in the backyard for weeks before the big day. Having seen his wild throws and fumbled catches at more than a few softball games, I feared he wouldn't make the team but said nothing, hoping for a miracle as we drove to the field. Tension mounted as parents vacated the premises until noon. Prepared for a rough afternoon, I returned, shocked to find Ben part of The Optimist team, managed by two brothers who wisely valued heart above skill.

When I look at Ben now, he's still all heart. His spirit and drive pull me from under the covers. He's the same strong, self assured human being who made the team, traveled the distance, proved his mettle. He's a brilliant filmmaker, a wise guy, a funny man, a sensitive soul. Who else but such a person could construct a magnificent life from so much anguish and create a legacy of the magnitude of Indestructible. More than a thousand people gave Ben a standing ovation at the Cinequest Film Festival, in awe of his contribution. Ben, beaming in his wheelchair, reminded me of a favorite quotation by Thomas Edison. "Everything comes to him who hustles while he waits."

Visit Barbara's Blog



Some Quotes About Indestructible


Thank you for making the documentary. I think it is one of the most amazing and beautiful things I've ever seen.
Laura Zinger

It was incredibly profound and moving. It really stayed with me for a couple of days, which is what great films should do. I was extremely moved by Ben's extraordinary journey and feel like the film is heartbreaking and beautiful at the same time.
Colleen Bell

I just spent the night watching "Indestructible" and I'm sitting here stunned, awed, devastated and rethinking the meaning of life. Thank you for making this movie, you have forever changed me.
Wendy Keller

I think I could watch it many times and observe and absorb different elements of it each time I see it--it's truly a work of art.
Jenny Boeder

This is TRULY an important documentary and piece of art.
Ross Travis

I watched "Indestructible" last night with my son (I might have told you that he has physical disabilities). We were both stunned and overwhelmed. Your courage in so honestly presenting your personal struggles, vulnerabilities and character is nothing short of amazing. I found it to be extraordinary.
Ken Moses, Ph.D.

We could not stop talking about the film last night...even laying in bed trying to fall asleep...AMAZING! WOW!
Adrienne Flentge

Freakin' awesome, great and put together tight. A great piece of work. Great movie.
Peter DeFaria

It's beyond moving. You have real talent, and you've used it for a sacred purpose. You've enriched us all, and I'm very grateful.
Daniel Gordis, Ph.D.

I can't get "Indestructible" out of my head. I keep hearing the music, seeing the images and thinking about the remarkable story. It's an incredibly brave and powerful piece of storytelling.
An incredible film.
Joanna Rudnick

Amazing film. I am so glad to have seen it, and I already feel marked by it. A very powerful film, you have already achieved what many filmmakers strive for. Even as I write this and I recall the film, I am moved once again.
Leslie Simmer

An engrossing, emotionally impactful film.
Justine Nagan

Your film will live in my heart while working on this disease. It was simply inspirational. Every second.
Clive Svendsen, Ph.D.

Watching "Indestructible" was the best film experience I've ever had. I was profoundly moved by your life and your attitude, not to mention the beautiful images that wove it all together. Thank you for sharing your truth with us.
Alison




We Still Need Your Money


While most of you have yet to see Indestructible, those who have are clearly moved and impressed by the power of this film.

For almost four years we have been asking you to donate your hard-earned money to help fund Indestructible. It is now in the final stages of completion and is already garnering high praise from the medical community. One prominent expert said it is the best film yet made on ALS. The support you have given us has been instrumental in making this happen, and we know that once you see the movie for yourself, you will have no question as to the impact this film can have on ALS and the change that needs to happen.

Please consider that the end is near, but we still need your help. We could not have gotten this far without you and are honored to have you by our side. Every single dollar helps - donate today, tell your friends to donate, and bring this movie to completion now.

Thank you for your support.

Ben Byer & Rebeccah Rush

Click Here To Donate Now.



How Have You Been Affected By ALS?


Whether you are an ALS patient, family member, friend, medical professional or have just read about ALS for the first time today, we want to hear from you. Please send us your stories.

In five hundred words or less tell our growing audience what you want them to know about ALS. Letters will be posted on our new website to be launched next month. At least one will be selected for our monthly newsletter series. Help open the public dialogue about ALS so this devastating disease can be brought to an end.

Letters will NOT be edited by ALS Film Fund. Authors may remain anonymous if it is requested. ALS Film Fund reserves the right to not publish certain letters for any reason. All letters become the property of ALS Film Fund to be used for any purpose to continue its mission.

Email letters to alsfilm@gmail.com



Quick Links...


Join our Email List
Newsletter Archive

About the Filmmakers
Indestructible Supporters

Facts about ALS
Donate



email: alsfilm@gmail.com
phone: 312-848-5919
web: http://www.indestructiblefilm.com