Gleason (2016)

Sorry, this movie sucks

Simply A Masterpiece

People are voting emotionally.

This is a gorgeous movie made by a gorgeous spirit.

I have spent my career seeing the end stages of ALS patients. Setting them up so they would be comfortable at home. Taking care of them in the hospital. I think ALS and Myasthenia Gravis are 2 of the scariest syndrome/diseases to have. There are a lot more scary ones that don't make it to adulthood. This documentary was raw and gritty. And was not wrapped up in a bow. The fears, insecurities, relationship issues of the spouse as the caregiver etc... I cried. Steve Gleason has given the world a hard look at debilitating neurological diseases. May God bless him and his family. I sincerely believe there is no real lesson in suffering and dying a lingering death. Or in dying young. I believe this family made a difference. With grace and dignity.

Every so often you see something that puts life in perspecpctive. This is the one.You watch this and come away reflecting on how you live, what you're doing with your life, and how your friends and family fit in with everything.I didn't have a clue who Steve is or what he'd done in the lead up to his ALS diagnosis, but I just watched this on a crowded plane and tried hard to hide the tears (not sure I succeeded!).Steve has achieved so much! Whilst ALS has changed his life drastically, he's fought and pushed hard to make a difference. Having said that, I don't think enough can be said for his wife, Michele, and what she's worked through- a new born and then growing son while her husband becomes more and more dependant in her- an amazing lady!Great movie. Watch it!

Greetings again from the darkness. Heroes come in many shapes and forms. Steve Gleason became a cult hero when he blocked a punt for his New Orleans Saints team in their first home game after Hurricane Katrina. For this, the team erected a life-sized statue outside the Superdome. In his time since that game, he has suffered more than any person should, and he has provided hope and assistance to more unfortunate folks than just about anyone. By now, just about everyone would consider him a hero.Director Clay Tweel takes a very direct approach to telling Steve's story. He guides us through the life of the undersized Washington State linebacker who, against all odds, carved out a 9 year career in the NFL; married a remarkable woman who was his equal as a free-spirit; was diagnosed with Amyotrophic Lateral Sclerosis (Lou Gehrig's disease); learned to live with the debilitating disease; established a foundation to provide assistance to others with ALS.Tweel pulls no punches in showing the progression of the devastating disease, and equally as importantly, in the toll such a disease takes on the loving caregiver after so many years. Gleason retired in 2008, and was diagnosed in 2011. Six weeks later, he and his wife Michel found out she was pregnant with their first child. Staring down the disease and the impending birth of their child, the couple took a 2 month expedition to the Alaska wilderness. This could be interpreted as their way of leaving their "old life" behind, but this couple is so full of life and spirit, that it was in fact, merely a next step.The diagnosis and the baby announcement motivated Gleason to begin filming video blogs/journals for his unborn child. His stated goal was to "share with you who I am", since the odds weren't good that father and son would ever be able to hold a conversation or play catch. Clips of these video entries are shown throughout and capture Gleason's charm, humor, sincerity and spirit of life.Son Rivers arrives in October 2011 just as the disease is creating severe challenges for Steve's physical and verbal capacities. We watch as Michel transitions from free-spirited newlywed to full-time care-giver and first time mother. Her coping methods are on display, as are the effects on her energy and outlook over the next few years.With the help of friends and family, Team Gleason is created as a foundation to provide assistance to ALS sufferers. The foundation finds its newest mission when Medicare announces that vocal/speech technology will no longer be covered for ALS. "No White Flags" becomes the calling card for the foundation, and these activities are blended with Gleason's medical and family hurdles … including his religious father who drags him to a 'faith healer'.Moments with Eddie Vedder and Drew Brees, among others, lead us to the global phenomenon known as "the ice bucket challenge" for ALS and finally the Microsoft Super Bowl commercial featuring Gleason and new speech technology. The film and story are simultaneously gut-wrenching and inspirational, and provide a rare behind-the-scenes look at the emotional and physical impact of disease on both patient and caregiver.

Just like a good sports movie should be (Weather it's a documentary or not) Gleason is very upbeat and makes you feel bad about not getting up off your ass to do something with your life.What I like especially about the film is Steve Gleason's positive tempo. He's a fighter and you can tell. The documentary keeps tabs on the amount of time Amyotrophic lateral sclerosis (ALS) is taking to effect his body. For a while I did not really notice that anything was changing, it was not until others in the documentary pointed things out, that I realized the effect it was taking.http://cinemagardens.com/Keeping an uptempo as he watched from a chair his son growing up was hard on him, so there were times when he broke down and that's understandable, cause he's human, that is the reason he was making this documentary, to show his son what type of man he is, and the best part is that he broke down but didn't break. He picked himself up and kept going.Same goes for his wife. She's a strong beautiful woman, who was going through it the same as him, and it was hard for her to keep it together but she's going strong. You can't help but to tear up a little over that.It's an inspirational story about what can happen if you never give up on life, and a touching story of a father making a connection with his son.