Life & Atrophy
 

 

Life & Atrophy

A Documentary Film following One Family's story to defy genetic fate

 

 
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abouT The Film

Life & Atrophy follows the journey of a family to find an experimental treatment for their son after he is diagnosed with Spinal Muscular Atrophy (SMA). This disease impacts 1 in every 10,000 births and is the leading cause of genetic death in infants by causing progressive muscle weakness. Once children are diagnosed with the condition families are told to go home and love their children because there is no treatment and no cure. The McIntosh family fights to find an experimental treatment for their son Miles in an effort to save him from this debilitating condition.

Long years of research have lead to promising clinical trials that might prove effective in combating SMA, giving families and patients hope. Families, scientists, and pharmaceutical companies work together to fix the genetic fate of SMA and provide life, hope, and strength to those affected by the condition. The families of SMA exemplify the fortitude of human strength and compassion, where together we can break out of our genetic shackles.

 
 
 
 
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Screeenings

Below is a list of film festivals and other events where the film will be screening. Please contact me if you are interested in screening the film!

 
 
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World Premiere

Date: Saturday, August 12th at noon

Location: RISD Museum in the Metcalf Auditorium, Providence RI

 

Boston Premiere

Date: Monday, October 2nd at 2:30 pm

Location: 500 Kendall Street Sanofi Genzyme First Floor, Boston MA

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Directors Statement

As the son of two geneticists, science has always been a part of my family. I never entirely knew the nature of my father's research, except that he worked on a disease called Spinal Muscular Atrophy (SMA). This disease is a rare, genetic, neuromuscular disease which causes progressive muscle weakness. It affects 1 in every 10,000 births and is the number one cause of genetic death in infants. While working in my father’s lab, I became entrenched in the science of SMA and started to learn that the field was on the verge of a huge breakthrough. I knew I had to start filming the community and follow the events as it lead up to new discoveries in the field. Then I met Miles and his family.

Miles is a five year old boy with type II SMA. Like many SMA families, his parents, Nikki and Tony, were shocked by the diagnosis but fought to find an experimental treatment for their son. Following the family into a clinical trial, I saw how their story embodied the hope and struggle all SMA families go through when faced with the disease. Miles enrolled in a clinical trial and began taking an experimental drug to help treat his disease, which would later go on to be the first FDA approved drug for SMA. This disease has gone from an orphan disease with nearly nothing known about it, to now having its first FDA approved drug on the market, as well as other treatments in the pipeline. This incredible achievement represents the dedication of a community towards finding a treatment. The film represents what can be accomplished when families, researchers, and pharmaceutical companies join together to solve complex diseases.

 
 
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CONTACT

Please contact us if you are interested in the film or would like to set up a community screening. 

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