Reviews

"Enero has been, and continues to be a trusted editor for many of our video projects. She always brings a contemporary look to a medium that can look corny in the wrong editorial hands."


"Great Results, High Integrity, Creative!"


"I know this will be a very different type of presentation at one of these strictly educational meetings of routine examples and regulation of clinical research. Because of you, this one will be lively and exciting while emotional, causing the listener to feel their purpose and renew their vision."


"Everyone truly enjoyed the DVD.  The sequence of events flowed very smoothly and the music was perfect!  Great Job!"

 

"The client loved the highlight and Beautiful Boy extra!  They were in tears!"


"Phenomenal job!!  Very moving.  My family is going to love our copy."


"I can't believe how you captured the feeling, happiness and fun we had those few days..."


"We just watched the DVD.  You did an excellent job.  I can tell you put a LOT of time into it, and it showed.  Great job, and thanks!"


"You are awesome...what talent!"



ABOUT THE FILMMAKER:

Enero is a Film Auteur and Visual Artist residing in Chicago, IL. She holds at Bachelors degree from Columbia College, Chicago in Film and Video. Enero has worked several independent and feature productions; and, is always in collaborative efforts with local musicians and artists.

ABOUT THE FILM:

Every week in the United States 200 people are diagnosed with Multiple Sclerosis. In Canada every day another 3 people are diagnosed with the same illness. Worldwide MS is thought to affect 2.5 million people. No two people have the same symptoms. MS is a chronic, unpredictable disease of the central nervous system. It is thought to be an autoimmune disorder. At this moment in history there is no cure for Multiple Sclerosis.

Most of the general public may know the initials MS and/or the words Multiple Sclerosis; however, do not understand what those words really entail. Upon my own diagnosis in 2007, I was confused and frightened. I had absolutely no concept of what this meant for my life and my body. Upon further research and getting to know others with MS, I found that I was not the only one. As I began to disclose to family and friends even more ignorance about the illness came to light. And so, I decided to use my skills and passion for filmmaking to tell this much needed story.

This documentary will follow many unique and powerful stories told by a person living with MS. As well, I will share my own story. The viewer will get to know the person behind the initials (M.S.) and follow his or her trek with the illness . "That Day" will also discuss the history of MS, the current treatments and the medical advancements on the horizon by incorporating expert interviews with medical professionals, specializing in Multiple Sclerosis.


The amount donated will go towards development and production, including but not limited to:

Hiring of crew
Equipment rental
Archival and stock footage
Research
Travel expenses and related
Expert interviews

Currently we are building our production team as well as coordinating travel and interviews with people who have offered to share their story.

Thus far five stories/interviews have been confirmed.
Two medical professionals are also confirmed, one of which is a leading expert in Multiple Sclerosis.

Your contribution will greatly help us reach our goal of completing a 90 minute feature documentary on MS.