Invisible Illness Documentary Film - You Are Not Alone
Invisible Illness Documentary Film - You Are Not Alone
Feature-length documentary sharing stories of hope, resilience, and courage from those living with and healing from Invisible Illness.
Feature-length documentary sharing stories of hope, resilience, and courage from those living with and healing from Invisible Illness. Read more
WHY THIS FILM?
Invisible Illness Film. A feature documentary of hope and resilience for and about people living with and healing from invisible illness.
Chronic pain. Lyme disease. Fibromyalgia. Diabetes. SIBO. Chronic Fatigue Syndrome. Endometriosis. Depression. PTSD. POTS. Hashimoto's. Infertility. Traumatic brain injury. The list goes on and keeps growing, in the number of illnesses and amount of people affected by them.
Millions of people around the world are suffering in silence.
In the United States alone, nearly one in two people (133 million) has a chronic medical condition. 96% of people with chronic medical conditions show no outward signs of their illness.
These and other conditions and illnesses don't necessarily manifest themselves in such a way where you can easily see the pain a person is suffering. This often results in friends, family, and even the medical community doubting or even dismissing the individual. So not only is the illness "invisible," often the person suffering feels invisible and invalidated.
Help us give a voice to the invisible and bring this project to life. Become a backer and share this much-needed project with your friends and community.
THIS FILM IS FOR...
...people living with invisible and/or chronic illnesses, who have lost their identity, dreams, jobs, sometimes even their friends, family and homes to the emotional, physical and financial ramifications of illness.
...people supporting those living with invisible illness, whose lives have been turned upside down as they take on the new role of caregiver and try to maintain career and family, while navigating complicated medical, insurance, and disability systems.
...friends, family, colleagues, and others who may know someone with a diagnosis, and not know how to support or encourage in a tangible way. People who aren’t dealing with health issues and feel unclear or confused about invisible illness, and want a practical way to show their support.
The main topics for the film include:
- Living with physical pain and chronic conditions
- Grieving identity loss and limitations
- Becoming your own advocate
- Vital role of caregivers and support people
- Working within medical and insurance systems
- Stigma and judgment of mental and physical illness
- Alternative healers and treatments
- Impact of stress, triggers and trauma
- Pain, movement, and listening to your body
- Creating connections and community
- Inspiring stories from survivors and healers
- Future vision of health care vs sick care
Our Message is Our Mission
Whether you have an illness yourself, or have friends or loved ones who do, everything changes when invisible illness becomes part of your life.
We want to let everyone affected by invisible illness know that they are not alone, that those who are healthy and well see them and support them in their suffering.
If you are dealing with chronic pain and illness, we want to inspire you to be a strong advocate for yourself or your loved ones when working within the medical system AND insurance companies.
You have the right to TRUST YOUR BODY and SPEAK UP for yourself.
This film will show you how to survive and thrive with invisible illness.
WHERE IT ALL BEGAN
When I stepped into the crosswalk five years ago, I had no way of knowing that my life would never be the same.
Although I landed on my feet, a distinctly different life is inevitable after a 2-ton vehicle crashes into you. The impact threw me six feet in the air.
Even now, after 5 years, 50+ specialists, 100+ medical tests, 500+ appointments, countless pills and failed treatments, being poked and prodded like a lab rat, I still carry the same pain that began that day. One thousand nine hundred seventy-five days of pain… so far. That’s just one of the consequences of a single moment of impact. The other consequences came later, from medical “care” and treatments.
Most of my injuries and illnesses are “invisible” and that changes everything about diagnosis, treatment, and recovery.
Over the past five years, I have felt confused, abandoned, betrayed, alone… and invisible. I never want anyone else to feel that way. And so, I’ve been working on a heart project, a project that a dear friend and mentor calls “soul important” work.
My husband, a professional filmmaker, and I have begun production on this feature-length documentary to tell the stories of people living with Invisible Illness.
Whether it’s chronic pain, Crohn’s, Lyme, CFS, IBS, SAD, OCD, TBI, BPD, ADHD, PCOS, POTS, SIBO, PTSD, or any other illness distilled into a 3- or 4-letter word, our stories need to be shared.
Stories of hope and resilience, courage and perseverance, and above all, a sense of community and belonging are sorely needed. We need to hear not only the stories from those suffering, but also from the people supporting and healing those who live with invisible illness.
Your illness may be invisible, but you don’t have to be.
To make matters worse, our healthcare system often doesn’t have the resources or definitive answers patients are seeking. Many times medical professionals aren't prepared to deal with invisible or rare illnesses, which may significantly delay diagnosis and treatment.
Perhaps you've experienced or can imagine the frustration involved with doctors repeatedly telling you “nothing is wrong" when your body is telling you otherwise. Or worse, they prescribe treatments that exacerbate your condition.
YOU ARE NOT ALONE... OR INVISIBLE
More than anything we want to inspire, encourage, and empower those living with an invisible illness to be resilient and have the confidence to be their own advocates. We want them to know they are not alone and there is a supportive, thriving community of invisible illness survivors and healers, going through the same challenges, creating a safe place where they can connect, find hope and feel support for their experience.
PLEASE SHARE THIS IMPORTANT MESSAGE
In addition to backing the project, you can support the film by sharing it...
Facebook. Click the "Share" button at the top of the page under the green "Back this Project" button. When you share, add a short blurb about why you think the project is important.
Twitter. Share a tweet below with just one click or write your own (click the links below to pre-populate your tweet. You'll be able to tweak it before sharing):
Email. Statistics suggest that you know at least two people who are suffering from an invisible illness. You can encourage friends and family simply by sharing this project.
IRL. You can share in real life too! Imagine that! Conversations at your workplace, school, doctor's office, yoga studio, place of worship, local library, community center, and more are perfect opportunities to spread the word about this life-changing film!
WHERE'S THE MONEY GOING?
Because we believe in this project, we've already invested hundreds of hours and tens of thousands of dollars into making it a reality. As we reach the finish line, we need support to finish the film and share it with the world.
Here's a breakdown of where the raised funds will go:
- 10% - Kickstarter and processing fees
- 15% - Reward fulfillment (e.g. fulfillment services, books, DVDs, photo boxes, shipping)
- 35% - Final principal photography costs (e.g. shooting additional interviews and b-roll and travel expenses)
- 25% - Post production (e.g. editing, color grading, sound design)
- 10% - Mandatory taxes
- 5% - Music licensing
From the very first interview we conducted two years ago, to the primary principal photography which began last summer, we have captured amazing stories and inspirational interviews with people living with invisible illness, their loved ones, and healers. We have collected ample material to turn this into a mini-documentary series if we surpass our funding goal.
If we succeed in funding, we plan to complete principal photography by May, and begin logging the hundreds of hours required to complete the editing of the film. Our goal is to finish editing in June and begin mastering the final film plus begin reward fulfillment in July. (See the individual reward descriptions for their respective delivery date estimates.)
WE'D LOVE TO HEAR FROM YOU
Reach out and say "hi" or ask as any questions you have about the campaign.
Ron Dawson (producer/dp)
- email: firstname.lastname@example.org
- Twitter: @DareDreamerRon
Tasra Dawson (writer/director)
Risks and challenges
Any creative project worth doing comes with risks and challenges. For this project, we are confident that the time and investment already put into filming and development will give us a solid base for completing this project within the anticipated timeline. There are always unexpected challenges that could arise, including new interviews we want to include and additional footage we want to capture. However, we are putting plans into place for keeping us on track with fulfilling all the rewards on time and on budget. Your support will help us meet that goal!Learn about accountability on Kickstarter
- (30 days)