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You are here: Home / Extra Spoons / Why you and your family should watch the Unrest Documentary

Why you and your family should watch the Unrest Documentary

Last Updated: February 5, 2018

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

Why You Should Watch The Documentary Unrest

I was sent a screener of the Unrest documentary back in December but by the time I got a chance to watch it the documentary was available on Netflix, so I watched it there.

After viewing it I have 5 reasons you should not only watch Unrest, but you should watch Unrest with your family. If you haven’t heard about Unrest yet, here’s the synopsis:

Jennifer Brea is an active Harvard PhD student about to marry the love of her life when suddenly her body starts failing her.

Hoping to shed light on her strange symptoms, Jennifer grabs a camera and films the darkest moments unfolding before her eyes as she is derailed by M.E. (commonly known as Chronic Fatigue Syndrome), a mysterious illness some still believe is “all in your head.”

In this story of love and loss, newlyweds Jennifer and Omar search for answers as they face unexpected obstacles with great heart.

Often confined by her illness to the private space of her bed, Jen is moved to connect with others around the globe.

Utilizing Skype and social media, she unlocks a forgotten community with intimate portraits of four other families suffering similarly. Jennifer Brea’s wonderfully honest portrayal asks us to rethink the stigma around an illness that affects millions of people.

Unrest is a vulnerable and eloquent personal documentary that is sure to hit closer to home than many could imagine.

 

Even while watching it I couldn’t help but share with others that they needed to see this film. So, why do you need to see it?

5 reasons you should watch unrest

 

1 . You’ll identify all too well.

From the opening scene, I identified all too well.

Even though Jennifer suffers from a different illness than I do – severe CFS/ME – I’ve lived with many of the same symptoms and can recall a time when I was just as ill.

 

2 . You’ll know you aren’t alone.

Often the hardest part of chronic illness is that feeling that you are alone in it.

Rarely do we know someone personally who suffers as we do.

We rely on the internet to find others who can relate (as Jennifer did) and we make lifelong friends who we will never meet in person.

If you’ve not done that yet, keep reaching out to others online, there are so many of us.

Related: The Importance of Support Groups for Fibromyalgia 

The internet is full of others who understand your experience. Reach out to them. Share on X

3 . You’ll learn about the history of these illnesses.

Unlike some documentaries that follow the life of someone with an illness, this documentary digs further.

Unrest digs into the history of our illnesses, and how CFS/ME (and similar illnesses like Fibromyalgia and even MS) have been misdiagnosed.

It also examines how those of us suffering from these illnesses have been called hypochondriacs and hysterical for hundreds of years.Still shot of Jennifer and Omar

4 . You’ll learn how differently these illnesses are treated internationally.

Jennifer also pays attention to how differently these illnesses are treated internationally.

It’s easy to take for granted that illness is treated the same everywhere, that different countries have a consensus on the cause and treatment for an illness, but that’s obviously not true.

5 . You’ll see a view from the other side.

This documentary isn’t just about Jennifer, bu also about her husband Omar and his journey through dealing with illness.

It also examines things from the point of view of other spouses and caregivers.

If you’ve not yet viewed Unrest, you can find it on most of the online video platforms, including Netflix, Amazon, Google Play, etc.

Unrest is not the first documentary about chronic illness, nor the first about CFS/ME.

Below is a list of those I’m aware of, if you know of others please leave a comment and share them. If you have thoughts on any of these please share those as well. By sharing we can all learn together.

  • I Remember Me – documentary about a man living with CFS/ME. (my review)
  • Under Our Skin – documentary about Lyme disease
  • The Connection – documentary by Shannon Harvey, examining the various ways we can combat chronic illness. (my review)
  • Fat, Sick, & Nearly Dead – documentary about juicing to improve symptoms of chronic illness. (my review)
  • Invisible: The Film – documents the life of Megan Dinsmore, who lives with and has overcome Fibromyalgia (not yet released).

 

Related Posts: 

  • Chronic illness does not mean you are a failure. You are a success story.
  • Learning to trust yourself in the face of chronic illness
  • Learning to trust yourself in the face of chronic illness

 

Leave a Comment Filed Under: Extra Spoons Tagged With: chronic fatigue, chronic illness, documentary, review

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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