Broken
Living with EDS and Other Chronic Conditions
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Narrated by:
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Marcia Brock
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Cassandra A Campbell
About this listen
Broken is an autobiography depicting elements of the author's experiences of living with chronic illnesses.
Marcia Brock has lived with hEDS, Raynaud's syndrome, lupus and has survived cancer several times. Cassandra A Campbell has been living with hEDS and fibromyalgia. Together they deliver workshops for Ehlers-Danlos.org. Both authors deliver this audiobook.
PLEASE NOTE: When you purchase this title, the accompanying PDF will be available in your Audible Library along with the audio.
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F--k Your Feelings: Master Your Mind, Accomplish Anything and Become a More Significant Human
- By: Ryan Munsey
- Narrated by: Ryan Munsey
- Length: 9 hrs and 15 mins
- Unabridged
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95 percent of decisions are based on feelings. Not logic. Not rational thought. Feelings. Can you feel the pull of emotions, hunger, guilt, pain, jealously, depression, and everything else weighing on every decision that you make? Business owners, entrepreneurs, regular people looking to get in shape, anyone with a goal that isn't terrified of tough love - you need to listen to F--k Your Feelings - as soon as possible! In this audiobook you'll learn how to use personal mind control techniques to control the way your brain is wired and much more.
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Science heavy for those of us who want the why
- By Beth T. Irwin on 10-29-18
By: Ryan Munsey
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The Finnish Guide to Happiness
- By: Melanie Dower
- Narrated by: Saskia Maarleveld
- Length: 2 hrs and 24 mins
- Original Recording
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If you ask a Finn, they will likely be as baffled as you are. That’s why Melanie Dower, an expat who has been living in Finland for the past decade, has taken up the charge. Her vantage as an outsider entrenched in Finnish culture uniquely positions her to identify the keys to Finnish happiness that elude the rest of the world and that Finns take for granted. From sauna to strong social safety nets, Finnish life is made up of a constellation of habits and structures that leave its residents relaxed, healthy, and fulfilled.
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INSPIRING BOOK. (Listening after Hurricane Helene)
- By Duchess on 10-21-24
By: Melanie Dower
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I Thought It Was Just Me (but it isn’t)
- Telling the Truth about Perfectionism, Inadequacy, and Power
- By: Brené Brown
- Narrated by: Lauren Fortgang
- Length: 10 hrs and 44 mins
- Unabridged
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Based on seven years of ground-breaking research and hundreds of interviews, I Thought It Was Just Me shines a long-overdue light on an important truth: Our imperfections are what connect us to each other and to our humanity. Our vulnerabilities are not weaknesses; they are powerful reminders to keep our hearts and minds open to the reality that we're all in this together.
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I'm sure its great if you are a mother ....
- By Leslie A Hill on 08-09-11
By: Brené Brown
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Ehlers-Danlos syndrome is known to be a condition in which people usually have hypermobile joints and stretchy skin. This is what physicians generally look for when they are considering EDS diagnoses. The truth is that EDS can present in many different ways. There are many different types and forms of EDS, and they affect very different parts of a person's body. A physician who looks for only two signs is missing the big picture of the family history and the patient's symptoms in relation to an EDS diagnosis.
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Aweful.
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Surviving and Thriving with an Invisible Chronic Illness
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Do you live with a chronic, debilitating, yet invisible condition? You may feel isolated, out of step, judged, lonely, or misunderstood - and that's on top of dealing with your actual illness. Take heart. You are not alone, although sometimes it can feel that way. Written by a blogger who suffers from an invisible chronic illness, Surviving and Thriving with an Invisible Chronic Illness offers peer-to-peer support to help you stay sane, be your own advocate, and get back to living your life. This compelling guide is written for anyone suffering with an illness no one can see.
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Great Reference Guide!
- By Heather D on 03-21-18
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POTS: What It Really Is & Why It Happens
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Postural orthostatic tachycardia syndrome (POTS) is currently defined as a "syndrome", a collection of symptoms for which the root cause has not yet been identified. This book aims to rectify this by arguing the case for POTS being considered a form of neurological injury to the limbic system following an antecedent trauma, such as a viral illness, pregnancy, surgery, or psychological trauma (or a combination).
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Only The Authors Opinions on Specific Treatment...
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Overall
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-
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Loses credit with misinformation
- By James on 10-10-16
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Holding It All Together when You're Hypermobile
- Achieve a Better Life Experience with EDS, POTS, and Joint Instability
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- Narrated by: Rebecca Winder
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This is not a false hope. You can turn pain into possibility with this life-changing book that can help everyone with elusive hypermobile Ehlers Danlos Syndrome (hEDS)–from those newly diagnosed to those who have suffered in silence for decades. Wherever you are on your journey navigating the complexities of chronic illness, you're not alone.
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Aweful.
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Surviving and Thriving with an Invisible Chronic Illness
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Performance
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Do you live with a chronic, debilitating, yet invisible condition? You may feel isolated, out of step, judged, lonely, or misunderstood - and that's on top of dealing with your actual illness. Take heart. You are not alone, although sometimes it can feel that way. Written by a blogger who suffers from an invisible chronic illness, Surviving and Thriving with an Invisible Chronic Illness offers peer-to-peer support to help you stay sane, be your own advocate, and get back to living your life. This compelling guide is written for anyone suffering with an illness no one can see.
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Great Reference Guide!
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Postural orthostatic tachycardia syndrome (POTS) is currently defined as a "syndrome", a collection of symptoms for which the root cause has not yet been identified. This book aims to rectify this by arguing the case for POTS being considered a form of neurological injury to the limbic system following an antecedent trauma, such as a viral illness, pregnancy, surgery, or psychological trauma (or a combination).
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Only The Authors Opinions on Specific Treatment...
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What listeners say about Broken
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- John A.
- 09-19-21
A great book
An odd disease that likely afflicts a great majority of the western populous. Great read!
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- Amy Orr
- 01-23-23
Great story’s
These story’s made me feel like I was not alone. My 2 daughters I have gone through life been told so many negative things. The main we are clumsy or it’s not that bad. This book will help so many who don’t realize they have this condition. Thank you
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- Colleen C
- 08-05-23
EDS definitely affects everyone differently
Enjoyed, however as a EDS patient "Zebra " myself, there is something missing. Maybe more Medical Facts.
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- Anonymous User
- 07-22-24
We deserve better 🦓
I REALLY wanted to love this book and give it high praise, instead, I find it a shallow, myopic marketing pamphlet for the authors. As a hEDS sufferer, I was looking for an informative book with intersectional perspectives, firmly grounded in science, reflected in personal experience. That is NOT what this is. Instead it's navel gazing, embarrassingly badly written, swamped with repetition, and worst of all, preaching pseudoscientific treatments of medical issues. This is inexcusable as it may put people at severe medical risk. Yes, the general medical system is deeply flawed and severely lacking in knowledge of, and effective treatments for EDS sufferers, the solution is however not to have your aura photographed and drink diluted tea. Educate yourself, make sure the references are founded in best practise scientific research, and find a doctor who actually does have competence to treat you. It's painstakingly hard work, but sadly the only option. We deserve better.
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