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Tired of being told there\\u2019s no name or treatment for your illness? That it\\u2019s\\n\'all in your head\' or that your pain can\\u2019t be real because you\\u2019re too\\nyoung/old/pretty/bright/healthy/normal to have a chronic disorder? \\n\\n

What if instead, there was someone who knew what you were going through\\nand could teach you strategies for coping with rare chronic illness? \\n\\n

This is not a false hope. You can turn pain into possibility with this\\nlife-changing book that can help everyone with elusive hypermobile\\nEhlers Danlos Syndrome (hEDS) \\u2013 from those newly diagnosed to those who have\\nsuffered in silence for decades. Wherever you are on your journey navigating\\nthe complexities of chronic illness, you\'re not alone. \\n\\n

Christie Cox explores not only the physical effects of hEDS but its emotional\\nimpact as well. As a fellow patient and medical rarity, known to doctors as\\nzebras, she\\u2019s experienced her body\\u2019s betrayal and suffered through the myriad\\ncomplications stemming from this disease. But she\\u2019s also found a way out from\\nthe depths of this life-altering disorder with wisdom you can turn into hope. \\n\\n

As a self-advocacy guide, she offers practical, no-nonsense advice about living\\nwith chronic illness and the concrete steps you can take to achieve a new\\nnormal. In her book, you\\u2019ll discover...\\n\\xa0\\xa0\\xa0\\xa0\\xa0\\xa0\\xa0\\n

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• A healing prescription for the miracle of the modern mindset
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• A look at the latest scientific research on the edge of answers
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• Q&A interviews with expert doctors and advocacy groups
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• Guidance for how to help loved ones better understand hEDS
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• Christie\\u2019s own inspiring story of how she came to live her best life
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• Lessons, questions and quotes to inspire your search for answers
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"This\\nbook gives you the tools and resources you need to get back to living the life\\nyou want."