Tired of being told there’s no name or treatment for your illness? That it’s
'all in your head' or that your pain can’t be real because you’re too
young/old/pretty/bright/healthy/normal to have a chronic disorder?
What if instead, there was someone who knew what you were going through
and could teach you strategies for coping with rare chronic illness?
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.
Christie Cox explores not only the physical effects of hEDS but its emotional
impact as well. As a fellow patient and medical rarity, known to doctors as
zebras, she’s experienced her body’s betrayal and suffered through the myriad
complications stemming from this disease. But she’s also found a way out from
the depths of this life-altering disorder with wisdom you can turn into hope.
As a self-advocacy guide, she offers practical, no-nonsense advice about living
with chronic illness and the concrete steps you can take to achieve a new
normal. In her book, you’ll discover...
"This
book gives you the tools and resources you need to get back to living the life
you want."
