 Not having a diagnosis for weeks, months, or years is torture.
The torment never stops when you’re stuck waiting for answers. The tests never stop, the questions never stop, the #Anxiety never stops. Most importantly, the pain and symptoms don’t stop. Nothing ever stops – until you finally get your answers. Or so I thought… Call me naive, but I really believed that once I received my confirmed diagnosis of #Endometriosis, things would start to get better, not worse. Once I had my answers, I could create a plan for my pain and symptoms then get back to living life as once before this nightmare started. My new chapter of putting all this behind me would finally begin. For a lot of us with chronic illnesses, that's simply not how it always goes. |
Endo-Sisters Unite As OneTrying to share how endometriosis affects women differently to increase disease awareness and shorten the long diagnosis time, one story at a time. Categories
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