I think connection is vital for those who live with a rare disease -- especially those of us whose disease is invisible to others. Kathi Timothy Myasthenia Gravis

Because of Sarcoidosis and other chronic illnesses, I can't do that anymore. But that doesn't mean I can't do anything. I just have to find different things to do and different ways to do them. Kerry Wong Sarcoidosis

The trauma of not being able to do anything -- other than meeting doctors and swallowing medicines -- was frustrating. Kalpen Shukla Hyper-IgE Syndrome (HIES, Job/Job's Syndrome)

Life becomes an endless cycle of finding strength to keep the faith. Ultimately, you realize that hope and strength come from sharing your story. Kristine DiDesidero Autoimmune Hepatitis

The writers in Kaleidoscope #RareDisease Stories show strength, courage, creativity, and, even through fear, hope.
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