
What Wouldn’t You Do Right Now For Your Child with a Rare Disease?
Founder of the Texas Rare Alliance, Khrystal Davis, has a child, Hunter, and Hunter has
Founder of the Texas Rare Alliance, Khrystal Davis, has a child, Hunter, and Hunter has
Kate Across America finds Debbie Healy of Pennsylvania; an advocate who gives us a strong
Brian has had HIV for more than 20 years. It wasn’t long ago that living
Occasionally we’ll hear stories about a heart transplant. What you rarely hear is the excruciating
“Social determinants of health” are about the environment in which people live, go to school,
Mast Cell Activation Syndrome (MCAS) isn’t an easy diagnosis to make if Tara’s journey is
Kate visited with Angela of Illinois. They talked about how Angela overcame some glaring inequities
The familiar narrative for treatment of a cancer diagnosis is that the process can be
Kate Across America takes us to Massachusettes this week to meet Kelly. Kelly did all
In a bit of a twist of events this week, I wanted my latest blog
To succeed as a patient in America, you cannot afford to be passive. Today Kate
In this installment of Kate Across America, Kate speaks with Lori Long of California. Lori
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