Check out and pass along the Editor’s Choice articles of the week!
In this interview ankylosing spondylitis heroine, Charis, explains her diagnosis, the everyday realities of living with A.S. and her sheer determination to make a difference.
Olivia Trueb lives every teenage girl’s dream. As in, she’s got a team of professional football players that are wrapped around her finger, and much to her surprise, she can thank her Common Variable Immune Deficiency (CVID) diagnosis for it.
One thing that almost every person living with or caring for someone living with hereditary angioedema (HAE) knows is that over time…
No one knows more about hereditary angioedema than those dealing it. So, here are 10 things every HAE patient strongly wants their healthcare providers to know.
This little girl with cystinosis got an unexpected gift from an unexpected giver. Her story will put a smile on your face. Guaranteed!
Pass the roundup along by choosing a social network below. Have a great weekend!