Happy Thursday!
This week, we’re highlighting a PW contributor’s story exploring blepharospasm and mental health and an article on two sisters with a rare connection. Following that, we have a story on new recommendations that recently came out for HAE patients, and an overview of the Glut 1 Deficiency Foundation conference.
Sit back and enjoy this week’s editor’s choice!
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Coming Through the Darkness: a Blepharospasm Story
One PW contributor shares a story on chronic illness and mental health. [/one_half_last]
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Scleroderma: The Skin-Hardening Disease Affecting Two UK Sisters
It’s rare for ONE sister to have scleroderma- let alone two!
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Study Findings Result in New Diagnostic Recommendations for Hereditary Angioedema in the ER
How should doctors treat HAE patients in the ER? New recommendations have come out regarding this question.
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Glut1 Deficiency Foundation 2019 Conference Highlights!
We recently had a chance to attend the Glut 1 Deficiencey Foundation conference. Here are the highlights! [/one_half_last] [one_half]
