Want some more news, events and announcements on SCID? We got ’em!
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The Expense of Scientific Progress: The Price of Gene Therapy for SCID
The Second Commercial Gene Therapy EVER: The Future of SCID
By Mid-2017, New Zealand Will be the Fourth Country Who Screens for SCID
What Gene Therapy Could Mean for SCID
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How This Kid with SCID was Able to Live a Normal Life
Day Zero: Read This Kid’s SCID Story
All in the Family: A Trio with SCID
SCID is Rare, But not for this Family
How this 70-Year-Old is an Advocate for the SCID Community
You Can’t Ignore SCID after Seeing this Little Girl’s Smile
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Are You Going to the World’s Largest PI Gathering in June?
Coming Together with Primary Immunodeficiency
How to Spend Your Summer Vacation with PI
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The First Six Things You Need to Know About Your Child’s SCID Diagnosis
A Resource You Can Use to Help Explain Your Child’s SCID Diagnosis to Others
Think Your Child May Have SCID? When to Call the Doctor
What to Expect Following Your Child’s SCID Diagnosis
What “The Boy in the Bubble” Really Means
SCID’s Science Explained: For the Patients Who Aren’t Scientists
Have a Child with SCID? A Transplant Could Help
Representation Is Only Good If its Accurate: Misinformation of SCID in the Media
The Basics of Screening for SCID
Raising a Child with SCID: What to Expect
Underdiagnosed? SCID may be Less Rare Than We Think
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