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Dedicated to bringing comprehensive healthcare information, immune globulin information, community lifestyle and reimbursement news.

Posted on 10. March 2016
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Happy Anniversary, IG Living!

Help IG Living celebrate 10 years of supporting patients with chronic illness who need life-saving plasma therapies to live [More]
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Categories: Fan Spotlight | In the News | Life With IG | Need to Know | People We Admire | Speaking Out | Support & Encouragement | Teen
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Posted on 28. January 2016
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Learning to Love Valentine’s Day

For a person with chronic illness, Valentine’s Day is about more than roses and candy; it is about loving someone who is there for you. [More]
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Categories: In the News | Life With IG | Need to Know | People We Admire | Speaking Out | Support & Encouragement | Teen
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Posted on 31. December 2015
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A Chance to Participate in a Gene Study for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

The Institute for Neuro Immune Medicine is conducting a gene study for people diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome [More]
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Categories: Fan Spotlight | In the News | Life With IG | Need to Know | People We Admire | Speaking Out | Support & Encouragement | Teen
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Posted on 1. October 2015
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PANDAS/PANS Awareness Week

IG Living and I Give for Kids are supporting the national PANDAS/PANS Network Awareness Day on October 9. PANDAS/PANS is a devastating childhood disease with profound symptoms that can be devastating for families [More]
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Categories: Fan Spotlight | In the News | Life With IG | Need to Know | People We Admire | Speaking Out | Support & Encouragement | Teen
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Posted on 11. July 2013
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Hello Baltimore!

Attending the annual Immune Deficiency Foundation (IDF) national conference can be eye-opening for a PIDD patient. Attending as a teen and meeting others who share your experience can be life changing. [More]
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Categories: Life With IG | Need to Know | Support & Encouragement | Teen
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Posted on 2. May 2013
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Learning To Cope With Pain

As parents, it is difficult to see our children cope with pain especially when they have a primary immune deficiency disease. Our job as parents is finding the best ways to help them through it. [More]
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Categories: Life With IG | Support & Encouragement | Teen
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Posted on 25. April 2013
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Indebted to the Doctor Who Saved My Life

Sometimes our lives are impacted by people who seem to be angels in disguise. For this young IVIG patient, that angel was a skilled physician with a warm Southern accent. [More]
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Categories: Life With IG | Need to Know | Teen
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Posted on 14. March 2013
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Rise, Shine and Pray for Strength

Getting kids out of bed in the morning can be challenging. When your child has primary immunodeficiency and wakes up feeling sick and exhausted, the task at hand can seem insurmountable. [More]
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Categories: Life With IG | Support & Encouragement | Teen
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