Help IG Living celebrate 10 years of supporting patients with chronic illness who need life-saving plasma therapies to live [More]

For most of my life, just the mention of Valentine’s Day would give me hives. Growing up, I wasn’t the kind of girl whom everyone wanted to be friends with. This was before teachers started requiring that everyone in the class be given a card. [More]

The Institute for Neuro Immune Medicine is conducting a gene study for people diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome [More]

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]

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]

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]

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]

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]