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

It’s hard. That’s what they don’t tell you when you get diagnosed. They tell you things like “It’s manageable.” Of course, that is what they’re supposed to do. They’re doctors. But nobody ever tells you that it’s hard. [More]

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

I’ve read many lists describing “what not to say to someone with chronic illness,” so I wanted to offer a new spin. These lists are valuable for the chronically ill and the healthy, but the lines of communication between us can be fraught with misunderstanding. [More]

The likelihood of your developing an autoimmune disorder increases if your family members suffer from these conditions. By looking at your family history, you can find out crucial information regarding the health history of your family members [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]

Immune Deficiency Foundation’s (IDF) National Conference helps patients and their families through education and research, while providing them with a wonderful social setting to interact with one another, physicians and sponsors [More]

The Immune Deficiency Foundation is hosting its annual national patient conference in New Orleans June 25-27. The conference will feature educational and social opportunities for patients and their families to further their knowledge about primary immune diseases. [More]