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

Posted on 19. May 2016
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A Mother’s Fear

How a mother copes with the possibility her child has inherited her immune deficiency [More]
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Categories: Life With IG | Speaking Out | Support & Encouragement
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Posted on 28. April 2016
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Rules for Living with Multiple Diagnoses

Joanna Tierno’s 10 rules on life for patients living with multiple diagnoses. They say that lightning rarely strikes the same place twice. But, that is a myth... The same is true for patients with primary immune deficiency diseases (PIs). [More]
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Categories: Life With IG | Support & Encouragement
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Posted on 21. April 2016
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Sick But Social: The Faithful Friend

Stacey Philpot shares how having a friend to share your experiences with makes having a chronic illness easier to live with. [More]
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Categories: Life With IG | Support & Encouragement
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Posted on 24. March 2016
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5 Tips on Coping with an Incurable Illness

Knowledge is power and can help you chart the best course of action, such as finding the best doctors and treatments for your conditions. I have a handful of chronic, incurable diseases and conditions at this time. Joanna Tierno’s blog gives patients five tips for living with their disease. [More]
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Categories: Life With IG | Need to Know | Speaking Out | Support & Encouragement
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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 25. February 2016
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Living with CVID

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]
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Categories: Fan Spotlight | In the News | Life With IG | Need to Know | Speaking Out | Support & Encouragement
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Posted on 28. January 2016
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Learning to Love Valentine’s Day

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]
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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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