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Meghan Bea

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Meghan Bea has lived with lupus for over a decade and is still learning about her disease. She began writing as part of her rehabilitation from a severe brain flare in 2014 and simply never stopped. Read more.

Scheduling My Life Around Lupus

When I first became sick at 21 years old, I was an active person balancing a job and my first year of...

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By Meghan Bea

3 min read
1comment
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Managing Lupus Hair Loss

Losing my hair was one of the first symptoms I noticed when I began to get sick. When I brushed my hair...

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By Meghan Bea

3 min read
21comments

Interview With Entrepreneur and Lupus Warrior Sara Gorman

As a newly diagnosed lupus patient in my early 20s, I used to hide my prescription bottles because I was so embarrassed...

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By Meghan Bea

3 min read
comments
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Why I Joined a Lupus Support Group

At my very first support group meeting, I walked into the Italian restaurant with sweaty hands. Not even the aroma of garlic...

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By Meghan Bea

3 min read
14comments
What A World Built For Lupus Patients Would Look Like image

What A World Built For Lupus Patients Would Look Like

As a sick person in a world built for the healthy and able-bodied, I’ve often struggled to keep up with my peers...

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By Meghan Bea

3 min read
2comments
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