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Amarissa at the 2014 Lupus Foundation of America Evening of Hope |
Two years ago, my vibrant thirteen year-old daughter Amarissa - an aspiring gymnast - could barely walk. She was so tired that she could hardly lift herself out of bed.
Her diagnosis was lupus. As she lay in a hospital bed with an enlarged heart and a failing liver, she told me she didn't want to die.
Fighting - that's what the Lupus Foundation of America does every day for the millions of people impacted by this devastating disease.
They are fighting lupus in children through the only research program dedicated to pediatric lupus. This month, the Lupus Foundation of America has been challenged by of the Wallace H. Coulter Foundation and the Louis Berkowitz Family Foundation to raise $100,000 to support research programs like this.
Your $25 gift becomes $50
Your $100 gift becomes $200
Your $500 gift becomes $1,000
Amarissa has fought hard. Today her lupus is under control thanks to the fourteen pills she takes daily. She has resumed gymnastics and has become a lupus advocate. Lupus is a cruel disease though, and we never know when it might become active again.
We're counting on you!
Dyan
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