Click on photo or name to
read their stories
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| Chris |
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My name is Chris. I was diagnosed with discoid lupus over
thirty years ago and developed systemic lupus a decade later.
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Over the years, I have learned to listen to my body
and advocate for myself. I believe that knowledge is
power. Thanks to the Lupus Foundation New England, I
benefit from new ways to live well with Lupus.
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This
is my story. One voice from many and it is my hope that
research will fund a cure. You can help me by contributing
a gift of any size to the Lupus Foundation New England.
Please click here
to make a donation. With your help, we are building
hope for a cure.
If you would like to submit your picture and share your
story of lupus with others please contact Beverly Jarosz
at the Foundation by emailing her at bjarosz@lupusne.org
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