Hollywood Phenom Maurissa Tancharoen Whedon Fights Lupus
Spring Issue of Lupus Now® Magazine highlight’s how she found support through her all-star network of friends and family
Washington, DC, April 05, 2012 --(PR.com)-- Maurissa Tancharoen Whedon has done it all--actress, singer, dancer, and television writer and producer. The 36 year-old Hollywood phenom started out as a singer during her teen years for a Motown band, and has gone on to write, act, and produce for shows, such as Fox’s Dollhouse, Lifetime’s Drop Dead Diva, and the widely successful Web series, Dr. Horrible’s Sing-Along Blog. But another one of her many titles: a person living with lupus. Diagnosed with lupus as a teenager, it wasn’t until the 2011 Lupus Foundation of America’s (LFA) WALK FOR LUPUS NOW® in Los Angeles, that this self-described “Lupus Warrior Princess” decided to face her disease one step at a time with the people who loved and supported her most.
The spring issue of Lupus Now® magazine, published by the Lupus Foundation of America highlights how Maurissa - also known as Mo to her friends – fought back against her disease and found support through her all-star network of friends and family. What started out as a bright red rash in her teen years manifested into central nervous system lupus, which affects the brain and nervous system, then pulmonary vasculitis and now, as lupus nephritis. Enduring chemotherapy, kidney failure, and fatigue among many other symptoms of the disease, Mo admitted that she, at times, felt alone.
“There have been times when I’ve succumbed to feeling hopeless or just plain angry about all of it. And alone,” Tancharoen wrote on her blog, itssonotsexy.tumblr.com. “Then there are moments like these that remind me that I’m not alone.”
That moment came in 2011 in an email from a friend asking Mo if she could start a team for the Los Angeles WALK FOR LUPUS NOW®, aptly named “Club Mo”. Mo’s family rallied quickly to join the walk team, including her brother Kevin Tancharoen, director of 2009’s Fame and 2011’s Glee: The 3D Concert Movie and brother-in-law, Joss Whedon, best known for Buffy the Vampire Slayer, Firefly, Serenity, and Dollhouse. Emails, social media, and word-of-mouth encouraged celebrity friends of Mo and her husband, Jed Whedon, to register to walk and reach out to their fans to donate money to support lupus research. Felicia Day, star of the Web series, The Guild, Eliza Dushku of Buffy and Dollhouse, and Nathan Fillion from ABC’s Castle, and of Firelfy, Dr. Horrible and Buffy fame were among those that supported Club Mo and helped raised nearly $80,000.
“This is the other power of the Lupus Walk,” says Joss Whedon. “The battle for new drugs continues. People see that. They aren’t stopping.”
The team hopes to walk again this year, especially if Mo is up for it and they plan on challenging themselves and their supporters to raise even more money for individuals with lupus and their families.
To read the complete article, or to order a subscription to Lupus Now® magazine, go online to lupusnow.org, contact your local LFA chapter, or call 866-4-THE-LFA. Published three times per year for people with lupus, their families, and health professionals, Lupus Now® includes the latest information on new treatments, clinical trial updates, lifestyle and wellness features, personal stories, and more.
About Lupus
Lupus is an unpredictable and potentially fatal autoimmune disease in which the immune system is out of balance, causing inflammation and tissue damage to any organ system in the body. The health effects of lupus include heart attacks, strokes, seizures, and organ failure. An estimated 1.5 million Americans and at least five million people worldwide have a form of lupus. For more information, visit www.lupus.org.
About the Lupus Foundation of America
The Lupus Foundation of America (LFA) is the nation’s foremost nonprofit voluntary health organization dedicated to finding the causes of and cure for lupus, and providing support, services, and hope to all people affected by lupus. The LFA and its network of chapters, branches, and support groups conduct programs of research, education, and advocacy.
Media Contacts:
Maggie Maloney, Maloney@lupus.org, 202-212-6766
Duane Peters, peters@lupus.org, 202-349-1145
The spring issue of Lupus Now® magazine, published by the Lupus Foundation of America highlights how Maurissa - also known as Mo to her friends – fought back against her disease and found support through her all-star network of friends and family. What started out as a bright red rash in her teen years manifested into central nervous system lupus, which affects the brain and nervous system, then pulmonary vasculitis and now, as lupus nephritis. Enduring chemotherapy, kidney failure, and fatigue among many other symptoms of the disease, Mo admitted that she, at times, felt alone.
“There have been times when I’ve succumbed to feeling hopeless or just plain angry about all of it. And alone,” Tancharoen wrote on her blog, itssonotsexy.tumblr.com. “Then there are moments like these that remind me that I’m not alone.”
That moment came in 2011 in an email from a friend asking Mo if she could start a team for the Los Angeles WALK FOR LUPUS NOW®, aptly named “Club Mo”. Mo’s family rallied quickly to join the walk team, including her brother Kevin Tancharoen, director of 2009’s Fame and 2011’s Glee: The 3D Concert Movie and brother-in-law, Joss Whedon, best known for Buffy the Vampire Slayer, Firefly, Serenity, and Dollhouse. Emails, social media, and word-of-mouth encouraged celebrity friends of Mo and her husband, Jed Whedon, to register to walk and reach out to their fans to donate money to support lupus research. Felicia Day, star of the Web series, The Guild, Eliza Dushku of Buffy and Dollhouse, and Nathan Fillion from ABC’s Castle, and of Firelfy, Dr. Horrible and Buffy fame were among those that supported Club Mo and helped raised nearly $80,000.
“This is the other power of the Lupus Walk,” says Joss Whedon. “The battle for new drugs continues. People see that. They aren’t stopping.”
The team hopes to walk again this year, especially if Mo is up for it and they plan on challenging themselves and their supporters to raise even more money for individuals with lupus and their families.
To read the complete article, or to order a subscription to Lupus Now® magazine, go online to lupusnow.org, contact your local LFA chapter, or call 866-4-THE-LFA. Published three times per year for people with lupus, their families, and health professionals, Lupus Now® includes the latest information on new treatments, clinical trial updates, lifestyle and wellness features, personal stories, and more.
About Lupus
Lupus is an unpredictable and potentially fatal autoimmune disease in which the immune system is out of balance, causing inflammation and tissue damage to any organ system in the body. The health effects of lupus include heart attacks, strokes, seizures, and organ failure. An estimated 1.5 million Americans and at least five million people worldwide have a form of lupus. For more information, visit www.lupus.org.
About the Lupus Foundation of America
The Lupus Foundation of America (LFA) is the nation’s foremost nonprofit voluntary health organization dedicated to finding the causes of and cure for lupus, and providing support, services, and hope to all people affected by lupus. The LFA and its network of chapters, branches, and support groups conduct programs of research, education, and advocacy.
Media Contacts:
Maggie Maloney, Maloney@lupus.org, 202-212-6766
Duane Peters, peters@lupus.org, 202-349-1145
Contact
Lupus Foundation of America
Maggie Maloney
202-212-6766
www.lupus.org
Maggie Maloney
202-212-6766
www.lupus.org
Contact
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