Like his brother, he was angry—that Mo should have to “put away” the dancer part of herself because the disease was attacking her body. Her doctor gave her the green light to walk, but mornings were slow going, full of fatigue and pain. After a mile, Jed brought her back to the booth to ensure she didn’t overextend herself.Even amid the joy and celebration that followed—the dance party that erupted between booths, the handshakes from walker to walker—the fact of Mo’s disease remained.“It’s such a positive and festive event that you can forget for a moment that this isn’t something that’s theoretical in Mo’s life,” Joss says. She was between takes and paused. “Then there are moments like these that remind me that I’m not alone.”Meanwhile, Jed Whedon, Mo’s husband, sent a short note to Adams with one message: Thank you.
The Los Angeles Walk to End Lupus Now® was seven weeks away. Walkers met others affected by the disease.“It seemed like every person I talked to about this Walk knew someone or was related to someone who has or had lupus,” Smith says. The Whedon brothers were there. Within two days, her fans had donated $5,000.“Tears of joy are streaming down my face right now,” Mo wrote on her blog the next day. She wrote for and acted on Fox’s Dollhouse. Subscribe to our emails.The Lupus Foundation of America works to improve the quality of life for all people affected by lupus through programs of research, education, support and advocacy. Joss has a lot of fans—and all of them would want to join. There are multiple chapters near you. They doubled back to retrieve it.When the couple finally appeared, a wall of people wearing Mo’s face on their chests greeted her. All told, the team had raised nearly $80,000.This is the other power of the Lupus Walk, says Joss. Above it, the team’s name. Jed is already worrying that the team may not reach the same heights.
She turned to Twitter—and her more than 1 million followers.“I’m participating in my first-EVER charity walk, for lupus,” she tweeted on Aug. 4. Gmail showed a new message from Nirvana Adams, a friend whom Tancharoen Whedon—Mo to her friends—hadn’t seen in months. Would Mo mind if Adams and their mutual friend Amy Smith started a team in her name?“Would that be okay?” Adams asked. A post shared by Maurissa Tancharoen (@motancharoen) on Jul 30, 2019 at 7:36am PDT View this post on Instagram Last day of #agentsofshield My god, I love these people.
She found herself checking the team page three times a day to watch the team break its own fundraising record. “I have the most amazingly wonderful friends.”A few weeks after her kidney flare began, Mo began That often meant she didn’t talk about the disease much when she wasn’t in a flare. In the rush to get out the door, Mo forgot her sun hat. 7 seasons
Maurissa Tancharoen Shares Behind-the-Scenes Photos From Her Guest Appearance on Agents of SHIELD . How Maurissa Tancharoen Whedon became an advocate for lupus On a Monday morning in early August, the sun was on its way to heating the Los Angeles basin to a glorious 80 degrees, but 36-year-old Maurissa Tancharoen Whedon was shut inside her home. Maurissa Tancharoen (/ m ə ˈ r ɪ s ə ˌ t æ n tʃ ə ˈ r oʊ n /; born November 28, 1975 in Los Angeles, California) is an American television producer, writer, actress, singer, lyricist and dancer.
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