Legend. Icon. Songstress. Diva.

Very few artists ever ascend to the rarefied heights that those four words symbolize. Toni Braxton is one of those few.

The multimillion-selling R&B/pop pioneer and seven-time Grammy Award-winner behind timeless hits such as “Love Shoulda Brought You Home,” “Another Sad Love Song,” “Breathe Again,” “Seven Whole Days,” “Un-Break My Heart” and “He Wasn’t Man Enough.” If that wasn’t enough, the multi-talented singer/songwriter has also expanded her skillset along the way: music producer, Broadway musical star, television actress/producer and best-selling author.

Braxton’s own mesmerizing voice remains constant with each project—the same sultry and smoky vocals that immediately turned heads in 1992. That’s when listeners first became aware of the newcomer who appeared on the soundtrack to the Eddie Murphy box office smash Boomerang. Helmed by songwriter/producers and LaFace Records founders Babyface and Antonio “L.A.” Reid, the soundtrack featured Braxton on two songs: “Give You My Heart,” a duet with Babyface, and “Love Shoulda Brought You Home.”

That set the stage for Braxton’s 1993 breakthrough with her self-titled debut LaFace album that’s now 8x platinum. The project also garnered the singer the first three of her seven Grammy Awards, including best new artist. Braxton, who began singing professionally in the ‘80s with her three sisters as The Braxtons, has since banked an enviable number of career-defining moments. Between 1996 and 2010, she released six more solo albums (Secrets, The Heat, Snowflakes, More Than a Woman, Libra and Pulse) and charted a string of hits (including “You Mean the World to Me,” “You’re Makin’ Me High” and “I Love Me Some Him”/ “I Don’t Want To”) before teaming with Babyface 2014 for the critically acclaimed duets album that won her a seventh Grammy for Best R&B Album.

Along the way, Braxton reinvented her game as she effortlessly segued into a theatrical acting career in 1998 as Belle in Beauty and the Beast. That barrier-breaking portrayal—the first black woman to play a leading role in a Disney Broadway production—led to a stint in a second Disney Broadway musical, Aida, and later a special guest star engagement with another Broadway musical, After Midnight.

Since then, Braxton has starred in three TV films for Lifetime including Twist of Faith, Toni Braxton: Unbreak My Heart (adapted from her same-titled best-selling memoir) and, most recently, Faith Under Fire: the Antoinette Tuff Story. In between, she and her three sisters have become popular reality stars via WE tv’s flagship series Braxton Family Values. Diagnosed with lupus several years ago, Braxton hasn’t allowed that to slow her career momentum nor her role as the proud mom of sons Denim and Diezel. She devotes time as spokesperson for Lupus L.A. and Autism Speaks, the latter on behalf of Diezel who is living with autism.

Reflecting on her silver anniversary of her career, Braxton says she’s still in love with music and the possibilities it affords. “There have been moments when I felt defeated; felt I let myself down,” she says. “Even if I fail, music gives me enough strength to try something different. I’ve come full circle—yet there are still so many things to do.”

Lindsay Sustarsic Cafritz is 28 years old and was born and raised in Los Angeles. She attended George Washington University in Washington DC and graduated with a BBA in marketing and business administration. After graduation she moved to New York City to pursue a career in the fashion/beauty industry, specifically in retail marketing, social media and creative content. She successfully launched that career working for Valentino and Burberry until her already volatile health began to rapidly deteriorate. She was formally diagnosed with Systemic Lupus Erythematosus in late 2014.

Shortly after the diagnosis, Lindsay moved back to Los Angeles. For the 4 years since moving back west she has worked as a freelance writer while spending the bulk of her time focused on improving her health.

Thankfully, since starting Benlysta infusions, her health has greatly improved. Lindsay started to get more immersed in the lupus community in late 2018 and organized a fundraiser for the LFA for Lupus Awareness Month with her then fiancé’s company, which is based in DC. She also set up a charity fund in lieu of a wedding registry to support the national clinical trials for mesenchymal stem cell research. She was married in June of this year and has since focused on stepping up her involvement in the LA Lupus community and becoming more active in Lupus LA.

Born and raised here in Los Angeles, Roger and Debbi Cowan both graduated from Stanford University and returned to Los Angeles to join family businesses. While at Stanford, Roger played football during the glory days of their 1970 and 1971 Rose Bowl teams where they notched back-to-back victories. Roger and Debbi married in 1979 and had their son, Jeff, and daughter, Amanda while starting their own real estate company, Rockdyne Enterprises. They now own and manage multiple apartment buildings on the westside of Los Angeles where they specialize in delivering superior apartments with unparalleled service.

Roger and Debbi joined Lupus LA soon after their daughter Amanda was diagnosed with lupus in 2006 and have been active members of the board. In addition to working closely on Lupus LA events, they enjoy traveling as much as possible, working out and staying in shape, golfing with friends, and attending cultural events in the city. Along with the joy they take in their daughter Amanda, they spend as much time as possible with their son Jeff, his wife Shannon, and their new granddaughter Clover Belle.

Born and raised here in Los Angeles, Roger and Debbi Cowan both graduated from Stanford University and returned to Los Angeles to join family businesses. While at Stanford, Roger played football during the glory days of their 1970 and 1971 Rose Bowl teams where they notched back-to-back victories. Roger and Debbi married in 1979 and had their son, Jeff, and daughter, Amanda while starting their own real estate company, Rockdyne Enterprises. They now own and manage multiple apartment buildings on the westside of Los Angeles where they specialize in delivering superior apartments with unparalleled service.

Roger and Debbi joined Lupus LA soon after their daughter Amanda was diagnosed with lupus in 2006 and have been active members of the board. In addition to working closely on Lupus LA events, they enjoy traveling as much as possible, working out and staying in shape, golfing with friends, and attending cultural events in the city. Along with the joy they take in their daughter Amanda, they spend as much time as possible with their son Jeff, his wife Shannon, and their new granddaughter Clover Belle.

Lauren Shuler Donner is a renowned and prolific film, TV, and theater producer, boasting an impressive array of credits, including the X-Men and Deadpool franchises, Pretty in Pink, Free Willy and You’ve Got Mail. She is currently developing several Broadway musicals based on her and her husband’s films. Lauren is a lupus patient and her dedication to the cause shines through her involvement with Lupus LA. Other influential roles include serving as Vice President for the Producers Guild of America and serving on the Board of The Motion Picture and TV Fund (MPTF).

Natalie Hariri is a true Angeleno, born and raised here and a graduate of USC where she majored in broadcast journalism at The Annenberg School of Communication and minored in The Classics thus becoming a Renaissance Scholar. She went on to work for Fox News during the Democratic National Convention here in Los Angeles along with various other television and radio shows. In 2005, she married her college sweetheart and best friend Sherwin Hariri, who at the time was an aspiring medical student; once Sherwin got accepted to Medical School in St Louis, MO, she moved with him and lived in Missouri for several years, before coming back home to Los Angeles, where Sherwin completed his medical training at Cedars Sinai and UCLA. Natalie was his biggest cheerleader and supported him fully in continuing his training at UCLA in allergy and immunology. In her free time, Natalie enjoyed volunteering at Cedars Sinai Medical Center and providing care and support to patients and their families. She also assisted Dr. Hariri in his early days in private practice and helped set up his first allergy & immunology practice in Beverly Hills, CA in 2014. It was in his clinic where she was exposed to patients with severe allergies and chronic/autoimmune illnesses. Dr. Hariri and Natalie have been married for 17 years and have three beautiful children, Marcel (11 years old and an avid basketball player), LaraLoren (10 years old, a dancer and aspiring “baby Doctor”) and Maximilian (15 months old and who was recently welcomed with much joy and happiness and who is everyone’s bundle of joy in the family). Natalie enjoys traveling, cooking, yoga, photography, fashion, reading medical journals and most of all cheering her kids on in their athletic activities. She is an advocate of staying fit to stay healthy both physically and mentally. As a young woman and mother, one of Natalie’s main goals in life is to help expedite the diagnosis of autoimmune diseases like lupus, as it is often delayed, and ultimately finding the cure. It is Natalie’s honor and pleasure to serve on this Board.

Amanda Palley is a lupus patient and Senior Vice President of Current Programs at CBS.

Adam Selkowitz is the founder and owner of Waterfall Films. He initially pursued an acting career, receiving a degree in Drama from Ithaca College. Adam then spent 6 years in New York, working mostly with an improv/sketch comedy group that he created called Spilt Milk. Spilt Milk performed across the country at comedy clubs, colleges and corporate events and was the official sketch comedy group at Caroline’s Comedy Club on Broadway for several years. Following his run with Spilt Milk, Adam moved to Los Angeles and switched from acting to production in creating Waterfall Films. The company’s original project, Greener Mountains, is an award-winning independent film available on Amazon Prime and other streaming services. Currently, the company has multiple projects in active development and has focused more recently on obtaining intellectual property rights around those projects.

In 1987 Adam was diagnosed with lupus and in 1999 he co-founded Lupus LA with Dr. Daniel Wallace and a small group of committed board members. Adam has led Lupus LA as Chairman of the Board for most of the last 20 years and has been at the forefront of the organization’s accomplishments, including raising over $10 million for lupus research, bringing a robust patient services program to Southern California and raising more global awareness for lupus than ever before. In addition, Adam is a member of the Cedars-Sinai Board of Governors and sits on their Leadership Council. He is also an Ambassador for Children’s Hospital Los Angeles.

Adam is most thankful to his wife Laurie, a corporate attorney in Los Angeles, and most proud of their two children, 3-year-old daughter Lucy and 1-month-old son Parker, the real stars of the family.

Stacey graduated from California State University Northridge in 1990 with a bachelor of science degree in Health Administration with a computer science minor. One of her most notable jobs was helping to establish the Industrial Care Center which is operational at San Pedro Hospital. In 1993 Stacey transitioned into the insurance industry where she owned and operated her own State farm Agency for over a decade. Stacey was diagnosed with lupus in 1994. She stays abreast of the disease and all related medical breakthroughs and advances in research. Stacey has been an active donor and Board member of Lupus LA. She has a passion for patient advocacy within the lupus and breast cancer communities. Stacey is an avid sports fan, and actually met her husband through her work at State Farm. Sports seems to be a family affair, as her husband is a prominent sports attorney who has represented some of the most iconic figures in professional sports. Her passion for sports was passed on to her twin boys, Grant and Tyler. Grant was an avid athlete in high school, participating in lacrosse, baseball and swimming. Tyler’s passion for baseball took him to Northwestern University, where he earned a spot in the team’s starting rotation. He was later drafted by the Boston Red Sox. Stacey resides in Manhattan Beach, where she can be seen taking strolls along the beach. She is an avid reader and spends a considerable amount of time supporting philanthropic causes close to her heart related to lupus and breast cancer.

Nancy Utley was appointed Chairman of Fox Searchlight Pictures in 2018. She jointly manages all aspects of the company including production, acquisitions, marketing and distribution alongside fellow Chairman Stephen Gilula. Ms. Utley has overseen many of Fox Searchlight’s most successful films to date, with a total of 116 Golden Globe® and 153 Oscar® nominations, including Best Picture winners “The Shape of Water,” “12 Years a Slave,” “Birdman” and “Slumdog Millionaire.”

Recent releases include “Ready or Not” and “Jojo Rabbit,” with upcoming releases including “A Hidden Life,” “Antlers,” “The Personal History of David Copperfield,” “Downhill” and “Wendy.” Past successful films include “The Favourite,” “Can You Ever Forgive Me?,” “The Old Man & The Gun,” “Isle of Dogs,” “Super Troopers 2,” “Three Billboards Outside Ebbing, Missouri,” “The Shape of Water,” “Gifted,” “Jackie,” “Brooklyn,” “Birdman,” “Wild,” “12 Years A Slave,” “The Grand Budapest Hotel,” “Beasts of the Southern Wild,” “The Best Exotic Marigold Hotel,” “The Descendants,” “The Tree of Life,” “Black Swan,” “127 Hours,” “Crazy Heart,” “500 Days of Summer,” “Slumdog Millionaire,” “The Wrestler,” “Juno,” “Once,” “Little Miss Sunshine,” “The Last King of Scotland,” “Sideways” and “Napoleon Dynamite.”

Prior to joining Fox Searchlight in 1999, Ms. Utley served in a variety of capacities for Twentieth Century Fox Film where she developed campaigns for films such as INDEPENDENCE DAY, THERE’S SOMETHING ABOUT MARY, MRS. DOUBTFIRE and THE STAR WARS TRILOGY. In her role as Executive Vice President of Marketing, she oversaw all aspects of media, research, publicity and promotion for Twentieth Century Fox’s theatrical releases. She also held posts as Vice President of Media, Senior Vice President of Media and Research, and Executive Vice President of Marketing, Media and Research.

Ms. Utley holds a Master’s degree in Journalism from Northwestern University and has been inducted into the Medill School of Journalism Hall of Achievement.

Daniel J Wallace MD, FACP, MACR is a board-certified internist and rheumatologist. A Clinical Professor of Medicine at the David Geffen School of Medicine at UCLA, he is the Associate Director of the Rheumatology Fellowship Program at Cedars-Sinai Medical Center where he also serves on the Board of Governors.

Dr. Wallace has authored nearly 450 peer reviewed manuscripts, 30 book chapters, eight textbooks (on lupus, osteoarthritis, Sjogren’s syndrome and fibromyalgia) and his practice includes caring for 2,000 lupus patients, the largest lupus cohort in the United States. With the four employees of the Wallace Rheumatic Studies Center, we have conducted numerous clinical trials, and have 3 current National institution of Health and a Department of Defense grants. Dr Wallace is co-chair of the Lupus Industry Council of the Lupus Research Alliance, past chair of the Lupus Foundation of America, and has served on the Board of Directors of the United Scleroderma Foundation and the Medical Advisory Board of the Sjogren’s Syndrome Foundation. He has been Chief of Rheumatology at the City of Hope and Cedars-Sinai Medical Center, and chairman of the Research and Education Foundation of the American College of Rheumatology.

Dr. Wallace is the recipient of the Lupus Foundation of America Humanitarian Award, Achievement Award of the Lupus Research Institute, Spirit Award of the Scleroderma Foundation, the Jane Wyman Humanitarian Award from the Arthritis Foundation, and the Healthcare Professional Leadership Award from the Sjogren’s Syndrome Foundation.

While a fellow at UCLA, Dr. Wallace conducted pioneering arthritis research and developed a close relationship with his mentor, Edmund Dubois. Dr. Dubois had the largest lupus practice in the United States at the time and was the principal editor of the only lupus textbook. He assumed Dr. Dubois’ practice upon his passing in 1985. Dr. Wallace is the author of eight medical textbooks (including the last six editions of Dubois’ Lupus Erythematosus, All About Fibromyalgia, The Lupus Book, All About Osteoarthritis, The New Sjogren’s Syndrome Handbook, and Fibromyalgia & Other Central Pain Syndromes). In addition, his work can be found in the New England Journal of Medicine, Annals of Internal Medicine, the Lancet, Journal of Clinical Investigation, Journal of Immunology and Journal of the American Medical Association.

Dr. Wallace has been recognized as among the 200 best doctors in the nation by Town and Country Magazine, and among the best doctors in Los Angeles by Los Angeles Magazine, Best Doctors in America editions since 1994. Dr. Wallace spends 20% of his time teaching and in clinics where he provides free medical care. His efforts have raised over $20 million for various rheumatic disease organizations.

Janice Brock Wallace received both her B.A. and M.A. in Public Administration and Public Health from the University of Southern California. Janice was one of the founders of Lupus LA and helped establish the Hollywood Bags Lady Luncheon and engineered the original relationship with Lupus LA and Children's Hospital. She has been involved in various support groups for Cedars Sinai Medical Center; was a past president of the former Amie Karen Cancer Fund, member of Women's Guild and is currently on the Board of Governors. Other work in the health field includes support for the Lupus Research Alliance, Arthritis Foundation, the United Scleroderma Foundation and the National Fibromyalgia Association. She co-authored Making Sense of Fibromyalgia with her husband, Dr. Daniel Wallace. Janice was the original book editor for The Lupus Book, All About Osteo-Arthritis and It's Not Just Growing Pains (Pediatric Rheumatology) all with Oxford University Press.

Currently, Janice is on the board of Center Theatre Affiliates (also a past president), MOCA Projects Council and Fellows for Contemporary Art Los Angeles. Janice has been married to Dr. Daniel Wallace for almost 48 years and has three married children and three delightful grandsons, Sam, Liam and Gabe.

Born and raised in Los Angeles, Maurissa Tancharoen Whedon has taken an unusual path to her work in television. With a background in music and dance, she's performed with the likes of Michael Jackson and Chaka Khan, and toured the country as a member of a pop group with Motown Records. At Occidental College, she became heavily involved in theater and wrote several award-winning plays. She then went on to write on Oliver Beene for FOX, and created and executive produced the MTV series Dancelife with Jennifer Lopez. With her husband and writing partner, Jed Whedon, she created and appeared in the Emmy-award winning musical, Dr. Horrible's Sing Along Blog. Together, their credits also include such shows as Dollhouse, Drop Dead Diva, and Spartacus. They also co-created and served as show runners and Executive Producers of Marvel's Agents of S.H.I.E.L.D. on ABC. The flagship Marvel Television series ran for seven seasons.

As an Asian-American female showrunner, her advocacy for diversity and representation is reflected in her work. Marvel's Agents of S.H.I.E.L.D. is not only touted as one of the most diverse shows on television, but as a show that celebrates layered, intelligent, powerful women. Maurissa is no stranger to adversity as she has been living with Lupus since she was fifteen years old. She is heavily involved in raising awareness and funds for those also suffering from this devastating illness. Maurissa still takes the occasional hip-hop class, makes music with Jed, and constantly marvels at their little superhero - their daughter, Benny Sue.

Denise Winner, CFA is president and CEO of Winner Squared. With over 15 years of experience developing technologies for the capital markets and entrepreneurial ventures, Ms. Winner founded Winner Squared in 2000 to provide cutting edge financial engineering, AI, and analytical solutions for banks, insurance companies, institutional traders, money managers, and entrepreneurs. Denise was formerly the director of Fixed-Income Analytics for Transamerica Investment Services, where she designed, implemented and managed the development of a real-time fixed income analytics platform, CBO trading systems, and transfer pricing models. Her prior experience includes: Quintelligent Corporation, where she was a founding partner and responsible for research and implementation of a fund of funds; and, Leland O’Brien Rubinstein/Geske Bock, where she was financial product manager.

Denise is a Chartered Financial Analyst. She holds a B.S. in Economics from Wharton, University of Pennsylvania and completed her Masters’ Thesis in Computer Science with a concentration in Artificial Intelligence from Brown University.

Denise serves as Treasurer for Lupus LA and Energize the chairs Penn Serves, Southern California Advisory Board for Penn, Penn’s Tennis Board, and Penn’s Momentum 2020. Denise She also launcher her own nonprofit Conquer our Run to heighten awareness and raise money for lupus and breast cancer.

As a computer scientist, Sheba has spent the last 20 years working in a technical software role with the quality department of pharmaceutical and life science companies. Her role spans from pre-sales technical information to professional services post-sale with the goal of digitizing critical data that can affect patient safety. She speaks regularly at industry conferences on data integrity and contamination control strategies for aseptic drug manufacturers. She was recently President of non-profit organization – the Parenteral Drug Association, SouthernCalifornia Chapter – for an elected term of 2 years. It is an educational organization dedicated to the connection of science, people, and regulation in a non-bias platform. In June of 2006, Dr. Dan Wallace diagnosed Sheba with Systemic Lupus Erythematosus and Nephritis following struggles with frequent fevers, joint/muscle pain, debilitating fatigue, visibly swollen lymph nodes, and hair loss. Born and raised in Montréal, she soon moved to Southern California to be closer to her family and support system. After grappling with the side effects of strong medications and some tough love counseling from her sister, she started to take her health into her own hands and has spent the last decade avidly reading and educating herself on Lupus and optimal health. Today, Sheba lives in Santa Monica and leads a very active lifestyle as a certified yoga instructor, scuba diver, tennis player, skier, beach volleyball player, runner, and global adventure traveler. She is now working to give back to the community and advocate for Lupus.