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Your Story Our Fight by Lupus LA

Your Story Our Fight by Lupus LA

LupusLA

Lupus LA enters the fastest growing media market with the new Your Story Our Fight® podcast which will give a voice to lupus patients while continuing Lupus LA’s mission to raise lupus awareness worldwide. Hosted by the Chairman of Lupus LA and lupus patient himself, Adam Selkowitz, patients from all walks of life will share stories about their unique lupus journeys. With a focus on inspiration and hope, Lupus LA’s podcast will provide support and optimism to a patient community looking for assurance that they are not alone.

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Top 10 Your Story Our Fight by Lupus LA Episodes

Goodpods has curated a list of the 10 best Your Story Our Fight by Lupus LA episodes, ranked by the number of listens and likes each episode have garnered from our listeners. If you are listening to Your Story Our Fight by Lupus LA for the first time, there's no better place to start than with one of these standout episodes. If you are a fan of the show, vote for your favorite Your Story Our Fight by Lupus LA episode by adding your comments to the episode page.

Season TWO Episode TWENTY-FOUR of the Your Story Our Fight® podcast welcomes Emmitt Henderson III. Emmitt Henderson III was diagnosed with Systemic Lupus and Lupus Nephritis in 1995 but had symptoms going back to 1980. Through the years, he has endured major complications from heart, liver, kidney and lung failures, avascular necrosis that led to a shoulder and knee replacement. He had a clinical trial, bone marrow stem cell transplant; he was on oxygen due to his lung failure and had a kidney transplant due to kidney failure. He was also diagnosed with Rheumatoid Arthritis, Sjogrens Syndrome, MTCD as well as he suffered from having a stroke, shingles, gout, chronic fevers, diabetes and hypertension. In 2019, Emmitt was diagnosed with a brain disease, that medically retired him from his career. He decided to advocate for the same disease that debilitated him since 1995 and to talk about how his mental health got him through it all. He created his organization called Male Lupus Warriors Corp to spread Lupus and Mental Health awareness. He holds a safe space for men to meet and talk about their hardships in life, he encourages everyone to not be a victim to their illness. Emmitt did an advocacy campaign in Tanzania Africa in 2022 which included climbing Mt. Kilimanjaro. During his climb, he suffered high altitude pulmonary edema and ended up going into kidney failure for the second time in his life. He is now currently doing dialysis and on the transplant list for another kidney. During this time, he still maintains his advocacy by being active on social media and facilitating support groups.

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Your Story Our Fight by Lupus LA - Episode #14 with Liz Morasso

Episode #14 with Liz Morasso

Your Story Our Fight by Lupus LA

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08/10/21 • 26 min

Episode FOURTEEN of the Your Story Our Fight® podcast welcomes Liz Morasso, a lupus patient and clinical social worker.

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Season TWO Episode TWENTY of the Your Story Our Fight® podcast welcomes Stacey Uberstine. 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.

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Season THREE Episode FIFTEEN of the Your Story Our Fight® podcast welcomes Shanelle Gabriel. Shanelle Gabriel is a spoken word poet, singer, education consultant, and lupus warrior from Brooklyn, NY. She has shared her fusion of poetry and soulful singing in esteemed venues from The Vatican to Lincoln Center, and has penned and featured in national poetry campaigns with Pandora Music, NFL Draft, and more. With over 18 years as an educator, she uses the arts to facilitate workshops on creating culturally supportive work and learning spaces. She is the mother of three albums, which are available on all streaming platforms, and aims to show others they can live a full life while battling a chronic illness.

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Your Story Our Fight by Lupus LA - Season 2 | Episode #8 with Legendary Producer, Lauren Shuler Donner
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08/30/22 • 33 min

Season TWO Episode EIGHT of the Your Story Our Fight® podcast welcomes Lauren Shuler Donner. Lauren Shuler Donner has produced many films, including Pretty in Pink, Free Willy, St Elmo’s Fire, Dave, You’ve Got Mail, Secret Life of Bees, and nine X-men movies. She was also an Executive Producer on another seven films and five tv shows including “Legion." Lauren has been honored with a star on Hollywood Blvd. and has received her honorary Doctorate from Boston University.

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Your Story Our Fight by Lupus LA - Episode #2 with Shannon Pawl Derby

Episode #2 with Shannon Pawl Derby

Your Story Our Fight by Lupus LA

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01/26/21 • 27 min

Episode TWO of the Your Story Our Fight® podcast welcomes Shannon Pawl Derby, a lupus patient, fitness, nutrition, and corrective exercise specialist.

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Season TWO Episode NINETEEN of the Your Story Our Fight® podcast welcomes Kellie Martin. Kellie began acting at the age of seven. She is most fondly remembered for playing Becca Thacher on the groundbreaking ABC family drama Life Goes On, for which she received an Emmy nomination. And, her portrayal of Lucy Knight, a precocious med student who met an untimely demise after two seasons on NBC’s ER, haunts viewers to this day. Kellie has been a been a regular on numerous series including, The Guest Book, Army Wives, Mystery Woman, and on Hallmark’s Hailey Dean, where she served as Executive Producer. Her television and feature film highlights include Troop Beverly Hills, A Goofy Movie, Malibu’s Most Wanted, Grey’s Anatomy, Private Practice, and Mad Men. She also served as leading lady for Hallmark’s beloved holiday movies, The Christmas Ornament and Christmas in Montana as well as rom-com favorites, Smooch, I Married Who?, and Hello It’s Me.
In 1999, Kellie lost her nineteen year old sister, Heather, to lupus. So, Kellie took on a new role, one that she continues passionately to this day: national spokesperson for the Autoimmune Association. She works to raise awareness, lobbies Congress, speaks, and meets personally with patients and their families. Kellie is a Yale graduate with a degree in Art History. She co-authored a novel, Madam, which was published by Penguin in 2014. She’s currently writing on a new novel.
Most recently, Kellie has been working with her Life Goes On co-star, Chad Lowe and All American show runner, Nkechi Okoro Carroll to reboot Life Goes On with Warner Brothers. She just directed Mistletoe in Montana for Lifetime and has been recording a new podcast with Chad Lowe entitled The Big Break. She lives on a suburban farm in California with her husband, Keith, daughters, Maggie (15), Olivia (5) and a bunch of goats, pigs, and horses.

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Season TWO Episode ONE of the Your Story Our Fight® podcast welcomes Elizabeth and Mia SantaCruz. Elizabeth became a passionate advocate for raising Lupus Awareness after her daughter was diagnosed with lupus at the young age of 8. As a parent and caregiver, she was invited by to participate as a Lupus Advocate at the Annual Advocacy Meeting and Hill Day in Washington D.C. to meet with Congressional members and their staff to discuss the support for Lupus research.

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Your Story Our Fight by Lupus LA - Episode #1 with Juana Mata

Episode #1 with Juana Mata

Your Story Our Fight by Lupus LA

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01/12/21 • 27 min

Episode ONE of the Your Story Our Fight® podcast welcomes Juana Mata, a lupus patient and lupus advocate to talk about her life as a patient and her work with Looms 4 Lupus, a popular support group within the lupus community.

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Season FOUR Episode FIVE of the Your Story Our Fight® podcast welcomes Sheba Family Zaman. 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.

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FAQ

How many episodes does Your Story Our Fight by Lupus LA have?

Your Story Our Fight by Lupus LA currently has 82 episodes available.

What topics does Your Story Our Fight by Lupus LA cover?

The podcast is about Non-Profit, Autoimmune, Podcasts, Self-Improvement, Education and Business.

What is the most popular episode on Your Story Our Fight by Lupus LA?

The episode title 'Season 2 | Episode #23 with Social Media Influencer and Lupus Patient, Samantha Boothe' is the most popular.

What is the average episode length on Your Story Our Fight by Lupus LA?

The average episode length on Your Story Our Fight by Lupus LA is 31 minutes.

How often are episodes of Your Story Our Fight by Lupus LA released?

Episodes of Your Story Our Fight by Lupus LA are typically released every 14 days.

When was the first episode of Your Story Our Fight by Lupus LA?

The first episode of Your Story Our Fight by Lupus LA was released on Jan 12, 2021.

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