Gali Health Ambassadors
The Gali Health Ambassador Program ensures that the inflammatory bowel diseases (IBD) community is directly involved in Gali’s design and development. Our ambassadors provide feedback, guidance and leadership within the Gali user community.
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Molly
Dunham-Friel
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Shawntel
Bethea -
Nathan
Smart -
Cindy
Coelho -
Nikki
Patel
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Amanda
Gildersleeve
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Sari
Guerrieri
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Myisha Malone
King
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Amber
Tresca -
Brooke
Abbott -
Amber Wallace
Ogle
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Alison
Rothbaum -
Kelly
Crabb -
Joe
Hinksman -
Amanda
Osowski -
Natalie
Hayden
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Mary
Horsley -
Krista
Deveau -
Ijmal
Haider -
Tim
Albert -
Lee
Martin
Molly
Dunham-Friel
Molly Dunham-Friel, known on Instagram as betterbelliesbymolly, was born and raised in Vermont and moved to Atlanta one week after graduating from the University of Vermont. Not long after she was diagnosed with ulcerative colitis. The initial diagnosis was overwhelming for Molly and every year has come with its own victories and struggles, but she has learned much along the way and hopes to help others on their IBD journey “so nobody feels defeated.” Molly wants to dedicate her career to creating advocacy programs and awareness for these “embarrassing diseases.” Building a stronger IBD community and telling her story make her feel powerful. She currently works at Emory University full time and Barre3 Druid Hills on the side. She has a Master’s degree in public health and wants to use it to build brighter futures for IBD warriors.
Shawntel
Bethea
Shawntel Bethea, also known as Shawn, is a health and lifestyle blogger and freelancer. Diagnosed with ulcerative colitis during her senior year of high school, Shawn now uses her story of strength to raise awareness, show that there is life beyond a diagnosis and empower others living with chronic illness to become partners in their own healthcare. Through her blog, Chronically Strong, Shawn gives an unfiltered view of what living with an autoimmune disease is truly like, sharing the trials and triumphs. When she’s not working, Shawn enjoys traveling and eating vegetarian pizza rolls.
Nathan
Smart
Nate Smart, also known as Mr. J-pouch on Instagram, is a survivor and thriver trying to navigate life with a J-pouch and Crohn’s disease while maximizing the quality of the life he lives both individually and together with his loved ones and associates. He hails from Salt Lake City, Utah and works as a registered nurse for a cancer clinic. Being a patient for almost half of his life has been his main focus, but it empowers him to support others in their struggle and to help them realize that “There is a light at the end of the tunnel, especially when it seems like there isn’t. They just haven’t reached it yet,” he says.
Cindy
Coelho
Cindy is a San Francisco Bay Area native and current resident. While she was an athlete playing tennis in college she developed an interest in metabolism and pursued a Bachelor’s and Master’s of Science in clinical nutrition. She is a registered dietitian helping people learn to manage medical conditions with nutrition modifications and loving what she does. She became her own case study when she was diagnosed with Crohn’s in 2017, following her first big flare while on a six-day boat tour of the Galapagos Islands. She was told that hers is a “challenging case,” and the gap in IBD research pushed her to get involved with fundraising for the Crohn’s and Colitis Foundation. IBD has impacted her life in many ways but she tries to not let it prevent her from doing what she loves. On a sunny day she can be found outside playing tennis, rock climbing, jogging or hiking. She also enjoys traveling, reading and growing food in her garden. Her supportive husband Chris helps her to stay fit and healthy.
Nikki
Patel
Nikki lives in Danville, California, but grew up in Santa Rosa. She recently graduated from the University of San Francisco and is pursuing a career as a digital marketer. She has lived with ulcerative colitis for nine years and overcame many challenges, but believes that her health journey has made her stronger. She considers her continued involvement with the Crohn’s and colitis community to be one of the best decisions she has ever made, allowing her to build a network and gain valuable experience and knowledge that help her live her best life. She hopes to pass her insights along to the IBD community and to continue her involvement with new advancements and technologies that improve quality of life for people with IBD.
Amanda
Gildersleeve
Amanda (or Andie) was born in Palmer, Alaska but has lived in Oregon for the past six years as she finishes college. Andie was diagnosed with severe and unremitting Crohn’s disease in 2008 when she was 13 years old. Her IBD journey has been quite eventful: in 2016, she spent three months in the hospital after “kicking her colon to the curb” for a permanent ileostomy in hopes of some alleviation from IBD. After ileus, perforations and a dash of other complications, she is about to finish nursing school and is living her happiest, healthiest life that she didn’t think would be possible. Andie knows that IBD can be a devastating and lonely disease, but now she hopes to work as a pediatric nurse practitioner to support other young people on their health journeys.
Sari
Guerrieri
Sari Guerrieri is a lifelong resident of New York’s Long Island. Born into a family rife with multiple serious diseases, her experience with chronic illness began long before her own Crohn’s disease diagnosis at the age of eight. After an ileostomy at 12, Sari has had numerous other bowel resections and surgeries over the past 25 years. Sari has at various times required alternative feeding methods and has participated in drug trials as both a pediatric and adult patient. November 2018 marked the beginning of Sari’s six-year-long remission. Sari has been actively involved with the Crohn’s and Colitis Foundation, United Ostomy Association of America, Youth Rally and lobbied on Capitol Hill for digestive diseases and ostomy insurance coverage. She has also volunteered with animal rescue groups, including fostering abandoned cats and kittens. She lives with her partner of 11 years and their cats.
Myisha Malone
King
Myisha Malone-King lives in Baltimore, Maryland. Diagnosed with Crohn’s disease and newly diagnosed with diverticulitis, her journey hasn’t been easy. Myisha runs a support group on Facebook called “Game of Crohn’s and Chronic Illness,” dedicating most of her energy to checking in with her friends in the IBD community, offering information and spreading awareness.
Amber
Tresca
Amber Tresca was diagnosed with ulcerative colitis at the age of 16. After 10 years of active disease and failed medical therapy she underwent 2 step j-pouch surgery. As a long-time j-poucher and mother of 2 children, Amber shares her experiences of living with ulcerative colitis on her blog, “About IBD.” She produces the “About IBD Podcast” that focuses on the IBD patient journey and has interviewed prominent people living with IBD and her own family members about various aspects of life with IBD. Amber also co-founded the IBD Moms social media groups with Brooke Abbott of “The Crazy Creole Mommy,” to support other women who live with IBD or have children who live with IBD. Amber works as a freelance writer and editor for medical web sites and publications specializing in IBD and other digestive disease.
Brooke
Abbott
Los Angeles native Brooke Abbott, better known as “the Crazy Creole Mommy,” is a single mother, health advocate and writer. Three years after being diagnosed with ulcerative colitis at age 24, Brooke was recommended for an emergency total colectomy and is currently living with a j-pouch. This surgery not only saved Brooke’s life, but also set her on a new path as an online advocate for the IBD community. Brooke now owns and operates The Crazy Creole Mommy Life blog, advocates on Capitol Hill for GI-related legislative agenda issues, writes for various outlets and teaches moms with disabilities and/or challenges how to baby wear. In 2018 she joined Amber Tresca of AboutIBD to form IBDMoms, a multifaceted resource program aimed at providing support to moms affected by IBD as a patient or caregiver. When she is not overanalyzing Mulder and Scully’s relationship on old episodes of the X-Files or volunteering at her son’s school, she is working toward a bachelor’s degree in public policy with an emphasis on health policy.
Amber Wallace
Ogle
Amber Wallace Ogle is a YouTuber and ostomy/Crohn’s disease advocate. She was diagnosed with Crohn’s Disease in 2008, when she was a junior in high school. She had a complete colectomy and received her ileostomy bag in 2016. Amber believes that sharing your story can be healing and strives to be transparent about her own health journey. She wants individuals living with IBD or an ostomy bag to know that they are not defined by their illness or condition. Amber uses positivity and her faith to show others that they too can live a full and happy life with IBD.
Alison
Rothbaum
Alison Rothbaum (@Empoweringpts9), a native of Ohio, is an ostomy and inflammatory bowel disease (IBD) advocate. She was diagnosed with Crohn’s disease in 1994 at the age of 15. She received her permanent ileostomy in 2003 and began her advocacy work in 2006. She works to overcome the many challenges IBD has brought her, and shares her successes and skills with others who are facing a health journey. Alison has a background in outpatient physical therapy and assisted in writing a protocol to help other patients who need a specific type of physical therapy rehabilitation related to illness and abdominal surgery. She formed Empowering Patients, LLC and advocates to clarify the healthcare world with patients across the globe. She is on the her local ostomy Board of Directors and is part of the IBD Social Circle (a Janssen Biotech initiative). She has created multiple in-person and virtual IBD and ostomy support forums and co-moderates the “MondayNightIBD” Twitter account with Dr. Aline Charabaty. She likes to remind herself and others that “It may not be ideal, but it’ll be ok.”
Kelly
Crabb
Kelly was diagnosed with Crohn’s disease in 2004. After struggling to accept that it is a lifelong illness, she began reaching out to the patient community to learn more about IBD. Fifteen years later, Kelly has helped many patients find resources and community support, camaraderie and friendship. Her goal is to provide information to new and seasoned patients like herself who were not supplied with educational materials or accurate information at the time of diagnosis. She hopes to help others normalize IBD and feel less isolated. In her spare time Kelly enjoys kayaking, hiking and running with the Crohn’s and Colitis Foundation’s Team Challenge. She has run two half-marathons and continues to train for triathlons to raise funds for IBD research.
Joe
Hinksman
Joe Hinksman, also known as @you.look.fine.to.me on instagram, resides on Vancouver Island in British Columbia, Canada. Navigating his way through his new diagnosis of IBD (Crohn’s disease) in 2016, Joe uses his passion for writing to practice gratitude, accountability and advocacy for chronic illness, mental health and addiction. By engaging with social media communities, and sharing his story, Joe strives to instill hope that even when the sky is falling, there’s so much to be grateful for.
Amanda
Osowski
Having suffered from disease-related symptoms for more than six years, Amanda Osowski (@amanda.osowski), a native of Chicago, was diagnosed with Crohn’s disease in January of 2016. Her path to diagnosis was incredibly trying and greatly impacted her mental health and support system. Amanda has spent the last decade sharing her experiences and fighting to help patients advocate for themselves and improve their quality of life. Amanda is passionate about creating content and sharing information on the realities of living with Crohn’s disease, including caring for one’s mental health, obtaining professional accommodations, exploring fertility, experiencing pregnancy, childbirth, and breastfeeding and managing health in remission. Amanda has a master’s degree in public health and currently works as both a postpartum doula and a consultant on clinical research strategy and project management for healthcare companies.
Natalie
Hayden
Natalie (Sparacio) Hayden, 36, is a former TV news anchor with Crohn’s disease living in St. Louis. She grew up in the Chicago suburbs with a big Greek and Italian family and holds a journalism degree from Marquette University. Her mission in life is to be an advocate for those battling inflammatory bowel disease. Natalie was diagnosed with Crohn’s at age 21 and has endured several hospitalizations, countless medications and flare ups. In August 2015, she underwent bowel resection surgery that involved the removal of 18 inches of her intestine. While it was a difficult chapter in her disease battle, it truly gave her a fresh start and enabled her to reach remission. Her blog “Lights, Camera, Crohn’s: An Unobstructed View” covers everything from overcoming struggles associated with chronic illness to celebrating small victories. As a passionate health advocate, journalist, wife and mom of two, she strives to show that there is more to life than your diagnosis and illness. In her free time, Natalie enjoys being involved with her local Crohn’s and Colitis Foundation chapter, public speaking, reading, running, traveling and spending time with family and friends.
Mary
Horsley
Mary Horsley, also known as @marywiththegreenhair and through her blog @itcouldbeworseblog on Instagram, is a Navy veteran, writer and model with IBD who lives in Georgetown, KY. Having been diagnosed with Crohn’s disease in 2016, Mary uses her passion for communication and journalism to share her patient perspective on living with chronic illnesses and other health issues such as fibromyalgia, migraines, and mental health. Mary also shares her insights on using the VA for her healthcare needs and documents both the good and the bad aspects of her IBD. As Mary says, for her, “it could be worse,” so she focuses on finding the positives and humor in difficult situations.
Krista
Deveau
Krista Deveau, also known as @my.gut.instinct on Instagram, is a 28-year-old kindergarten teacher and IBD and ostomy advocate from Calgary, Canada. Diagnosed with Crohn’s disease at the age of 9, Krista has tried many different approaches to managing IBD, including enteral feeds, specialized diets and biologic medication. When all else failed and life was no longer normal due to pain, fatigue and incontinence, Krista went the temporary ileostomy route and considers that to have been the best decision she has ever made. Over the last two years, she has felt the healthiest and strongest ever since her diagnosis. While the ostomy life also has its ups and downs, Krista makes the best of it and continues pursuing her passion for building a safe and inclusive classroom in which children can focus on their uniqueness while embracing their differences.
Ijmal
Haider
Ijmal Haider lives in Canada and was diagnosed with ulcerative colitis in 2015. He is an entrepreneur and business owner. In his time off, he volunteers and speaks publicly about chronic illness and mental health. Ijmal is the president of his local Crohn’s and Colitis Canada chapter, an ambassador for Lyfebulb and Gali Health, and the founder of @HiddenSpoons on Instagram. He hosts a podcast and runs a YouTube channel called “Help Us YYC,” which focuses on tackling mental and physical health issues. He also publishes a personal blog @raziblog where he documents his personal experience living with IBD.
Tim
Albert
Tim Albert (@bad_gut_tim) is a software developer living in Milwaukee, WI. He was diagnosed with Crohn’s Disease in 2002. He graduated from Saint Louis University and in November of 2019, after months of flaring, underwent ostomy surgery to get the disease back under control. In his spare time, he likes to hang out with family, write, golf, and cheer on the Milwaukee Bucks. Tim has a passion for patient advocacy and wants everyone living with a digestive disease to believe that IBD doesn’t have to define them, hold them back, or keep them from leading full and exciting lives. You can follow Tim’s advocacy efforts on Facebook, Twitter, Instagram, YouTube, and his blog BadGutTim.com
Lee
Martin
Lee Martin, known on Instagram as @theloveleecrohnie, is a blogger and IBD/ostomy advocate from Ontario, Canada. Diagnosed with indeterminate Crohn’s colitis at age 27, she tried various approaches to managing her IBD till she had to be rushed into emergency surgery in 2018. She’s had many complications and hospital stays since her subtotal colectomy with end ileostomy surgery, but has since achieved remission for the first time in her IBD journey. Through her online presence, Lee hopes to help others with IBD and ostomies not feel alone and to raise awareness of “invisible illnesses.”
