Built by patients. Guided by lived experience.
Focused on real change.
Born from one patient’s frustration and one doctor’s determination to do better, GSGA has grown into a national community where you can learn, connect, and feel heard.
Our roots are personal, but our mission is shared: to change how gout is understood, supported, and treated, and to empower every person living with it to take back their story.
GSGA was co-founded by gout patient advocate Gary Ho and rheumatologist Dr. Christopher Parker, who came together to close the gap between what patients live and what clinicians see. Their shared vision is simple: a community where your story matters, your questions are heard, and real progress starts with the people living with gout.
When his pain was dismissed, he pushed for answers, turning one fight into a mission that’s helping thousands.
Gary Ho was only 24 when he began experiencing symptoms of gout. Having seen his father live with the disease, he suspected what it was, but when he went to the doctor, he was told, “You’re too young to have gout.” No tests were ordered. The attacks were occasional at first, but over time they became more severe and frequent. For 16 years, Gary lived with escalating pain, often relying on crutches or a wheelchair to get through the day. Still, his concerns were dismissed.
Everything changed when he finally met a rheumatologist who listened. Tests confirmed what he had suspected all along. By then, the damage was significant, he had developed chronic gout, with joint deterioration and reduced kidney function.
Determined to take back his health, Gary began treatment and joined a clinical trial that helped restore his mobility and dramatically improve his quality of life. He realized that if he didn’t manage gout, gout would manage him.
But the damage wasn’t just physical. Gary had endured years of stigma, from friends, employers, and even healthcare providers. His pain was ignored, his experience minimized. That isolation was just as hard to carry as the disease itself.
In 2015, alongside his rheumatologist Dr. Chris Parker, Gary co-founded the Gout Support Group of America (GSGA), a place for people with gout to connect, learn, and feel less alone. What began in a single doctor’s office has now grown into a nationwide community helping others take control of their health, reclaim their confidence, and improve their quality of life.
His partnership with patients began with Gary, and grew into a commitment to better understanding and better care.
Dr. Chris Parker is a rheumatologist, speaker, and physician educator. He is Board Certified by the National Board of Osteopathics Medical Examiners, American Board of Internal Medicine, Subspecialty Rheumatology.
Dr. Parker has treated those with gout for many decades and has seen the social stigmas and misinformation surrounding gout and a gout diagnosis. His passion is providing accurate information to patients, physicians, caretakers, and others through education.
Dr. Parker believes in taking a comprehensive approach to treating his patient’s gout symptoms and flares through a combination of healthy eating, weight management, and effective treatments. Dr. Parker believes that controlling and managing gout includes maintaining a healthy regimen and seeking treatment from a physician.
Through his work with gout patients over the years, Dr. Parker has found that the patient voice is extraordinarily strong in relaying information and support to other gout patients. Dr. Parker knew it was important to support this dialogue and ensure that accurate and trustworthy information was being shared. So, in partnership with patient advocate Gary Ho, Dr. Parker co-founded Gout Support Group of America.
Wesley Mizutani, MD, is a practicing Rheumatologist who received a Medical Degree at UCLA School of Medicine, 1983 and went on to finish his residency in Internal Medicine at USC/LA County Medical Center. He completed a fellowship at UCSD School of Medicine in Rheumatology. He began his career in rheumatology as Department Chairman of Rheumatology for FHP health plan. He then obtained his MBA degree from Cal State University, San Marcos. When Talbert Medical Group became a physician owned group he served as Treasurer for the Group for 5 years. He served as Chairman of the Board of Talbert Medical Group and sat on the Board of Directors for 7 years. Clinically he served as the Medical Director of Specialties. He founded the Clinical Research Department at Talbert Medical Group and participated in over 100 clinical trials. He served as Rheumatology Lead at Optum Medical Group. He also held an appointment at UCSD School of Medicine as an Associate Clinical Professor of Medicine.
His passion has always been patient advocacy. He has testified at numerous legislative hearings both at the California State Capitol and Capitol Hill. He serves as a Board Member of Alliance for Patient Access. He has also been heavily involved with the Arthritis Foundation currently serving on the National Board of Directors and National Advocacy Committee. He currently serves as the Board Chairman of the Gout Support Group of America and on the Executive Leadership Council of National Association of Managed Care Physicians as well as the Medical Advisory Board of Lupus LA. He was the recipient of the 2024 Star Advocacy Award from the California Chronic Care Coalition and the 2025 Medical Visionary Award from Lupus LA.
Jasmine Patel, MPH, is a patient advocacy professional with a decade of experience working with patient organizations, advocacy groups, professional societies, public affairs firms, and pharmaceutical companies. Her expertise in patient engagement and advocacy has driven meaningful improvements in patient care and treatment access across various diseases.
Jasmine is a strong collaborator with a unique ability to bring different people together around a common cause, fostering a shared sense of purpose and commitment to improving patient outcomes.
Jasmine’s passion for patient empowerment is the driving force behind her work. She firmly believes that patient voices must be heard and is dedicated to ensuring that they have a seat at the table when important healthcare decisions are being made on their behalf.
Jen was only 26 when a mysterious, intense pain first hit her foot and turned her world upside down. It took two frustrating years to get a proper diagnosis, and then over another year of relentless monthly flares that became worse and worse, before she finally found the right doctor, the right treatment, and a way forward. With her gout now well managed, Jen has been flare-free for years and is passionate about helping others reach that same turning point.
As a board member of the Gout Support Group of America, Jen brings a unique blend of personal experience and creative energy to the team. She plays a key role in shaping the brand, website, and outreach strategy, making sure the group’s voice is as bold, supportive, and patient-focused as its mission.
Jen especially advocates for women with gout, who are too often dismissed or misdiagnosed. She’s a vocal believer that patient stories matter, and that humor and honesty can be powerful tools for change. When she’s not creating or connecting with the gout community, you’ll probably find her in the ocean, planning her next tropical trip, or cheering for fellow transplant athletes chasing big goals, just like she is.
Why this work matters
Support that meets you where you are
Whether you’re newly diagnosed or years into your journey, you’ll find the tools, knowledge, and encouragement to move forward with confidence.
A space for honest conversations about life with gout, from questions and frustrations to small wins and everything in between. You belong here.
Science and treatment options explained in plain language, so you can understand what’s happening in your body and make informed choices with confidence.
Expert-backed tools and next-step direction tailored to where you are in your gout journey, helping you move forward with clarity instead of confusion.
Patients. Leading. Period.
Too often, gout patients are treated like data points instead of human beings. GSGA exists to rewrite that narrative. We believe the people who live with this disease are the ones best equipped to shape the future of gout care. Your lived experience, your insights, and your reality are what drive meaningful progress.
And that leadership isn’t symbolic, it’s active. Behind the scenes, we work with researchers, data teams, advocacy organizations, and clinical experts to turn patient experience into real influence. We help shape patient engagement strategies, review educational materials before they’re released, and contribute to conversations about trial design, access barriers, stigma reduction, and more. From policy meetings to data projects to national awareness efforts, we’re making sure the healthcare system reflects the needs and realities of the people living with gout, starting with you.
It began with a Facebook group
The GSGA community started in one online space where people with gout could finally talk openly, and it’s been growing ever since. Today, new members join every day looking for connection, answers, and a place to be real about what living with gout is actually like.
If you want judgment-free support from people who truly get it, you’ll find it here.
We’re grateful for the generous support of the companies who partner with us to expand access to reliable information, elevate patient voices, and strengthen the resources this community deserves.
We’re proud to be supported by organizations that believe in better outcomes for people living with gout.
Change starts here. Let’s do it together.
Support from sponsors helps us amplify patient voices and shift the narrative around gout.
GSGA isn’t here to play small. We’re building a future where people living with gout are seen, supported, and equipped with the clarity they’ve been missing. Whether you’re here for community, guidance, advocacy, or reassurance that what you’re feeling is real, this is a place where your voice matters, and where real change begins.
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