We’re honored to work with dedicated leaders, all of whom have professional experience and a strong commitment to helping people affected by sarcoma.

Philip was an inaugural member of the Sarcoma Alliance Board of Directors, and after Suzanne passed away in 2002, Philip took over her duties as the President of the organization for three years. He continued to serve on the Board through 2011, and recently returned to Board service and the Presidency as the Alliance celebrates its 25th year.
Throughout his career, Philip has maintained an interest in the intersections of Law and Medicine, with a special emphasis on sarcoma and HIV/AIDS. He was also proud to work for many years on the litigation and appeals that ultimately resulted in legal recognition of the rights of same-sex couples to marry.

Motivated by this journey, Natasha has become a vocal advocate voice for the rare disease community—particularly in addressing the critical gaps adolescents face when navigating care transitions. She is committed to ensuring that no patient or caregiver feels alone, and that everyone has access to clear information, meaningful support, and empowered decision-making.
In her advocacy and volunteer work, Natasha draws on both her industry experience and lived perspective to uplift families and promote equity in care. As a board member of the Sarcoma Alliance, she brings compassion, insight, and a relentless commitment to advancing the Alliance’s mission to guide, educate, and support those affected by sarcoma.

Caroline passed away on November 6, 2024 after a 4 ½ year illness. Michael is now passionate about raising money in Caroline’s honor and memory to help fund much needed sarcoma research, awareness and patient assistance programs.
Michael received his BS in Finance from the University of Virginia and his Master of Business Administration from the University of North Carolina at Chapel Hill. Michael’s interests include travel, tennis, acoustic guitar and spending time with his two sons.


Dr. Christ brings a wealth of expertise, having trained at top institutions such as Yale University, the Hospital for Special Surgery, and Memorial Sloan Kettering Cancer Center. He practices at UCLA Medical Center and Children’s Hospital Los Angeles.

She is a pediatric bone cancer survivor and above-knee amputee who remains committed to supporting those in the oncology and limb loss communities. She is an advocate for recreational adaptive sports access and support network access for amputees. She frequently publishes articles about the lived experience of being a young adult with limb loss.
She appreciates the unique challenges that come with navigating a sarcoma diagnosis and pursuing limb salvage vs amputation. She is excited to join The Sarcoma Alliance to further advocate for patients and families within the sarcoma community.

After serving in Operation Enduring Freedom, Brandi was diagnosed in 2009 with a rare and aggressive cancer (ewing sarcoma). Navigating treatment as a young veteran reshaped her life and clarified her purpose. Experiencing the emotional, physical, and structural gaps patients face during and after treatment gave her a deep understanding of how essential strong support networks are to long-term healing.
Since 2019, Brandi has served on the Board of Directors for the Sarcoma Alliance. In this role, she is focused not only on advocacy, but on identifying unmet needs within the cancer ecosystem — and developing collaborative solutions to bridge those gaps. She is particularly passionate about strengthening survivorship support, expanding patient education, and cultivating partnerships that create shared value across patients, providers, researchers, and advocacy organizations.
Brandi believes meaningful progress happens at the intersection of relationship-building and strategic alignment. She actively works to cultivate synergy between stakeholders, bringing people, ideas, and resources together to build initiatives that are sustainable, measurable, and beneficial to the broader community.
She also serves as a Consumer Advocate on the Department of Defense’s Peer Reviewed Cancer Research Program (PRCRP) Programmatic Panel, where she contributes to national funding decisions and ensures that patient voice and military health priorities remain central to research strategy.
Professionally, Brandi brings more than a decade of corporate marketing experience to her work, combining data-driven strategy with disciplined execution. Whether in advocacy, business, or real estate, her mission remains the same: to serve with integrity, build with intention, and help transform survivorship into strength.

Dr. Kyri is also a stage IV Ewing Sarcoma thriver, diagnosed during the height of the COVID-19 pandemic. Receiving a life-threatening diagnosis at a time when cancer care was largely overshadowed by the global crisis meant navigating treatment with limited access to in-person support. This experience profoundly shaped her perspective and strengthened her commitment to ensuring that patients and families—particularly those facing rare cancers—are supported with dignity, transparency, and compassion.
In addition to her advocacy for sarcoma and cancer patients, Dr. Kyri applies a trauma-informed lens to her work, recognizing the lasting effects of serious illness, isolation, and major life disruption. She is deeply committed to improving how healthcare systems respond not only to medical needs, but also to the emotional, psychological, and social realities patients face during and after diagnosis.
Throughout her career, Dr. Kyri has worked alongside healthcare organizations and leaders to promote ethical practices, clear communication, and patient-focused decision-making. Her dual perspective—as both a healthcare compliance professional and a survivor—allows her to thoughtfully bridge policy, practice, and lived experience.
As a member of the Sarcoma Alliance Board, Dr. Kyri is honored to serve as a voice for individuals and families affected by sarcoma. She is dedicated to strengthening support structures, advancing equitable access to resources, and helping ensure that patient experiences meaningfully inform advocacy, education, and organizational priorities.

Healey is the author of The Resilience Mindset: How Adversity Can Strengthen Individuals, Teams, and Leaders (9/9/2025 – ECW Press/Simon & Schuster), At Face Value: My Triumph Over A Disfiguring Cancer (2nd Edition 1/6/2006 - Caveat Press), and is a contributing author to Open My Eyes, Open My Soul: Celebrating Our Common Humanity, Make Your Own Miracle: Surviving Cancer, an Anthology, and Reading Lips and Other Ways to Overcome a Disability.
His work has appeared in the following publications: CEO World Magazine, Newsweek, Fast Company, The American, Authority Magazine, Psychology Today, Metro UK, The San Francisco Chronicle, Guideposts, NurseWeek, U.S. News and World Report, MarketingProfs, Coping and CURE Today. He has appeared on dozens of national and local TV networks and has been interviewed on more than 150 podcasts and radio stations across the U.S. and Canada.

In March 2024, Tim’s wife, Lindsay, was diagnosed with CIC-DUX4 sarcoma after discovering the tumor during the birth of their son. Her strength through radiation, surgery, and chemotherapy during their son’s first year of life continues to inspire their family and fuels Tim’s commitment to helping others through similar challenges.
Throughout his career, Tim has led various small businesses focused on improving people, process, and technology. He has also contributed to larger healthcare organizations, including Exact Sciences - a leader in cancer diagnostics.
In addition to aiding sarcoma awareness via the Sarcoma Alliance, Tim and Swish BI have developed several technologies, including INDEXALIGN, a platform designed to bring transparency to corporate political contributions and advocate for eliminating the influence of money in politics.
Tim looks forward to drawing on his experience as a caregiver to support others who are helping loved ones through cancer treatment.

Since 2001 she has volunteered for a variety of children’s cancer groups, including the Children’s Oncology Group (COG), ACOR Rhabdo-Kids, and Lincoln Candlelighters.
On the Sarcoma Alliance Board she represents pediatric sarcoma patients, who make up roughly 15% of all sarcoma patients, helps manage the Sarcoma Alliance Facebook news feed, and has served as an Officer of the organization.

Dave joined the Sarcoma Alliance Board of Directors in October of 2002 and in 2020 was given the title of Honorary Board Emeritus. He has represented the Sarcoma Alliance at conferences like American Association of Cancer Research, Oncology Nursing Society, Society of Gynecologic Oncology and the Connective Tissue Oncology Society.
Dave is a retired Computer Lab Specialist from El Camino Community College in Torrance, California where he was in charge of nearly 400 computers in 9 computer labs on campus. He is conversant in Italian, French, and Spanish.

In 1998 he created the original Sarcoma Alliance web site when his wife, Wendy, a sarcoma patient, and Suzanne Leider, first conceived the idea of a sarcoma support organization. He is the creator of our original logo seen on the “Our Founders” page and the artwork for Sage Cuisine. Today he helps maintain the Alliance web site and oversees the production of our newsletter and various printed materials for the organization.

She wrote for the Alliance’s website, newsletters, blog, press releases and survivor profiles. She continues to write on her WordPress site, Twitter and Facebook. Suzie has represented the Alliance at meetings of the Connective Tissue Oncology Society, American Society of Clinical Oncology, American Association for Cancer Research, Society of Gynecologic Oncology and Association of Oncology Social Work.
She became a peer volunteer for MD Anderson Cancer Center in 2004 and added Imerman Angels and Friend for Life along the way. She was a founding board member of Moffitt Cancer Center’s Patient and Family Advisory Program.
Suzie has a bachelor of journalism degree from the University of Missouri and a master’s in women’s studies from the University of South Florida. She received National Press Foundation fellowships to study Spanish and multiculturalism. Her poetry has been published online and in Rolling Stone and various literary journals.

While working, she volunteered as a literacy tutor and a mentor for junior staff. She also supported a colleague during his battle with carcinoma, attending doctors’ visits with him and researching the disease and its treatments. After retirement, Suzanne has been volunteering with the Sarcoma Alliance, as well as with another nonprofit organization, the Medical Musician Initiative, which is dedicated to providing healing music to critical care patients. She also volunteers at a local school where she assists a kindergarten class with reading, and is a member of a local charitable organization that supports local schools, students, food banks, and other causes.
In her spare time she enjoys going to concerts, spending time with family and friends, and hanging out with her German Shepherd dog, Leica.

Marites earned her BS in Nursing from the University of California, Los Angeles in 1992 and her Master’s degree in Nursing from UCLA in 2006. She is Board certified in Acute Care and Palliative Care and has over 25 years of nursing experience with hospitalized patients in various settings. She is currently a Nurse Practitioner at Olive View-UCLA Medical Center, a county facility which provides health care to the uninsured, indigent and medically underserved population of Los Angeles.
As a founding board member, Marites remains dedicated to advancing the mission of the Alliance in honor of Suzanne and all those affected by sarcoma.