Behind every #sarcoma story is strength, love, and community. Through Sarcoma Connect, the Facebook Tribute Wall, and Patient Stories, SFA helps patients and families find the support and inspiration they deserve. Whether you’re connecting with others or honoring a loved one,

Before the year ends, give a gift that makes a difference. By joining the Seeds of Hope Society, your monthly donation fuels awareness, provides critical patient resources, and advances life-saving research. As a member, you’ll receive exclusive updates on the impact you’re

During #BoneCancerAwarenessWeek, we stand with everyone affected by primary bone sarcomas. Among these cancers, Osteosarcoma and Ewing Sarcoma are the most common types seen in children. Though rare, they demand greater awareness and stronger research investment to improve

SFA is here to help people impacted by #sarcoma every step of the way. From clinical trial information and treatment center listings to financial assistance, SFA offers resources designed to support your needs. Find more details about these and other resources on our website.

Join us at 9:00 AM ET on Monday, November 3, 2025, for the upcoming live expert discussion about circulating tumor DNA (ctDNA) in sarcomas. Submit any questions you have in advance or use the Q&A feature during the event. You can also share questions on social media anytime

In the last 14 years, the Race to Cure Sarcoma has engaged more than 68,000 participants and raised nearly $12 million. These funds directly support SFA’s research grants, fueling progress for the #sarcoma community. Join us for the final races of the year to walk, run, and make

In case you missed it, the first webinar of our pediatric sarcoma series is now available on YouTube! Hear from Dr. Damon R. Reed, Dr. Katherine A. Janeway, and Care Partner and Advocate Jenny Sage as they discuss what makes pediatric #sarcomas unique. Link in bio. #curesarcoma

#RareCancerDay: Rare cancers account for ~25% of diagnoses but receive far less funding. Sarcoma, ~1% of adult cancers, urgently needs more research. Join SFA in advancing research: https://t.co/NzlFFSpDSx #sarcoma #CureSarcoma #cancer

This Childhood Cancer Awareness Month, we honor all families touched by pediatric sarcoma, including those who carry the memory of loved ones no longer with us. On this episode of Sarcoma Stories, Maria Peña shares the journey of her daughter, Aubrie, who was diagnosed with

Recently diagnosed with #sarcoma? Our Diagnosis Discussion Guide is here to help. It provides key questions and considerations to support informed conversations with your doctor and empower you in your care decisions. Learn more at https://t.co/CQM5ID9Q2y #curesarcoma

On #WorldCancerResearchDay, we're sharing Mike Cacioppo's story about how research in drug repurposing led to a treatment that gave him more time with his family. The science of finding new uses for existing treatments is critical for the #sarcoma community. Every dollar invested

In honor of World Cancer Research Day, we're highlighting the crucial role of research in the #sarcoma community. Meet our 2024 SFA John W. O’Brien Memorial Research Award Recipient, Dr. Mike Stacey. His work on chondrosarcoma focuses on how cancer cells influence normal cells,

Faces Behind the Ribbon continues with Jason’s experience as a childhood Ewing’s Sarcoma survivor. September is Childhood Cancer Awareness Month, and SFA continues to honor and support those impacted by childhood sarcoma. As Jason says, you do not have to go through this alone.

Highlights from the 2025 Stand Up to Sarcoma Gala! From inspiring speakers to honoring this year’s award recipients and the silent auction, the evening was full of moments of hope, impact, and energy. Thank you to everyone who helped make this night possible! Save the date! The

The countdown is on! Race to Cure Sarcoma Chicago is just one week away. Register today to secure your spot at https://t.co/BQ9RDpIkjH and join us on 09/27! Can’t make it? Spread the word! #RCTSChicago #curesarcoma #sarcoma

Join us for our first Pediatric Sarcoma Webinar, happening Sept. 24 from 5–6 PM EST! Hear from top experts and Care Partner and Advocate, Jenny Sage, on treatment, care, and what makes pediatric #sarcomas unique. Save your spot through the link in bio! #curesarcoma

Today is Wear Gold Day! Join SFA in raising awareness for childhood cancer and pediatric sarcoma. Put on gold, snap a photo, and share it using #WearGoldDay, #pediatricsarcoma, and #CureSarcoma. You can also send your photos to communications@curesarcoma.org to be featured.

Congratulations to our Adolescent Young Adult Committee member, Sean Cincotta, and his wife Meg on their recent marriage! Your SFA family celebrates this special moment and is inspired by your love and commitment. Sean and Meg have been pivotal in raising funds for sarcoma

Thank you to Good Morning America for honoring Natasha Allen and raising awareness of #sarcoma. Natasha, who passed away at age 28 after a five-year battle with synovial sarcoma, was a fierce advocate, especially for young people with cancer. At SFA’s annual Stand Up to Sarcoma