¿Qué debo hacer si presento fátiga?
"¿Qué debo hacer si presento fátiga?" aportado por Fundación GIST México.
"¿Qué debo hacer si presento fátiga?" aportado por Fundación GIST México.
Our theme for 2020 was Hope. 2020 presented a challenge to us all, but most especially to our patients and caregivers who are seeking to survive this rare cancer. In 2020, The Life Raft Group needed to provide a lifeline to our community, and to offer them hope in the form of increased support as we navigate the challenges of living in a COVID-19 world. #GISTHope
It's time to shorten the time to effective treatment access. Fundación GIST Chile shares their story.
The LRG will be collaborating with the NIH again in 2021 to hold the Virtual GIST Tumor Board in place of the NIH's Pediatric & Wildtype GIST Clinic normally held in the DC area. Applications to have cases reviewed are now open.
It's time to to recognize the value of a more precise diagnosis. GISTer Jon Treder shares his story.
The Life Raft Group is delighted to welcome two phenomenal new members to our Board of Directors: Ms. Kay Stolzer and Dr. Monica (mOe) Anderson.
It's time to fully unleash the power of biomarker testing to support precision oncology - all GIST patients should have biomarker (mutational) testing for the best possible personalized treatment plan.
Each member has a unique story, but all reflect the intrinsic courage of one facing the challenge of GIST. Vicenta Salinas shares her story.
Understanding the role of mutations and biomarker testing is one of most important things patients must learn. Uncovering the driving force behind each individual’s tumors is not just important, it is critical. This video shows the action steps of our It's Time campaign.
Lea el artículo para Colectivo GIST España sobre la importancia de conocer la mutación de tu gist - succinato deshidrogenasa - Abril 8, 2021