Featured Videos
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Paying With Our Lives: The Impact of Federal Funding Cuts On Rare Cancer Research
Cancer affects everyone and should never be political. Yet recent federal funding cuts to cancer research are having both immediate and far-reaching consequences on the rare cancer community. In this Rare Cancer Day Lunch and Learn webinar, the inspiring panelists discuss the impact of these cuts based on their own personal experiences and how you can get involved to support rare cancer research.
Linds Brown (ocular melanoma patient and advocate) and Sara Selig, MD, MPH (public health physician, Brigham and Women’s Hospital, caregiver, and advocate) joined Gillian Parrish (President, Parrish Public Relations) for this important and meaningful conversation.
The Power of Advocacy: Collective Strength Through the Rare Cancer Patient Voice
In this TargetCancer Foundation Lunch and Learn Webinar, four rare cancer patients and advocates who are making a powerful impact in the field discussed their personal experiences and insights regarding the importance of advocacy for awareness and progress in the treatment of rare cancers.
TargetCancer Foundation President Kristen Palma was joined by rare cancer patients and advocates Dana Deighton (Director, Communications & Engagement, Melanoma Research Alliance), Katie Doble (Stage 4 Rare Cancer Survivor and Patient Advocate), Naomi Natale (Co-Founder, cureMEC: The Myoepithelial Carcinoma Project) and Suzanne Vincze (Vice President, Max Vincze Foundation) for this important discussion.
TargetCancer Foundation at 15 Years: Celebrating our Community
Four community members share their rare cancer experiences in this short video as they reflect on the impact being a part of the TargetCancer Foundation community had on them and their families. We are grateful for the support of our community, which strengthens our efforts as we continue to make a difference for those facing a rare cancer diagnosis. We hope you will be inspired to get involved!
https://targetcancer.org/get-involved/
TargetCancer Foundation at 15 Years: Reshaping the Rare Cancer Research Landscape
TargetCancer Foundation at 15 years: Looking back at our history
Browse our Library
Paying With Our Lives: The Impact of Federal Funding Cuts On Rare Cancer Research
The Power of Advocacy: Collective Strength Through the Rare Cancer Patient Voice
TargetCancer Foundation TRACK Molecular Tumor Board: Salivary Duct Carcinoma
Success Stories & Ethics of Expanded Germline & Cascade Testing in Pediatric Cancer
Closing the Book on Readers and Writers in NUT Carcinoma | Christopher French
The Power of Personal Experience: Patients and Caregivers as Drivers of Rare Cancer Research
The Precision Patient: Seeking Out Innovative, Science-Based Therapy for Patients with Rare Cancers
Dr. Razelle Kurzrock: N-of-1 Patient Centric Clinical Trials
Revolutionizing Rare Cancer Drug Development with Novel Tumour-Agnostic Classifiers & AI Innovations
Patients and Practitioners as Partners: Initial Steps for Navigating a Rare Cancer Diagnosis
TargetCancer Foundation at 15 Years: Celebrating our Community
TargetCancer Foundation at 15 Years: Reshaping the Rare Cancer Research Landscape