Are you a cancer patient, survivor, or caregiver who wants to make healthcare care?
Join our research registry with hundreds of others and be the first to learn about our new project opportunities to share your experience to impact real change.
Are you ready to lend your voice to influence the future of cancer care?
How This Resource Supports You
Gryt Health was created by cancer survivors for patients, survivors, and caregivers facing cancer diagnoses. Our goal is to provide support and resources to improve experiences while engaging our community in ground-breaking research opportunities that strengthen the role of the patient voice in healthcare decision-making.
How You Make An Impact
Through questionnaires, digital focus groups, and patient journey research, the GRYT Project helps its partners better understand the patient, survivor, and caregiver experience so that cancer care can be improved and positively impact health outcomes, from early-stage treatments through long-term survivorship.
Transparency With Our Partners
You can think of Gryt Health as a mediator between the healthcare industry and patients. However, unlike other companies catering to pharma needs, Gryt Health always puts patients, survivors, and caregivers first because we are patients, survivors, and caregivers.
Pharmaceutical and biotechnology companies come to us to understand the patient perspective and experience in everything from interacting with the healthcare system to treatment, diagnosis, and post-treatment concerns and burdens. We integrate your experience into what they produce so that information is more tailored to patient needs, side effects and impacts of treatment are better understood, and, ultimately, cancer care and health outcomes are improved.
CAR T-Cell Therapy Clinical Trial Patient Experience Research Opportunity
Received Chimeric Antigen Receptor (CAR) T-cell therapy? Talking with your doctor about CAR T-cell therapy? Share your CAR T-cell therapy clinical trial experience to help improve the experiences of future patients! We are looking for patients who are considering or participating in CAR T-cell therapy clinical trials within the United States to participate in virtual engagements about their experiences and unmet needs. For more information and/or to participate, please contact us at firstname.lastname@example.org.
Patient Advisory Panel for Clinical Trial Insights
GRYT Health is looking for patients who have undergone a clinical trial for the treatment of their cancer in the United States within the past 5 years to sit on a virtual patient advisory panel for approximately 12 months. The purpose of this project is to better involve the patient voice in clinical trial development by enabling healthcare companies to hear from patients who have firsthand clinical trial experience. Your participation in this project will help to make clinical trials more patient-friendly, equitable, and efficient so that more patients can access and benefit from new medications and technologies. For more information and/or to participate, please contact us at email@example.com.
From Our Partners
Fertility & Family-Building After Cancer
What are your options for building a family after cancer? The Roadmap to Parenthood study will help you learn about fertility and family-building options after cancer, and what you can do to plan for the future.
The study is for US women only. Participants will have access to a website that was developed for and with women affected by cancer and will be asked to complete three brief surveys over three months. This project is supported by the National Cancer Institute (NCI).
Frequently asked questions about The GRYT Project
Tap or click on the question to see an answer.
We fully believe in the power of the patient, survivor, and caregiver voice. By integrating your experience into research projects, we can move healthcare forward. Our projects focus on compiling information that helps advance the treatment, care, and the experiences of those affected by cancer. Together, we can improve health outcomes.
The trust of our Gryt Health community is paramount in everything we do. Even if you choose to participate in a research project, we will never sell or share your personal information without your permission. We will always offer full transparency concerning whom we are working with and the purpose of the research study.
The research we are doing in collaboration with our partners will move healthcare forward, and we intend to share information that will improve health outcomes broadly. With that being said, some of our projects are confidential and cannot be immediately shared.
When you sign up to join The GRYT Project, you will be added to a research registry of those interested in working with us on research projects. It is important to note that each research project has its unique parameters, and while you may be qualified for one, it does not guarantee entry into other collaborations. We will contact you by email when projects become available to meet the selection criteria.
Our research projects are conducted throughout the year. The projects available will vary from month to month. Unfortunately, we cannot predict how often you will be eligible to participate within a given year. Make sure to add firstname.lastname@example.org to your address book to avoid our emails going to spam.
Yes! Absolutely! As long as you meet the project requirements, you are eligible to participate in multiple research projects, even if that means participating in overlapping projects.
While we try very hard to make sure we can compensate those who participate in our projects as much and as often as possible, not all of our projects are compensated. Sometimes our partners have very limited resources and cannot offer compensation. You will know which projects are compensated and which are not, upfront and the choice to participate is yours.