It’s Lung Cancer Awareness Month! Across the country, our patient speakers have been sharing their journeys providing hope and inspiration to all.
Looking to get involved? Send us a PM to learn about our ALK+ mNSCLC patient speaker bureau.
#ALKmNSCLC#LungCancer#LCAM
NEW! Join our speaker bureau of patients living with cGVHD to share your diagnosis and treatment journey. To learn more, send us a private message or contact us at [email protected]. #cgvhd#patientadvocacy#patientvoices
NEW OPPORTUNITY! Are you currently living with ALK+ mNSCLC and currently on your first line of treatment? VPR POP wants to hear from you! Join our bureau of fellow ALK+ speakers sharing their story to educate and inspire others.
**OPEN TO US RESIDENTS ONLY**
Throughout March, the VPR POP team has been proud to show our support for our multiple myeloma patient ambassadors! To learn more about multiple myeloma, its causes, and how to get involved visit https://t.co/5uGnr83DhP.
#multiplemyeloma#multiplemyelomaawarenessmonth
This March VPR POP is proud to show our support for our patient ambassadors with bleeding disorders! To learn more about bleeding disorders and how to spread the word visit https://t.co/jfPSsmjpgS.
#hemophilia#bleedingdisorders#bleedingdisordersawarenessmonth
@SabrinaYRenfro Hi Sabrina, thanks for re-sharing our post! Would love to connect with you and/or your husband about our open patient and caregiver speaker opportunity.
@SabrinaYRenfro We are creating a program for patients and/or their caregivers to share their prostate cancer story. We’d love to hear more about your experience. Please message us!
Share your prostate cancer journey!
Have you or a loved one been diagnosed with prostate cancer and had a PSMA PET Scan? We want to hear from you.
For more information, please contact VPR POP at [email protected] or 833-436-2844.
#prostatecancer#PSMAPETScan
Thank you for all who expressed interested in this opportunity. The spots for this advisory session have now been filled.
For more opportunities like this, please follow our page.
Are you or someone you know living with Hemophilia B? We are looking for individuals to participate in a virtual advisory board on March 6th, 2024 to share their story and experiences. Participants will be compensated for their time. Please reach out to us for more information!