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Daniel Ndibou shares his journey with sickle cell disease, focusing on positivity and curiosity to overcome challenges.
Nana and Mame Qhartey share how they manage their sickle cell disease and cope with tough days by reading books, watching K-dramas, and resting to feel better.
Nana Qhartey stresses the importance of mental health, encouraging breaks and rest without feeling guilty.
Nana Qhartey shares her experience with sickle cell anemia, aiming to educate others about the condition and its challenges.
Nana and Mame Qhartey talk about their journey with sickle cell anemia and how their experience helped them bond and support each other.
Sickle cell disease patient McKenley Allen tells other patients to not be afraid to ask for help when pain crises happen. Learn more from McKenley.
Nia Mullins shares how she gradually learned about her sickle cell disease and why it caused her to have pain. Learn more about Nia’s story.
Ricky, a teen with cancer, talks about how having a team of people that support you gives a strong foundation to face cancer.
Whitney was diagnosed with Li-Fraumeni Syndrome (LFS) as a teenager. She shares how laughter helped in her journey.
Ricky, a teen with cancer, shares how he moved forward after his diagnosis and accepted a new normal.
Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome. Mary shares her perspective on how being proactive can empower patients.
Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome. Kate shares how she felt when she learned her brother had LFS.
Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome. Hear how one family copes by staying close to family and connecting with others who have LFS.
Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome. Mindy and Breanna talk about continuing to live your life and making each day count.
Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome. Anne discusses the decision to have her children tested for LFS after her husband's diagnosis.