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Don’t Be Afraid to Ask for Help

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.

Learning About Sickle Cell Disease

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 on Having a Support Team

Ricky, a teen with cancer, talks about how having a team of people that support you gives a strong foundation to face cancer.

Li-Fraumeni Syndrome (LFS): Laughter is Good Medicine

Whitney was diagnosed with Li-Fraumeni Syndrome (LFS) as a teenager. She shares how laughter helped in her journey.

Ricky on Accepting a New Normal

Ricky, a teen with cancer, shares how he moved forward after his diagnosis and accepted a new normal.

Li-Fraumeni Syndrome (LFS): Knowledge is Power

Li-Fraumeni Syndrome (LFS) is a hereditary cancer syndrome. Mary shares her perspective on how being proactive can empower patients.

Supporting a Sibling with Li-Fraumeni Syndrome (LFS)

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): Staying Close to Family

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.

Living with Li-Fraumeni Syndrome (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.