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Melanoma survivor T.J. Sharpe shares why patients should know their treatment options.
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Ron Hollander, president of the International Neuroendocrine Cancer Alliance, talks to us about patient advocacy.
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Groups of people doing communal exercises are an everyday sight in Japan, but for one woman they are a very public way to show she is fighting back.
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Parents and doctors can help children understand rare diseases like TSC and SJIA with the help of cartoon dogs and comic book superheroes.
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We surveyed 7,000 people in seven countries to find out what they know about multiple sclerosis (MS). Our survey identified several surprising misconceptions.
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Learn about how digital is changing the face of patient advocacy.
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Lisa, a patient living with CML, shares her experience and discusses the importance of speaking up about unmet needs in your disease.
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Melanoma survivor T.J. Sharpe discusses the importance of clinical trials to help raise awareness among the community.
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Global Oncology Patient Insights Panels (GOPIPs) are giving patients and advocates a critical voice in advancing lung cancer trials.
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