Pregunte al doctor sobre el linfoma – 17 de abril del 2025

Ask the Doctor

Pregunte al doctor sobre el linfoma

Pregúnte al Doctor sobre el linfoma es un programa virtual de dos horas que combina una descripción general y accesible del linfoma realizada por un experto con una extensa sesión de preguntas y respuestas.

Fecha: Jueves, 17 de abril del 2025

Hora: de 2:00 PM a 3:00 PM, hora del este

Este es un evento virtual de Zoom, accesible en línea y por teléfono. Las instrucciones de acceso se enviarán por correo electrónico después de inscribirse.

También puede registrarse llamando o enviando un correo electrónico a nuestra línea de ayuda al 800-500-9976 or lymphoma@lymphoma.org.

Descripción general del programa

Este programa proporciona a los pacientes recién diagnosticados una base sólida para comenzar su trayectoria como pacientes.

  • Descripción del linfoma
  • Pruebas de diagnóstico
  • Opciones de tratamiento
  • Sesión de preguntas y respuestas

Participantes

Enrique Diaz, MD
The University of Texas Health Science Center at San Antonio

This program is for patients, survivors, care partners, and program supporters. If you are a pharmaceutical industry professional who is interested in attending but your company is not listed as a sponsor, please email vgonzalez@lymphoma.org to learn more about sponsorship.

Disclaimer: The Lymphoma Research Foundation is a national nonprofit organization based in the United States (U.S.) with educational programs and resources which are intended for a U.S. based audience. These programs and resources are intended for educational purposes only and are not a substitute for medical advice. Individuals who use Foundation programs and services are advised to consult a medical professional for medical advice, diagnoses, or treatment. Foundation programs and resources address available lymphoma/CLL treatments in the United States and information on drug approvals by the U.S. Food and Drug Administration (FDA).

The Foundation does not endorse any treatments, products, or services mentioned in its resources. The information provided is for informational purposes only and should not be considered as an endorsement. The Foundation shall not be liable for any direct, indirect, incidental, special, consequential, or punitive damages arising out of the use of its programs and resources, to the extent permitted by law. You assume full responsibility for any actions taken based on the information provided.

For individuals outside of the U.S. seeking information, the Foundation recommends the Lymphoma Coalition. The Lymphoma Coalition is a global network of worldwide nonprofit/NGO lymphoma patient organizations with information appropriate for non-U.S.-based audiences. Additional information can be found by visiting their website at https://lymphomacoalition.org.

All content provided by the Foundation is protected by intellectual property laws. You may not reproduce, distribute, or otherwise use the content without the Foundation’s prior written consent.

Colaboradores