NCCN Member Institutions

The National Comprehensive Cancer Network (NCCN) is a not-for-profit alliance of 21 of the world’s leading cancer centers. We are dedicated to improving the quality and effectiveness of care provided to people with cancer.

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Printed Copies of the NCCN Guidelines for Patients™

The NCCN Guidelines for Patients™, which are based on the world-renowned NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for cancer care professionals, are meant to help people with cancer and their friends and family understand cancer, to help them talk with their cancer care team about the best treatment options.

In addition to the NCCN Guidelines for Patients™ versions available for online reading or immediate download, NCCN is pleased to announce that printed copies are available for many of the NCCN Guidelines for Patients™, including Breast Cancer, Chronic Myelogenous Leukemia, Malignant Pleural Mesothelioma, Melanoma, Multiple Myeloma, and Prostate Cancer.

 

 

*Please email This e-mail address is being protected from spambots. You need JavaScript enabled to view it   to request your FREE copies

 

 


NCCN.com Begins The Year Helping You Cope With Change...

UPDATED: NCCN Guidelines for Patients: Prostate Cancer

Understanding Early Introduction of Palliative Care Options

Intimacy and Sexual Issues for Patients Undergoing Cancer Treatment

Making the Transition From Hospital to Home

NCCN Treatment Summaries: Non-Hodgkin's Lymphoma VIDEO: About Hospice Care for Cancer Patients

Financial Assistance for People With Cancer

NCCN.com Tip of the Month

Although flowers and cards are always nice to give, sometimes the most helpful and appreciated gestures involve a helping hand with everyday activities that are usually taken for granted. While it’s important to always ask the person first in order to make sure your good intentions will be welcomed, there are many thoughtful ways to show someone with cancer that you care and want to help. Click here to see some ways you can pitch in to help ease some of the burden on your loved one.

If you have a tip you would like to submit for consideration, please click here.

 

 

Louis Spino, pancreatic cancer survivor

Louis Spino, a pancreatic cancer survivor, carefully considered his treatment options before choosing a plan offered by the U-M Cancer Center

NCCN Member Institution Spotlight

Louis Spino was still recovering from open-heart surgery in 2005 when his buddy asked him why his eyes were yellow. A CT scan confirmed that Spino, then 80, had pancreatic cancer.

A local oncologist told Spino he needed to go somewhere where they see a lot of cases like his. So Spino’s five daughters kicked into gear. They opened a third volume in a series of binders they were keeping about their father’s health: Dad’s Recovery Notes.

“We sat down that day and started calling people,” said Margie Spino, who lives a block away from her father in Toledo, Ohio. “We weren’t shy.”

The Spinos talked to the nation’s leading pancreatic cancer specialists at cancer centers in several city. Each offered opinions. The centers that were farther away were eliminated first, given the distance. The decision came down to another large cancer center and the University of Michigan (U-M). U-M recommended chemotherapy and radiation followed by surgery; the other center recommended surgery first.

Read more...

 


 

 

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What types of questions should I ask my doctor about my cancer?

Click here for the answer...
 
 
Answer provided by:
Terry S. Langbaum, MAS
Chief Administrative Officer
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Baltimore, Maryland

See more NCCN Cancer Answers...

 

 
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Ask Jai

Advice For Caregivers


The latest Ask Jai:

Dear Jai: My wife has pancreatic cancer. Her visitors are coming less and less. What can I do?
For the answer, click here.
Jai Pausch became a caregiver for her husband, Randy, during his 23-month battle with pancreatic cancer. Using her experiences to help others, Jai has written about the unique challenges caregivers face, dealing with loss, and creating a new life from shattered dreams. Her book, Dreaming New Dreams, will be published by Crown Publishing Group and is due out May 15, 2012. Currently, Jai is a writer, speaker and advocate for caregivers. She actively participates with several cancer organizations and serves as a board member for the Pancreatic Cancer Action Network and the NCCN Foundation. She lives with her new husband and three children in southern Virginia.
To hear Jai Pausch speak more about her experience and the "Ask Jai" column, watch this video.
Have a concern or question to share? Email Jai at askjai@nccn.org.
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