Lymphoma

In the U.S., ACS is a community-based voluntary health organization dedicated to eliminating cancer as a major health problem.

• Provides educational materials both online and in print about cancer, including blood cancers, as well as related information on topics such as diet, exercise, complementary and alternative medicine, and disease statistics
• Offers support services via online discussion boards and in-person support groups through local chapters
• Cancer Survivors NetworkSM, a global online community, transcends geographic boundaries and builds bonds among cancer survivors and caregivers through shared experiences and feelings
• Road to Recovery, a program offered locally by some chapters, has volunteer drivers who transport patients to and from treatment appointments
• Hope Lodges are temporary housing accommodations for patients traveling far from home for treatment. There are more than 30 lodges.

To abolish chronic lymphocytic leukemia (CLL) as a threat to the life and health of patients.

• Aims to fund patient-oriented projects with rapid clinical applications and to expand the knowledge of CLL on a global scale
• Provided seed money for the formation of two CLL Research Consortiums, one in Australia and one in Israel.

To address the unmet needs of the CLL patient and related blood cancer communities

• Provides disease, treatment and clinical trial information
• Offers quarterly newsletter “The CLL Tribune”

To support every person with cutaneous lymphoma by promoting awareness and education, advancing patient care, and facilitating research.

• Provides education and support to patients diagnosed with CL
• Information on website is designed to help physicians, nurses and other health professionals access resources related to cutaneous lymphoma.

To provide expert-mediated information on current and emerging cancer management options in order to empower patients, caregivers, and health professionals to become direct partners in cancer care.

• Offers cancer information and video library, podcasts, email newsletter and online discussion forums.

To offer mutual support and encouragement to the Waldenstrom's macroglobulinemia community and others with an interest in the disease.

• Provides information and educational programs that address patients' concerns
• Promotes and supports research leading to better treatments, and ultimately, a cure
• Hosts online forum, telephone and email lifeline network
• Offers support groups for patients, caregivers and families.

To help lymphoma patients and families, and to fund research for a cure.

• Registered nurses provide medical information and resources
• Provides online list of lymphoma specialists in the US
• Online survivor stories and lists of recommended books
• Funds research grants and awards to scientists at leading universities and cancer centers.

To realize the promise of science to eradicate lymphoma and serve the community touched by this disease.

• Provides Lymphoma Helpline and Clinical Trials Information Service
• Provides educational materials, conferences, webcasts
• Offers limited financial assistance to patients in active treatment
• Lymphoma Support Network is a one-to-one peer support program that matches lymphoma patients or caregivers with volunteers who have had similar lymphoma-related experiences
• Funds biomedical research focused on the origins, treatment and identification of a cure for lymphoma
• Raises public awareness of the disease.

To provide accurate, up-to-date, and reliable information on cancer that is easy to understand; this free service is a federally funded cancer education program.

• Offers trained information specialists who can answer cancer-related questions on a range of cancer topics (but is not a substitute for medical advice).

NORD is leading the fight to improve the lives of rare disease patients and families. We do this by supporting the rare community – its people and organizations – and by working together to accelerate research, raise awareness, provide direct assistance and drive public policy.

• Administers Patient Assistance Programs to help patients obtain life-saving or life-sustaining medication they could not otherwise afford
• The Patient Information Center provides information on thousands of rare disorders and resources
• The Rare Caregiver Respite Program offers limited financial assistance to eligible caregivers so that they can take a break from caregiver responsibilities
• Hosts regional and national meetings for patients and families
• Works collaboratively with a growing roster of member organizations.

To provide cancer patients with the resources and information needed to live well with cancer.

• Provides an online portal of cancer information in a library of programs, organized into ‘health centers’. Information from medical conferences as well as interviews featuring top medical experts are continually added to the site.

To create a world-class center of excellence for patients and their families diagnosed with ocular tumors, macular degeneration, and related ophthalmic conditions.

• Provides Find A Doctor search tool to locate an eye cancer specialist
• Offers an online support community through Facebook
• Funds research to find cures for patients with ocular tumors and related eye diseases
• Provides eye cancer specialists for unserved and underserved countries.