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National Organizations That Offer Services to People With Cancer and Their Families

People with cancer and their families sometimes need assistance coping with the emotional as well as the practical aspects of their disease. This fact sheet includes some of the national organizations that provide this type of support. It is not intended to be a comprehensive listing of all organizations that offer these services in the United States, nor does inclusion of any particular organization imply endorsement by the National Cancer Institute, the National Institutes of Health, or the Department of Health and Human Services. The intent of this fact sheet is to provide information useful to individuals nationally. For that reason, it does not include the many local groups that offer valuable assistance to patients and their families in individual states or cities.


Alliance for Lung Cancer Advocacy, Support, and Education (ALCASE)

Post Office Box 849
Vancouver, WA 98666 
360–696–2436
1–800–298–2436 
info@alcase.org
www.alcase.org
ALCASE offers programs designed to help improve the quality of life of people with lung cancer and their families. Programs include education about the disease, psychosocial support, and advocacy about issues that concern lung cancer survivors.

American Brain Tumor Association (ABTA)

2720 River Road
Des Plaines, IL 60018
847–827–9910
1–800–886–2282(1–800–886–ABTA)
info@abta.org
www.abta.org
The ABTA funds brain tumor research and provides information to help patients make educated decisions about their health care. The ABTA offers printed materials about the research and treatment of brain tumors, and provides listings of physicians, treatment facilities, and support groups throughout the country. A limited selection of Spanish-language publications is available.

American Cancer Society (ACS)

1599 Clifton Road, NE.
Atlanta, GA 30329–4251 
404–320–3333
1–800–227–2345 (1–800–ACS–2345)
www.acs.org
The ACS is a voluntary organization that offers a variety of services to patients and their families. The ACS also supports research, provides printed materials, and conducts educational programs. Staff can accept calls and distribute publications in Spanish. A local ACS unit may be listed in the white pages of the telephone directory under "American Cancer Society."
American Cancer Society (ACS) Supported Programs:
This is both a telephone and Web-based service for cancer survivors, their families, caregivers, and friends. The telephone component (1–877–333–HOPE) provides survivors and families access to pre-recorded discussions. The Web-based component offers live online chat sessions, virtual support groups, pre-recorded talk shows, and personal stories.
I Can Cope
I Can Cope is a patient education program that is designed to help patients, families, and friends cope with the day-to-day issues of living with cancer.
This program assists people who have lost their voice as a result of cancer. It provides information on the skills needed by laryngectomees and works toward total rehabilitation of patients.
This program was developed by the Cosmetic, Toiletry, and Fragrance Association Foundation in cooperation with ACS and the National Cosmetology Association. It focuses on techniques that can help people undergoing cancer treatment improve their appearance. The entire program is also available in Spanish.
Reach to Recovery
The Reach to Recovery Program is a rehabilitation program for men and women who have or have had breast cancer. The program helps breast cancer patients meet the physical, emotional, and cosmetic needs related to their disease and its treatment.

American Foundation for Urologic Disease (AFUD)

Suite 410 
1000 Corporate Boulevard
Linthicum, MD 21090
410–689–3990
1–800–828–7866
www.afud.org
The AFUD supports research; provides education to patients, the general public, and health professionals; and offers patient support services for those who have or may be at risk for a urologic disease or disorder. They provide information on urologic disease and dysfunctions, including prostate cancer treatment options, bladder health, and sexual function. They also offer prostate cancer support groups (Prostate Cancer Network). Some Spanish-language publications are available.

American Institute for Cancer Research (AICR)

1759 R Street, NW.
Washington, DC 20009 
202–328–7744
1–800–843–8114
aicrweb@aicr.org
www.aicr.org
The AICR provides information about cancer prevention, particularly through diet and nutrition. They offer a toll-free nutrition hotline and funding of research grants. The AICR also has a wide array of consumer and health professional brochures, plus health aids about diet and nutrition and their link to cancer and cancer prevention. The AICR also offers the AICR CancerResource, an information and resource program for cancer patients. A limited selection of Spanish-language publications is available.

The Brain Tumor Society

Suite 3–H
124 Watertown Street
Watertown, MA 02472 
617–924–9997
1–800–770–8287 (1–800–770–TBTS) 
info@tbts.org
www.braintumor.org
The Brain Tumor Society provides information about brain tumors and related conditions for patients and their families. They offer a patient/family telephone network, educational publications, funding for research projects, and access to support groups for patients.

Cancer Care, Inc.

National Office
275 Seventh Avenue
New York, NY 10001
212–712–8080
1–800–813–4673 (1–800–813–HOPE)
212–712–8400 (Administration)
info@cancercare.org
www.cancercare.org
Cancer Care is a national nonprofit agency that offers free support, information, financial assistance, and practical help to people with cancer and their loved ones. Services are provided by oncology social workers and are available in person, over the telephone, and through the agency’s Web site. Cancer Care’s reach also extends to professionals—providing education, information, and assistance. A section of the Cancer Care Web site and some publications are available in Spanish, and staff can respond to calls and e-mails in Spanish.
Cancer Care also operates the AVONCares Program for Medically Underserved Women, which provides financial assistance to low income, under- and uninsured, underserved women throughout the country who need supportive services (transportation, child care, and home care) related to the treatment of breast and cervical cancers.

Cancer Hope Network

Two North Road
Chester, NJ 07930
1–877–467–3638 (1–877–HOPENET) 
info@cancerhopenetwork.org
www.cancerhopenetwork.org
The Cancer Hope Network provides individual support to cancer patients and their families by matching them with trained volunteers who have undergone and recovered from a similar cancer experience. Such matches are based on the type and stage of cancer, treatments used, side effects experienced, and other factors.

Cancer Information and Counseling Line (CICL) 
(a service of the AMC Cancer Research Center)

1600 Pierce Street
Denver, CO 80214
1–800–525–3777
ciclhelp@amc.org
www.amc.org
The CICL, part of the Psychosocial Program of the AMC Cancer Research Center, is a toll-free telephone service for cancer patients, their family members and friends, cancer survivors, and the general public. Professional counselors provide up-to-date medical information, emotional support through short-term counseling, and resource referrals to callers nationwide between the hours of 8:30 a.m. and 5:00 p.m. MST, Monday through Friday. Individuals may also submit questions about cancer and request resources via e-mail.

Cancer Research and Prevention Foundation

Suite 500
1600 Duke Street
Alexandria, VA 22314 
703–836–4412
1–800–227–2732 (1–800–227–CRFA) 
info@preventcancer.org
www.preventcancer.org
The Cancer Research Foundation of America seeks to prevent cancer by funding research and providing educational materials on early detection and nutrition.

Candlelighters Childhood Cancer Foundation (CCCF)

Post Office Box 498
Kensington, MD 20895–0498 
301–962–3520
1–800–366–2223 (1–800–366–CCCF)
info@candlelighters.org
www.candlelighters.org
The CCCF is a nonprofit organization that provides information, peer support, and advocacy through publications, an information clearinghouse, and a network of local support groups. A financial aid list is available that lists organizations to which eligible families may apply for assistance.

Children’s Brain Tumor Foundation (CBTF)

Suite 1301 
274 Madison Avenue
New York, NY 10016
212–448–9494
1–866–228–4673 (1–866–228–HOPE)
info@cbtf.org
www.cbtf.org
The CBTF is nonprofit organization that funds research and provides support, education, and advocacy for children with brain and spinal cord tumors and their families. It also provides educational materials (including a Spanish-language publication) and cosponsors conferences and seminars for families, survivors, and health care professionals that offer the latest information about research, treatments, and strategies for living. Through CBTF’s Parent-to-Parent Network, families share their experiences with others in similar situations.

Children’s Hospice International®

Suite 230
901 North Pitt Street
Alexandria, VA 22314
703–684–0330
1–800–242–4453 (1–800–2–4–CHILD)
chiorg@aol.com
www.chionline.org
Children’s Hospice International provides a network of support for dying children and their families. It serves as a clearinghouse for research programs and support groups, and offers educational materials and training programs on pain management and the care of seriously ill children.

Colon Cancer Alliance (CCA)

175 Ninth Avenue
New York, NY 10011
212–627–7451 (Main office)
1–877–422–2030 (Helpline)
info@ccalliance.org
www.ccalliance.org
The CCA is an organization of colon and rectal cancer survivors, their families, caregivers, and the medical community. The Alliance provides patient support and public education, supports research, and advocates for the needs of cancer patients and their families. The CCA offers information including brochures and booklets, a newsletter, a toll-free Helpline, and weekly online chats. It also offers the CCA Buddies Network, which matches survivors and caregivers with others in a similar situation for one-on-one emotional support. The CCA has volunteers who speak Spanish.

Colorectal Cancer Network

Post Office Box 182
Kensington, MD 20895–0182 
301–879–1500 
ccnetwork@colorectal-cancer.net
The Colorectal Cancer Network is a national advocacy group that raises public awareness about colorectal cancer and provides support services to colorectal cancer patients and their families, friends, and caregivers. Services include support groups; an Internet chat room; e-mail listservs for survivors, caregivers, and advocates; hospital visitation programs; and a "One on One" service that connects newly diagnosed individuals with long-term survivors. The Network also provides literature on screening, diagnosis, treatment, and supportive care for colorectal cancer.

ENCOREPlus®

YWCA of the USA
Office of Women’s Health Advocacy
Suite 700
1015 18th Street, NW.
Washington, DC 20036 
202–467–0801
1–800–953–7587 (1–800–95E–PLUS) 
cgould@ywca.org
www.ywca.org
ENCOREPlus is the YWCA’s discussion and exercise program for women who have had breast cancer surgery. It is designed to help restore physical strength and emotional well-being. A local branch of the YWCA, listed in the telephone directory, can provide more information about ENCOREPlus.

Gilda’s Club® Worldwide

Suite 1402
322 Eighth Avenue
New York, NY 10001
1–888–445–3248 (1–888–GILDA–4–U) 
info@gildasclub.org
www.gildasclub.org
Gilda’s Club Worldwide works with communities to start and maintain local Gilda’s Clubs, which provide social and emotional support to cancer patients, their families, and friends. Lectures, workshops, support and networking groups, special events, and children’s programs are offered. Services are available in Spanish.

HOSPICELINK

Three Unity Square
Post Office Box 98
Machiasport, ME 04655–0098 
207–255–8800
1–800–331–1620
HOSPICEALL@aol.com
www.hospiceworld.org
HOSPICELINK helps patients and their families find support services in their communities. They offer information about hospice and palliative care and can refer cancer patients and their families to local hospice and palliative care programs.

International Myeloma Foundation (IMF)

Suite 206
12650 Riverside Drive
North Hollywood, CA 91607–3421
818–487–7455
1–800–452–2873 (1–800–452–CURE) 
TheIMF@myeloma.org
www.myeloma.org
The IMF supports education, treatment, and research for multiple myeloma. They provide a toll-free hotline, seminars, and educational materials for patients and their families. Although the IMF does not sponsor support groups, they do keep a list of other organizations’ support groups and provide information on how to start a support group. A section of the IMF Web site and some printed materials are available in Spanish.

International Waldenstrom’s Macroglobulinemia Foundation (IWMF)

Suite 301
2300 Bee Ridge Road
Sarasota, FL 34239–6226
941–927–4963
IWMF1@juno.com
www.iwmf.com
The IWMF provides encouragement and support to people with Waldenstrom’s Macroglobulinemia (WM) and their families, and works to increase awareness of issues related to WM. The IWMF also encourages and supports increased research toward finding more effective treatments and ultimately a cure. The IWMF offers publications, including a quarterly newsletter, The IWMF Torch, and bulletins. Through its Internet Talklist, regional support groups, and telephone Lifeline Project, the Foundation also helps people with WM contact others with this disease. People may also participate in the IWMF’s annual Educational Forum to hear prominent researchers and other speakers, and to share their experiences with other participants.

Kidney Cancer Association

Suite 203
1234 Sherman Avenue
Evanston, IL 60202–1375 
847–332–1051
1–800–850–9132 
office@kidneycancerassociation.org
www.kidneycancer.org
The Kidney Cancer Association supports research, offers printed materials about the diagnosis and treatment of kidney cancer, sponsors support groups, and provides physician referral information.

Lance Armstrong Foundation (LAF)

Post Office Box 161150
Austin, TX 78716–1150 
512–236–8820
www.livestrong.org
The LAF, a nonprofit organization founded by cancer survivor and cyclist Lance Armstrong, provides resources and support services to people diagnosed with cancer and their families. The LAF’s services include Cycle of Hope, a national cancer education campaign for people with cancer and those at risk for developing the disease, and the Cancer Profiler, a free interactive treatment decision support tool. The LAF also provides scientific and research grants for the better understanding of cancer and cancer survivorship.

The Leukemia and Lymphoma Society

1311 Mamaroneck Avenue
White Plains, NY 10605–5221 
914–949–5213
1–800–955–4572
infocenter@leukemia-lymphoma.org
www.leukemia-lymphoma.org
The goal of The Leukemia and Lymphoma Society is to find cures for leukemia, lymphoma, Hodgkin’s disease, and multiple myeloma and to improve the quality of life of patients and their families. The Society supports medical research and provides health education materials, as well as the following services: patient financial aid for specified treatment expenses and transportation, family support groups, First Connection (a professionally supervised peer support program), referrals, school re-entry materials, and public and professional education. The Society also provides audiotapes in English and some Spanish-language publications.

Living Beyond Breast Cancer (LBBC)

Suite 204
10 East Athens Avenue
Ardmore, PA 19003
610–645–4567
1–888–753–5222 (1–888–753–LBBC)(Survivors’ Helpline)
mail@lbbc.org
www.lbbc.org
The LBBC is an educational organization that aims to empower women with breast cancer to live as long as possible with the best quality of life. The LBBC offers an interactive message board and information about upcoming conferences and teleconferences on its Web site. In addition, the organization has a toll-free Survivors’ Helpline, a Young Survivors Network for women diagnosed with breast cancer who are age 45 or younger, and outreach programs for medically underserved communities. The LBBC also offers a quarterly educational newsletter and a book for African American women living with breast cancer.

The Lustgarten Foundation for Pancreatic Cancer Research

1111 Stewart Avenue
Bethpage, NY 11714
516–803–1000
1–866–789–1000
www.lustgarten.org
The Lustgarten Foundation funds research, advocates for research funding, and raises awareness of pancreatic cancer diagnosis, treatment, and prevention. The Foundation assists patients and their families in obtaining the most accurate, up-to-date information about pancreatic cancer. It provides educational materials and publications about pancreatic cancer, including a Spanish-language publication. It also has an on-staff social worker available to make referrals to cancer support services.

Lymphoma Research Foundation (LRF)

For patient services:
Suite 207
8800 Venice Boulevard
Los Angeles, CA 90034
310–204–7040
1–800–500–9976 
LRF@lymphoma.org (general information)
helpline@lymphoma.org (patient services)
www.lymphoma.org
For research and advocacy: 
19th Floor
111 Broadway
New York, NY 10006 
212–349–2910
1–800–235–6848
researchgrants@lymphoma.org (research program)
advocacy@lymphoma.org (advocacy)
In 2001, the Lymphoma Research Foundation of America (LRFA) and the Cure For Lymphoma Foundation (CFL) merged to become the Lymphoma Research Foundation (LRF). The LRF’s mission is to eradicate lymphoma and serve those touched by this disease. The LRF funds research, advocates for lymphoma-related legislation, and provides educational and support programs for patients and their families.

The Multiple Myeloma Research Foundation (MMRF)

Suite 201
51 Locust Avenue
New Canaan, CT 06840 
203–972–1250 
info@themmrf.org
The MMRF supports research grants and professional and patient symposia on multiple myeloma and related blood cancers. The MMRF publishes a quarterly newsletter, and provides referrals and information packets free of charge to patients and family members.

Mesothelioma Guide

121 S. Orange Ave - Suite 1450
Orlando, FL 32801
888-572-9011
webmaster@mesotheliomaguide.com

www.MesotheliomaGuide.com

www.MesotheliomaGuide.com/Asbestos

 
The Mesothelioma Guide is a new site reaching out to provide up-to-date support to mesothelioma patients and family members. Mesothelioma is a rare cancer, only affecting 2,000 – 3,000 patients a year. Although this number may be small relative to other cancerous diseases, it is almost always 100% fatal. Any individual or family that is diagnosed with or knows someone with cancer deserves to have the best information and support available. Our goal at Mesothelioma Guide is to increase mesothelioma awareness.

Mesothelioma - Asbestos

20 N. Orange Ave- Suite 1450
Orlando, FL 32801
800-615-2270
webmaster@asbestos.com

www.asbestos.com
 
The Mesothelioma Center is here to help you. Whether you, a family member or a friend are diagnosed with mesothelioma or another asbestos-related disease, this site was designed for you. The Mesothelioma Center is committed to being a comprehensive one-stop resource for all asbestos- and mesothelioma-related issues, from occupational exposure to treatment options. We understand that being diagnosed with cancer, especially a cancer as rare as mesothelioma, can be overwhelming.

MesotheliomaHelp

546 Fifth Ave
New York, NY 10036
1-877-637-6843

www.mesotheliomahelp.org
 
MesotheliomaHelp, America’s Mesothelioma Resource, is one of the web’s primary resources for information on malignant mesothelioma and other asbestos-related diseases. Our team of writers, supporters and sponsors of this site are dedicated to bringing the latest, most comprehensive mesothelioma information to patients, families and caregivers.
Our goal is to provide the appropriate information to families battling mesothelioma to empower them to participate in making the decisions about their care, and to offer some measure of hope and support.

Pleural Mesothelioma Center

1-800-381-1772
outreach@pleuralmesothelioma.com 
patients@pleuralmesothelioma.com

PleuralMesothelioma.com
 
PleuralMesothelioma.com is an informative website and advocacy group that helps people affected by pleural mesothelioma cancer. We provide free resources and assistance to help patients and their loved ones cope with medical, emotional and financial challenges.

Mesothelioma Resource Online

One William Street
New York, NY 10004
855-584-0411
webmaster@mesotheliomasymptoms.com

www.mesotheliomasymptoms.com
 
Mesothelioma Resource Online has created and developed this site to provide answers and support for people diagnosed withmesothelioma, as well as their families and loved ones. Mesothelioma is a rare form of cancer that is caused by exposure to asbestos and has long been considered a mystery and incurable. However, over the past two decades, physicians, scientists and researchers have begun to unravel this mystery and help people diagnose mesothelioma in its earlier stages, while providing more extensive forms of treatment, vast resources, and general information to make coping and survival more about optimism rather than uncertainty.
 
National Asian Women’s Health Organization (NAWHO)

Suite 900
250 Montgomery Street
San Francisco, CA 94104 
415–989–9747 
nawho@nawho.org
The NAWHO is working to improve the health status of Asian women and families through research, education, leadership, and public policy programs. They have resources for Asian women in English, Cantonese, Laotian, Vietnamese, and Korean. Publications on subjects such as reproductive rights, breast and cervical cancer, and tobacco control are available.

National Bone Marrow Transplant Link (nbmtLink)

Suite 108
20411 West 12 Mile Road
Southfield, MI 48076
1–800–546–5268 (1–800–LINK–BMT)
nbmtlink@aol.com
www.nbmtlink.org
The nbmtLink motto is "A second chance at life is our first priority." The nbmtLink operates a 24-hour, toll-free number and provides peer support to bone marrow transplant (BMT) patients and their families. It serves as an information center for prospective BMT patients as well as a resource for health professionals. Educational publications, brochures, and videos are available. Staff can respond to calls in Spanish.

National Brain Tumor Foundation (NBTF)

Suite 612 
22 Battery Street
San Francisco, CA 94111–5520
415–834–9970
1–800–934–2873 (1–800–934–CURE) 
nbtf@braintumor.org
www.braintumor.org
The NBTF provides patients and their families with information on how to cope with their brain tumors. This organization conducts national and regional conferences, publishes printed materials for patients and family members, provides access to a national network of patient support groups, and assists in answering patient inquiries. The NBTF also awards grants to fund research. Staff are available to answer calls in Spanish, and some Spanish-language publications are available.

National Breast Cancer Coalition (NBCC)

Suite 1300
1101 17th Street, NW.
Washington, DC 20036 
202–296–7477
1–800–622–2838 
info@stopbreastcancer.org
www.stopbreastcancer.org
The NBCC is a breast cancer advocacy group that educates and trains individuals to become advocates who effectively influence public policies that affect breast cancer research and treatment. It also promotes breast cancer research, and works to improve access to high-quality breast cancer screening, diagnosis, and treatment for all women.

National Childhood Cancer Foundation (NCCF)

440 East Huntington Drive
Post Office Box 60012
Arcadia, CA 91066–6012
626–447–1674
1–800–458–6223
info@nccf.org
www.nccf.org
The NCCF supports research conducted by a network of institutions, each of which has a team of doctors, scientists, and other specialists with the special skills required for the diagnosis, treatment, supportive care, and research on the cancers of infants, children, and young adults. Advocating for children with cancer and the centers that treat them is also a focus of the NCCF. A limited selection of Spanish-language publications is available.

National Coalition for Cancer Survivorship (NCCS)

Suite 770
1010 Wayne Avenue
Silver Spring, MD 20910–5600
301–650–9127
1–877–622–7937 (1–877–NCCS–YES)
info@canceradvocacy.org
www.nhpco.org

National Hospice and Palliative Care Organization (NHPCO)

Suite 625
1700 Diagonal Road
Alexandria, VA 22314 
703–837–1500
1–800–658–8898 (Helpline)
info@nhpco.org
The NHPCO is an association of programs that provide hospice and palliative care. It is designed to increase awareness about hospice services and to champion the rights and issues of terminally ill patients and their family members. They offer discussion groups, publications, information about how to find a hospice, and information about the financial aspects of hospice. Some Spanish-language publications are available, and staff are able to answer calls in Spanish.

National Lymphedema Network (NLN)

Suite 1111
1611 Telegraph Avenue
Oakland, CA 94612–2138
510–208–3200
1–800–541–3259
nln@lymphnet.org
www.lymphnet.org
The NLN provides education and guidance to lymphedema patients, health care professionals, and the general public by disseminating information on the prevention and management of primary and secondary lymphedema. They provide a toll free support hotline, a referral service to lymphedema treatment centers and health care professionals, a quarterly newsletter with information about medical and scientific developments, support groups, pen pals, educational courses for health care professionals and patients, and a computer database. Some Spanish-language materials are available.

National Marrow Donor Program® (NMDP)

Suite 500
3001 Broadway Street, NE.
Minneapolis, MN 55413–1753 
612–627–5800
1–800–627–7692 (1–800–MARROW–2)
1–888–999–6743 (Office of Patient Advocacy)
www.nmdp.org
The National Marrow Donor Program (NMDP), which is funded by the Federal Government, was created to improve the effectiveness of the search for bone marrow donors. It keeps a registry of potential bone marrow donors and provides free information on bone marrow transplantation, peripheral blood stem cell transplant, and unrelated donor stem cell transplant, including the use of umbilical cord blood. The NMDP’s Office of Patient Advocacy assists transplant patients and their physicians through the donor search and transplant process by providing information, referrals, support, and advocacy.

National Ovarian Cancer Coalition (NOCC)

Suite 14
500 Northeast Spanish River Boulevard
Boca Raton, FL 33431
561–393–0005
1–888–682–7426 (1–888–OVARIAN)
NOCC@ovarian.org
www.ovarian.org
The NOCC raises awareness about ovarian cancer and promotes education about this disease. They have a toll-free telephone number for information, referral, support, and education about ovarian cancer. They also offer support groups, a database of gynecologic oncologists searchable by state, and educational materials. A limited selection of Spanish-language publications is available.

National Patient Travel Center (NPTC)

Suite One
4620 Haygood Road
Virginia Beach, VA 23455
1–800–296–1217
mercymedical@erols.com
www.patienttravel.org
The NPTC provides the National Patient Travel Helpline, a telephone service which facilitates patient access to charitable medical air transportation resources in the United States. The NPTC also offers information about discounted airline ticket programs for patients and patient escorts, operates Special-Lift and Child-Lift programs, and brings ambulatory outpatients to the United States from many overseas locations.

The Oral Cancer Foundation

Number 205
3419 Via Lido
Newport Beach, CA 92663
949–646–8000
info@oralcancerfoundation.org
www.oralcancerfoundation.org
The Oral Cancer Foundation is a nonprofit organization that is dedicated to saving lives through education, research, prevention, advocacy, and support for persons with oral cancer. The Foundation provides an online Oral Cancer Forum, which includes a message board and chat room that connect newly diagnosed patients, family members, and the public.

Ovarian Cancer National Alliance (OCNA)

Suite 413
910 17th Street, NW.
Washington, DC 20006 
202–331–1332
ocna@ovariancancer.org
www.ovariancancer.org
The Alliance works to increase public and professional understanding of ovarian cancer and to advocate for research to determine more effective ways to diagnose, treat, and cure this disease. The Alliance distributes informational materials; sponsors an annual advocacy conference for survivors and families; advocates on the issues of cancer to the ovarian cancer community; and works with women’s groups, seniors, and health professionals to increase awareness of ovarian cancer.

Pancreatic Cancer Action Network (PanCAN)

Suite 131
2221 Rosecrans Avenue
El Segundo, CA 90245 
310–725–0025
1–877–272–6226 (1–877–2–PANCAN) 
information@pancan.org
www.pancan.org
PanCAN, a nonprofit advocacy organization, educates health professionals and the general public about pancreatic cancer to increase awareness of the disease. PanCAN also advocates for increased funding of pancreatic cancer research and promotes access to and awareness of the latest medical advances, support networks, clinical trials, and reimbursement for care.

Patient Advocate Foundation (PAF)

Suite B
753 Thimble Shoals Boulevard
Newport News, VA 23606
757–873–6668
1–800–532–5274
help@patientadvocate.org
www.patientadvocate.org
The PAF provides education, legal counseling, and referrals to cancer patients and survivors concerning managed care, insurance, financial issues, job discrimination, and debt crisis matters. The Patient Assistance Program is a subsidiary of the PAF. It provides financial assistance to patients who meet certain qualifications. The toll-free number is 1–866–512–3861.

The Patient Story

415-857-0931 
www.thepatientstory.com
Our mission with The Patient Story is to humanize cancer diagnoses for new patients and give them a sense of calm and control, through in-depth interviews, videos, and timelines from recent survivors. We've also been recommended as a resource by organizations like the Leukemia & Lymphoma Society.


Prostate Cancer Foundation

1250 Fourth Street
Santa Monica, CA 90401
310–570–4700
1–800–757–2873 (1–800–757–CURE) 
info@prostatecancerfoundation.org
www.prostatecancerfoundation.org
The Prostate Cancer Foundation is a nonprofit organization that provides funding for research projects to improve methods of diagnosing and treating prostate cancer. It also offers printed resources for prostate cancer survivors and their families. The mission of the Prostate Cancer Foundation is to find a cure for prostate cancer.

R. A. Bloch Cancer Foundation, Inc.

4400 Main Street
Kansas City, MO 64111 
816–932–8453 (816–WE–BUILD)
1–800–433–0464 
hotline@hrblock.com
www.blochcancer.org
The R. A. Bloch Cancer Foundation matches newly diagnosed cancer patients with trained, home-based volunteers who have been treated for the same type of cancer. They also distribute informational materials, including a multidisciplinary list of institutions that offer second opinions. Information is available in Spanish.

Sisters Network®, Inc.

Suite 4206
8787 Woodway Drive
Houston, TX 77063 
713–781–0255
1–866–781–1808
sisnet4@aol.com
www.sistersnetworkinc.org
Sisters Network seeks to increase local and national attention to the impact that breast cancer has in the African American community. All chapters are run by breast cancer survivors and receive volunteer assistance from community leaders and associate members. The services provided by Sisters Network include individual/group support, community education, advocacy, and research. The national headquarters serves as a resource and referral base for survivors, clinical trials, and private/government agencies. Teleconferences are held to update chapters with the latest information and share new ideas. An educational brochure designed for underserved women is available. In addition, a national African American breast cancer survivors newsletter is distributed to survivors, medical facilities, government agencies, organizations, and churches nationwide.

The Skin Cancer Foundation

Suite 1403
245 Fifth Avenue
New York, NY 10016
212–725–5176
1–800–754–6490 (1–800–SKIN–490)
info@skincancer.org
www.skincancer.org
Major goals of The Skin Cancer Foundation are to increase public awareness of the importance of taking protective measures against the damaging rays of the sun and to teach people how to recognize the early signs of skin cancer. They conduct public and medical education programs to help reduce skin cancer.

STARBRIGHT Foundation

Suite 500
11835 West Olympic Boulevard
Los Angeles, CA 90064 
310–479–1212
1–800–315–2580
ford@starbright.org
www.starlight.org
The STARBRIGHT Foundation creates projects that are designed to help seriously ill children and adolescents cope with the psychosocial and medical challenges they face. The STARBRIGHT Foundation produces materials such as interactive educational CD-ROMs and videos about medical conditions and procedures, advice on talking with a health professional, and other issues related to children and adolescents who have serious medical conditions. All materials are available to children, adolescents, and their families free of charge. Staff can respond to calls in Spanish.

Support for People with Oral and Head and Neck Cancer (SPOHNC)

Post Office Box 53
Locust Valley, NY 11560–0053 
1–800–377–0928
info@spohnc.org
www.spohnc.org
The SPOHNC is a self-help organization that serves oral and head and neck cancer patients, survivors, and their families. The organization offers support group meetings, information, newsletters, and teleconferences. The SPOHNC also offers a "Survivor to Survivor" network which pairs survivors or their family members with volunteers who have had a similar diagnosis and treatment program.

The Susan G. Komen Breast Cancer Foundation

Suite 250
5005 LBJ Freeway
Dallas, TX 75244
972–855–1600
1–800–462–9273 (1–800–I’M AWARE®)
helpline@komen.org
www.komen.org
The Susan G. Komen Breast Cancer Foundation’s mission is to eradicate breast cancer as a life-threatening disease by advancing research, education, screening, and treatment. This organization operates a national toll-free breast cancer helpline (1–800–I’M AWARE®) that is answered by trained volunteers whose lives have been personally touched by breast cancer. Breast health and breast cancer materials, including pamphlets, brochures, booklets, posters, videos, CD-ROMs, fact sheets, and community outreach materials are available. Staff can respond to calls in Spanish, and some publications are available in Spanish.

Thyroid Cancer Survivors’ Association, Inc. (ThyCa)

Post Office Box 1545
New York, NY 10159–1545
1–877–588–7904 
thyca@thyca.org
www.thyca.org
ThyCa offers a network of services to thyroid cancer survivors, caregivers, family members, and friends. These services include e-mail support groups, person-to-person support, local support groups, and a toll-free survivors’ telephone line. ThyCa also offers a low-iodine cookbook, newsletters, conferences, and workshops. The organization has volunteers who are fluent in Spanish.

United Ostomy Association, Inc.

Suite 200
19772 MacArthur Boulevard
Irvine, CA 92612–2405
949–660–8624
1–800–826–0826 (6:30 a.m.– 4:30 p.m., Pacific time)
uoa@deltanet.com
www.ostomy.org
The United Ostomy Association helps ostomy patients through mutual aid and emotional support. It provides information to patients and the public and sends volunteers to visit with new ostomy patients.

US® TOO! International, Inc.

5003 Fairview Avenue
Downers Grove, IL 60515
630–795–1002 (in the Chicago area)
1–800–808–7866 (1–800–80–US TOO)
ustoo@ustoo.com
www.ustoo.com
US TOO is a prostate cancer support group organization. Goals of US TOO are to increase awareness of prostate cancer in the community, educate men newly diagnosed with prostate cancer, offer support groups, and provide the latest information about treatment for this disease. A limited selection of Spanish-language publications is available.

Vital Options® International TeleSupport® Cancer Network

Suite 645
15821 Ventura Boulevard
Encino, CA 91436–2946 
818–788–5225
1–800–477–7666 (1–800–GRP–ROOM)
info@vitaloptions.org
www.vitaloptions.org
The mission of Vital Options is to use communications technology to reach people dealing with cancer. This organization holds a weekly syndicated call-in cancer radio talk show called "The Group Room®," which provides a forum for patients, long-term survivors, family members, physicians, and therapists to discuss cancer issues. Listeners can participate in the show during its broadcast every Sunday from 4 p.m. to 6 p.m. Eastern time by calling the toll-free telephone number. A live Web simulcast of "The Group Room" can be heard by logging onto the Vital Options Web site.

The Wellness Community

Suite 412
35 East Seventh Street
Cincinnati, OH 45202
513–421–7111
1–888–793–9355 (1–888–793–WELL) 
help@thewellnesscommunity.org
www.thewellnesscommunity.org
The Wellness Community provides free psychological and emotional support to cancer patients and their families. They offer support groups facilitated by licensed therapists, stress reduction and cancer education workshops, nutrition guidance, exercise sessions, and social events.

Y-ME National Breast Cancer Organization, Inc.

Suite 500
212 West Van Buren Street
Chicago, IL 60607 
312–986–8338
1–800–221–2141 (English)
1–800–986–9505 (Spanish) 
askyme@y-me.org (English); latino@y-me.org (Spanish)
www.networkofstrength.org
The Y-ME National Breast Cancer Organization provides information and support to anyone who has been touched by breast cancer. Y-ME serves women with breast cancer and their families through their national hotline (available 24 hours a day), open-door groups, early detection workshops, and support programs. Numerous local chapter offices are located throughout the United States. A section of the Y-ME Web site, a toll-free hotline, and publications are available in Spanish.