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Newly Diagnosed
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Newly DiagnosedPeople who have recently received a diagnosis of a blood cancer often have questions about the disease, the prognosis and the treatments available. This section of the Web site is arranged to provide information to answer some of these questions and assist patients in finding additional resources.

It is important to learn about the disease, but also to learn about your insurance coverage, healthcare facilities and how to obtain support for yourself and your family. Specific questions may also be answered by information specialists at The Leukemia & Lymphoma Society's  Information Resource Center. The center is open every business day, 9 a.m. to 6 p.m. ET, at (800) 955-4572.

The word "diagnosis" means to distinguish or identify a disease. Patients usually arrive at the doctor's office with a series of complaints or symptoms. Through questioning and examination the physician may also observe abnormal "signs," such as an enlarged spleen. The results of laboratory tests provide further information. The accumulated evidence leads the physician to a decision about the final diagnosis.

Patients who receive a diagnosis often wish to learn more about the disease and the tests used to determine the diagnosis. This section is here to assist.




Find Support - Need comfort and support? This section will help.

For Caregivers - When someone is diagnosed with a blood cancer it will dramatically affect the lives of families and all others who have a relationship with the patient

What to Ask - Taking an active role in choosing a healthcare provider and in making other treatment decisions can have a positive effect on your health and your quality of life. Here are some key questions related to treatment that patients and families will want to ask following diagnosis.

Choosing a Blood Cancer Specialist or Treatment Center - The physician that you choose to provide cancer treatment, and the center or clinic where you choose to get cancer care, are important. Information and resources are presented to help you make informed choices.

Communicating with A Blood Cancer Specialist - It is important to have good communication with your blood cancer specialist and your treatment team. Taking an active role in treatment decision-making can have a positive effect on your health and quality of life. Information is presented to help you communicate better with your doctor.

Stories of Hope/Mosaic - We at The Leukemia & Lymphoma Society want to share personal stories of courage and hope with you. By telling us your experiences, hopes and frustrations, you join a community of special people that understands the cancer journey and who, in turn, can reach out to you.

Blood Cancer Resource Directory - Follow the links to organizations that can help you cope with blood cancers

Calendar - Calendar of upcoming events

Education Programs - The Leukemia & Lymphoma Society offers patient and family education and information for individuals living with cancer



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last updated on 12/09/05

The Leukemia & Lymphoma Society® (LLS) is the world's largest voluntary health agency dedicated to blood cancer. The LLS mission: Cure leukemia, lymphoma, Hodgkin's disease and myeloma, and improve the quality of life of patients and their families. LLS funds lifesaving blood cancer research around the world and provides free information and support services.
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