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This document serves as a resource guide highlighting major sources of routine follow-up data available for population-based cancer registries, focusing on large-scale record linkage and passive forms
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How to fill out Follow-up resource guide

01
Obtain a copy of the Follow-up resource guide.
02
Read the introduction to understand the purpose of the guide.
03
Identify the section relevant to your needs.
04
Fill out personal information, if required, including name and contact details.
05
Follow the prompts in the guide step by step, providing necessary information.
06
Review your entries to ensure all information is accurate.
07
Submit the completed guide to the designated contact or organization.

Who needs Follow-up resource guide?

01
Individuals seeking support after receiving medical treatment.
02
Patients who require additional resources for recovery.
03
Caregivers looking for guidance on how to assist others.
04
Healthcare providers needing a structured approach to follow-up care.
05
Organizations offering support services for continuous care.
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Survivors of childhood cancers have a higher risk of depression and other mental health problems later in life. It's important to make sure kids have the support they need. They often struggle with these problems alone, too afraid to talk to someone about them.
Among the hypothetical cohort of 5-year survivors of childhood cancer representative of the Childhood Cancer Survivor Study participants (44% female and 56% male; mean [SD] age at diagnosis, 7.3 [5.6] years), conditional life expectancy was 48.5 years (95% uncertainty interval [UI], 47.6-49.6 years) for 5-year
A follow-up care plan is a summary of your treatment, along with recommendations for your cancer care after treatment ends. Your plan may also include suggestions to help meet other needs, such as emotional, social, or financial issues.
During follow-up visits During a follow-up visit, the doctor usually asks questions about the side effects of treatment and how the child is coping. The doctor may do a physical exam, including: feeling the abdomen to check for a larger than normal liver or spleen. checking the lymph nodes for swelling.
A survivorship care plan (also called a follow-up care plan) is developed for each child. Survivorship care plans are based on the type of cancer and treatment your child received. For example, some children may need to return for visits each month for the first year after they have completed treatment.

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The Follow-up resource guide is a document designed to provide structured information and resources for follow-up actions regarding a specific process or event.
Individuals or organizations involved in a process that requires monitoring or reporting must file the Follow-up resource guide.
To fill out the Follow-up resource guide, users should provide all required information accurately, follow the provided instructions, and ensure all relevant data is included.
The purpose of the Follow-up resource guide is to track progress, ensure accountability, and provide necessary information for decision-making and future actions.
The information that must be reported includes the details of the event, actions taken, follow-up measures, responsible individuals, and any relevant deadlines.
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