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This form allows individuals registered with the NDSS to apply for an extension of access to continuous glucose monitoring (CGM) and flash glucose monitoring (Flash GM) products through the NDSS scheme, specifically for those with type 1 diabetes who are planning pregnancy.

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What is continuous and flash glucose?

Continuous glucose monitoring (CGM) involves a small sensor placed under the skin that measures glucose levels in real-time, while flash glucose monitoring allows users to scan a sensor worn on the body to get glucose readings.

Who is required to file continuous and flash glucose?

Individuals with diabetes who use continuous or flash glucose monitors to manage their blood sugar levels may be required to file this information for insurance purposes or medical records.

How to fill out continuous and flash glucose?

To fill out continuous and flash glucose forms, users typically need to provide their glucose levels data from the monitoring device, along with personal information and usage details.

What is the purpose of continuous and flash glucose?

The purpose of continuous and flash glucose monitoring is to provide real-time insights into glucose levels, allowing for better management of diabetes and reducing the risk of hypoglycemia or hyperglycemia.

What information must be reported on continuous and flash glucose?

Users must report their glucose readings, sensor calibration dates, time spent within target glucose range, and any significant events affecting glucose levels.

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