Systems and methods are provided for treating cervical and/or uterine cancers in brachytherapy with an intracavitary brachytherapy applicator. The system comprises a tandem adapted for insertion into a cervix of a patient. An ovoid assembly comprises first and second inflatable ovoids and an ovoid support mechanism. The first and second inflatable ovoids are adapted for insertion within fornices of a patient. First and second retractors are adapted to be coupled to the ovoid assembly. The first retractor is adapted to be positioned to retract the bladder of a patient during treatment. The second retractor is adapted to be positioned to retract the rectum of a patient during treatment. The tandem and the first and second inflatable ovoids are adapted to be coupled to a radioactive source to deliver an implant radiation dose suitable for cancer treatment at a cancerous cervical treatment site in a patient.

The present disclosure provides systems, methods and apparatuses for inducing a desired biological response in an organism through the use of one or more repetitive signals from one or a series of LED lights designed to emit the signal with multiple pulsed components. Each component of the signal contains a one or more light color spectrum or wavelength that is within 50 nm of the peak absorption of a photon receptor of the organism corresponding to the desired biological response. Each component has a repetitive ON duration with an OFF duration and an intensity where the relationship between the ON duration and OFF duration of the first component and the second component induces the desired response in the organism through the stimulation or excitation of a molecule associated with a photoreceptor and the reset of the molecule.

Methods, systems, and devices for illness detection are described. A method may include identifying a menstrual cycle model associated with a menstrual cycle for a user, and receiving physiological data for the user collected throughout a first time interval and a second time interval by a wearable device. The method may include inputting the physiological data and the menstrual cycle model into a classifier, and identifying a satisfaction of deviation criteria between first and second subsets of the physiological data collected throughout the first and second time intervals, respectively, based on the menstrual cycle model. The method may include causing a graphical user interface (GUI) of a user device to display an illness risk metric associated with the user based on the satisfaction of the deviation criteria, the illness risk metric associated with a relative probability that the user will transition from a healthy state to an unhealthy state.

Samples, systems for collecting samples, and methods of preserving samples from menstrual fluid are provided.

A mechanism for estimating windows for menstrual cycles and fertility. The mechanism tracks menstrual cycles based on accuracy of predictions as compared to user input logging the start and stop of a cycle; this user input and the accuracy of prior cycle predictions is used to improve and update future predictions. Thus, as the mechanism receives additional data, it refines its predicted fertility window and period. A user's heart rate may be used to estimate fertility windows, periods, and other portions of a menstrual cycle.

An electronic system for non-invasive monitoring of estrogen of a female human comprises a wearable device (1) and a processor (13, 30, 40). The wearable device (1) includes a first sensor system (101) configured to be worn in contact with the skin of the female human and to determine a level of perfusion of the female human. The processor (13, 30, 40) is configured to receive and store the level of perfusion of the female human from the first sensor system (101) for a respective point in time. The processor (13, 30, 40) is further configured to determine a change in the level of perfusion of the female human, using the levels of perfusion of the female human stored for a plurality of respective points in time. Furthermore, the processor (13, 30, 40) is configured to detect a change in estrogen level of the female human based on the change in the level of perfusion of the female human.

Embodiments of the present disclosure provide systems, apparatuses and methods for synchronous communication and control of LED lights and sensors in an LED light array containing two or more LED lights. Through the use of a master clock within a gateway and/or a master controller that is in communication with LED lights in an array that is in a facility, such as in a greenhouse, hot house, poultry egg production facility, a hospital, dairy production or other lighting facilities, the gateway and/or master controller is capable of synchronizing the emission of light or photons from an LED light array by generating a master signal that contains commands and time from a master clock within the signal that is transmitted to each of the LED lights within an array.

An electronic system for non-invasive monitoring of estrogen of a female human comprises a wearable device and a processor. The wearable device includes a first sensor system configured to be worn in contact with the skin of the female human and to determine a level of perfusion of the female human. The processor is configured to receive and store the level of perfusion of the female human from the first sensor system for a respective point in time. The processor is further configured to determine a change in the level of perfusion of the female human, using the levels of perfusion of the female human stored for a plurality of respective points in time. Furthermore, the processor is configured to detect a change in estrogen level of the female human based on the change in the level of perfusion of the female human.

Provided are a medical diagnosis apparatus and a medical diagnosis method using the same. According to an embodiment, the medical diagnosis apparatus may include: a main body; a chair unit movably supported by the main body and on which an object is positioned; a diagnosis part that is movably connected to the main body and is spaced apart from the chair unit by a preset first distance in one plane; a controller configured to generate a control signal for moving the diagnosis part according to preset information; and a first driving device configured to generate a driving force for moving the diagnosis part according to the control signal.

According to certain embodiments, an electronic device comprises: a sensor module; a processor operatively connected to the sensor module; and a memory operatively connected to the processor, wherein the memory stores instructions that, when executed, cause the processor to perform a plurality of operations comprising: acquiring sensor information through the sensor module, determining sleep information of a user, based on the sensor information, and determining a biorhythm of the user, based on the sleep information.