Abstract: A computer-implemented method that includes receiving, by a computer system, current medical data from at least one electronic source; identifying, by the computer system, at least one medical-related filtering criterion related to an individual or a group of individuals; filtering, by the computer system, the current medical data based, at least in part, on at least one medical-related filtering criterion to identify current personalized medical data, where the current personalized medical data is related to the individual or the group of individuals; and presenting, by the computer system, the current personalized medical data to the individual or the group of individuals.

Abstract: A computer-implemented method that includes receiving, by a computer system, current medical data from at least one electronic source; identifying, by the computer system, at least one medical-related filtering criterion related to an individual or a group of individuals; filtering, by the computer system, the current medical data based, at least in part, on at least one medical-related filtering criterion to identify current personalized medical data, where the current personalized medical data is related to the individual or the group of individuals; and presenting, by the computer system, the current personalized medical data to the individual or the group of individuals.

Abstract: The present invention provides for a computer system that includes at least one server having software stored on a non-transient computer readable medium; where, upon execution of the software, the at least one server is at least configured to: i) receiving, in real-time, an input from a user; ii) receiving, in real-time, physiological data representative of a physiological measurement of physiological characteristic of the user; iii) comparing, in real-time, the physiological measurement of the user to a pre-determined physiological value associated with the physiological characteristic retrieved from a database; iv) based on the comparing, determining, in real-time, that a difference between the physiological measurement of the user and the pre-determined physiological value is higher or smaller than the predetermined threshold value, and then: v) generating, in real-time, at least one alert; vi) transmitting, in real-time, the at least one alert.

Abstract: In some embodiments, the instant invention provides for a computer-implemented method, including: providing, to a user, in real time, by at least one specialized computing device being specifically programmed with wellbeing management software, at least one personalized breathing instruction via a graphical user interface displayed on the at least one specialized computing device, receiving, in real time, by the at least one specialized programmed computing device, user sensor data from at least one heart rate sensor being associated with the user, determining, in real time, by the at least one specialized programmed computing device, user heart rate variability of the user (user HRV), based, at least in part, on the user sensor data, automatically calculating, by the at least one specialized programmed computing device, a parameter status percentage; providing, to the user, at least one personalized breathing recommendation being configured to modify the parameter status percentage.

Abstract: In some embodiments, the instant invention provides for a computer-implemented method, including: providing, to a user, in real time, by at least one specialized computing device being specifically programmed with wellbeing management software, at least one personalized breathing instruction via a graphical user interface displayed on the at least one specialized computing device, receiving, in real time, by the at least one specialized programmed computing device, user sensor data from at least one heart rate sensor being associated with the user, determining, in real time, by the at least one specialized programmed computing device, user heart rate variability of the user (user HRV), based, at least in part, on the user sensor data, automatically calculating, by the at least one specialized programmed computing device, a parameter status percentage; providing, to the user, at least one personalized breathing recommendation being configured to modify the parameter status percentage.

Abstract: The present invention provides for a computer system that includes at least one server having software stored on a non-transient computer readable medium; where, upon execution of the software, the at least one server is at least configured to: i) receiving, in real-time, an input from a user; ii) receiving, in real-time, physiological data representative of a physiological measurement of physiological characteristic of the user; iii) comparing, in real-time, the physiological measurement of the user to a pre-determined physiological value associated with the physiological characteristic retrieved from a database; iv) based on the comparing, determining, in real-time, that a difference between the physiological measurement of the user and the pre-determined physiological value is higher or smaller than the predetermined threshold value, and then: v) generating, in real-time, at least one alert; vi) transmitting, in real-time, the at least one alert.

Abstract: A system and method that includes receiving data from sensors such as electroencephalography, heart rate, accelerometer, blood oxygen saturation, pressure, temperature, and galvanic skin response sensors; determining user physiological information such as brain activity patterns during sleep, quantity of movement during sleep, breathing depth and rate, blood pressure, heart rate and stroke volume, heart rate variability, perspiration level and stress level based, at least in part, on sensor data; evaluating the physiological information to determine at least one of sleep quality, sleep apnea potential, quality of physical activity, and need for stress management for a user; and providing to user based, at least in part, on the evaluation, at least one recommendation such as timing, intensity, level, and type of physical activity to improve sleep quality, time and type of food consumption to improve sleep quality, relaxation techniques to reduce stress level, and nutritional supplements to improve sleep qualit

Abstract: A system and method that includes receiving data from sensors such as electroencephalography, heart rate, accelerometer, blood oxygen saturation, pressure, temperature, and galvanic skin response sensors; determining user physiological information such as brain activity patterns during sleep, quantity of movement during sleep, breathing depth and rate, blood pressure, heart rate and stroke volume, heart rate variability, perspiration level and stress level based, at least in part, on sensor data; evaluating the physiological information to determine at least one of sleep quality, sleep apnea potential, quality of physical activity, and need for stress management for a user; and providing to user based, at least in part, on the evaluation, at least one recommendation such as timing, intensity, level, and type of physical activity to improve sleep quality, time and type of food consumption to improve sleep quality, relaxation techniques to reduce stress level, and nutritional supplements to improve sleep qualit

Abstract: A computer-implemented method that includes receiving, by a computer system, current medical data from at least one electronic source; identifying, by the computer system, at least one medical-related filtering criterion related to an individual or a group of individuals; filtering, by the computer system, the current medical data based, at least in part, on at least one medical-related filtering criterion to identify current personalized medical data, where the current personalized medical data is related to the individual or the group of individuals; and presenting, by the computer system, the current personalized medical data to the individual or the group of individuals.

Abstract: The present invention provides for a computer system including at least one server having software stored on a non-transient computer readable medium; where, upon execution of the software, the at least one server is at least configured to: i) receiving physiological data representative of a first physiological measurement of at least one physiological characteristic of an epileptic user; ii) receiving physiological data representative of a second physiological measurement of at least one physiological characteristic of the epileptic user; iii) comparing the first physiological measurement of the epileptic user to the second physiological measurement of the epileptic user; iv) based on the comparing, determining that a difference between the first physiological measurement of the epileptic user and the second physiological measurement is: a) higher than a predetermined threshold value, or b) smaller than the predetermined threshold value; and v) generating at least one alert; vi) transmitting the at least one

Abstract: A computer-implemented method that includes receiving, by a computer system, current medical data from at least one electronic source; identifying, by the computer system, at least one medical-related filtering criterion related to an individual or a group of individuals; filtering, by the computer system, the current medical data based, at least in part, on at least one medical-related filtering criterion to identify current personalized medical data, where the current personalized medical data is related to the individual or the group of individuals; and presenting, by the computer system, the current personalized medical data to the individual or the group of individuals.

Abstract: In some embodiments, the instant invention provides for a computer-implemented method, including: providing, to a user, in real time, by at least one specialized computing device being specifically programmed with wellbeing management software, at least one personalized breathing instruction via a graphical user interface displayed on the at least one specialized computing device, receiving, in real time, by the at least one specialized programmed computing device, user sensor data from at least one heart rate sensor being associated with the user, determining, in real time, by the at least one specialized programmed computing device, user heart rate variability of the user (user HRV), based, at least in part, on the user sensor data, automatically calculating, by the at least one specialized programmed computing device, a parameter status percentage; providing, to the user, at least one personalized breathing recommendation being configured to modify the parameter status percentage.

Abstract: The present invention provides for a computer system including at least one server having software stored on a non-transient computer readable medium; where, upon execution of the software, the at least one server is at least configured to: i) receiving physiological data representative of a first physiological measurement of at least one physiological characteristic of an epileptic user; ii) receiving physiological data representative of a second physiological measurement of at least one physiological characteristic of the epileptic user; iii) comparing the first physiological measurement of the epileptic user to the second physiological measurement of the epileptic user; iv) based on the comparing, determining that a difference between the first physiological measurement of the epileptic user and the second physiological measurement is: a) higher than a predetermined threshold value, or b) smaller than the predetermined threshold value; and v) generating at least one alert; vi) transmitting the at least one

Abstract: The present invention provides for a computer system that includes at least one server having software stored on a non-transient computer readable medium; where, upon execution of the software, the at least one server is at least configured to: i) receiving, in real-time, an input from a user; ii) receiving, in real-time, physiological data representative of a physiological measurement of physiological characteristic of the user; iii) comparing, in real-time, the physiological measurement of the user to a pre-de-termined physiological value associated with the physiological characteristic retrieved from a database; iv) based on the comparing, determining, in real-time, that a difference between the physiological measurement of the user and the pre-determined physiological value is higher or smaller than the predetermined threshold value, and then: v) generating, in real-time, at least one alert; vi) transmitting, in real-time, the at least one alert.

Abstract: The invention is directed to a mobile hand held miniature laboratory system in general, and to fluid testing apparatus for performing a parameter measurement in a fluid sample and methods of use in particular. The apparatus comprising: a strip adapted to absorb a fluid sample and to produce a signal indicative of said parameter level in said sample; and adaptor adapted to connect said strip to a smart phone to allow delivery of the produced signal or a correlated signal to said smart phone for obtaining a measurement of said fluid parameter displayed on said smart phone, wherein said testing apparatus relies on said smart phone at least for power supply and display means. The fluid may be a physiological fluid such as blood, urine, saliva or amniotic fluid, or a non-physiological fluid such as fluid obtained from industrial pools for fish or algae growth, or entertainment swimming pools.

Abstract: A system for effecting ischemic necrosis in a foreskin of a penis includes an inner ring having an inner surface comprising an inner diameter and an outer surface comprising an outer diameter and at least one circumferential groove; and an outer ring configured to substantially fit around the circumferential groove of the inner ring, wherein the inner ring is configured to fit to a portion of a glans of the penis that lies between an inner surface of the foreskin and the glans of the penis and the at least one outer ring is configured to fit an outer surface of the foreskin, the inner ring and the outer ring thereby compressing the foreskin in the circumferential groove with a compression force, and wherein the compression force is sufficient to effect ischemic necrosis in the foreskin.

Abstract: A system for effecting ischemic necrosis in a foreskin of a penis includes an inner ring having an inner surface comprising an inner diameter and an outer surface comprising an outer diameter and at least one circumferential groove; and an outer ring configured to substantially fit around the circumferential groove of the inner ring, wherein the inner ring is configured to fit to a portion of a glans of the penis that lies between an inner surface of the foreskin and the glans of the penis and the at least one outer ring is configured to fit an outer surface of the foreskin, the inner ring and the outer ring thereby compressing the foreskin in the circumferential groove with a compression force, and wherein the compression force is sufficient to effect ischemic necrosis in the foreskin.

Abstract: The invention is directed to a mobile hand held miniature laboratory system in general, and to fluid testing apparatus for performing a parameter measurement in a fluid sample and methods of use in particular. The apparatus comprising: a strip adapted to absorb a fluid sample and to produce a signal indicative of the parameter level in the sample; and adaptor adapted to connect the strip to a smart phone to allow delivery of the produced signal or a correlated signal to the smart phone for obtaining a measurement of the fluid parameter displayed on the smart phone, wherein the testing apparatus relies on the smart phone at least for power supply and display device. The fluid may be a physiological fluid such as blood, urine, saliva or amniotic fluid, or a non-physiological fluid such as fluid obtained from industrial pools for fish or algae growth, or entertainment swimming pools.

Abstract: The present disclosure provides a support element (110) for use in effecting ischemic necrosis in a foreskin of a penis, being a closed-loop member defining an opening dimensioned to permit a penis glans to pass therethrough and having an inner surface and an outer surface; the outer surface comprising a circumferential support (118) for an elastic ring (150) to be mounted thereon, said circumferential support being formed within a groove (120) in at least part of the outer surface; at least one first segment of the outer surface having an outer curvature of a radius larger than that of its flanking second segments. Also provided herein is a system (100) for effecting ischemic necrosis in a foreskin of a penis, comprising the support element (110) and elastic ring (150), and optionally a deployment element (160) for mounting the elastic ring over the foreskin and support element.

Abstract: The invention is directed to a mobile hand held miniature laboratory system in general, and to fluid testing apparatus for performing a parameter measurement in a fluid sample and methods of use in particular. The apparatus comprising: a strip adapted to absorb a fluid sample and to produce a signal indicative of said parameter level in said sample; and adaptor adapted to connect said strip to a smart phone to allow delivery of the produced signal or a correlated signal to said smart phone for obtaining a measurement of said fluid parameter displayed on said smart phone, wherein said testing apparatus relies on said smart phone at least tor power supply and display means. The fluid may be a physiological fluid such as blood, urine, saliva or amniotic fluid, or a non-physiological fluid such as fluid obtained from industrial pools for fish or algae growth, or entertainment swimming pools.