An aural water removal suction apparatus for removing water from within ears includes a mouthpiece that has a principal opening extending into a mouth portion and a stem aperture extending from the principal opening through a stem portion. A tubing is coupled to the mouthpiece. A pair of ear tubes comprising a right ear tube and a left ear tube is coupled to the tubing. A pair of ear buds that is configured to be inserted into a user's ears is coupled to the pair of ear tubes. The canal aperture of each of the pair of ear buds, the pair of ear tubes, the tubing, and the stem aperture of the mouthpiece are all in fluid communication. The user creates suction through the canal aperture of the pair of ear buds with her mouth on the principal opening of the mouthpiece to draw water from her ears.

A droplet delivery device with a small volume drug ampoule and related methods for delivering precise and repeatable dosages to a subject for pulmonary use is disclosed. The droplet delivery device is configured to facilitate the ejection of small, e.g., single use, volumes of a therapeutic agent. The droplet delivery device includes a housing, a mouthpiece, a small volume drug ampoule, an ejector mechanism, and at least one differential pressure sensor. The delivery device is automatically breath actuated by the user when the differential pressure sensor senses a predetermined pressure change within housing. The droplet delivery device is then actuated to generate a plume of droplets having an average ejected particle diameter within the respirable size range, e.g, less than about 5-6 m, so as to target the pulmonary system of the user. The small volume drug ampoule may include a reservoir which comprises an internal flexible membrane separating two internal volumes, a first background pressure fluid volume and a second drug volume.

A pulmonary drug delivery system is disclosed, including a breath-powered, dry powder inhaler, with or without a cartridge for delivering a dry powder formulation. The inhaler and cartridge can be provided with a drug delivery formulation comprising, for example, a diketopiperazine and an active ingredient, including, small organic molecules, peptides and proteins, including, hormones such as insulin and glucagon-like peptide 1 for the treatment of disease and disorders, for example, diseases and disorders, including endocrine disease such as diabetes and/or obesity.

A device, a system and a method are provided to accurately apply a medically beneficial substance directly to a laterally or superiorly located paranasal sinus cavity. When the device is assembled with a solution in a reservoir, and inverted such that the reservoir is above an input apparatus and a housing, weight of the solution pushes down on a diaphragm creating a negative pressure on the diaphragm, which prevents air from entering the reservoir and prevents a liquid from flowing out of the reservoir. Applying a positive pressure to a bottom of the diaphragm causes the diaphragm to open and allows air to flow into the reservoir. When a user creates the positive pressure by exhaling air into the device the act of exhaling causes the user's choana to close. Thereby any solution introduced into the user's sino-nasal cavity will remain contained within the user's sino-nasal cavity increasing effectiveness of treatment and decreasing user discomfort including gagging, choking, and inner ear disturbance. When the positive pressure on the bottom of the diaphragm is removed, the flow of the liquid from the reservoir stops.

The hiccup relieving apparatus includes a body with a first end having a mouthpiece, a second end having a restriction in the body between the first end and the second end. The restriction makes it difficult to draw fluid through the body to the user's mouth. The fluid can be air or the body can be immersed in water or other potable liquid in a container. The restriction requires an adult user, using the mouthpiece, to produce a threshold suction of for example water before water can flow from the water in the water container, through the body, through the mouthpiece, and to the user.

A device, a system and a method are provided to accurately apply a medically beneficial substance directly to a laterally or superiorly located paranasal sinus cavity. When the device is assembled with a solution in a reservoir, and inverted such that the reservoir is above an input apparatus and a housing, weight of the solution pushes down on a diaphragm creating a negative pressure on the diaphragm, which prevents air from entering the reservoir and prevents a liquid from flowing out of the reservoir. Applying a positive pressure to a bottom of the diaphragm causes the diaphragm to open and allows air to flow into the reservoir. When a user creates the positive pressure by exhaling air into the device the act of exhaling causes the user's choana to close. Thereby any solution introduced into the user's sino-nasal cavity will remain contained within the user's sino-nasal cavity increasing effectiveness of treatment and decreasing user discomfort including gagging, choking, and inner ear disturbance. When the positive pressure on the bottom of the diaphragm is removed, the flow of the liquid from the reservoir stops.

A device, a system and a method are provided to accurately apply a medically beneficial substance directly to a laterally or superiorly located paranasal sinus cavity. When the device is assembled with a solution in a reservoir, and inverted such that the reservoir is above an input apparatus and a housing, weight of the solution pushes down on a diaphragm creating a negative pressure on the diaphragm, which prevents air from entering the reservoir and prevents a liquid from flowing out of the reservoir. Applying a positive pressure to a bottom of the diaphragm causes the diaphragm to open and allows air to flow into the reservoir. When a user creates the positive pressure by exhaling air into the device the act of exhaling causes the user's choana to close. Thereby any solution introduced into the user's sino-nasal cavity will remain contained within the user's sino-nasal cavity increasing effectiveness of treatment and decreasing user discomfort including gagging, choking, and inner ear disturbance. When the positive pressure on the bottom of the diaphragm is removed, the flow of the liquid from the reservoir stops.

A device that reduces human energy loss in the breathing process, without requiring external energy such as electricity. The device transfers motion, elastic or heat energy by conveying air volume and pressure between the exhaling and inhaling phases in the breathing process in order to adjust the air pressure or temperature in these phases so as to improve air perfusion or the body's thermal homeostatic conditions as required, in addition to reducing the air resistance in masks or respirators used for protection against contaminants. The invention pertains to the field of healthcare. The invention comprises inhalation and exhalation chambers that are associated with air pumps, besides having elastic energy accumulation walls to minimize air flow resistance.

A supplemental nutrition apparatus is disclosed herein. The supplemental nutrition apparatus may comprise a reservoir coupled to and in fluid communication with a fluid passageway, wherein the fluid passageway is configured to communicate fluid from the reservoir to a fluid passageway outlet, and a support element configured to engage a user, to at least partially support the fluid passageway, and to position the fluid passageway outlet proximate to the user's nipple.

Devices and methods are described that aid in harmonizing a person with their bodies and/or their environment.