Abstract: A stent includes a first tubular unit that has a cylindrical tubular shape and a mesh circumferential surface; and a second tubular unit that has a cylindrical tubular shape and a mesh circumferential surface, and is connected to the first tubular unit in a longitudinal axis direction of the stent. The first tubular unit has a first-first direction bent portion which is bent to be convex toward the first direction side that is one side of the longitudinal axis direction, the second tubular unit has a second-second direction bent portion which is bent to be convex toward the second direction side that is the other side of the longitudinal axis direction, and the first-first direction bent portion and the second-second direction bent portion form a first connecting portion that is connected so as to be relatively movable.

Abstract: Apparatus and method for delivering and deploying an intravascular device into the vessel including an outer and inner tube that are axially linked by a housing structure at the proximal end of the catheter, and a retractable sleeve structure having a middle tube and sleeve tip. The sleeve tip is sealed to the inner tube at the distal end, and continuously extends into the middle tube. At the proximal end of the sleeve structure, the middle tube is sealed to either a housing structure or slideable proximal ring, forming a sealed chamber between the inner tube and the sleeve structure. A radial space is formed between the sleeve tip and the inner tube optimized for intravascular device placement. During retraction of the sleeve structure, the fold of the sleeve tip peels away from the device, which expands to its deployed state while minimizing axial forces and friction.

Abstract: A flexible compressive orthopedic knee sleeve of stretchable fabric having an exterior surface webbing material at least partially covering the sleeve to provide targeted compressive force similar to athletic taping and to also provide kinetic retention.

Abstract: A sleeve has a tubular body formed from an elasticized textile and has first and second ends. The first end defines a locking cuff having a tacky band extending about an exterior surface of the sleeve; a non-tacky band located adjacent to and extending distally from the tacky band; and a receiving band located adjacent to and extending distally from the non-tacky band. The textile body further defines a central portion adjacent to and extending distally from the receiving band to the second end. The central portion includes an anatomical band arranged to contour to the anatomy of a user having at least one different elastic property different from an elastic property of the central portion outside of the anatomical band.

Abstract: Ankle foot orthoses and methods of manufacturing an ankle foot orthosis. In one embodiment, an ankle foot orthosis is disclosed that includes a foot plate constructed to have both a trimmable portion and a non-trimmable portion. The ankle foot orthosis includes a spiral strut coupled with either the hindfoot region of the foot plate laterally of a mid-line for the foot plate or the midfoot region of the foot plate laterally of the mid-line. The spiral strut includes a transition portion that spirals by approximately sixty-five degrees (65°) over less than one-hundred sixty millimeters (160 mm) in height from the bottom surface of the foot plate. The spiral strut also includes an adjustable portion that enables a cuff coupled thereto to be height adjustable. Methods of manufacturing the aforementioned ankle foot orthoses are also disclosed.

Abstract: An appendage pressurization device includes an appendage strap and one or more artificial muscles communicatively coupled to a controller. Each artificial muscle includes a housing having an electrode region, an expandable fluid region, a dielectric fluid housed within the housing, and an electrode pair positioned in the electrode region of the housing. The electrode pair includes a first electrode fixed to a first surface of the housing and a second electrode fixed to a second surface of the housing, wherein the electrode pair is actuatable between a non-actuated state and an actuated state. Actuation from the non-actuated state to the actuated state directs the dielectric fluid into the expandable fluid region. A pressure sensor is communicatively coupled to the controller, wherein the pressure sensor outputs a current pressure value to the controller and actuation of the electrode pair is based on the current pressure value.

Abstract: An improved orthopedic casting slipper kit for custom molding of a foot casting, wherein the kit includes a low-cut casting slipper shaped to extend upwardly on a patient's foot from a plantar surface of the foot to an open end. and a quantity of curable resin for impregnation into the fabric of the casting slipper, the improvement comprising a sheer removal sock which is first placed on the patient's foot, prior to the casting slipper to facilitate removal of the hardened mold.

Abstract: A monitor device for an ostomy system comprising an ostomy appliance with a base plate and a method of monitoring an ostomy appliance is disclosed.

Abstract: The present invention relates to an inserter for an intrauterine system comprising a handle (3), and an insertion tube (6) having a first end and a second end, and being arranged in connection with the handle. The inserter is characterized in that the first end of the insertion tube (6) comprises at least one frame slot for receiving a frame of the intrauterine system. The invention also relates to a kit comprising an inserter according to the present invention and an intrauterine system, wherein the intrauterine system (1) comprises a therapeutic component (1b) and a continuous, closed frame (1a), the therapeutic component (1b) being connected to the frame (1a) at least one point, and therapeutic component (1b) of the intrauterine system (1) is at least mainly arranged inside the first end of the insertion tube (6) and the frame (1a) of the intrauterine system (1) is at least mainly arranged outside the first end of the insertion tube (6).

Abstract: Continuous core body temperature measurements are made during hypothermic operations, where the core body temperature of the patient is lowered to reduce swelling. Caregivers monitor the patient's core body temperature to prevent damage that can occur to the patient if the patient's core body temperature becomes too low. To accurately determine the core body temperature of the patient, a temperature monitoring system measures the temperature at or near the surface of the patient and through at least a portion of a thermal block at multiple locations.

Abstract: A micro drop adapter that is adapted to engage with dropper bottles. The micro drop adapter engages with and surrounds the original tip of the bottle. The micro drop adapter comprises at least one inner tube that is urged against the original tip of the bottle forming a seal and a channel in fluid connection with the bottle. The micro drop adapter comprises an adapter tip that dispenses micro drops, which are drops having a volume of less than approximately 50 microliters. The micro drop adapter further comprises a cap.

Abstract: Described here are systems and methods for accessing Schlemm's canal and for delivering an ocular device, tool, or fluid composition therein. The ocular devices may maintain the patency of Schlemm's canal without substantially interfering with transmural fluid flow across the canal. The fluid composition may be a viscoelastic fluid that is delivered into the canal to facilitate drainage of aqueous humor by disrupting the canal and surrounding trabeculocanalicular tissues. Some systems described here may be configured to cut or tear the trabecular meshwork with the body of an elongate member located within Schlemm's canal. Other tools for disrupting these tissues and minimally invasive methods for treating medical conditions associated with elevated intraocular pressure, including glaucoma, are also described.

Abstract: A phacoemulsification surgical console, and a related system and method. The console, system and method may include a cassette receiver suitable for receiving a surgical cassette, a controller suitable for controlling provided aspects of the phacoemulsification; and a pre-alignment feature along a lower portion under and proximate to the cassette receiver, extending outwardly from the lower portion, and suitable for aligning the surgical cassette to the cassette receiver. The pre-alignment feature may comprise a shelf.

Abstract: An implantable amina cribrosa crossing pressure balance maintainer for constantly balancing the lamina cribrosa crossing pressure difference, an implantation device, and a method for balancing the lamina cribrosa crossing pressure difference. The lamina cribrosa crossing pressure balance maintainer is placed at the lamina cribrosa to balance the lamina cribrosa crossing pressure difference so as to enable the deformed lamina cribrosa to recover or even reverse deformation, so that the tolerance of glaucoma patients to intraocular hypertension is improved, nerve damage caused by the lamina cribrosa crossing pressure difference is relieved and reduced, and primary factors of the glaucoma optic nerve damage are eliminated. New ideas are provided for the treatment of the glaucoma in the middle and advanced periods.

Abstract: An ophthalmic surgery laser system and method of laser delivery for an ophthalmic surgery laser system are disclosed herein. Embodiments of the system and method are directed to an ophthalmic surgery laser system including a laser engine, a laser guide, and a laser shaper. Embodiments of the system and method are directed to a laser delivery system for an ophthalmic surgery laser system. Embodiments of the system and method are directed to an ophthalmic surgery laser system including additional functionality such as laser scanning confocal microscopy, 3D laser scanning, and laser beam diagnostics. Embodiments further include the use of a lower power illumination source.

Abstract: Methods and apparatus are configures to measure an eye without contacting the eye with a patient interface, and these measurements are used to determine alignment and placement of the incisions when the patient interface contacts the eye. The pre-contact locations of one or more structures of the eye can be used to determine corresponding post-contact locations of the one or more optical structures of the eye when the patient interface has contacted the eye, such that the laser incisions are placed at locations that promote normal vision of the eye. The incisions are positioned in relation to the pre-contact optical structures of the eye, such as an astigmatic treatment axis, nodal points of the eye, and visual axis of the eye.

Abstract: A magnetic positioning system and related method for automated or assisted eye-docking in ophthalmic surgery. The system includes a magnetic field sensing system on a laser head and a magnet on a patient interface to be mounted on the patient's eye. The magnetic field sensing system includes four magnetic field sensors located on a horizontal plane for detecting the magnetic field of the magnet, where one pair of sensors are located along the X direction at equal distances from the optical axis of the laser head and another pair are located along the Y direction at equal distances from the optical axis. Based on relative magnitudes of the magnetic field detected by each pair of sensors, the magnetic field sensing system determines whether the patient interface is centered on the optical axis. The system controls the laser head to move toward the patient interface until the latter is centered on the optical axis.

Abstract: Disclosed herein are modules for performing hyperbaric oxygen therapy (“HBOT”) on a patient submerged in pressurized water where substantially no gas is present in the module. The modules generally have an entry, a fluid inlet for introducing water into the module, first and second fluid outlets positioned substantially at a base and a top of the module respectively, and a utilities inlet and outlet in part for transferring breathing air to and from the patient. The module permits HBOT treatment on a patient submerged in water with no air in the module, thus reducing the risk of fire or explosion. Methods and systems are also contemplated. Disclosed herein are methods of filling a module with water until there is substantially no gas in the module, and providing the patient in the module with treatment air during HBOT treatment.

Abstract: An aerodynamic rail cover for an operating room with laminar airflow is provided. The rail cover comprises a rail cover component configured to be movably attached to a support rail of a ceiling mounted support arrangement of a medical imaging system. The rail cover component comprises a base element and an air guiding surface element connected to the base element. The base element is configured to be attached to a portion of the support rail of the ceiling mounted support arrangement. The air guiding surface element forms an air guide to be mounted at least temporarily to cover a portion of the support rail of the ceiling mounted support arrangement. The air guiding surface element comprises two surface parts that extend from starting edges on opposite sides of the base element to a common trailing edge.

Abstract: A medical chair with height adjustable armrest comprises a lifting mechanism, a base coupled to a bottom side of the lifting mechanism, a sitting part coupled to an upper side of the lifting mechanism, and a backrest part coupled rotatably to the upper side of the lifting mechanism. An armrest comprises an armrest stop with the armrest rotatably coupled to the backrest part adjustable to an upper position and a bottom position, where, in the bottom position, the armrest stop bears on the first stop coupled to the backrest part, and in the upper position, the armrest stop does not bear on the first stop.

Abstract: The embodiments described and claimed herein include an automated securement system that lock a wheeled mobility device into a designated station aboard an autonomous public transit vehicle, thus preventing unintended movement that is discomforting and potentially dangerous for both the WMD user and other passengers. The automated securement system includes features that integrate with typical autonomous public transit vehicles to minimize obstruction during stowage while maximizing effectiveness during deployment.

Abstract: A stair lift, including: a carrier portion, configured for carrying a person or an object; a lift portion, configured for moving relative to the carrier portion; and a driver mechanism, configured for inducing the relative movement. The carrier portion and the lift portion are connected and supported via a guide mechanism, and are configured for freely translating along an X-Z plane relative to each other. The driver mechanism includes a circulation moving mechanism, and the circulation moving mechanism includes a driving pin (moving member), configured for moving along a predetermined closed track under the driving of a single gear motor. The driving pin (moving member) is connected to the lift portion, such that the carrier portion and the lift portion are configured for moving relative to each other along the track, whereby enabling the stair lift to go upstairs or downstairs.

Abstract: A user module for a patient support apparatus is provided. The user module has a user interface operably coupled thereto. The user interface includes an input device and an output device. The output device includes a visual display including textual and non-textual elements. The non-textual elements include enhanced, graphical, and animated portions relating to one or more operational features of the patient support or to a person positionable on the patient support. The input device includes one or more touch sensors corresponding to defined regions of the visual display.

Abstract: Disclosed herein is a patient lift system. The patient lift system includes a housing enclosing a frame, a geared spool mounted within the frame, a strap, a first carry bar and a second carry bar. The first carry bar attaches to the frame and extends external to the housing. The first carry bar encloses an electric motor having a drive shaft. The drive shaft is associated with a gear arranged to cooperate with the geared spool to, responsive to activation of the motor, turn the geared spool, thereby altering an amount of strap on the geared spool, thereby altering a distance between the housing and the connector. The second carry bar attaches to the frame and extends external to the housing. The second carry bar encloses a battery to provide electrical power to the electric motor.

Abstract: A device (1) that supports the mobility of a person with restricted mobility comprises a trolley (3) and a mast (4) attached to the trolley (3). The mast (4) comprises a backrest (6) and armrests (5) for receiving the person.

Abstract: A movement system for use with an overhead patient lift system includes a motor. A drum is operatively coupled to the motor. The drum is configured to be selectively driven by the motor to rotate in one of a clockwise direction and a counter-clockwise direction. A lifting strap is coupled to the drum. The lifting strap is extendable and retractable with respect to a carriage of the overhead patient lifting system as the drum rotates. A manual release operatively coupled to the drum is actuatable to selectively disengage the drum from the motor to allow the lifting strap to be manually extended. Also disclosed is an overhead patient lift system including the movement system and a method for manually extending a lifting strap of an overhead patient lift system.

Abstract: Provided is a main unit of a nursing machine, including a sewage bucket accommodating sewage, a water blocking device, a first water tank, a second water tank, a water pump, a first waterway, a second waterway, and a third waterway. The water blocking device includes a labyrinth-type channel communicating with a water storage cavity and a float accommodation cavity, and multiple division boards extending up and down to perform separation to form the labyrinth-type channel. The labyrinth-type channel is located between the water storage cavity and the float accommodation cavity, and communicates between the water storage cavity and the float accommodation cavity. The second water tank is provided with a first water inlet and a first water outlet. The water pump joins the third waterway.

Abstract: A method for performing lower limb rehabilitation training comprises the steps of: (a) placing a training object's feet on a pedal in a limb rehabilitation training system, wherein the pedal comprises a pressure sensor and a location information sensor; (b) standing stably on the pedal to enable the pressure sensor on the pedal to record the body weight of the training object; and (c) sitting down on the saddle, thereby enabling: the pressure sensor on the pedal to monitor pressure variation between the training object and the pedal throughout the training of the training object, wherein the rehabilitation evaluating unit evaluates the physical status and rehabilitation status of the training object according to the physiological information and exercise information of the same collected by the sensing unit, and adjusts the exercise frequency and the exercise duration of the training object according to the physical status.

Abstract: The present invention comprises a device for supporting at least one arm of a user, wherein the device has at least one main body (2) for arranging on a torso (4) of the user and at least one supporting device (8) for supporting the arm, wherein the supporting device (8) is arranged on the main body (2) via at least one joint (10) so that it can be moved relative to the main body (2), wherein, in every position within a predetermined position range of the supporting system (8) relative to the main body (2), the joint (10) allows a movement of the supporting system (8) relative to the main body (2) in a first direction and prevents a movement in an opposite second direction.

Abstract: A rotational joint of intra-extra rotation for assistance of the movement of intra-extra rotation of a shoulder of a user. The rotational joint features a first circular guide arranged to rotate about a first rotation axis and a second circular guide arranged to rotate about a second rotation axis that is parallel to the first rotation axis. A support element is arranged to support the first and the second circular guides. The first and the second circular guide are pivotally connected by a conical wheel having a third rotation axis perpendicular to the first rotation axes and said conical wheel being pivotally constrained to the support element.

Abstract: A mounted massage roller comprising in one example: a mounting assembly configured to be mounted to a fixed structure; a pivot assembly attached to the mounting assembly at a hinge forming a horizontal hinge axis about which the hinge rotates; the pivot assembly rotatable about the hinge axis relative to the mounting assembly; the pivot assembly comprising at least one handle configured to be grasped by a patient to rotate the pivot assembly about the hinge; the pivot assembly at least one roller configured to roll about a roller axis parallel to the hinge axis; each roller having a radially outward surface configured to roll against the patient as the patient moves the pivot assembly about the hinge axis.

Abstract: Provided is a device useful for facial beauty treatment by efficiently releasing ligaments, SMAS fascia, and the like, and having a compact structure with multiple functions and an ease for a user to use at home. The present invention provides a device (1) that has a massage function by rolling of a roller (3), a suction function by a suction portion (4), and a stimulation function by outputting a stimulation signal by a conductive element (34) fixed to a bottom surface (23) or a roller (3), and can efficiently and reliably implement an effect such as releasing the ligaments such as a facial skin of a user. In addition, since a circumferential protrusion (61) is formed on the peripheral edge of an opening portion (24) for performing suction so as to surround the opening portion (24), it is possible to enhance confidentiality during suction by the suction portion (4), and the effect described above can be efficiently exhibited.

Abstract: A percussion paddle device for use in chest physical therapy-comprising a handle and cup positioned at one terminal end of the handle. The cup is made of a pliable plastic and has a cushion positioned long its exterior rim. In use, the percussion paddle is swung at a patient such that the cushion is flush with the patient creating seal. The resulting build up of pressure mimics the force of a cupped hand.

Abstract: A lower limb (1) of an ambulatory exoskeleton comprising at least a pelvis segment (10). a leg segment (20) and a foot segment (30), the leg segment (20) being hinged at the First end (21) of same to the pelvis segment (10) and at the second end (24) of same to the foot segment (30). the leg segment (20) comprising a spring element (25) and means (40. 44) for varying the distance (d) separating the ends (21. 24) of the leg segment (20), the means (40. 44) for varying the distance (d) separating the ends (21. 24) of the leg segment (20) being carried by the pelvis segment (10).

Abstract: A robotic system configured to, in response to a state transition intention input, change the robotic system from operating in a first mode with sensitivity to detecting state transitions at a first sensitivity level to operating temporarily in a second mode with sensitivity to detecting state transitions at a second sensitivity level that is more sensitive than the first sensitivity level. The state transition intention input indicates an intention to make a state transition from a first state to a second state, with the second state being possible from a plurality of possible different states.

Abstract: A crutch includes an arm rest having an elbow end and a front end, the front end defining a front face having a first opening formed therein, and a bottom edge forming a second opening. The crutch has a handle extending outwardly from the front end of the arm rest, but not from the first or second openings. A leg is received into one of the first and second openings in a first configuration, and into the other of the first and second openings in a second configuration. The leg is selectively convertible between the first and second configuration.

Abstract: A rollable user-support device comprising a rigid frame with first legs and second legs, each with a rollable and swivelable wheel, a seat with a seat folding mechanism and/or a seat manipulation mechanism. The seat manipulation mechanism can be operable to move the seat, with a user seated thereon, between a lower rearward seating position and an elevated forward seating position, and the seat folding mechanism can be operable to move the seat between the elevated forward seating position and a folded position, at least one of the devices being connected to a swivel prevention mechanism associated with the first wheels. The device can constitute a bi-directional rollable user-support device operable in three modes.

Abstract: A steam physiotherapy mechanism includes a receptacle having a chamber formed in a housing, a steam pipe disposed in the housing, a steam generating device connected to the steam pipe for generating and supplying a steam into the chamber of the housing, a number of tiles disposed in the housing, and a number of retainers engaged with the tiles for anchoring the tiles in the housing, the tiles each include a number of casings each having a compartment, and one or more of the compartments of the casings are filled with an ore mud. The tiles each include a number of passages formed in the casings and communicating with the compartments of the casings.

Abstract: Provided herein is a massage device having a sound output module. According to an embodiment of the present disclosure, there is provided a sound output module including a sound generating part configured to generate sound, a sound emitting member configured to emit transmitted sound to the outside, an actuator configured to provide a driving force to allow movement of the sound emitting member, and an external driven member configured to receive the driving force from the actuator and move linearly, wherein the sound emitting member is seated on the external driven member and allowed to protrude outward due to linear movement of the external driven member. There is also provided a massage device including the sound output module.

Abstract: A reservoir assembly is disclosed. The reservoir assembly includes a reservoir; a port connector comprising: an inlet extending from an interior volume of the reservoir; an outlet wherein fluid contained in the interior volume of the reservoir exits the reservoir; and a filling port configured wherein the reservoir may be filled with a fluid.

Abstract: A tamper evident seal structure for a vial septum or other cover having a housing including a sidewall terminating in oppositely disposed open and closed ends. A retainer is fixedly disposed within the housing and structured for retaining engagement with a portion of a vial, substantially adjacent the vial cover. The housing also includes a pressure member disposed within an interior thereof in attached, relation to the closed-end. The pressure member and the retainer are cooperatively disposed and structured to respectively exert pressure on the vial cover concurrent to retaining engagement with the vial. Tamper evident capabilities are at least partially defined by a detachment of a removable sidewall section from a remainder of said sidewall.

Abstract: A glass tube semi-finished product or a hollow glass product manufactured from the glass tube semi-finished product is provided with a first marking with information regarding origin and manufacture of the glass tube semi-finished product and a second marking, the information of which second marking is linked to the information of the first marking, so as to enable a determination regarding authenticity of the glass tube semi-finished product, origin of the glass tube semi-finished product, and/or origin of an apparatus with which the first and/or second marking was generated on the glass tube semi-finished product. The first marking is a marking that is produced at temperatures above the transformation temperature of the glass in a counterfeit-proof manner. The combination of two markings provides a high level of protection against counterfeiting.

Abstract: According to embodiments, a method of making a coated pharmaceutical container, may include: forming a glass tube; forming the glass tube into a pharmaceutical container comprising an interior surface and an exterior surface; and applying a coating to the exterior surface. The coating has a coefficient of friction less than or equal to 0.7 relative to a second pharmaceutical container when tested in a vial-on-vial testing jig under a normal load of 30 N. The coated pharmaceutical container may be thermally stable after depyrogenation at a temperature of at least 260° C. for 30 minutes in air.

Abstract: Nutritional formulas comprising long-chain polyunsaturated fatty acids (LC-PUFAs) are provided, along with methods and devices for preparing and/or administering nutritional formulas. In some embodiments, a percentage of the LC-PUFAs in the nutritional formula are in the form of monoglycerides and/or free fatty acids. In some embodiments, the nutritional formulas do not comprise added lipase. Also provided are methods for providing nutrition to a subject, methods for improving fat absorption, methods for improving cognitive ability, methods for preventing chronic lung disease, and methods for reducing the length of time a patient requires total parenteral nutrition.

Abstract: Disclosed herein are methods for treating a subject afflicted with a cancer having an activating RET alteration by administering an effective amount of a selective RET inhibitor, e.g., Compound 1 or pharmaceutically acceptable salts thereof, including, e.g., administering an amount of 60 mg to 400 mg of the selective RET inhibitor once daily.

Abstract: The present invention relates to a method for the mass-production of exosome comprising a cargo protein, a vector for preparing the exosome, exosome including a cargo protein prepared by the method, and a method for loading the cargo protein to cytosol by using the exosome prepared thereby. According to the method for preparing an exosome comprising a cargo protein provided by the present invention, the exosome loaded with a cargo protein can be produced with a high yield, so that it can be used broadly in the treatment of disease using the exosome.

Abstract: Disclosed are methods and compositions related to immunoconjugates. Particularly disclosed are immunoconjugates that comprise the Fc portion of IgG3 as well as Factor VII light chain or Factor VII. Also disclosed is an immunoconjugate protein, wherein said immunoconjugate protein comprises a hybrid Fc region of an IgG1 and an IgG3 immunoglobulin conjugated to Factor VII. These immunoconjugates can target Tissue Factor (TF) expressing cells.

Abstract: Compositions and methods that rapidly and selectively modify hematopoietic stem cells (or cells derived therefrom) to achieve therapeutic objectives by providing for transient expression of nucleic acids are described. The transient expression leads to permanent therapeutic changes in the modified cells, referred to herein as “hit and run” effects.

Abstract: The present invention belongs to the field of medicine, and relates to use of cannabidiol (CBD) in the treatment of pulmonary arterial hypertension. The CBD can be used as the only active ingredient or combined with other active ingredients to prepare a medicament for treating pulmonary arterial hypertension. Specifically, the present invention relates to use of any one selected from (1) to (3) in the preparation of a medicament for treating and/or preventing pulmonary arterial hypertension: (1) CBD, (2) a plant extract containing the CBD; and preferably, the plant extract is a cannabis extract, and (3) a pharmaceutical composition containing the CBD and one or more pharmaceutically acceptable adjuvants. In the present invention, upon experimental researches, it has found that the CBD has the function of inhibiting pulmonary arterial hypertension, and is especially suitable for treating the pulmonary arterial hypertension caused by hypoxemia.

Abstract: A method of treating or alleviating symptoms of disease, disorder or condition associated body wasting in a subject, including disease, disorder or condition associated body wasting in the subject, the disorder or condition identified based on initial measures of body mass, body mass index, or a bloodstream concentration of a substance, orally administering to said subject an amount of curcumin over a period of time effective treat or alleviate the disease, disorder or condition associated body wasting, diminishing or reversing the body wasting in the subject, and assessing efficacy of treating or alleviating symptoms of the disease, disorder or condition associated with body wasting by comparing final measures of body mass, body mass index, or a bloodstream concentration of a substance after the treatment period time to the initial measures of body mass, body mass index, or bloodstream concentration of the substance.