A pelvic prolapse treatment belt may include a main structural member having an inner and outer layer. The main structural member may include a plurality of through-hole regions positioned to be located on respective sides of a wearer's spine and a single through hole positioned at an approximate center of a rear of the main structural member. A compression pad may be attached to the main structural member. The compression pad may be configured for placing over a pelvic cavity of the wearer. A single strap may be attached to a bottom end of the compression pad and have a length sufficient for extending over the wearer's intergluteal cleft. The single strap may be sized for inserted through the single through-hole and have a distal end attached to a waist strap. The waist strap may include attachment features for attaching to the outer side of the main structural member.

A pelvic prolapse treatment belt may include a main structural member having an inner and outer layer. The main structural member may include a plurality of through-hole regions positioned to be located on respective sides of a wearer's spine and a single through hole positioned at an approximate center of a rear of the main structural member. A compression pad may be attached to the main structural member. The compression pad may be configured for placing over a pelvic cavity of the wearer. A single strap may be attached to a bottom end of the compression pad and have a length sufficient for extending over the wearer's intergluteal cleft. The single strap may be sized for inserted through the single through-hole and have a distal end attached to a waist strap. The waist strap may include attachment features for attaching to the outer side of the main structural member.

In order to provide efficient support for a user's back, the belt of the present application includes structures to help align and maintain the position of three portions of the users body—an upper abdominal region, a lower abdominal region and the lower back. To provide this support, a belt has an abdominal panel configured to be positioned over the user's abdomen, and a belt member wrapping around the waist region. The abdominal panel has a specific configuration and size to cause an upper portion of the abdomen is held in position and a lower portion of the abdomen to be held in position, with forces being applied so that these portions remain in a preferred alignment. The belt member includes a strap that is configured so that it can be positioned within the user's waist groove, and will provide additional supporting forces. In this way, the belt provides support to three critical locations on the user's body, thus insuring optimum alignment and support of the user's central body region.

A hemostatic device includes a flexible band adapted to be wrapped around a patient's limb at a site on the limb where bleeding is to be stopped, a portion for securing the band in a wrapped state to the limb, a curved plate which is made of a material more rigid than the band and at least a portion of which is curved toward the inner peripheral side thereof, a main balloon which is provided on the inner peripheral side of the curved plate and which inflates when a fluid is introduced therein, and a pressing member which is provided between the curved plate and the main balloon so that at least a portion thereof overlaps with the balloon and which is adapted for pressing against the balloon. The device provides an excellent hemostatic effect and prevents numbness and poor circulation in areas peripheral to the site of attachment.

A hemostatic device includes a flexible band adapted to be wrapped around a patient's limb at a site on the limb where bleeding is to be stopped, a portion for securing the band in a wrapped state to the limb, a curved plate which is made of a material more rigid than the band and at least a portion of which is curved toward the inner peripheral side thereof, a main balloon which is provided on the inner peripheral side of the curved plate and which inflates when a fluid is introduced therein, and a pressing member which is provided between the curved plate and the main balloon so that at least a portion thereof overlaps with the balloon and which is adapted for pressing against the balloon. The device provides an excellent hemostatic effect and prevents numbness and poor circulation in areas peripheral to the site of attachment.

A Diastasis Recti Splinting Garment is described which includes a plurality of attached torso straps and pelvic straps which the user wraps around their body and connects to the garment so as to approximate the 2 sides of the abdominal wall, providing support to the linea alba and fascial sheathes to allow for tissue healing. Furthermore, the adjustable angled straps encircle the torso and pelvis of the user to restore the integrity of the core, providing stability to the ribcage, spine and pelvis. Restoring the integrity of the core lends itself to optimal activation of the deep core stabilizers, including the abdominal muscles as well as the musculature of the pelvic floor, back, and diaphragm. This in turn aids in dynamic stability of the spine, ribcage and pelvis. This allows maximum support of the diastasis recti, consequently facilitating tissue healing through balancing intra-abdominal pressure, while still supplying support to the vulnerable pelvic floor and stability to the spine, ribcage and sacroiliac joints.

Device for external directional support of the female urethra under stress, consisting of a rigid cushion (1) fixed to a rigid counter-support (2) placed in the rear part of a belt or briefs, and comprising a partial rear perineal support part, the rigid counter-support (2) being connected at the front by adjustable straps (2) supporting it to a belt (5) or briefs whose rear periphery is rigidified by an insert or other non-folding material.

A Diastasis Recti Splinting Garment is described which includes a plurality of attached torso straps and pelvic straps which the user wraps around their body and connects to the garment so as to approximate the 2 sides of the abdominal wall, providing support to the linea alba and fascial sheathes to allow for tissue healing. Furthermore, the adjustable angled straps encircle the torso and pelvis of the user to restore the integrity of the core, providing stability to the ribcage, spine and pelvis. Restoring the integrity of the core lends itself to optimal activation of the deep core stabilizers, including the abdominal muscles as well as the musculature of the pelvic floor, back, and diaphragm. This in turn aids in dynamic stability of the spine, ribcage and pelvis. This allows maximum support of the diastasis recti, consequently facilitating tissue healing through balancing intra-abdominal pressure, while still supplying support to the vulnerable pelvic floor and stability to the spine, ribcage and sacroiliac joints.

Systems and methods are provided for mitigating and/or preventing a hernia using a wearable device worn by a user such that an output device is positioned at a predetermined location corresponding to a target hernia mitigation site on the user's body. One or more physical parameters of the user are monitored to identify when the user is about to perform a predetermined physical activity, and the output device is activated to provide an output to mitigate a hernia or prevent a hernia from occurring at the mitigation site when the predetermined activity is performed.

Systems and methods are provided for mitigating and/or preventing a hernia using a wearable device worn by a user such that an output device is positioned at a predetermined location corresponding to a target hernia mitigation site on the user's body. One or more physical parameters of the user are monitored to identify when the user is about to perform a predetermined physical activity, and the output device is activated to provide an output to mitigate a hernia or prevent a hernia from occurring at the mitigation site when the predetermined activity is performed.