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By being proactive in creating a stress-free household where we actively seek to cooperate and solve problems instead of trying to fix blame, we can make it unnecessary for them to point fingers and rally against each other.


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Inside: What are the causes of sibling rivalry? Are sibling rivalries normal? What are examples of sibling rivalry behaviours? Three mistakes that parents make when managing siblings arguments and how do you deal with sibling rivalries.


While it is almost impossible to completely eliminate sibling rivalry, you can definitely put some strategies in place to reduce the frequency of it as well as to handle it in a more peaceful and restful manner.


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Another effective way to reduce sibling rivalry is by strengthening the connection between the kids themselves. These games focus on building relationships in a fun and positive way, rather than always focusing on their negative interactions.


If the sibling rivalry in your home is beyond what you can manage alone, schedule an Online Parent Coaching session. We will sit down and talk through your challenges, become curious about what each sibling needs, and find solutions that will ease the tension and build connection in your family. Schedule a session today!


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One useful approach for revealing tactile influences on vision is to add tactile signals while the visual system is confronted with ambiguous visual inputs and unable to resolve a stable percept16,17. A standard way to induce perceptual ambiguity in vision is by using binocular rivalry18,19,20, the name given to the perceptual bistability that arises when each eye is presented with a different image. The incompatible monocular images prevent binocular fusion and trigger an irregular series of perceptual oscillations in which one image is perceived and then the other, in an ongoing stochastic alternation18,19,20. A number of studies have shown that tactile signals congruent with one of the competing visual images can help stabilize the perceptual ambiguity by biasing the alternation dynamics in favour of the crossmodally congruent stimulus21,22,23. In one study22, two visual gratings with orthogonal orientations were presented to each eye to produce binocular rivalry and participants continuously monitored the perceptual fluctuations between one grating and the other. Subjects intermittently explored for several seconds a tactile grating which was congruent with one of the visual stimuli. Tactile exploration extended the dominance duration of the matching visual stimulus (if it was currently dominant), or shortened its suppression duration when it was suppressed so that visual perception quickly changed to match the tactile stimulus. Subsequently, Lunghi and Alais21 showed this visual-haptic interaction in rivalry is tightly orientation tuned, with the effect declining rapidly as the visual-tactile orientation difference increases.


The exploration of crossmodal influences on binocular rivalry is informative for several reasons. One is that with visual perception unresolved and bistable, the role of crossmodal signals is more evident as even a relatively small input to vision can tilt the balance in favour of the congruent image and thus stabilize visual perception. Another reason is that the alternating monocular suppression that underlies the perceptual alternations in binocular rivalry is thought to occur early in visual processing where left- and right-eye signals are first combined24,25. Any crossmodal influence on rivalry therefore implies an early interaction. Consistent with this argument are results showing that the tactile interaction with rivalry is spatially localized and spatial-frequency tuned22,26 as well as orientation tuned21, reflecting the characteristics of neurons in early visual cortex. A final point of interest is that the tactile influence on binocular rivalry operates on both the dominant and the suppressed percept. This is significant because most modulatory effects on rivalry dynamics operate by extending the duration of the consciously perceived image and do not influence the competing percept that is suppressed from awareness. That a congruent tactile stimulus will rescue the matching visual stimulus from suppression21,22,26,27 also suggests an early visual-tactile interaction as it must interact with a stimulus that is thought to be suppressed early in visual processing and at a level preceding conscious awareness.


Here we extend the recent work on tactile influences on binocular rivalry by measuring whether visual contrast thresholds in rivalry are altered by congruent tactile input. Measuring contrast sensitivity for suppressed stimuli is widely done in rivalry research as it can be compared with sensitivity during dominance to obtain a measure of suppression strength known as suppression depth. Typically, the loss in contrast sensitivity during rivalry suppression is in the range of 0.3 to 0.5 log units relative to dominance sensitivity. Given the findings suggesting that congruent tactile input acts on the suppressed visual image and that tactile and visual signals can combine to boost signal strength14,15, we test the prediction that the visual grating undergoing suppression will maintain higher contrast sensitivity when it is paired with a congruent tactile grating than when paired with an incongruent one.


Two extra experimental sessions were acquired for each observer in which rivalry alternation dynamics were recorded. In these sessions, the probe stimuli were presented but participants were instructed to ignore them and to report their visual perception continuously by pressing appropriate keys on the keyboard with their left hand. These sessions enabled estimates of the proportion of contrast increment probes presented during dominance and suppression for each condition (visual-only and visuo-haptic stimulation), which in turn are used as weights in the model shown below (see Equation 1). Specifically, in order to obtain the weights, we asked observers to continuously report their visual perception although we only recorded the percept reported at the time of each probe presentation. Note that this step may not be necessary given equal stimulus contrasts in each eye and interocular counterbalancing to control for differences in ocular dominance, as weights of 0.5 could be justifiably assumed. Also, the rivalry dynamics could have differed slightly for the two tasks because of different attentional loads (asking observers to report rivalrous perception may have slowed switching rate31, however this would affect overall switching rate rather than one of the stimuli selectively and thus would not change the dominance/suppression proportion).


Psychometric functions plotting probe detection performance as a function of the probe's contrast increment (black symbols) are shown for a single subject: (A) visual-only condition, (B) parallel visuo-haptic condition (red lines). The black functions show performance obtained during rivalry without observers indicating their fluctuating perceptual states. A new model30, as shown in Equation 1, was used to decompose the compound function shown in black to recover the component psychometric functions for dominance (solid lines) and suppression (dashed lines) and their threshold (μ) and slope (σ) parameters. Average and single subjects' contrast discrimination thresholds measured during dominance (C, D) and suppression (E, F): parallel visuo-haptic stimulation improved contrast discrimination sensitivity during binocular rivalry suppression (*** represents p 2ff7e9595c


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