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Thread: Sleep Paralysis

  1. #1

    Sleep Paralysis

    I have been affected by sleep paralysis since I was in my early teenaged years. It is not a constant affliction and I am not troubled by it much, but occasionally it rears its ugly head.

    I would like to know why it occurs.

    For me (I don't know if it is like this with everyone) it happens when I am trying to wake up in the morning. Everything in this hsort space of time seems SO real, and yet I am unable to move a muscle. I have seen people in the room with me and talked to them. I have been absolutely positive that I am beating my sleeping husband with my fist to shake me so I can come out of it. I have fallen on the floor (this is all in my head, mind you; it's not ACTUALLY happening at all!) and jarred myself out of it. The worst feeling is that I am trying to move my arms and cannot do a thing.

    Is there any explanation why this happens?

  2. #2

    Sleep Paralysis

    Sleep Paralysis
    January 26, 1999

    What is sleep paralysis?
    Sleep paralysis consists of a period of inability to perform voluntary movements either at sleep onset (called hypnogogic or predormital form) or upon awakening (called hypnopompic or postdormtal form).

    Sleep paralysis may also be referred to as isolated sleep paralysis, familial sleep paralysis, hynogogic or hypnopompic paralysis, predormital or postdormital paralysis

    What are the symptoms?
    • A complaint of inability to move the trunk or limbs at sleep onset or upon awakening
    • Presence of brief episodes of partial or complete skeletal muscle paralysis
    • Episodes can be associated with hypnagogic hallucinations or dream-like mentation (act or use of the brain)
    • Polysomnography (a sleep recording) shows at least one of the following:
      • suppression of skeletal muscle tone
      • a sleep onset REM period
      • dissociated REM sleep

    Is it harmful?
    Sleep paralysis is most often associated with narcolepsy, a neurological condition in which the person has uncontrollable naps. However, there are many people who experience sleep paralysis without having signs of narcolepsy. Sometimes it runs in families. There is no known explanation why some people experience this paralysis. It is not harmful, although most people report feeling very afraid because they do not know what is happening, and within minutes they gradually or abruptly are able to move again; the episode is often terminated by a sound or a touch on the body.

    In some cases, when hypnogogic hallucinations are present, people feel that someone is in the room with them, some experience the feeling that someone or something is sitting on their chest and they feel impending death and suffocation. That has been called the “Hag Phenomena” and has been happening to people over the centuries. These things cause people much anxiety and terror, but there is no physical harm.

    What else can you tell me about sleep paralysis?
    • Some people with disrupted sleep schedules or circadian rhythm disturbances experience sleep paralysis
    • A study found that 35% of subjects with isolated sleep paralysis also reported a history of wake panic attacks unrelated to the experience of paralysis
    • Sixteen percent of these persons with isolated sleep paralysis met the criteria for panic disorder

    How can I stop the sleep paralysis?
    In severe cases, where episodes take place at least once a week for 6 months, medication may be used.

    You may be able to minimize the episodes by following good sleep hygiene:
    • getting enough sleep
    • reduce stress
    • exercise regularly (but not too close to bedtime)
    • keep a regular sleep schedule

    Sleep Paralysis Articles & Web Sites
    What is sleep paralysis?
    Sleep Paralysis and Lucid Dreams Research
    Sleep Paralysis and Associated Hypnagogic and Hypnopompic Experiences Page
    Sleep Paralysis/Hag Phenomena
    Sleep paralysis is normal
    Last edited by Daniel; January 27th, 2008 at 11:11 PM.

  3. #3

    Sleep Paralysis and hypnagogic and hypnopompic states

    Sleep Paralysis and Associated Hypnagogic and Hypnopompic Experiences

    Sleep Paralysis
    Sleep paralysis, or more properly, sleep paralysis with hypnagogic and hypnopompic hallucinations have been singled out as a particularly likely source of beliefs concerning not only alien abductions, but all manner of beliefs in alternative realities and otherworldly creatures. Sleep paralysis is a condition in which someone, most often lying in a supine position, about to drop off to sleep, or just upon waking from sleep realizes that s/he is unable to move, or speak, or cry out. This may last a few seconds or several moments, occasionally longer. People frequently report feeling a "presence" that is often described as malevolent, threatening, or evil. An intense sense of dread and terror is very common. The presence is likely to be vaguely felt or sensed just out of sight but thought to be watching or monitoring, often with intense interest, sometimes standing by, or sitting on, the bed. On some occasions the presence may attack, strangling and exerting crushing pressure on the chest. People also report auditory, visual, proprioceptive, and tactile hallucinations, as well as floating sensations and out-of-body experiences (Hufford, 1982). These various sensory experiences have been referred to collectively as hypnagogic and hypnopompic experiences (HHEs). People frequently try, unsuccessfully, to cry out. After seconds or minutes one feels suddenly released from the paralysis, but may be left with a lingering anxiety. Extreme effort to move may even produce phantom movements in which there is proprioceptive feedback of movement that conflicts with visual disconfirmation of any movement of the limb. People may also report severe pain in the limbs when trying to move them. Several recent surveys including our own suggest that between 25-30% of the population reports that they have experienced at least a mild form of sleep paralysis at least once and about 20-30% of these have had the experience on several occasions. A few people may have very elaborate experiences almost nightly (or many times in a night) for years. Aside from many of the very disturbing features of the experience itself (described in succeeding sections) the phenomenon is quite benign. It was thought in the past that it was a significant part of the so-called "narcoleptic tetrad", but recent surveys of non-clinical populations, such as ours, suggest that the prevalence may be as high among the general population as among diagnosed narcoleptics. For a summary of SP Characteristics see Table 1.

    Sleep paralysis most often has an adolescent onset. Earlier research had generally studied student populations leaving open the possibility that this might have been an artifact of the fact that only young people were surveyed. In several surveys with older samples, (Mean age of approximately 30) we have corroborated a very clear tendency for people at all ages to report an adolescent onset for their episodes. Several large samples have produced consistent means of 17 years of age, with a sharp increase after 10 and an even sharper decline from 17 to the mid-twenties. The results do suggest, however, that sleep paralysis episodes can begin at virtually any age, although it is rare for this to happen after 30.

    "Hallucinations" and Sleep Paralysis
    Our research has led us to conclude that hallucination is probably not too strong a term for the experiences associated with sleep paralysis. We take our definition of hallucination from Slade & Bentall (1988). A hallucination is an experience of perception in the absence of an appropriate stimulus, but which has the impact of a conventional perception and is not under the control of the experient. A hallucination has the quality of being a sensation related to external event rather than merely a product of the imagination. It does not seem to be merely an idea. It has the quality of objectivity, that is, something beyond the willing and wishing of the experient. The "object" of the hallucination" is taken to exist independently of the will of the experient. The experience is, in principle, a publicly available phenomenon. The hallucinator should also believe that any appropriately situated person should be able to confirm these experiences. These qualities of sensation, objectivity, existence, and independence, are among the defining qualities of hallucinations (Aggernaes, 1972).

    There are probably several degrees of a hallucinatory experience, as distinct from illusions and normal or conventional sensations. A "full-blown" hallucination seems like a real experience and is believed to be a real experience. One might say the individual is both hallucinating and is deluded by the hallucination in to accepting it as a real experience. A hallucination proper may be said to have occurred if the sensation seems quite authentic even if the experient judges the experience to be, for some reason, suspect. It seems real but there is also something counterfeit about the experience. A pseudo-hallucination also has this counterfeit quality but it also lacks the fullness of a conventional sensation. It has an ethereal, "as-if" quality, lacking the richness of a true sensation. An illusion is simply a misinterpretation of a conventional stimulus.

    Sleep paralysis related experiences appear to range from what might be best termed fleeting illusions to true hallucinations. The distinction between illusions and hallucinations is one of long standing harking back at least to Esquirol (1832). Most of the experiences associated with sleep paralysis appear to be hallucinations and quasi-hallucinations (e.g., Slade & Bentall, 1988). People experiencing HHEs are sometimes convinced of their reality but are often able to take a more critical sense, at the same time. This appears to be more common after people have read something about SP and HHEs and come to believe that the experiences are of a hallucinatory nature. Often however, there is no loss of intensity or vividness of the experience. The knowledge or belief that the experience is illusory reduces, for some, the terror of the experiences but appears to have relatively little impact on the apparent reality of the experiences. The quasi-hallucinatory HHEs, though frequently vivid, often have an ethereal and insubstantial quality. These quasi-hallucinations probably best describe the large majority of sleep paralysis and range from vaguely disturbing to extremely terrifying. They usually also motivate a least some search for meaning. The HHEs of sleep paralysis would include misinterpretations of shadows and indistinct objects in a dark room. Finally there may be some people who experience full-blown hallucinations during sleep paralysis in which they not only have vivid and complex imaginative experiences but are also convinced that these experiences have objective external sources. Such people are unlikely to describe their experience as one of sleep paralysis but perhaps as one of demon possession or alien abduction.

    Frequency of Associated hallucinations
    Depending on the nature of the question and the populations surveyed between 20 - 40 % of people report having had such an experience. For about a third of these people that is about the extent of the experience and other than a momentary concern about being paralyzed many of these people do not appear to give the matter much thought. It is entirely possibly that almost everyone has experienced such a state but has scarcely noticed and soon forgotten the experience. Another two-thirds of those experiencing sleep paralysis, however, have associated experiences sometimes referred to as hypnagogic and hypnopompic hallucinations. These hallucinations may be tactile, kinesthetic, visual, or auditory. The most common of these experiences is the "sensed" presence accompanied by fear. Individuals vary considerably in the extent to which they report such symptoms. A rather small proportion (>5%) report all the associated components.

    Sleep Paralysis as an Anomalous REM State
    REM and Dreaming: A major distinction of sleep states, for close to a half century, has been accepted between REM and NREM sleep (Aserinsky & Kleitman, 1953; Jouvet, 1967). REM periods are characterized by desynchronized cortical characterized by low-voltage fast EEG patterns with synchronized hippocampal activity characterized by slow (4-8 Hz) theta activity (e.g., Culebras, 1994). It is also widely accepted that dreaming is more common and more vivid during REM than during NREM sleep (Dement & Kleitman, 1957). In addition to the characteristic desynchronized cortical low-voltage fast EEG activity, there are numerous physiological, behavioral, and sensory features associated with REM such as muscle atonia, gating of sensory input, rapid eye and middle ear movements, as well as heart rate and respiration changes (Carskadon & Dement, 1989; Symons, 1993).

    Within REM periods a distinction is sometimes made between a background tonic state (TREM) and bursts of phasic REM (PREM) every 16-120 seconds and lasting from 2-9 seconds (Aserinsky, 1971, Molinari & Foulkes, 1969). Specifically, PREM is characterized by bursts of rapid eye and middle ear movements and characteristic cortical and hippocampal EEG patterns. PREM is associated with, and may be preceded by, ponto-geniculo-occipital EEG waves (PGO spikes in animal preparations) originating in the bilateral, dorsolateral pons and projecting rostrally through the lateral geniculate nucleus and other thalamic nuclei (Hobson, Alexander, Frederickson, 1969). It has been conjectured that the most vivid dreams, or most vivid events within dreams, are associated with PREM (Molinari and Foulkes, 1969).

    REM and SP: SP has also been associated with REM states, particularly with sleep-onset and sleep-offset REM (SOREM) (Nan'no, Hishikawa, & Koida, 1970). In both REM dreams and SP hallucinations a general atonia is maintained during REM by marked and sustained hyperpolarization of the motoneurons (Chase & Morales, 1989). One likely function of the general atonia is the prevention of the physical enactment of the motor components of dreaming. There are at least two major traditional hypotheses concerning the connection between neurophysiological events and visual imagery in dreams. The visual imagery of dreaming may arise either from the direct stimulation of visual areas of the cortex during the PGO spike, in which case the rapid eye movements may reflect attempts to scan the images (Ladd, 1892; Roffwarg, Dement, & Muzio, 1962), or conversely, the mages may be produced by the oculomotor impulses in response to direct stimulation from the gigantocellular pontine reticular field (Hobson & McCarley, 1977; McCarley & Hobson, 1979).

    REM is thought to be generated in the lateral portions of the nucleus reticularis pontis oralis (RPO) immediately ventral to the locus ceruleus in the pontine reticular formation. The neurotransmitters in this region have not been clearly determined, but are neither cholinergic nor monoaminergic. The RPO receives projections from cholinergic regions in the laterodorsal tegmental nucleus (LDT) and the pedunculopontine tegmental nucleus (PPT) as well as from ventromedial portions of the medulla. The RPO, LDT, and PPT are collectively thought to be part of the REM-on neural population (Steriade & McCarley, 1990). These populations are hypothesized to interact with REM-off noradrenergic neurons in the locus ceruleus and seratonergic neurons in the raphe system. These latter populations are most active during waking and least active during REM. Interactions between the REM-on and REM-off populations are thought to control REM onset and offset (Steriade & McCarley, 1990).

    SP may reflect an anomaly of the functioning of the monoaminergic systems and/or their inhibition of the REM-on cholinergic system. Experimental and clinical dissociations have been demonstrated among major components of REM: namely, PGO activity, atonia, and EEG desynchronization (Hishikawa & Shimizu, 1994). Hishikawa & Shimizu speculate that SP may be produced by hyperactivation of the Sleep-on populations or, they deem more likely, hypoactivation of the Sleep-off populations. That SP may be alleviated by serotonin and adrenergic reuptake inhibitors is taken to be consistent with this hypothesis. Also involved may be suprapontine systems involving the reticular system, including the hippocampus and amygdala.

    REM SP with HHEs differs from REM dreams in that during SP there is little or no blocking of exteroceptive stimulation and there is no loss of waking consciousness. SP with HHEs differs from dream experience in that the sensory cortex may be receiving both externally and internally generated information. The peculiarity of the HHEs in SP may, in part, be a result of the brain's attempts to integrate endogenous cortical arousal originating in the pons with normal sensory input. A similar peculiarity may exist for motor pattern arousal during SP. McCarley and Hobson argue that, during dream generation by internal stimulation of motor programs, we interpret the activity of the pattern generators and their corollary discharge as movement. The lack of peripheral feedback, though not normally necessary for effective control, may contribute to a sense of unreality to the apparent movement and hence to the "bizarreness" of dreams. Pontine activation of motor patterns during SP appears to be less common in SP than in dreams, if subjective reports of illusory movement are to be taken as evidence. Volitional attempts at movement during SP are common, however, and the absence of feedback is most often, though not always, experienced as paralysis rather than illusory movement. Thus it appears that, during SP, the frontal cortex is more sensitive to the absence of feedback than during dreaming. When motor programs are spontaneously activated during SP these might be extremely resistant to coherent interpretation am may be experienced as very unusual bodily states. In concluding sections we will relate more specifically the phenomenology of various HHEs to the underlying neurophysiology.

  4. #4

    Sleep Paralysis

    Thanks for all the details. SP did begin in my teens, probably when I was 14 or l5. I was sent to Toronto to have a CAT scan at that time.

    It happens a lot less frequently now. Even when it is happening I seem to know what it is and I am not particularly terrified after I get myself out of it.

    My perceived movements and the movements of others during my bouts of SP have never been particularly threatening, though. Whatever goes on during that brief time span, though, is VERY, VERY real! When I get up, I start asking questions! "Didn't I make any noise?", "If ever you hear me making noise and I'm asleep, SHAKE ME!" "Did you just walk in the room and throw a blanket over me while I was lying here just now?"......things of that nature.

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