Sleep: When at night you can no longer find your way back to yourself
Falling asleep, staying asleep, not waking up rested. Three faces of one story that tells more than a diagnosis. And a path that begins with listening, not with a pill.
It seems to have become normal that you don't sleep. That you lie awake at three in the morning with your head running calculations on projects no one is paying you for. That after seven hours in bed you get up as if you'd just run a marathon. That is not normal. It has only become average.
I bet you know this feeling. You lie down, exhausted to the bone. The body wants to. The mind doesn't. It keeps spinning. It plans. It remembers. It sorts. And eventually, when it does sleep, something rips you back out at three. You lie there, your heart beats faster than it should, and you think: why is my body doing this?
Or the other one. You sleep seven, eight, nine hours. And you still feel as if you were never gone. As if the sleep took place, but did not mean you.
These are three completely different problems sitting under one word: sleep disorder. In a consultation there is often little time for this distinction, even though it makes a great deal of difference. I take that time, because I believe therapy starts exactly here.
The three faces of your night
Before we can even talk, we have to know what we are talking about. Because trouble falling asleep is, neurobiologically and emotionally, something completely different from trouble staying asleep. And both are again something different from sleep that does happen, but does not nourish you.
Trouble falling asleep
You lie awake. Your head spins. You can't let go of yourself. The mind doesn't find the way into the body.
Trouble staying asleep
Falling asleep works. But between two and four you are awake. Heart faster, thoughts loud, hours before you find your way back.
Non-restorative sleep
You sleep. Long enough. But you wake up wrung out. Sleep took place. It did not reach you.
Clinical sleep medicine puts all of this under the heading of insomnia in the ICSD-3. The German AWMF S3 guideline Insomnia in adults (registry no. 063-003) puts the figure for diagnostic insomnia in Germany at 8 to 15 percent. The largest analysis to date, Kocevska and colleagues 2021 in Nature Human Behaviour with more than 1.1 million people from three countries, shows that sleep complaints increase with age and that women are more often affected than men.
First, rule out: what conventional medicine must not miss
Before we talk about Anthroposophy, KPNI and liver rhythms, we have to do one thing: take the organic causes seriously and rule them out. Not because conventional medicine has the last word. But because it would be unfair to recommend a meditative breathing rhythm to you when what sits behind your night is an untreated sleep apnea.
Obstructive sleep apnea (OSA)
Pauses in breathing at night. Prevalence up to 38 percent. STOP-BANG questionnaire, polysomnography as gold standard.
Restless legs syndrome
Tingling, urge to move the legs in the evening. Ferritin target often above 75 µg/l. 5 to 15 percent of the population.
Periodic limb movement
Unconscious leg movements during sleep. Fragments the sleep architecture without you noticing.
Narcolepsy & hypersomnias
Daytime sleepiness despite night sleep. Cataplexy as the key symptom. Multiple sleep latency test.
Thyroid
Both over- and underactivity. TSH, fT3, fT4, plus antibodies. Isolated TSH is not enough.
Depression, anxiety disorder
Early-morning waking is classic in depression. Ruminative wakefulness in anxiety. PHQ-9, GAD-7.
Nocturia, BPH, heart failure
Frequent night-time urination. Prostatic hyperplasia, cardiac decompensation, diabetes insipidus.
Parasomnias & chronic pain
Sleepwalking, nightmares. Persistent pain systematically fragments deep sleep.
A large epidemiological analysis in The Lancet Respiratory Medicine estimates that nearly one billion people worldwide have obstructive sleep apnea. Only a fraction know it. Anyone who snores, falls asleep during the day, wakes up with a dry mouth and has a thick neck belongs in a sleep lab or at least on an outpatient polygraphy device. And one important addition: anyone who has to fight off sleep during the day should not drive and should not operate machinery until this has been clarified. Marked daytime sleepiness can limit fitness to drive, which in Germany is regulated in the driving licence ordinance.
Holistic does not mean leaving conventional medicine out. Holistic means speaking conventional medicine as one of several languages. If the cause is a mechanical breathing problem, no lavender oil will help. If the cause is a life that the body has to work through at night, no CPAP will help.
Trouble falling asleep: when the mind does not want to enter the body
In Rudolf Steiner's view of the human being, the human consists of four members. The physical body, the living etheric body, the soul-feeling astral body, and the I. At night something very beautiful happens: the astral body and the I detach a bit from the body, go into the spiritual world, and the body is allowed to regenerate. In the morning they return.
Trouble falling asleep, in this picture, is not a brain-chemistry problem. It is a disturbance of the transition. The astral body, which is everything that thinks, plans, remembers, does not want to let go. It holds itself in the body. And as long as it does, the body cannot sleep.
The question is: why does it hold on.
Two variants, one movement
In Anthroposophy there are two basic directions for this. Either there is too much spirit in the body that cannot let go. You are entirely in your head, you have not closed the day, you are still carrying the conversation from 6pm with you. Or there is too little body to catch the spirit. You haven't exerted yourself physically. The body is not tired enough to invite the spirit to come to rest.
That sounds old-fashioned. But it is precisely described in modern neurobiology.
Dieter Riemann, one of the leading European sleep researchers, summarized the hyperarousal model of insomnia in Sleep Medicine Reviews in 2010.
What his team showed in an overview of many individual studies: in chronic trouble falling asleep, the autonomic nervous system in the evening is not in the parasympathetic state but overactive. Heart rate stays elevated, skin conductance high, EEG activity in the fast frequencies instead of the slow ones. Hormonally, immunologically, in imaging, everywhere the same signal: continuous alarm.
What this means for you: your trouble falling asleep is not a character flaw. It is a nervous system that cannot find the switch. And there are reasons for that, reasons we can find.
Riemann D et al. The hyperarousal model of insomnia: a review of the concept and its evidence. Sleep Med Rev. 2010;14(1):19–31. DOI: 10.1016/j.smrv.2009.04.002In KPNI language: the nervous system is in continuous sympathetic tone. The parasympathetic, your vagus nerve, doesn't get its turn. This can keep evening cortisol up, can delay melatonin release, and can weaken the calming effect of GABA. How strongly this chain works in any single person varies a great deal.
On the GABA question itself the data are contradictory. One small spectroscopy study found about 30 percent less GABA in the brain in insomnia and explicitly called this preliminary (Winkelman 2008, 16 affected people against 16 healthy ones). A second study found 12 percent more occipital GABA and read it as an adaptive response to chronic hyperarousal (Morgan 2012). Both are preliminary. What follows from this is a hypothesis so far, not an explanation.
Vgontzas and colleagues at the Sleep Research and Treatment Center of Pennsylvania State University in Hershey measured the cortisol of eleven people with chronic insomnia across 24 hours in 2001 and compared it with thirteen healthy controls.
What they found: ACTH was on average about 27 percent higher (P = 0.04). Cortisol was arithmetically about 14 percent higher, but at P = 0.07 this difference missed statistical significance. The largest swings were in the evening and the first half of the night. Important for context: in the timing pattern itself the authors found no difference, the circadian rhythm of cortisol was preserved.
What this means for you: your night is not only subjectively restless. It may be that your system is hormonally set higher overall. This is not imagination. It is a finding you can measure, although it was obtained in a very small group.
Vgontzas AN et al. Chronic insomnia is associated with nyctohemeral activation of the hypothalamic-pituitary-adrenal axis. J Clin Endocrinol Metab. 2001;86(8):3787–3794. DOI: 10.1210/jcem.86.8.7778Exam phase. Lying awake. And a long way back.
During the exam phase in medical school I experienced myself what I see in patients today. The body was tired. The mind wasn't. I lay in bed and worked through cases that weren't even coming up. I wanted to let go. I couldn't. That was the first time I understood what an astral body that does not detach from the body means. I felt it.
What helped me back then was not sleeping pills. It was a botanical and anthroposophic combination remedy. There is no body of studies I could offer you as evidence for it, and my own experience is not evidence. I write it down only so that you know I have felt this state from the inside.
You do not have a sleep-onset disorder. You have a nervous system that did not get the chance to come down during the day. The question is not how you fall asleep faster. The question is whether you have been in your life enough during the day so that you can re-enter it again at night.
Trouble staying asleep: the hour between the liver and the soul
You fall asleep. All good. Then around three something pulls you back out. You lie awake, sometimes in panic, sometimes only with this strange here-I-am-again feeling. And you don't get back into sleep for an hour, two hours.
Old Chinese medicine has named this hour for centuries. Between 1 and 3 in the morning, it says, is the time of the liver. Between 3 and 5 the time of the lung. Between 5 and 7 the time of the large intestine. For each hour an organ, each organ with an emotional theme, each organ with a physiological task.
The organ clock, Chinese and chronobiological
Is this just old magic? Not entirely. Modern chronobiology has by now shown that almost every cell in your body carries its own clock. In 2014 a paper in PNAS published a circadian gene-expression atlas across twelve mouse tissues. Result: the liver, the heart, the kidney, the fat tissue, all have their own peaks of gene activity. The liver expresses its detoxification enzymes especially strongly in certain time windows.
Zhang and colleagues measured in 2014 in PNAS, in twelve mouse tissues, how strongly which gene is active at which time of day.
What they observed: about 43 percent of all protein-coding genes show a circadian rhythm somewhere in the body. The liver is particularly rhythmic in this. CYP enzymes, glucose metabolism, detoxification cascades have clearly defined peak times. More than that: many of the best-selling medications target genes with strong day-night rhythm.
What this means for you: if you regularly wake up between 1 and 3, it is not absurd to ask what your liver is doing right then. TCM described a temporal rhythm without being able to measure it. Chronobiology measures today that many organs carry their own day-night rhythms, so far above all in the mouse model, and mice are nocturnal. Whether the hourly grid of TCM is found in humans in this form is open. I use the question as a prompt, not as proof.
Zhang R, Lahens NF, Ballance HI, Hughes ME, Hogenesch JB. A circadian gene expression atlas in mammals. Proc Natl Acad Sci USA. 2014;111(45):16219–16224. DOI: 10.1073/pnas.1408886111Trouble staying asleep rarely has one cause. It usually has three to five. And every single one of them can be examined.
The nocturnal cortisol peak, shifted
In a healthy rhythm cortisol drops low in the evening, has its low point around two in the morning, and then slowly rises to wake you up around seven. In chronic stress, in HPA dysregulation, in perimenopause, this rise can move forward. The cortisol surge can come too early, sometimes around half past two. You wake up with the feeling something is important, and nothing is really important. To be honest about it: the insomnia study cited above found higher levels overall, but no shifted circadian pattern. The advanced rise is therefore an explanatory model from practice, not an established finding.
Healthy vs. shifted cortisol rhythm
The model behind this: in HPA dysregulation the 4h rise can slide forward. A working hypothesis, not an established rule.
The nocturnal hypoglycemia that no one measures
Here comes something I see often in the practice and almost never find in textbooks. People who eat little in the evening or very early have no glucose supply during the night. Between two and three the blood sugar falls below a critical threshold. The body, evolutionarily wise, releases adrenaline and cortisol to mobilize glucose from the liver. Adrenaline can wake you up. You think you have trouble staying asleep. Behind it there can also be a nocturnal drop in blood sugar. Whether that applies to you can only be measured, not assumed. And other causes such as heart rhythm, thyroid or breathing belong ruled out first.
Philip Cryer described this counter-regulation meticulously in the diabetes literature. In Diabetes in 2003, Banarer and Cryer deliberately lowered blood sugar during sleep in eight people with type 1 diabetes and eight healthy controls. In the people with diabetes the adrenaline response during sleep was attenuated, in the healthy controls it was not. And the people with diabetes precisely did not wake up: their sleep efficiency was 77 percent against 26 percent in the control group. So this counter-regulation is well studied in type 1 diabetes. Whether it affects people without diabetes in the same way is not established. I see the pattern in practice with unstable blood sugar, but I say it plainly: that is clinical observation, not a body of evidence.
A racing heart at night that looks like panic
I know this pattern: heart racing, sweating, wide awake in the middle of the night. It looks like a panic attack, and sometimes that is exactly what it is. In such cases it is worth measuring nocturnal blood sugar as well, before explaining the night in psychological terms alone. That does not replace psychiatric assessment.
And it does not replace ongoing medication. If a doctor has prescribed you a sedative, you never stop it on your own and never abruptly. With benzodiazepines and Z-drugs, sudden withdrawal can trigger seizures and confusional states. Every change belongs in the hands of the prescribing doctor.
A second important point: if you take insulin or sulfonylureas, nocturnal hypoglycemia is a potentially life-threatening event. It is not managed with an evening snack. It belongs with the treating doctor, who adjusts the dose.
Progesterone and the forgotten allopregnanolone
For women, a second major factor comes in. Progesterone, the second female cycle hormone, is converted in the body into a metabolite called allopregnanolone. And allopregnanolone is one of the strongest natural modulators of your GABA-A receptor. Put more simply: it binds where benzodiazepines also bind. Only naturally, endogenously, rhythmically.
In perimenopause, progesterone falls first. Allopregnanolone falls with it. The GABA receptor then gets less of its natural calming signal. In women from 40 onwards a fall in progesterone can therefore play a role when trouble staying asleep newly appears. Whether that is the driving factor in your case is decided by the findings, not by your age.
Kravitz and colleagues in 2008 in Sleep followed more than 3,000 women through the menopausal transition, multi-ethnic and longitudinal.
What they observed: sleep disturbances increased markedly during perimenopause and correlated with vasomotor symptoms like hot flushes, but also independently of these with the hormonal shifts of the transition.
What this means for you: if as a woman in your late 30s or early 40s you suddenly stop staying asleep, that is no coincidence. It is physiology giving a signal. And the signal can be captured in the lab.
Kravitz HM et al. Sleep disturbance during the menopausal transition in a multi-ethnic community sample of women. Sleep. 2008;31(7):979–990.Caufriez and the Brussels sleep lab in 2011 in the J Clin Endocrinol Metab gave eight healthy postmenopausal women progesterone or placebo double-blind, and measured the night with polysomnography. Important for context: these women had no sleep complaints of their own and no hot flushes.
What they found: on the night when sleep was artificially disturbed by blood sampling every 15 minutes, wake time after sleep onset under progesterone was 53 percent lower, deep sleep duration almost 50 percent higher and slow-wave activity about 45 percent higher. Growth hormone rose, TSH fell. The decisive limitation is in the authors' own conclusion: progesterone had no effect on undisturbed sleep.
What this means for you: progesterone is not just a cycle hormone. Through its metabolite allopregnanolone it can play a part at the GABA axis. This study says nothing about perimenopausal women with trouble staying asleep, however, because it did not study them. It is a pointer, not evidence for a therapy.
Caufriez A et al. Progesterone prevents sleep disturbances and modulates GH, TSH, and melatonin secretion in postmenopausal women. J Clin Endocrinol Metab. 2011;96(4):E614–E623. DOI: 10.1210/jc.2010-2558Histamine, thyroid, liver detoxification
Three more candidates that can play a role in the practice. Histamine has a peak at night between two and three. Anyone who eats very histamine-rich food, who has DAO deficiency, can get restless in this phase. An overactive thyroid (Hashimoto can show both faces) can drive the heart rate up at night. And a heavily taxed liver can, so the reasoning goes, reach its limit during the deep phase. For this liver connection there are no robust human studies. It is a working hypothesis, not an established mechanism.
Trouble staying asleep is rarely a sleep problem. It is a measurement point. Your body shows you at night what it could not show during the day. Sugar, hormones, liver, stress axis. The question is not how you sleep through the night. The question is what your body is trying to clear at night.
Non-restorative sleep: when you were present, but not nourished
The third face is the trickiest. You sleep seven hours. But you get up as if after a bad night. No dreams, no feeling, no letting go. Coffee becomes a crutch. The afternoon is a fight.
Non-restorative sleep is almost always one of three things: an undetected apnea, a fragmented REM phase, or too low parasympathetic activity at night. All three are measurable.
What we check when you wake up unrested
- Screening for sleep apnea, starting with STOP-BANG and, if positive, outpatient polygraphy or polysomnography
- HRV measurement at home over several nights, to document parasympathetic regeneration
- Ferritin, vitamin D, B12, magnesium, selenium, iodine, TSH with fT3 and fT4, hs-CRP as inflammation marker
- Evening and morning cortisol, 4-point daily profile if HPA dysregulation is suspected
- For women: progesterone, estradiol, cycle-dependent, and DHEA
- Stool analysis for dysbiosis, parasites, histamine breakdown (DAO)
- Trauma screening: when REM is chronically fragmented, the body is asking about something older
HRV: the window into your night that you can have at home
Now to a topic that has often surprised me in practice. I analyze the sleep of my patients through heart-rate variability, HRV. Across several nights. At home. In their own bed. And I get information from it that comes very close to the sleep lab in many dimensions.
Why does this work? Because your heart beats differently in every sleep stage. In deep sleep it becomes slow, very regular, variability rises. In REM it becomes irregular, breathing becomes more chaotic, the sympathetic system mixes in. In waking: different again. The pattern of the heart rhythm tells you which sleep stage is happening right now.
Radha, Fonseca and colleagues validated a sleep-staging model based on heart-rate variability against polysomnography in Scientific Reports in 2019.
What they found: across 292 participants and 584 nights, the HRV-based algorithm reached an agreement with the gold standard PSG of about 77 percent accuracy on four sleep classes. The spread was considerable, however, and Cohen's kappa was 0.61, which is only moderate agreement. The authors themselves note that performance can decline in people aged 50 and over. And a disclosure belongs with it: all the authors worked for a manufacturer of sleep-tracking technology.
What this means for you: we can approximate your sleep architecture without you having to spend a night in a strange bed with electrodes on your forehead. And we can do it across several nights, not just one. But an approximation is not a measurement. Where breathing is the question, the sleep lab remains the place for it.
Radha M, Fonseca P, Moreau A et al. Sleep stage classification from heart-rate variability using long short-term memory neural networks. Sci Rep. 2019;9:14149. DOI: 10.1038/s41598-019-49703-y- Measures brain waves, airflow, oxygen saturation, leg movements very precisely
- Indispensable for suspected apnea, narcolepsy, parasomnias
- First-night effect: a night in the lab is not your night at home
- Usually only one or two nights, large organizational effort
- Sleep stages with good approximation, parasympathetic regeneration measured precisely
- Several nights, patterns instead of a snapshot, weekend vs. weekday rhythm
- No foreign environment, no wiring, your real sleep behavior
- Complements PSG, does not replace it when apnea is suspected
I do not use HRV to prove that you sleep badly. You know that yourself. I use it to see when your body is not sleeping. When it falls out of REM. Whether your parasympathetic system becomes dominant at all. What your deep-sleep density looks like at three. These patterns are often what makes the diagnosis possible in the first place.
For many questions you do not need a sleep lab. You need a measurement method that means you, in your bed, across several nights. HRV can do that. But if there are signs of sleep apnea, narcolepsy or a parasomnia, HRV cannot replace the sleep lab. Then the path leads first into polygraphy or polysomnography, and HRV comes in afterwards.
The causes nobody expects
I have worked with many people on sleep problems over the past years. And I have learned that the causes often sit in places where nobody looks for them. Classical sleep medicine looks at the brain, the breathing, the bed. The functional and KPNI view also looks at the gut, the liver, the hormones, at biographical stories that are still awake at night.
Nocturnal hypoglycemiaThe sugar that crashes at 3am
What looks like panic can also be falling blood sugar that adrenaline and cortisol respond to. A CGM measurement over 14 days can show more here than a single blood draw. That does not rule out a panic disorder. Both belong looked at.
ParasitesWhen someone is still awake in the gut
Enterobius classically becomes symptomatic at night. Whether intestinal parasites play a role in an isolated sleep disorder is not scientifically settled. Blastocystis is also found in many people without complaints. I mention it only because I keep it in mind in individual cases, not because it is an established connection.
Trauma and PTSDREM that still carries the old material
Fragmented REM phases, nightmares, early-morning startles. Sleep problems are very common in post-traumatic stress. For objectively measured sleep parameters the data are less clear than for self-reported ones. Trauma therapy can improve sleep alongside, when the trauma is the driving factor.
ThyroidMetabolism that does not switch off at night
Hashimoto can go in both directions. Latent hyperthyroidism can drive the heart rate up at night. Hypothyroidism with low fT3 can reduce deep sleep. TSH alone is not enough.
Progesterone deficiencyGABA without its partner
Allopregnanolone, a breakdown product of progesterone, can strengthen the GABA-A receptor, similar to the way sedatives do, only endogenously and rhythmically. Perimenopausal trouble staying asleep can therefore be a GABA-A story and not only a melatonin story.
Liver detoxificationThe night as a cleaning shift
Phase 2 detoxification of the liver follows circadian peaks. Alcohol, medication, xenoestrogens and chronic inflammation can put a heavy load on this shift between 1 and 3. In humans this is not established. It is a consideration I keep in mind during the history.
Psychological burdenThe day you did not close
Unspoken conflicts, untaken tears, undecided choices become loud at night. The default mode network activates, the medial prefrontal cortex keeps thinking. The soul only comes to rest when the day takes a form.
Too little movementA body that is not tired
Kredlow showed meta-analytically in 2015: physical activity improves sleep with moderate to clear effect sizes. A body that was not asked anything during the day cannot deeply let go at night.
The list is incomplete. It is meant to show you something else. If everything in your case was within the reference range and you still do not recover, that does not mean the measurement was wrong. It can mean that additional parameters are missing. Or that a value sits within the reference range but not in the range where people tend to feel well. That is an addition, not a correction.
I do not want to pretend in this article that everything is equally well documented. It is not. Hyperarousal, perimenopause sleep, nocturnal hypoglycemia in people with diabetes and the connection between blue light and melatonin are supported by well-designed human studies. Anthroposophic remedies, the TCM organ clock and the role of intestinal parasites in isolated insomnia are clinical experience plus mechanistic plausibility. I use them when they fit, and I tell you transparently what I know and what I suspect. Only that way can medicine stay honest.
Rhythm as the foundation: light, blue light, movement
Now to the part you find in every sleep guide. I write it anyway because it is important. But I write it with one caveat up front: sleep hygiene alone almost never solves your sleep disorder. It is foundation, not therapy. If your foundation is leaky, no roof helps. If your foundation stands, that does not mean a house has been built on it yet.
Light in the morning, darkness in the evening
Your suprachiasmatic nucleus in the hypothalamus is the central pacemaker. It reads light through special ganglion cells in the retina that respond most sensitively to blue between 460 and 480 nanometers. Bright light in the morning can stabilize your rhythm, and outdoors 10 to 20 minutes is often enough. Strong blue screen light in the evening can push it back. If you have a bipolar illness, a retinal condition or medication that makes you light-sensitive, discuss light therapy with a doctor first.
Anne-Marie Chang and the Harvard team measured in 2015 in PNAS what two hours of reading on an iPad before sleep do.
What they found: those reading on the light-emitting device took longer to fall asleep, were less sleepy in the evening, released less melatonin, had a later-timed internal clock and were less alert the next morning than after the printed book.
What this means for you: if you scroll on your phone late in the evening, your brain can misjudge the time of day. Melatonin can come later, sleep can shift back, and the next morning can feel heavier.
Chang AM et al. Evening use of light-emitting eReaders negatively affects sleep. PNAS. 2015;112(4):1232–1237. DOI: 10.1073/pnas.1418490112Movement as foundation, not as a trick
Kredlow and colleagues published a meta-analysis of 23 randomized studies in 2015. Physical activity improves sleep parameters with effect sizes that are clinically relevant. Strength training and endurance both work. High-intensity training right before bed is too activating for many. Moderate movement in the afternoon or early evening seems to be the sweet spot.
The basics, in one sentence
Sleep hygiene, in brief
- Get outside within the first hour of the morning, 10 to 20 minutes are enough
- Last big meal about three hours before bed, but do not sleep on an empty stomach if you tend toward nocturnal hypoglycemia
- Caffeine ideally only until midday, the half-life is very individual
- Alcohol in the evening is one of the most common disruptors of staying asleep, it can make falling asleep easier and can make the second half of the night restless
- From 8pm onwards dimmed, warm light, screen on night mode or glasses with a blue-light filter for evening work
- Bedroom on the cool side, for many people that range is around 16 to 18 degrees, plus dark, quiet, no work in bed
- As far as possible the same bedtime, also on weekends, a stable rhythm can matter just as much as the sheer number of hours
The bridges: what can help at night
I am deliberately not going to give doses here. Dosing belongs in the consultation, not in a blog. But I would like to show you the directions we can go in the practice. It is always a combination of biochemistry, nervous system, and rhythm.
On magnesium there is a small study in older people with insomnia that points to a favourable effect (Abbasi 2012). On glycine there is a small investigation in which time to fall asleep became shorter and participants rated their sleep as subjectively better (Yamadera 2007). These are pointers, not robust evidence. And neither substance is free of interactions. With impaired kidney function magnesium belongs in the plan only after medical advice, because it can accumulate, and it can impair the absorption of certain antibiotics and of thyroid hormones, which is why spacing them apart makes sense. Vitamin D, B6, zinc and selenium are co-factors of many synthesis steps. Depending on the history it can make sense to measure them as well. They are not a mandatory programme for every sleep workup.
Valerian showed moderate effects on falling asleep in the meta-analysis by Fernandez-San-Martin in 2010, methodically not flawless. Passiflora, lemon balm and hops are traditionally used. All of these can make you tired and can impair fitness to drive, and their effect can add to that of sedating medication and of alcohol. Anthroposophic combination remedies like Calmedoron and Bryophyllum follow a different approach: they aim not to dampen but to support rhythm. They are medicines too, and they can have side effects. A small observational study by Simões-Wüst and colleagues in 2015 in Integrative Cancer Therapies documented, in 20 evaluable cancer patients under Bryophyllum pinnatum, a fall in the Pittsburgh Sleep Quality Index from 12.2 to 9.1, so an improvement, but still not good sleep. There was no control group, and 6 of the 20 reported complaints such as fatigue, dry throat, agitation or digestive problems. A first data point, no more than that. None of this belongs in self-medication.
Ashwagandha (Langade 2019, a small randomized study) can reduce perceived stress. The other side belongs with it: in several European countries signals of liver injury under ashwagandha are being discussed, it can affect thyroid values, and it is not for use in pregnancy or while breastfeeding. Rhodiola, Schisandra and ginseng come into play situationally. The decisive factor is not the adaptogen itself, but whether it fits your findings and the rest of your medication. That belongs discussed, not tried out.
Whether a progesterone deficiency plays any role in your case can be shown by a cycle-dependent lab. What follows from that belongs in the consultation. German advertising law does not allow me to write publicly about prescription-only therapies. We decide that in conversation and on the basis of findings, and always after weighing contraindications and risks.
True freedom
Here is a sentence I will say to my daughter one day. Sleep is not a duty you fulfill. Sleep is the conversation between your body and yourself that you could not have during the day. When you sleep well you are freer. Not more efficient, not more productive, that comes as a side effect. Freer.
You make different decisions when you have slept. You are more patient. You are more courageous. You are yourself, and not an exhausted version of yourself.
What you can do differently from today
Which face are you carrying?
Write down for three days: when do I go to bed, when do I fall asleep, when do I wake up, how do I feel in the morning. After only three days you see the pattern. Falling asleep, staying asleep, or not rested. Therapy starts with this distinction.
Light and movement as foundation
One week, consistently: 20 minutes outside in the morning, ideally on an empty stomach. 30 minutes of moderate movement in the afternoon. From 8pm onwards warm light, screen with filter or away. This does not solve every sleep disorder. But it builds the foundation on which we can build everything else.
Measure, don't guess
If your sleep has been bad for weeks, you need data. HRV across several nights, a targeted lab for thyroid, cortisol, iron, vitamin D, and for women sex hormones. Gut feeling alone is often no longer enough in acute exhaustion, and that is okay. Data is not coldness. It is the way out of feeling powerless.
If you want not only to read but to start directly: below this article you will find the option to book an appointment. Then we will look together at which face your night is carrying. And what we can do about it together.
Sources and context
- American Academy of Sleep Medicine. International Classification of Sleep Disorders, 3rd ed. (ICSD-3), Darien IL, 2014. Guideline
- AWMF S3 Guideline Insomnia in Adults. Registry no. 063-003, Version 2017, valid until 2022. German Society for Sleep Research and Sleep Medicine. Guideline
- Kocevska D, Lysen TS, Dotinga A et al. Sleep characteristics across the lifespan in 1.1 million people from the Netherlands, United Kingdom and United States. Nat Hum Behav. 2021;5(1):113–122. DOI: 10.1038/s41562-020-00965-x Meta-analysis
- Benjafield AV, Ayas NT, Eastwood PR et al. Estimation of the global prevalence and burden of obstructive sleep apnoea. Lancet Respir Med. 2019;7(8):687–698. DOI: 10.1016/S2213-2600(19)30198-5 Epidemiology
- Riemann D, Spiegelhalder K, Feige B et al. The hyperarousal model of insomnia: a review of the concept and its evidence. Sleep Med Rev. 2010;14(1):19–31. DOI: 10.1016/j.smrv.2009.04.002 Review
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Context and transparency: for every statement I name the source and its level of evidence, so that you can look it up yourself. For anthroposophic combination remedies there are so far no published human studies with sleep as a primary endpoint, for Bryophyllum there is a single small observational study without a control group. The role of intestinal parasites in isolated insomnia is largely clinical experience, not a controlled study. The TCM organ clock as an exact time grid is not scientifically validated in this form, while the underlying circadian cell biology is well documented, although in humans in less detail than in animal models. I make this gradation deliberately visible so that you can place every statement according to its evidentiary weight. And finally the most important point: this article is general information. It does not replace an individual medical examination, a diagnosis or a treatment, and it is not an instruction for self-treatment.