Sanandarhea/ Vision of Life

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healing your inner aspects-
finding your destiny-
manifesting your Vision of Life-
living yourself❣

*Heilung innerer Aspekte*
*deine Bestimmung erkennen*
*manifestieren deiner Lebensvision*
*dich selbst leben*

MYSTERIOUS CELLS IN OUR BODIES May this cells in our bodies be another explanation for transgenerational traumas?What do...
06/01/2026

MYSTERIOUS CELLS IN OUR BODIES

May this cells in our bodies be another explanation for transgenerational traumas?
What do you think about it?

"You carry literal pieces of your mom—and maybe your grandma, and your siblings, and your aunts and uncles.

Some 24 years ago, Diana Bianchi peered into a microscope at a piece of human thyroid and saw something that instantly gave her goosebumps. The sample had come from a woman who was chromosomally XX. But through the lens, Bianchi saw the unmistakable glimmer of Y chromosomes—dozens and dozens of them. “Clearly,” Bianchi told me, “part of her thyroid was entirely male.”

The reason, Bianchi suspected, was pregnancy. Years ago, the patient had carried a male embryo, whose cells had at some point wandered out of the womb. They’d ended up in his mother’s thyroid—and, almost certainly, a bunch of other organs too—and taken on the identities and functions of the female cells that surrounded them so they could work in synchrony. Bianchi, now the director of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, was astonished: “Her thyroid had been entirely remodeled by her son’s cells,” she said.

The woman’s case wasn’t a one-off. Just about every time an embryo implants and begins to grow, it dispatches bits of itself into the body housing it. The depositions begin at least as early as four or five weeks into gestation. And they settle into just about every sliver of our anatomy where scientists have checked—the heart, the lungs, the breast, the colon, the kidney, the liver, the brain. From there, the cells might linger, grow, and divide for decades, or even, as many scientists suspect, for a lifetime, assimilating into the person that conceived them. They can almost be thought of as evolution’s original organ transplant, J. Lee Nelson, of the Fred Hutchinson Cancer Center in Seattle, told me. Microchimerism may be the most common way in which genetically identical cells mature and develop inside two bodies at once.

These cross-generational transfers are bidirectional. As fetal cells cross the placenta into maternal tissues, a small number of maternal cells migrate into fetal tissues, where they can persist into adulthood. Genetic swaps, then, might occur several times throughout a life. Some researchers believe that people may be miniature mosaics of many of their relatives, via chains of pregnancy: their older siblings, perhaps, or their maternal grandmother, or any aunts and uncles their grandmother might have conceived before their mother was born. “It’s like you carry your entire family inside of you,” Francisco Úbeda de Torres, an evolutionary biologist at the Royal Holloway University of London, told me."

Article by Katherine J. Wu








MUTTERMILCH ist ein Wunder!In 2008, Katie Hinde stood in a California primate lab staring at hundreds of milk samples. M...
28/11/2025

MUTTERMILCH ist ein Wunder!

In 2008, Katie Hinde stood in a California primate lab staring at hundreds of milk samples. Male babies got richer milk. Females got more volume. Science had missed half the conversation.
She was a postdoctoral researcher at the California National Primate Research Center, analyzing milk from rhesus macaque mothers. For months, she'd been measuring fat content, protein levels, mineral concentrations. The data showed something she hadn't expected: monkey mothers were producing completely different milk depending on whether they'd given birth to sons or daughters.
Sons received milk with higher concentrations of fat and protein—more energy per ounce. Daughters received more milk overall, with higher calcium levels. The biological recipe wasn't universal. It was customized.
Hinde ran the numbers again. The pattern held across dozens of mother-infant pairs. This wasn't random variation. This was systematic.
She thought about what she'd been taught in graduate school. Milk was nutrition. Calories, proteins, fats. A delivery system for energy. But if milk was just fuel, why would it differ based on the baby's s*x? Why would mothers unconsciously adjust the formula?
The answer shifted everything: milk wasn't passive. It was a message.
Hinde had arrived at this question through an unusual path. She'd earned her bachelor's degree in anthropology from the University of Washington, then completed her PhD at UCLA in 2008. While most lactation research focused on dairy cattle or developing infant formulas, Hinde wanted to understand what milk actually did in primate mothers and babies.
At UC Davis, she had access to the largest primate research center in the United States. She could collect milk samples at different stages of lactation, track infant development, measure maternal characteristics. She could ask questions that had never been systematically studied.
Like: why do young mothers produce milk with more stress hormones?
Hinde discovered that first-time monkey mothers produced milk with fewer calories but higher concentrations of cortisol than experienced mothers. Babies who consumed this high-cortisol milk grew faster but were more nervous and less confident. The milk wasn't just feeding the baby's body—it was programming the baby's temperament.
Or: how does milk respond when babies get sick?
Working with researchers who studied infant illness, Hinde found that when babies developed infections, their mothers' milk changed within hours. The white blood cell count in the milk increased dramatically—from around 2,000 cells per milliliter to over 5,000 during acute illness. Macrophage counts quadrupled. The levels returned to normal once the baby recovered.
The mechanism was remarkable: when a baby nurses, small amounts of the baby's saliva travel back through the ni**le into the mother's breast tissue. That saliva contains information about the baby's immune status. If the baby is fighting an infection, the mother's body detects the antigens and begins producing specific antibodies, which then flow back to the baby through the milk.
It was a dialogue. The baby's body communicated its needs. The mother's body responded.
Hinde started documenting everything. She collected milk from over 250 rhesus macaque mothers across more than 700 sampling events. She measured cortisol, adiponectin, epidermal growth factor, transforming growth factors. She tracked which babies gained weight faster, which were more exploratory, which were more cautious.
She realized she was mapping a language that had been invisible.
In 2011, Hinde joined Harvard as an assistant professor. She began writing about her findings, but she also noticed something troubling: almost nobody was studying human breast milk with the same rigor applied to other biological systems. When she searched publication databases, she found twice as many studies on erectile dysfunction as on breast milk composition.
The world's first food—the substance that had nourished every human who ever lived—was scientifically neglected.
She started a blog: "Mammals Suck...Milk!" The title was deliberately provocative. Within a year, it had over a million views. Parents, clinicians, researchers started asking questions. What bioactive compounds are in human milk? How does milk from mothers of premature babies differ from milk produced for full-term infants? Can we use this knowledge to improve formulas or help babies in NICUs?
Hinde's research expanded. She studied how milk changes across the day (fat concentration peaks mid-morning). She investigated how foremilk differs from hindmilk (babies with bigger appetites who nurse longer get higher-fat milk at the end of feeding). She examined how maternal characteristics—age, parity, health status, social rank—shaped milk composition.
In 2013, she created March Mammal Madness, a science outreach event that became an annual tradition in hundreds of classrooms. In 2014, she co-authored "Building Babies." In 2016, she received the Ehrlich-Koldovsky Early Career Award from the International Society for Research in Human Milk and Lactation for making outstanding contributions to the field.
By 2017, when she delivered her TED talk, she could articulate what she'd discovered across a decade of research: breast milk is food, medicine, and signal. It builds the baby's body and fuels the baby's behavior. It carries bacteria that colonize the infant gut, hormones that influence metabolism, oligosaccharides that feed beneficial microbes, immune factors that protect against pathogens.
More than 200 varieties of oligosaccharides alone. The baby can't even digest them—they exist to nourish the right community of gut bacteria, preventing harmful pathogens from establishing.
The composition is as unique as a fingerprint. No two mothers produce identical milk. No two babies receive identical nutrition.
In 2020, Hinde appeared in the Netflix docuseries "Babies," explaining her findings to a mass audience. She'd moved to Arizona State University, where she now directs the Comparative Lactation Lab. Her research continues to reveal new dimensions of how milk shapes infant outcomes from the first hours of life through childhood.
She works on precision medicine applications—using knowledge of milk bioactives to help the most fragile infants in neonatal intensive care units. She consults on formula development, helping companies create products that better replicate the functional properties of human milk for mothers who face obstacles to breastfeeding.
The implications extend beyond individual families. Understanding milk informs public health policy, workplace lactation support, clinical recommendations. It reveals how maternal characteristics, environmental conditions, and infant needs interact in real time through a biological messaging system that's been evolving for 200 million years—longer than dinosaurs.
Katie Hinde didn't just study milk. She revealed that the most ancient form of nourishment was also the most sophisticated. What science had treated as simple nutrition was actually a dynamic, responsive communication between two bodies—a conversation that shapes human development one feeding at a time.

24/11/2025

DATES
✍🏻 The effect of late pregnancy consumption of date fruit on labour and delivery by O Al‑Kuran et al. (2011) — DOI: 10.3109/01443615.2010.522267
🍎

An incredible study found that women who ate 6 dates a day in the last 4 weeks of pregnancy were...

• 74% more dilated when they arrived at the hospital
• Had a 77% shorter first stage of labor
• And were 42% less likely to need a C-section

So what makes dates so powerful?

Dates are packed with nutrients that actually prepare the cervix and uterus for labor.
They influence oxytocin receptors, which means the body responds more effectively to the natural hormones that trigger labor.

They also contain prostaglandins that help ripen (soften and thin) the cervix,
and tannins that encourage stronger, more efficient contractions.

On top of that, dates provide natural sugars and fats for energy during labor,
plus calcium and serotonin to support the body through the intensity of birth.

Some studies even suggest dates make the uterus more sensitive to oxytocin—
leading to smoother, more effective contractions and shorter labors.

This is also why women who eat dates late in pregnancy are far less likely to need a C-section.

The most common recommendation is to start eating 6 dates a day from 37 weeks until birth.

I’m a midwife and a home birthing mama,
and I was encouraged to eat dates in my own pregnancy and honestly, I think it helped me.

Share this with a pregnant mama, or save it for later 🖤

Did you eat dates in late pregnancy?
What was your experience?

WIE T3 ENTSTEHT UND WARUM LEBER UND DARM SO WICHTIG SIND:"Die Schilddrüse ist ein kleines, aber sehr leistungsstarkes Or...
21/11/2025

WIE T3 ENTSTEHT UND WARUM LEBER UND DARM SO WICHTIG SIND:

"Die Schilddrüse ist ein kleines, aber sehr leistungsstarkes Organ im vorderen Halsbereich. Sie produziert zwei wichtige und zentrale Hormone:

T4 (Thyroxin) – das Speicherhormon oder die inaktive Vorstufe

T3 (Trijodthyronin) – das biologisch aktive Hormon

Damit der Körper auf Energie, Temperatur oder Belastung reagieren kann, braucht er vor allem T3, denn nur T3 kann in den Zellen an den Hormonrezeptoren andocken und dort Stoffwechselprozesse aktivieren.

Die Schilddrüse selbst produziert ungefähr 80 bis 90 Prozent T4 und nur 10 bis 20 Prozent T3.

Das bedeutet: Der größte Teil des aktiven T3 entsteht nicht in der Schilddrüse, sondern durch Umwandlungsprozesse in anderen Organen, vor allem in Leber und Darm.

Damit T4 aktiv wird, muss es in T3 umgewandelt werden.
Dieser Vorgang heißt Dejodierung, weil dabei ein Jodatom abgespalten wird (T4 in T3).
Das geschieht durch spezielle Enzyme, die Dejodasen heißen.

Es gibt drei Arten dieser Enzyme:
• Typ I (v. a. in der Leber, Niere und Schilddrüse)
• Typ II (v. a. im Gehirn, Muskel und Fettgewebe)
• Typ III (wandelt T4 in reverse T3, eine inaktive Form)

Der Körper steuert diese Enzyme fein abgestimmt. Je nach Situation (z. B. Stress, Krankheit, Fasten) kann er die Aktivität der Dejodasen verändern, so entscheidet der Körper, wie viel aktives T3 wirklich im Umlauf ist.

Etwa 60 Prozent des gesamten T3 entstehen in der Leber.
Die Leber ist also das Hauptorgan für die Aktivierung der Schilddrüsenhormone.

Damit das funktioniert, braucht sie:
ausreichend Nährstoffe, vor allem Selen (Cofaktor der Dejodasen), Zink, Eisen und Magnesium, eine gute Entgiftungsleistung
ausreichende Eiweißzufuhr (für den Hormontransport und Enzymbildung)
eine gesunde Durchblutung und Gallenfunktion

Wenn die Leber überlastet ist, etwa durch Medikamente, Alkohol, hormonelle Belastung, Zucker, Entzündungen oder Schadstoffe, wird die Umwandlung von T4 zu T3 gehemmt.
Dann bleibt mehr T4 ungenutzt im Blut, während weniger aktives T3 entsteht

Der Körper kann stattdessen vermehrt rT3 (reverse T3) bilden.
Das ist eine inaktive Variante von T3, die an den gleichen Rezeptoren andockt, sie aber blockiert, ähnlich wie ein Platzhalter. So entsteht trotz scheinbar normaler Schilddrüsenwerte eine funktionelle Unterfunktion: Die Hormone sind da, aber sie wirken nicht.

Der Darm ist bei der Schilddrüsenfunktion viel wichtiger, als man lange dachte.
Etwa 20 Prozent des zirkulierenden T3 entstehen durch Umwandlungsprozesse im Darm.

Hier wirken vor allem die Darmbakterien (Mikrobiom) mit.
Bestimmte Bakterienarten können T4 zu T3 aktivieren, andere sind daran beteiligt, die Hormone aus der Galle und dem enterohepatischen Kreislauf wieder zurück in den Körper zu bringen.

Wenn die Darmflora gestört ist, durch Antibiotika, ungesunde Ernährung, chronischen Stress, Entzündungen oder eine undichte Darmschleimhaut („leaky gut“), sinkt die Umwandlungsleistung, die Leber wird stärker belastet und es können Entzündungsstoffe entstehen, die wiederum die Schilddrüsenrezeptoren hemmen.

Ein gesunder Darm ist also eine Voraussetzung für eine gute T3-Versorgung. Ohne eine stabile Darmflora kann selbst die beste Schilddrüsenfunktion nicht optimal wirken.

Neben Leber und Darm findet auch in anderen Geweben eine lokale Umwandlung statt:
in den Muskeln (wichtig für Energie und Muskelkraft)
im Gehirn (relevant für Konzentration, Stimmung, Gedächtnis)
im braunen Fettgewebe (für Wärmeproduktion)
in Herz und Nieren

Diese lokale Umwandlung ermöglicht es dem Körper, fein abgestimmt auf seinen Energiebedarf zu reagieren
Zum Beispiel kann das Gehirn seine eigene T3-Produktion aufrechterhalten, selbst wenn der Blutspiegel niedrig ist. Eine Art Selbstschutz für die kognitive Funktion.

Viele Einflüsse können diesen Prozess blockieren oder verlangsamen:

Physische und psychische Belastungen:
• Chronischer Stress (erhöht Cortisol hemmt Dejodasen)
• Schlafmangel
• Entzündungen (z. B. Darm, Zähne, Gelenke)

Stoffwechsel- und Ernährungsfaktoren:
• Eiweißmangel
• Diäten, Fasten, Unterernährung
• Nährstoffmängel (Selen, Zink, Eisen, Vitamin A, D, B-Komplex)
• Überlastete Leber (Medikamente, Alkohol, Schadstoffe)
• Dysbiose oder leaky gut

Hormonelle Einflüsse:
• Hohe Östrogenspiegel (z. B. durch Pille oder Leberstau)
• Cortisolüberschuss (Stress, Nebennierenschwäche)
• Niedriges DHEA oder Progesteron

All das kann dazu führen, dass zu wenig aktives T3 gebildet wird, obwohl die Schilddrüse selbst gut arbeitet.

Die Schilddrüse ist also nicht isoliert zu betrachten.
Sie steht in enger Wechselwirkung mit der Leber (Stoffwechselzentrum und Entgiftungsorgan), dem Darm (Mikrobiom, Nährstoffaufnahme, Immunmodulation) und dem autonomen Nervensystem (Stressregulation, Cortisolsteuerung)

Ein dauerhaft überreiztes Nervensystem durch Stress, innere Unruhe, Überforderung kann die Hormonumwandlung bremsen und gleichzeitig die Leber belasten.
Das erklärt, warum viele Menschen mit Schilddrüsenproblemen sich in Stressphasen deutlich schlechter fühlen, obwohl ihre Laborwerte gleich bleiben.

Die Menge an aktivem T3 im Körper hängt weniger davon ab, wie viel die Schilddrüse produziert, sondern vielmehr davon, wie gut Leber und Darm funktionieren.
Eine überlastete Leber, eine gestörte Darmflora oder chronischer Stress können die Umwandlung blockieren und zu einem „versteckten“ T3-Mangel führen, auch bei normalen Laborwerten.

Deshalb ist eine ganzheitliche Sicht entscheidend:
Eine gesunde Verdauung, gute Nährstoffversorgung, Leberpflege und Stressregulation sind genauso wichtig für die Schilddrüsengesundheit wie das Organ selbst."

Obiger Text von Alexandra Nau -Heilpraktikerin- Danke!!!
🌟

Das Bild ist von 05/23 als bei mir in der Szintigrafie ein heißer Knoten befundet wurde.
Mit Ayurveda Medizin und Geduld habe ich alle damaligen Probleme in Griff bekommen.

Shankapushpi wurde mein treuer Begleiter, als es mal länger vergriffen war, hatte ich mir mal gleich 2kg aus Indien einführen lassen.

Falls du Unterstützung brauchst in stressigen Zeiten, kann ich dir diese Pflanze sehr empfehlen. Auch zur Steigerung der Gehirnleistung u.v.m.

Gerne gebe ich auch etwas von meiner großen Menge ab!

Bdi Interesse PN!

Negative thinking doesn’t just affect your mood—it physically alters your brain. Studies from major neuroscience centers...
17/11/2025

Negative thinking doesn’t just affect your mood—it physically alters your brain. Studies from major neuroscience centers show that chronic worry and rumination flood the brain with cortisol, the body’s main stress hormone. When cortisol stays high for long periods, it damages neurons, shrinks the hippocampus (your memory center), and weakens the prefrontal cortex, which controls logic, focus, and emotional stability. Over time, this slow chemical attack leads to poorer decision-making, heightened anxiety, and early cognitive decline.

What makes this even more dangerous is how negativity rewires the brain. Repeated pessimistic thoughts carve deeper neural pathways around fear, doubt, and worst-case scenarios, making these patterns automatic. Your brain literally becomes trained to look for danger—whether it’s real or not. But because the brain is plastic, the cycle can be reversed. Mindfulness, gratitude practices, reframing thoughts, and surrounding yourself with emotionally healthy people strengthen new neural circuits that protect memory, boost resilience, and improve long-term brain health.

Interrupting isn’t always a sign of rudeness. Research suggests that many people interrupt because of faster cognitive p...
15/11/2025

Interrupting isn’t always a sign of rudeness. Research suggests that many people interrupt because of faster cognitive processing, anxiety, or impulsivity rather than intentional disrespect. Those with quick processing speeds may form responses before others finish speaking, while anxious individuals worry they’ll forget their point if they wait. Studies also link impulsive interruptions to ADHD, where rapid idea flow and limited short-term retention make pausing difficult. In many cases, the brain is simply moving faster than the conversation.

Sources: Eysenck, M.W. (2012). Anxiety and Cognition; Barkley, R.A. (2015). Attention-Deficit Hyperactivity Disorder; YourTango (2024). People Who Can’t Stop Interrupting Usually Have These Reasons.

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Mein Angebot und Hintergrund

Ich bin gerne für dich und deine Anliegen da, bei Beziehungsthemen, ganz alltäglichen Themen oder beim Klären und Umsetzen deiner persönlichen Visionen, bei Fragen und Anliegen aus deinem beruflichen Kontext sowie auch in Krisen.

Settings: Einzelsitzungen, Paar- und Gruppensitzungen sowie Supervision und Beratung.

Als Psychotherapeutin setze ich mich für die Heilung von Ängsten, Depressionen und anderen psychische Erkrankungen ein. Deine Fragen und Herausforderungen haben Raum in Ruhe betrachtet und erkannt zu werden, um so in eine Lösung, Erleichterung und auch Heilung geführt zu werden! Dies ist mein Hauptberuf!

Auch die Auseinandersetzung mit Themen wie Tod und Spiritualität sind wesentlich in jedem Leben, um den eigenen Weg ganzheitlich betrachten zu können!