Brain Disease

La vida contemporánea nos brinda infinitas oportunidades de satisfacer nuestros deseos, aunque también numerosas tentaciones. Y en un mundo saturado de pantallas, inmersos en rutinas que no nos permiten alimentarnos adecuadamente, descansar o ejercitarnos, nuestros cerebros libran una dura batalla cuyos resultados nos han dejado más solitarios, ansiosos, deprimidos y propensos a las enfermedades y al sobrepeso. Pero no tenemos que vivir así.

Many people–maybe even most people—know someone who has what they call Alzheimer’s disease. Alzheimer’s seems to be everywhere. That people are living longer today—long enough for it to manifest itself—is often given as the reason for its prevalence. But some of those people who have puzzling brain changes are surprisingly young; in their fifties—the middle of their lives. And what they have is not the “traditional” Alzheimer’s disease.

Sebbene la principale preoccupazione relativa al COVID-19 riguardasse le sue conseguenze, soprattutto in termini di problemi respiratori, i progressi nella conoscenza di questa malattia hanno permesso di capire come i suoi effetti si estendono oltre i polmoni, e possono raggiungere ed influenzare il sistema nervoso. Questo testo affronta le conseguenze che il COVID-19 ha nel cervello, da una doppia prospettiva.

I have had Parkinson’s disease (PD) for 22 years. I am told I have a mild case, but it is still my PD, and I live with it 24/7. It would be a gross understatement to say my life was changed forever. Interestingly, many of these changes have made me a more compassionate, empathetic, and caring person. In part, this book was motivated by the following premise: Many of us will experience a life-changing event that will cause us to pause and reassess where we are, what we do, and why we do it. For some, it might be the death of a loved one or a personal tragedy.

It’s hard to know what’s meant to be healthy. If you read the news, you’ll see headlines praising a food one day, and then condemning it the next. You’ll see people selling you miracle cures for conditions that they’ve invented. You’ll realize that powerful industries control the information that’s given the most airtime, and that ultimately, you’re better off trying to find out the truth for yourself.

Dr. Matthias Ennenbach hat aus unzähligen Patientengesprächen ein allgemein gültiges Erklärungsmodell entwickelt, das die Psychosomatik aus der "Psychoecke" holt. Die erleichternde Botschaft: Jeder Mensch funktioniert psychosomatisch! Es gibt weder rein körperliche noch rein psychisch-nervliche Erkrankungen, sondern immer nur ein Wechselspiel von beidem. Und das lässt sich anschaulich darstellen.

La serie de libros Seis Anillos está interesada en analizar las complejidades del cerebro, y cómo mantenerlo en óptima salud. El cerebro es el centro de atención, y estos libros proporcionan información para ayudar a comprender cómo los factores psicológicos y fisiológicos afectan a su salud y a su rendimiento óptimo.

If you have certain illnesses or symptoms, a poorly functioning vagus nerve could be the culprit; that’s particularly true of inflammatory and autoimmune diseases. This nerve is the longest cranial nerve in the body, running from the brain stem to the colon and affecting many organs in the body. The good news is that you can take simple actions to stimulate your vagus nerve to function better. This information can be especially important for people with treatment-resistant depression; vagus nerve stimulation (VNS) seems to reset chemical imbalances in the mood centers of the brain.

Are you struggling with fatigue, brain fog, or depression? Is there something wrong with your stomach or gut? It may be your vagus nerve malfunctioning! The vagus nerve is a large, branching nerve that begins in your brain and sends signals to your body’s major organs such as your heart, lungs, and digestive system. It’s responsible for your heart rate, digestion, reaction to stress, and many other things. That’s why, a lot can go wrong in your body if the vagus nerve doesn’t function perfectly.

Di fronte a una malattia per la quale non è ancora disponibile un rimedio risolutivo, pazienti, familiari e medici si trovano a intraprendere un cammino lungo e impegnativo. Che cos'è il Parkinson? Come si manifesta? Come è possibile affrontarlo? Il libro descrive le varie fasi della malattia, gli aspetti diagnostici, le terapie, ma anche le modalità per rendere meno ardua la vita dei malati e dei loro familiari, senza dimenticare uno sguardo al domani e alla ricerca.

This quick-consult self-help book goes beyond describing which herbs, vitamins, and nutrients help specific ailments. In this book, you’ll find the best ways to take these products, as well as the correct dosages. You’ll also discover a host of other modalities like exercise, mindfulness, and meditation that alleviate the distress associated with anxiety and stress. This practical guide is formulated to give you the help you need in an easy-to-use format.

Explicar el mundo a su hijo Cris, que nació con parálisis cerebral hace más de treinta años, es para Andrés Aberasturi una tarea dura y dolorosa. Pero el autor de estas páginas honestas y sin adornos, que solo pretende dejar testimonio de una parte de su verdad, la considera esencial para combatir el desasosiego. "Andrés hace hablar a Cris. A sus manos, a su silla, a sus movimientos, a su siempre implorada sonrisa, a su mutismo, Andrés les da vida," como bien explica Javier Sádaba en el prólogo.

Imagine what it would be like to one day wake up and find that you were suddenly completely blind. This is what happened to Vanessa Potter. Her condition is unique. It has no name. Over the course of the next six months, Vanessa slowly recovered her vision. This mesmerising account tells the story of Patient H69 in her own words, based on these detailed diaries she kept during her time of blindness and through the scientific research that was to follow.

Lina was a precocious toddler - charming, chatty, joyful. At the age of three, in the aftermath of her second MMR vaccine, first came a seizure, and then, to her parents’ horror, the loss of Lina’s ability to play, use language, and control her impulses. Over the next few years they continued to lose Lina. She communicated her acute discomfort by biting, screaming, hitting, laughing maniacally, and throwing violent tantrums.

The Thinking Moms’ Revolution (TMR) is a group of 23 moms (and one awesome dad) from Montana to Malaysia who all have children with developmental disabilities. Initially collaborating online about therapies, biomedical intervention, alternative medicine, special diets, and doctors on the cutting edge of treatment approaches to an array of chronic and developmental disabilities, such as autism, sensory processing disorders, food allergies, ADHD, asthma, and seizures, they've come together into something far more substantial.

Written with a poignant blend of honesty, dry humor, faith, and inquisitiveness, Smiling Again is a story of the persistence of life and beauty in spite of pain. Sally recounts the shock of diagnosis, a long and painful recovery from invasive brain surgery, her eventual retirement due to disability, and ultimately contentment and acceptance of a new life journey.

While fighting an aggressive brain tumor, Deirdre must care for her mother with advanced Alzheimer’s, raise her teenage daughter, and help her husband chase a new dream - opening a barbecue restaurant. Her greatest defense is her sense of humor in this tender memoir chronicling life struggles that are often tragic - but can still be very funny. Grab a tissue and take a ride as one batty broad battles her way through the tragicomic trials of her most perilous adventure yet - brain cancer.

My first migraine hit me in high school, and I was unsure what to do. I have a pretty high pain tolerance from being picked on, beat up, and the everyday of having older siblings. I can put up with bumps, bruises, and scrapes, but one day when I got home from school a migraine hit me like a spike in my brain. I had bright lights in my field of view which I found out about later was called an “aura” then I started to see stars. Then the PAIN HIT!

Before you read this, think for a moment: Do you know where your keys are? What was the name of that last visitor to your office? We rely on memory every moment of the day, but many of us constantly complain that we're losing it faster than we ever imagined.

Are you struggling to understand why your neurodivergent loved one thinks and acts the way they do? Does ignorance in autism leave you feeling frustrated, isolated, and unsure of how to bridge the communication gap? In a world where autism is often misunderstood, not knowing how to approach a loved one who is unaware of their condition can leave you doubting whether you can provide them with the life that they deserve.