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Alzheimer's is a type of dementia that causes problems with memory, thinking and behavior. Symptoms usually develop slowly and get worse over time, becoming severe enough to interfere with daily tasks. Alzheimer's disease is the most common cause of dementia. The word dementia describes a set of symptoms that can include memory loss and difficulties with thinking, problem-solving or language. These symptoms occur when the brain is damaged by certain diseases, including Alzheimer's disease. This factsheet describes the symptoms of Alzheimer's disease, how it is diagnosed, and the factors that can put someone at risk of developing it. It also describes the treatments and support that are currently available. Alzheimer's disease, named after the doctor who first described it (Alois Alzheimer), is a physical disease that affects the brain. There are more than 520, 000 people in the UK with Alzheimer's disease. During the course of the disease, proteins build up in the brain to form structures called 'plaques' and 'tangles'. This leads to the loss of connections between nerve cells, and eventually to the death of nerve cells and loss of brain tissue. People with Alzheimer's also have a shortage of some important chemicals in their brain. These chemical messengers help to transmit signals around the brain. When there is a shortage of them, the signals are not transmitted as effectively. As discussed below, current treatments for Alzheimer's disease can help boost the levels of chemical messengers in the brain, which can help with some of the symptoms. Alzheimer's is a progressive disease. This means that gradually, over time, more parts of the brain are damaged. As this happens, more symptoms develop. They also become more severe. Symptoms The symptoms of Alzheimer's disease are generally mild to start with, but they get worse over time and start to interfere with daily life. There are some common symptoms of Alzheimer's disease, but it is important to remember that everyone is unique. Two people with Alzheimer's are unlikely to experience the condition in exactly the same way. For most people with Alzheimer's, the earliest symptoms are memory lapses. In particular, they may have difficulty recalling recent events and learning new information. These symptoms occur because the early damage in Alzheimer's is usually to a part of the brain called the hippocampus, which has a central role in day-to-day memory. Memory for life events that happened a long time ago is often unaffected in the early stages of the disease. Memory loss due to Alzheimer's disease increasingly interferes with daily life as the condition progresses. The person may: lose items (eg keys, glasses) around the house struggle to find the right word in a conversation or forget someone's name forget about recent conversations or events get lost in a familiar place or on a familiar journey forget appointments or anniversaries. Although memory difficulties are usually the earliest symptoms of Alzheimer's, someone with the disease will also have – or go on to develop – problems with other aspects of thinking, reasoning, perception or communication. They might have difficulties with: language – struggling to follow a conversation or repeating themselves visuospatial skills – problems judging distance or seeing objects in three dimensions; navigating stairs or parking the car become much harder concentrating, planning or organising – difficulties making decisions, solving problems or carrying out a sequence of tasks (eg cooking a meal) orientation – becoming confused or losing track of the day or date. A person in the earlier stages of Alzheimer's will often have changes in their mood. They may become anxious, irritable or depressed. Many people become withdrawn and lose interest in activities and hobbies.
Aphthae (or canker sores) are ulcers that are typically round or oval and occur on the inside of the lips or underneath the tongue. They are very common and affect between 30-60% of the population. The cause of aphthae is still uncertain but hereditary factors are certainly significant with approximately 40% of people who get them having a family history of aphthae. The main causes of aphthous ulcers include: emotional stress and lack of sleep, local injury by an accidental self-inflicted bite, nutritional/vitamin deficiencies (especially iron and folic acid, vitamins B1, B2, B6, B12 and vitamin C), the menstrual cycle and certain foods (including coffee and chocolate). Aphthae can be divided into three types of ulcers.
Ankylosing spondylitis is a type of arthritis that affects the spine. Ankylosing spondylitis symptoms include pain and stiffness from the neck down to the lower back. The spine's bones (vertebrae) may grow or fuse together, resulting in a rigid spine. These changes may be mild or severe, and may lead to a stooped-over posture. Early diagnosis and treatment helps control pain and stiffness and may reduce or prevent significant deformity. Who Is Affected by Ankylosing Spondylitis? Ankylosing spondylitis affects about 0.1% to 0.5% of the adult population. Although it can occur at any age, spondylitis most often strikes men in their teens and 20s. It is less common and generally milder in women and more common in some Native American tribes. What Are the Symptoms of Ankylosing Spondylitis? The most common early symptoms of ankylosing spondylitis include: Pain and stiffness. Constant pain and stiffness in the low back, buttocks, and hips that continue for more than three months. Spondylitis often starts around the sacroiliac joints, where the sacrum (the lowest major part of the spine) joins the ilium bone of the pelvis in the lower back region. Bony fusion. Ankylosing spondylitis can cause an overgrowth of the bones, which may lead to abnormal joining of bones, called "bony fusion." Fusion affecting bones of the neck, back, or hips may impair a person's ability to perform routine activities. Fusion of the ribs to the spine or breastbone may limit a person's ability to expand his or her chest when taking a deep breath. Pain in ligaments and tendons. Spondylitis also may affect some of the ligaments and tendons that attach to bones. Tendonitis (inflammation of the tendon) may cause pain and stiffness in the area behind or beneath the heel, such as the Achilles tendon at the back of the ankle.
MIRACULOUS SUCCESSFULLY CURED critical Case of 2 BRAIN TUMOUR GRANULOMATOS BY MODERN HOMOEOPATHY WITHOUT SURGERY OUR AIM - COMPLETE, PERMANENT , EASY, SAFE , FAST & COSTEFFECTIVE PERMANENT MODERN HOMOEOPATHY CURE Thanks with Regards DR ARPIT CHOPRA (MD HOMOEOPATHY) Chief Consultant Homoeopath & Biochemic AAROGYA SUPERSPECIALITY MODERN HOMOEOPATHIC CLINIC(Computerised) 102, First Floor, Krishna Tower, Opposite Curewell Hospital, Newpalasia, Indore (M.P.) Mob 9713092737 / 9713037737/ 9907527914(whats up no) PH - 0731-2532737, 3961737 website-
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MODERN HOMEOPATHY CURE IN COMPLETE, PERMANENT , EASY, SAFE , FAST & COSTEFFECTIVE MODE. Addison’s disease, also known as primary adrenal insufficiency and hypocortisolism, is a long-term endocrine disorder in which the adrenal glands do not produce enough steroid hormones.[1] Symptoms generally come on slowly and may include abdominal pain, weakness, and weight loss. Darkening of the skin in certain areas may also occur. Under certain circumstances, an adrenal crisis may occur with low blood pressure, vomiting, lower back pain, and loss of consciousness. An adrenal crisis can be triggered by stress, such as from an injury, surgery, or infection.[1] Addison's disease arises from problems with the adrenal gland such that not enough of the steroid hormone cortisol and possibly aldosterone are produced, [1] most often due to damage by the body's own immune system in the developed world and tuberculosis in the developing world.[4] Other causes include certain medications, sepsis, and bleeding into both adrenal glands.[1][4] Secondary adrenal insufficiency is caused by not enough adrenocorticotropic hormone (ACTH) (produced by the pituitary gland) or CRH (produced by the hypothalamus). Despite this distinction, adrenal crises can happen in all forms of adrenal insufficiency. Addison's disease is generally diagnosed by blood tests, urine tests, and medical imaging. DR ARPIT CHOPRA (MD HOMOEOPATHY) Chief Consultant Homoeopath & Biochemic AAROGYA SUPERSPECIALITY MODERN HOMOEOPATHIC CLINIC(Computerised) website-
Amenorrhoea is the absence of menstrual periods. Apart from during childhood, pregnancy, breastfeeding and menopause, the absence of periods may be caused by a problem with the reproductive system. One of the most common causes of amenorrhoea is when the body’s hormones are disrupted. The body’s ability to make the female sex hormones oestrogen and progesterone can be affected by a range of factors, including certain reproductive disorders, losing or putting on weight, emotional stress or exercising too much. It may be physiological as before the menarche, after the menopause or in pregnancy, or it may be postoperative if the patient has had a hysterectomy. Amenorrhoea can be divided into primary and secondary: Primary amenorrhoea is when menses have not occurred by the time of the expected menarche. This may be taken as age 14 years in the absence of secondary sexual characteristics, but it is worth waiting until age 16 years if other features are developing normally. Secondary amenorrhoea is when menstruation has previously occurred but it has stopped for at least six consecutive months.
Acromegaly is a hormonal disorder that results from too much growth hormone (GH) in the body. The pituitary, a small gland in the brain, makes GH. In acromegaly, the pituitary produces excessive amounts of GH. Usually the excess GH comes from benign, or noncancerous, tumors on the pituitary. These benign tumors are called adenomas. Acromegaly is most often diagnosed in middle-aged adults, although symptoms can appear at any age. If not treated, acromegaly can result in serious illness and premature death. Acromegaly is treatable in most patients, but because of its slow and often "sneaky" onset, it often is not diagnosed early or correctly. The most serious health consequences of acromegaly are type 2 diabetes, high blood pressure, increased risk of cardiovascular disease, and arthritis. Patients with acromegaly are also at increased risk for colon polyps, which may develop into colon cancer if not removed. When GH-producing tumors occur in childhood, the disease that results is called gigantism rather than acromegaly. A child's height is determined by the length of the so-called long bones in the legs. In response to GH, these bones grow in length at the growth plates—areas near either end of the bone. Growth plates fuse after puberty, so the excessive GH production in adults does not result in increased height. However, prolonged exposure to excess GH before the growth plates fuse causes increased growth of the long bones and thus increased height. Pediatricians may become concerned about this possibility if a child's growth rate suddenly and markedly increases beyond what would be predicted by previous growth and how tall the child's parents are. What are the symptoms of acromegaly? The name acromegaly comes from the Greek words for "extremities" and "enlargement, " reflecting one of its most common symptoms—the abnormal growth of the hands and feet. Swelling of the hands and feet is often an early feature, with patients noticing a change in ring or shoe size, particularly shoe width. Gradually, bone changes alter the patient's facial features: The brow and lower jaw protrude, the nasal bone enlarges, and the teeth space out. Overgrowth of bone and cartilage often leads to arthritis. When tissue thickens, it may trap nerves, causing carpal tunnel syndrome, which results in numbness and weakness of the hands. Body organs, including the heart, may enlarge. Other symptoms of acromegaly include joint aches thick, coarse, oily skin skin tags enlarged lips, nose, and tongue deepening of the voice due to enlarged sinuses and vocal cords sleep apnea-breaks in breathing during sleep due to obstruction of the airway excessive sweating and skin odor fatigue and weakness headaches impaired vision abnormalities of the menstrual cycle and sometimes breast discharge in women erectile dysfunction in men decreased libido
Addison’s disease (also Addison disease, chronic adrenal insufficiency, hypocortisolism, and hypoadrenalism) is a rare, chronic endocrine system disorder in which the adrenal glands do not produce sufficient steroid hormones (glucocorticoids andmineralocorticoids). It is characterised by a number of relatively nonspecific symptoms, such as abdominal pain and weakness, but under certain circumstances, these may progress to Addisonian crisis, a severe illness which may include very low blood pressureand coma. An adrenal crisis often occurs if the body is subjected to stress, such as an accident, injury, surgery, severe infection or illness; death may quickly follow.