miércoles, 20 de junio de 2012

MORDEDURAS DE DIFERENTES INSECTOS

3 Black-legged, or deer ticks, on human skin

Ticks

Many bugs give us reason for pause, including poisonous spiders, chiggers, bees and lice. But few get under our skin -- quite literally -- like the tick. If you enjoy the outdoors, be careful of ticks -- they can attach as you brush past grass and plants. Ticks don't always carry diseases, and most bites are not serious. But they can carry diseases including Lyme disease and Rocky Mountain spotted fever.
Tick burrowing into human skinOnce a tick latches onto skin, it often moves to the warm, moist armpits and groin -- feeding on blood and passing on any disease it carries. A tick bite can also trigger an allergic reaction. If you have a tick, it is important to remove it properly. To prevent tick bites, keep your arms, legs, and head covered when outdoors. Use tick repellant with DEET on skin or clothing, or products with permethrin on clothing. Check for ticks after spending time in grassy or wooded Bull's-eye rash indicating Lyme disease
In the U.S., the Western black–legged tick and the deer tick can carry Lyme disease bacteria. Infected ticks usually don't spread the disease until they've been attached for at least 36 hours. The first sign of infection is usually a circular skin rash. Early symptoms may also include fever, headache, and fatigue. Untreated Lyme disease may spread to other parts of the body, including the muscles, joints, heart, and nervous system. Most cases of Lyme disease can be treated sucBlack widow spider on tree branchcessfully with antibiotics.

Black Widow Spiders: Poisonous!

Wood piles and tree stumps -- that's where poisonous female black widows hide. She is long-legged and glossy black, with a distinctive orange, red, or yellow "hourglass" shape on her underside. These spiders are roughly ¼ inch wide and 1.5 inches long, counting their long legs.Close-up of black widow spider bite on fingerBlack widow spider bites may cause sharp, shooting pain up the limb, but they can also be painless. Look for one or two red fang marks, redness, tenderness, and a nodule at the bite site. Severe muscle cramps, nausea, vomiting, seizure, and a rise in blood pressure may follow soon after. Get medical care immediately. Anti-venom medicine is available. If possible, bring the spider with you for positive identification.Brown recluse spiderHiding in attics and closets -- in Midwestern and South central states -- that's where you'll find brown recluse spiders. The spiders range in color from yellowish-tan to dark brown, with darker legs. Their venom is extremely poisonous, and their bite can cause serious wounds and infection. Yet you may not feel their bite.Brown recluse spider biteWhen the brown recluse bites, it is often painless -- then skin reddens, turns white, develops a red "bull's–eye," blisters, and becomes painful. These bites can be deadly in rare cases. Get medical care immediately. If you can, bring the spider with you for positive identification.Head louse crawling out of hair onto a combIn hair -- that's where you'll find lice. They like to hide in the neck area of the scalp and behind the ears. If you have lice, you likely got it from sharing a hat, brush, or other item with a person who has lice. Lice are itchy, but scratching can lead to infection. In severe cases, hair may fall out.Head lice infestation

Head Lice Remedies

To kill lice and their eggs (called nits), use lotions, creams, or shampoos from the drug store or prescribed by your doctor. Wash clothing, bedding, and brushes to prevent the spread of lice. Check all household members, and treat everyone who has nits or lice. Side view of cat flea

Fleas: Not for Pets Only

Fleas are small, wingless, agile insects that live off the blood of their host -- and they don't just bite pets. They dine on people, too.Flea bites on leg

Flea Bites

Some people are very sensitive to flea bites -- but scratching can cause a wound or infection. The best solution is to get rid of fleas on pets and in your home. Keep pets out of your bed and be sure to vacuum rugs daily. Spray insecticides on infested areas. Consider using a once-a-month insecticide on your pet.Yellowjacket wasp

Bee, Wasp, Hornet, Yellow Jacket

When a bee stings, it loses the stinger and dies. But a wasp, hornet, or yellow jacket can inflict multiple stings becausDetails of wasp sting and swollen upper lipe it does not lose the stinger. These stings can cause serious reactions in people who are allergic to them.

Bee, Wasp, Hornet, Yellow Jacket Stings

If you don't have an allergic reaction, simply remove the stinger, clean the sting site, apply ice, take oral antihistamine for itching, and take ibuprofen or acetaminophen for pain relief. If you have a severe anaphylactic reaction, lie down and carefully remove the stinger. Use an EpiPen (epinephrine) if you have one. Get immediate medical care.fire ant

Fire Ants: Ouch!

Fire ants look much like ordinary ants -- and are found in most of the Southeastern states. They produce large mounds in open areas and are aggressive when disturbed. During an attack, the fire ant latches onto the skin with its jaw, then Fire ant bites showing with white pustulesstings from its abdomen. It 

Fire Ant Stings

The fire ant sting typically causes red hive-like lesions that burn and itch. Painful pus-filled lesions can also occur. Cold packs, pain relievers, and antihistamines can help relieve the discomfort. A large number of stings may trigger a toxic or severe life-threatening allergic reaction. Get emergency care.may inject venom many times.Scanning electron micrograph of chiggers

Chiggers: Itchy!

Contrary to popular belief, chiggers are not insects; they are arachnids. Specifically, chiggers are the juvenile (or larval) form of a family of mites called Trombiculidae. They only dine on humans in their juvenile form, they later become vegetarians as adults. Their bites are painless, but lesions are very itchy. Itching usually peaks a day or two after the biRed, itchy chigger bites on man's legte occurs.

Chigger Bites

After a few days of being attached to the skin, chiggers fall off -- leaving itchy red welts. Over-the-counter products can help relieve itching. See your doctor if the skin appears infected or the welts appear to be spreading.Scabies mites burrowed in skin

Scabies: Stealthy Pests

When scabies mites get into the skin, they can cause a big skin problem. The mites spread through skin-to-skin Scabies mite infestation on wrist and armcontact with an infected person -- or by sharing towels, bed linens, and other objects.

Treating Scabies

Intense itching and skin sores don't appear until several weeks after mites get into skin. The itching is very severe and usually worse at night. The rash typically is seen on the sides and webs of the fingers, the wrist, elbows, genitals, and buttock. You'll need prescription lotion or pills to get rid of scabies. Wash all clothes, towels, and bedding in hot waterBedbug feeding on human skin

Bedbugs: Hitching a Ride

Their name tells the tale, as these tiny insects tend to hide in bedding. They are often found in hotels, shelters, and apartment complexes -- and can hitch a ride into your home aboard luggage, pets, and boxes.Bedbug bites on person's arm

Bedbug Bites

Bedbugs leave itchy, red bites on the skin, usually on the arms or shoulders. More of a nuisance than a health hazard, it is possible to develop an infection from scratching. If you have an allergic skin reaction, use creams with corticosteroids and take oral antihistamines -- and see your doctor.Puss caterpillar or hive producing caterpillar

Puss Caterpillar: Southern Stinger!

The most poisonous caterpillar in the U.S., puss caterpillars can be found in Southern states where they feed on shade trees like elm, oak, and sycamore. The poison is hidden in hollow spines among the hairs.

Puss Caterpillar Stings

When a puss caterpillar stings, you may get waves of intense pain, rash, fever, vomiting, and muscle cramps. Remove the broken-off spines by using cellophane tape or a commercial facial peel -- and call your doctor.Hive on human skin from puss caterpillar

Puss Caterpillar Stings

When a puss caterpillar stings, you may get waves of intense pain, rash, fever, vomiting, and muscle cramps. Remove the broken-off spines by using cellophane tape or a commercial facial peel -- and call your doctor.Arizona bark scorpion

Scorpions: Deadly!

Not all scorpions are poisonous, but those that are can be deadly. Scorpions are found mostly in the Southwest and Western states. Symptoms of a sting include pain, swelling, itching, vomiting, increased sweating, and vision problems. Get medical care immediately.Close Up of a Deerfly Biting Into Human Skin

Deerflies: Painful!

These biting flies live in wetlands, forests, and other damp environs. Treat the painful bites with alcohol to prevent infection. Deerflies spread Tularemia, an infectious bacterial disease that requires medical attention. Insect repellant and protective clothing help prevent deerfly bites.Close-up of mosquito feeding on human skin

Mosquitoes: More Than Irritating!

Mosquitoes aren't just annoying. Scratching a bite can cause a skin infection. Also, mosquitoes can carry West Nile virus, dengue fever, and other diseases. To protect yourself from mosquitoes, apply insect repellent and cover up when you go outdoors. Use window screens, and get rid of standing water in your yard.House Fly or Domestic Fly (Musca domestica)

Houseflies: Dirty, Hairy!

A housefly is a dirty insect -- carrying more than 1 million bacteria on its body. It can spread intestinal infections by contaminating food. To control flies, keep food and garbage in closed containers and use window screens on your home.Cockroach

Cockroaches: Ugly Trouble

They're not just ugly. Cockroaches carry diseases like salmonella. When they die, the carcasses can trigger allergic reactions and asthma. If you live in a warm climate, getting rid of cockroaches can be difficult. It helps to use pesticides, keep a clean kitchen, and repair cracks and holes in floors and walls.

lunes, 18 de junio de 2012

TIZA contiene el carcinogeno talco, el polvo de tiza causa enfermedades de los pulmones (TALC in CHALK a Carcinogen, Chalk dust causes pulmonary disease)

Los riesgos del talco son muchos.
Es un problema grande tanto en la casa como en el trabajo.  Para los maestros que trabajan con tiza por mucho tiempo, puede afectar sus pulmones.  Para los ninos con asma puede resultar en un "ataque asmatico" o empeorimiento de su condicion.  El talco, un componente de tiza tiene un componente semajante al asbestos, carcinogeno que causa mesotelioma.  Hay tiza sin polvo, la cual tiene menos riesgo para los pulmones y los computadores (el abanico del cual atrae los particulos calentando la maquina).  Lo que sigue en ingles tiene mas informacion........

Risks of Talcum Powder
Q. What is talc?
A. Talc is a mineral, produced by the mining of talc rocks and then processed by crushing, drying and milling. Processing eliminates a number of trace minerals from the talc, but does not separate minute fibers which are very similar to asbestos.
Q. What kinds of consumer products contain talc?
A. Talc is found in a wide variety of consumer products ranging from home and garden pesticides to antacids. However, the products most widely used and that pose the most serious health risks are body powders Talc is the main ingredient in baby powder, medicated powders, perfumed powders and designer perfumed body powders. Because talc is resistant to moisture, it is also used by the pharmaceutical industry to manufacture medications and is a listed ingredient of some antacids. Talc is the principal ingredient home and garden pesticides and flea and tick powders. Talc is used in smaller quantities in deodorants, chalk, crayons, textiles, soap, insulating materials, paints, asphalt filler, paper, and in food processing.
Q. Why is talc harmful?
A. Talc is closely related to the potent carcinogen asbestos. Talc particles have been shown to cause tumors in the ovaries and lungs of cancer victims. For the last 30 years, scientists have closely scrutinized talc particles and found dangerous similarities to asbestos. Responding to this evidence in 1973, the FDA drafted a resolution that would limit the amount of asbestos-like fibers in cosmetic grade talc. However, no ruling has ever been made and today, cosmetic grade talc remains non-regulated by the federal government. This inaction ignores a 1993 National Toxicology Program report which found that cosmetic grade talc, without any asbestos-like fibers, caused tumors in animal subjects.1 Clearly with or without asbestos-like fibers, cosmetic grade talcum powder is a carcinogen.
Q. What kind of exposure is dangerous?
A. Talc is toxic. Talc particles cause tumors in human ovaries and lungs. Numerous studies have shown a strong link between frequent use of talc in the female genital area and ovarian cancer. Talc particles are able to move through the reproductive system and become imbedded in the lining of the ovary. Researchers have found talc particles in ovarian tumors and have found that women with ovarian cancer have used talcum powder in their genital area more frequently than healthy women.2
Talc poses a health risk when exposed to the lungs. Talc miners have shown higher rates of lung cancer and other respiratory illnesses from exposure to industrial grade talc, which contains dangerous silica and asbestos. The common household hazard posed by talc is inhalation of baby powder by infants. Since the early 1980s, records show that several thousand infants each year have died or become seriously ill following accidental inhalation of baby powder.3
Q. What about infants?
A. Talc is used on babies because it absorbs unpleasant moisture. Clearly, dusting with talcum powder endangers an infant's lungs at the prospect of inhalation. Exposing children to this carcinogen is unnecessary and dangerous.
ACTIONS YOU CAN TAKE:
1. Do not buy or use products containing talc. It is especially important that women not apply talc to underwear or sanitary pads.
2. Contact your pediatrician and/or local hospital and find out if they have a policy regarding talc use and infants.
3. Write to the FDA and express your concern that a proven carcinogen has remained unregulated while millions of people are unknowingly exposed.
References:
1.National Toxicology Program. "Toxicology and carcinogenesis studies of talc (GAS No 14807-96-6) in F344/N rats and B6C3F, mice (Inhalation studies)." Technical Report Series No. 421. September 1993.
2. Harlow BL, Cramer DW, Bell DA, Welch WR. "Perineal exposure to talc and ovarian cancer risk." Obstetrics & Gynecology, 80: 19-26, 1992.
3. Hollinger MA. "Pulmonary toxicity of inhaled and intravenous talc." Toxicology Letters, 52:121-127, 1990.



LAS FRACTURAS


LAS FRACTURAS DE LOS NINOS OCURREN MUCHAS VECES
EN EL VERANO CUANDO EMPIEZAN A CORRER, SALTAR Y HACER LO QUE HAN HECHO LOS NINOS DESDE QUE EMPIEZAN A CAMINAR.  ESTAN EXPLORANDO SU AMBIENTE.  ESTE PUESTO ES PARA EXPLICAR LO QUE PASA A VECES.  ACUERDENSE QUE LOS NINOS SON FUERTES, TIENEN MUCHOS RECURSOS PARA CURARSE PERO HAY VECES CUANDO PUEDA SER UN PROBLEMA QUE REQUIERE ATENCION INMEDIATA:


1.  FRACTURA ABIERTA
2.  FRACTURA DEL CODO
3.  FRACTURA DE LA COSTILLA QUE PENETRA AL PULMON
4.  FRACTURA QUE RESULTE EN PROBLEMAS CON LA CIRCULACION
5.  FRACTURAS DE LA CABEZA


Las fracturas (Fractures)
Fracturado quiere decir quebrado, el hueso está roto ya sea que la fractura es parcial o total. El hueso puede fracturarse total o parcialmente de diversas maneras (transversa, longitudinal o en el medio).
¿Cómo ocurren las fracturas?
Las fracturas pueden ocurrir de diversas formas, pero hay tres que son las más comunes:
  • El trauma es lo que más fracturas causa. Por ejemplo, una caída, un accidente motociclístico, una caída practicando un deporte, todo eso puede causar fractura.
  • La osteoporosis también puede causar fracturas. La osteoporosis es una enfermedad ósea en la cual los huesos "se afinan," son más frágiles y se rompen con más facilidad.
  • El uso excesivo también puede causar fracturas, lo cual es muy común de ver en los atletas (fracturas por stress o fatiga).
Cómo se diagnostica una fractura
Si se quebrar un hueso se dará cuenta casi inmediatamente. Puede ser que oiga un chasquido o un ruido como si se quebrara, la zona alrededor de la fractura le causará dolor y estará inflamada, se puede tal vez deformar una extremidad o el hueso puede salir a través de la piel, los médicos generalmente utilizan radiografías para diagnosticar. Una fractura por stress será más difícil de diagnosticar, puede no aparecer inmediatmente en los rayos X. Sin embargo, puede haber dolor, dolor al presionar y un poco de hinchazón.
Tipos de fracturas
  • Fractura cerrada o simple. El hueso está roto pero la piel intacta.
  • Fractura abierta o compuesta. La piel está perforada ya sea por el hueso o por el golpe al momento de la fractura, en este tipo de fractura el hueso puede o no estar visible.
Tipos especiales de fracturas
  • Fractura transversa. Fractura en ángulo recto con el eje del hueso.
  • Fractura en tallo verde. Fractura en la cual se rompe un lado del hueso y el opuesto se encorva solamente. Se ven más en los niños.
  • Fractura conminuta. Fractura del hueso en tres o más fragmentos.

Proceso de curación
Tan pronto ocurre la fractura, el cuerpo comienza a proteger la zona herida, formando un coágulo de sangre protector, tejido calloso o fibroso. Comienzan a crecer nuevas "extensiones" de las células óseas a ambos lados de la fractura, éstas extensiones crecen unas hacia otras, la fractura se cierra y el callo se reabsorbe.
Tratamientos de las fracturas
Los médicos utilizan yesos, férulas, clavos u otros dispositivos para mantener la fractura en posición correcta mientras el hueso suelda.
  • Los métodos externos de fijación incluyen emplasto, molde de fibra de vidrio, férulas de yeso, férulas, u otros dispositivos. Como los fijadores externos, que son unas barras por fuera de la piel unidas a clavos finos en el hueso.
  • Los métodos internos de fijación se utilizan para inmovilizar los trozos de hueso mediante placas metálicas, clavos o tornillos métálicos mientras el hueso suelda.
Recuperación y rehabilitación
Las fracturas pueden tardar varias semanas o meses en soldar, depende del tipo de herida y si el paciente sigue las instrucciones del médico. El dolor desaparece mucho antes de que el hueso esté lo suficientemente sólido como para soportar actividades normales y presión.
Aún después de haberse quitado el yeso o la tablilla, deberá restringir las actividades hasta que el hueso esté lo suficientemente soldado como para comenzar con sus actividades normales. En términos generales, cuando el hueso de la pierna o del brazo está suficientemente sólido como para retomar sus actividades normales, los músculos estarán débiles por falta de uso, sentirá que los ligamenteos están "endurecidos" por falta de uso y por eso necesitará un período de rehabilitación con ejercicios. Deberá aumentar gradualmente las actividades hasta que esos tejidos pueden funcionar normalmente y se haya completado el proceso de curación.

ESTERIOTIPIAS

Una de mis amigas, hija de una amiga bien querida desde siempre, me mando una pregunta sobre este complejo tema.  Mis colegas ya tiene menos informacion que ella.   La respuesta va a ser en ingles (mejor que en espanol....para mi)

http://youtu.be/8tv7hI8RtwQ

Stereotypies non Autistic


Resumen de los movimientos incluidos en este padecimiento


EN ESPANOL:
(mi amiga va a ayudar con la traduccion)



Background

Stereotypies are repetitive, purposeless actions that are most commonly seen in childhood. Stereotypies do not have a clear definition due to the wide range of possible stereotyped behaviors and the overlap with other movement or behavioral disorders.[1]
The Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) strictly defines a stereotypy as a repetitive, nonfunctional motor disorder that interferes with normal activities or results in injury. It must persist for more than 4 weeks and not be due to another medical condition, drugs, or a developmental disorder.[2]
However, some definitions of stereotypies are extremely broad, and it is therefore helpful to classify them to distinguish between the different movements. Three categories are proposed.[3]
  • Common stereotypies are by far the most frequent type and comprise habits, such as nail-biting and bruxism.
  • Complex motor stereotypies are the second main type, and these consist of various repetitive limb movements.
  • Head nodding is a separate stereotypy that shares some characteristics with complex motor stereotypies.
Complex motor stereotypies and head nodding fulfill the DSM-IV-TR criteria and are the focus of this review.
Complex motor stereotypies are further subdivided into primary or secondary. Primary stereotypies occur in otherwise developmentally normal children and usually remain stable or regress. Secondary stereotypies are those that occur in conjunction with a neurologic or behavior disorder. They are seen in autism, mental retardation, Tourette syndrome, and rare neurodevelopmental syndromes, such as Rett syndrome. In older children they may be associated with schizophrenia, obsessive-compulsive disorder, or early-onset neurodegenerative diseases.
Other involuntary movements that may present similarly to stereotypies include tics and automatisms. Tics are by far the most common misdiagnosis. Complex motor tics are also repetitive, involuntary actions. However, they usually have a later age of onset, greater variability in movements and rhythms, and are briefer. More importantly, unlike tics, stereotypies are not associated with premonitory urges and subsequent relief from those urges.
Voluntary repetitive movements mimicking stereotypies include attention deficit hyperactivity disorder (ADHD), mannerisms, and compulsions. ADHD tends to be characterized by more generalized and restless actions than stereotypies. Mannerisms are rarely continual and accompany a normal activity. Compulsions comprise repeated ritualistic movements to relieve anxiety or fear, and may occur with tics and stereotypies.
For common stereotypies, the mechanisms are unclear and also dependent on the specific type. For example, head banging may develop from frustration and temper tantrums in early childhood. In contrast, thumb sucking develops as a physiological action in early infancy, but may persist due to reinforcement from its comforting effect.
Research on the mechanisms of complex motor stereotypies has been from 2 different approaches. Psychogenic hypotheses aim to explain the cause of stereotypies from a behavioral standpoint and are discussed later. Neurobiological hypotheses look at the structural and molecular basis for stereotypies.
Anatomically, the basal ganglia is implicated in stereotypic disorders.[4] In monkeys, stereotypies are correlated to neuronal activity in the striatum, especially the putamen. Intrastriatal injection of amphetamine, which increases dopamine levels, causes stereotypies in rodents.[5] In humans, case reports of stereotyped movements have spontaneously emerged after lesions of the putamen, orbitofrontal cortex, or thalamus. A volumetric MRI study in children with complex motor stereotypies has shown a reduction in the size of the caudate nuclei and also in frontal white matter.[6] Precise localization within the basal ganglia and corticostriatal circuitry is yet to be elucidated.
Dopaminergic pathways appear to mediate complex motor stereotypies.[7] In the treatment of Parkinson disease, patients on high doses of levodopa sometimes perform repetitive, purposeless actions, known as punding. In addition, levels of plasma homovanillic acid, a dopamine metabolite, are reduced in adults with stereotypies.[8] Studies in rodents have shown that administration of dopamine can produce repetitive behaviors such as sniffing or head bobbing.[1] From investigating the effect of selective dopamine agonists, D2 dopamine receptors are known to be important in enhancing stereotypies.[5]

United States

Data on the prevalence of stereotypies are limited, especially internationally, and this varies according to the exact definition used by the researchers. Nevertheless, habits or common stereotypies are thought to occur in up to two-thirds of infants. In children, 20-50% display them.[9]
Thumb and hand sucking are seen in 17-59% of children younger than 15 years. Approximately 10% of developmentally normal infants exhibit head banging. Body rocking is seen in 6-19% of children younger than 3 years.[10] Nail biting has a prevalence of more than 60% in 8-year-olds in one study and is the most common stereotype in school-age children and college students. Trichotillomania is present in 1% of college students, although chronic hair pulling is reported in up to 13%.[11] Bruxism has a prevalence of 8% worldwide.[12]
The prevalence of primary complex motor stereotypies is unknown, but it may be as high as 3-4% of preschool children in the United States.[13]
Secondary stereotypies are of course determined by the associated disorder. Rett syndrome and autism each occur in 1 in 20,000 live births. In Rett syndrome, all affected children have hand stereotypies. In autism, more than 60% of preschool children show stereotypies. In contrast, they are seen in only 25% of nonautistic children of a similar mental ability.[14]

Mortality/Morbidity

Mortality has not been reported as a direct result of stereotypies.
Stereotypic movements can lead to social stigmatization of the child by peers. There may be embarrassment or anxiety in the child or the parents.
Self-injurious stereotypies are unusual in developmentally normal children, although they occur in up to 40% of children with autism.[15] They include hand biting, severe trichotillomania, and self-hitting.

Race

There are no known racial differences in the frequency of stereotypies.

Sex

Many common stereotypies show no predilection for either sex. Amongst the different types, thumb sucking, nail biting, and bruxism are slightly more common in females. Head banging is more common in males.
Overall, complex motor stereotypies are nearly twice as likely to occur in males as in females. The increased prevalence of conditions such as autism or mental retardation in males is a confounding factor, but even in primary stereotypies, males are more likely to be affected.

Age

Common stereotypies occur within different age groups. Thumb or hand sucking occurs in early infancy. Head banging usually begins at around 9 months of age, and may last up to 3 years. Body rocking develops in the first year of life, usually as a transient phenomenon during gross motor development. Nail biting begins much later, at the age of 4 years. It has peak prevalence between 8 and 11 years, but still persists in 28% of 18-year-olds. Bruxism and trichotillomania begin in later childhood, although they are less common.
More than 80% of complex motor stereotypies begin before 2 years of age, with a peak incidence at 6 months of age.[16, 17] Another 10% begin in the following year. The outcome is variable, and approximately a third show resolution or improvement of stereotypies. Mostly this happens in the first year but may take 10 years or longer; 60% proceed to have stable stereotypies, and a minority have worsening of their stereotypies.
Complex motor stereotypies may comprise flapping, waving, opening and closing of a fist, finger wiggling, or wrist flexion and extension. They can be primary or secondary, and the main concern for parents and professionals is that they are the manifestation of an underlying disorder. No clinical features enable differentiation of stereotypies between normally developing children and those with autism or developmental delay.
In both groups, the movements can last for more than a minute, and can occur multiple times in a day. In autism, they tend to occur for a longer duration overall.[18] The movements can be associated with other clinical features. These include skin picking, mouth opening, facial grimacing, and involuntary noises.
The most common trigger is excitement or being happy. Concentration on a task, tiredness, and anxiety are also triggers. More than one trigger is present in most children. In most cases, movements cease if the child is distracted, for example by calling out his or her name. Movements also do not occur in sleep.

Other secondary stereotypies

Atypical gazing at objects or fingers has been described in children with autism.[14] These have been termed complex visual stereotypies and appear to occur only as secondary stereotypies. Abnormal pacing, running, or skipping have also been considered to be secondary stereotypies. Again, they are strongly associated with autism rather than other disorders.[14]

Head nodding

Head nodding has slightly different characteristics than complex motor stereotypies of the limbs. It comprises a regular rhythmical movement of the head and neck, which is either up-and-down, side-to-side, or shoulder-to-shoulder. It has an earlier age of onset, and episodes occur more than once a day. Head nodding is unlikely to be associated with a family history, unlike other forms. Also, in most cases it regresses in later childhood.

Common stereotypies

The range of habits or common stereotypies is described below in chronological order. These rarely require medical attention. In some children, a natural progression is seen. This begins with thumb or hand sucking, then body rocking and head banging, and later still, with nail biting and foot or finger tapping.
  • Thumb or hand sucking is first seen in utero, and is the earliest common stereotypy.[19] Hand sucking rarely persists beyond infancy. Thumb sucking is not usually associated with medical sequelae unless it persists beyond the age of 4. It can then lead to dental malocclusion, digital deformities, temporomandibular disorders, and social stigmatization.
  • Head banging is the repeated action of hitting the head against a wall or the bed when lying. It often occurs during teething, ear infections, and temper tantrums. Head banging may cause abrasions and callus formation, but only rarely does it lead to fractures or more serious injury.
  • Body rocking is a rhythmic side-to-side or to-and-fro rocking of the body. It is usually seen just before sleeping or after waking.
  • Nail biting is the most common stereotypy of later childhood. It leads to shortened, irregular fingernails that may be aesthetically unpleasant. It also predisposes to paronychia and herpetic whitlow. Again, the behavior is increased with anxiety and stress.
  • Trichotillomania is the repeated plucking of scalp or body hair leading to clinically significant hair loss. Most sufferers have no other comorbidities, but it is related to body dysmorphic disorderspersonality disorders, and eating disorders.[11] The most common sites, in order of decreasing frequency, are scalp, eyelashes, eyebrows, and pubic hair.
  • Bruxism is the act of grinding teeth and/or clenching the jaw. It can happen subconsciously at night as well as during the day. Complications include mechanical wear, teeth fractures, temporomandibular disorder pain, headache, and neck pain.[12]

Other movements

The presence of other stereotypies, tics, or obsessive tendencies should also be sought in the history since they are associated in more than one third of children with complex motor stereotypies.

Developmental history

A birth and developmental history should always be taken. This includes pregnancy, gestation, delivery, and developmental milestones. These may identify underlying disorders and so are essential to differentiate primary and secondary complex motor stereotypies. In autism, children show limited social and communication skills and a restricted range of activities. Interestingly, even children with primary stereotypies may have mild language delay despite normal intelligence.[20]

Family history

A comprehensive family history is important because 25% of children have at least 1 affected family member.[16] This should also include asking about the presence of other developmental and movement disorders.

Drug history

Although drugs are rarely implicated, clinicians should be aware that chronic neuroleptic drug use can lead to stereotypies, usually as part of a tardive dyskinesia. Amphetamine poisoning in children has been reported to cause self-injurious stereotypies, including head banging and hand biting.
Physical examination is guided by the history and types of stereotypies present. In most cases no physical findings are apparent, except for the movements themselves. One must look for other movement disorders, such as tics or chorea. Sensory and motor examination identify underlying pathology. Blindness, deafness, hemiparesis, and cerebral palsy are causes of secondary stereotypies.
After weeks of waiting, today was our appointment for Olivia at Children’s Hospital with a Pediatric Neurologist.
(This fall, I noticed Olivia wasexperiencing what I thought were facial tics. Our doctor sent us to a Pediatrician, who ordered an EEG, which led to our appointment today with a Pediatric Neurologist. Earlier this week,I posted about her worsening symptoms.)

The Diagnosis

The Pediatric Neurologist believes that Olivia is experiencing stereotypy.
Until yesterday, I had never heard the term stereoytpy. But, a reader actually emailed me yesterday after reading my post about Olivia’s tics, (or what I assumed were tics,) and told me that her daughter had the same symptoms and was diagnosed by a Pediatric Neurologist with stereotypy. She wrote to tell me not to worry, that stereotypy can occur in healthy children.
A stereotypy (pronounced /ˈstɛriː.ɵtаɪpi/) is a repetitive or ritualistic movement, posture, or utterance, found in patients with mental retardation, autism spectrum disorders, tardive dyskinesia and stereotypic movement disorder. Stereotypies may be simple movements such as body rocking, or complex, such as self-caressing, crossing and uncrossing of legs, and marching in place.[1] Several causes have been hypothesized for stereotypy, and several treatment options are available.[2]
Stereotypy is sometimes called stimming in autism, under the hypothesis that it self-stimulates one or more senses.[3] Related terms include punding and tweaking to describe repetitive behavior that is a side effect of some drugs.[4]
Distinction from tics:
Like tics, stereotypies are patterned and periodic, and are made worse by fatigue, stress, and anxiety. Unlike tics, stereotypies usually begin before the age of three, involve more of the body, are more rhythmic and less random, and are associated more with engrossment in another activity rather than premonitory urges. Examples of early tics are things like blinking and throat clearing, while arm flapping is a more common stereotypy. Stereotypies do not have the ever-changing, waxing and waning nature of tics, and can remain constant for years. Tics are usually suppressible for brief periods; in contrast, children rarely consciously attempt to control a stereotypy, although they can be distracted from one.[5]
Proposed causes:
There are several possible explanations for stereotypy, and different stereotyped behaviors may have different explanations. A popular explanation is stimming, which hypothesizes that a particular stereotyped behavior has a function related to sensory input. Other explanations include hypotheses that stereotypy discharges tension or expresses frustration, that it communicates a need for attention or reinforcement or sensory stimulation, that it is learned or neuropathological or some combination of the two, or that it is normal behavior with no particular explanation needed.[3]
The doctor assured us that while stereotypy does present in children with other disorders such as autism, it is also common in typically developing children. (Her own daughter experienced stereotypy.)
She said that as Olivia gets older, she may learn to inhibit her stereotypies and do them more when she is alone. She may stop doing them altogether.

Now what?

The neurologist is referring Olivia to a pediatric psychiatrist who specializes in stereotypy, tics and Tourette’s, as well as ADHD, etc.
OliviaI am glad that we will be able to receive some sort of follow up care. Neurology doesn’t treat stereotypy and considers it benign.
I am so grateful that my daughter doesn’t require medication or treatment! But, considering our family history, I do prefer to have her receive some sort of longer term follow up with a specialist. (Olivia’s brother Jackson has ADHD, ODD and Anxiety, and one of Olivia’s cousins is on the Autism Spectrum.)
I just prefer to stay as educated and aware of what my children are experiencing as possible. Even if there isn’t anything I “can do,” knowledge just makes me feel better.
I have been reading tonight about stereotypy, and indeed it does seem to occur often in developmentally healthy children.
Here is an excerpt from an informative article I found and it describes how stereotypies can affect children who do not have mental retardation or pervasive developmental disorders:
“…The stereotypies seen in these children were associated especially with periods of engrossment such as when playing a game or participating in an activity, but also at times of excitement, stress, fatigue, and boredom. They usually lasted in the range of seconds to minutes (but could go on for hours in some cases) and appeared many times per day. In practically all cases, the stereotypies could be suppressed by sensory stimuli or distraction…
Stereotypies usually develop in early life, mostly before 2 years of age, whereas tics begin to occur in children at age 6 7 years. Unlike tics, which rapidly change from one thing to another (blinks, grimaces, twists, shrugs), stereotypies are prolonged episodes of the same iterated movement.
People with a tic disorder often will stop their tics during engrossing activities, but individuals with stereotypies often will start their repetitive movements during such periods. Distraction usually interrupts stereotypies but not tics.
Many of the children in the study had a comorbidity, including ADHD (15%), obsessive-compulsive disorder or obsessive-compulsive behavior (20%), tics (13%), learning disability (4%), or had an early language or motor developmental delay that resolved itself (12%).
The biologic basis for stereotypies remains unclear, although some evidence suggest that there is a dysfunction in the circuitry between the cortex and the striatum, Dr. Singer said (Pediatr. Neurol. 2005;32:109-12).
If a child’s stereotypy doesn’t interfere with his activity, Dr. Singer said that he doesn’t recommend any particular therapy…”

Relief

I didn’t expect to leave the hospital feeling relieved. Going in, I felt hopeless.
Watching my daughter get lost in repetitive movements, her body clenched and her face contorted, is incredibly upsetting. It interrupts her constantly throughout her day and some episodes go on and on.
OliviaBut knowing that these episodes are not damaging her brain, that they aren’t seizures and I didn’t leave the hospital with a prescription for medication, is such a relief.
Life isn’t perfect. Life isn’t typical. We all have our unique challenges, experiences and blessings.
As difficult as it is to watch my daughter clench and contort her face and her body, even as I hold her or we walk down the street, I am trying to have peace that this is just part of the plan the Lord has for her life.
I need to have faith and let Olivia thrive in the life God has planned for her.
THANK YOU again for all your loving support! Your comments, messages and prayers mean so much to us!!!

UPDATE ON OLIVIA

Olivia is now four years old. She is a happy, energetic, and extremely friendly little girl who keeps us in constant laughter.
Olivia still has her stereotypies. They have not lessened — she still experiences them regularly and is now aware that she has them. There are certain situations and stimuli that always brings on her stereotypic movements, such as driving in a car, waiting in a line up, being in the shower or getting out of the bath/shower, and getting bored. Stress and fatigue do seem to make them worse, but are not as much of a factor as the stimulation around her.
I can “call her out” of a stereotypy by calling her name firmly. She will then “come back” and look at me as if she just came from another place. But, unless I continue to hold her hand and engage her, she will immediately go back into her stereotypic movements.
Olivia will sometimes go for an hour or more and not have any stereotypic movements, but at other times they are far more frequent.
It isn’t easy to watch my daughter struggle with stereotypic movement disorder. It is hard when people stare at her, kids and adults alike, confused by what they are seeing, or ask me if she is special needs.
But, even though I feel a slight panic sometimes when I see my daughter “go away” into a place I don’t understand as she experiences her stereotypies, I constantly thank God. My daughter is alive. She is not experiencing seizures or anything that is hurting her. She is happy. She is here. And I am so very very grateful.
If your child is experiencing stereotypic movements or tics, please don’t despair. Yes, it is hard. I know the pain and panic I felt when I first realized something was going on with Olivia. We want the best for our children. We want to keep them from all suffering.
But we can’t. Life sometimes hurts. And a diagnosis of stereotypy or tics??? Well — it isn’t the end of their world or yours. As Julia’s cousin told Olivia, it is just a part of who she is.

Written by Janice, co-founder of 5 Minutes for Mom.

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Email Author    |    WebsiteAbout Janice
Janice is co-founder of 5 Minutes For Mom. Along with her twin sister Susan and their mother Joan, Janice also owns two online toy stores -- one specializing in Ride on Toys and the other in Rocking Horses. Janice has a spunky little girl and a rambunctious boy who love to make it difficult for her to work from home.
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{ 60 comments… read them below or add one }
1laura January 29, 2010 at 4:16 am
Happy for your family! Wahoo!
2Eileen January 29, 2010 at 5:17 am
First of all I have to say your little darlin’s award winning BREAK OUT smile there just made me smile… and it’s 4 am and not a happy insomniac right now…
I am sorry I missed your post about Olivia before and your very worries that all mom’s have when we intuitively or otherwise know that something is “amiss” with our kids. My daughter is 10 and had some strange type of “pass out” seizures when she was barely walking…they passed them off as her HOLDING HER BREATH when she was frustrated. I was like…you have GOT to be kidding! She would also have febrile seizures, so I was not going to just be blase’ about this. THey really didnt find anything but we are now dealing with horrible migraines with Morgan. She is smart, funny, seems physically healthy…but just breaks down with head pain often. Nothing is showing up. SO…I know how you feel, hearing there is nothing physically damaging showing up and hoping the doctors are right in saying they “will probably” go away. Some things really ARE simple and kids grow out of it. I also know how you reach when you already have a child with issues. (We have another child that struggles with school and ADD or social anxiety disorder…they really dont know WHAT it is and nothing has helped for 8 years. She works VERY hard and has overcome a lot of the stigma and is very confident now.)
Just wanted you to know there are lots of brilliant, beautiful little angels out there who might have simple or not so simple issues…and their wonderful moms/dads are there to get them through, to protect them… to love them no matter what and do any work at all to help them. I can hear your love for Olivia in your words and know that no matter what your kids have to brave,no matter what triumphs they feel, you will be there by their side.
So scary to go through. Just a couple pointers. I would get video or audio of any kids health issues you may think should be tended to, dont think a second about getting a second opinion. AND you are ALREADY reading all you can get your hands on—be informed. Knowledge is power, and in the age of the communication web, sometimes we find research and studies that doctors dont have TIME to look at.
You will be OK. God will answer yours and our prayers for your little girl…so she will always smile from her heart like your beautiful photo above. God bless your family, always Janice!
eileen
3Mom24 January 29, 2010 at 6:28 am
Lots of hugs and compassion. I’m sorry that she has this, I’m sorry that you’re struggling with yet another worry, yet I’m happy that the news wasn’t much, much worse and that she’s over-all healthy.
4Christine Holroyd January 29, 2010 at 6:54 am
I feel relieved that you feel relieved KWIM? It is still a hurdle I’m sure, but you’re right about being educated on the subject. Knowledge and finally having a diagnosis can help to relieve so much anxiety.
Hugs to you from afar.
5Debbie January 29, 2010 at 7:11 am
Thankful the news was not worse. Praying for you all and the Dr.’s as you move forward with this diagnosis and deal with the condition problems she is facing in the future. Praying it will lessen and disappear in the coming months or years. Praying for peace for you all.
6Kelly Tirman January 29, 2010 at 7:27 am
wow – I had never heard of this before. Thanks for sharing.
7TheAngelForever
Twitter: 
January 29, 2010 at 7:49 am
So glad that you have an answer and know that Oliva is not in danger from what is going on. More hugs coming your way from a parent that know even after relief from a neurologist your brain still races a mile a minute.
8Deb - Mom of 3 Girls January 29, 2010 at 8:34 am
Oh I’m so glad that you have a diagnosis and that it’s something treatable and ‘benign’! It’s got to feel good just to have answers and be working toward a plan to help Olivia overcome this. Hugs…
9Susie's Homemade January 29, 2010 at 8:53 am
I am so glad that she has something that can be worked out in therapy! That’s great news!
10A Cowboy's Wife January 29, 2010 at 9:33 am
At least knowing what it is helps. It’s not knowing I think that makes it harder.
((Hugs)) to you all. Hoping they can do more to relieve them…
11Christine Jensen January 29, 2010 at 10:14 am
I am so glad to hear that you have gotten a diagnosis that gives you relief!
I too had the scare of my little one (My 3 year old) needing to see a neurologist. He had a seizure this summer and has since has small odd twitching at night. The neurologist think he has a benign form of epilepsy that only occurs when waking from sleep or falling asleep. It is scary, but having more information always makes you feel better than when you don’t know and you are imagining all sorts of scary diseases!
12Carissa January 29, 2010 at 10:41 am
I am so glad to hear that there is a diagnosis and that you are already on top of everything! I agree that it is hard to watch our children do things that we know do not normally happen. Good luck with all of the future treatment and please keep us posted! I will keep praying for your family!
13Jenean January 29, 2010 at 10:42 am
Crazy! I think my son has that. We’ve never taken him to a specialist, though, because I didn’t think his symptoms were severe enough and they didn’t accompany some other type of behavior. I can remember him doing strange things since he was about 3 or 4. He did eye blinking, throat clearing, scrunching up his nose, and now he kind of flaps one of his arms. Not in a wide arc, but kind of against his body. I think we notice it more because we’re around him.
14Marj McClendon January 29, 2010 at 10:56 am
I am so glad to hear Olivia has no seizures or anything that requires medication. Thank you Lord. Big Hugs to you and Olivia.
15Nancy T. January 29, 2010 at 11:17 am
Oh what a relief to get a diagnosis! So glad to hear it’s something that can be managed.
16Jessica Harwood January 29, 2010 at 11:22 am
I’m so glad that you have a diagnosis and that you feel like knowledge helps you. I’m also glad to know that little Olivia won’t need to be on medications or anything like that. I wish your family the best as you continue to learn about this & work through it together.
17Renee January 29, 2010 at 12:30 pm
A dear friend of mine have had the same experience with her son a couple years ago. Same symptoms and borderline ADD and autism spectrum. At age 2 is started is tics and repetitive MVTs and parents were concern and got him check.
His vocabulary was behind and he was not obeying simple command. After 3 years of speech therapy, 3 days of week with a special behavioral therapist and a special diet (no sugar, no white bread, no gluten all pro et pre biotic and all organic diet) he shown lots of improvement and is now attending public school.
He did not receive any vaccination after 2 years old and his parents decided not to pursue any vaccination in the future (after recherche they believed that their son little body is not tolerating them !!!)
So that is their story, and what did work for them might or might not work for your family… each case ans child is different.
May the Lord grant you some wisdom concerning the health and training of your child.
18Blessing January 29, 2010 at 12:32 pm
I am so happy there is no damaging effect to the diagnosis. I read up some things online and it doesnt seem like it would affect her that much.
Here are some few tips shared by the Mayo Clinic. Hopefully it helps, the more information you have, the better prepared you are to handle it.
19Lisa L January 29, 2010 at 12:32 pm
I’ve been praying and praying for Olivia Janice. So glad to hear this good news.
20Katie January 29, 2010 at 12:40 pm
I’m so happy to hear about Olivia’s diagnosis. If I were there, I think I’d dance around and hug you lots. But, since I’m not I’m just going to have to dance around by myself and send you lots of virtual hugs.
Being educated is a very good thing. It was once said to me that as a mom, I am my child’s greatest advocate. You are too and while it’s a lot of responsibility, it’s the best job in the world.
*hugshugshugs*
21Lucretia M Pruitt January 29, 2010 at 12:41 pm
So happy that you have more information and that you got to leave the doctor’s relieved!
There is nothing that makes us feel more helpless than watching things happen to our children and not knowing what, if anything, we should do.
((hug))
22suburbangranola January 29, 2010 at 12:53 pm
I also have a almost 8 year old child that has a tic. She throws her head back. She has been doing it off and on for about 2 years. She has asthma and eczema but other than that she is very healthy. Our pediatrician told us that it is nothing to worry about. He did send us to a neurologist (to ease my mind I think) and he concurred.
23Pamela January 29, 2010 at 1:15 pm
As a parent, I know how important it is to have a diagnosis. What a sweet little girl you have here. So full of life!
24Christi January 29, 2010 at 2:12 pm
So thankful that this is something that can be dealt with! Praising the Lord with you!
25Stacie January 29, 2010 at 2:22 pm
I am so happy that it is nothing too serious!
((hugs))
26The Mom Jen January 29, 2010 at 2:23 pm
I’m so glad it’s this and nothing worse. My husband always says “we all have something” and it’s the way we deal with it is what matters. You are strong, you are educating yourself and you are a amazing mother full of love, keep it all up and we’re hear whenever you need to talk!
27Jon Gray January 29, 2010 at 3:28 pm
Praying for all the best for Olivia and you guys. Glad to read that the prognosis is good. Hang in there!
28Mindy January 29, 2010 at 4:03 pm
Oh Janice, isn’t it a relief to at least KNOW something at last? Even if the news is devastating ( your news isn’t thank the Lord! ) it is simply better to know…always.
You know, you didn’t have to share this with us at all…but thank you for doing so. There might be a mama who reads your story and is comforted/educated/inspired to act etc…knowledge is power and support is strength.
You have my complete support. Always!
I am glad for the Olivia update!
mindy
29Tarasview January 29, 2010 at 4:19 pm
Janice- I am so happy for you that it is not something too serious and scary. But I know it is still so hard to see your child going through something “atypical” or “abnormal”… no matter how “benign” it may be. I’ll be praying with you that Olivia is one of those kids where it just goes away. Soon.
Hugs.
30Rachel January 29, 2010 at 5:21 pm
What wonderful news! I’m so glad that it is benign and much less serious than you had feared. That’s so excellent!
31Jennifer, Snapshot January 29, 2010 at 6:06 pm
It is great to have support, and I know that you are relieved to have a diagnosis so that you can rest in that.
32Mary January 29, 2010 at 9:43 pm
Praise God for a diagnosis! I know that he has a good plan for Olivia.
I bet you were so comforted to hear the word “benign”. It doesn’t make watching her contortions more fun but hopefully the road ahead will not be too hard.
33Muthering Heights January 29, 2010 at 10:51 pm
I’m so sorry that she has this, but I’m glad that now you can move on with a course of treatment!!!
Hugs to you!
34Bailey's Leaf January 29, 2010 at 11:13 pm
So happy for you that Olivia is okay! Always good to run for the extra advice, particularly in light of family history. Hoping that as she grows older, she will be able to tweak the movements a bit herself so they are less interrupting to her life.
Praise that she is healthy as we had all prayed!
35Debbie January 30, 2010 at 4:21 am
Janice – thanks for sharing this information. I had not heard of stereotypy, either, and appreciate the detailed information you provided. So glad you are relieved – she’s such a sweet little thing.
36Caren January 30, 2010 at 5:56 am
Glad to hear that she is ok. I have trichotillomania (hair pulling) which gets worse with stress. I have had several friends who have had good luck with brain types of disorders by altering their diet and using supplements. Getting rid of dairy and wheat, eating more raw vegetables and fruit, more proteins like quinoa, spirulina and peas, and taking a probiotic has helped many children. Some also recommend ambertose. God bless you and your family, and I hope her episodes stop soon.
37MommyNamedApril January 30, 2010 at 7:55 am
I’ve been thinking about you and your family – I’m so glad you got a benign diagnosis… what a fantastic word to hear from the doctor! I know you’ll all come through this just fine :-)
((hugs))
38Shannon January 30, 2010 at 8:13 am
as a mom to another mom, I can imagine it is frustrating, but you are doing an amazing job just being a mom. You are doiing an amazing job just realizing that she needed some additional help.
I am glad that you have a piece of “closure” so to say that you know whats going on!
Hugs to you and your fmily!
39Deanne January 30, 2010 at 8:33 am
I love this comment you made……
“I need to have faith and let Olivia thrive in the life God has planned for her.”……that is beautiful.
((hugs))
40Stacey Kannenberg January 30, 2010 at 8:51 am
I went from Kindergarten to College with a girl who was a “rocker”. When she was stressed she rocked back and forth without being in a rocking chair. Her face would get flushed but she seemed alert to everything around her. It calmed her almost like a type of mediation. After she would be refreshed, relaxed and very at peace! It wasn’t until we were in college together that she shared that her rocking was a type of illness. None of her friends never thought much about it nor ever really commented on it, other than to say we would make a great mother! Some of us would rock slightly when she was rocking to keep up with her conversation, it was kinda “catchy”. She has a masters in education and today is a successful mom business owner who still ROCKS!
41Wendy K January 30, 2010 at 9:18 am
Thinking of you and your family and wihsing you the best!
42fidget January 30, 2010 at 9:50 am
im glad to hear it’s not something that requires medication
My daughter stims, she is on the spectrum. She is high functioning, fabulous and successful in her endeavors.
Since you have a family history, please make sure your doctor is familiar with the differences in autism when it comes to girls. Many of the diagnostic tests we do are geared towards DXing boys and “classic” autism. According to those tests she’s not even on the spectrum but when grouping her various issues, it’s clearly the best diagnosis for her.
We had to FIGHT to get her DXd, some docs still refuse to acknowledge that autism happens in girls. Girls often WANT to be social and some can even socialize successfully to a certain extent and still are spectrum.
Since Mira has been in the autism program at school she has grown by leaps and bounds.
feel free to email me if you have any questions. Mira has been DXd for 4 years now. For me, her diagnosis was a relief, I finally understood what was going on and we could roll up our sleeves and get to work on making her life better
43shelly January 30, 2010 at 10:33 am
SO happy to hear that they have figured out what it is! It’s so worrisome to have an issue and not know what to do or how to help. I will keep praying for you and for little Olivia.
44oh amanda January 30, 2010 at 1:02 pm
Oh, I just got chills reading your post. I’m glad you got a diagnosis, but know that I’m praying for her!!
45Shop with Me Mama (Kim) January 30, 2010 at 2:24 pm
Glad to hear you finally got some answers. Yeah for no treatment or medication. Hugs and continued prayers to you and your daughter :)
46Sarah January 30, 2010 at 3:39 pm
I’m so happy to know that she’s healthy, and she is fortunate to have a caring and supportive family who will help her cope and thrive despite any challenges she may face! I’ll be thinking of you both.
47Angie January 30, 2010 at 4:16 pm
I’m glad it’s nothing serious! I’ll keep you all in my prayers!
48Farrah January 30, 2010 at 5:03 pm
That’s good to hear it’s not too serious. I know what it’s like to see your child do something off and worry while they’re pinpointing what could be wrong. My son was recently diagnosed with tics this past fall. He’ll be 9 next month and what started out as constant blinking which he still does it has now progressed to neck jerks. We’ve been trying to find the right med to help suppress it but have yet to discover one. They say it may eventually get worse but I’m trying to keep the faith.
49Naomi January 30, 2010 at 6:02 pm
So happy to hear the diagnosis is not a life-threatening condition and that she may very well outgrow it.
50JamericanSpice
Twitter: 
January 30, 2010 at 7:54 pm
It is hard to watch our kids hurt or be uncomfortable ot just now know what’s wrong. I’m so glad you have a diagnosis and can now focus on research and follow up care for your baby.
51Kate January 31, 2010 at 12:04 am
Sounds like good news? It must be somewhat comforting to have an answer – and one that doesn’t involve neurological intervention. I hope that you continue to find answers.
52Rachel - Busy Mommy Media January 31, 2010 at 2:25 am
As hard as that must be, I’m glad you at least got some answers. We went through nearly a year of testing with my 3 year old before we got a diagnosis and I know how scary the waiting can be.
53Debra January 31, 2010 at 2:25 am
Thanks for keeping us updated with the news. I’m sure it feels so much better having the knowledge you do now.
HUGS!
54Mikki January 31, 2010 at 7:13 pm
Janice~
I remember the day that I was told that my oldest daughter may have Autism. I can honestly say that I didn’t remember driving home or calling my husband in tears asking him to come home, but I did all those.
I remember sitting on the floor in my living room in the fetal position cussing out God for messing with my life again.. but at the end of that night, I found myself naked before God.. not literally, but spiritual.. I was stripped FINALLY of my need to control everything and gave my life and my family’s life to Christ.
I know you have this same faith, and it will be what carries you through the days ahead.
PTL for an answer right.. Now you know what’s causing these tics and can go from there..
One thing that God CONTINUES to whisper in my ear on those days when I cry out ‘why’.. is this.. ” Mikki, I created her this way.. for MY purpose.. not yours. Your job is to love her the way I do.”
May God continue to guide you, hold you, strengthen you and most of all.. shape you into a great Mommy!!
My oldest is no longer considered autistic. She was so young with they tried diagnosing her anyways.. but she is AWESOME.. just like your little Olivia!!
Looking forward to seeing God’s amazing work in her life!!
Can’t wait to meet you next week!!
Blessings.. and sorry for rambling on.. LOL
55Stephanie February 2, 2010 at 5:47 pm
So happy to hear that you have a diagnosis and that your little Olivia won’t require medication. Just sent a prayer up for her – that the tics will disappear and she’ll be in the pink of health…today and always.
P.S. Beautiful pictures! She is precious.
56Lorie Shewbridge February 4, 2010 at 9:34 am
Please know that my heart goes out to you and Olivia, Janice. You are doing the best thing that you can do: educating yourself and loving your daughter unconditionally.
I have found some extrememly helpful and unbiased info on health matters whenever I’ve needed some by going to the NIH. I hope this is helpful:
http://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=stereotypy
God bless your whole family and know that you are all in my prayers.
57Julie May 11, 2010 at 10:41 pm
Thank you for sharing your story. My daughter’s name is Harmony Faith, and she just turned 4 in Feb. We have been going to doctors in our area to try and find out why she flaps her arms and her face contorts. She also holds her breath. All this happens when she gets excited, and it all started when she was 10 months old. I have been looking online for answers, and I saw some u-tube videos of children with this. I also read your story on here. We have an appt. with another neurologist next week, and I am bringing all the info I found on this. I know in my heart she has this. It fits her perfectly. I am really struggling to admit my beautiful, bright, loving daughter has this because there is no cure. She is advanced in all areas with her milestones, and is very social. I am praying that God heals your daughter, and I am praying that He heals ours as well. Thank you again for sharing your story because your strength is giving me hope.
58Amanda May 17, 2010 at 8:49 pm
Hi there-
My daughter was diagnosed with complex motor stereotypies a few years back and at first, I was terrified. The lack of information outside of the autistic population was sparse, and after finally piecing what I could together I posted my daughter’s video on YouTube. After receiving so many emails from parents, I was convinced that I should bring together what info I could, so I started a blog athttp://www.motorstereotypy.com.
I still try to post new info as I get it, and recently Dr. Singer finished his website athttp://www.hopkinsmedicine.org/neurology_neurosurgery/specialty_areas/pedsneuro/conditions/motor-stereotypies/. It has tons of info on this condition, and is very reassuring about the benign nature of the movement. Such a comfort to finally get some information out there, so thanks for sharing your story!!
Amanda
Thankfully,
59Christina Lopez February 26, 2012 at 8:36 pm
Wow! Years ago back in 2009 when I tried to google this diagnosis I couldn’t find much information. My son symptoms started at 22 mo old, was diagnosed w/ stereotypies w/ possible tourettes but in the beginning it was very scary because of the unknown. Our neurologist had him tested many times for epilepsy in the beginning (for safety and acute concerns) and also w/ a neuropsych to check his development and any other concerns for Autism. I only ended up googling again because I am filling out insurance paperwork and I wasn’t sure what they (insurance) considered this a behavioral diagnosis or neurological.
Thanks for posting your story and it’s comforting to find others out there. My son just turned 5 and is doing great, neuropsych eval came out very positive and his symptoms have decreased significantly. I am only to return if his symptoms worsen or it becomes a social concern. My understanding too, was that because he could be distracted during his symptoms this was why he it was more stereotypies than tourettes. My son’s symptoms was to abruptly sit up, turn his head, point his index finger up on one hand and the other arm would come in as well as a dreamy odd look on his face w/ an odd grin, over and over starting at first lasting seconds to eventually increased to many many minutes and repeating over a period of hours of these episodes. Even in the middle of the night. I also found fatigue increased his symptoms. What a crazy time life can be during the time your looking for a diagnosis.
I was told that 1/3 rule will get worse, get better or go away by puberty/adolescents. No medication is required for my son and he continues to progress academically/socially/and behaviorally.
During the diagnosis process I also noted another symptom, when the neurologist observed this she wanted to diagnosis him w/ motor tourettes since again no medication is required, she just wanted more testing to confirm the “new” symptoms was not epilepsy I declined the very expensive test and am confident he does not have epilepsy.
Many prayers and positive thoughts to every family that is going through this diagnosis and letting others know that things can be great at least they are here at my home.
60tabatha May 19, 2012 at 1:49 am
Thankyou so much for posting this blog.
My 3 year old son Brody has this. I was so terrified when I heard the diagnosis back in October. I have spent months coming across information online that hasn’t eased my nerves one bit. Reading you blog has brought me great comfort. Thankyou and God bless.
-Tabatha