ADHD Attention Deficit Hyperactivity Disorder

Parenting is a daunting responsibility even when things are running smoothly. When a child shows behavior requiring medical intervention, it becomes more difficult.

In order to help those who suspect their child may have this disorder, here are a few clues that a problem is ADHD rather than another disorder.

Does the child have difficulty paying attention to you or staying focused on a task?
Does the child have difficulty controlling themselves or appears hyperactive?
Does the child’s behavior seem out of sync with peers?

The average onset of ADHD is 7 years old. It is more prominent in boys than girls. The disorder manifests itself in 9.0 per cent of American children age 13 to 18.

 

 Clues

 

In order to help those who suspect their child may have this disorder, here are a few clues that a problem is ADHD rather than another disorder.

Does the child have difficulty paying attention to you or staying focused on a task?
Does the child have difficulty controlling themselves or appears hyperactive?
Does the child’s behavior seem out of sync with peers?

 

Similar Conditions

 

The average onset of ADHD is 7 years old. It is more prominent in boys than girls. The disorder manifests itself in 9.0 per cent of American children age 13 to 18.

Before rushing to a diagnosis of ADHD, there are several conditions that need to be ruled out. A pediatrician can determine if the child:

Has a middle ear infection. This could cause hearing problems and lack of interest.
Has recently had a change or disruption, such as a family member passing away, parents divorcing or other stressful situation.
Has vision problems making it difficult to concentrate.
Has seizures or other medical problems.
Has any other learning disabilities.

 

Symptoms

 

Observations that may indicate ADHD include the most common symptoms of inattention, hyperactivity and impulsive behavior. To receive a diagnosis of ADHD, the child must exhibit these behaviors for at least six months.

Inattention is indicated when a child often forgets things, switches from one activity to another and is easily distracted. If a child is easily bored with a task after a short time or has difficulty completing a job, it may be a sign of ADHD. Not listening when being spoken to, becoming easily confused, moving slowly and appearing to daydream may also be suspect.

Hyperactivity include symptoms such as fidgeting and squirming in their chair, talking nonstop, and dashing around. They may play with one toy for a short time then move quickly to another. The child feels the need to be constantly moving.

Impulsivity is shown through interrupting another child’s activities or an adult conversation, with no regard to consequences. They may blurt out comments unrelated to the subject. The child has difficulty waiting for their turn and shows disregard for another child’s needs or wishes.

 

Assessment

 

The disorder ADHD is derived from the above behaviors (Attention deficit hyperactivity disorder). It can continue through adolescent years and even into adulthood.

Children have different personalities and mature at different rates. They also exhibit various temperaments and have different energy levels. Most child exhibit one or more of the symptoms of ADHD at one time or other, but if it is persistent and disruptive to teachers, parents, classmates and siblings, it may need treatment.

There is no single diagnostic test for ADHD. It is assessed over time by parents with the help of pediatricians or mental health specialists. The child can be evaluated in social situations or be given academic and intellectual tests to determine if it is a learning disability or another disorder.

Concurrent Conditions

 

Other possible conditions which may manifest themselves at the same time as ADHD include:

Oppositional defiant disorder
Conduct disorder
Anxiety
Depression
Bipolar disorder
Tourette syndrome
Learning disability
Sleep disorder
Bed-wetting

A diagnosis of ADHD may require sessions of therapy, visits to the doctor, and alterations in personal and family behavior.

At this time, there is no known cure for ADHD, but with medication, therapy, social skills training and establishing routines, a child can show improvement and make life easier for all concerned.

Epilepsy in the 21st Century

Many myths and beliefs abound concerning epilepsy, and for anyone that has witnessed a full-fledge grand mal epileptic seizure, as I have, this is understandable. “Epilepsy is the most common serious neurological disorder and is one of the world’s most prevalent noncommunicable diseases”, yet few conditions carry the same stigma as this disorder. Victims either try to conceal it or struggle with embarrassment and rejection throughout their lives. Furthermore, 70 percent of people with epilepsy receive no treatment. Developing countries are home to the significant majority of people with epilepsy and, paradoxically, are the ones least prepared to provide care". Awareness of the conflicts between medical and spiritual realities of epileptics in developing countries will contribute to better health care and alleviate suffering. Revealing some of the misconceptions about epilepsy, the associated stigma that goes along with it, current remedies in third world countries, and presenting ways it can be better dealt with is the purpose of this paper.

Misconceptions

More than 50 million people worldwide suffer from epilepsy, yet erroneous beliefs about epilepsy are numerous. Murthy reported that in developing countries, patients with epilepsy encounter several significant barriers to adequate treatment and are more often managed according to local ethnic, racial, religious, economic, educational, and cultural diversities. Fadiman in her book “The Spirit Catches You and You Fall Down”, points out that a Hmong (Laos) who has epilepsy is considered to be an anointed one, has an elevated social status, and usually becomes a shaman (spiritual healer) later in life because the condition gives them intuitive sympathy for the suffering of others and lends them emotional credibility as healers. However, this positive attitude regarding epilepsy is the not the norm throughout the world. Jallon indicated, “The patient’s experience of epilepsy is closely related to his or her culture. In Africa, epilepsy is usually considered a dangerous and shameful disease because it is believed to be transmitted by saliva, urine, and expired air”.

In Uganda it is believed that epilepsy is caused by a lizard spinning around in circles in the head disturbing the brain and causing dizziness, usually followed by a seizure . Another belief in Malawi is that an insect that is moving inside the stomach causes epilepsy. In an area of Kenya that is inhabited by nomadic people a 14 year old girl was buried alive by her own parents because they believed that she was possessed and was harboring evil spirits. The abuse is not limited to the physical, as people with epilepsy are often shunned and verbally abused as well, told that they will get nowhere in life – that they are outcasts and failures. Some regions of the world consider epilepsy to be a metaphysical phenomenon and believe the only way to cure it is through sorcery. This is definitely a distressing situation for a person who has no idea how they came to have the disorder.

Throughout the years, epileptics have been regarded as different from the rest of humanity. Thanks to modern medicine, however, this belief is slowly changing. In reality, epilepsy in developing countries is found to be caused by poor living conditions where victims are exposed to a host of parasitic and infectious disease largely absent in industrialized countries. Malaria may indirectly lead to epilepsy as may malnutrition and under-resourced health care at the pre-, peri-, and postnatal levels. Neurocystercosis is another cause of epilepsy that is an infection of the central nervous system with cysticerci of the pork tapeworm. Studies from Latin America have shown that infection of the brain by the larvae of the pork tapeworm Taenia solium is an important cause of epileptic seizures in endemic communities. Trauma, a tumor or cyst, poisoning and infection can also cause it.Epilepsy is a disorder, not a disease. In about 70% of cases, it can be treated with medication, which can cost as little as US$5 a year per person. Studies from developing countries suggest that significant number of patients with epilepsy receive traditional therapy even when access to medical services is readily available. It is definitely a positive step to take in understanding the truth when it comes to epilepsy rather than listening to myths and cultural beliefs.

Stigma

Shame is widespread amongst epileptics as well as other negative emotions. Some aspects of the stigma that go along with epilepsy are “Fear of a seizure, injury, death, and embarrassment; of loss of employment, educational opportunities, or a driving license; or of limited marital prospects and social horizons. Sahni mentioned that with respect to family and friends, overprotection and restriction of activities interfere with their daily lives, as they are often seen as socially and intellectually less capab le than the remainder of the population. Many perceive negative public attitudes as a greater burden than seizures”. Jallon suggested that many health professionals often are ignorant about epilepsies (their causes, diagnoses, treatments and psychosocial aspects, and that it may rank with leprosy and mental illness in regards to the stigma. In China, epilepsy has been reported to threaten the aspirations of the entire family as well as the opportunities of the individual with epilepsy. Some parents even object to their children playing with a person with epilepsy. It is understandable then that many people try to hide their epilepsy.

Ignorance is hazardous and can cause a loss of self-esteem in a person with epilepsy. India (until recently) and other countries have laws that discriminate against people with epilepsy–for example, with regard to marriage, employment, and insurance. Engagements are often canceled. The parents of epileptic girls have to give heavy dowry at the time of marriage, even if the boy is handicapped. As a result, many girls do not disclose their problem before marriage. They take the medicine secretly. One of the most important aspects of a normal life and aspirations of young men and women is to have a family and children, Yet in India, persons with epilepsy were denied this fundamental right by prejudiced legislation enacted as late as 1976. Unbelievable but true, 18 states in America provided eugenic sterilization of people with epilepsy until 1956. Until the 1970s, it was also legal to deny people with seizures access to restaurants, theatres, recreational centers and other public buildings. It is understandable then that developing countries are still under a cloud of prejudice for the epileptic and their need for proper education regarding the disorder.

Remedies

Current remedies in third world countries are numerous. In Fadiman’s book, it was believed that the epilepsy of a baby girl was caused by the loud noise of a slamming door that frightened her soul out of her body. The parents felt the only way to get her soul back was to beckon the shaman who would sacrifice animals, ride on an imaginary horse over mountains and call her soul back. When they were faced with the seemingly cold American medical personnel who took vials of blood from their baby and prescribed medicines that seemed to make the child sicker rather than better, they felt more comfortable sticking with the traditions they had become accustomed to.

There is a plethora of horror stories about the treatment of people with epilepsy in underdeveloped countries. In certain parts of Nigeria an epileptic is forced to drink a mixture made of cow urine, thrusting their limbs into a fire, or rubbing pepper into their eyes and face. They also undergo dietary restrictions since they believe that the excess foam in the stomach rises to the head ultimately resulting in seizures. In Cameroon they believe that epilepsy is contagious, as do many inhabitants of other African countries. Treatment generally entails visiting a healer and undergoing dietary restrictions to help prevent the production of foam in the stomach since they believe that excess foam in the stomach rises to the head ultimately resulting in seizures. In India and China they practice Ayurvedic medicine, which focuses on opening the heart and mind, relieving the stresses and negative energies that are causing the seizures. This is done with enemas and purgatives, as well as ingesting purified butters (ghees) and oils. Chinese folk medicine for epilepsy, known as Dan Fang, suggests drinking a young girl’s urine and eating fresh human brain or goat’s heart. In Nepal, bystanders who witness a seizure will often spray water on the forehead of the person experiencing the seizure or make him or her smell a leather shoe. In the Netherlands in 1996, a person was whipped and put into isolation because her seizures were thought to result from magic. So much needless suffering has resulted from ignorance in regards to the true nature of epilepsy.

While four-fifths of the potential market for anti-epileptic drugs is in the developing worlds, up to 90% of people with epilepsy in developing countries receive no treatment at all. There may be various reasons for this, but poverty may be viewed as the root cause of the treatment gap. Lack of education regarding epilepsy also appears to be an epidemic. Everyday conditions for most of the worlds poor are radically different from the experience of the western hospital outpatient. The primary concern of families is often subsistence, and this shapes their attitudes to health and their contact with health services. Poor female literacy, often associated with underdevelopment, is an important influence whereas cultural and religious beliefs may also impinge on health related attitudes and practices.

Sahni indicated that herbal therapy is the most popular form of traditional medicine in Africa which includes mixtures of plants having an anti-seizure, antipyretic, or antibacterial effect. Spiritual healers are also common since epilepsy is thought to be related to a visitation by the devil, to witchcraft or to spirits. Scott pointed out that people might not seek treatment with antiepileptic drugs if epilepsy is not seen as a condition that can be treated by western medicine. There is a need to know that traditional healing is not the best or only way to remedy all disorders.

Dealing with it

There are many roadblocks that need to be cleared in educating the developing countries of the world regarding epilepsy. Palmini expounded “whenever doctors do not take the time to explain to epilepsy patients and their families the characteristics of the disease and the concepts and bases of treatment, there is a great risk that treatment failure will ensue”. The patient must be treated with respect and given every chance possible to live a normal life. “People with epilepsy need more than drug treatment because their local cultural context adds a social and economic burden to the physical burden of their seizures. The education of health workers, patients, and the wider community is therefore essential.” Appropriate interventions must consider the medical, developmental, and psychosocial needs of people with epilepsy, as well as being financially, geographically and culturally accessible. It seems like an insurmountable problem, but with continued effort it can be improved.

Hospitals in Wisconsin and Minnesota allow shamans (spiritual healers) to come in and perform healing rituals at the patient’s bedside. This puts them more at ease and willing to accept other forms of treatment from foreign doctors if they are shown respect for their own beliefs. A survey done at a Medical School in Nigeria showed that 40% of medical students were not sure that epilepsy was not contagious. It is clear that the dedication of doctors working in the public health system in developing countries mirrors the level of respect that society has for its members, whatever the social stratum. Thus, it is imperative that social changes do occur in these countries to enhance greater mutual respect. There appear to be few studies in developing countries aimed at professionals dealing with epileptics and conducting collaborative studies could enable epilepsy awareness groups to evaluate and compare the success of their medical education programs by appraising cross-cultural differences.

I have a niece who has epilepsy and has been able to marry and have five children. She takes medication daily and tries to do all that her doctors advise, but she still has seizures on occasion, which is a worry for her and her family. A third of people with epilepsy have physical or cognitive difficulties. Whether or not seizures can be controlled, people with epilepsy need to resume as normal a life as possible. This requires a holistic assessment and formulation of an action plan with the community. People need to be educated how to treat someone who has a seizure to alleviate the possibility of injury to anyone.

As with any chronic disorder, if it is proven to be so, medication and visits to the doctor need to continue. The treatment and rehabilitation of people with epilepsy is a long-term matter, and so it is essential that services, once started, continue in a predictable way. It also impacts societies as a whole, since our safety can depend on whether an epileptic when driving is taking his/her appropriate medication.

One of the main ideas in Fadiman’s book was the lack of ability to translate an idea from the American doctors to the Lee family. Even when they had an interpreter, some things just were not understandable according to their life experiences. That is why it is very important to try to understand a culture, including their spiritual and medical beliefs before trying to force new remedies on them.

Although many steps have been taken to try and reduce the stigma attached to epilepsy, more must still be done. A project in China is underway. Some of the key aspects of the programme are focused on knowledge, attitudes, and practices. It is intended to bring about a change in traditional and cultural attitudes so that stigma of epilepsy is reduced and more people are prepared to receive treatment.

Many misconceptions abound in the minds of people throughout the world regarding epilepsy even though it has been proven to be a treatable neurological condition. The challenges are great, but efforts on many levels are being put in place to alleviate unnecessary suffering for epileptics and their families. Education as well as awareness of different cultural beliefs and better communication between patients and the medical personnel can bring epilepsy into the 21^stcentury.

Sources Cited

Fadiman, Anne. The Spirit Catches You and You Fall Down. New York: Farrar, Straus and Giroux, 1997.

Jallon, P. “Epilepsy in Developing Countries.” International League Against Epilepsy Workshop Report, Epilepsia 38 (1997): 1142-1151.

Murthy, J.M.K. “Some Problems and Pitfalls in Developing Countries” Epilepsia44:s1 (2003): 38-42.

Nag D. “Gender and epilepsy: A Clinician’s experience”. Neurol India 48 (2000): 99-104.

Pal, Deb, Arturo Carpio, Josemir W A S Sander. “Neurocysticerosis and epilepsy in developing countries.” Neurological Aspects of Tropical Disease. (2000): 137-143. JNNP. March 16, 2006.

Palmini, André. “Medical and Surgical Strategies for Epilepsy Care in Developing Countries,” Epilepsia, 41 (2000) S10-217.

Press, Anna. “Ignorance is not Bliss: Epilepsy in Third World Countries,” Epilepsy Ontario (2000) March 16, 2006. http://epilepsyontario.org/client/eo/eoweb.nsf/

Reynolds, Edward. “Sudden death in the shadows of epilepsy.” BMJ (March 7, 2006): 349-350 http://bmj.com/cgi/content/full/326/385/349

Sahni, Puja. “Epilepsy in Africa and the African American Community.” Epilepsy Ontario. March 18, 2006

---“The Importance of Cultural Competency and Epilepsy,” Epilepsy Ontario: Multicultural Outreach Projecthttp://epilepsyontario.org/client/EO/EOWeb.nsf/web/Multicultural+Outreach+Project.

Scott, Robert A. Samden D. Lhatoo, Josemir W.A.S. Sander. “The treatment of epilepsy in developing countries: where do we go from here?” Bulletin of the World Health Organization (2001): 79.4.

Symonds, Patricia. Calling in the Soul. Seattle and London: University of Washington Press, 2004.

“Epilepsy: social consequences and economic aspects.” World Health Organization February 2001.

I Am Not Spina Bifida, I Am Lily

I am Loved

My grandma said she loved me before I was born. That is truly conceivable, since she was there together with my parents and siblings for my first sonogram. My family was giddy with excitement to discover if they would be adding a new sister or brother to their tribe. The sonogram Monitors were well placed so all could see me wiggle around inside my mother’s womb. The technician shared in the exuberance of the little crowd, and started the magic machine which could reveal images of me. Oohs and aahs were uttered as my tiny hand, foot or other little body part was recognized. Mommy, Daddy, my sisters, brother and Grandma saw images of my cute face, and discovered that I would most probably be a little girl. At first there was so much joy and anticipation, until a sudden hush fell over the room.

What about me?

The tech had noted classic characteristics of Spina Bifida, a birth defect in my spine and brain. All of a sudden, a doctor entered and suggested that grandma take the children to another room, while my Daddy stayed with mother. What had been a very happy occasion turned into tears and worries in an instant. My poor mother lie there emotionally injured. While grandmother tried to entertain my brother and sisters, a well-meaning physician shared the blatant facts with my parents. My spirit was housed in a broken and bent physical body. He encouraged them to abort me (calling me a fetus), since the likelihood of my being severely handicapped was imminent. What? What about me? My spirit was strong! I would be good and try to not cause too much trouble.

My "condition"

My parents thought about it only for a brief moment, and declared that they could not abort an innocent baby. Just the thought of it (to them) was bizarre and inhumane. They mustered up the courage and determination to raise a less than perfect baby. Years of operations, medical bills, daily cathetering, wheelchairs, were only part of what they faced. They were given a glimmer of hope that there was a possibility the defect could be fixed in utero, but it was highly unlikely. It was later confirmed that the defect was at L7, so the operation was impossible. My families hopes and dreams for me were sorely challenged, but they never wavered in their faith that my spirit would be strong.

I am Lily

I am Lily! I was born December 15, 2008 with all my fingers and toes, and an adorable little face with bright blue eyes. My spinal cord had not developed properly, and was partially outside of my back, encased in a little sac. I was adored and loved as much, and even more (out of compassion) than most babies. My family supported me through many years of medical procedures and daily, even hourly extraordinary care. Now I am five years old. I have my own pink wheelchair, and can go faster than most people can walk. I have great upper body strength developed from many years of pulling myself around by my arms and hands. I love to sing and dance. Yes, I dance in my wheelchair. My parents took me to dance lessons to learn how to be graceful and meet other children like me.

I can do it!

http://elayne001.hubpages.com/hub/I-Am-Not-Spina-Bifida-I-Am-Lily
I spent much of my earthly life on the floor, on my skateboard, on the couch or in my hot pink chair. There is also a gizmo called the kangaroo which helps me jump around. I attend preschool and I am very witty. My parents got me a great playground that I can climb by myself and go down the slide. I have worn braces on my legs since I was tiny, because I have club feet. My upper body is a size larger than my lower body since the lower muscles are not used. My grandma used to pinch my legs to see if I could feel anything. It is okay, because it doesn’t hurt. My grandma thinks I am a bit bossy, because I always tell her what to do, but she usually does it anyway.