Myasthenia Gravis is a neuromuscular disease causing fluctuating muscle weakness and fatigue due to a breakdown in communication between nerves and muscles. There is no cure, but treatment can relieve symptoms. Signs include weakness of specific muscles like eyes and throat, as well as limbs, worsened by exertion and stress. Physical therapy focuses on aerobic exercise, strength training, swimming, posture, and breathing to build functional capacity and decrease fatigue while avoiding overexertion that worsens symptoms. The goal is improved mobility, balance, and ability to perform daily activities.
Hierachical theory- says that higher centers control on lower center; but when higher center damage then this inhibitory control from the higher center is loss which leads to exageration of the movt.
In normal individual, these occur a smooth, rhythmic movt. Because there is a presence of control from higher center on lower center.
Duchenne Muscular Dystrophy (DMD) is a genetic disorder caused by mutations in the dystrophin gene leading to progressive muscle weakness. It mainly affects boys and symptoms start between ages 2-3. Affected children become wheelchair bound by age 12 and have life-threatening heart, respiratory, and orthopedic complications if not properly managed. Management involves monitoring for cardiomyopathy, respiratory support, orthopedic care, corticosteroids which can prolong ambulation, and future therapies like gene therapy aim to treat the underlying genetic cause.
Peripheral neuropathy is a condition that results from damage to the peripheral nerves outside of the brain and spinal cord. It can cause numbness, tingling, pain or weakness in the hands, feet or other areas. There are several types including peripheral, autonomic and focal neuropathies. The most common cause is diabetes, through mechanisms such as increased aldose reductase activity and oxidative stress damaging nerves over time. Diagnosis involves physical exams, nerve conduction tests and ruling out other potential causes. Treatment focuses on managing pain, slowing progression, and preventing complications through good glucose control, medications, physical therapy and foot care.
Pes planus, or flat feet, is a loss of the medial longitudinal arch of the foot. It can be flexible or fixed, developmental or acquired. Treatment is usually only needed if pes planus is new, painful, progressing, or associated with other problems. Non-surgical treatments include stretching exercises, orthotics, and addressing contributing factors like tight heel cords or obesity. Surgery is considered for rigid, painful pes planus or conditions that may worsen without intervention.
Neurodevelopmental Therapy
Neurodevelopmental treatment (NDT) is a hands-on treatment approach used by physical therapists, occupational therapists, and speech-language pathologists
Without NDT interventions, the patient likely will develop a limited set of movement patterns that he or she will apply to nearly all tasks.
This document discusses current trends in the management of spasticity in hemiplegic patients. It defines spasticity as a velocity-dependent increase in muscle tone caused by damage to the central nervous system. Spasticity can range from mild muscle stiffness to severe, painful muscle spasms. If left untreated, spasticity may lead to muscle contractures, deformities, and other complications. Common treatments discussed include oral medications, botulinum toxin injections, physical therapy, and the modified Ashworth scale for assessing spasticity severity.
Physiotherapy management for rheumatoid arthritissenphysio
Rheumatoid arthritis is an autoimmune disease that causes chronic inflammation of the joints. It most commonly affects women and can lead to joint damage, deformity, and disability over time. Physiotherapy plays an important role in managing rheumatoid arthritis by providing pain relief, preventing deformities, improving flexibility and strength, and maintaining functional ability. Treatment involves heat/cold therapy, exercises, joint protection techniques, and alternative therapies to help reduce inflammation and preserve joint function. The goals of physiotherapy are to protect joints, relieve pain, and prevent disability through regular exercise and mobility work.
Myasthenia Gravis is a neuromuscular disease causing fluctuating muscle weakness and fatigue due to a breakdown in communication between nerves and muscles. There is no cure, but treatment can relieve symptoms. Signs include weakness of specific muscles like eyes and throat, as well as limbs, worsened by exertion and stress. Physical therapy focuses on aerobic exercise, strength training, swimming, posture, and breathing to build functional capacity and decrease fatigue while avoiding overexertion that worsens symptoms. The goal is improved mobility, balance, and ability to perform daily activities.
Hierachical theory- says that higher centers control on lower center; but when higher center damage then this inhibitory control from the higher center is loss which leads to exageration of the movt.
In normal individual, these occur a smooth, rhythmic movt. Because there is a presence of control from higher center on lower center.
Duchenne Muscular Dystrophy (DMD) is a genetic disorder caused by mutations in the dystrophin gene leading to progressive muscle weakness. It mainly affects boys and symptoms start between ages 2-3. Affected children become wheelchair bound by age 12 and have life-threatening heart, respiratory, and orthopedic complications if not properly managed. Management involves monitoring for cardiomyopathy, respiratory support, orthopedic care, corticosteroids which can prolong ambulation, and future therapies like gene therapy aim to treat the underlying genetic cause.
Peripheral neuropathy is a condition that results from damage to the peripheral nerves outside of the brain and spinal cord. It can cause numbness, tingling, pain or weakness in the hands, feet or other areas. There are several types including peripheral, autonomic and focal neuropathies. The most common cause is diabetes, through mechanisms such as increased aldose reductase activity and oxidative stress damaging nerves over time. Diagnosis involves physical exams, nerve conduction tests and ruling out other potential causes. Treatment focuses on managing pain, slowing progression, and preventing complications through good glucose control, medications, physical therapy and foot care.
Pes planus, or flat feet, is a loss of the medial longitudinal arch of the foot. It can be flexible or fixed, developmental or acquired. Treatment is usually only needed if pes planus is new, painful, progressing, or associated with other problems. Non-surgical treatments include stretching exercises, orthotics, and addressing contributing factors like tight heel cords or obesity. Surgery is considered for rigid, painful pes planus or conditions that may worsen without intervention.
Neurodevelopmental Therapy
Neurodevelopmental treatment (NDT) is a hands-on treatment approach used by physical therapists, occupational therapists, and speech-language pathologists
Without NDT interventions, the patient likely will develop a limited set of movement patterns that he or she will apply to nearly all tasks.
This document discusses current trends in the management of spasticity in hemiplegic patients. It defines spasticity as a velocity-dependent increase in muscle tone caused by damage to the central nervous system. Spasticity can range from mild muscle stiffness to severe, painful muscle spasms. If left untreated, spasticity may lead to muscle contractures, deformities, and other complications. Common treatments discussed include oral medications, botulinum toxin injections, physical therapy, and the modified Ashworth scale for assessing spasticity severity.
Physiotherapy management for rheumatoid arthritissenphysio
Rheumatoid arthritis is an autoimmune disease that causes chronic inflammation of the joints. It most commonly affects women and can lead to joint damage, deformity, and disability over time. Physiotherapy plays an important role in managing rheumatoid arthritis by providing pain relief, preventing deformities, improving flexibility and strength, and maintaining functional ability. Treatment involves heat/cold therapy, exercises, joint protection techniques, and alternative therapies to help reduce inflammation and preserve joint function. The goals of physiotherapy are to protect joints, relieve pain, and prevent disability through regular exercise and mobility work.
Important structures associated with neural control of locomotion- CPGs, Peripheral receptors and afferents, Basal ganglia, Cerebellum, Brainstem, Cerebellar Cortex.
Rood's approach is a neurophysiological technique developed in 1940 based on reflex models of motor control. It uses sensory stimulation to normalize tone and elicit desired muscle responses based on developmental sequences. The key concepts are:
1. Categorizing muscles as tonic or phasic for stability or mobility.
2. Using ontogenic sequences of motor and vital functions development.
3. Applying appropriate sensory stimuli like touch or vibration to proprioceptive, exteroceptive, and vestibular receptors.
4. Manipulating the autonomic nervous system with techniques like icing or warming.
This document discusses different types of gait abnormalities and their causes. It defines gait as the pattern of limb movement during locomotion. Gait abnormalities deviate from normal walking and can indicate neurological or musculoskeletal issues. Several specific gait abnormalities are described, including scissor gait caused by spastic cerebral palsy, antalgic gait indicating pain with weight bearing, festinant gait seen in Parkinson's disease, and Trendelenburg gait caused by abductor muscle weakness. The document provides examples of medical conditions associated with each abnormal gait pattern.
Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle weakness. It is caused by an absence of the protein dystrophin due to mutations in the dystrophin gene on the X chromosome. The disease mainly affects boys and results in the breakdown of skeletal muscles. While there is no cure, treatment aims to manage symptoms and improve quality of life through physical therapy, bracing, medication, and respiratory/nutritional support. Research continues on new therapies such as gene therapy to replace the missing dystrophin protein.
Muscular dystrophy is a genetic disease that causes the muscles to weaken over time. There are several types but Duchenne muscular dystrophy is the most common and severe, affecting boys. It is caused by an absence of dystrophin protein which leads to muscle cell damage. Symptoms start in early childhood and include difficulty walking, joint contractures, and loss of ambulation in the teen years. Management is multidisciplinary and focuses on maintaining mobility and function as long as possible, treating complications, and palliative care as the condition progresses. Life expectancy for Duchenne patients is usually early 20s.
This document provides information on diagnostic investigations and assessments for cerebellar ataxia. It lists various tests that can be done as part of the diagnostic workup including blood tests, imaging studies, genetic testing, and neurological exams. Specific tests are described to evaluate factors like balance, coordination, gait, dysmetria, and oculomotor performance that may be impaired with cerebellar ataxia. A thorough patient history and neurological exam incorporating several assessment scales are important for evaluating ataxia.
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder characterized by progressive muscle degeneration and weakness. It is caused by the absence of the protein dystrophin due to mutations in the DMD gene. Symptoms usually begin between ages 2-6 and include difficulty walking, climbing stairs, and rising from the floor. Affected individuals lose the ability to walk by age 12 and often die in their 20s from respiratory or cardiac failure. Diagnosis involves testing for elevated creatine kinase levels and detecting dystrophin abnormalities through muscle biopsy or genetic testing. Currently there is no cure, but treatment focuses on symptom management through bracing, steroids, respiratory support, and physical therapy
NDT, BOBATH TECHNIQUE, BASIC IDEA OF BOBATH, CONCEPT OF BOBATH, NEUROPHYSIOLOGY OF NDT, ICF MODEL, PRINCIPLES OF TREATMENT OF NDT IN STROKE AND CP, AUTOMATIC AND EQUILIBRIUM REACTIONS, KEY POINTS OF CONTROL, FACILITATION, INHIBITION AND HANDLING IN NDT
As part of a class presentation, we attempted to make this to briefly explain what Torticollis meas, the Types of presentation of Torticollis, and Management strategies for a Physiotherapist for Congenital Torticollis especially.
I hope this helps. :)
The pictures and information had been taken from internet, complied to make a brief presentation for the purpose of class presentation.
I do not own any content.
Cerebral Palsy: PT assessment and ManagementSurbala devi
Cerebral palsy (CP) is a group of disorders caused by damage to the developing brain before, during or after birth. It affects movement and posture, and can cause physical disability. The main types are spastic, athetoid, ataxic and hypotonic CP. Symptoms vary depending on the type and severity. CP is diagnosed based on signs of impaired motor development and abnormal muscle tone or movement. There is no cure for CP, but treatment aims to improve ability and quality of life through therapies and medications.
Emery-Dreifuss muscular dystrophy (EDMD) is a rare genetic muscle disease that causes progressive weakness and wasting of the muscles. It affects both the skeletal muscles used for movement and the heart muscles. The main symptoms are weakness of the shoulder and upper arm muscles and calf muscles, which can lead to difficulty walking and abnormal spine curvature. Heart problems also commonly occur. EDMD is caused by mutations in genes that produce proteins important for muscle cell structure and is typically inherited in an X-linked or autosomal dominant/recessive pattern. Physical therapy focuses on exercises to maintain strength and flexibility and can include assistive devices as the condition progresses.
This document presents a research paper on the female athlete triad among female basketball players in India. The paper defines the three components of the triad as disordered eating, menstrual dysfunction, and osteoporosis. It describes administering a screening questionnaire to 80 female basketball players and analyzing the results. The results found that most players did not exhibit high-risk behaviors or symptoms of the triad, though a few had minor issues. The paper concludes there is no prevalence of the triad among these players but recommends continued education to prevent problems in athletes.
1. Neurodevelopmental therapy (NDT) was developed in 1948 by Berta and Karel Bobath to treat patients with central nervous system damage like hemiplegia and stroke.
2. NDT uses a problem-solving approach involving examination of posture, movement, functional skills, and systems to develop individualized treatment plans. The goal is to minimize impairments and prevent secondary disabilities.
3. The NDT examination process evaluates clients holistically, incorporates their family/environment, and identifies both limitations and competencies to inform treatment planning.
Cerebellar ataxia is a lack of muscle coordination caused by lesions in the cerebellum. It can result from genetic conditions, infections like chickenpox, brain tumors, head trauma, or exposure to toxins. Symptoms include unsteady walking, slurred speech, dizziness, and uncoordinated eye movements. While the condition cannot be cured, treatment focuses on managing symptoms through physical therapy, lifestyle adaptations like walkers or wheelchairs, and addressing any underlying causes.
This document discusses athetosis and dystonia. It defines athetosis as irregular, slow writhing movements, often of the extremities and fingers. Dystonia is defined as an abnormal sustained muscle contraction causing twisting movements and abnormal postures. The document describes the clinical presentations and patterns of movement seen in athetosis. It discusses the potential pathophysiology of athetosis involving lesions in the frontal lobes, parietal lobes, and putamen. Causes of athetosis in children and adults are provided. Dystonia is similarly defined and classified. Potential pathology, types, hereditary forms, and secondary causes of dystonia are outlined in detail.
Cerebral palsy is a neurodevelopmental condition characterized by impaired muscle tone, movement, and motor skills, caused by non-progressive disturbances in the developing fetal or infant brain. It is a heterogeneous syndrome with varied presentations. Management requires a multidisciplinary approach including physical therapy, medications to manage spasticity and other symptoms, surgery, nutrition support, and social services. Prognosis depends on factors like severity of impairment, birth weight, intelligence, physical and communication abilities, and access to care.
CIMT involves constraining the unaffected limb, along with intense therapy, in order to force the use of the affected limb with intent to improve motor function.
This document discusses carpal tunnel syndrome, which is caused by compression of the median nerve as it passes through the carpal tunnel of the wrist. It can cause numbness, tingling, and weakness in the hand. The presentation outlines the causes, clinical features, diagnosis, and treatment options for carpal tunnel syndrome, which include wrist splints, oral anti-inflammatory medications, local steroid injections, and carpal tunnel release surgery if conservative measures fail. The document provides details on physical exam findings and special tests like Tinel's and Phalen's maneuvers used to diagnose carpal tunnel syndrome.
The Brunnstrom concept is a theoretical model of motor recovery following central nervous system injury developed by physical therapist Signe Brunnstrom. It is based on the hierarchical reflex theory and assumes that lower level reflexes get incorporated into purposeful movements through higher centers. Recovery proceeds from primitive reflexive movement to voluntary isolated movements. Treatment involves facilitating this progression using reflexes, associated reactions, proprioceptive and exteroceptive stimuli, and resistance. Motor and sensory function is evaluated using Brunnstrom's staging which characterizes recovery in a sequential progression.
Educational needs for Children with EpilepsyA.J. Lawrence
In order to make well thought out decisions for children with epilepsy, it is necessary to acknowledge all objective data including scores from testing, observations, outside therapists, history, emotional and personality variables, family and school data. One must pay close attention to their child and look for early signs of epilepsy in order to address specific educational needs and prevent hindered development.
HIV/AIDS Stigma & Discrimination by Dr Munawar Khan SACPDr Munawar Khan
The document discusses HIV/AIDS related stigma and discrimination. It defines stigma and discrimination, and explains how stigma works by labeling, stereotyping and devaluing individuals. It discusses the different types of stigma including external stigma of discrimination from others and internal stigma of low self-esteem. Root causes of stigma are discussed as lack of HIV knowledge and moral judgments of those with HIV. Addressing stigma requires educating healthcare workers and the community to correct misinformation and promote compassion.
Important structures associated with neural control of locomotion- CPGs, Peripheral receptors and afferents, Basal ganglia, Cerebellum, Brainstem, Cerebellar Cortex.
Rood's approach is a neurophysiological technique developed in 1940 based on reflex models of motor control. It uses sensory stimulation to normalize tone and elicit desired muscle responses based on developmental sequences. The key concepts are:
1. Categorizing muscles as tonic or phasic for stability or mobility.
2. Using ontogenic sequences of motor and vital functions development.
3. Applying appropriate sensory stimuli like touch or vibration to proprioceptive, exteroceptive, and vestibular receptors.
4. Manipulating the autonomic nervous system with techniques like icing or warming.
This document discusses different types of gait abnormalities and their causes. It defines gait as the pattern of limb movement during locomotion. Gait abnormalities deviate from normal walking and can indicate neurological or musculoskeletal issues. Several specific gait abnormalities are described, including scissor gait caused by spastic cerebral palsy, antalgic gait indicating pain with weight bearing, festinant gait seen in Parkinson's disease, and Trendelenburg gait caused by abductor muscle weakness. The document provides examples of medical conditions associated with each abnormal gait pattern.
Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle weakness. It is caused by an absence of the protein dystrophin due to mutations in the dystrophin gene on the X chromosome. The disease mainly affects boys and results in the breakdown of skeletal muscles. While there is no cure, treatment aims to manage symptoms and improve quality of life through physical therapy, bracing, medication, and respiratory/nutritional support. Research continues on new therapies such as gene therapy to replace the missing dystrophin protein.
Muscular dystrophy is a genetic disease that causes the muscles to weaken over time. There are several types but Duchenne muscular dystrophy is the most common and severe, affecting boys. It is caused by an absence of dystrophin protein which leads to muscle cell damage. Symptoms start in early childhood and include difficulty walking, joint contractures, and loss of ambulation in the teen years. Management is multidisciplinary and focuses on maintaining mobility and function as long as possible, treating complications, and palliative care as the condition progresses. Life expectancy for Duchenne patients is usually early 20s.
This document provides information on diagnostic investigations and assessments for cerebellar ataxia. It lists various tests that can be done as part of the diagnostic workup including blood tests, imaging studies, genetic testing, and neurological exams. Specific tests are described to evaluate factors like balance, coordination, gait, dysmetria, and oculomotor performance that may be impaired with cerebellar ataxia. A thorough patient history and neurological exam incorporating several assessment scales are important for evaluating ataxia.
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder characterized by progressive muscle degeneration and weakness. It is caused by the absence of the protein dystrophin due to mutations in the DMD gene. Symptoms usually begin between ages 2-6 and include difficulty walking, climbing stairs, and rising from the floor. Affected individuals lose the ability to walk by age 12 and often die in their 20s from respiratory or cardiac failure. Diagnosis involves testing for elevated creatine kinase levels and detecting dystrophin abnormalities through muscle biopsy or genetic testing. Currently there is no cure, but treatment focuses on symptom management through bracing, steroids, respiratory support, and physical therapy
NDT, BOBATH TECHNIQUE, BASIC IDEA OF BOBATH, CONCEPT OF BOBATH, NEUROPHYSIOLOGY OF NDT, ICF MODEL, PRINCIPLES OF TREATMENT OF NDT IN STROKE AND CP, AUTOMATIC AND EQUILIBRIUM REACTIONS, KEY POINTS OF CONTROL, FACILITATION, INHIBITION AND HANDLING IN NDT
As part of a class presentation, we attempted to make this to briefly explain what Torticollis meas, the Types of presentation of Torticollis, and Management strategies for a Physiotherapist for Congenital Torticollis especially.
I hope this helps. :)
The pictures and information had been taken from internet, complied to make a brief presentation for the purpose of class presentation.
I do not own any content.
Cerebral Palsy: PT assessment and ManagementSurbala devi
Cerebral palsy (CP) is a group of disorders caused by damage to the developing brain before, during or after birth. It affects movement and posture, and can cause physical disability. The main types are spastic, athetoid, ataxic and hypotonic CP. Symptoms vary depending on the type and severity. CP is diagnosed based on signs of impaired motor development and abnormal muscle tone or movement. There is no cure for CP, but treatment aims to improve ability and quality of life through therapies and medications.
Emery-Dreifuss muscular dystrophy (EDMD) is a rare genetic muscle disease that causes progressive weakness and wasting of the muscles. It affects both the skeletal muscles used for movement and the heart muscles. The main symptoms are weakness of the shoulder and upper arm muscles and calf muscles, which can lead to difficulty walking and abnormal spine curvature. Heart problems also commonly occur. EDMD is caused by mutations in genes that produce proteins important for muscle cell structure and is typically inherited in an X-linked or autosomal dominant/recessive pattern. Physical therapy focuses on exercises to maintain strength and flexibility and can include assistive devices as the condition progresses.
This document presents a research paper on the female athlete triad among female basketball players in India. The paper defines the three components of the triad as disordered eating, menstrual dysfunction, and osteoporosis. It describes administering a screening questionnaire to 80 female basketball players and analyzing the results. The results found that most players did not exhibit high-risk behaviors or symptoms of the triad, though a few had minor issues. The paper concludes there is no prevalence of the triad among these players but recommends continued education to prevent problems in athletes.
1. Neurodevelopmental therapy (NDT) was developed in 1948 by Berta and Karel Bobath to treat patients with central nervous system damage like hemiplegia and stroke.
2. NDT uses a problem-solving approach involving examination of posture, movement, functional skills, and systems to develop individualized treatment plans. The goal is to minimize impairments and prevent secondary disabilities.
3. The NDT examination process evaluates clients holistically, incorporates their family/environment, and identifies both limitations and competencies to inform treatment planning.
Cerebellar ataxia is a lack of muscle coordination caused by lesions in the cerebellum. It can result from genetic conditions, infections like chickenpox, brain tumors, head trauma, or exposure to toxins. Symptoms include unsteady walking, slurred speech, dizziness, and uncoordinated eye movements. While the condition cannot be cured, treatment focuses on managing symptoms through physical therapy, lifestyle adaptations like walkers or wheelchairs, and addressing any underlying causes.
This document discusses athetosis and dystonia. It defines athetosis as irregular, slow writhing movements, often of the extremities and fingers. Dystonia is defined as an abnormal sustained muscle contraction causing twisting movements and abnormal postures. The document describes the clinical presentations and patterns of movement seen in athetosis. It discusses the potential pathophysiology of athetosis involving lesions in the frontal lobes, parietal lobes, and putamen. Causes of athetosis in children and adults are provided. Dystonia is similarly defined and classified. Potential pathology, types, hereditary forms, and secondary causes of dystonia are outlined in detail.
Cerebral palsy is a neurodevelopmental condition characterized by impaired muscle tone, movement, and motor skills, caused by non-progressive disturbances in the developing fetal or infant brain. It is a heterogeneous syndrome with varied presentations. Management requires a multidisciplinary approach including physical therapy, medications to manage spasticity and other symptoms, surgery, nutrition support, and social services. Prognosis depends on factors like severity of impairment, birth weight, intelligence, physical and communication abilities, and access to care.
CIMT involves constraining the unaffected limb, along with intense therapy, in order to force the use of the affected limb with intent to improve motor function.
This document discusses carpal tunnel syndrome, which is caused by compression of the median nerve as it passes through the carpal tunnel of the wrist. It can cause numbness, tingling, and weakness in the hand. The presentation outlines the causes, clinical features, diagnosis, and treatment options for carpal tunnel syndrome, which include wrist splints, oral anti-inflammatory medications, local steroid injections, and carpal tunnel release surgery if conservative measures fail. The document provides details on physical exam findings and special tests like Tinel's and Phalen's maneuvers used to diagnose carpal tunnel syndrome.
The Brunnstrom concept is a theoretical model of motor recovery following central nervous system injury developed by physical therapist Signe Brunnstrom. It is based on the hierarchical reflex theory and assumes that lower level reflexes get incorporated into purposeful movements through higher centers. Recovery proceeds from primitive reflexive movement to voluntary isolated movements. Treatment involves facilitating this progression using reflexes, associated reactions, proprioceptive and exteroceptive stimuli, and resistance. Motor and sensory function is evaluated using Brunnstrom's staging which characterizes recovery in a sequential progression.
Educational needs for Children with EpilepsyA.J. Lawrence
In order to make well thought out decisions for children with epilepsy, it is necessary to acknowledge all objective data including scores from testing, observations, outside therapists, history, emotional and personality variables, family and school data. One must pay close attention to their child and look for early signs of epilepsy in order to address specific educational needs and prevent hindered development.
HIV/AIDS Stigma & Discrimination by Dr Munawar Khan SACPDr Munawar Khan
The document discusses HIV/AIDS related stigma and discrimination. It defines stigma and discrimination, and explains how stigma works by labeling, stereotyping and devaluing individuals. It discusses the different types of stigma including external stigma of discrimination from others and internal stigma of low self-esteem. Root causes of stigma are discussed as lack of HIV knowledge and moral judgments of those with HIV. Addressing stigma requires educating healthcare workers and the community to correct misinformation and promote compassion.
This presentation brings together 3 currents in my approach to treating pediatric epilepsy: a recognition of the importance of epilepsy comorbidities, partnering with families in patient assessment and decision making, and creative use of informatics/EHR's to gather information about clinical aspects of epilepsy. A presentation to the Missouri Valley Child Neurology Colloquium, March 2012.
The document discusses physical fitness and its benefits. Physical fitness includes cardiovascular endurance, muscular endurance, muscular strength, flexibility, and lean body composition, achieved through regular exercise. Maintaining physical fitness provides numerous health benefits such as reduced risk of disease, more energy, better stress management, stronger bones and muscles, improved sleep and digestion, and a longer lifespan.
This document discusses the physical fitness test (PFT) that is administered in schools. It provides information about the two types of PFT - the pre-test at the beginning of the school year and the post-test at the end to measure changes. It outlines the various components that are tested, including agility, speed, flexibility, leg power, abdominal strength, and cardio endurance. The document also discusses the different physical fitness components for athletes versus ordinary individuals and provides tips for exercising safely and effectively. Finally, it debunks some common myths about physical fitness.
SPORTS MEDICINE SEMINAR PRESENTATION NDUTH RESIDENCY.pptxdaughter awala
This document discusses sports medicine and exercise physiology. It defines sports medicine as the branch of medicine concerned with exercising individuals, dealing with fitness, injuries from sports and exercise, and their treatment and prevention. It describes the health benefits of regular exercise, including improved cardiovascular health, glycemic control, bone mineral density, and mental health. It also discusses gender-specific considerations, such as the female athlete triad and exercise during pregnancy. The physiological adaptations to different types of exercise like aerobic and anaerobic activity are also summarized.
Physical exercise includes any activity that maintains or improves physical fitness and overall health. It is performed for reasons such as strengthening muscles, cardiovascular health, weight control, and enjoyment. There are three main types of exercise: flexibility, aerobic, and anaerobic. Regular physical exercise provides important health benefits, but excessive exercise without proper rest and nutrition can cause harm and injuries over time.
Physical exercise includes any bodily activity that enhances physical fitness and overall health. There are three main types of exercise: flexibility, aerobic, and anaerobic. Physical exercise provides numerous benefits such as strengthening muscles and the cardiovascular system, reducing stress, improving sleep, and helping to prevent chronic conditions. However, excessive exercise without proper rest can potentially cause harm through overtraining or injury. Exercise needs to be tailored to each individual's physical limitations.
Regular physical activity is associated with lower risk of cardiovascular disease. Engaging in moderate physical activity for at least 150 minutes per week or vigorous activity for 75 minutes per week provides significant health benefits by reducing risk factors like high blood pressure and improving heart function. Exercise training leads to improvements in cardiac health and symptoms for those with coronary artery disease or chronic heart failure compared to procedures like percutaneous coronary intervention alone. Maintaining physical activity throughout life is important for ongoing cardiovascular protection.
Exercise offers an effective treatment for mental health issues without requiring a prescription. Studies show that exercise reduces stress by releasing endorphins and improving cardiovascular health. It also benefits conditions like anxiety, depression, and ADHD by increasing the brain's production of dopamine, norepinephrine, and serotonin. In addition to improving mood and cognitive functions, exercise reduces inflammation and enhances brain structure and function.
Stroke is the third leading cause of death in the US and the leading cause of severe disability. Rehabilitation after a stroke aims to prevent complications, maximize functional independence, and facilitate a return to normal life roles and community integration. Post-stroke rehabilitation includes physiotherapy, medication management, and psychological support. The goals are to address impairments, prevent issues like contractures, and train new skills to manage daily living. A variety of rehabilitation techniques and technologies are used depending on individual needs and impairments. Outcomes vary based on neurological deficits and rehabilitation received, though many patients achieve significant functional gains.
This document discusses cerebral palsy (CP), a group of permanent disorders caused by damage to the developing brain that affects body movement and muscle tone. CP symptoms can range from mild to severe and vary depending on the location and degree of brain damage. It is classified in different ways including by the affected body parts (topographical), type of movement abnormality (neuromotor), and functional ability. While CP is non-progressive, physical therapy and management of symptoms can help reduce impairments and secondary complications over the lifespan.
This document discusses the many health benefits of exercise for older adults. It summarizes that exercise can help reduce the risks and effects of diseases like diabetes, hypertension, stroke, heart disease, osteoporosis, arthritis, and some cancers. It recommends both aerobic exercise like walking or dancing for 30 minutes a day, as well as strength training two times a week, to improve health, mobility, and quality of life as people age. The document emphasizes that exercise is the best way for older adults to stay healthy and independent.
Special consideration in cardiac rehabilitation in heart failure patientsQuratBenu1
1) The document discusses special considerations for cardiac rehabilitation programs for patients with heart failure.
2) It outlines three main types of heart failure and explains the muscle hypothesis, which links reduced cardiac function to peripheral skeletal muscle abnormalities.
3) Key factors for exercise programs discussed include extensive medical screening, monitoring drug regimens, using low-intensity exercise testing and prescriptions, and providing education to patients about symptom recognition and disease management.
This document discusses the pathological effects of excessive physical exertion in athletes. It defines excessive physical exertion as pushing the body beyond its threshold, which can lead to overtraining syndrome and cause physical and mental exhaustion. The physical effects include muscle fatigue, joint pain, injury, and decreased immunity. The mental effects are depression, anxiety, and burnout. Prevention is achieved through proper training, nutrition, and rest so athletes can perform their best without compromising their health.
3. Physical Activity in Diabetes management - Copy.pptxVEERESHKADEMANI1
The document discusses the role of physical activity and exercise in diabetes management. It covers topics like the benefits of aerobic and resistance training in improving health outcomes, components of an exercise prescription including frequency, intensity and time, assessing a patient's exercise needs, different types of exercise, strategies to prevent hypoglycemia during or after exercise, and concludes that physical activity should be recommended to all individuals with diabetes.
This document discusses performance enhancing drugs in sports. It defines drugs as substances that can produce physical or psychological effects when taken. It then discusses why athletes may be tempted to take performance enhancing drugs, noting the high stakes of competition and potential financial rewards. The document categorizes performance enhancing drugs into prohibited classes of substances like stimulants, narcotics, anabolic steroids, and diuretics. It also discusses prohibited methods like blood doping. Side effects of various drugs are explained.
The document discusses several endocrine disorders and their relevance to physiotherapy. It covers topics like:
- The three main types of endocrine diseases: gland hyposecretion, hypersecretion, and tumors.
- The challenges of diagnosing endocrine diseases given difficulties directly assaying hormone levels.
- An overview of the major endocrine glands like the hypothalamus, pituitary gland, thyroid, parathyroids, adrenals, pancreas, ovaries and testes.
- Some common endocrine diseases that may benefit from physiotherapy interventions like Cushing's syndrome, hypothyroidism, hyperthyroidism, amenorrhea, and polycystic ovary syndrome.
Exercise as a prescriptive medicine in Non Communicable Diseases Tinuade Olarewaju
Exercise is a prescriptive medicine. Physiotherapists use it as a potent tool to combat several NCD's also referred to as diseases of civilisation. Thanks to all references who made their work publicly available.
If de-adaptation occurs due to overtraining it is usually too late to effectively reverse the condition of the athlete. Therefore, the key issue in dealing with overtraining syndrome is prevention.
Similar to Epilepsy and phsical exercise debate (20)
The document discusses neuroimmunology and provides information on the immune system and its normal functions and disorders. It describes the innate and adaptive immune systems, including skin, phagocytes, natural killer cells, the complement system, antibodies, B cells, antigen presenting cells, major histocompatibility complex, toll-like receptors, T lymphocytes, cluster of differentiation markers, cytokines, chemokines, initiation and regulation of the immune response, termination of the immune response, self-tolerance, central tolerance, peripheral tolerance, anergy, regulatory T cells, immune privilege in the central nervous system, and several immune-mediated disorders of the nervous system including multiple sclerosis, myasthenia gravis, Guillain-Barré syndrome
Recent Modalities of Neuro-imaging discusses various imaging techniques used to image the brain and spinal cord, including:
- Computed tomography perfusion which uses contrast to generate maps of cerebral blood flow, volume, and transit time to identify ischemic tissue.
- Myelography which uses intrathecal contrast for spinal imaging.
- Magnetic resonance techniques like quantitative MRI, diffusion tensor imaging, and MR spectroscopy which provide microstructural data on tissues.
- Perfusion imaging uses ultrasound contrast to assess cerebral blood flow.
Imaging findings are discussed for conditions like multiple sclerosis, epilepsy, and stroke.
This document summarizes higher cortical functions including language, calculations, spatial awareness, memory, executive function, music and creativity. It discusses the cerebral cortex and different types of association cortices. It then examines various neurological functions like sensory processing, attention, motor programming, language, memory, agnosias, apraxia, aphasia and alexia. Key areas discussed include the visual and auditory systems, object recognition networks, spatial attention, praxis, types of agnosia and aphasia, and the neuroanatomy underlying different language functions.
The document discusses the importance of carefully considering alternative diagnoses to multiple sclerosis (MS) when evaluating patients. Common causes of MS misdiagnosis include nonspecific white matter abnormalities on brain MRI and vague neurological symptoms. Other disorders like neuromyelitis optica spectrum disorders, acute disseminated encephalomyelitis, and inherited disorders can mimic MS clinically and radiologically. A thorough evaluation of demographic, clinical, laboratory, and imaging factors is necessary to avoid misdiagnosis, as an MS diagnosis has significant implications for treatment.
This document discusses remyelinating therapies for multiple sclerosis (MS). It begins by explaining how MS results in demyelination and how remyelination can restore neuronal function. Several potential remyelinating therapies currently in preclinical or clinical trials are described, including clobetasol, opicinumab, guanabenz, and olesoxime. Biomarkers for measuring remyelination like diffusion tensor imaging, magnetization transfer imaging, and positron emission tomography are also summarized. The document concludes that while challenges remain, promising remyelinating strategies exist to provide benefit throughout the entire course of MS.
approach to Dystonia and myoclonus movement disordersOsama Ragab
This document provides an overview of the clinical approach to diagnosing dystonia and myoclonus. It discusses classifying dystonia based on characteristics like distribution, temporal pattern, age of onset, and etiology. Common causes of dystonia include inherited genetic forms, acquired causes like brain injuries, and idiopathic cases. The document also outlines an 8-step approach to diagnosing myoclonus that involves determining if symptoms are truly myoclonus, identifying anatomical substrates, defining the etiology, checking for medication involvement, running routine labs and imaging, considering mitochondrial or neurodegenerative causes, and potentially using next-generation sequencing.
Alzheimer disease , is there any hope for cureOsama Ragab
- Alzheimer's disease affects over 100 million people worldwide and is projected to increase significantly by 2050. While much research has focused on amyloid plaques and tau tangles as potential causes, treatments targeting these pathways have yet to successfully slow or stop the progression of the disease.
- Alternative hypotheses for Alzheimer's causation include neuroinflammation, oxidative stress, metabolic dysfunction, and aging. Strategies targeting these pathways also have not resulted in effective treatments.
- The exact causes and mechanisms of Alzheimer's remain unclear as amyloid and tau are normal brain proteins and their roles are still being understood. Further research is still needed to determine the root causes and identify effective treatments for this devastating disease.
Systemic infections may increase the risk of stroke through several mechanisms. Bacterial infections like infective endocarditis and meningitis have been linked to strokes, often due to inflammation and endothelial injury. Viruses such as HSV, VZV, HCV and HIV can cause vasculitis and coagulopathies leading to hemorrhagic or ischemic strokes. Fungi sometimes form cerebral abscesses or invade arteries, predisposing to aneurysms and thrombosis. Parasitic infections including Chagas disease are also associated with cardioembolic strokes. Overall, infections may exacerbate traditional stroke risk factors or directly cause strokes through inflammatory and thrombotic pathways.
This document provides an overview of ischaemic stroke, including its definition, risk factors, pathophysiology, clinical presentation, diagnosis and management. Key points include:
- Ischaemic stroke accounts for 80% of strokes and results from focal brain infarction due to obstruction of cerebral blood flow.
- Major risk factors include hypertension, atrial fibrillation, diabetes, hyperlipidemia and previous stroke or TIA.
- Clinical syndromes depend on the location of brain infarction and can include motor/sensory deficits, aphasia and visual field cuts.
- Diagnosis involves neuroimaging such as CT, MRI and vascular imaging to identify the cause.
- Acute
This document summarizes recent investigations in epilepsy, including various imaging and functional techniques. Neuroimaging techniques like fMRI, DTI, and PET can help localize epileptogenic foci and assess language dominance, memory function, and metabolic changes. SPECT and ictal-interictal subtraction can identify regions of hyperperfusion during seizures. MEG can localize irritative zones from magnetic fields generated by epileptic activity. Combined with MRI, these functional techniques provide valuable information to plan management of epilepsy.
Skeletal muscle disorders can be classified as either primary muscle diseases or secondary disorders caused by other conditions like inflammation, metabolic abnormalities, or drugs. Progressive muscle dystrophies are a primary cause and include Duchenne muscular dystrophy and Becker muscular dystrophy, which are caused by mutations in the dystrophin gene. Symptoms include weakness, wasting, and pseudohypertrophy. Management focuses on rehabilitation, steroids, respiratory support, and future gene therapies. Myasthenia gravis is an autoimmune disorder where antibodies target acetylcholine receptors, causing fluctuating weakness. Diagnosis involves the Tensilon test and repetitive nerve stimulation with treatment consisting of cholinesterase inhibitors, steroids, plasma exchange,
Approach to disturbance of consciousnessOsama Ragab
This document provides an overview of consciousness and approaches to disturbances of consciousness such as coma. It defines key terms like coma, stupor, and delirium. Coma can be caused by structural brain insults, metabolic derangements, infections, drugs or toxins. The clinical approach involves stabilizing vital functions, assessing severity using scales like Glasgow Coma Scale, and evaluating for immediate life-threatening causes through diagnostic tests and empirical treatment when needed to prevent further brain damage. A thorough neurological exam evaluates factors like consciousness level, pupil size and reactivity, ocular motility, motor responses and more to localize the cause. Distinguishing features between toxic/metabolic vs. structural comas are discussed.
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system characterized by breakdown of the myelin sheath covering nerve axons. It affects over 400,000 people in the US and more than 2.1 million worldwide. Genetic factors, autoimmunity, infection, vitamin D levels, and loss of protective childhood infections may play a role in MS etiology. Clinically, MS presents with a variety of neurological symptoms depending on the location of lesions in the brain and spinal cord, including visual, motor, sensory and cognitive impairments. Disease courses include relapsing-remitting MS, secondary progressive MS, primary progressive MS and progressive-relapsing MS.
This document discusses viral encephalitis and provides examples of imaging findings. It begins with an overview of virus structure and taxonomy. It then focuses on specific neurotropic viruses like herpesviruses. For HSV-1, imaging may show temporal and frontal lobe lesions and hemorrhage. HSV-2 commonly causes neonatal encephalitis seen as white matter abnormalities. VZV can cause meningoencephalitis, vasculitis, and leukoencephalopathy. EBV occasionally causes non-specific cortical or deep nuclei abnormalities. Overall, the document examines viral encephalitis from multiple angles including virus properties, neuroanatomy, and characteristic imaging patterns.
non motor manifestation of parkinson diseaseOsama Ragab
This document discusses non-motor symptoms of Parkinson's disease. It begins by providing background on the original description of Parkinson's disease in 1817 and defines it as primarily affecting motor functions. However, it notes that nearly 90% of Parkinson's patients experience non-motor manifestations as well, including neuropsychiatric symptoms, sleep disorders, autonomic dysfunction, sensory symptoms, and other issues. The document then examines the roles of different neurotransmitter systems including dopamine, serotonin, norepinephrine, glutamate, and GABA in both motor and non-motor features of the disease.
This document discusses the effects of epilepsy and anti-epileptic drug (AED) use on reproductive health and pregnancy outcomes. It notes that women with epilepsy have an increased risk of gestational hypertension, preterm delivery, fetal malformations, and low birthweight infants. During pregnancy, AED levels may decrease due to changes in metabolism and clearance, increasing seizure risk. Close monitoring of drug levels and seizures is recommended during pregnancy to adjust dosages as needed. Folic acid supplementation is also advised to reduce the risk of neural tube defects.
This document discusses higher cortical functions and the neuroanatomy that supports them. It describes how different areas of the cerebral cortex are involved in functions like memory, language, reasoning and more. It discusses the primary and association areas, and how they communicate to allow for complex functions. It also summarizes different types of agnosias that can occur from damage to various cortical areas, disrupting abilities like object recognition, face recognition, and spatial attention.
These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
Lecture 6 -- Memory 2015.pptlearning occurs when a stimulus (unconditioned st...AyushGadhvi1
learning occurs when a stimulus (unconditioned stimulus) eliciting a response (unconditioned response) • is paired with another stimulus (conditioned stimulus)
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
low birth weight presentation. Low birth weight (LBW) infant is defined as the one whose birth weight is less than 2500g irrespective of their gestational age. Premature birth and low birth weight(LBW) is still a serious problem in newborn. Causing high morbidity and mortality rate worldwide. The nursing care provide to low birth weight babies is crucial in promoting their overall health and development. Through careful assessment, diagnosis,, planning, and evaluation plays a vital role in ensuring these vulnerable infants receive the specialize care they need. In India every third of the infant weight less than 2500g.
Birth period, socioeconomical status, nutritional and intrauterine environment are the factors influencing low birth weight
Co-Chairs, Val J. Lowe, MD, and Cyrus A. Raji, MD, PhD, prepared useful Practice Aids pertaining to Alzheimer’s disease for this CME/AAPA activity titled “Alzheimer’s Disease Case Conference: Gearing Up for the Expanding Role of Neuroradiology in Diagnosis and Treatment.” For the full presentation, downloadable Practice Aids, and complete CME/AAPA information, and to apply for credit, please visit us at https://bit.ly/3PvVY25. CME/AAPA credit will be available until June 28, 2025.
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
NAVIGATING THE HORIZONS OF TIME LAPSE EMBRYO MONITORING.pdfRahul Sen
Time-lapse embryo monitoring is an advanced imaging technique used in IVF to continuously observe embryo development. It captures high-resolution images at regular intervals, allowing embryologists to select the most viable embryos for transfer based on detailed growth patterns. This technology enhances embryo selection, potentially increasing pregnancy success rates.
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
- Video recording of this lecture in Arabic language: https://youtu.be/uFdc9F0rlP0
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
2. The practice of physical exercise by persons with epilepsy (PWE) has been a
matter of debate for health professionals.
Some surveys performed in the last decade showed that PWE perceive their
health as poor and exercise less than the population without epilepsy.
PWE still carry the burden of psychosocial stigmatization, in both developed
and developing countries.
Epilepsy and physical exercise
3. Does physical activity worsen epilepsy?
Seizure precipitating factors exist in relation to physical exercise:
fatigue.
Stress.
repeated head injury during contact sports.
hyperventilation.
changes in the metabolism of antiepileptic drugs (AEDs).
metabolic disturbances.
Epilepsy and physical exercise
4. Does physical activity worsen epilepsy?
No link has been established between post exercise fatigue and increased seizure
frequency.
stress also activate hypothalamic CRH, which in turn stimulates deoxycorticosterone
production and Increased levels of allotetrahydrodeoxycorticosterone which
activates GABAA receptors in certain brain regions, with decreased seizure
susceptibility.
Epilepsy and physical exercise
5. Does physical activity worsen epilepsy?
exercise-induced hyperventilation, an adaptive reaction to acidosis, may even produce
suppression of interictal abnormalities. Therefore, hyperventilation during exercise appears
to deter seizure onset.
studies showed only slight variations in serum levels, especially for phenytoin (small
decrease) and valproic acid and phenobarbital (small increase) between the exercise and
pre-exercise periods, not statistically relevant and without effect on seizure frequency.
There are no studies showing a link between these metabolic disturbances (hypoxia,
dehydration, hyperthermia, hypoglycemia and hyponatremia) and the increase of true
epileptic seizures in PWE during exercice.
Epilepsy and physical exercise
6. Influence of the type of physical exercise
There is no evidence in literature that minor head trauma exacerbates seizures,
implying that contact sports are not harmful for PWE.
Interictal epileptiform activities usually remain unchanged or even decrease during
or immediately after aerobic exercise.
Epilepsy and physical exercise
7. Risks associated with physical exercise
persons with epilepsy have a higher risk of injuries, the most common being head
trauma, submersion injuries, burns and fractures.
Most of injuries reported in PWE during exercise are soft tissue injuries.
We should put in consideration two point :
1- seizure type
2- is seizure controlled or not?
Epilepsy and physical exercise
8. Does physical activity benefit epilepsy?
The effect of acute and chronic physical exercise was evaluated on the development
of amygdala kindling, showing that more stimulus were necessary to provoke
seizures in rats submitted to exercise than controls.
The therapeutic effect of exercise training on depression in PWE has been studied
with promising results. Some explanations for that consist in the increase and
regulation of neurotransmitter systems involved in depression physiopathology.
Epilepsy and physical exercise
9. Does physical activity benefit epilepsy?
it is well known that physical activity induces osteoprotection. Indeed, it increases
bone growth in width and mineral content, so protect against osteoporosis and AEDs
induced bone changes.
PWE can benefit of weight a reduction with physical training, as well as risk factors
reduction for diabetes, hypertension, obesity and coronary heart diseasese.
Epilepsy and physical exercise
13. sports Recommendation
Swimming and water
sports
• Always swim in supervised pools with direct
supervision of trained professionals .
• Do not swim in unsupervised open waters.
• Always wear a life-vest when in a boat, when
water-skiing or any other similar sport .
• avoid these sports in uncontrolled epilepsy.
• Scuba diving is generally not recommended.
Epilepsy and physical exercise
14. sports Recommendation
Sports at heights • Hand-gliding, parachuting, sky-diving are not
recommended.
• horseback-riding permitted if under supervision .
• (bicycling, gymnastics at parallel bars or involving
acrobatic activities, rock climbing) perform them with the
necessary safety equipment and not alone.
• Not recommended for those with uncontrolled epilepsy.
Epilepsy and physical exercise
15. sports Recommendation
Motor sports • No formal restrictions if epilepsy is controlled and according to the
driving regulations of each country, however the safety of others and
not only of the PWE should be accounted for.
• Not recommended for those with uncontrolled epilepsy.
Shooting sports • For PWE with controlled epilepsy may be permitted.
• Not recommended for those with uncontrolled epilepsy.
Epilepsy and physical exercise
16. sports Recommendation
Contact sports
• Contact sports Generally recommended with the exception of boxing,
• Not recommended for those with uncontrolled epilepsy
Aerobic sports
(e.g.: running,
basketball,
stationary bike,
aerobics,
gymnastics)
• No restrictions with the use of appropriate safety equipment when
advised.
Epilepsy and physical exercise