Huntington’s disease symptoms can be broken down into many different categories such as: Motor, Cognitive, Psychiatric, Metabolic, and others. It also includes three different stages, which can show how the person is responding to the disease and as it progresses the symptoms may worsen and affect the individuals daily life activities and more.
Motor Symptoms:
• There are two categories in which your motor abilities are affected with Huntington’s disease: Involuntary movements (chorea) and impaired voluntary movements, which is the beginning of limb incoordination and an impaired ability to use your hand. As the symptoms worsen the postural reflexes are affected. As chorea (involuntary movements) decrease and other symptoms such as dystonia,
She yelled for help because it was hard for her to breathe. She noticed that the left side of her arm was weak and useless, which is sign of motor deterioration. Parkinson's disease is a type of condition that starts off very slowly, and later on, it progressively takes control of all body movements. Some early signs of Parkinson’s disease are depression, emotional changes, major headaches, and trouble sleeping at night, and inexplicable aches and pains (Levy, 30).
The condition is progressive and worsens over time; in the later stages, people with dementia become unable to carry out everyday activities and find it difficult to convey their thoughts and feelings. As the symptoms become more profound, they
This disease also breaks down brain cells, which are imperative for everyday functioning and intelligence. Symptoms of this disease include, developmental mental delay, seizures, stiff limbs, Optic atrophy: wasting of a muscle of the eye, resulting in vision difficulties, deafness, irritability, spasms, and ataxia which is the
Early signs of dementia Early signs of dementia aren 't as severe as they can be as the diseas in the person sometimes people have bad memory loss and can potentially forget their daily routines (go to work, pick up kids from school have confusion with the date, time or place and the people with dementia could have trouble understanding simple conversations Younger-onset dementia Younger- onset dementia is when the age of 65 get dementia and this is mostly caused by Huntington 's people under disease when your brain cells die off and leave you being unable or hardly able to move or talk people can Huntington 's disease is or 30 to 50. This disease is also an inherited disease meaning that it has get Huntington 's disease at the more common age come through the genes of your family Dejectedly Huntington 's disease is like dementia as is has no cure but researchers are still working on it to make the suffering lives better. This disease is also called Early-onset dementia Statistics of dementia by 2025 There are more than 413,106 Aussies that have to live forms of dementia and that is anticipated to rise to 536,164 60,000 The amount of People suffering from Early onset dementia is also expected to rise to
Parkinson’s affects the central nervous system eventually leads to triggering in the hand. Alzheimer 's is a disease that affects the memory and important mental functions. Dementia is when a person think a lot which interferes with their daily functions. Huntington’s an inherited condition when nerve cells starts to lose the ability over a period of time. Athletes who come in contact with sports are more like like to get it because in a game there is usually hitting each other or even getting injured dramatically.
Parkinson’s disease is a “disorder of the nervous system that affects movement” (Staff, 2015), but does not have an acute onset. Usually symptoms start with a slight tremor in the hands and then slowly progresses to other parts of the body (Staff, 2015). Even though most people have fast, shaking, movements, Parkinson’s can also cause stiffness or slow movements. According to Mayo Clinic Staff, early signs of Parkinson’s disease may include diminished facial expressions, absence of swaying arms when walking, and “speech may become soft or slurred” (2015). Unfortunately, Parkinson’s does not have a cure, but there are medications out there to help symptoms as well as brain surgeries.
The brain is complex, but vulnerable. Over sixty million US citizens have brain issues such as developmental diseases, which include: learning disorders, and autism spectrum disorders. Others include antisocial behaviour and schizophrenia that originates in childhood and continues throughout his or her life. Degenerative diseases of adult life include: Alzheimer’s disease, amyotrophic lateral sclerosis (ALS), Huntington’s disease, and Parkinson’s disease, among others. These diseases often affect elderly adults and are caused by the deterioration of nerve cells, eventually leading to the death of cells.
This was very obvious when he showed the doctors that the patients could indeed move. The disease that the patients had showed symptoms very similar to Parkinson's disease. Almost all of the patients were previously diagnosed with encephalitis lethargic, seemed to be "frozen", and had reflex-like movements like catching a ball. Some were able to move after experiencing things like certain types of music or human contact.
Depending on which part is damaged by dementia there are different signs and symptoms. For example the frontal lobe controls emotional expression, personality, language,
Last accessed 3rd Nov 2014.). This disease effects the brain and spinal cord. There are some difference symptoms of MS such as; tiredness, bladder and bowel problems, speech problems, blurry vision, memory and thinking are affected, balance, chronic pain and tremors. MS can be treated quite well when the person starts to realise patterns and triggers to their symptoms. It gradually effects the whole body depending what stage the person is in.
The nervous system is made up of two systems that work together to help the body function. One of the systems is the Central Nervous System (CNS) which consists of the spinal cord and the brain. The other system is the Peripheral Nervous System (PNS) which is made up the nerves that connect to the rest of the body. Working together they both contribute to the wonder known as the nervous system, but how? (Better Health Channel, 2014).
According to WebMD, the first type of spinal muscular disease is the most serious variant due to the fact that most children with type 1 fail to live past two years of age from breathing issues because the muscles that control breathing are feeble. Symptoms of type 1 include limp arms and legs as well as the trouble swallowing. Moreover, type 2 spinal muscular atrophy occurs with children from six to eighteen months old. According to the National Organization for Rare Diseases, children with type 2 are able to sit on their own, but fail to walk more than 10 feet, however, once they mature to a teenager, they will be unable to sit independently. A symptom common for people diagnosed with type 2 is the fingers quivering (National Organization for Rare Diseases).
Neuromotor Impairments, under Individuals with Disabilities Education Act (IDEA), is one of the divisions that fall under the category of orthopedic impairment, others being degenerative diseases and musculoskeletal disorder (Gargiulo, 2015, p. 495). Neuromotor impairments are abnormalities of the central nervous system which includes brain and spinal cord or the ability of descending-nervous-tracts from the brain or spinal cord to innervate the muscles of the body. These impairments are congenital (present at or before birth) and severely impair coordination of limb movements, urinary control and proper alignment of the spinal cord and vertebrae. It is however quite possible that individuals with neuromotor impairments have additional impairments
In the final stage of this disease, individuals lose the ability to respond to their environment, to carry on a conversation and,
Introduction Amyotrophic lateral sclerosis (ALS) which is also known as Lou Gehrig's disease is a rapidly progressive neurological disease that attacks the nerve cells (neurons) in charge of controlling voluntary muscles in the body. The disease is classified to a group of disorders known as motor neuron diseases. Lou Gehrig’s disease causes weakness with a broad assortment of disabilities that eventually cause all muscles under voluntary control to be affected. The patient will eventually lose their strength and not have the ability to move their arms, legs, or any other body part. When muscles in the diaphragm and chest wall fail, patients lose the ability to breathe without a ventilator for support.