How do people cope with Huntington's disease?

Keep life simple - Rest, Exercise, Nutrition, A daily laugh Carry earplugs with you when you are out (Some people with HD are sensitive to noise) Carry calendars with you to write down everything you must do for the day and any information you get from other people.

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What is everyday life like for someone with Huntington's disease?

Other symptoms may include insomnia (having trouble sleeping), loss of energy, fatigue, and seizures. Eventually the person will need to stay in bed or in a wheelchair. Changes in thinking (cognitive changes) may include problems with attention or judgment and having difficulty solving problems or making decisions.

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How does a person act with Huntington's disease?

Huntington's disease brain changes lead to alterations in mood, especially depression, anxiety, and uncharacteristic anger and irritability. Another common symptom is obsessive-compulsive behavior, leading a person to repeat the same question or activity over and over.

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How does Huntington's disease change your life?

Huntington's disease is a condition that damages nerve cells in the brain causing them to stop working properly. It's passed on (inherited) from a person's parents. The damage to the brain gets worse over time. It can affect movement, cognition (perception, awareness, thinking, judgement) and mental health.

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How does Huntington's disease affect you socially?

Huntington's disease (HD) commonly presents with impaired social functioning. Specifically, many patients exhibit social withdrawal, or decreased engagement in social activities.

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Living with Huntington’s disease

39 related questions found

How does Huntington's disease affect you emotionally?

memory lapses. depression – including low mood, a lack of interest in things, and feelings of hopelessness. stumbling and clumsiness. mood swings, such as irritability or aggressive behaviour.

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Are people with Huntington's disease aware?

Unawareness of motor, cognitive, behavioral, and functional aspects of HD has been documented throughout the disease course. This can occur at motor and cognitive onset but is more pronounced as the disease progresses.

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Are people with Huntington's aware?

Surprisingly, many people with Huntington's disease aren't aware that the involuntary movements are happening, or don't notice them as much as other people do. That's because Huntington's disease can affect people's awareness of their own bodies.

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What are 3 interesting facts about Huntington's disease?

Huntington's Disease Facts
  • Huntington's Disease (HD) is an inherited brain disorder.
  • HD typically begins between the ages of 30-45, though onset may occur as early as the age of two or as late as the 70s.
  • HD affects males and females equally and affects all ethnic and racial groups.

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Is Huntington's disease classed as a terminal illness?

Huntington's disease is a condition that stops parts of the brain working properly over time. It's passed on (inherited) from a person's parents. It gets gradually worse over time and is usually fatal after a period of up to 20 years.

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Is Huntington's painful?

The most painful conditions in Huntington's, said Achterberg, are limb pain, headache, abdominal pain and fractures. “I think we should do more work in validation of pain tools, including observational pain instruments,” he said. “And for clinicians, I suggest you be especially aware of abdominal pain.”

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What is end-of-life Huntington's disease?

Common end-of-life signals include significant weight loss, difficulty swallowing or breathing, recurrent aspiration pneumonia, and uncontrolled pain.

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What can make Huntington's disease worse?

Weight loss can make symptoms worse and weaken the patient's immune system, making them more vulnerable to infections and other complications. Huntington's disease itself is not usually fatal, but it can lead to choking, pneumonia, or other infections that can lead to death.

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What celebrity has Huntington's disease?

Famous People with Huntington's Disease
  • Woody Guthrie. Woodrow Wilson Guthrie (July 14, 1912– October 3, 1967) was an American musician and songwriter whose legacy involves hundreds of children's songs, traditional songs, ballads as well as improvised works. ...
  • Charles Sabine.

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What famous person died of Huntington's disease?

Woody Guthrie was an American songwriter, musician, writer, and political activist who died with Huntington disease (HD) in 1967 at age 55. His relatively brief creative life was incredibly productive with countless songs and a tremendous volume of letters to his name.

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What is the mental decline of Huntington's disease?

Early in the disease, cognitive decline may manifest as memory and learning difficulties, judgment impairment, and trouble with driving, answering questions or making decisions. As the disease progresses, concentration and focus on intellectual tasks become increasingly difficult.

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What are the 5 stages of Huntington's disease?

What Are The 5 Stages Of Huntington's Disease?
  • Stage 1: Preclinical Stage.
  • Stage 1: Early Stage.
  • Stage 2: Early Intermediate Stage.
  • Stage 3: Late Intermediate Stage.
  • Stage 4: Early Advanced Stage.
  • Stage 5: Advanced Stage.
  • Treating Someone With Huntington's Disease.

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Should someone with Huntington's disease be driving?

HD can affect the ability to self evaluate and it is advised that driving be discussed with family members and your doctor. They may have a different perception of your driving skills.

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Does Huntington's disease affect mental health?

Overview of HD's Behavioral and Psychiatric Symptoms

People with HD may suffer from depression and other conditions found in the general population, such as mania, obsessive compulsive disorder, or various forms of psychosis.

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Is Huntington's disease like autism?

Young people with JHD are often misdiagnosed with ADHD or autism spectrum disorder before being diagnosed with Huntington's, or it is assumed that their behavior is the result of a stressed home environment caused by having a parent with Huntington's.

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Can stress make Huntington's disease worse?

(For more information on Complications of HD, click here.) It is important to know that stress can lead to complications and the worsening of symptoms in people with HD.

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Does Huntington's cause anger issues?

Huntington's disease impairs the functioning of the brain, which can result in apathy, trouble organizing, impulsivity, irritability and anger, unawareness, disinhibition, preservation, and other psychiatric symptoms. These emotional and behavioral symptoms can further complicate the caregiver's role.

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Why is Huntington's disease so devastating to the patient?

Huntington's disease (HD) is one of the most devastating diseases of mankind. It incapacitates patients by affecting their ability to move, think, and behave normally. It causes uncontrollable and disabling movements of the face, neck, trunk and limbs, loss of balance, and uncoordinated movements.

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What limitations does a person with Huntington's disease have?

About Huntington's Disease

Motor issues often include involuntary movements, difficulty with speech and swallowing, lack of coordination, and fatigue and weakness. Many cognitive functions become limited, such as memory, decision making, critical thinking, multitasking and concentration.

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