By Darlene Mitchell Dementia, Donald J. Trump, President
It certainly looks as if the president of the United States has a dangerous condition.
Tagged #Frontotemporal Dementia, #PSP, Donald Trump.
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Self-isolating has forced us to turn even more to telecommunication and social media.
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DEADPOOL QUOTES: 1.) “Never underestimate the stupidity of idiots.” 2.) “Today was about as much fun as a sandpaper dildo.” 3.) “My common sense is tingling.” 4.) “You can’t buy love, but you can rent it for three minutes.” 5.) “I’m gonna eat until I’m tired. Then I’m going to sleep until I’m hungry.” 6.) “I can say chimichanga in seven languages.” 7.) “Do you have an off switch?” 8.) “That’s a face I can sit on.” 9.) “Daddy needs to express some rage.” 10.) “I seriously need a speed bump between my brain and my mouth.” 11.) “I’m a bad guy who is paid to fuck up worse guys.” 12.) “Life is an endless series of train wrecks with only brief commercial like breaks of happiness.” Marvel Comics. Deadpool created by Fabian Nicieza & Rob Liefield
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What is PSP form of frontotemporal dementia? ›
Progressive supranuclear palsy (PSP) is a condition that causes both dementia and problems with movement. It is a progressive condition that mainly affects people aged over 60. The word 'supranuclear' refers to the parts of the brain just above the nerve cells that control eye movement.Is progressive supranuclear palsy a frontotemporal dementia? ›
Progressive supranuclear palsy (PSP) is a frontotemporal dementia. It is characterised by difficulties with balance, movement, vision, speech and swallowing. It is caused by progressive damage to the cells in the brain that control eye movements.Is PSP a type of FTD? ›
Progressive supranuclear palsy (PSP) belongs to the category of FTD disorders that primarily affect movement. Some symptoms of both PSP and corticobasal syndrome — another FTD disorder associated with a decline in motor function — resemble those often seen in people with Parkinson's disease.How long do you live with PSP? ›
PSP typically progresses to death in 5 to 7 years,1 with Richardson syndrome having the fastest rate of progression.What are the 4 stages of PSP? ›
- Early stage.
- Mid stage.
- Advanced stage.
- End of life stage.
- sudden loss of balance when walking that usually results in repeated falls, often backwards.
- muscle stiffness, particularly in the neck.
- extreme tiredness.
- changes in personality, such as irritability, apathy (lack of interest) and mood swings.
The final stages of PSP are usually dominated by an increasingly severe dysarthria and dysphagia. These features are usually described as being part of a pseudo-bulbar palsy, as brisk jaw and facial jerks may be present.How long does a person live with frontal lobe dementia? ›
People with FTD typically live six to eight years with their condition, sometimes longer, sometimes less.What causes death in PSP? ›
The disease gets progressively worse, with people becoming severely disabled within three to five years of onset. Affected individuals are predisposed to serious complications such as pneumonia, choking, head injury, and fractures. The most common cause of death is pneumonia.What are 5 extreme behavior changes found with FTD? ›
Loss of empathy and other interpersonal skills, such as having sensitivity to another's feelings. Lack of judgment. Loss of inhibition. Lack of interest (apathy), which can be mistaken for depression.
Does alcohol cause PSP? ›
There was no significant association between PSP and alcohol drinking, smoking habits, anti- inflammatory agent use or specific occupations.Can you recover from PSP? ›
There's currently no cure for progressive supranuclear palsy (PSP), but there are lots of things that can be done to help manage the symptoms. As PSP can affect many different areas of your health, you'll be cared for by a team of health and social care professionals working together.Does PSP run in families? ›
Most cases of progressive supranuclear palsy are sporadic, which means they occur in people with no history of the disorder in their family. However, some people with this disorder have had family members with related conditions, such as parkinsonism and a loss of intellectual functions (dementia).Does stress cause PSP? ›
PSP patients were found to be three times more likely to report high exposure to highly stressful events than controls. This suggests that these highly stressful events may have a role in the etiopathogenesis of PSP.Do PSP patients hallucinate? ›
Only 2 out of 22 PSP patients (9.1%) reported visual hallucina- tions. Case 1 had auditory in addition to visual hallucinations.Do PSP patients sleep a lot? ›
Poor sleep is common with PSP. It takes longer for patients to fall asleep, and they wake more frequently during the night, resulting in a shorter time asleep. Neuroanatomical areas affected in PSP are also the same areas of the brain that house the sleep/wake regulation system.Is there pain with PSP? ›
Pain is more common and more intense in PD and MSA than PSP. Differences in distribution of neurodegenerative pathologies may underlie these differential pain profiles.How do you get PSP disease? ›
Affected individuals frequently experience personality changes and cognitive impairment. Symptoms typically begin after age 60 but can begin earlier. The exact cause of PSP is unknown. PSP is often misdiagnosed as Parkinson disease, Alzheimer disease, corticobasal degeneration and other neurodegenerative disorders.What is the most common cause of supranuclear palsy? ›
Cause of supranuclear palsy
Deterioration of cells in the brainstem, cerebral cortex, cerebellum and basal ganglia — a cluster of cells deep within your brain — is what causes the coordination and movement issues of progressive supranuclear palsy.
MRI scans can also detect changes to the brain that are consistent with a diagnosis of PSP, such as shrinkage of certain areas. Scans that show the build-up of the tau protein in the brain that's associated with PSP are currently under development.
Is PSP worse than Parkinson's? ›
On average, PSP gets worse quicker than Parkinson's and doesn't respond as well to medications. People with Parkinson's usually bend forward, while people with PSP stand very straight, or even slightly backwards. Problems with swallowing and with speaking appear early with PSP and they are far more severe.What famous people have progressive supranuclear palsy? ›
A famous person with PSP was Dudley Moore, the actor.How can I help someone with progressive supranuclear palsy? ›
Physical therapy and occupational therapy, to improve balance. Facial exercises, talking keyboards, gait and balance training also can help with many of the symptoms of progressive supranuclear palsy.What is end stage frontotemporal dementia? ›
In later stages, patients develop movement disorders such as unsteadiness, rigidity, slowness, twitches, muscle weakness or difficulty swallowing. Some patients develop Lou Gherig's disease or amyotrophic lateral sclerosis (ALS). People in the final stages of FTD cannot care for themselves.What causes death in frontotemporal dementia? ›
Pneumonia is the most common cause of death, with FTD. People are also at increased risk for infections and fall-related injuries. As FTD progressively worsens, people may engage in dangerous behaviors or be unable to care for themselves.Do people with frontal lobe dementia get violent? ›
Physical aggression among people with dementia is not unusual. A study showed that one-third of patients with the diagnosis Alzheimer's disease or frontotemporal dementia were physically aggressive towards healthcare staff, other patients, relatives, animals and complete strangers.Do people with PSP go blind? ›
Involuntary eye closure is common in PSP. It can be mild and irritating or severe with functional blindness. It may be caused blepharospasm (especially pretarsal blepharospasm) or apraxia of lid opening—the inability to open the eyes voluntarily despite normal peripheral levator function.What are the disadvantages of PSP? ›
- Larger and heavier.
- Slightly slower than later models.
- Discontinued, so Sony support is limited or nonexistent.
- Screen not as bright when compared to PSP-3000.
- No internal memory for storage.
- No video out.
- Does not run Skype.
Physical therapy and occupational therapy, to improve balance. Facial exercises, talking keyboards, gait and balance training also can help with many of the symptoms of progressive supranuclear palsy.How fast does frontotemporal dementia progress? ›
Most studies show that FTD is steadily progressive, with declining function in everyday life and accumulation of social, cognitive, and neurological disabilities leading to complete dependency requiring institutional care over a course of 6–8 years.
Do people with FTD know they have it? ›
People with FTD often lack insight, which means they can't recognize their symptoms or condition. Because they can't see the problem, they often don't believe they need medical care or treatment. That lack of understanding can lead to frustration or fear for the person with the symptoms and their loved ones.How long does end stage frontotemporal dementia last? ›
However, end-stage dementia may last from one to three years. As the disease advances, your loved one's abilities become severely limited and their needs increase. Typically, they: have trouble eating and swallowing.Can I drive with PSP? ›
Can I drive? Depending on your symptoms, you may be able to continue driving for a while with PSP or CBD. However, you are legally required to disclose your diagnosis to the DVLA and your insurer. You may need to be assessed at a driving centre if you wish to continue to drive.How does PSP affect the eyes? ›
A person with PSP will begin to experience eye problems, such as difficulty opening and closing their eyes, blinking, blurry vision, or moving their eyes side to side or up and down. Later in the disease, people with PSP may feel increasing weakness in their limbs.Is coughing a symptom of PSP? ›
Swallowing difficulties are also common in PSP. These include: Coughing or choking on food or drink.Does exercise help with PSP? ›
Structured exercises can improve strength, mobility, and balance in people living with PSP (9). Physical therapy (11) and physical activities, such as walking (12, 13), music-cued movement (14), dancing (15), and cycling (16), can also improve fitness, community ambulation, and social participation in parkinsonism.What's the most common age for someone to be diagnosed with PSP? ›
Most cases of PSP develop in people who are over the age of 60.Can a PSP be tracked? ›
On the PSP Tracking app, users can:
Easily log in using PSP platform credentials. View ships under accounts or sub-accounts on a map or in list view. Select a specific ship and view its movement history and details. Change the device's reporting frequency (with relevant permissions)
Speech changes are common in PSP. Speech can become slurred or speech rate can become too fast, leading to difficulties being understood. Changes in voice quality can also occur: strained or harsh voice, or quiet and breathy voice.
It involves damage to many cells of the brain. Many areas are affected, including the part of the brainstem where cells that control eye movement are located. The area of the brain that controls steadiness when you walk is also affected. The frontal lobes of the brain are also affected, leading to personality changes.
Does PSP cause paranoia? ›
Most commonly, PSP presents with axial rigidity, vertical gaze palsy, frequent falls, pseudobulbar affect, frontal executive disabilities, and neuropsychiatric disturbances including depression, anxiety, impulsivity, and paranoia.What are the three types of frontotemporal dementia? ›
There are three types of frontotemporal disorders (FTD): behavioral variant frontotemporal dementia (bvFTD), primary progressive aphasia (PPA), and movement disorders.What is the difference between dementia and frontotemporal dementia? ›
While Alzheimer's disease generally affects most of the brain, frontotemporal dementia primarily affects the frontal and temporal lobes of the brain – the areas generally associated with personality and behaviour.Is frontotemporal dementia the same as dementia? ›
Frontotemporal dementia is an uncommon type of dementia that causes problems with behaviour and language. Dementia is the name for problems with mental abilities caused by gradual changes and damage in the brain. Frontotemporal dementia affects the front and sides of the brain (the frontal and temporal lobes).What is another name for frontotemporal dementia? ›
Frontotemporal dementia (FTD) is one of the less common types of dementia. It is sometimes called Pick's disease or frontal lobe dementia. The first noticeable FTD symptoms are changes to personality and behaviour and/or difficulties with language.What is the life expectancy of frontal lobe dementia? ›
People with FTD typically live six to eight years with their condition, sometimes longer, sometimes less.What happens in the last stages of frontotemporal dementia? ›
In later stages, patients develop movement disorders such as unsteadiness, rigidity, slowness, twitches, muscle weakness or difficulty swallowing. Some patients develop Lou Gherig's disease or amyotrophic lateral sclerosis (ALS). People in the final stages of FTD cannot care for themselves.Which is worse frontotemporal dementia or Alzheimer's? ›
AD is the most common dementia in older people. Therefore, it is often one of the first diseases a doctor considers. But Alzheimer's disease usually begins with memory loss, while FTD is typically a behavior or language disorder. The probability of AD is strongly affected by the age of the person showing the symptoms.Is frontotemporal dementia aggressive? ›
However, individuals with frontotemporal dementia were physically aggressive more often -- and the violence exhibited by the people suffering from frontotemporal dementia could also be more serious, and this was particularly evident towards complete strangers.Does frontotemporal dementia show on a brain scan? ›
Brain imaging is indicated in all individuals with symptoms of FTD to rule out structural causes. MRI scanning will identify small vessel ischemia, subdural hematomas, strategically placed tumors and hydrocephalus. Additionally, the pattern of brain atrophy can support the diagnosis.
What are some of the first symptoms noticed in frontal lobe dementia? ›
- Loss of inhibitions. This means a person has trouble controlling themselves. ...
- Apathy. This usually causes a lack of interest or motivation. ...
- Loss of empathy. ...
- Compulsive behaviors. ...
- Changes in diet or mouth-centered behaviors. ...
- Loss of executive function.
Medications. Antidepressants. Some types of antidepressants, such as trazodone, may reduce the behavioral problems associated with frontotemporal dementia. Selective serotonin reuptake inhibitors (SSRIs) — such as citalopram (Celexa), paroxetine (Paxil) or sertraline (Zoloft) — also have been effective in some people.Does frontotemporal dementia show on MRI? ›
Atrophy or shrinkage of specific regions of the brain that might be suggestive of FTD can be identified by MRI.Can stress cause frontotemporal dementia? ›
When both anxiety and depression were entered as variables, a significant increase in the risk of developing FTD was observed in patients who had reported anxiety on the HADS (p = 0.017; OR: 2.947, 95% CI: 1.209–7.158).