Symptoms, Stages and Treatments

Dementia is an umbrella term for a group of progressive neurological disorders that affect memory, thinking, behaviour, and the ability to perform everyday activities. The most common types include Alzheimer's disease, vascular dementia, dementia with Lewy bodies (DLB), and frontotemporal dementia (FTD). Each type has distinct causes, but they share overlapping symptoms that worsen over time, typically progressing through early (mild), moderate, and severe stages.
These stages are not always linear or uniform - progression can vary based on individual health, genetics, and environmental factors. Recognising symptoms early is crucial because it allows for timely diagnosis, which can improve quality of life through interventions, planning, and support.
Early detection often involves consulting a healthcare professional for cognitive assessments, brain imaging, and blood tests to rule out reversible causes like vitamin deficiencies or thyroid issues.
Management focuses on symptom relief, as there is no cure for most dementias, but treatments like medications, therapies, and lifestyle changes can slow progression and enhance well-being. Actions at each stage include medical care, lifestyle adjustments, safety measures, and emotional support for both the individual and caregivers.
Dementia Hub explores the symptoms of the four main types of dementia across stages, drawing from reliable sources and incorporating real-life examples to illustrate how these symptoms manifest in everyday situations. We will also outline practical actions to take, emphasising a holistic approach that includes medical, social, and environmental strategies.
Remember, Dementia Hub is not a substitute for professional medical advice - always consult a doctor for personalised guidance.



Signs of Alzheimer's Disease
Alzheimer's disease is the most prevalent form of dementia, accounting for 60-80% of cases. It involves the build up of amyloid plaques and tau tangles in the brain, which disrupt cell communication and lead to neuron death. This primarily affects areas responsible for memory and cognition, spreading gradually throughout the brain.
Early Stage (Mild Alzheimer's):
In the early stage, individuals often maintain independence in daily activities like driving or working, but subtle cognitive changes emerge. Common symptoms include memory lapses, such as forgetting recently learned information, struggling to find the right words during conversations, or misplacing items more frequently than usual. For instance, someone might forget a familiar name when meeting new people or have trouble recalling what they just read in a book. In one real-life case, a woman named Jacquelyn, diagnosed at 57 with early-onset Alzheimer's, began repeatedly asking her daughter about everyday details like meal plans, even after just discussing them minutes earlier, leading to frustration but no major disruptions yet. Other signs include increased difficulty with planning or organizing, like managing finances or following a recipe, and minor challenges in social or work settings. These symptoms may not be obvious to outsiders but can be noticed by close family or through diagnostic tools like cognitive tests. At this stage, the brain changes are beginning but haven't caused widespread damage yet. Mood changes, such as mild frustration from these lapses, might occur, but personality remains largely intact. It's easy to mistake these for normal aging, but if they interfere with daily life, it's a red flag. Another example comes from a retiree who started losing track of appointments, like missing a doctor's visit but later vaguely recalling it, prompting his family to notice the pattern.
Actions to Take in the Early Stage:
Early intervention is key to maximizing quality of life. First, seek a professional diagnosis through a doctor who can conduct neuropsychological tests, brain scans (like MRI or PET to detect plaques), and lab work to confirm Alzheimer's and rule out other causes. Once diagnosed, focus on empowerment: the individual should participate in legal and financial planning, such as creating advance directives, power of attorney, and living wills, while they can still make informed decisions. Lifestyle changes are vital - adopt a heart-healthy diet (e.g., Mediterranean style with fruits, vegetables, and omega-3s), engage in regular physical exercise (at least 150 minutes weekly), and stimulate the brain with activities like puzzles or learning new skills to build cognitive reserve.
Medications like cholinesterase inhibitors (e.g., donepezil) may be prescribed to boost brain chemicals for better memory and judgment. Join support groups through organizations like the Alzheimer's Association for education and emotional support. Caregivers should learn about the disease to provide subtle assistance without undermining independence, such as using reminders or calendars. Overall, this stage is about maintaining autonomy and planning ahead to reduce future stress.
Moderate Stage (Middle Alzheimer's):
As the disease advances, symptoms become more pronounced, lasting several years and requiring increased assistance. Memory issues deepen, with forgetfulness of personal history or recent events—someone might not recall their address, phone number, or the school they attended. Confusion about time and place is common, leading to disorientation, such as not knowing the date or where they are. Behavioural changes emerge, including mood swings, withdrawal in challenging situations, or unfounded suspicions (e.g., accusing others of theft). In a documented case, a man in the middle stage became convinced his wife was hiding his belongings, leading to arguments and him searching the house obsessively at odd hours. Sleep patterns disrupt, with daytime sleeping and night time restlessness, increasing the risk of wandering. Physical symptoms like bladder or bowel control problems may start, and routine tasks become harder, such as choosing appropriate clothing or managing hygiene without prompts.
Personality shifts can be distressing, like compulsive behaviours (e.g., repetitive hand-wringing) or delusions. These stem from nerve cell damage affecting judgment and emotional regulation, making social interactions strained.
Actions to Take in the Moderate Stage:
Care needs intensify, so involve a multi disciplinary team including doctors, occupational therapists, and social workers. Continue medications, possibly adding memantine to regulate brain chemicals and slow symptom progression. Therapies like occupational therapy can teach adaptive strategies for daily tasks, such as simplifying routines or using labelled drawers. Environmental modifications are essential: reduce clutter to minimize confusion, install safety features like grab bars or wander-prevention locks, and use monitoring devices for safety.
Caregivers should prioritise respite care or adult day centres to prevent burnout, allowing breaks while ensuring the individual receives structured activities. Encourage engagement in simplified hobbies, like listening to music or gardening, to maintain purpose. Address behavioural symptoms with non-drug approaches first, such as validating feelings to reduce agitation, and use antidepressants if depression arises. Regular check-ups monitor for complications like infections. This stage emphasises balancing support with dignity, adapting to the person's abilities to foster independence where possible.
Severe Stage (Late Alzheimer's):
In the final stage, profound cognitive and physical decline occurs, with individuals needing round-the-clock care. Communication falters—they may utter words but struggle to express needs or pain. Awareness of surroundings diminishes, leading to loss of recent memory and recognition of loved ones. Physical abilities erode: walking becomes unsteady, then sitting and swallowing difficult, increasing risks of aspiration pneumonia or infections. In one poignant account, a patient in late-stage Alzheimer's refused food due to swallowing issues, resulting in rapid weight loss and dehydration that required tube feeding. Personality changes peak, with possible apathy or agitation, and basic self-care is impossible.
Brain damage is extensive, affecting motor control and vital functions, often leading to bed-bound states and vulnerability to health issues. Caregivers often report loved ones becoming non-verbal, responding only to touch or music.
Actions to Take in the Severe Stage:
Shift focus to comfort and dignity through palliative or hospice care, which provides pain management, emotional support, and end-of-life planning. Ensure 24/7 supervision, possibly in a specialised facility if home care is overwhelming. Nutritional support, like soft foods or feeding assistance, prevents malnutrition. Therapies such as music or gentle touch can offer comfort even if verbal response is limited.
Caregivers need robust support - join groups, seek counselling for grief, and use community resources. Monitor for infections vigilantly, as they are common causes of death. Legal plans from earlier stages ease decisions now. Hospice benefits families by emphasizing quality over curative efforts, helping navigate emotional challenges.
Signs of Vascular Dementia

Vascular dementia, the second most common type, results from reduced blood flow to the brain, often due to strokes, mini-strokes (TIAs), or conditions like atherosclerosis. This causes patchy brain damage, leading to stepwise progression where symptoms may stabilise then suddenly worsen after vascular events.
Early Stage (Mild Vascular Dementia):
Corresponding to stages 1-3 in the 7-stage model, symptoms are subtle or absent initially. In stage 1, behaviour is normal despite underlying brain changes. By stage 2, mild forgetfulness appears, like misplacing items or slowed thinking, often dismissed as aging. Stage 3 brings increased confusion, such as forgetting appointments, with a vague sense of something amiss. Unlike Alzheimer's, early symptoms may include judgment issues or concentration problems rather than pure memory loss, stemming from disrupted blood supply to cognitive areas. An example involves a man post-mini-stroke who began struggling with simple math at the grocery store, like calculating change, but attributed it to stress.
Physical signs might include slight weakness on one side if a small stroke occurred. Mood changes like apathy can appear, as seen in a woman who lost interest in her weekly book club, sitting quietly instead of engaging.
Actions to Take in the Early Stage:
Prevention and early detection are paramount. If risk factors like high blood pressure, diabetes, or smoking are present, address them immediately through lifestyle changes: adopt a balanced diet low in salt and fats, exercise regularly (e.g., walking 30 minutes daily), quit smoking, and limit alcohol. Seek medical evaluation if symptoms arise - tests like MRI can detect vascular damage.
Medications for underlying conditions (e.g., blood thinners or statins) can prevent further strokes. Brain-stimulating activities, such as reading or social groups, build resilience. Diagnosis here allows for multidisciplinary care, including dieticians and therapists, to slow progression. Plan for future needs while the person is cognitively able.
Moderate Stage (Moderate Vascular Dementia):
Stages 4-5 mark noticeable decline. In stage 4, forgetfulness affects finances or recent events, like not remembering meals. Daily life impairs, but basic self-care remains possible. Stage 5 brings severe challenges: forgetting personal details, difficulty dressing, or following instructions. Communication slows, and depression or irritability may emerge. Progression can be abrupt after a stroke, with symptoms like poor judgment or hallucinations. For instance, a patient after a TIA started wandering into traffic while trying to "go home" from a familiar park, highlighting sudden disorientation.
Brain flow disruptions cause varied symptoms based on affected areas, often including mobility issues, such as a man who could no longer prepare a simple meal, burning food repeatedly due to lapsed attention.
Actions to Take in the Moderate Stage:
Intensify vascular risk management with regular doctor visits to monitor blood pressure and cholesterol. Cholinesterase inhibitors or memantine might help cognitive symptoms, though evidence is mixed. Occupational therapy adapts tasks, like using visual aids for dressing. Group activities stimulate the brain and combat isolation.
Safety is key - install home modifications to prevent falls, and use reminders for medications. Caregivers should access respite services and support groups. If a stroke occurs, immediate medical intervention can limit damage.
Severe Stage (Severe Vascular Dementia):
Stages 6-7 involve total dependence. Stage 6 features high confusion, incontinence, swallowing difficulties, and behavioural changes like bouts of aggression. Independence is lost, with possible paralysis. Stage 7 is rare, with complete communication failure and bed - bound state, often ending in death from complications. In a severe case, a woman became unable to recognize her children, leading to distress and requiring constant reassurance through photos and voices.
Physical frailty increases infection risks, as seen in patients who develop pneumonia from immobility.
Actions to Take in the Severe Stage:
Provide 24-hour care, possibly in a facility. Focus on palliative measures: assist with eating to avoid choking, manage incontinence, and monitor for infections. Medications address behaviours, but avoid over - sedation. Hospice supports comfort and family grief. Multidisciplinary teams ensure holistic care, emphasizing dignity.



Signs of Lewy Bodies Dementia

DLB arises from alpha-synuclein deposits (Lewy bodies) disrupting brain chemicals, often overlapping with Parkinson's or Alzheimer's. Symptoms fluctuate daily, distinguishing it from other dementias.
Early Stage (Mild DLB):
Symptoms start with cognitive fluctuations, like varying levels of alertness or delirium-like episodes. Visual hallucinations (seeing non-existent things) and REM sleep behaviour disorder (acting out dreams) are common early. Movement issues emerge, such as rigidity or shuffling gait. Memory loss is less prominent than in Alzheimer's, but attention and visual processing falter, e.g., trouble interpreting spatial information. Autonomic problems like dizziness or incontinence may appear due to nervous system malfunctions. One family's story describes a mother in her 80s who began kicking during sleep as if fighting off intruders in her dreams, a classic REM disorder sign later linked to DLB.
These stem from Lewy bodies affecting multiple brain regions early on. Another example: a man noticed his handwriting shrinking and becoming shaky, alongside brief episodes of staring blankly during conversations.
Actions to Take in the Early Stage:
Diagnosis requires expert evaluation, as no single test confirms DLB - use clinical judgment, scans, and sleep studies. Avoid antipsychotics, which can worsen symptoms severely; opt for cholinesterase inhibitors to aid cognition. Manage sleep with behavioural strategies or medications.
Lifestyle: exercise for mobility, environmental changes to reduce fall risks (e.g., better lighting). Join support like LBDA for resources. Genetic testing if family history. Plan disability benefits via SSA's compassionate allowance.
Moderate Stage (Moderate DLB):
Fluctuations intensify, with disorganized thinking and illogical ideas. Hallucinations become recurrent, and parkinsonism worsens, causing coordination loss and reduced facial expressions. Sleep disorders like insomnia disrupt routines. Cognitive decline affects reasoning, with increasing confusion and behavioural changes. A caregiver recounted their loved one mistaking a coat rack for a person and conversing with it, leading to falls when reaching out.
Autonomic issues escalate, leading to frequent falls or digestive problems, as in a case where constipation became chronic, exacerbating discomfort.
Actions to Take in the Moderate Stage:
Collaborate with physicians for tailored meds—SSRIs for depression, careful monitoring for side effects. Therapies: physical for movement, speech for communication. Home adaptations: remove hazards, use assistive devices.
Caregiver support is crucial; use respite and education from Alzheimer's Association. Address hallucinations gently without confrontation.
Severe Stage (Severe DLB):
Advanced decline includes inability to concentrate, severe movement impairment, and constant hallucinations. Communication and independence cease, with risks of infections from immobility. In end-of-life scenarios, patients often experience heightened paranoia, like believing family members are imposters, complicating care.
Actions to Take in the Severe Stage:
Hospice for comfort-focused care. Manage symptoms with minimal meds, emphasize soothing therapies like music. Family support groups help cope with end-of-life.



Signs of Frontotemporal Dementia
FTD targets frontal and temporal lobes with tau or TDP-43 build up, affecting behaviour, language, and motor functions. It often strikes younger people (40s-60s), with subtypes like bvFTD, PPA, and motor variants.
Early Stage (Mild FTD):
Symptoms vary by subtype. In bvFTD, personality changes dominate: impulsivity, lack of empathy, or inappropriate behaviours (e.g., overeating or rude comments). PPA involves language issues—hesitant speech or word loss. Motor types show tremors or balance problems. Memory is spared early, unlike Alzheimer's, but planning falters. A husband's early diagnosis at 42 revealed itself through sudden bursts of irritability, like snapping at colleagues over minor errors, alienating friends.
These reflect lobe-specific damage. In another account, a mother in her 50s began calling objects by wrong names, like labelling a fork a "spoon-tool," confusing family dinners.
Actions to Take in the Early Stage:
Seek specialist diagnosis via MRI and exams. No cures, but meds reduce agitation. Genetic counselling if inherited. Join AFTD for support. Plan legally early; therapies like speech help maintain skills.
Moderate Stage (Moderate FTD):
Behaviours worsen: emotional flatness or excesses in bvFTD; severe language loss in PPA; stiffness or weakness in motor types. Daily functioning impairs, with possible apathy or compulsions. A daughter described her mum's progression to compulsive hand-washing rituals, lasting hours and isolating her socially.
Actions to Take in the Moderate Stage:
Symptom management with antidepressants. Occupational therapy for routines; environmental cues for safety. Caregiver respite; community services like CurePSP for motor issues.
Severe Stage (Severe FTD):
Total dependence: swallowing issues, incontinence, bed confinement. Infections rise from immobility. One caregiver noted constant apologies for their partner's aggressive outbursts toward strangers, as recognition faded completely.
Actions to Take in the Severe Stage:
Palliative care for comfort; assist with feeding/bowel control. Support families through helplines; focus on dignity.