POLG Mitochondrial Disease Home Care in Greater Noida | Support
POLG-Related Mitochondrial Disease: Structured Home Care for Fatigue, Coordination and Daily-Living Support
Mr. Saurabh Tandon (fictional name) is a 39-year-old man from Greater Noida, Uttar Pradesh, living with a POLG-related mitochondrial disease. His biggest day-to-day challenges were severe fatigue, coordination difficulty and reduced activity tolerance. Over four weeks of structured home support, he learned to pace his energy, move more safely around his home, and keep doing daily activities as independently as possible. His underlying genetic condition remains, and regular specialist follow-up continues. Home care supported his daily life. It did not replace medical treatment.
- Patient Age
- 39 years
- Gender
- Male
- Location
- Greater Noida, Uttar Pradesh
- Primary Condition
- POLG-related mitochondrial disease
- Duration of Care
- 4-week structured programme, then continuing support
- Final Clinical Outcome
- Preserved independence, safer routine, better energy pacing
Case Summary at a Glance
What happened
A 39-year-old man with a confirmed POLG-related mitochondrial disease struggled with severe fatigue, balance changes toward the end of the day, and mild coordination problems when tired.
Why home care
The condition shows itself during everyday life: bathing, cooking, walking and turning. Support in the real home environment allows coaching, hazard removal and early recognition of new neurological signs.
How it was managed
Energy conservation (Plan, Prioritize, Pace, Rest), individually tailored physiotherapy, occupational therapy adaptations, fall prevention, nutrition and medication monitoring, and family education.
Result
After four weeks, he participated in several personal and household activities, recognised his physical limits better, and the family assisted without taking away independence. The routine became safer and more predictable.
Patient Background
Mr. Saurabh Tandon is a 39-year-old resident of Greater Noida. He lived an active family life and handled most of his own daily tasks without help. His medical history included no major orthopedic injury and no documented hospital admissions for this condition during the period described here.
His first noticeable problem was energy. Ordinary activities such as walking through a shopping centre or standing for long periods left him unusually tired. This was not the tiredness a healthy person feels after a long day. It arrived quickly and recovered slowly.
Over the following months, his family noticed two more things. He occasionally appeared unsteady while turning. And some movements became harder to coordinate when he was fatigued. Activities he once enjoyed were quietly dropped. Rest periods between household tasks grew longer.
After extensive neurological evaluation, metabolic investigations and genetic testing, he was diagnosed with a POLG-related mitochondrial disease. His family then arranged structured home support with three aims: manage fatigue, keep him safe while moving around the house, and preserve as much independence as possible.
Families in and around Noida and Greater Noida often face the same situation with rare neurological conditions: the diagnosis is clear, but daily life at home still needs to be rebuilt around the illness. That is exactly where this case begins.
Understanding POLG-Related Mitochondrial Disease
Mitochondria are tiny energy factories inside almost every cell. They convert food and oxygen into usable energy. The POLG gene carries instructions for DNA polymerase gamma, an enzyme that maintains the DNA inside these mitochondria. When this gene changes, the energy supply of cells can become unreliable, especially in tissues with high energy demands such as muscles, nerves, the brain, the eyes and the ears.
POLG-related disease is not one single illness. It is a group of related mitochondrial disorders caused by changes in the same gene. Symptoms differ substantially between individuals. Doctors group them into several recognised patterns, from mainly eye-movement and muscle problems to forms with ataxia (unsteady movement), nerve involvement (neuropathy) and, in some cases, seizures or liver involvement.
Depending on the specific disorder, people may experience combinations of:
- Muscle weakness
- Exercise intolerance
- Severe fatigue
- Coordination problems
- Balance difficulties
- Seizures
- Vision or eye-movement problems
- Hearing difficulties
- Neuropathy
- Liver involvement in some forms
- Cognitive or neurological changes
Because the group is broad, care must be individualized. What helps one person may not help another. This single fact shaped every decision in Mr. Tandon’s home support plan.
The family was advised from the beginning that mitochondrial disorders can affect different body systems. New symptoms should be reported to the treating team rather than assumed to be ordinary fatigue. This instruction became the backbone of home monitoring, because early recognition matters far more than early treatment at home.
Clinical Diagnosis and Findings
Confirmed diagnosis
The diagnosis of a POLG-related mitochondrial disease was established by his specialist team after neurological evaluation, metabolic investigations and genetic testing. The precise subtype and the genetic report were interpreted by the treating specialists.
Neurological and functional findings observed at home
- Fatigue: the most limiting symptom. It was not sleepiness. Both physical and mental activities could leave him depleted.
- Coordination: mild difficulties that became more noticeable when tired, especially with turning, carrying objects while walking, doing several movements together, and walking on uneven surfaces.
- Balance: generally adequate indoors during slow movement, but risk of losing balance rose with fatigue, quick turns, crowded environments, uneven flooring and reduced attention.
- Endurance: difficulty with prolonged standing, several consecutive household tasks, long shopping trips and long cooking sessions.
- Self-awareness: he sometimes forgot to rest until he was already exhausted.
Important observations from the family
- He became tired quickly during household activities.
- His balance was less reliable toward the end of the day.
- He sometimes needed support when changing direction.
- He avoided long walks.
- He needed frequent breaks while showering and dressing.
- Family members occasionally completed tasks for him unnecessarily, which quietly reduced his practice and independence.
Laboratory results, imaging and genetic reports
His stated goal was simple and realistic: keep participating in daily life without repeatedly pushing himself beyond his physical limits.
Specialist Treatment and Follow-Up
There was no hospital admission for this condition during the documented period. The diagnosis was reached through outpatient specialist evaluation, and his treatment has remained under the care of that specialist team since.
The specialist team’s standing advice to the family was clear:
- Continue ongoing neurological and metabolic follow-up.
- Report new symptoms rather than assuming they are ordinary fatigue.
- Keep the medication plan entirely with the treating specialists. The family maintained an updated medication list and made no independent changes.
- Understand that some POLG-related conditions can involve seizures or other neurological complications, which makes adherence and specialist review especially important.
When travelling to every review became tiring, the family also learned how doctor home visits can support care between scheduled hospital appointments, under the direction of the treating specialists.
In POLG-related disease, medicine choices carry real weight. For example, valproate, a commonly used anti-seizure medicine, is generally avoided in POLG-related disease because of liver risk. This is exactly why medication decisions stayed with the specialists, and why the home team’s role was monitoring and adherence support, never prescribing.
Why Home Healthcare Was Needed
A mitochondrial disease cannot be managed by a hospital visit. It is managed, hour by hour, inside a home: in the bathroom, in the kitchen, on the stairs, during a trip to the market. That is where fatigue accumulates and where falls happen. Structured home support was chosen for five specific clinical reasons.
1. Fatigue-driven fall risk
Balance was weakest exactly when the day was busiest: evenings, after exertion, in the bathroom. Risk reduction had to happen in the rooms where the risk lived.
2. Energy habits cannot be taught in a clinic
Pacing, resting before exhaustion and splitting tasks are habits. They form only when practised in the real environment, with real objects and real distances.
3. Family behaviour needed gentle correction
Well-meaning relatives were finishing his tasks. Over-assistance reduces practice, confidence and independence. Coaching the family is part of the treatment.
4. Early recognition of neurological change
New weakness, new seizures, swallowing or vision changes must never be dismissed as tiredness. Trained home visitors observe real function daily and escalate early.
The support was delivered through coordinated home nursing services and trained patient care taker support for daily-living assistance, always within the limits set by his specialist team.
His symptoms were stable but functionally limiting. Adding more hospital visits would have exposed him to infections and exhaustion without fixing the actual problem, which was how energy was spent at home. Supportive home care, connected to specialist follow-up, was the clinically appropriate middle path.
The Home Care Plan by AtHomeCare
The programme used structured patient care services at home with clear goals. Nothing in the plan replaced his specialist treatment. Everything in it protected his safety and independence between specialist visits.
Goals of home support
- 1. Reduce excessive fatigue
- 2. Maintain safe mobility
- 3. Improve coordination during daily activities
- 4. Prevent falls
- 5. Adapt household tasks
- 6. Preserve independence with personal care
- 7. Establish appropriate rest periods
- 8. Monitor changes across body systems
- 9. Support emotional well-being
- 10. Maintain regular specialist follow-up
Energy conservation: the foundation
Energy management became the foundation of the daily routine. Instead of completing all tasks consecutively, activities were divided across the day using one simple framework.
Important activities were identified in advance. Each day had one or two “must-do” items.
Less important tasks were postponed or delegated to family members.
He worked at a comfortable, steady speed instead of rushing.
Planned breaks were taken before severe exhaustion arrived, not after.
A sustainable daily rhythm
At first, Saurabh believed resting meant becoming inactive. The therapist reframed it: planned rest actually buys energy for more activity. A day was sequenced like this:
This rhythm was far more sustainable than completing several demanding tasks continuously.
Physiotherapy support
Physiotherapy was tailored to his functional ability. The aim was maintaining movement and safety without causing excessive exhaustion. Depending on his response, the professionally selected programme could include:
- Gentle range-of-motion exercises
- Postural exercises
- Balance activities
- Functional transfers
- Controlled walking
- Flexibility exercises
Families considering this route can read about physiotherapy at home in Greater Noida and why guided, planned movement matters more than intensity.
In mitochondrial disease, tired muscle cells recover slowly. Exhaustive training can worsen weakness and coordination for hours or days afterwards. Evidence on exercise in mitochondrial disease generally supports gentle, regular, submaximal activity with rest, and warns against pushing to exhaustion. Exercise intensity was therefore adjusted based on how Mr. Tandon responded during and after activity, never increased on a fixed schedule.
Avoiding excessive exertion
Unusual exhaustion, increased weakness after exercise, dizziness, new coordination problems, or any significant worsening of symptoms. The routine was then adjusted rather than intensified.
A related guide on sudden weakness and its warning signs helped the family understand that new weakness is information, not an excuse to push harder.
Coordination and functional training
Rather than using complicated exercise drills, therapy used practical tasks he already needed to do every day:
- Controlled sit-to-stand movements
- Safe turning technique
- Walking around household obstacles
- Reaching for objects
- Moving between rooms
- Performing one activity at a time
The goal was to make everyday movement safer, the same principle used in movement assistance for other neurological conditions.
Fall prevention
Because coordination and fatigue affected his balance, the home was reviewed carefully. Preventive work of this kind follows the same logic described in this fall prevention guide and in practical home modification advice.
- Removed unnecessary clutter
- Secured loose electrical cables
- Reduced trip hazards
- Improved lighting, especially at dusk
- Kept walking pathways clear
- Stored commonly used objects within easy reach
- Removed unstable furniture from walking areas
- Rule added: never walk quickly when fatigued
Structured daily movement planning gave the family a repeatable way to keep walking safe as energy levels changed through the day.
Bathroom safety
The bathroom needed special attention because fatigue and balance problems become more noticeable during bathing.
- Appropriate non-slip surfaces
- Stable support rails where professionally appropriate
- Shower seating if needed
- Easy access to toiletries
- Good lighting
- Floors kept dry
- Standing reduced wherever a seated option was possible
He was encouraged to take breaks rather than rushing through personal care. Guidance on personal care and hygiene support at home helped the attendant make bathing safer without making it feel dependent.
Occupational therapy support
Kitchen
Seated preparation was used for longer tasks. Frequently used utensils were moved to waist-height, easy-reach shelves.
Dressing
Clothing was organised so he could dress without unnecessary bending or prolonged standing.
Household work
Large chores were divided into smaller activities spread across the day.
Shopping
Long shopping trips were avoided where possible. Help was arranged in advance for the physically demanding parts of the task.
Families who want to understand this kind of daily-living support in depth can read about trained attendants at home and who actually needs one.
Communication and cognitive support
Saurabh remained able to make his own decisions. However, fatigue occasionally affected his concentration. The family therefore avoided giving several complicated instructions at once. Important information was written down when needed, presented one step at a time, and reviewed when he was rested. This reduced unnecessary mental fatigue without reducing his authority over his own life.
Nutrition and hydration
There is no single diet that treats all POLG-related mitochondrial diseases. His nutrition was managed according to his medical team’s advice. The family monitored:
- Appetite and meal regularity
- Weight
- Hydration
- Gastrointestinal symptoms
- Changes in energy around meals
A structured approach to nutrition and hydration monitoring gave the family simple daily checkpoints. Unexplained weight loss, persistent vomiting, difficulty eating or other new symptoms were to be reported to his medical team immediately.
Unexplained weight loss, persistent vomiting, difficulty eating, or new swallowing difficulty. In mitochondrial conditions, these are never treated as minor digestive complaints at home.
Medication safety
His medication plan was managed entirely by his treating specialists. The family maintained an updated medication list and made no independent changes. Medication routines of this kind follow established medication monitoring practices and recognised medication safety principles for home care.
Because some mitochondrial disorders can include seizures or liver involvement, both adherence and specialist review carry extra weight in POLG-related disease. The home team’s role was to support the plan, record observations and escalate concerns. Prescribing authority never left the specialist team.
Monitoring for seizures and neurological changes
Depending on the specific POLG-related disorder, seizures can occur. His family was educated to recognise unusual events such as:
- Sudden episodes of unresponsiveness
- Repetitive abnormal movements
- Unexplained falls
- New confusion following an episode
- Recurrent unusual staring episodes
Recognising sudden neurological events is a skill every neurological household needs, as explained in this guide to sudden neurological signs and recovery. Any suspected seizure or significant change was to be discussed promptly with the treating team.
Stay calm and protect the head. Do not restrain the person. Do not put anything in the mouth. Once movements ease, turn the person onto one side. Time the episode. Call emergency help if a seizure lasts beyond about five minutes, repeats, or if breathing or injury is a concern. If the specialist team had provided an individualised emergency plan, that plan would always take priority.
Fatigue and sleep
Poor sleep worsens daytime fatigue, so his sleep pattern was reviewed. The family encouraged a consistent sleep routine, appropriate daytime rest, avoiding excessive late-day exertion, and a comfortable sleeping environment. Persistent excessive daytime sleepiness or major sleep changes were to be discussed with the medical team.
Emotional support
Saurabh sometimes felt guilty when he could not keep pace with other family members. His family was coached to separate ability from effort. Needing more rest did not mean he was unwilling to participate. Responsibilities were divided according to energy levels, and he continued the tasks that were meaningful and safe. Families in similar situations often also value companionship and emotional support at home as part of the care plan.
Mobility equipment planning
A mobility aid was considered only if functional assessment showed it would improve safety or independence. Needs can change over time, and reassessment was planned if he developed frequent falls (a pattern also described in recurrent falls in neurological conditions), increasing balance problems, difficulty walking necessary distances, severe fatigue during mobility, or difficulty moving safely outdoors. Any equipment would be selected and fitted by an appropriate rehabilitation professional, with options such as medical equipment rental in Greater Noida and safe wheelchair transfer and hygiene support available if ever required.
Four-Week Home Support Timeline
The documented programme ran across four weeks, each with a distinct clinical focus. The care team also agreed a continuing maintenance plan for the months that followed.
Initial functional assessment
The home team assessed activity tolerance, recovery time after activity, daily energy pattern, sleep routine, and the effect of exertion on coordination. Fatigue was confirmed as the most limiting symptom. Initial goals were agreed with Saurabh and his family, and the first home safety walkthrough began.
Establishing energy baselines
The family recorded activity duration, rest periods, walking tolerance, coordination changes, sleep quality and daily energy patterns. The purpose was simple: find out exactly which activities caused excessive fatigue, so the plan could be built on facts rather than guesswork.
Mobility and safety
Saurabh practised safe transfers, controlled walking, turning, balance activities and gentle mobility exercises. The home was reviewed for fall hazards and the hazard checklist was completed. Therapist guidance kept every session within his energy budget.
Daily-living adaptation
Dressing, meal preparation and household tasks were divided into smaller steps. He learned to sit during tasks when practical and to rest before becoming exhausted. The family stepped back from unnecessary over-assistance, deliberately giving him room to complete what he safely could.
Long-term planning
The family consolidated a sustainable routine. The continuing plan included regular specialist follow-up, individualized physiotherapy, energy conservation, fall prevention, nutritional monitoring, medication review, monitoring for neurological changes, and periodic reassessment of daily-living assistance.
Maintenance phase (planned, as agreed with the family)
The formal documented review period covered four weeks. Beyond that, the agreed plan was to continue the established routine, attend all scheduled specialist reviews, report any new symptom immediately, and request reassessment whenever the reassessment triggers appeared. Outcomes in later months were therefore planned checkpoints rather than recorded results.
Clinical Evidence
| Area | Documented observation | Care implication |
|---|---|---|
| Fatigue | Most limiting symptom. Physical and mental activity both depleted him. Recovery was slow. | Energy conservation (Plan, Prioritize, Pace, Rest) became the foundation of the plan. |
| Coordination | Mild difficulties, worse when tired. Turning, carrying while walking, and dual tasks were hardest. | Task simplification, one activity at a time, seated options where possible. |
| Balance | Adequate indoors at slow pace. Risk rose with fatigue, quick turns, crowds, uneven floors, reduced attention. | Home hazard review, lighting and pathway changes, no fast walking when tired. |
| Endurance | Long shopping, prolonged standing and long cooking were difficult. Frequent breaks needed in showering and dressing. | Task splitting, seated preparation, scheduled rests before exhaustion. |
| Self-monitoring | Sometimes forgot to rest until already exhausted. | Scheduled rests and family cueing, rather than relying on his internal warning signals. |
| Period | Clinical focus | What was recorded or practised |
|---|---|---|
| Week 1 | Energy baselines | Family recorded activity duration, rest periods, walking tolerance, coordination changes, sleep quality and daily energy patterns. |
| Week 2 | Mobility and safety | Practised safe transfers, controlled walking, turning, balance activities and gentle mobility exercises. Home fall-hazard review completed. |
| Week 3 | Daily-living adaptation | Dressing, meal preparation and chores divided into smaller steps. Sitting during tasks when practical. Resting before exhaustion. |
| Week 4 | Long-term planning | Sustainable routine established. Continuing plan agreed: specialist follow-up, physiotherapy, energy conservation, fall prevention, nutrition monitoring, medication review, neurological monitoring, periodic reassessment. |
Warning signs requiring medical review
- New or rapidly worsening weakness
- Significant change in coordination
- Repeated falls
- New seizures or unusual episodes
- Persistent vomiting
- Unexplained weight loss
- New vision or hearing changes
- Increasing difficulty swallowing
- Significant changes in alertness
- New severe abdominal or other systemic symptoms
The family kept this list visible at home, alongside a wider reference on early warning signs that require urgent attention. A sudden neurological or systemic change was never to be assumed to be normal fatigue. Practical guidance on emergency warning signs and response was also reviewed with them.
- Severe breathing difficulty
- Loss of consciousness
- A prolonged or repeated seizure
- Serious injury following a fall
- Sudden severe neurological deterioration
- Persistent vomiting with significant weakness or reduced alertness
If the specialist team had provided an individualised emergency plan, the family would follow that plan above everything else. If any deterioration ever required higher-acuity support, families can also learn about ICU-level care at home in Greater Noida, arranged only under medical guidance.
After any fall at home, a short period of structured observation is standard practice, similar to post-fall nursing observation, even when the person appears unhurt.
Medical Review Team
Reviewed and Authored By
Dr. Ekta Fageriya, MBBS
This case study has been medically reviewed for clinical accuracy, safe home-care reasoning and alignment with specialist-led management of POLG-related mitochondrial disease.
Supporting Clinical Documents
The documentation for this case was kept in two layers, which mirrors how good home care should work alongside specialist medicine.
With the treating specialist team
- Neurological evaluation summary
- Metabolic investigation reports
- Genetic test report confirming the POLG-related diagnosis
- Prescriptions and the current medication plan
In the home-care record
- Initial functional assessment notes
- Family-maintained energy and activity diary
- Physiotherapy session notes and response records
- Home fall-hazard checklist
- Updated family medication list (no changes made at home)
Recovery Outcome
After four weeks of structured home support, Saurabh’s underlying mitochondrial condition remained present. That was expected. What changed was how he lived with it.
- Mobility: he continued to participate in several personal and household activities, moving around his home safely with the routines established in Week 2.
- Fatigue management: instead of repeatedly exhausting himself, he divided activities into manageable periods and recognised his physical limits earlier.
- Nutrition and hydration: monitored daily by the family as advised; any concerning change was to go straight to the medical team.
- Medical stability: stable under specialist follow-up, with the medication plan unchanged and fully specialist-managed.
- Family feedback: the family became more confident about providing assistance without taking away his independence.
Remaining challenges
Endurance remains limited by the condition itself. Good weeks and bad weeks still alternate. This is the honest reality of a chronic genetic disorder: home support improved safety, pacing and quality of daily life. It did not, and could not, remove the disease. Long-term care therefore continues with periodic reassessment and regular specialist reviews.
The overall approach created a safer and more predictable daily routine, which is exactly the realistic outcome a well-run supportive home-care programme should deliver.
Key Clinical Learnings
- POLG-related mitochondrial diseases can have varied neurological and functional presentations, so assessment must come before any care plan.
- Fatigue, not weakness, was the symptom that most limited daily independence in this case. Plans must be built around energy, not just muscles.
- Activity should be paced according to the person’s tolerance, measured from their own recorded baselines rather than a generic schedule.
- Physiotherapy should focus on safe functional movement. In mitochondrial disease, over-exertion can set progress back, so response guides intensity.
- Coordination and balance problems rise with fatigue, which means fall risk is highest in the evening and after exertion. Prevention must match that pattern.
- Occupational therapy converts medical advice into practical changes: seated cooking, organised wardrobes, split chores and planned shopping help.
- Nutrition and hydration should be monitored according to individual medical needs, with clear red flags for the medical team.
- New seizures or major neurological changes always require medical attention and must never be dismissed as tiredness.
- Medication decisions belong to the treating team. Some anti-seizure medicines are unsafe in POLG-related disease, which makes specialist review critical.
- Home support should complement specialist care, never replace it. The two layers, working together, produced the outcome described here.
- Family coaching matters as much as patient training. Reducing unnecessary over-assistance protects independence.
Frequently Asked Questions
Can a person with a POLG-related mitochondrial disease receive home care?
How should fatigue be managed at home?
Divide activities into smaller periods and schedule rest before becoming severely exhausted. Important activities can be planned for times when energy is usually better. Sitting during suitable tasks and avoiding unnecessary physical effort also conserve energy. The framework used in this case was Plan, Prioritize, Pace, Rest.
Is physiotherapy safe for people with mitochondrial disease?
Physiotherapy may be useful for maintaining mobility, flexibility, balance and functional ability, but the programme should be individualized. Exercise intensity should take the person’s symptoms and recovery response into account. Severe or prolonged post-exercise fatigue should be discussed with the rehabilitation team.
What should families do if coordination becomes worse?
First reduce immediate fall risks and provide appropriate supervision if needed. New or rapidly worsening coordination problems should be reported to the treating medical team because they may require further assessment. They should not automatically be assumed to be ordinary tiredness.
When should home-care needs be reassessed?
Can seizures happen at home, and how should families respond?
Some POLG-related disorders can involve seizures, so families should know the warning signs: sudden unresponsiveness, repetitive abnormal movements, unexplained falls, confusion after an episode, or unusual staring. During a convulsive seizure, protect the head, do not restrain the person, do not put anything in the mouth, turn the person to one side once movements ease, and time the episode. Urgent emergency care is needed for a seizure lasting beyond about five minutes, for repeated seizures, or when breathing or injury is a concern. Always follow the treating team’s individual emergency plan.
Is there a special diet for POLG-related mitochondrial disease?
No single diet treats all POLG-related mitochondrial diseases. Nutrition should follow the treating medical team’s advice. Families can monitor appetite, weight, hydration, meal regularity, gut symptoms and energy, and report unexplained weight loss, persistent vomiting or difficulty eating promptly.
Who should manage medicines in a POLG-related condition?
The treating specialists manage the medication plan. Families should keep an updated medication list and never make independent changes. Some mitochondrial disorders carry seizure or liver risks, and certain anti-seizure medicines are known to be unsafe in POLG-related disease, which makes specialist review particularly important.
When should emergency care be sought at home?
Seek urgent medical attention for severe breathing difficulty, loss of consciousness, a prolonged or repeated seizure, serious injury after a fall, sudden severe neurological deterioration, or persistent vomiting with significant weakness or reduced alertness. If the specialist team has provided an individualized emergency plan, follow that plan.
How can families support emotional well-being alongside physical care?
Separate ability from effort. Needing more rest does not mean a person is unwilling to participate. Divide responsibilities according to energy levels, allow the person to continue meaningful and safe tasks, avoid unnecessary over-assistance, and seek professional support if low mood or caregiver stress builds up.
Contact AtHomeCare, Greater Noida
If your family is supporting someone with a mitochondrial or other neurological condition at home, a structured assessment is the right first step. Every plan is built around the treating specialist’s advice.
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Medical Disclaimer
This fictional case study is intended for educational and informational purposes only. Mr. Saurabh Tandon is a fictional patient, and the case is presented to explain supportive home-care considerations for an adult living with a rare mitochondrial disorder.
POLG-related mitochondrial diseases are a diverse group of inherited disorders, and symptoms, complications and progression vary considerably between individuals. Every patient is unique. Physiotherapy, exercise, nutrition, medication management, seizure care, mobility assistance and other interventions should be individualized by qualified healthcare professionals. Treatment decisions must always be made by qualified healthcare professionals.
Emergency symptoms require immediate hospital care. Home healthcare complements, but does not replace, emergency medical services. This content does not replace diagnosis, treatment or advice from a medical professional.