Meet some of our experienced and dedicated healthcare professionals
15 Years Experience
SPECIALIZATIONS
Experienced in Neurological rehabilitation, Orthopaedic physiotherapy, and Paediatric care
Delivers structured, high-impact treatment plans across neuro, ortho, and paediatrics—ensuring safety, comfort, and measurable recovery at every stage.
15 Years Experience
SPECIALIZATIONS
Experienced in Neurological rehabilitation, Adult physiotherapy, and Paediatric care
Combines deep clinical expertise with a compassionate approach, supporting both adults and children through neuro and physical rehabilitation that promotes long-term independence and recovery.
12 Years Experience
SPECIALIZATIONS
Skilled in Orthopaedic rehabilitation, Manual therapy techniques, and Paediatric physiotherapy
Brings a personalised, hands-on approach to healing—combining structural expertise with paediatric sensitivity to restore movement, relieve pain, and improve everyday function.
3 Years Experience
SPECIALIZATIONS
Trained in Pain management, Cardiac and Orthopaedic rehabilitation, Neurological care, and Neural tissue mobilisation
Brings clinical precision and empathy together—designing science-backed recovery protocols for pain relief, nerve mobilisation, and cardio-neuro-ortho rehabilitation across all age groups
2 Years Experience
SPECIALIZATIONS
Holds an MPT in Orthopaedics with a focus on Musculoskeletal rehabilitation and strength recovery
Delivers focused, movement-oriented therapy grounded in orthopaedic science—helping patients rebuild strength, restore function, and return to daily life with confidence
Muscular Dystrophy presents with progressive muscle weakness, loss of coordination, and difficulty in movement. Common symptoms include frequent falls, difficulty climbing stairs, muscle wasting, and joint stiffness. Depending on the type of MD, specific muscles such as the quadriceps, biceps, or calf muscles (gastrocnemius) may be affected. Duchenne Muscular Dystrophy (DMD), one of the most severe forms, primarily affects boys and leads to loss of ambulation by early adolescence.
Muscular Dystrophy is caused by genetic mutations that interfere with the production of proteins necessary for healthy muscle function. Mutations in the dystrophin gene are responsible for DMD, while other types of MD result from defects in different genes. The condition is usually inherited in an X-linked, autosomal dominant, or autosomal recessive manner. In some cases, spontaneous genetic mutations can also lead to MD.
The primary risk factor for Muscular Dystrophy is a family history of the disease. Males are more commonly affected by certain types like DMD due to its X-linked inheritance. Other risk factors include genetic predisposition, prenatal exposure to harmful substances, and lack of early intervention. The disease progression can lead to severe complications such as respiratory failure, cardiac dysfunction, and scoliosis.
Since Muscular Dystrophy is a genetic disorder, prevention primarily involves genetic counseling and prenatal screening for at-risk families. Early detection can help in planning appropriate interventions to slow disease progression. Maintaining a healthy lifestyle, avoiding excessive strain on muscles, and engaging in guided physical therapy can aid in managing symptoms effectively.
Diagnosis of Muscular Dystrophy involves genetic testing, muscle biopsy, electromyography (EMG), and creatine kinase (CK) blood tests. There is no cure for MD, but treatment focuses on symptom management. Medications like corticosteroids can help slow muscle degeneration, while assistive devices such as braces and wheelchairs improve mobility. In severe cases, surgical interventions may be needed to correct musculoskeletal deformities.
Physiotherapy is essential in managing Muscular Dystrophy by maintaining muscle strength, preventing contractures, and improving mobility. Techniques such as stretching exercises, resistance training, and aquatic therapy help slow muscle deterioration. Breathing exercises and postural training assist in preventing respiratory complications. Assistive devices and adaptive techniques enable individuals to retain independence for as long as possible. Regular physiotherapy sessions can enhance the quality of life and delay functional decline.
At Portea, we understand the challenges of living with Muscular Dystrophy. Our home-based physiotherapy services are tailored to the specific needs of each individual, providing personalized care to help them regain mobility and independence in a safe and supportive environment.
We also specialize in providing expert physiotherapy services for post-surgical rehab, arthritis, neuro-rehab, sports injury, orthopedic physiotherapy, physiotherapy for the elderly, for respiratory disorders, and more – all delivered conveniently at your home. Our dedicated team ensures you receive the personalized care you need for a smooth and successful recovery.
Yes, some types like limb-girdle or facioscapulohumeral muscular dystrophy can develop in adulthood, causing gradual muscle weakness and mobility issues.
A balanced diet helps maintain muscle strength, manage weight, and support overall health, especially in preventing complications like obesity and constipation due to limited mobility.
Yes, consistent physiotherapy helps preserve muscle function and flexibility, often delaying or reducing the need for wheelchairs, braces, or mobility aids.
No, symptoms, severity, and progression vary depending on the type of MD and individual genetics. Each case requires a personalized care and therapy plan.
Devices like power wheelchairs, home lifts, communication tools, and adaptive utensils can improve safety, independence, and quality of life at home.
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