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Cerebral Palsy Orthopaedic Surgery in India

Specialized surgical procedures to improve mobility, function, and quality of life in children with cerebral palsy through soft tissue and bony corrections.

Overview

Cerebral Palsy (CP) is a group of permanent movement disorders appearing in early childhood caused by abnormal brain development or damage to the developing brain. While CP itself cannot be cured, orthopaedic surgery plays a crucial role in managing musculoskeletal complications that arise from spasticity, muscle imbalance, and abnormal growth patterns. These surgical interventions aim to improve function, reduce pain, facilitate care, and enhance the quality of life for children with CP. At Arthroscenter, Dr. Gurudeo Kumar specializes in comprehensive orthopaedic management of cerebral palsy, offering both soft tissue procedures (muscle lengthening, tendon transfers, and releases) and bony procedures (osteotomies and corrective surgeries). Our multidisciplinary approach integrates surgical intervention with intensive physiotherapy, occupational therapy, and family education to optimize outcomes. We assess each child according to the Gross Motor Function Classification System (GMFCS) levels I-V to determine the most appropriate surgical strategy. The surgical approach for CP is highly individualized based on the type of CP (spastic, dyskinetic, ataxic, or mixed), severity, affected body parts (hemiplegia, diplegia, or quadriplegia), age, and functional goals. Single-event multilevel surgery (SEMLS) is often preferred for children with multiple deformities, allowing comprehensive correction in one operation and reducing the need for multiple surgeries. Success depends on careful patient selection, precise surgical technique, and dedicated postoperative rehabilitation. In Bihar's context, early intervention and accessible rehabilitation services are essential for maximizing surgical benefits.

Symptoms & Indications

This surgery may be recommended if you experience:

Persistent muscle spasticity causing difficulty with movement and positioning

Progressive joint contractures limiting range of motion

Equinus foot deformity (toe walking) preventing heel contact during gait

Hip subluxation or dislocation causing pain and affecting sitting balance

Scissoring gait pattern due to hip adductor spasticity

Crouch gait with excessive knee and hip flexion during walking

Scoliosis or spinal deformity affecting sitting posture and balance

Upper limb spasticity interfering with hand function and self-care

Progressive bone and joint deformities despite conservative management

Pain or difficulty with hygiene, dressing, and daily care activities

Procedure Details

Duration

2-5 hours depending on the number of levels addressed; single-event multilevel surgery (SEMLS) addressing multiple joints may take 4-6 hours

Anesthesia

General anesthesia; epidural or caudal analgesia may be added for postoperative pain control

Preparation for Surgery

Comprehensive preoperative assessment includes detailed physical examination, gait analysis (video or instrumented if available), GMFCS level classification, assessment of spasticity using Modified Ashworth Scale, X-rays to evaluate bone deformities and hip displacement, and sometimes CT or MRI for complex deformities. Multidisciplinary team consultation with physiotherapists, occupational therapists, and orthotists helps establish realistic goals. Children are optimized medically, with attention to nutritional status, seizure control, and respiratory function. Preoperative physiotherapy establishes baseline function and educates families about postoperative expectations. The surgical plan is individualized—soft tissue procedures for younger children with primarily spasticity-related issues, bony procedures for older children with established skeletal deformities, or combined single-event multilevel surgery (SEMLS) for comprehensive correction.

Surgical Steps

1

General anesthesia is administered with careful positioning to prevent pressure sores in children with poor nutritional status

2

For lower limb procedures: Multilevel soft tissue releases may include gastrocnemius/soleus lengthening for equinus, hamstring lengthening for knee flexion contracture, hip adductor release for scissoring, and psoas lengthening for hip flexion contracture

3

Tendon transfers are performed to rebalance muscle forces—common transfers include posterior tibialis transfer for varus foot deformity and rectus femoris transfer to improve knee extension during gait

4

Bony procedures address fixed skeletal deformities: Femoral derotational osteotomy corrects excessive internal rotation, proximal femoral varus osteotomy treats hip subluxation, distal femoral extension osteotomy corrects crouch gait, and tibial osteotomy addresses rotational or angular deformities

5

Hip procedures for subluxation/dislocation include femoral varus derotational osteotomy, pelvic osteotomy (Dega or Pemberton), and open reduction with soft tissue releases to achieve stable hip reduction

6

Foot and ankle procedures may include calcaneal lengthening osteotomy, midfoot osteotomies, triple arthrodesis (in older children), or talectomy for severe rigid deformities

7

Upper limb procedures address thumb-in-palm deformity, wrist flexion contracture, elbow contracture, and shoulder internal rotation through selective muscle releases, tendon transfers, and sometimes osteotomies

8

Wounds are closed meticulously, and appropriate immobilization is applied—typically long leg casts for lower limb procedures or splints/casts for upper limb surgeries, with careful padding to prevent pressure sores

Recovery Timeline

What to expect during your recovery journey

Hospital Stay (2-7 days)

Immediate Postoperative Care

Initial recovery in hospital with pain management, wound monitoring, and prevention of complications. Early mobilization begins with physiotherapy guidance, focusing on positioning, gentle range of motion exercises within cast limitations, and respiratory care. Nutritional support is critical. Parents receive education about cast care, positioning, pressure sore prevention, and recognition of complications. Hospital stay duration depends on extent of surgery and child's overall health.

Weeks 1-6

Immobilization and Initial Healing

Casts or splints maintain surgical correction during initial healing. Regular cast checks prevent pressure sores—critical in children with sensory impairment. Home physiotherapy begins with passive range of motion exercises for non-operated joints, positioning programs, respiratory exercises, and maintaining strength in unaffected limbs. Pain management continues as needed. Weekly or biweekly clinic visits monitor healing and address any concerns. For multilevel surgery, this is a challenging period requiring significant family support.

Weeks 6-12

Cast Removal and Intensive Rehabilitation

Casts are gradually removed and replaced with removable splints or orthoses. This phase marks the beginning of intensive physiotherapy—the most critical determinant of surgical outcome. Therapy includes stretching to maintain surgical gains, strengthening exercises, gait training with assistive devices, functional activities practice, and orthotic training. Frequency: 5-6 sessions per week initially. Serial casting may continue for some joints. Gradual progression from non-weight bearing to partial then full weight bearing under therapist supervision.

Months 3-6

Progressive Function and Gait Training

Continued intensive physiotherapy focusing on functional goals—independent sitting, standing, walking (with or without aids depending on GMFCS level), transfers, and activities of daily living. Strengthening programs intensify as healing consolidates. Orthotic management is refined—AFOs, KAFOs, or other braces as needed. Some children may require adjustment of orthoses or serial casting for residual contractures. Occupational therapy addresses upper limb function and self-care skills. Progress is monitored objectively through video gait analysis and functional assessments.

Months 6-12

Functional Consolidation and Community Reintegration

Therapy transitions to 3-4 sessions weekly with emphasis on community ambulation, school activities, and social participation. Focus shifts to maintaining range of motion, preventing recurrence of contractures, optimizing gait pattern, and building endurance. Home exercise programs are essential for long-term maintenance. Orthotic adjustments accommodate growth. Assessment of surgical goals achievement—improved gait, reduced energy cost, easier caregiving, reduced pain, better positioning for functional activities.

Year 1 and Beyond

Long-term Maintenance and Growth Monitoring

Regular follow-up every 3-6 months to monitor for recurrence of deformities, assess growth-related changes, adjust orthoses, and modify therapy programs. Lifelong commitment to stretching, strengthening, and functional activities is essential to maintain surgical gains. Some children may require additional procedures during growth spurts. Transition planning for adolescents addresses adult care, vocational training, and independence. Success is measured not just by radiographic correction but by meaningful functional improvements, reduced caregiver burden, and enhanced quality of life.

Tips for Faster Recovery

Intensive, consistent physiotherapy is THE most important factor determining surgical success—commitment to 5-6 sessions weekly for first 3-6 months is essential

Maintain meticulous cast care and pressure sore prevention—check skin regularly, especially over bony prominences

Family education and support are critical; consider arranging help during the intensive rehabilitation phase

Continue stretching exercises lifelong to prevent recurrence of contractures as child grows

Ensure proper nutrition to support healing and bone health—calcium, vitamin D, and adequate protein

Use prescribed orthoses consistently as directed; proper fitting and regular adjustments are essential

Set realistic expectations aligned with GMFCS level—surgery improves function but does not cure CP

Coordinate care among orthopaedic surgeon, physiotherapist, occupational therapist, and pediatrician

Monitor for complications: infection, pressure sores, loss of correction, over-lengthening weakness

Celebrate functional improvements—easier dressing, better sitting balance, reduced pain—not just radiographic changes

Frequently Asked Questions

Common questions about this procedure

Q1.What are the different types of cerebral palsy and how does this affect surgical planning?

Cerebral palsy is classified into four main types based on movement patterns: Spastic CP (70-80% of cases) characterized by increased muscle tone and stiffness—further divided into spastic hemiplegia (one side affected), spastic diplegia (primarily legs affected, most common in premature babies), and spastic quadriplegia (all four limbs affected). Dyskinetic CP (10-15%) involves involuntary, uncontrolled movements including athetosis and dystonia. Ataxic CP (5-10%) causes problems with balance and coordination. Mixed CP shows features of multiple types. Surgical planning differs significantly: Spastic CP responds best to soft tissue releases and tendon lengthening to address fixed contractures; these children are the best surgical candidates. Dyskinetic CP has less predictable surgical outcomes because the primary problem is abnormal movement control rather than fixed deformity—surgery is selective, focusing on specific functional goals. Ataxic CP rarely requires orthopaedic surgery. The distribution pattern (hemiplegia, diplegia, quadriplegia) determines which limbs require intervention and the complexity of surgery. GMFCS level (I-V) is critical: ambulatory children (GMFCS I-III) have different surgical goals (improve gait efficiency, independence) compared to non-ambulatory children (GMFCS IV-V) where goals focus on positioning, care facilitation, and pain prevention.

Q2.At what age is cerebral palsy surgery typically performed?

Age considerations for CP surgery are complex and depend on the procedure type and goals. Soft tissue procedures (muscle/tendon lengthening, releases) can be performed as early as 3-4 years when contractures interfere with function, gait, or positioning. However, there is a risk of recurrence with growth, potentially requiring repeat procedures. Single-Event Multilevel Surgery (SEMLS) for ambulatory children is optimally performed between ages 6-10 years, when gait pattern is mature enough to assess comprehensively but before fixed bony deformities develop and while rehabilitation potential is high. Bony procedures (osteotomies) are typically performed after age 6-8 when skeletal maturity is sufficient, though specific procedures like femoral osteotomy for hip subluxation may be done earlier (4-6 years) to prevent hip dislocation. Hip surveillance and early intervention for hip dysplasia should begin by age 2-3 to prevent painful dislocation. Upper limb surgery is often delayed until age 6-8 or later when the child can participate in goal-setting and intensive hand therapy. Spinal surgery for scoliosis is typically performed in adolescence when growth is nearly complete, though severe progressive curves may require earlier intervention. In Bihar's context, many children present late, and surgery may need to be performed at older ages to address established deformities. The guiding principle is: operate when contractures or deformities interfere with current function or threaten future function, and when the child can participate meaningfully in rehabilitation.

Q3.What is Single-Event Multilevel Surgery (SEMLS) and is it better than staged procedures?

Single-Event Multilevel Surgery (SEMLS) involves performing multiple soft tissue and/or bony procedures at different anatomical levels during a single operation under one anesthetic. For example, a child with spastic diplegia might undergo hamstring lengthening, hip adductor release, psoas lengthening, and gastrocnemius recession all in one surgery. The alternative is staged procedures—addressing one or two levels at a time over multiple separate operations. SEMLS advantages include: one hospitalization and anesthetic exposure rather than multiple, simultaneous correction of all deformities allows balanced rehabilitation, more cost-effective overall, less disruption to school and family life, potentially better functional outcomes because all components of the gait pattern are addressed together. Disadvantages include: longer single operation (4-6 hours), more intensive immediate postoperative care, more complex rehabilitation initially, higher initial cost. Research evidence generally favors SEMLS for ambulatory children (GMFCS II-III) with multiple level involvement—studies show comparable or better functional outcomes with fewer total surgeries compared to staged approaches. However, SEMLS requires: comprehensive preoperative gait analysis, experienced surgical team, strong rehabilitation infrastructure, and committed family support. Not all children are SEMLS candidates—very young children, those with severe medical comorbidities, or those with limited single-level problems may be better served by staged procedures. At Arthoscenter, we use comprehensive gait analysis and multidisciplinary assessment to determine the optimal surgical strategy for each child, whether that is SEMLS or staged approach.

Q4.What are the realistic goals and outcomes of cerebral palsy surgery?

Setting realistic expectations is crucial for family satisfaction. Cerebral palsy surgery CANNOT cure CP, normalize movement completely, or eliminate the need for ongoing therapy. What it CAN do: reduce spasticity-related contractures, improve joint alignment and range of motion, enhance gait efficiency and reduce energy cost of walking, facilitate transfers and positioning, reduce pain from joint deformities, make hygiene and dressing easier for caregivers, delay or prevent secondary complications like hip dislocation or severe scoliosis, and improve quality of life. Specific outcomes depend on GMFCS level: For GMFCS I-II (community ambulators), goals include improving gait aesthetics, reducing compensatory movements, increasing walking speed and endurance, and reducing long-term joint stress. Success rates for improved gait kinematics: 70-80%. For GMFCS III (household/limited community ambulators with aids), goals include maintaining or improving walking ability with assistive devices, easier transfers, better standing tolerance. Success in maintaining ambulatory status: 60-75%. For GMFCS IV-V (non-ambulatory), goals focus on improving sitting balance and posture, preventing painful hip dislocation, facilitating positioning and caregiving, reducing pain from contractures. Success in achieving these goals: 75-85%. Overall, studies show 60-80% of children achieve their primary functional goals after CP surgery, but success heavily depends on: appropriate patient selection, comprehensive surgical planning, intensive postoperative physiotherapy (THE most critical factor), family commitment, and realistic goal-setting aligned with GMFCS level. Functional improvements may be modest but meaningful—walking independently for household distances instead of requiring assistance, sitting comfortably for classroom activities instead of requiring special positioning equipment, or reducing caregiver burden for hygiene and dressing.

Q5.How does orthopaedic surgery differ from SDR (Selective Dorsal Rhizotomy) for cerebral palsy?

These are complementary approaches targeting different aspects of CP. Selective Dorsal Rhizotomy (SDR) is a neurosurgical procedure that permanently reduces spasticity by cutting selected sensory nerve rootlets in the spinal cord. It addresses the neurological cause of spasticity but does not correct established contractures or bony deformities. SDR is best for: young children (typically 3-8 years) with pure spastic diplegia, good strength, minimal fixed contractures, and good selective motor control. Benefits include permanent spasticity reduction, improved ease of movement, and reduced energy expenditure. Limitations: does not correct fixed deformities, requires intensive post-SDR physiotherapy, and has risks including sensory changes, bladder/bowel dysfunction, and spinal deformity. Orthopaedic surgery addresses the musculoskeletal consequences of CP—contractures, deformities, and mechanical malalignment. It can be performed at any age and is suitable for all CP types. Benefits include correction of fixed deformities, improved joint alignment, and addressing specific functional limitations. Limitations: does not reduce spasticity at its source, and contractures may recur if spasticity persists. Many children benefit from BOTH approaches sequentially: SDR first (at age 4-6) to reduce spasticity and facilitate therapy, followed by orthopaedic surgery later (age 8-10) to address any residual contractures or deformities that develop despite therapy. This combined approach can produce excellent outcomes in carefully selected patients. However, SDR availability is limited in India including Bihar—few centers offer it, and cost is high (₹6-10 lakhs). At Arthoscenter, we work with neurosurgical colleagues when SDR is appropriate, but most of our CP patients are managed primarily with orthopaedic interventions, therapy, and sometimes botulinum toxin injections for spasticity management.

Q6.What is hip surveillance in cerebral palsy and why is it important?

Hip surveillance refers to systematic monitoring of hip development in children with CP through regular clinical examination and X-rays. It is critically important because hip displacement (subluxation/dislocation) is one of the most common and serious complications of CP, occurring in 30-40% of children overall and up to 60-90% of non-ambulatory children (GMFCS IV-V). Hip displacement develops gradually due to muscle imbalance—spastic hip adductors and flexors pull the femoral head out of the acetabulum, especially when combined with poor weight-bearing and abnormal positioning. The process is often painless initially, so without surveillance it goes undetected until severe dislocation occurs. Consequences of untreated hip dislocation include: severe pain from arthritis, difficulty with positioning and sitting, pressure sores, impaired perineal hygiene, pelvic obliquity contributing to scoliosis, and significantly reduced quality of life. Hip surveillance protocols recommend: clinical hip examination and anteroposterior pelvis X-ray at age 2-3 years for all children with CP (except GMFCS I who walk independently), then repeated every 6-12 months depending on GMFCS level and hip migration percentage. X-rays are measured for Migration Percentage (MP)—the percentage of femoral head not covered by acetabulum. Normal MP is <10%; MP >30% indicates progressive displacement requiring intervention; MP >40% usually requires surgery. Early intervention when hip displacement is detected (MP 30-40%) may involve soft tissue procedures alone (adductor and psoas release). More advanced displacement (MP 40-70%) requires femoral osteotomy ± pelvic osteotomy. Established dislocation (MP >90%) may require complex reconstructive surgery or in severe cases, salvage procedures for pain management. The key principle: hip surveillance allows early detection and preventive intervention before painful dislocation occurs. Unfortunately, systematic hip surveillance is not yet widely implemented in Bihar, and many children present with established painful dislocations requiring complex surgery. At Arthoscenter, we advocate strongly for hip surveillance and work to implement it through our CP clinics.

Q7.What is the role of physiotherapy after cerebral palsy surgery?

Physiotherapy is absolutely THE MOST CRITICAL factor determining surgical success—more important than surgical technique itself. Surgery creates the mechanical opportunity for improved function by lengthening tight muscles, correcting deformities, and rebalancing forces. But realizing that potential requires intensive, expert physiotherapy to: maintain the range of motion gained surgically, strengthen muscles that may be weakened by lengthening procedures, retrain gait patterns to take advantage of improved alignment, prevent compensatory abnormal movement patterns from developing, and gradually progress to functional activities. The intensity required is much higher than many families expect: First 3 months post-surgery: 5-6 sessions per week of structured physiotherapy plus daily home exercises. Months 3-6: 4-5 sessions weekly with continued home program. Months 6-12: 3-4 sessions weekly. Beyond 1 year: 2-3 sessions weekly plus lifelong daily stretching and exercise routine. Each session is typically 45-60 minutes. Without this intensity, contractures recur, surgical corrections are lost, and functional goals are not achieved. Studies show that inadequate post-surgical physiotherapy is the number one cause of poor outcomes after otherwise technically successful CP surgery. The challenges in Bihar's context: Limited number of physiotherapists trained specifically in pediatric neurological rehabilitation. In rural areas, accessing regular physiotherapy is extremely difficult. Cost of intensive therapy over many months can be prohibitive for many families—private physiotherapy in Patna typically costs ₹500-800 per session, meaning 5-6 sessions weekly for 3 months = ₹30,000-60,000 just for therapy. At Arthoscenter, we address this through: in-house physiotherapy department with pediatric neurological specialists, family training programs where parents learn to continue therapy at home, subsidized therapy costs for economically disadvantaged families, and connecting families with government rehabilitation facilities. We emphasize to families before surgery: the commitment to intensive physiotherapy is as important as the decision for surgery itself. Without that commitment, surgery should be delayed or reconsidered.

Q8.Can cerebral palsy surgery be performed for adults, or is it only for children?

While CP surgery is most commonly performed in childhood, adults with CP can definitely benefit from orthopaedic procedures, though goals and outcomes may differ. Adult CP surgery addresses: progressive painful contractures that develop despite previous surgery or therapy, hip pain from subluxation or dislocation that was undetected or untreated in childhood, painful foot deformities interfering with footwear or ambulation, upper limb contractures affecting hygiene or self-care, and spinal deformity causing pain or sitting imbalance. The differences in adult CP surgery include: goals are often more focused on pain relief, maintaining current function, and facilitating care rather than improving function, bony deformities are more established and may require more extensive surgery, rehabilitation potential may be less than in children due to longstanding adaptive patterns and muscle changes, but adults can be more motivated and compliant with therapy, surgery may be combined with pain management strategies like neurolysis or botulinum toxin, and realistic expectation-setting is even more critical. Common adult CP procedures include: hip reconstruction or salvage procedures (arthroplasty, proximal femoral resection) for painful dislocated hip, tendon releases for contractures affecting hygiene, foot fusion procedures for severe rigid deformities, and spinal fusion for painful progressive scoliosis. Outcomes can be very satisfying when goals are appropriate—many adults achieve significant pain reduction, easier caregiving, better positioning, and improved quality of life. At Arthoscenter, Dr. Gurudeo Kumar has extensive experience with adult CP surgery and takes a comprehensive approach including pain management, realistic goal-setting, and planning for long-term maintenance. One challenge in Bihar is that many adults with CP never received any surgical intervention in childhood despite clear indications, presenting with severe neglected deformities that are more complex to treat. Even in these cases, surgery can often provide meaningful improvements in pain, positioning, and quality of life, though expectations must be carefully managed.

Q9.What are the risks and complications of cerebral palsy surgery?

As with any major orthopaedic surgery, CP surgery carries risks that must be weighed against potential benefits. General risks include: infection (2-5% depending on extent of surgery and nutritional status), wound healing problems (higher risk in malnourished children or those with skin sensitivity), anesthesia complications (careful preoperative assessment needed for children with seizures, respiratory issues, or swallowing problems), blood loss requiring transfusion (more common with multilevel or pelvic surgery), pressure sores during prolonged immobilization (prevention crucial in children with sensory impairment), and venous thromboembolism (rare in children but possible with prolonged immobilization). Specific orthopaedic complications include: Over-lengthening weakness—excessive muscle lengthening can create new weakness and actually worsen function; requires careful surgical judgment. Under-correction—insufficient release leaves residual contracture requiring revision. Recurrence of deformity—occurs in 20-30% of cases over years, especially with continued growth and persistent spasticity; emphasizes importance of ongoing therapy and spasticity management. Neurovascular injury—rare but can occur with procedures near nerves and vessels. Loss of correction—casts or fixation may slip, allowing deformity to recur during healing. Fracture—can occur through weakened or osteoporotic bone during surgery or postoperatively. Specific to certain procedures: Hip surgery may result in avascular necrosis of femoral head (rare), nerve injury (sciatic nerve during hip surgery ~1%), or recurrent dislocation if soft tissue balance not achieved. Foot surgery may result in stiffness, overcorrection creating new deformities, or wound complications. Spinal surgery carries higher risks including neurological injury, implant complications, and pseudarthrosis. To minimize complications, Dr. Gurudeo Kumar employs: meticulous preoperative assessment and optimization, careful surgical technique with intraoperative monitoring, appropriate postoperative protocols including pressure sore prevention, experienced anesthesia team familiar with CP patients, and close postoperative monitoring. Families should understand: some degree of surgical complications is unavoidable in complex multilevel surgery, but serious permanent complications are rare (<2%) in experienced hands. The benefits of appropriately indicated surgery typically far outweigh risks.

Q10.What is the cost of cerebral palsy surgery and what financial support is available in Bihar?

CP surgery costs vary widely based on extent and complexity. At Arthoscenter in Patna: Single-level soft tissue procedure (e.g., hamstring lengthening): ₹75,000-1,25,000 including surgeon fees, hospital stay (3-5 days), anesthesia, and medications. Multi-level soft tissue procedures (SEMLS without bony surgery): ₹1,50,000-2,50,000. Complex procedures including osteotomies: ₹2,50,000-4,00,000. Hip reconstruction surgery: ₹2,00,000-3,50,000. These costs cover surgery only—additional expenses include: preoperative assessments and imaging (₹10,000-20,000), postoperative physiotherapy (₹30,000-60,000 for first 3 months if done 5-6x weekly), orthoses/braces (₹15,000-50,000 depending on type), follow-up visits and any adjustments or minor procedures. Total first-year cost for comprehensive CP surgery and rehabilitation can range ₹2,00,000-6,00,000 depending on complexity. This is financially challenging for most Bihar families. Available financial support: Government health insurance schemes—Ayushman Bharat PMJAY covers up to ₹5 lakhs annually for empaneled hospitals; check if your hospital is empaneled and CP surgery is covered. State government disability schemes—Bihar State Disability Pension and various disability welfare programs may provide limited financial assistance. NGO support—organizations like Bhagwan Mahaveer Viklang Sahayata Samiti (BMVSS/Jaipur Foot), Rotary clubs, and local charitable organizations sometimes support CP surgeries. Crowdfunding platforms—Ketto, Milaap, and others have been successfully used by Bihar families to raise funds for CP surgery. Corporate CSR programs—some companies support medical treatment for underprivileged children under CSR mandates. At Arthoscenter, we work with families to: navigate insurance and government schemes, provide cost-effective treatment without compromising quality, arrange subsidized or free physiotherapy for economically disadvantaged patients through our charitable programs, and connect families with NGOs and support organizations. Dr. Gurudeo Kumar believes every child deserves the opportunity for improved function regardless of economic status, and we make every effort to make surgery accessible. Families should discuss financial concerns openly during consultation—solutions can often be found.

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