Pain assessment and relief (using medications and non-drug approaches)

Management of symptoms like breathlessness, nausea, fatigue

Regular doctor and nurse visits (home-based or clinic)

Coordination with hospitals for advanced care when needed

Home visits by nurses, doctors, and caregivers

Assistance with daily living (bathing, feeding, mobility)

Basic medical equipment support (oxygen, hospital beds, etc.)

Training family members in caregiving

Counseling for patients dealing with anxiety, fear, or depression

Support for caregivers experiencing burnout

Grief and bereavement counseling for families

Comfort-focused care in the last stages of life

24/7 on-call support

Guidance for families on what to expect

Dignified end-of-life planning

Help accessing government schemes or financial aid

Connecting families with community resources

Legal guidance (advance directives, wills, etc.)

Support aligned with the patient’s beliefs and values

Access to spiritual counselors or local faith leaders

Day centers where patients can receive care, therapy, and social interaction

Respite care to give family caregivers a break

Physiotherapy for mobility and comfort

Occupational therapy to maintain independence

Speech and swallowing support when needed

24/7 phone or video consultation for urgent concerns

Follow-ups and monitoring without travel

Training programs for caregivers and volunteers

Awareness programs about palliative care

Partnerships with hospitals and NGOs