Palliative care is about making life easier when illness brings tough symptoms. It doesn’t only mean end-of-life care — you can get palliative help alongside treatments that aim to cure or slow disease. The goal is simple: control pain and other symptoms, support emotional needs, and help you make care choices that match what matters to you.
Start by asking direct questions. Who is on the palliative team? What symptoms can they treat right now? How will they help with pain, breathlessness, nausea, or sleep problems? Ask for clear next steps: a phone number for urgent issues, who manages medications, and when to expect follow-up. A short checklist like this makes conversations with doctors much easier in stressful moments.
Pain relief is often the first thing people worry about. Palliative teams use medicines, but also non-drug options — positioning, heat/cold packs, breathing exercises, or massage. For breathlessness, small changes help: using a fan, sitting upright, and controlled breathing. Nausea often improves with anti-nausea meds and eating smaller, bland meals. Ask the team for simple home strategies you can use right away.
Medications should be practical and reviewed regularly. Keep a single medication list everyone can see — times, doses, and why each drug is used. If a medicine causes drowsiness or confusion, tell the team; often a small dose change or different drug fixes it. If swallowing is tough, ask about liquids, patches, or injectable options. Practical tweaks matter more than complicated plans when comfort is the goal.
Conversations about goals and wishes are awkward but useful. Palliative care helps you name what matters: staying at home, avoiding hospital stays, or getting a reduce-symptom focus. Write down your priorities and share them with family and your care team. Ask for help making an advance care plan and a simple summary your doctor can upload to your records.
Care at home or in hospice both have pros. Home care keeps you in familiar surroundings and can be scaled with visiting nurses. Hospice focuses fully on comfort and extra support when life is short. The palliative team will explain options and help you choose what fits your goals and budget.
Finally, don’t ignore caregiver needs. Ask the team about respite, practical help at home, and local support groups. Small supports — a visiting nurse, a short-term care worker, or counseling — stop burnout and improve care for the person who’s unwell. Palliative care aims to make every day better, not just manage the medical side but the whole life around it.
In my recent blog post, I discussed the importance of HIV and palliative care in ensuring comfort and quality of life at every stage of the illness. I highlighted how palliative care focuses on relieving physical, emotional, and spiritual suffering for individuals with life-limiting conditions like HIV. I also emphasized the need for a personalized and holistic approach, involving both medical and non-medical interventions. Additionally, I shared insights on how early integration of palliative care can help improve the overall well-being of patients and their families. Lastly, I called for increased awareness and support for palliative care services within our healthcare system to help those affected by HIV lead a more comfortable and fulfilling life.