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Living With a Tracheostomy
Coming home with a tracheostomy is a major adjustment for you and the people caring for you. These resources from trusted clinical organisations cover daily care, communication, eating, bathing, and the signs that mean it's time to call for help.
⚠️ This is general information only: not medical advice. Always follow your healthcare team's specific instructions.
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Resources from NHS & the National Tracheostomy Safety Project
Last reviewed: August 2026 · Free to use · No data collected
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Great Ormond Street Hospital (NHS): Living with a tracheostomy
Comprehensive NHS guide to home tracheostomy care, suctioning, tube changes, and communication.
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National Tracheostomy Safety Project: Principles of care for adults in the community
Clinical guidance on community/home tracheostomy care for adults.
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Suctioning
Suctioning clears airway secretions and keeps the tube patent. Use a clean technique, wash your hands before and after, and insert the catheter only to the length your care team has shown you: the trachea lining is sensitive and can be damaged if the catheter goes too far or suction is applied too long.
Tape and tie changes
Ties secure the tube and are usually changed daily or whenever soiled. Tension should allow one finger to slip comfortably between the tie and the neck, not tighter, not looser. Tape/tie changes are a two-person job: one holds the tube steady while the other changes the tie.
Tube changes
Full tube changes (commonly monthly for silicone tubes, but follow your own schedule) need two trained people and careful preparation. Avoid changing a tube immediately after a meal.
Stoma (opening) care
Check the skin around the tracheostomy opening daily for redness or irritation, use a protective dressing behind the tube flange, and change it regularly. Don't apply creams near the stoma without your nursing team's specific approval. It's normal for a new stoma to look red and slightly inflamed for about the first week.
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Communication and Eating
Communication
Speech can be affected at first, and usually improves with speech therapy input over time. Options your team may introduce include speaking valves, sign language, or an electrolarynx device, depending on the type of tracheostomy and your individual situation.
Eating and swallowing
Many people can eat normally with a tracheostomy but should be monitored, particularly early on. Suction before meals where possible, and avoid suctioning immediately after eating to reduce the chance of vomiting.
Bathing and showering
Keep water below the level of the tube, avoid splashing directly onto the stoma, and keep a manual suction option nearby. For hair washing, lean the head back in shallow water or use a shampoo shield your care team recommends.
Contact your GP, community nurse, or tracheostomy team if
Secretions change colour, become thicker, increase noticeably in amount, develop an odour, or show blood specks; the skin around the stoma becomes increasingly red, sore or swollen; or you notice new difficulty breathing that isn't resolved by routine suctioning.
Emergency
⚠️ If you have severe bleeding, sudden severe pain, chest pain, difficulty breathing, or any sign of a medical emergency, call your local emergency number immediately: 000 (AU) · 999 (UK) · 911 (US & Canada) · 112 (EU). A blocked or dislodged tube causing breathing difficulty that doesn't resolve with your usual emergency steps (as shown to you by your team) needs urgent emergency care.
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Support helplines
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Tracheostomy care essentials
Practical products that make living with a tracheostomy more comfortable.
🫁Tracheostomy care supplies: ties, dressings, cleaning kits and humidification filters (HMEs) are the items people managing a trach at home tend to need most.
Shop tracheostomy care supplies →
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