Speaking after laryngectomy
This page tells you about speaking after laryngectomy. You can go to sections about
Speaking after laryngectomy
If you have had your larynx completely removed you will lose your voice. Before your operation a speech and language therapist will discuss the possible ways you can communicate after your surgery. There are three main ways to learn to speak again.
Voice prosthesis (Tracheo oesophageal puncture – TEP)
This is the most common way to restore speech after laryngectomy. Your surgeon makes an opening between your windpipe and food pipe (oesophagus), at the back of your stoma. They put a small, one way valve into the opening. It allows you to make sounds by pushing air from your lungs through the valve and up into your mouth. With practice, you may be surprised at how well you can be understood.
To speak in this way, you move air down into your food pipe (oesophagus) and then back up into your mouth and you shape your mouth to create speech. Nowadays, many people find it easier to use a voice prosthesis, but oesophageal speech has the advantage of not needing any equipment.
An electrolarynx (electronic larynx) is a battery operated machine that produces sound for you. They are usually about the size of a small electric razor. You hold the machine against your neck, or fit a small tube into the corner of your mouth. When you press the button on the machine, it makes sound. If you move your tongue and mouth you can form the sounds into words.
You can view and print the quick guides for all the pages in the Living with laryngeal cancer section.
Losing your voice is likely to be a great shock if you have had your larynx completely removed (a total laryngectomy). Your surgeon will have separated your windpipe (trachea) from your mouth and food pipe (oesophagus) during the operation. You will have a hole in your neck, called a stoma, that you breathe through. You can no longer force air from your lungs through your mouth to speak. So you will need to learn new ways of communicating.
A speech and language therapist will visit you before your operation to discuss the possible ways you can communicate after your surgery. You may be able to meet someone who has had similar surgery or see videos of people communicating after their laryngectomy. The type of communication you can use will depend on your individual situation, the type and amount of surgery you have, and what you yourself prefer.
There are three main ways to help you make sound and learn to speak again. These are
- Voice prosthesis or tracheo oesophageal puncture (TEP)
- Oesophageal speech
The main aim will be to keep your life as normal as possible. This means helping you to feel confident speaking with people in everyday situations, including using the telephone. Some options are likely to be better suited to your work and home situation than others.
Tracheo oesophageal puncture (TEP) is the most common way to restore speech after laryngectomy, but it is not suitable for everyone. You usually have TEP as part of the operation to have your larynx removed. Or you can go back for a minor operation to have it done later. This is usually at least 8 weeks after you have had surgery to remove your larynx.
In TEP, your surgeon makes a tiny hole called a fistula at the back of your stoma. The hole creates an opening between your windpipe and food pipe (oesophagus). Your surgeon may put a tube (catheter) into the hole to keep it open. Or they may put a small valve (voice prosthesis) into the hole during the operation. If you don't have a catheter into the hole, you will need to have a feeding tube down your nose (nasogastric tube) for a while.
If you have a catheter into the puncture (hole), you may be able to have liquid food down the tube. But once the area has healed and you are eating and drinking, the doctor takes the catheter out and they put a small, one way valve into the hole.
If you have the tracheo oesophageal puncture some time after your laryngectomy, the catheter will only need to be in place for a few days, or you may have the valve (voice prosthesis) put in straight away.
The voice prosthesis is a valve that allows you to make sounds by pushing air from your lungs through the valve and up into your mouth. You have to cover your stoma with your fingers so that the air goes through the valve and not out of the stoma. Once you can use this type of voice prosthesis, you may be able to use other types of valve which are hands free. They automatically close the stoma when you are using your speaking valve. So you won't have to put your hand up to cover the hole when you want to say anything. But hands free valves are not suitable for everyone.
Using a voice prosthesis takes practice. After a while, the muscles deep in your throat will grow stronger and vibrate more easily as the air passes through. Your speech therapist will help you. When you have got used to it, you may be surprised at how well you can be understood.
3 main types of valve are used in the UK
- Blom-Singer valve
- Provox valve
- Groningen valve
Blom-Singer valves and some Provox valves are external valves. This means that they are meant to be taken out to be cleaned and many people look after these themselves. Your valve must be kept clean. If it gets blocked, air can't pass through it easily and you won't be able to speak. Your nurse will show you how to take out the valve, clean it and put it back. You will be able to practice this until you are confident enough to do it on your own. There is a section about caring for your stoma.
Groningen and some types of Provox valve are internal valves. You leave them in place until they need changing – about every 6 months, or sooner if they are leaking. A specially trained therapist, doctor or nurse must change them. They can do this at one of your follow up appointments.
Sometimes you may need to switch from one type of valve to another if your needs change.
Your medical team will make sure you know what to do if your valve falls out and that you know who to contact for advice.
Occasionally people have difficulty speaking with a speech valve in place. This is usually because the muscles in their pharynx go into spasm. Your speech and language therapist will help you to try and overcome the spasm. Your surgeon may also suggest a treatment to inject some botulinum toxin (Botox) into the muscle to relax it. Sometimes the problem with speech is caused by swelling of the area around the valve caused by acid indigestion. Your doctor or specialist nurse can prescribe anti indigestion medicines if you have acid indigestion.
This used to be the most common way that people learned to speak after a laryngectomy. To speak in this way, you move air down into your food pipe (oesophagus). The air passes through the muscles in your throat and causes vibrations. You learn to use these vibrations and turn them into speech by moving your mouth and lips as you would when speaking normally.
If you use this method, your speech and language therapist will begin teaching you soon after you recover from your operation. Some people are able to do it more quickly than others. Sometimes it may seem that you will never get the hang of it. But keep trying, and you should eventually be able to do it. The biggest difficulty is moving down enough air to be able to produce continuous speech. About 1 in 3 people manage this very well. Some people can even go back to work – even to jobs that need a lot of talking. Your speech and language therapist can be a great support during this time. They will understand that you need a lot of practice.
Nowadays, many people find it easier to use a voice prosthesis than oesophageal speech, but oesophageal speech has the advantage of not needing any equipment. This may be better for you than valve speech if you have difficulty with fiddly things. Or better than an electrolarynx if you think it might be difficult for you to hold something to your throat every time you need to speak.
An electronic larynx (electrolarynx), is a battery operated machine that produces sound for you to create a voice. There are many different makes and types, but they are usually about the size of a small electric razor. You hold the machine against your neck, or fit a small tube into the corner of your mouth. When you press the button on the machine, it makes sound. If you move your tongue and mouth you can form the sounds into words. This method of speech after laryngectomy may be best for you if
- You are not able to have a voice prosthesis (TEP) for medical reasons
- You did not have a voice prosthesis put in at the time of your laryngectomy but are waiting to have one put in later
To be able to use this method you need training from a speech and language therapist and plenty of practice. The speech has a mechanical sound to it but most people can make themselves understood. One patient told us
"Don't be afraid to use the telephone. Start a telephone
conversation with "I have a speech problem, can you understand
me? and then it will go as normal. Difficulties can arise
with numbers and it pays to ask the recipient to repeat them back to you"
Some of the machines have buttons to vary the pitch or tone of the sound made by the electronic larynx. This will make your voice sound more varied. Your speech and language therapist will advise you on the best type for your situation and can arrange for you to have an electrolarynx on loan. You can look at the laryngeal cancer organisations page for companies that supply these machines.
You may find it useful to carry a small notebook and pen so that you can always write notes to people if you need to. Laptop computers, tiny typewriters, electronic notebooks or electronic keyboards are other ways you can communicate. A number of small portable machines are available. Your speech and language therapist can advise you on which may suit you best. It may help you to speak to someone who uses the same type of voice restoration that you have chosen. The National Association of Laryngectomee Clubs is an organisation that offers support before and after surgery to the larynx.
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