THIS may not be immediately obvious. Some warning signs are the presence of a neck covering of some sort — perhaps a cravat or a scarf. Many laryngectomees wear a Medic Alert bracelet or necklace to draw attention to their special needs. Once the clothing around the neck is loosened and the throat exposed, the stoma — the hole in the neck — makes it obvious the patient is in need of special care.
IT is vital to remember that the nose and the mouth are no longer connected to the lungs, so resuscitation through the mouth or nose is not possible. Air must be passed through the stoma to reach the lungs. Once the stoma is exposed check for several possible signs.
For further information refer to the LANSW website
A LARYNGECTOMEE is someone who, usually because of cancer, has had his or her larynx or voice box surgically removed. Cigarette smoking is acknowledged as one of the major causes of this type of cancer. Laryngectomees permanently lose the capacity for normal speech, but can use other methods to speak, as described below.
GENERALLY the physical changes are not immediately noticeable. The larynx, at the top of the trachea — or windpipe — is removed and an opening, called a stoma, is made in the front part of the neck, below the collar line. The trachea is joined to this opening. As there is no longer any connection between the lungs and the nose and mouth, the laryngectomee breathes through the stoma and coughs and sneezes through it. Eating and drinking continue orally as normal.
LARYNGECTOMEES can do most things they did before the operation. Swimming, unless using special equipment, is an exception because water cannot automatically be prevented from entering the stoma and the lungs. The sense of smell may be diminished because air does not pass through the nose. Heavy lifting and straining are difficult as breath cannot be "locked in".
VARIOUS alternatives are available, including the use of compact hand held devices that produce a tone in the mouth (either via and oral tube or via a vibrator applied to the neck) which the laryngectomee can convert to speech using the lips, tongue, palate and teeth in the normal way. These devices. however, cannot produce variations in tone. The clarity of speech is very good and the listener will become accustomed to it quite quickly.
There are two other methods — oesophageal and tracheo-oesophageal speech.
The first involves the "swallowing" of air and using it to produce vibrations in the wall of the oesophagus and the pharynx which are converted into speech in the normal way.
The second method involves the use of a plastic valve which is inserted in a surgically created hole between the trachea and the oesophagus. The valve enables the laryngectomee to use air from the lungs to create vibrations in the oesophagus and convert them to speech.
Both these methods create speech that is usually lower in pitch and, while softer, they allow tone variation and are of quite good quality.
THERE are many ways you can help. Mostly they require more than a little patience and sensitivity.
Permanent loss of one's voice is quite traumatic and the use of new methods of speech outside the immediate circle of family and friends is not easy. In the early stages the attitude and reaction of strangers can affect the person's confidence in speaking in public. Some basic guidelines are