Researchers estimate that 89% of people with Parkinson's disease (PD) have speech and voice disorders. A similar, or slightly higher percentage have swallowing problems, with both speech and swallowing problems increasing in frequency and intensity as the disease progresses. Yet, despite evidence regarding the prevalence of these problems,
the number of individuals referred for speech treatment is estimated to be around 3-4%. (Expert Rev Neurother. 2008;8(2):297-309.)
This past year, I have had the opportunity to speak at several Parkinson's conferences as well as host some Voice Aerobics seminars. In all instances, I have asked those in attendance, with a diagnosis of Parkinson's disease for a year or less or greater than five years, if they received a referral for a speech and swallowing consult. Consistently, the number of people indicating that they were referred by their physicians for a speech pathology evaluation has been less than 5%. This has been particularly distressing, since
more than half of the individuals in attendance will usually acknowledge that they are experiencing changes in speech and/or swallowing function. When interacting with participants, I have noticed that greater than 75% have some impairment in speech, including those who may have DBS ( deep brain stimulation) for control of motor symptoms.
Changes in speech, voice, and swallowing function, in many ways reflect the "sneaky" or insidious nature of Parkinson's disease. Because, even though a newly diagnosed individual may not be expressing
noticeable speech and swallowing symptoms
( typical symptoms include: voice and speech which is not as loud or as clear, choking when eating or drinking, stuttering like problems with speaking, etc.), the physiological changes in the muscles of respiration, speech, and swallowing, are nevertheless, taking place.
So, whether your physician, or you, as a person with Parkinson's, wait until you are expressing symptoms to be evaluated by a speech - language pathologist,
you have really waited too long. This does not mean that therapy will not still be effective, but, what it means is that doing the
work of therapy will be harder.
I have recently been working with two individuals with a diagnosis of Parkinson's disease for approximately 7 years. They both report a decline in speech and swallowing over the last couple of years, and at the present time, both have rather severe problems with generating enough volume to be heard by their spouses. Both have obvious problems with choking with liquids, and both have to be mindful about drooling. Both patients express interest in making improvements, but, their voice habits have become quite set, and the amount of effort to generate greater loudness and speech clarity requires almost constant attention. While Medicare may be currently providing both of them the gift of 30 days of treatment, I fear that the improvements they make will not be long-lasting unless they are able to commit to daily practice.
This same therapy and same practice would have been so much easier for both of these individuals when first diagnosed, and when muscles were not as rigid, overall movement not as difficult, and their spouses not as burdened by other aspects of the disease.
So, why do physicians wait to refer patients for a consultation with a speech- language pathologist? And, why do some individuals wait, until they are having symptoms, to engage in a voice strengthening program?
If you have not yet consulted with a speech-language pathologist, ask your physician for a referral, and put it on your list of resolutions for 2011!