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Feb 23 2010

Loss of Smell and Parkinson’s Disease

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Question:

A pre-diagnosed Parkinson symptom was the loss of my sense of smell.  It rarely appears on medical information forms, and if brought up during  examination noted but never gone further in discussion.

I wonder about this. If it was a matter of lose of touch, hearing or sight, would this be treated differently?  Why is it downplayed?   Are there any known recovery  methods, studies or treatments concerning this condition?

Thanks, any information will be appreciated.

Daniel

Response:

Researchers have known for at least 30 years that persons with the symptoms of Parkinson’s have an impaired sense of smell. Several studies were released in 2008 confirming the link. The impairment in ability to smell involves more than being able to take in the full essence of a scent. Individuals with the symptoms of Parkinson’s have greater difficulty distinguishing one order from another, or are unable to detect any order whatsoever.

There is currently considerable research interest in the link between Parkinson’s symptoms and the loss of smell now that it has become clear that the two are inextricably linked. Loss of specific smells in particular have also been linked to Parkinson’s symptoms, which is interesting in itself.

Some researchers are currently working on designing a diagnostic smell test for Parkinson’s. There is no definitive test at present that gives a clear  indication of Parkinson’s.  A smell test will also not be definitive,  but it can be used in conjunction with other evidence.  I suspect such tests will soon be routinely offered to patients.

The Pennsylvania Smell Identification Test is often used by many neurological clinics to evaluate neurological imbalances. This test evaluates a person’s ability to detect 40 scents.  People who take the test can are able to identify on average 35 of the 40 odors correctly. Parkinson’s patients can identify 20 of the 40 odors or less.

Researchers predict that people with seriously impaired olfactory functions have five times the risk of developing Parkinson’s than those with the highest olfactory function.

In light of your interest in this question, I will set my intention to interview some of the researchers who are currently conducting studies to evaluate the connection between the ability to smell and the symptoms of Parkinson’s. To be sure, it is an interesting line of inquiry which may  lead to understanding the underlying factors that are at play.

Robert Rodgers, Ph.D.
Parkinsons Recovery

Resources

Cruise to Alaska
Jump Start to Wellness
Parkinsons Recovery Chat Room
Symptom Tracker
Parkinsons Recovery Radio Network
Aqua Hydration Formulas

Books

Road to Recovery from Parkinsons Disease
Pioneers of Recovery

Five Steps to Recovery
Meditations for Parkinsons

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Nov 05 2009

Healing at Jump Start is for Everyone

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I have had a number of calls from people asking about the two for one offer to attend Jump Start to Wellness. If you are a persons with the symptoms of Parkinson’s and wish to attend Jump Start to Wellness on November 30th and December 1st, you are most welcome to attend with another person – whether it be a spouse, family member or friend. The other person attends for free.

For more information, visit:  http://www.parkinsonsrecovery.com/jumpstart.html

If you are a caretaker or family member who has been affected by Parkinson’s Disease, you are most welcome to attend Jump Start to Wellness with or without the family member or friend who has Parkinson’s. The program  is designed to help everyone who attends.  Bring a friend or family member for free.

I have learned from experience that the best thing I can do for my the health of my own family is to take care of my own needs. When I heal myself, I heal my entire family.

Robert Rodgers, Ph.D.
Parkinsons Recovery

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