Skip to content


    Attention All WebMD Community Members:

    These message boards are closed to posting. Please head on over to our new WebMD Message Boards to check out and participate in the great conversations taking place:

    Your new WebMD Message Boards are now open!

    Making the move is as easy as 1-2-3.

    1. Head over to this page:

    2. Choose the tag from the drop-down menu that clicks most with you (and add it to any posts you create so others can easily find and sort through posts)

    3. Start posting

    Have questions? Email us anytime at [email protected]

    Parkinson's without tremors
    fsuokie posted:
    I was diagnosed with Parkinson's last year and put on medication. I do not have tremors. Is that unusual. Have all the other symptoms and the medication has helped a lot
    granbaker responded:
    I have been diagnosed for about 5 years. It was based on my tremors. I take requip and that works well. However, at my last apointment the Neurologist has began to doubt that I have Parkinson's. He blames the medication I was on for mental health. He is now talking about the tremors being what he calls essental tremors and has perscribed a different medication. I really don't know the answer to your question, only my own experience.
    lovedogs1955 responded:
    I have very fine tremors constantly, that become more noticeable when I am tired, stressed or anxious. If you are able to do some research, you will notice that not everyone gets tremors. PD is a very individualized disease process, so we all have different symptoms and experiences.
    granbaker replied to lovedogs1955's response:
    Dear lovedogs1955, I also have fine tremors constantly however they do not escalate with stress. My last visit to the neuro he suggested that I might have "essential tremors" which are not a PD thing and perscribed a different medication. I am presently taking requip with very good results. Just starting this new medication. He suggested I might be misdiagnoised with PD. That threw me into a tailspin. I really don't have a lot of the symptons that go along with PD, but I thought the requip was taking care of them. What do to next? He suggested we wait and watch and see how I progress. I sure wish that blood test was available. As you say we all have different symptons and I have heard it say PD is very hard too diagnos. Scary isnt it.
    lovedogs1955 replied to granbaker's response:
    PD affects SO many parts of the body. Not everyone gets affected the same way. Heck, I am a retired RN with over 30 years of experience and didn't really know about all of the various things that can happen. For example, I never knew that it is common for PD patients to lose their sense of smell. There are several good websites to look at for other symptoms, including methods of coping and special portions for our caregivers.

    Helpful Tips

    doctor/patient experience with rytary
    Hi- I am a cc physician who was diagnosed 6 years ago at age 41--I have not had tremor or dyskinesia but certainly have significant off ... More
    Was this Helpful?
    1 of 1 found this helpful

    Related Drug Reviews

    • Drug Name User Reviews

    Report Problems With Your Medications to the FDA

    FDAYou are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    For more information, visit the Duke Health Neurological Disorders Center