Unpleasant feelings as meds take effect

Posted by bromy @bromy, Feb 11 5:58pm

I have been taking carob/levo for over a year and take it three times a day. As the meds start to “sunset” and the new ones start to take effect, in addition for my tremor starting up , I have a dull sensation in my right ear, a headache and start to yawn ..sometimes for as long as 20 min. Then I often cough for a few minutes. This is very unpleasant as well as exhausting. What is causing this? Is it normal? I always drink plenty of water and try to just keep moving or doing something.

Interested in more discussions like this? Go to the Parkinson's Disease Support Group.

Hello @bromy and welcome to the PD support group on Mayo Connect. From what you indicated it sounds like this is a new symptom for you. Is this correct? Perhaps one of our other members will share with you, however, this is nothing that I have experienced. As Mayo Connect is a patient to patient support group we cannot diagnose problems, just share our experiences.

As this problem is recent, it might be a good idea to contact your doctor's office through the patient portal or by phone and let them know about this. Have you seen your neurologist recently for an evaluation?

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@hopeful33250

Hello @bromy and welcome to the PD support group on Mayo Connect. From what you indicated it sounds like this is a new symptom for you. Is this correct? Perhaps one of our other members will share with you, however, this is nothing that I have experienced. As Mayo Connect is a patient to patient support group we cannot diagnose problems, just share our experiences.

As this problem is recent, it might be a good idea to contact your doctor's office through the patient portal or by phone and let them know about this. Have you seen your neurologist recently for an evaluation?

Jump to this post

Actually this problem is at least 6 months old. Just wondered if anyone else experienced it. I told my neurologist but no suggestions..

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@bromy

Actually this problem is at least 6 months old. Just wondered if anyone else experienced it. I told my neurologist but no suggestions..

Jump to this post

I'm sorry to hear that you do not have any answers for this symptom. I know how frustrating that can be. You might want to post this experience in another PD discussion group where your post will have a greater audience. Here is the link to that group:
--Living with Parkinson's Disease, Meet Others...
https://connect.mayoclinic.org/discussion/living-with-parkinsons-disease-meet-others-come-say-hi/

If you would continue asking your question in this group, you will have a larger group of members to connect with. I wish you well.

Will you keep posting if you have other PD questions or concerns?

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