Parkinson's, Migraines And Deja Vu? | MyParkinsonsTeam

Connect with others who understand.

sign up Log in
Resources
About MyParkinsonsTeam
Powered By
Real members of MyParkinsonsTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
Parkinson's, Migraines And Deja Vu?
A MyParkinsonsTeam Member asked a question ๐Ÿ’ญ

I've noticed that when I try to control my right hand with my brain/mind and try very hard to forcibly stop or control the Parkinson's tremors I get this feeling of deja vu and nausea like I used to when I had a very bad migraines prior to being diagnosed. When I try to do movement exercises with my fingers and try to get them to do minor tasks like touching tip to tip I get a feeling of being nauseous. Also, don't get migraines anymore since I've been diagnosed and started the Parkinson's medsโ€ฆ read more

posted May 21, 2017
โ€ข
Be the first to like/hug
A MyParkinsonsTeam Member

@BobDeBellis-----the PD meds can cause nausea------i don't take any yet because i deal with this on my own----i would definitely check in with you doc----there may be some help for you----good luck and keep on touch----Bonnie

posted May 22, 2017
A MyParkinsonsTeam Member

I hope you feel better . My problem is I keep loosing my legs I during planing on a steep hill in my yard I fell down a 5 foot wall thank God I'm just very sore. But for the most part exercise is the ticket and being stress free

posted May 22, 2017
A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member
I have more headaches than ever before. I asked my Neurologist about it he said to exercise my head an neck with light exercise.Know I looked at him like he had grown an extra head .Exercise my neck & head. You can turn your head side to side , roll it around on your shoulders, tuck your chin in towards your chest.Try to touch your shoulder with your chin.You can start with 5 an add 5 more in aweek.No more than 10 in the morning and if you tolerate it ok you can do 10 more in the evening It helped me maybe it can bring you some relief.Am adding you to my team Take Care God Bless Hugs ๐Ÿ˜‚๐Ÿ˜‚๐Ÿ˜‚๐Ÿ˜‚

posted June 1, 2017
A MyParkinsonsTeam Member

Thanks, everyone for your answers. I have known for a long time that those chemicals can effect PD, they also cause cancer and probably many other diseases. I would like to have a definite answer to what causes PD, but i am not hopeful about getting one. My priority is finding the cure. I have known a number of researchers at the University of Toronto, where I worked. One of these professors is married to a PD patient. That, of course, is his motivation for his work. Through these people I know that research takes a long, long time, and that's just to find a very small part of a potential answer. I can't even feel angry about chemical exposures because I think back then (in my youth) people just didn't know the dangers. We played in that stuff, ate the food that grew in it, drank the well water that leached through it, and breathed it in every day for years. And to some extent we still do.
Julianne

posted May 25, 2017
A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member There have been several studies connecting PD to Ag sprays, especially herbicides and fungicides. Look it up on the internet. Good hunting. :-)

posted May 25, 2017

Related content

View All
Parkinsons And Deja Vu?
A MyParkinsonsTeam Member asked a question ๐Ÿ’ญ
In 3 Mos.my Husbands Neurologist Went From Saying He Was First Steps Of PD To Dementia. This Is In Form Of A Question?
A MyParkinsonsTeam Member asked a question ๐Ÿ’ญ
How Many Out There Have Parkinsonism? Do You Know The Difference Between Parkinsonism And Parkinson's?
A MyParkinsonsTeam Member asked a question ๐Ÿ’ญ
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in