poll what have you done to manage dyskinesia and Parkinson's disease | MyParkinsonsTeam
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Top 10 search results for "poll what have you done to manage dyskinesia" in Q&A. To see all results and access other features, sign up for free.

Who Has Been Using Sinemet (carbodopa/levodopa) For More Than Five Years? Dyskinesias? Please Mention Dose And Other Pd Meds.
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A MyParkinsonsTeam Member

I’d like to give you information but all I know about Sinemet is that I start vomiting and cant quit. If he’s doing better that’s a good thing but definitely let his prescribing doctor knows so he… read more

I Have Had PD 16 Yrs, Suffer Dyskinesia And Need A Hip Replacement. Is It Advisable?
A MyParkinsonsTeam Member asked a question 💭

The last few years I have suffered much hip pain and I have been on a waiting list for a replacement hip. I was taking 300mg Stalevo total daily, but have reduced to 250 (50mg x 5 Times) + Mirapexin. (1 slow release nightly) in order to reduce severity of dyskinesia. Has reduced dyskinesia but also reduced mobility etc. and still prone to it when under stress. My surgeon witnessed this the day before my hi op was due and is afraid my uncontrolled writhing could put my new hip out and makes… read more

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A MyParkinsonsTeam Member

Linda. Bless you. I won’t complain after reading your message. I am 86 and no hip pain. But I am small, don’t weigh much, have exercised a lot for 20+ yrs and maybe that has helped my hips… read more

I Have Been Reading That Too Much Levodopa Can Lead To Dyskinesia? Is Dyskenisia The Same As Tremors?
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I was prescribed 25/100 carbidopa/levodopa for my PD tremors. Should I stop taking if tremors are my only symptom?

A MyParkinsonsTeam Member

That is great bews Evan, thanks for sharing. Hope things stay this way for you forever, sincerely.

Any Good Treatments For Dyskinesia?
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A MyParkinsonsTeam Member

I will never forget it. I lost several weeks of living

Anyone With Dyskinesia And Visited The Dentist? How Do Stay Still So They Can Clean, Drill Or Pull A Tooth?t
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my dentist prescribed 1 valium pill to be taken before my appt. didn't work, my dyskinesia was going full on. tried gas no luck still the same.

my husband suggested next time ehrn I go to the dentist to take 1 anxiety pill prescribed by my neurologist. I try not to take it, using Reiki and meditation. If need be I take a half pill and I sleep well. Anyone suggestions for me?

A MyParkinsonsTeam Member

I don’t take any anesthesia at dentist office and I just let him get on it I’m convinced anesthetic makes me feel sick and shaky

How Do You Get Your Body To Relax While Experiencing Dyskenias In Your Entire Body?
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I have advanced Parkinson's with my main symptoms being debilitating fatigue and dystonia in my legs. I had bilateral DBS surgery 3 years ago and then a Duopa pump added to the mix a year ago. The dyskenias are relatively new. I get botox shots in my mouth, neck and shoulder. These are partially for the dystonia in my neck and shoulder and partially for the dyskenias in my mouth. Recently, I have begin having dyskenias on a daily basis. I find them exhausting. How do you relax? Help
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A MyParkinsonsTeam Member

I believe that I should include the past couple of years and the journey that I am on. I think the pandemic caused a lot of grief to many. I was no different. I think that it cut both my… read more

Does Anyone Get Jerks In There Legs?
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A MyParkinsonsTeam Member

Ask your Neurologist!
It may be RLS 'Restless Leg Syndrome'. It can happen to any of us.

https://www.google.com/search?client=firefox-b-...

Is There Anyone Who Refuses DBS Surgery?
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I have very severe, unlivable dyskinesias from Levodopa that i'm on for the past almost 10 years. I was told by my doctor that the only thing that will help is DBS surgery. Does anyone who needs DBS badly for dyskinesias not want it? How does a person live the rest of their life jumping around and not being able to function? Gocovri or any other medication does not help.

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A MyParkinsonsTeam Member

Thank you.

My Husband Will Suddenly Get Have Bouts Of Severe Uncontrollable Shivering. Anyone Else Experience This? Advice?
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A MyParkinsonsTeam Member

I’m cold ALL the time, but rarely shivers.

Has Anyone Had To Wean Off Mirepex? If So, How Slow Was Your Schedule And What Were Your Experiences Doing It?
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Every time my MDS tries to wean me off Mirepex, I get anxious. Anyone had success getting off this drug?

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A MyParkinsonsTeam Member

SOOINTERESTING; MANY THANKS!