micrographia handwriting difficulties and parkinsons and Parkinson's disease | MyParkinsonsTeam

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Top 10 Search Results for "micrographia handwriting difficulties and parkinsons"

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Apokyn Injectable -about To Start On It. Anyone Use This Drug?
A MyParkinsonsTeam Member asked a question 💭

My sister is about to start Apokyn which is a rescue drug that is injected( like diabetes’ injectable with small thin needle that doesn’t hurt). It supposed to kick in within 10-20 minutes and last about an hour while other carbidopa-levodopa kicks in ( takes about an hour for that). Anyone have experience with this drug?

A MyParkinsonsTeam Member

I have never heard of these drugs. I will stick to THC it alot more natural.

Has Anybody Found Any Solution To Micrograpia Using Brain Plasticity Or Something Similar ?
A MyParkinsonsTeam Member asked a question 💭

I have limiting micrographia - slow and small handwriting eventually jumbling up after a couple of lines. Wondering has anybody found any solution to micrograpia using brain plasticity or something similar ?

A MyParkinsonsTeam Member

Great news, thanks for sharing, I´ll give it a try. Rgds

STAGE IV Parkinson's- HELP -severe Wheezing And Trouble Breathing. What Helps With This?
A MyParkinsonsTeam Member asked a question 💭

chest x rays are clear; gasping and wheezing. have an albuterol nebulizer that helps some--any body else have this or know what helps? Thanks feeling desperate

A MyParkinsonsTeam Member

My Primary care prescribed Spiriva Respimat 1.25MCG. INH SPR. 2 puffs daily. I also use VENTOLIN. HFA. 90MCG Inhaler for shortness of breath and wheezing. I also use a CPap and keep a canned supply… read more

Hi What Cough Medicine Can I Take That Wont Conflict With My Meds.
A MyParkinsonsTeam Member asked a question 💭

coughing with some congestion. this is in addition to usual parkinson's related cough

A MyParkinsonsTeam Member

Low doses of DXM are beneficial for PD. Higher doses (like the ones found in cough syrup) are detrimental. Neurologist =1 PR = 0

The Lemon Tea and Whiskey sound like the best alternative.

Any One Who Is Taking Levidopa ER..... Can You Tell Me How/when You Take It I Am A Little Confused About This Thanks
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

I take the Extended-Release carbidopa. Levodopa 3 times a day (6am or upon waking up if it is later than 6am,, 2pm and 8pm) I take regular C/L twice a day, but I chew it since they no longer make the… read more

I Suffer From Severe Wear Offs Every 2 Hours.
A MyParkinsonsTeam Member asked a question 💭

Does anyone here go through this? Im at my wits end and so is my wife. Feels like i am going to die everytime.
Im at the point where I cant breathe, cant move, in pain and extremely nervous. This lasts until the next dose kicks in whenever it decides to that is.

A MyParkinsonsTeam Member

I take ER C/L, but then take a regular C/L in between doses and I chew that one so that it gets into my system faster, since the dissolvable one is no longer available. It starts working within 10… read more

Handwriting Difficulties
A MyParkinsonsTeam Member asked a question 💭

Ugh, I'm really just venting. I had to write an important number down and of course, when I needed it, I could not read it.

Does anyone else have this annoying problem?

A MyParkinsonsTeam Member

voice activation on phone and computer has saved my husband who has this problem

How To Speed Up The Absorption Period Of Levadopa After Food
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

benefit is is quick absorption

Can Anyone Enlighten Me On The Term Parkinsons Plus Please?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

This is what I found . The timing of protein intake during levodopa administration is crucial. While some individuals may not experience issues with protein intake affecting medication absorption, for… read more

After Being On Carbidopa Levodopa For 3 Months, 1/2 Tablet 3 Times A Day. I've Been Experiencing Daily Dizziness, Is This Common?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

I, too, have been dealing with it. I’m in physical therapy for it now. Told me, it’s balance and eye movement, and can be an ear blockage.,