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Top 10 Search Results for "telling work that you have 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.

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

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

Can Parkinson's Be Fatal?
A MyParkinsonsTeam Member asked a question 💭

I get tired of hearing people say that you don't die from Parkinson's. Instead you die from losing your balance and falling. You die from choking because you no longer can swallow. You die from sepsis or multiple system failure.

Following that logic can you say that someone didn't die from COVID? Instead they died from sepsis, pneumonia or many other related illnesses?

From my point of view, I recognize that many people with Parkinson's can live many years after their diagnosis. Albeit with… read more

A MyParkinsonsTeam Member

you are a brave brave soul

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 💭
A MyParkinsonsTeam Member

I'm so glad Parkinson's has been kind to you. My prayers for you to continue your journey as well as you are. HUGS.

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

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

Are There Specific Exercises PD Patients Should Do?
A MyParkinsonsTeam Member asked a question 💭

My husband was diagnosed in December at age 69. He has been going to the gym -- mostly walking on the treadmill and using the rowing machine. I'm wondering if there are specific exercises he should be doing and if a trainer would help. Thank you and warm wishes for your journey.

A MyParkinsonsTeam Member

@A MyParkinsonsTeam Member Thank you for the 🫂 hug and here's a hug 🫂 for you.Have a wonderful day today 😀. Julie Olson 2.