how parkinsons disease can affect your mental health and Parkinson's disease | MyParkinsonsTeam

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Top 10 Search Results for "how parkinsons disease can affect your mental health"

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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.

How Many Out There Have Parkinsonism? Do You Know The Difference Between Parkinsonism And Parkinson's?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

Erinanne! 🤗🤗🤗🤗🤗🤗🤗🤗

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.

Https://www.healthing.ca/diseases-and-conditions/parkinsons-disease/early-onset-parkinsons-disease-this-disease-can-affect-anyone-despite-ag
A MyParkinsonsTeam Member asked a question 💭
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.

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

Do I Have Parkinsons Or Not?
A MyParkinsonsTeam Member asked a question 💭

One neurologist says I have Parkinson's and put me on Sinemet. Another neurologist from the same office says that I don't have it and thinks my neck, lower back and anxiety are what is causing problem's with my shaking and my walking. So he will be taking me off the Sinemet gradually to see if he can tell what my problem really is. I've also had other tests. My question is once I'm off the meds will I know whether I have the Parkinson's or not? If my symptoms stay the same and don't get… read more

A MyParkinsonsTeam Member

Possibly. Not som
eveilevodopa

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

Freaking Out A Bit
A MyParkinsonsTeam Member asked a question 💭

Apologies up front, but I'm kind of freaking out. Seeing my neuro in a few weeks and thinking of starting medication. Tremors are getting worse but the side effects of meds make me nervous. Saw my GP dr last week and she asked why I was not on meds yet and she went into how this isn't going to get any better, it'll only get worse until my body shuts down and I'll be "locked in" within a few years. I'm 62 years old and on my own. I work full time and don't have an option of retirement. I was… read more

A MyParkinsonsTeam Member

I'm blessed to have found a M.D.S. who is empathetic and knowledgeable to help guide me on this unexpected journey in my golden years. I canceled a recent appointment with my primary. Her concerns… read more

What Is PSP
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

Progressive supranuclear palsy (PSP) is a rare neurological disorder that affects body movements, walking and balance, and eye movements. PSP is caused by damage to nerve cells in areas of the brain… read more