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Top 10 Search Results for "fatigue"

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Is Muscle Fatigue A Symptom Of PD?
A MyParkinsonsTeam Member asked a question 💭

I have noticed in the last year I have muscle fatigue. Walking from the parking lot to my apartment causes it as well as walking in Walmart. Does anyone else have this symptom?

A MyParkinsonsTeam Member

I do also and I can't go much any longer it's hard to walk to the mall box

Pain
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

Lunesta? Thoughts?

Talk amongst yourselves 😄

Does Your PD Leave You Tired All The Time?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

I find myself needing to fight fatigue more often than I would like to. When I wake up in the morning and find myself tired I try to fight through it. Usually, by evening time, I am not so tired.

Do You Know The Impact Of Fatigue On Those With PD?
A MyParkinsonsTeam Member asked a question 💭

Below is a summary of an article posted on the The Parkinson's News Forum

If you live with PD you might often feel run-down, ut of energy or even a bone-deep kind of tired. You may even feel like you are getting lazy or turning into a self-proclaimed chronic napper.

You may be surprised to know that 'you are more normal than you thought' since at least 50% of those with PD are also affected by fatigue which is a non-motor PD symptom and this fatigue can be chronic.

Fatigue in PD can be… read more

A MyParkinsonsTeam Member

Thank you Lucky for sharing. I had nausea with C-L also but my doc gave me med for the nausea and in 1 mo, my body adjusted to the C-L, I stopped the nausea med and C-L has worked well to help manage… read more

Fatigue
A MyParkinsonsTeam Member asked a question 💭

Question: Seem to have a new symptom. I get up around 10. Around 1pm I crash - have to hit the couch . This may last for a couple hours or all day.
Is this common? I've read about the Parkinson fatigue symptom , but finding it hard to accept that this will be my daily life. Be upfront , honest. I want to know. Thanks.

A MyParkinsonsTeam Member

I also have pd fatigue but it was much worse when I was diagnosed and it first started. It was one of my early symptoms. Over the last few months its actually gotten somewhat better for the most… read more

I Can't Seem To Get My Husband Motivated, He Is Fatigued.
A MyParkinsonsTeam Member asked a question 💭

I want to suggest activities but he doesn't feel like it, so now I feel like not asking so he won't feel bad in saying no.

A MyParkinsonsTeam Member

My husband is 78 and has sleep apnea and won’t wear a mask so he gets disturbed sleep and sleeps often in the day. Melatonin helped a little. A pill called Clonazapam caused headaches which made his… read more

Is Fatigue On Some Days Normal? There Are Days I Can Barely Put One Foot In Front Of The Other. Almost Debilitating.
A MyParkinsonsTeam Member asked a question 💭

I have a mild case with only a left hand tremor. Not on meds.

A MyParkinsonsTeam Member

Yes Sue fatigue is normal for me and many others every day all day. I even feel tired when I'm asleep . Someone posted recently about C12 ??? I can't remember who and I'm too tired to search 😄 that's… read more

Does Anybody Else Have Days Like This Too?
A MyParkinsonsTeam Member asked a question 💭

I'm on carbidova lipidova and I have been diagnosed with Parkinson's for a year. I'm still struggling with fatigue.
Is there anybody dealing with this?

A MyParkinsonsTeam Member

Fatigue is one of the major things I have to deal with. You have to deal with it by making yourself exercise and keep active as best you can. I play pickleball and feel much when I do. If I go too… read more

Does Stimulate S Effect PD. C To Help With Fatigue
A MyParkinsonsTeam Member asked a question 💭
Parkinson’s Disease and Alcohol: Your Guide Read Article...
Anyone Have Overwhelming Fatigue?. Some Evenings, I Have To Leave Dinner So I Don’t Fall Asleep .
A MyParkinsonsTeam Member asked a question 💭

This after 12 hours total sleep and at least hour’s nap.

A MyParkinsonsTeam Member

The other thing they don’t understand is how different it can be from one patient to the other. Some of us look good because of PD manifests with non-motor symptoms.