where in california or nevada is the best medical care for parkinsons and Parkinson's disease | MyParkinsonsTeam

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Top 10 Search Results for "where in california or nevada is the best medical care for 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.

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

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.

Seeking Name Of Neurologist Versed In "The Movement Non Visible Symptoms" Especially GI .
A MyParkinsonsTeam Member asked a question 💭

I live in the 93012 area and have not as yet found a Doctor versed in this aspect of Parkinsons. They are not fluent in understanding the interactive issues with RX and the potential results which can happen when wrong. Note: Movement disorder specialized doctors, so far I have found, are not versed in GI complications.

A MyParkinsonsTeam Member

Also the Parkinsons Association of Northern California (PANC). they have a lot of information.

If You’re Happy With Your Neurologist, Why Do U Have To See A MDS?
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

U are doing the right thing. Ur doctor can help

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! 🤗🤗🤗🤗🤗🤗🤗🤗

End Stage Of Parkinson Help
A MyParkinsonsTeam Member asked a question 💭

My mum is in the end stage of Parkinsons. The doctors have now taken her off most of the medication she was on as they say that because she has had Parkinsons for almost 22 years the medications do not work as they should. I could do with talking to others that have had or know someone that has had Parkinsons for this length of time. I'm so worried at the moment as last week mum was put on another drug to help keep her calm its called Trazadone but it has made her even worse she has been like a… read more

A MyParkinsonsTeam Member

Sandy, some injections are given in the calf and others in the feet

If Parkinson’s Won’t Kill You Why Is There An End Stage Where They Tell You To Bring Hospice In And Get Your Ducks In A Row????????
A MyParkinsonsTeam Member asked a question 💭
A MyParkinsonsTeam Member

Thank you all for your answers. It answered a lot of my questions

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

Parkinson's Plus With Lewy Body
A MyParkinsonsTeam Member asked a question 💭

My mom was diagnosed with parkinson's without the tremors 5 years ago. At a recent neurologist appt., the doctor said that it's not the typical Parkinson's but rather Parkinson Plus with Lewy Body. (She's rapidly losing motor abilities which was the reason for the new diagnosis.) This was the first I've ever heard of the "plus". Anyone else hear of this? Thanks.

A MyParkinsonsTeam Member

I was told I have Parkinsonism with Lewey body dementia