Watch CBS SUNDAY MORNING : Michael J Fox... - Cure Parkinson's

Cure Parkinson's

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Watch CBS SUNDAY MORNING

JMitch1950 profile image
9 Replies

Michael J Fox joins Jane Pauley on CBS Sunday Morning tomorrow. Check your time zone. 9AM Eastern Time- a research panel sharing experiences will be present- will be informative.

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JMitch1950 profile image
JMitch1950
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9 Replies
healthabc profile image
healthabc

i found the segment disappointing

Cbgs profile image
Cbgs in reply tohealthabc

Why?

nelo23 profile image
nelo23 in reply tohealthabc

I agree. I would have liked to know more about the treatments, meds, etc. that he has tried or that his foundation is testing, trialing, etc.

seamus60680 profile image
seamus60680

I thought he looked great! One of the most inspirational and influential men of our time.

I'll be quite happy if I'm doing as well as MJF in 25 years time!

au contraire

The first thing we learned is that John Pepper does have Parkinson's, MJ Fox does boxing and your brain can not process all the info it takes in. Communication is tiring because we have to shut down the brain that helps with calming. I found it more informative than most of his interviews.

youtu.be/CFdJza0AbeA

can not wait to see it again

New revelations upon watching it a second time: I am going to be pigeon toed as I loose control, he to ( like me ) has a little fat in the middle. ( with as much as he moves he should be a pole, must be cortisal fat. ) ANXIETY....

When he can not focus on staying calm his synapses start firing causing movement / for me pain. I also saw others who looked normal but as soon as the spotlight was on them lost control.

Now to watch it again.

I have been wondering if I should start a time line bio on myself and what I believe to be the start of my PD.

Michele11 profile image
Michele11

If I did not have PD I am not sure I would understand from his interview what it was exactly. It was presented by the show in a way like everyone knows what Parkinson's is. . I understood what he was saying about controlling his dyskinesia by focusing his mind and not talking, but I think it would make me confused about the disease if I did not have it.

When I saw the panel of ordinary PD people, I got excited that they were showing all sorts of PD people, but they did not say too much.

I would of liked to hear a little on any progress on finding a cure and details on what are obstacles. Maybe the fact there was no update speaks volume.

Perhaps the interview fit in with the style of the show..kind of breezy. Perhaps I was expecting too much? After all MJF is just one person who has done a great deal to raise PD awareness.

Nobody can understand us, that's the problem.

youtu.be/xpFC9uziVhE

and it is not just the right who do not understand

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