Michael J. Fox on Parkinson's and life - electric toothbrush for adults

By Dr.
When I went to Michael J. , chief medical correspondent for Sanjay Gupta
I don't know when we will start the interview this morning.
I was told: "He has to time the medicine . ".
"He will be ready when his medication starts.
"As far as I know, Fox's medication is starting right away, and we talked about everything in the next 90 minutes.
Fox said his first thing in the morning was to wear hard shoes because his feet and legs were too stiff.
He humorously added that he just put the toothbrush in his mouth and let the movement of the head finish the rest of the work.
As a neurosurgeon, it is fascinating to hear Michael describe his own brain surgery so clearly and his fear of having another surgery.
"Well, this is brain surgery . . . . . . " He said cheerfully.
There's a lot we don't know about Parkinson's disease.
First of all, no one knows what causes it.
A person's genes may load a gun and something in the environment will pull the trigger. But what?
You might be surprised that four of Fox's first TV series, Leo and I, had early Parkinson's disease.
Is it a statistical anomaly or a clue?
Michael and the scientists at his foundation are not sure yet.
When I asked him about it, Michael paused and shrugged and said, "I don't care much about a few people.
I am concerned about everyone who has this disease.
To that end, he put $0. 2 billion raised by his foundation into use.
You won't hear much about stem cells from Michael or the foundation, but he will describe in detail the efforts of five people
His foundation is funding international biomarker research.
The aim is to find more clues about the disease by collecting samples from patients.
In fact, most treatments are just covering up the symptoms, and Fox believes that if they find new targets for the disease, it will greatly speed up the speed of existing treatments.
Influence Your World: Learn more about Michael J.
Today, I asked Fox if he was sure he had Parkinson's disease.
After all, there is no blood test or imaging study.
It was only a clinical diagnosis. at the age of 30, Fox was diagnosed.
He has officially developed the disease for nearly 20 years.
Fox told me he was pretty sure he had Parkinson's, but even today Parkinson's is not a precise science.
Michael looks good today.
Good days and bad days, he told me.
It is believed that the natural state of Parkinson's disease is a symptom of stiffness, tremor and lack of facial expressions.
When Michael took the medicine, the situation was different.
He is smiling, passionate, smooth, not stiff.
"These are physical disorders," he told me . ".
"But it gives me time to do what I want to do," he added with his unique smile.
8 tomorrow night. m.
You will hear Michael J.
Fox has made plans for the future.
Editor's note: "Sanjay Gupta MD reports: With Michael J.
Fox aired at 8: 00 on Thursday night. m. ET on CNN.
I watched a TV show about Michael and his optimism, and part of it was him playing golf with Bill Murray.
As you can imagine, it's hard for Michael to stay still to handle the ball, but he still loves the game and enjoys the part he can handle, be optimistic that the next attempt will have a good effect.
He said he just wanted to do "the next right thing ".
"The attitude is great. I adopted it.
This is something worth working on.
Michael is a unique person. I have always been a fan of him.
It's a pleasure to see such a Capiltalist-loving God-
Afraid of Republicans fighting such a weak disease!
Tea in southern Alabama
The party extended its best wishes for a comprehensive recovery. Fox!
Let the Eagle continue to fly! Uh. .
He said he was a Republican!
This Michael J. Fox is not Alex P. Keaton.
I'm pretty sure he's a free agent. Oh well.
No one is perfect.
But he's a great actor. .
Hank, how do you know he's a "God fearing Republican "?
I don't believe he is, but you might want to do some research so you don't sound like an idiot, oh wait, you sound like an idiot already.
On the other hand, I'm glad the tea party split the Republican Party and will make it possible for Obama to win a second term.
Yugo moves well but next time "South Alabama tea-
The party sends you the best wishes for a full recovery "-you may want to do a little research.
Currently, there is no rehabilitation for Parkinson's patients.
There is nothing more than politicizing a insensitive comment.
I apologize to Ugo-it was Hank Leiden who politicised the matter. Sorry.
Why is South Alabama Tea Party not donating money to his foundation and best wishes?
There may be the possibility of "full recovery.
He's Hank from Canada.
Canada/USA).
From what I can find out, if his point of view is more free, he is not interested in both parties.
Also, as said before, this is not something he is going to recover from.
In my opinion, Michael is an excellent spokesperson/advocate for a better understanding and elimination of this terrible debilitating disease. His efforts -
He tried to keep his thoughts more in the "reality" area --
Will only improve his reputation as a great person, not just an actor.
Now, if only people with equal status in the field of entertainment or sports will come forward and provide the same level of publicity in eliminating equally weak but more common diseases --mental illness.
This is the complete reference to the end site. . .
"Do the next right thing, not the next right thing. "-
Bill Murray can want to contact Rush University in Chicago. they are conducting a study on the nexNeuro smart mat in IL Schaumburg to provide "passive nerve stimulation" through passive and non-passive enhancement and transmission of natural doping"
Escape the process of stimulating the brain and the nervous system, they got a lot of results, I have been using it for nearly two years, and did a very good job, and my story happened in libande.
I was diagnosed at Rush University about 10 years ago. . .
You have to fight Parkinson's with all your power, eat and exercise correctly every day, even if it's all you can do, a little bit. . .
I ate wheat straw and alfalfa tablets from Pines International to help alleviate the side effects of Parkinson's drugs.
Thanks to God people like Michael Fox who helped bring more awareness, his work Channel 7 news tells a story in a hurried study. . . .
I think you can find it here: abc local. go. com/wls/story?
Section = news/health & id = 7691254one, hope to help some of you. . .
Saw him play in a professional.
The Am tournament earlier this year.
This person is inspiring for anyone with a weak illness.
It is very sad that in this era, people need to raise money from donors to study the disease.
Socialized medical care is not only the best way to ensure the health of the United States, but also the right thing to do.
I agree that MJF is inspiring.
I have a twist tension barrier & lack of coordination
Onset, slowness, freezing, etc. related to Parkinson's disease.
Tension disorders and symptoms of Parkinson's disease are often associated.
Many doctors and the public have never heard of tension disorders, although it is the 3rd most common movement disorder after Parkinson's disease and primary tremor.
You can develop tension disorder at the same time as Parkinson's disease.
I am taking Parkinson's medication with many people with tension disorders to help ease the symptoms and inject Botox and DBS. (The Bachmann-
Foundation for Parkinson's disease
If you want to learn more, you can search for more information on Google. Thank-You Mr.
All your courage and inspiration comes from Fox.
Hope for love and peace
Fox is in my 3 rooms.
The favorite movie of The Times, wrote 3 of the coolest books, my grandfather got Parkinson's disease and these books helped me try to understand everything grandpa went through (
Still, I'm like the most confused person in my family)
I also think Micheal J.
One of all the foxes
The disease did not affect his sense of humor.
I love all his movies and shows and have always been very respectful to him, however, I am very sad to learn that he is suffering from this disease, when I read the article and read about the part where he put his toothbrush in his mouth and asked his head to do the rest, I didn't shed tears, but crashed in laughter.
Michael J. Fox.
You have to admire this guy.
Michael J. Fox is an inspiration for all of us and I have always been a fan.
Love him in future and family relationships.
Michael is a true gentleman and we thank you for your efforts to find a way to treat this devastating disease.
Your positive attitude is extraordinary and I wish you all the best. .
I have always been a fan of Michael and scientific research.
I just lost my dad because of Parkinson's.
He has been begging for death for the past few years.
Mayo's damn Drs won't listen to him.
I have been taking care of him all these years and now I am almost 40 years old and I have to start my life.
No doctor will let me take medicine for 21 years!
I'm sorry for your loss; I know first-
How painful it has been to see a loved one suffer from this disease for many years.
But what would you do if the doctor did not prescribe your father?
I know you're angry.
I just don't understand why your anger is directed at doctors who can't cure Parkinson's, not because they don't want to, but because there is no cure yet.
My father died recently after more than 25 years of Parkinson's disease.
I miss him so much, but I really believe that doctors and medical researchers are doing everything they can to find ways to treat the disease and make the daily life of those diagnosed easier.
I am only 22 years old and my father's life inspires me to make the most of my life.
Michael J. Fox and his family are a real source of inspiration.
My mom has PD. M. J.
Fox is amazing-thank you very much for your sincere efforts under the Foundation and other ways to help PD patients.
There you are, Michael!
Stem cell research, my friend, will save the day!
After my doctor, I went through all the changes for a few months
I said I have Parlinson's and all I can think of is how Micheal J Fox plays his part in everyday activities.
I 've always been a fan of him, read most of his books, and he's also on the list of people I know.
In a very strange way, he helped me put it together. The Dr.
It turned out to be incorrect for me, but I'm not quite sure.
I survived and wondered if the time would come back.
Keep writing your book Micheal and maybe try to write a book for young people. Best regards. . . . How old are you?
In order for a doctor to diagnose you with Parkinson's disease, you must have shown Parkinson-like symptoms.
How long have you had symptoms?
Have you ever taken Parkinson's medicine?
Did the symptoms disappear?
How long have you been relieved now?
What do they think is the initial symptom?
Best of all, SandyWe is a medical family.
We don't believe in Michael J.
Fox has Parkinson's disease.
He is obviously suffering from a degenerative disease, but probably not Parkinson's.
If you haven't been seen by a doctor studying Parkinson's for a while, you'll never be sure of the diagnosis.
For Alison, there are a lot of things related to Parkinson's disease, such as disorders, which is a difficult problem. I was diagnosed at 34 in 1983 and you can't read Michael is. .
He is a role model for other patients. . .
He has won the admiration and respect of all of us.
I hope Michael Angelo is still alive today and he will draw a portrait that he will call "innocent patients ". My father is a huge fan of Michael's work.
My father asked me every day if Michael J. Fox had cured Parkinson's disease.
I haven't told him yet.
My father is 83 years old and has Parkinson's disease.
To do something great, Michael.
Here is a $ to reverse the review.
Go somewhere else to play trolls
Whether you believe it or not, Ed, not everyone in this world only cares about him or herself.
Would Michael care about it if he had not been troubled by Parkinson's disease?
I believe his current behavior shows that he cares about all the people.
He has every right to use his celebrity status to raise awareness and raise money for what he has to live every day.
Thank God, like Michael, Jerry Lewis and others, they "adopted" a variety of medical causes.
I can only hope that someone will care about you if you unfortunately have a similar illness.
My grandfather died of Parkinson's disease recently.
The side of Parkinson's patients who are not shown in the media is the state at the end of life.
In the last year of life, this person slowly becomes less and less functional and becomes active in the body rather than the mind.
From facial expressions to language, to intestinal control, they lost control of everything.
For a few months, I drove seven days a week to my grandparents' home after work to help grandma get ready for sleep as we refused to let Grandpa die in a nursing home.
Imagine that you have to change adult diapers for the strongest man you know.
Imagine that you have to convince your grandfather that your father thinks you are his grandson, not someone who takes him to a hospital or a nursing home.
Imagine what little food you have to give your grandfather.
Imagine seeing your grandfather's limbs shrink into skin and bones due to not being able to swallow food.
This is just a small glimpse of the horror that exists at the end of Parkinson's life.
When a person has a doctor who is proficient in Parkinson's disease, it is possible to live a fairly long meaningful life.
There is no doctor who is proficient in Parkinson's disease, which is more like a guessing game, because the body is used to the medicine it is taking, which leads to the fact that the medicine needs to be replaced frequently, but there is no certain result.
Michael J. Fox: For everything you do to raise your awareness of Parkinson's disease and everything you do to help find a cure, I applaud you.
You're a saint. Thank you.
It wasn't until my father got the PD about 10 years ago that I really focused on it.
What Robert is saying is so real-it's painful to look at people I 've always thought so powerful to reach the point where he can't even get a fork.
My father's mind is still sharp and the rest of his body is healthy, which basically makes him a prisoner in his own body.
I can't imagine how frustrating life is.
Frankly, I'm afraid that this gene is lurking somewhere in me.
I welcome any attention to this disease.
Although it may be too late for my father, I hope that for all those who are in the early stages of PD or have not yet shown symptoms of this terrible disease, the answer comes sooner rather than later.
You described my father's death to T.
My dad was sick and died. Very hard.
Say to Robert Wells: God bless you, I don't need to imagine what you are describing because I live with my own father now.
He was diagnosed in 2006 and has fallen rapidly over the past six months.
Looking at Dad, protector, provider wasting on skin and bones is the most tragic thing in the world.
He is now almost at a point where he can't swallow and lost his ability to speak a few days ago.
There is no way.
I'm glad that PD has an outspoken advocate like Fox.
Without research and progress, we can never find a reason that is more important than treatment.
Robert, it's too late for our loved ones, but let's hope that the lessons learned from them will help someone else's dad or grandpa beat this thing.
I extend my deepest condolences to you and your family.
While the medicine helped to extend the time, my father was full of contempt and pain for the great man.
More vulnerable than flowers, these precious moments let us hold together tightly, I pick up a rose, it goes through my clothes, along the winding streets, I feel a brief joy to hear the deafening voice, I know they are not what they look like in this earth field, full of disappointment and pain, you will never see me frown, I owe your heart, that is to say, this is true, I will be with you when the transaction fails
My mom died of Parkinson's last year, and your comments brought tears to my eyes.
That's what my mom is. . .
She is a very energetic woman.
It's hard to see the people you love from being very active to not being there at all.
She would look at me and say "Where's Cheryl ". . . . that was tough.
It's a terrible disease and I hope Michael J. Fox can find a cure.
He is a great actor.
Thank you for your words.
Bless you and your family. Mr.
Wells, with you. Mr.
Robert Wells, I know exactly what you and your grandfather are going through.
My mother was 61 years old and was diagnosed with Parkinson's disease six years ago.
At first she could speak easily and move her hands and feet, but now she can't speak and the whole body is completely paralyzed.
Even though we have physical therapists coming to our house every day, she just doesn't have the motivation to exercise her hands and legs. .
The only positive is that her brain is still working properly and we only communicate through gestures. .
Can someone please let me know if it is possible for her speech to be withdrawn? ?
I just learned from CNN that Michael Fox has been fighting this disease for the last 20 years and I'm just amazed and in awe of the strength of his daily persistence in life. . .
I hope his foundation will eventually find a way to treat the disease.
Like Michael, I was also diagnosed with early Parkinson's disease.
My symptoms started when I was 34, when I was sergeant, a US Air Force army, and I ran 5-
50 miles a day.
70 hours a week, I feel invincible.
Over the years, I have learned to slow down and cope with life calmly.
I spent 12 more years in the air force with Parkinson's disease.
I retired after 27 years of military sergeant in February 2007.
Every day is a new challenge for me to accept and move on.
I believe a positive attitude has helped me and my family overcome Parkinson's disease.
I pray that our doctors will find a cure, but I will continue to shake until then, but will not shake and remain positive.
I do agree with Michael, though, that the morning can be fun and painful, and I can brush my teeth faster than an electric toothbrush, and learned to drink 12 ounces of beer in a 22 ounce glass and not sprinkle a drop.
God bless everyone.
Michael, I read your post earlier today but didn't have time to reply.
You sound like a very brave person and I admire your spirit in the face of PD.
I wish you all the best. michael. .
Sorry for the delay, but we are already behind in living in Hi. .
Anyway, you have such a wonderful view of life. .
Especially when it comes to not spilling a drop. . . .
It is a part of our lives and a part of our lives.
First of all, thank you for your encouragement and for your service over the years! !
On top of that, it's amazing that after you discover PD, you have the courage and strength to be able to continue your career at AF! !
I wish you good luck and am glad to hear that you have still found a way to enjoy your life.
You are lucky to have a family that helps you and stands with you!
Dana, Kkat and EMilyThank thank you for your kind words and I will remember them and take them to find inspiration.
It is likely that your question will not always be answered by Michaelto.
But what he cares about now is not like you only care about yourself. My brother was diagnosed with Parkinson's disease at the age of 34 through the elimination process.
I can contact the doctor.
Gutpa's observation of morning medication is "guess" as I have seen my brother disabled by this situation many times!
Thank you, Michael J.
Fox and his candor and optimism about the disease.
I'm a fan of Michael.
I know about his Parkinson's and I'm sorry for that.
I have been praying for him after I watched his opera.
All attempts to write and email him failed.
Nevertheless, God is almighty and he loves all his children, even the ashiti and thechristians too.
Let's all pray for him, please join me in prayer for Michael Sunday, October 3. 00am to 10. 00a. m (
Eastern time zone).
May God bless you
Dear Mr. Cooper:. . .
You're a great professional. . . . comunicators . . . . so commited . .
Participate so seriously. . . . . . . . . and Mr. Michael Fox . . . . .
You are the embodiment of courage and dignity. . . . .
May God bless you and your family. . .
Special Greetings
In fact, I am a fox fan and I do know very well that he is suffering from this terrible, terrible and weak condition. . . all too well. . .
I am not perfect myself and not close to Saints, but sometimes I think that those who have money need to get diseases or something to care, care or think about and start spending money and advocating research, this is a shame. .
If Michael does not have Parkinson's, he may not be an advocate for Parkinson's, but it is likely that he will still contribute to the world in another way.
There are other celebrities with the disease who do little to nothing in terms of publicity, so it shows that Micheal is a disease.
I'm a fan of Michael J.
But I will never regret the money of a celebrity.
He has enough money to forget which year he lives in, not to mention Parkinson's.
How many low-income people will swap places with this guy? (all of them)
I take your money and your house, you can get my house because so I can take medicine to stop shaking, but when you wake up at my house with my money, you will hit your head on the wall on purpose.
You're right. you don't know much about the disease.
If you do, you will realize that what you are saying is ridiculous.
I have a young Parkinson's disease, and believe me, money can't make up for the challenges of Parkinson's disease in any way, shape or form.
The medicine you are talking about does not completely eliminate the symptoms and almost always has some challenging side effects.
As for Michael J.
Fox, I am very grateful for everything he has done for the Parkinson's community.
He made the disease public as others could not.
It is undeniable that I thank him for everything he has done in his fight against Parkinson's disease.
You are so ignorant that it is useless to solve your problem of a complete lack of understanding of this terrible disease.
No wonder you have no money.
You're too stupid to be hired. Anywhere. By anyone.
You have to live a very sad life before you think what you just said is true. First off.
Didn't you watch the video?
In the end, they said the medication he was taking made him shake like this.
I assure you that all the money in the world will not take away the pain of not being able to do what you like normally.
Michael seems brave about the disease, but I believe he will get hurt inside.
He has a wonderful soul and it makes me very sad to see him like this, but let me see his hope of staying strong.
Bless him and I hope that one day he will get what he wants.
If not for yourself, suffer for others.
My friend has Parkinson's disease and she says even the poorest people won't spend any money on Parkinson's.
Parkinson's disease is painful and weak for her, she said.
Like being stuck in your body and not moving (
No medicine).
It will work even if you take the medicine.
This could eventually lead to Michael J. Fox has (
Drugs, not Parkinson's disease, are responsible for this).
I certainly hope science can find a way to help my friends and all the people with Parkinson's disease as soon as possible.
Thank you, Michael J.
The Fox found a cure for your efforts.
You are an inspiring person and my frienddi was recently diagnosed after several months of trial and error in clinical work.
While this is always an uncertain diagnosis, there are two constants for me: first, almost every reaction I get from my family and friends to my diagnosis mentions Mr. Fox.
Second, mentioning Michael J. Fox is always an example of courage and optimism.
It means everything to me, and he has my deep gratitude.
I have been told that I have been suffering from Parkinson's disease in the past January. 2010.
I'm 57 years old this year, but looking back at the signs a few years ago, we just didn't put two or two together.
I took Azilect and it helped a lot to lower my stiffness and trembling.
Most people don't know I have it unless I'm tired and then I get really bad.
I tend to lean on or balance myself instead of helping to "hide" things that are wobbling.
I'll check it out next week and I wish I could stay on one more pill.
I hate the decline in fine motor skills and my lack of endurance.
I can't make myself too tired and I can't make myself pay for it.
I call myself the Weeble of man.
I can't swing, but I haven't fallen yet.
When I leaned forward and pulled the weeds out of the flower bed, my dog had knocked me down twice.
I hate stiffness.
It gets harder and harder to move once I stop or sit down.
I try not to think about the future and my future.
I 've been in love with Michael for years and his movies still make me smile.
I wish I could keep this positive attitude as much as I can, but I feel scared sometimes.
I don't want my husband to worry too much.
I am glad to know that I am not alone on this trip.
When I was driving a limo in Los Angeles, I used to drive this car from Los Angeles International Airport to the hotel long enough. I know this guy is as good as a man.
If people put money into his foundation, I wouldn't doubt it.
I suspect this guy has an enemy in this world. . . .
Hi, I just wanted to say that I also have Parkinson's and I agree it's hard to accept but I always say that as long as I can still move my body, whether it's stiff or hard to pick up I just know I'm fine and I also want you to know that I read your book and I think your book is awesome. The question is adult stem cells or embryonic stem cells?
As a former Catholic, this comes first in my mind because my faith is very important in moral terms.
I don't want to draw a line with embronic stellar cell studies at all, because it's not correct with the Catholic Church.
Of course, in key issues such as cancer, Parkinson's disease, blindness, deafness, psychological and cognitive disabilities, and some physical diseases, funds need to be raised in health research.
Even though they will find a cure, I suspect I am blind because my illness is very rare and no one has it.
Propaganda of it is not the reason for this fact.
Nevertheless, good luck with the treatment of Parkinson's disease.
What is "preconceived "?
Are you learning to be a Catholic?
I have never heard of the term before.
Peter Wolfe, do you have a body or yourself with Parkinson's disease?
Interesting comments, but can you really know how people feel about staus? God knows I will be favored because I can afford 1st classes when the plane crashes. I think not! ! ! ! P. s.
Sandy, 44, don't know how to get back to you! ! !
It is indeed a terrible disease, like cancer, with only one result.
Michael is great. he has more wealth than most people.
Remember, he basically didn't.
His income is good compared to other actors, but if he is a healthy actor, the income will not be that big.
I 've had PD or 10 years now, counting the rest of my time, and I'm hoping to die with dignity and grace like possibe instead of falling into hell.
My experts and PCP told me to keep working as long as possible, not to retire, stay active and move on. . . .
I will continue the traffic jam.
I just finished a music video of a song about Parkinson's disease, which was written by a friend of mine who was diagnosed with a young Parkinson's disease.
Thank you for your work, Michael! [
Youtube was diagnosed earlier this year and decided to retire at 59.
I now work 4 hours a day to be as strong as possible and spend more time with my family.
I may have only 15 years left, but I think the next 10 years will be the best.
I'm sorry to hear that, but you seem to be a strong person.
Yes, enjoy every day.
I always liked Michael J.
Since I was a kid, Fox.
I remember I was 9 when Spin City was canceled, so I really didn't understand what he was going through, but my parents explained what a terrible illness he was suffering from.
At the end of the last episode of the Spin City series, when he started talking about Parkinson's, I called out my eyes.
Now that I'm older, his illness has developed and I see the real impact it has on him, it breaks my heart.
He always looks like a good guy, and of course he's funny.
He is not worthy of what happened to him. No one does.
I think everything he does for those who have this disease is fantastic.
To correct my mistake, I was 11 when the show was canceled.
I think I remember correctly.
Thanks to michael for his great achievements in pd.
I hope that people will think of cloning as well.
I have been diagnosed and dealt with for 10 years and have confidence in God and your doctor that I am dead without them.
Once a day, Michael, thank you for your support for everything Michael has done.
Thanks to Michael for talking and helping others for this disease, pain, daily fatigue and weakness, people should know that money can't buy perfect health, Michael won't get a promise tomorrow, only God knows everything about our future, thank you for being brave once a day!
Good information about PD.
Sadness, waste of disease.
Fortunately, there is such a capable person to get the news (MJF)
About disease.
God bless all the people associated with the disease by helping others or putting up with the disease on their own.
Comment on "We all know how it will end.
Hey, we're all over! !
He also used his foundation to pay himself a generous salary so that he could maintain his luxurious lifestyle because he could no longer get the same generous performance income.
A lot of people may benefit from his work, but don't be fooled and he will make sure he benefits first.
Ed, do you want to know what's wrong with America today?
Look in the mirror.
Ed, I'm disappointed in you.
Tax documents of the Foundation (990's)
Public documents.
Schedule J clearly lists Michael as an officer and indicates that he does not accept compensation from the Foundation (page 2, Line 1).
As a concern (now deceased)
I can tell you that what is relevant to PD is that the study is very much in urgent need and scoffs at a person who has gone out of his way to fund the study.
Actually, Ed does have a point.
Fox does have all the luxury items that money can buy-including private physical therapists, nurses, and more if needed in the future.
I have to say that there are so many other people living on disability check-ups, and in isolation, unemployed people are asking for help every day.
Where are these services for all these orgs in ET, PD and tension disorders?
All non-profit organizations report the salaries of their trustees/directors and their well-paid employees in IRS Form 990, which are posted on their website.
It's a great honor to see such a liar-loving God-
Afraid of Republicans fighting such a weak disease!
Tea in southern Alabama
The party extended its best wishes for a comprehensive recovery. Fox!
Let the Eagle continue to fly!
You know, saying over and over again won't make this comment less ridiculous.
Why don't you live a good life and do something useful?
Otherwise, there is no need to remind us of how ignorant you are to the rest of us.
Hank, take a break.
You sound like a 12-year-old.
Conservative for a long time
This guy got MJF mixed up with his role on TV.
He is known to be a true rock time traveler.
My wife and I have always been a big fan of Michael.
Michael and I were both born in Edmonton the same year and married to twins. . .
I have Parkinson's, too.
Finding out that I have PD is a relief because it finally explains to me why I can't work as much as I can before.
I am worried that I used to have MS like my mother.
I have been worried that I will get MS.
The effect of PD on the family is similar to that of MS.
It is important to know that 30% of Parkinson's patients are depressed due to Parkinson's disease.
Call it a side effect!
Fortunately, there are pills to control the situation.
However, it does become humiliating when I cry in front of your family.
I'm the breadwinner, Rock!
But I can handle the body part of my life because it's under my control. . . for now.
What I can't control is the economic needs, as many other PD suffer.
I have a very successful IT career and am very popular.
I have been worried that I will be disabled because of MS.
My insurance agent solved the problem. . .
That's what I think.
He sold me a limited company policy to guarantee the benefits I can no longer work in my current job.
This policy costs me more than $400 a month! But guess what? . .
No insurance company!
I am from a net worth 1.
Less than $50 k for 5 factories, credit rating completely destroyed, no home.
So the thing I wake up every day is. . .
When will the insurance company finally pay? . .
When can I leave purgatory and go to heaven or hell!
My father's first symptom was depression;
Too bad.
He is a successful vet with mixed practices for large and small animals.
Depression is difficult to treat because the side effects of many anti-depression drugs make him unbearable.
This is a very difficult problem. he was hospitalized and had to accept ECT (
What was previously called "shock treatment ")
Affecting his memory.
I think since then, the anti-depression drugs have evolved and the doctors who prescribed them have been better educated in using them, so I hope PD patients don't have to endure what my father did.
It's hard to see the people who raise you so strong and smart, so invincible and so vulnerable.
My heart is really open to anyone with PD and their family.
I can only hope that one day, career and treatment will become a reality.
I work in the insurance industry and deal with disability claims, and yes, I am sad when the benefits paid are not the insurance that the agent first informed them.
If your policy is a group policy (
Through your employer)
The amount of your benefits is likely to be limited to two years of your own professional benefits.
If this is the personal policy you pay for, you should revisit the agent.
Have you talked to laywer to see if you can at least get the premium back?
You're such a jerk!
It has nothing to do with taking the dollar from his foundation.
He made enough royalties in his voice.
And his past performances and movies.
If you stick your head out of your back and look at the man, you will know that he will not be slightly past the checkout counter.
Not everyone on this planet is a thief!
I think there's something else in this person's mind!
He is a great person, very touching and inspiring.
The part that caught my attention most was being a doctor.
Gupta said that when he did what he had learned a long time ago, such as playing the guitar, the shock disappeared, and it was amazing for me.
How complicated our brains are.
A beautiful person with good attitude. . .
He is using his celebrity and monetary status to raise awareness and promote research, which ultimately benefits everyone who deals with the disease, and for me it's the best of all possible outcomes for Mr.
Fox's dilemma (besides a CURE! ). Well done, Mr. Fox.
Continue to fight well!
Hank Ryden, you're a stupid fool.
One of those horrible, obsessed politicians, right?
Believe me, there are more ways to go in life. Get a dam clue.
Thank God for giving micheal j.
Fox, my husband was diagnosed ten years ago with financial inability to do surgery, and the medication didn't help him.
He now has to get help on every task he tries and even eats.
Two studies are currently under way, one at Harvard and the other at the University of North Carolina, to study possible links between statins and Parkinson's disease.
My husband is probably in the beginning.
He's been on statins for nine years. . . .
I'm pretty sure he has a contract with Diet Pepsi.
Look at what assweet did to his brain. Thanks M. J. F.
You have given us all so much enjoyment over the years and we all wish you all the best.
As a Canadian, your situation is not bad. . =)
Do you know that Michael J. Fox was diagnosed with Lyme disease 3 years ago with Parkinson's disease?
It can lead to many neurological symptoms, from MS, ALZ, ALS to Parkinson's disease.
It is called the great imitator.
I hope that Michael and anyone with this disease hope that perhaps through medical research, the foundation established, there will be more help and understanding for this disease.
It's a shame to have some negative comments here.
This guy is trying to help everyone with this disease, he suffers as much as the poor, he is trying to help everyone.
Just like Christopher reeve tried to help the paralyzed.
Give credit to the people where they are due.
They can use their celebrities to help them.
Absolutely inspiring!
"Life can only be understood backwards;
But it must be forward. " -
Solon kerkeguor: "The truth is a trap: You can't have it without being caught.
You cannot get the truth in such a way, but only in such a way that it catches you. " -
Soren Kierkegaard "The irony is a disciplined, and only those who don't know it are afraid, but those who know it cherish it.
The person who does not understand the irony, has no ears to its whispers, he lacks eo ipso, which may be called the absolute beginning of personal life.
He lacks what is indispensable in his personal life, lack of regeneration and revival, ironic clean baptism, living in limited by boldness and positivity, and redeemed souls living in limited. " -
Solon kerkeguor "because of its great seriousness of death, great passion, good or bad, becomes transparent and no longer limited by appearance. " -
The function of "prayer is not to influence God, but to change the nature of the people who pray. " -
I was told that Soren Kierkegaard "He has to time the medicine ".
"He will be ready when his medication starts.
"Unless he has a personal political goal in mind.
You're a low man.
Regardless of time and dose, there is no medicine to cure the disease.
Just do a favor.
It is clear that you have no education about Parkinson's disease or drugs for Parkinson's disease.
These drugs must go through the blood-brain barrier and the only way to take them is to swallow them.
Stress, physical activity, protein consumption, etc. . . . . . .
All of this affects how many drugs you receive.
If you don't absorb fast enough, you freeze and tremble. . . . . . .
But if it absorbs too fast, you will have movement disorders.
Spontaneous, unconscious movements).
Every person who takes a PD medication will experience it.
"The period in which drugs start or stop working suddenly and unpredictably.
This is a guessing game.
My husband in his early 30 s is suffering from Parkinson's and he doesn't have a TV show to play and can't control the side effects of the medication.
He must be "pretending" so he can't work and play with the children. . . . . . . . RIGHT? ! I think not!
When you make such a statement, you insult and hurt millions of people who deal with PD.
I think he did it. . .
He's a good comedian! ! !
Don't joke about this.
You, people can't pretend that this thing is obviously a disciple of Limburg in a hurry.
No matter how good an actor you are, this disease is not something you can fake.
You can't pretend the sudden, uncontrollable movements and other symptoms of the disease.
People like you should be ashamed, but you don't really know what shame is.
I would like to say that your comment is too much.
Crossed the line in my book.
Are you true? Appallled.
Understand Parkinson's disease.
Trust me, it's not funny about the symptoms and negative effects of your daily life.
There is also no movement disorder called Tension Disorder.
I have cervical tension disorder (
One of many types of tension disorders)
From the time I wake up to sleep, my symptoms affect my life every day. . . . .
CD is a less serious type of tension disorder.
I believe MJF is dealing with every minute of his every day.
Thank God he can find humor in his days.
When will Carol have a cure for it?
My grandfather died of a set meal for Alzheimer's and Parkinson's.
I can't help but wonder why your brain crashes and why does it look more now than ever?
I'm not sure if it's going up.
I think people just live longer and don't die because of something else;
Diseases in the elderly are more likely to occur because more people live long enough.
I hope they can find a cure soon, but the truth is, it's hard because they don't even know what causes it.
But the MJF Foundation is the biggest hope.
He changed the way he studied, and his basic research would not be so fast.
You're right. many people think PD is growing at an amazing rate.
Many data show that the number of young patients is increasing.
It is believed that 20% of the people currently diagnosed are under 50 years of age, with an average onset time of 56 years.
Statistics are unreliable, which is why it is important to push the government to track all nervous system diseases and see if there is anything in the environment, food that leads to an increase in the incidence of nervous system diseases, etc.
My husband is in his 30 s and has a fight with the police.
I'm sorry you lost your grandfather because of this terrible disease.
We need to take a closer look at what's in the food and take out aluminum and unknown additives.
Next time you buy deodorant, look at the warning on the back of it.
Then you will go to the store to buy a Thai salt stick, I have one, and I have one after two years, and then count.
Your body is destined to sweat, but you can stop stinking without these chemicals. chloraphyll (sp)
Natural ingredients in green plants.
If you buy it at the health food store, you will drop a drop in tea or water and frequent use will eliminate all kinds of body odors.
Naturally, deoderant is not needed.
Plus all the anti-carginegent effects.
Why did no reporter ask?
Why hasn't he received deep brain stimulation that can relieve most of Parkinson's symptoms?
He's a celebrity, not a guinea pig.
He will have some other poor patients react to drugs and movement disorders. . .
Identify candidates for DBS!
Any neurosurgeon should be disappointed to see him like this, and neurologists should be ashamed.
He had more than 80,000 implants around the world.
The Fox won't be a guinea pig. The Fox already has DBS.
In his diagnosis
I tried to recall when but it was in 1st 10 years.
They mentioned brain surgery in the reporter's article).
He did have DBS in the horse a few years ago.
He was very frank about the matter and the fact that it did not work for him.
Subsequently, drs improved the timing of the operation-the key to disease progression-and the operation itself.
I was wrong. he had a different brain operation to eliminate his tremor.
He continued tonight why there was no DBS.
Contrary to what you may have read or heard, DBS has many shortcomings;
Obviously, this is brain surgery, which is dangerous in itself.
I once thought, "Why don't people with PD have surgery? ".
Then I saw a man very early.
Starting PD with DBS;
Before the operation, he was still working, a parent of young children and a member of society.
After the operation, he never recovered his previous cognitive abilities, and because his family could not take care of him, he had to live in a nursing home (He will wander).
There are many benefits, but there are many other things to consider. Dr.
Gupta did ask about DBS.
I think it's related to his previous surgery.
1998 incision of the trachea
I heard it clearly.
Gupta mentioned magnets.
Deep brain stimulation magnet
See DBS in the image article.
They asked him.
DBS does not work for everyone.
It can help make the tremor and exercise better, but has no effect on all other Parkinson's symptoms.
Also, it only works 5-in a short period of time-
After 10 years, you will be worse than before surgery.
There are also possible side effects, such as the decline in executive functions and problems with raw words, attention and learning.
About 9% of patients suffer from mental illness, ranging in severity from peeping to attempted suicide.
I also know people whose Parkinson's disease has deteriorated.
This is largely a personal decision to weigh risks and side effects and to decide whether the results of DBS are worth it.
DBS has brought great stories to people's lives for several years, but there are also many people who regret it.
If the drug works for him, there is no reason to have DBS.
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