This is incredibly good news! And I need to comment that there’s a great interview on UA-cam of a PD patient, an older guy who had advanced problems bc of the disease, after many years, he was declining a lot. So he went on a keto diet, as an experiment, and found that he got better and better, and better, reversing the neurological damage, and is now 90 or 95% improved!!!. It’s very very hopeful news! And I hope every person who is suffering w/ PD finds the story on YT.
I was diagnosed with Parkinson's about ten years ago & I to started isolating my self to avoid the stares. After having DBS in February I feel great & I'd like to thank all the doctors at the University of Maryland medical Center in Baltimore Md
The surgery can now be done while asleep. Both electrodes can be implanted in a single surgery in cases and sometimes even the generator. Also it is being done much earlier in the persons progression to give better benefits.
I'm house bound also for the past 4 years was diagnosed 20 years ago, I fight every day, but I'm getting worse and no one understands what it's like, I'm gonna look into these things with my Neurologist 😊
Absolutely BRILLIANT, oh my goodness ! Such a gateway of HOPE !!!! Ode to the science and those able to im0lament it. Tremendous GRATITUDE to say the least.
For those of you wondering. Del Maxson died January 25, 2015 at the age of 68 from a “lengthy illness”. There’s no mention of Parkinson’s in his obituary. Also the family “request memorial donations be made to a canine rescue and humane society.” Maybe I’m just reading too much into this but if this was such a great thing for him and his family don’t you think it would have been mentioned in the obituary and donations be made to medical “stuff”? Again I’m probably reading too much into it…. This is just sad though. I really want to believe this worked for him.
I really appreciated the quality of Education and mastery gained by these doctor during there acedmics now finally paid off....so moral of the story's says that God bless each and everyone with sound mind so use this brain to gain mastery in you education and see what education will going to reward you after the example is infront in a form of those brilliant surgeon.
This interview was filmed over 20 years ago, clearly this treatment didn't work too well over time. Many of the people in this comment section need to start reading the descriptions on videos.
Yeah my dad got this treatment and hes gotten a lot worse, his movement is a lot better but he can’t function the same, mentally he is much worse and it’s really sad to see, I wish he never got the surgery.
Lost my mom 6 years ago to a 21 year battle with Parkinson’s Disease. The Dyskinesia was brutal as were the Requip and Carbo/Levo. The problem with the surgery is that it’s a bandage and doesn’t cure the disease and eventually the issues come back. The memory goes even with the surgery. A temporary fix.
My husband was misdiagnosed with PD. He has essential tremors. My advice is simple: Get a second opinion or even a third or fourth one. My husband was on carbadopa/levodopa for over a year all the while never actually having PD. The second neurologist we found ordered a DatScan which confirmed that he had been misdiagnosed. Upon further research I discovered that the percentage of misdiagnosis of PD is 30%!!
The patient I am looking after has undergone Parkinson's surgery but his condition is still the same as before the surgery, he has difficulty sleeping, has difficulty urinating, has difficulty defecating and his body is unstable.
I think a lot of people went there as he’s such an advocate for making society aware of the disease . It would be great if he did get the opportunity to have this operation and give hope to other sufferers .
Looking around, I see that there is assistive device for cerebral palsy people….a pull on sleeve for arms and legs to curb spasticity. It’s not only here, it’s BEEN here. As we go ga-ga over these things……..remember we lost the super computer because Senators Obstruction wouldn’t fund, went to other countries instead. Stem cell research quashed same reason. Senator No said no. We are far behind where we should be because of the pharmaceutical-industrial complex.
I was going to ask the same question. I mean, come on, look at the difference, it is a miracle and MJF should see at Steve Jobs’ story and try to avoid bad decisions. With all due respect.
Here in Houston, eight years ago I made a new friend with Parkinson's as I would drive her to doctors appointments and Parkinson's seminars and events. Carolyn had a DBS when I first met her, and her tremors were well under control for the entire time I knew her. One time while she was still living alone, her DBS battery lost its regular recharge and she ended up in the hospital until the technician showed up and reset her software. She was jerking so much in those few hours, so unhappy, she said if she stays this way she just wants to be dead. The most unbelievable thing I learned from attending multiple Parkinson's lectures and product shows by the DBS companies: Of all the Parkinson's patients that are candidates for DBS, only 10% agree to get it. Yes, you read that right. The average Parkinson's patient is just too intimidated by the procedure to have it done. That is the saddest thing about Parkinson's disease today.
God bless the hands of the doctors and their brains. I ponder would that work for those with short term memory. I know a Dr Of Chemistry young man has probs with short term memory which is destroying his life and given all he did for people I'd love if it worked for him I truly would
Parkinson's sufferers are benefiting from vitamin B1 therapy. See the book "Parkinson's and the B1 Therapy" - I would suggest giving this a good try before embarking on pharmaceutical route. But be patient because this approach requires it as the book states.
Lmfao everytime I hear a surgeon say “anchor” something to something else in your body…he bout to hammer that ish in and definitely not be delicate about it 🤣
This is so amazing! So cool what technology can do now! The hope it has brought to so many people! I am so Excited for all these Parkinsons Patients! They all have a new lease on life! Thrilled! Love it so much! CATHERINE MAGEE
My blind sister and I had Multiple sclerosis And she got her sight back the same way I did mine by a back adjustment. We had both had a back injury as a child and flipped over backwards 3 times as an adult. But I'm a quad because no doctor will touch me because Researchers say it is not a bad injury.
My goodness! I'm so sorry this happened to you and your sister! You deserve the best treatment available! Keep fighting! Get an advocate or case manager for yourself, honey. Ask your Dr or insurance company to get you one.
I wonder if it works for everyone. I have seen that cannabis has a similar effect . I do hope this is a new technique and a lot of sufferers get the option to get this operation.
This year I met the fourth mother with a down syndrome child. And asked if she had used wheat germ In unlimited amounts before enduring pregnancy. All for said yes. But I can't get a researcher to ask that question because that's not how research is done.
I'd love to meet Michael J. Fox. I hear he lives in Oregon, Like I do. My state, and people like governor Kitzhaber, and Julie Kelley, have definitely helped the disabled like myself.
May God bless Ali Rezai and other compassionate doctors who tirelessly help their patients.
KEEP UP THE PROMISING WORK!
What a fantastic story!! Praise God for those who study to help others improve their life. What a TRUE BLESSING 🙌
This is incredibly good news! And I need to comment that there’s a great interview on UA-cam of a PD patient, an older guy who had advanced problems bc of the disease, after many years, he was declining a lot. So he went on a keto diet, as an experiment, and found that he got better and better, and better, reversing the neurological damage, and is now 90 or 95% improved!!!. It’s very very hopeful news! And I hope every person who is suffering w/ PD finds the story on YT.
So change in diet can really help wow
This brings tears to my eyes...
I was diagnosed with Parkinson's about ten years ago & I to started isolating my self to avoid the stares. After having DBS in February I feel great & I'd like to thank all the doctors at the University of Maryland medical Center in Baltimore Md
👍
Bless your heart.....
WOW! Totally astounding! God bless every one of his medical team and especially his wonderful surgeons! ❤️❤️❤️❤️❤️❤️🙏🙏🙏🙏🙏🙏
My dad is having surgery this morning starting at 8 am pray everything go well
🙏🙏🙏
🙏🏻💝🙏🏻💝🙏🏻💝🙏🏻
😢Any positive Update, how is he?
😢😢 🙏🏽 How is he 🙏🏽🙏🏽🙏🏽❤
How is he 🙏
I’m so happy for you. You’re an amazing person.
What a wonderful gift to be freed of this affliction.
Absolutely amazing im so happy for them . The Best Doctors .
Amazing..I'm so happy to see him go out and be with people😀❤️
Thank you sharing
60 Minutes, please follow up on this. What are the newest breakthroughs and how are these same patients doing today?
The surgery can now be done while asleep. Both electrodes can be implanted in a single surgery in cases and sometimes even the generator. Also it is being done much earlier in the persons progression to give better benefits.
I'm house bound also for the past 4 years was diagnosed 20 years ago, I fight every day, but I'm getting worse and no one understands what it's like, I'm gonna look into these things with my Neurologist 😊
@cynthiafrockowiak1364 my husband was diagnosed in 2005 - dbs in 2012. Was miraculous in the beginning. Only lasted about 3 yrs or so
@@cynthiafrockowiak1364 I know what it's like! Prayers for you
I wonder if Dale still a life
Absolutely amazing im so happy for them 💗 🎉
This is amazing!
That’s so wonderful! I’m hoping our beloved actor Michael J. Fox sees this. He deserves a better life!!
I'm almost to the point of doing the DBS it's nice to see this post it's comforting to see what can be possible for me.
Absolutely BRILLIANT, oh my goodness !
Such a gateway of HOPE !!!!
Ode to the science and those able to im0lament it.
Tremendous GRATITUDE to say the least.
Great episode👏
For those of you wondering. Del Maxson died January 25, 2015 at the age of 68 from a “lengthy illness”. There’s no mention of Parkinson’s in his obituary. Also the family “request memorial donations be made to a canine rescue and humane society.” Maybe I’m just reading too much into this but if this was such a great thing for him and his family don’t you think it would have been mentioned in the obituary and donations be made to medical “stuff”? Again I’m probably reading too much into it…. This is just sad though. I really want to believe this worked for him.
You're reading way too much into this. It's just a medical procedure.
Thank you Doctors
I say THANK GOD for this..for giving the doctors the wisdom they need to fight this disease
I also think what you EAT..is also what can get you on the feet..
Eat less...and get more..yess..
Get healthy my Friends❤
I really appreciated the quality of Education and mastery gained by these doctor during there acedmics now finally paid off....so moral of the story's says that God bless each and everyone with sound mind so use this brain to gain mastery in you education and see what education will going to reward you after the example is infront in a form of those brilliant surgeon.
Well done sir, this is wonderful ! Great doctors.
😢🙏🙏🙏❤️this is amazing.
Thank God for these doctors
If only my 80- yr-old immobile Sweetheart could receive this surgery. He's had Parkinsons for 8 yrs. Needs 24-7 care. 😢
AMAZING!❤
Who’s calling Michael J. Fox?? God Bless these doctors!!
I am happy for you. I hope you enjoy your mobility and freedom. 🙏🙏💯
Got diagnosed three years ago. This diease has affected me with immense fatigue, low appetite, nausea, vomiting, depressing and debilitating
Amazing!
Thats amazing
Thanks
This interview was filmed over 20 years ago, clearly this treatment didn't work too well over time. Many of the people in this comment section need to start reading the descriptions on videos.
Don't take yourself so seriously! 😮
Yeah my dad got this treatment and hes gotten a lot worse, his movement is a lot better but he can’t function the same, mentally he is much worse and it’s really sad to see, I wish he never got the surgery.
😢 oh no just reading these comments, someone I love is in stage 2 PD
God bless these folks…
The science of modern medicine and the resilience of the human body are truly awe inspiring.
Truly life changing
The Best Doctors 🥼
I appreciate you sharing.
Lost my mom 6 years ago to a 21 year battle with Parkinson’s Disease. The Dyskinesia was brutal as were the Requip and Carbo/Levo. The problem with the surgery is that it’s a bandage and doesn’t cure the disease and eventually the issues come back. The memory goes even with the surgery. A temporary fix.
Are you talking about this surgery?
Thank you.
Excellent!
My husband was misdiagnosed with PD. He has essential tremors. My advice is simple: Get a second opinion or even a third or fourth one. My husband was on carbadopa/levodopa for over a year all the while never actually having PD. The second neurologist we found ordered a DatScan which confirmed that he had been misdiagnosed. Upon further research I discovered that the percentage of misdiagnosis of PD is 30%!!
If your husband's problem wasn't Parkinson's did they figure out what the problem was?
@@philochristos as I said I'm my post, he has essential tremors...
*pathogen (h. pylori etc) -> biofilm -> ulcer -> Parkinson's* , research Medical Gaslighting
@@Julieglam3caused by what?
@philochristos good question!
Im happy for this man
Wow! Amazing. ❤
Bless them
I love it!
AMAZING! I hope that Techniques have GREATLY IMPROVED?
Very nice.
Amazing, just amazing🤓
I'm so surprised how good we today can help people, I just wish that all people were able too get the same help with out paying all that mony.
This is the first one that intrigues me
The patient I am looking after has undergone Parkinson's surgery but his condition is still the same as before the surgery, he has difficulty sleeping, has difficulty urinating, has difficulty defecating and his body is unstable.
❤ im happy for you man!
Amazing
et....getting ready for a mri guided ultrasound treatment consult..non invasive used for et/pd and others
Science is amazing!
Wow what a life changing procedure. Has Michael J Fox had this procedure? I haven’t heard him speak about it, and if he hasn’t I wonder why?
I thought of him right away.
I think a lot of people went there as he’s such an advocate for making society aware of the disease . It would be great if he did get the opportunity to have this operation and give hope to other sufferers .
Michael says he doesn’t want this. When asked why he responds “It’s brain surgery!”
Looking around, I see that there is assistive device for cerebral palsy people….a pull on sleeve for arms and legs to curb spasticity. It’s not only here, it’s BEEN here.
As we go ga-ga over these things……..remember we lost the super computer because Senators Obstruction wouldn’t fund, went to other countries instead.
Stem cell research quashed same reason. Senator No said no.
We are far behind where we should be because of the pharmaceutical-industrial complex.
I was going to ask the same question. I mean, come on, look at the difference, it is a miracle and MJF should see at Steve Jobs’ story and try to avoid bad decisions. With all due respect.
Here in Houston, eight years ago I made a new friend with Parkinson's as I would drive her to doctors appointments and Parkinson's seminars and events. Carolyn had a DBS when I first met her, and her tremors were well under control for the entire time I knew her. One time while she was still living alone, her DBS battery lost its regular recharge and she ended up in the hospital until the technician showed up and reset her software. She was jerking so much in those few hours, so unhappy, she said if she stays this way she just wants to be dead. The most unbelievable thing I learned from attending multiple Parkinson's lectures and product shows by the DBS companies: Of all the Parkinson's patients that are candidates for DBS, only 10% agree to get it. Yes, you read that right. The average Parkinson's patient is just too intimidated by the procedure to have it done. That is the saddest thing about Parkinson's disease today.
God bless the hands of the doctors and their brains. I ponder would that work for those with short term memory. I know a Dr Of Chemistry young man has probs with short term memory which is destroying his life and given all he did for people I'd love if it worked for him I truly would
Wow so amazing 😅
Has Michael J Fox been made aware of this treatment
Yes he is very aware of it
@@lyndagibson9699I wonder why he hasn’t gotten it?
It’s amazing what medicine can do then. This being twenty years ago. Where are we now in these treatments.
Parkinson's sufferers are benefiting from vitamin B1 therapy. See the book "Parkinson's and the B1 Therapy" - I would suggest giving this a good try before embarking on pharmaceutical route. But be patient because this approach requires it as the book states.
Legend
Incredible... but no mention of cost of surgery, etc. Guessing it's for the ultra rich only?
Medicare covers this
Sounds perfect for Neurolink?
AAAAAAAMEN IN JESUS CHRIST THANK YOU ALL YOU BE BLESSED AND ALL YOU FAMILIES WOW!!!!!
Plz tell how much total cost of ths operation
Lmfao everytime I hear a surgeon say “anchor” something to something else in your body…he bout to hammer that ish in and definitely not be delicate about it 🤣
The poor man, but I’m so grateful that he’s gotten so much relief.
the surgical magic trick
DBS is used for essential tremor…looking at this in late fall
How does a person with Parkinson's disease get this DBS? I can only hope my brother can get this.❤️
This is so amazing! So cool what technology can do now! The hope it has brought to so many people! I am so Excited for all these Parkinsons Patients! They all have a new lease on life! Thrilled! Love it so much! CATHERINE MAGEE
Why this video is in 4:3 format ? Not 16:9 ? 😮😮😮
A triathlon?😮😮😮😮 OMG
My dad had Parkinsons, but not as bad as that, he passed at 88
My blind sister and I had Multiple sclerosis And she got her sight back the same way I did mine by a back adjustment. We had both had a back injury as a child and flipped over backwards 3 times as an adult. But I'm a quad because no doctor will touch me because Researchers say it is not a bad injury.
My goodness! I'm so sorry this happened to you and your sister! You deserve the best treatment available! Keep fighting! Get an advocate or case manager for yourself, honey. Ask your Dr or insurance company to get you one.
Wow!
I have a dear friend, husband diagnosed with Parkinson. But no tremors. He just can't keep bp up high enough to walk
Wow it's kinda like the nerve stimulus for seizures.....
Wow, and I hope Mr. Michael J. Fox can try on it cause he earned it.
Would this work for Michael J. Fox?
Old video? (what is the date)
Seems to be old story..hope he is doing better and better....🤲🏻💐
He’s dead
My brother in law passed away from this disease, I whis he could of had this operation
I want this
I wonder if it works for everyone. I have seen that cannabis has a similar effect . I do hope this is a new technique and a lot of sufferers get the option to get this operation.
It doesn't work as well for everybody.
Is there a percentage of the probe’s success rate?
What about Michael J Fox and Linda Ronstadt?
The people at his church should have shown more compassion, he shouldnt have felt embarrased
Case in point: Michael J. Fox
This year I met the fourth mother with a down syndrome child. And asked if she had used wheat germ In unlimited amounts before enduring pregnancy. All for said yes. But I can't get a researcher to ask that question because that's not how research is done.
I was hoping he would say what he wanted to do with his wife. 😂 What a chad.
What is the cost of DBS in India?
Doctor I have Parkinsonism. My problem is Freezing. So is there anyway you could tell me that there is cure for this
0:14 🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉🎉❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤
Nice.....Michael j. Fox, your next buddy.
I'm hiding away hate parkinson's 😢
what about immunotherapy ?
I'd love to meet Michael J. Fox. I hear he lives in Oregon, Like I do. My state, and people like governor Kitzhaber, and Julie Kelley, have definitely helped the disabled like myself.