Hi Michael you’re an inspiration to everyone out there battling any kind of disease or cancer to see how much courage you have and I have you and your family in my prayers that you find a cure soon God bless you all🙏❤️🙏❤️🙏❤️🙏❤️🙏
I live in Japan. I was diagnosed with Parkinson's disease in July 2015. The activities of MJFF are also attracting attention in Japan. In Japan, even if Parkinson's disease is mild, social participation is very often restricted. I want to be able to actively participate in society and support people who are more in need than I am, even if I have an intractable disease or disability.
I give my brother about 30 grams of ktc coconut oil each day and the oil is only £2 a tub in Asda and it's 500ml in each tub, it stopped his tremors within an hour and it worked for other people and people don't need the drugs to stop tremors
I just finished reading Michael's book, no time like the future and wanted to learn more. I have no personal stake in Parkinson's but I must say I am compelled with Michael and Debra's work. Michael is the perfect spokesman for this disease and it is his attitude and positivity and drive which leads his life. I really appreciate it his book and found myself laughing out loud at certain parts because of this humor mixed with an insight which is incredible. He put into words something most people couldn't even begin to put into words even living with the disease. He's got the greatest family cuz he's the greatest dad. A fellow Canadian appreciates Michael and Debra.
Thank you Andy. I think it was yesterday that I subscribed here and am enjoying the information here bc I have had Parkinson’s a few years now. Haven’t read the book bc my eyes are as though I’m crying right now just from reading on here, as between my Parkinson’s and TED, I see as though looking through water, like swimming with my eyes open. Optometrist says it’s all medical so no need for new glasses and I’m safe to drive my car, although my respect for human life prevents me doing much of that. Don’t want to wreck my car either haha! Bad allergies also, so ride with my ex more than I drive. Michael J. Fox and I live in two different worlds in many ways, but watching him in this interview and listening to him talk, I sure feel a kindred spirit. My being an unknown person has made it easy for me, although I was a type A personality, to become a shut in these past few years. Quarantine didn’t change my life and the 6 foot rule was a blessing to me, being a petite person. Less likely to be crushed haha. Due to medical issues, I’ve shrunk tremendously. Found myself wishing the large woman who used to lived in my home would please remove her clothes from my closets and replace them with some for this little old lady in my mirrors LoL! Parkinson’s requires a sense of humor, as there is no way to know what to expect next. DID learn the APDA isn’t there to help people in my position. They got my address to try to solicit more research funding. Yes, I stopped that haha. Between medical bills that Medicare doesn’t cover and my living expenses, wrong person to solicit. I’m behind on medical bills bc my utilities are on auto pay so I don’t forget. Parkinson’s is bad on the memory. They aren’t researching symptoms from patients, so I suppose just a money grab is my opinion. Was happy to find this information source. GBU and your family. Thank you for your time and pardon typos please. ~
P.S. I agree that Michael is a perfect spokesperson. His pain and Parkinson’s is very real. The old saying of, “it takes one to know one” applies here. I admire him being able to go public, sit through an interview that long without having to get up and walk a bit and keep his composure. I’m reclusive now bc I don’t know when pain may leak from my eyes, although I’m smiling. Not cool, I know. Just a line I’ve crossed and haven’t yet found the road back from so stay home usually. ;) Haha caught THAT typo so edited. Seen I turned that road into a rod! Kids live next door with only a field between us I used to run. Now I refer to it as “the green mile” so REALLY need to gain self discipline to make myself do some PT and more walking, regardless of the pain. Do not want to die yet, and more importantly don’t want to trade my house in for assisted living. So doing research. Wish I had treated this body better earlier in life. If you’re young, please consider this. Broke every bone in my left wrist in my twenties on roller skates to later break that index finger than that thumb at a different time. Feel it all now and it doubles down for rain. That’s just one limb so I’m a train wreck rusting HAHA! If you have time for an extra prayer, please add me to your list as Crystal is my real name. I sure believe in the power of prayers. Thank you very much in advance. ~
@@crystalbelle2349 I am sorry that you have to deal with this terrible disease. I cannot fully comprehend how terrible and debilitating it must be. I've had a small struggle when I was younger. I had my leg amputated 4 days before my 23rd birthday. I have been able to deal quite well with it and it does not come close to what you or Michael deal with daily. I wish you all the best and some very good days ahead of you. 🤗
@@mrsaskriders thank you. My phone got old and I had lost many of my UA-cam Subscriptions somehow, and just found this one this evening. My son & his family bought a new phone for me for Christmas! 🎄 😃 As you can see, it has taken me awhile to get back, but I wanted to thank you for your communication. I’m sorry that you had to have that leg amputated, as I had an uncle who did many years ago. I realize what a hardship it can be, although I didn’t suffer his pain I did drive him when I lived there & we were friends as well as family. He had been in a car wreck back in the early eighties, so that was long ago. I’ve been in NC since the early nineties, relocated from WV, my home state. This is my home now, with my son & his family nearby. I hope that you are doing well. GBU and your family. ~
I just subscribed to your channel and I hope to learn more about the foundation and the effort that is put into finding a cure. I love the work that you guys are able to put into helping with this disease.
I live in Saskatchewan and I first started experiencing symptoms of blepharospasm when I was 28, close to 8 years ago now. I woke up one morning with horrible stabbing eye pain in my left eye and the only way I can describe it is it felt like my eye was exploding inside my head and I was surprised when I was able to open my eye and see. I don't know anyone who has the same issue as me and while other family members like my great great uncle and my late aunt had Parkinson's and my dad's first cousin has Parkinson's, no-one in my family has ever had similar issues with blepharospasm, so it does get lonely sometimes not knowing anyone who can personally relate to the pain I have experienced. I myself have not been diagnosed with Parkinson's, but have participated in the site's surveys. Thank you Michael and Debbie for all that you do!
Sadly I first learned about Parkinson when Michael J Fox was diagnosed. A year and a half ago I was diagnosed with Parkinson. I'm trying to learn more about this terrible illness 🤒
I just subscribed to your channel. Thank you Michael and Debbi for everything you are doing. This is so wonderful! We need a government that will definitely support stem cell research. I realize this is highly controversial to many people. I have always been very hesitant about it myself but when you put it in to prospective it shouldn't be an issue. The science and new treatments until there is a cure.
Minha mãe têm Parkinson já faz cinco anos. É verdade que você J Michael encontrou a cura do Parkinson?? Você patrocinou pesquisas para cura do Parkinson e encontrou É verdade? DEUS te abençoe J Michael!! Sou Brasileiro 🇧🇷não falo inglês só português!! Speak português from Brazil🤝
IAM JOELFERNANDEZ SUFFERING XDP DYSTONIA PARKINSON DISEASE I NEED YOUR HELP FOR DBS JOEL DOLING FERNANDEZ MY ADDRESS: HERNANDEZ COMPOUND CORNER KASOY ST. VERDANT SUBDIVISION PAMPLONA TRES LAS PIÑAS CITY PHILIPPINES MY CELPHONE NUMBER 09356034826 MY EMAIL ADDRESS FERNANDEZ.JOEL1965@GMAIL.COM
Hey Michael, I sent a message to your research department. I've got something you should look into ASAP. Dr L Wilson posted a Parkinson's article in 2019 on his site. He's been setting up development programs for people through the years using an HTMA (hair tissue mineral analysis). On his Parkinson's page- "...hair analysis research indicates that the causes are chronic manganese or lead toxicity. Other nutrient deficiencies and constipation also play a role." I've personally been working through one of his practitioners since 2017. I hope you'll be able to read this, Mr Fox! By the way, did you happen to live on well water at any point growing up in Canada, starting with Edmonton?? I ask because well water can have abnormally high levels of manganese.
💭 If there's no need to head in the direction you are, all of your discussion is about troubles and suffering and there can't be any progress, and that's defeatist.
Hi Michael you’re an inspiration to everyone out there battling any kind of disease or cancer to see how much courage you have and I have you and your family in my prayers that you find a cure soon God bless you all🙏❤️🙏❤️🙏❤️🙏❤️🙏
P
This channel is wonderful and My father is Parkinson's Patients.i hope every Parkinson patient in this planet will get better one day.
İnşallah !!!
Coconut oil stopped my brothers tremors and only £2 a tub
Gratefulness is a healthy balance for living a fulfilling life. Blessings
I live in Japan. I was diagnosed with Parkinson's disease in July 2015. The activities of MJFF are also attracting attention in Japan. In Japan, even if Parkinson's disease is mild, social participation is very often restricted. I want to be able to actively participate in society and support people who are more in need than I am, even if I have an intractable disease or disability.
Coconut oil stopped my brothers tremors
@@MIKEDAYLIGHT Thank you very much. Thanks for the information.
I give my brother about 30 grams of ktc coconut oil each day and the oil is only £2 a tub in Asda and it's 500ml in each tub, it stopped his tremors within an hour and it worked for other people and people don't need the drugs to stop tremors
I just finished reading Michael's book, no time like the future and wanted to learn more. I have no personal stake in Parkinson's but I must say I am compelled with Michael and Debra's work. Michael is the perfect spokesman for this disease and it is his attitude and positivity and drive which leads his life. I really appreciate it his book and found myself laughing out loud at certain parts because of this humor mixed with an insight which is incredible. He put into words something most people couldn't even begin to put into words even living with the disease. He's got the greatest family cuz he's the greatest dad. A fellow Canadian appreciates Michael and Debra.
Thank you Andy. I think it was yesterday that I subscribed here and am enjoying the information here bc I have had Parkinson’s a few years now. Haven’t read the book bc my eyes are as though I’m crying right now just from reading on here, as between my Parkinson’s and TED, I see as though looking through water, like swimming with my eyes open. Optometrist says it’s all medical so no need for new glasses and I’m safe to drive my car, although my respect for human life prevents me doing much of that. Don’t want to wreck my car either haha! Bad allergies also, so ride with my ex more than I drive. Michael J. Fox and I live in two different worlds in many ways, but watching him in this interview and listening to him talk, I sure feel a kindred spirit. My being an unknown person has made it easy for me, although I was a type A personality, to become a shut in these past few years. Quarantine didn’t change my life and the 6 foot rule was a blessing to me, being a petite person. Less likely to be crushed haha. Due to medical issues, I’ve shrunk tremendously. Found myself wishing the large woman who used to lived in my home would please remove her clothes from my closets and replace them with some for this little old lady in my mirrors LoL! Parkinson’s requires a sense of humor, as there is no way to know what to expect next. DID learn the APDA isn’t there to help people in my position. They got my address to try to solicit more research funding. Yes, I stopped that haha. Between medical bills that Medicare doesn’t cover and my living expenses, wrong person to solicit. I’m behind on medical bills bc my utilities are on auto pay so I don’t forget. Parkinson’s is bad on the memory. They aren’t researching symptoms from patients, so I suppose just a money grab is my opinion. Was happy to find this information source. GBU and your family. Thank you for your time and pardon typos please. ~
P.S. I agree that Michael is a perfect spokesperson. His pain and Parkinson’s is very real. The old saying of, “it takes one to know one” applies here. I admire him being able to go public, sit through an interview that long without having to get up and walk a bit and keep his composure. I’m reclusive now bc I don’t know when pain may leak from my eyes, although I’m smiling. Not cool, I know. Just a line I’ve crossed and haven’t yet found the road back from so stay home usually. ;)
Haha caught THAT typo so edited. Seen I turned that road into a rod! Kids live next door with only a field between us I used to run. Now I refer to it as “the green mile” so REALLY need to gain self discipline to make myself do some PT and more walking, regardless of the pain. Do not want to die yet, and more importantly don’t want to trade my house in for assisted living. So doing research. Wish I had treated this body better earlier in life. If you’re young, please consider this. Broke every bone in my left wrist in my twenties on roller skates to later break that index finger than that thumb at a different time. Feel it all now and it doubles down for rain. That’s just one limb so I’m a train wreck rusting HAHA! If you have time for an extra prayer, please add me to your list as Crystal is my real name. I sure believe in the power of prayers. Thank you very much in advance. ~
@@crystalbelle2349 I am sorry that you have to deal with this terrible disease. I cannot fully comprehend how terrible and debilitating it must be. I've had a small struggle when I was younger. I had my leg amputated 4 days before my 23rd birthday. I have been able to deal quite well with it and it does not come close to what you or Michael deal with daily. I wish you all the best and some very good days ahead of you. 🤗
@@mrsaskriders thank you. My phone got old and I had lost many of my UA-cam Subscriptions somehow, and just found this one this evening. My son & his family bought a new phone for me for Christmas! 🎄 😃 As you can see, it has taken me awhile to get back, but I wanted to thank you for your communication. I’m sorry that you had to have that leg amputated, as I had an uncle who did many years ago. I realize what a hardship it can be, although I didn’t suffer his pain I did drive him when I lived there & we were friends as well as family. He had been in a car wreck back in the early eighties, so that was long ago. I’ve been in NC since the early nineties, relocated from WV, my home state. This is my home now, with my son & his family nearby. I hope that you are doing well. GBU and your family. ~
@@crystalbelle2349 I'm glad your son got a new phone for you and thank you for the well wishes. I wish you well too! Take care 🙏
I just subscribed to your channel and I hope to learn more about the foundation and the effort that is put into finding a cure. I love the work that you guys are able to put into helping with this disease.
Thank you for being there
I live in Saskatchewan and I first started experiencing symptoms of blepharospasm when I was 28, close to 8 years ago now. I woke up one morning with horrible stabbing eye pain in my left eye and the only way I can describe it is it felt like my eye was exploding inside my head and I was surprised when I was able to open my eye and see. I don't know anyone who has the same issue as me and while other family members like my great great uncle and my late aunt had Parkinson's and my dad's first cousin has Parkinson's, no-one in my family has ever had similar issues with blepharospasm, so it does get lonely sometimes not knowing anyone who can personally relate to the pain I have experienced. I myself have not been diagnosed with Parkinson's, but have participated in the site's surveys. Thank you Michael and Debbie for all that you do!
Sadly I first learned about Parkinson when Michael J Fox was diagnosed. A year and a half ago I was diagnosed with Parkinson. I'm trying to learn more about this terrible illness 🤒
Hi, it is a Nice channel and informative session.
Keep it up.
Mohsin
I just subscribed to your channel. Thank you Michael and Debbi for everything you are doing. This is so wonderful! We need a government that will definitely support stem cell research. I realize this is highly controversial to many people. I have always been very hesitant about it myself but when you put it in to prospective it shouldn't be an issue. The science and new treatments until there is a cure.
No speak english.🤔 Não têm legendas em português!! from Brazi🇧🇷l português! God bless you J Michael Fox🤝
Minha mãe têm Parkinson já faz cinco anos. É verdade que você J Michael encontrou a cura do Parkinson?? Você patrocinou pesquisas para cura do Parkinson e encontrou É verdade? DEUS te abençoe J Michael!! Sou Brasileiro 🇧🇷não falo inglês só português!! Speak português from Brazil🤝
IAM JOELFERNANDEZ SUFFERING XDP DYSTONIA PARKINSON DISEASE I NEED YOUR HELP FOR DBS
JOEL DOLING FERNANDEZ
MY ADDRESS: HERNANDEZ COMPOUND CORNER KASOY ST. VERDANT SUBDIVISION PAMPLONA TRES LAS PIÑAS CITY PHILIPPINES
MY CELPHONE NUMBER 09356034826
MY EMAIL ADDRESS FERNANDEZ.JOEL1965@GMAIL.COM
What is the best medications for a parkinson disease
Have you looked into focused ultrasound ???
Hey Michael, I sent a message to your research department. I've got something you should look into ASAP. Dr L Wilson posted a Parkinson's article in 2019 on his site. He's been setting up development programs for people through the years using an HTMA (hair tissue mineral analysis). On his Parkinson's page- "...hair analysis research indicates that the causes are chronic manganese or lead toxicity. Other nutrient deficiencies and constipation also play a role." I've personally been working through one of his practitioners since 2017. I hope you'll be able to read this, Mr Fox! By the way, did you happen to live on well water at any point growing up in Canada, starting with Edmonton?? I ask because well water can have abnormally high levels of manganese.
Pls let knoe if u were on L ropapa
Its freetoo
Mike...
💭 If there's no need to head in the direction you are, all of your discussion is about troubles and suffering and there can't be any progress, and that's defeatist.
I hate when people dig their heels into their audacity like this.
Michael was a sweet man, but don't use his warm spirit as an excuse for centering this whole campaign around aiming for a moral victory.
чё?
How could Michael make such light of the height of his folly like this?
I'm disappointed.
Stop holding his spirit hostage in dishonesty and just give me back my fox.