Wao, the best intro Parkinson’s information given I have ever heard. Thank you. You couldn’t explain it better. Straight plain English. I appreciate you. 🙏
We're glad you found this information helpful! For more information on the basics of Parkinson's, know you can visit our website: www.parkinson.org/understanding-parkinsons
Im seven years post diagnosis. My first symptom was a jaw tremor. Things have progressed and many common PD symptoms have taken hold, but im very thankful for C/L. My newest issue in memory loss.
Know that we're here for you 💙 We have more information on cognitive changes with PD on our website here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/cognitive
I was diagnosed with tremor dominant Parkinson's about six years ago. It began with a slight tremor in my right forefinger and today I have tremors in all my limbs and jaw. I had been doing Parkinson's foundation exercises, a six kilometre walk and an hour's yoga everyday regularly for the past several years. However a few months ago I have developed clenching of abdominal muscles and difficulty breathing at times. I have lost 20 kilos and get easily fatigued. Is any of this a side effect of c/ l that I take or is it just a progression of the disease?
Hi @@vinaypratapsingh1436 - While there's not currently a cure for Parkinson's disease, there are ways to treat the symptoms of PD. We have more information on treatments at: www.parkinson.org/living-with-parkinsons/treatment If you'd like to learn more about the research we are doing to find a cure, we encourage you to visit www.parkinson.org/advancing-research
One of my family members think I have Parkinson's disease, I suffer from other disabilities such as 'cerebral palsy, epilepsy, etc, etc', in the last few years my mobility has decreased and I fall quite a lot. I have tremours occassionally in my right hand and numbness and tingling through out my limbs, jumping from one arm to another, or to a leg or foot, very randomly and sparadically. Are these some of the things Parkinson's disease can do?
Hi there - To learn about early signs of Parkinson's, we encourage you to visit: www.parkinson.org/understanding-parkinsons/10-early-signs No single one of these signs means that you should worry, but if you have more than one sign you should consider making an appointment to talk to your doctor.
I'm being sent to the university of South Florida neurology department to get tested to figure out what is wrong and I have several of these symptoms 😢
Hi Dennis - Know that we're here for you if we can be of assistance! If you're interested, we have more information on early signs of Parkinson's disease here: www.parkinson.org/understanding-parkinsons/10-early-signs
Hi there - While there's not currently a cure for Parkinson's disease, there are ways to treat the symptoms of PD. We have more information on treatments at: www.parkinson.org/living-with-parkinsons/treatment
Medications are only covering up symptoms, they never adresses rootcauses-at best they cover up some lacks, but never adresses why the lack. It’s the buissness model of big pharma. To address rootcauses you have to look into functional medicine, it’s lifstyles and stress mangement based. “Let food be thy medicine or you have to let medecine be thy food” (Hippocrates-ironically the Father of medicine)
I'm 7 years post diagnosis with PD and feel like crap. Exposed to Agent Orange in Vietnam. Tired every day my legs are weak and horribly stiff. Don't have much of an appetite. Have a metric shit ton of anxiety. No ambition. My Sinemet doesn't seem to work any more. I feel apprehensive all day. S.O.S.
Know that we're here for you. 🩵 We have resources designed specifically for veterans living with Parkinson's disease at www.parkinson.org/living-with-parkinsons/finding-care/veterans. We also have information to help manage anxiety in PD here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/anxiety
The best thing you can do is just accept the anxiety, so its on your own terms. Don't try to run away from it, because that only makes it worse. No s.o.s. is needed because its you that saves yourself. I have been through this hell. It stopped the day I gave up looking for a savior or a magic pill. Now I don't care if I have anxiety because it doesn't own me anymore.
Hi there - Some people with Parkinson's disease do experience changes in vision. We have more information on this symptom here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/vision
Wao, the best intro Parkinson’s information given I have ever heard. Thank you. You couldn’t explain it better. Straight plain English. I appreciate you. 🙏
We're glad you found this information helpful! For more information on the basics of Parkinson's, know you can visit our website: www.parkinson.org/understanding-parkinsons
thank you doc for nice information
Im seven years post diagnosis. My first symptom was a jaw tremor.
Things have progressed and many common PD symptoms have taken hold, but im very thankful for C/L. My newest issue in memory loss.
Know that we're here for you 💙 We have more information on cognitive changes with PD on our website here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/cognitive
@@ParkinsonDotOrg I can't thank you enough!
I have Parkinson’s now for 13 yrs
I was diagnosed with tremor dominant Parkinson's about six years ago. It began with a slight tremor in my right forefinger and today I have tremors in all my limbs and jaw. I had been doing Parkinson's foundation exercises, a six kilometre walk and an hour's yoga everyday regularly for the past several years. However a few months ago I have developed clenching of abdominal muscles and difficulty breathing at times. I have lost 20 kilos and get easily fatigued. Is any of this a side effect of c/ l that I take or is it just a progression of the disease?
Hi there - We encourage you to contact our free Helpline to discuss these symptoms in more detail: 1-800-4PD-INFO (473-4636) | Helpline@Parkinson.org
Is this disease curable...??
Hi @@vinaypratapsingh1436 - While there's not currently a cure for Parkinson's disease, there are ways to treat the symptoms of PD. We have more information on treatments at: www.parkinson.org/living-with-parkinsons/treatment
If you'd like to learn more about the research we are doing to find a cure, we encourage you to visit www.parkinson.org/advancing-research
Oo
One of my family members think I have Parkinson's disease, I suffer from other disabilities such as 'cerebral palsy, epilepsy, etc, etc', in the last few years my mobility has decreased and I fall quite a lot. I have tremours occassionally in my right hand and numbness and tingling through out my limbs, jumping from one arm to another, or to a leg or foot, very randomly and sparadically. Are these some of the things Parkinson's disease can do?
Hi there - To learn about early signs of Parkinson's, we encourage you to visit: www.parkinson.org/understanding-parkinsons/10-early-signs
No single one of these signs means that you should worry, but if you have more than one sign you should consider making an appointment to talk to your doctor.
I'm being sent to the university of South Florida neurology department to get tested to figure out what is wrong and I have several of these symptoms 😢
Hi Dennis - Know that we're here for you if we can be of assistance! If you're interested, we have more information on early signs of Parkinson's disease here: www.parkinson.org/understanding-parkinsons/10-early-signs
Is Parkinson cure completely or only slowdowns the disease progression by using medication
Hi there - While there's not currently a cure for Parkinson's disease, there are ways to treat the symptoms of PD. We have more information on treatments at: www.parkinson.org/living-with-parkinsons/treatment
Medications are only covering up symptoms, they never adresses rootcauses-at best they cover up some lacks, but never adresses why the lack. It’s the buissness model of big pharma. To address rootcauses you have to look into functional medicine, it’s lifstyles and stress mangement based.
“Let food be thy medicine or you have to let medecine be thy food” (Hippocrates-ironically the Father of medicine)
Por favor no lo pueden traducir
Hola. Puedes encontrar nuestros videos en español aquí: th-cam.com/play/PLDGRDRM479GtQ90xFlF2Ca6HljwfeY_u7.html
I'm 7 years post diagnosis with PD and feel like crap. Exposed to Agent Orange in Vietnam. Tired every day my legs are weak and horribly stiff. Don't have much of an appetite. Have a metric shit ton of anxiety. No ambition. My Sinemet doesn't seem to work any more.
I feel apprehensive all day. S.O.S.
Know that we're here for you. 🩵 We have resources designed specifically for veterans living with Parkinson's disease at www.parkinson.org/living-with-parkinsons/finding-care/veterans.
We also have information to help manage anxiety in PD here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/anxiety
The best thing you can do is just accept the anxiety, so its on your own terms. Don't try to run away from it, because that only makes it worse. No s.o.s. is needed because its you that saves yourself. I have been through this hell. It stopped the day I gave up looking for a savior or a magic pill. Now I don't care if I have anxiety because it doesn't own me anymore.
❤
Does it affect the eyes???
Hi there - Some people with Parkinson's disease do experience changes in vision. We have more information on this symptom here: www.parkinson.org/understanding-parkinsons/non-movement-symptoms/vision