Has any research been done on the Hyperbaric Oxygen Therapy to assisting the Parkinson’s Disease to digress the symptoms? Please respond at your earliest convenience. Thanks in advance for your response to my question.
We understand and regret that medication access is hard for many people around the world. Unfortunately, we are unable to facilitate access to medications directly. If you email us at blog@dpf.org, we might have resources we could recommend in your area.
I really wish that people would answer questions on this format. Recent studies on light and how it affects the benefits of Parkinson's. F a v a beans and their inherent amazing equality for increasing dopamine levels. Phenomenal nobody's talking. Nobody's talking about the Monty Python research study that study Parkinson's patients and a special kind of walk that if you can do for 11 minutes is equal to a 75 minute workout the research came out in December of 2022. We need to know more than we do as patients. One way that can happen is by having someone respond to these comments. I've mentioned it before and no one has followed up on it and I fault Davis Phinney for that because of the impact of social media is a two-way street not one way. Not just information overload downward communication there has to be a report built and there's plenty of room for improvement.
For me the the way rigidity and dystonia effect my GI tract, is really frustrating and a weird second short uncontrollable sleep that happens shortly after I'm up for the day and midway through getting dressed and ready to go outside for errands. A weird tingling sensation happens during that strange not like real sleep interlude. I try to put myself in a safe place and let it pass. It knocks me out longer the more I fight it. I still have the tingling sensation when I become alert enough to get the rest of the way ready and out the door. This doesn't happen later through the rest of the day (the uncontrollable sleep part). I do have swallowing difficulty sometimes. Have to consciously keep my windpipe clear.
@@davisphinneyfdnI will have to come back to this because it is more involved while I'm thinking about it and I'm trying to get out the door to an appointment. Am in the fog of it again right now. Trying to get going. :)
You have explained it so well,I have learnt a lot and understand my Parkinson's better than I did before. You've given me hope for the future.Thanksx
This was a really good interview and i learned a bit from it. Thank you.
interesting thanks
Thank you. 😊
Very Interesting...Thank you .
Two of my sisters each have one son diagnosed within the past year with Parkinson's Disease. It was diagnosed two years
Has any research been done on the Hyperbaric Oxygen Therapy to assisting the Parkinson’s Disease to digress the symptoms? Please respond at your earliest convenience. Thanks in advance for your response to my question.
Hi Gwendolyn, Thank you for watching. Here's an article to get you started: www.mdpi.com/2218-273X/12/5/661
I am suffering from Parkinsonism plus can’ I get any medication please
We understand and regret that medication access is hard for many people around the world. Unfortunately, we are unable to facilitate access to medications directly. If you email us at blog@dpf.org, we might have resources we could recommend in your area.
I really wish that people would answer questions on this format. Recent studies on light and how it affects the benefits of Parkinson's.
F a v a beans and their inherent amazing equality for increasing dopamine levels. Phenomenal nobody's talking. Nobody's talking about the Monty Python research study that study Parkinson's patients and a special kind of walk that if you can do for 11 minutes is equal to a 75 minute workout the research came out in December of 2022. We need to know more than we do as patients. One way that can happen is by having someone respond to these comments. I've mentioned it before and no one has followed up on it and I fault Davis Phinney for that because of the impact of social media is a two-way street not one way. Not just information overload downward communication there has to be a report built and there's plenty of room for improvement.
You can watch Sleep, Light, and Neurodegeneration here: ua-cam.com/video/W4tSV1HU9-I/v-deo.html
For me the the way rigidity and dystonia effect my GI tract, is really frustrating and a weird second short uncontrollable sleep that happens shortly after I'm up for the day and midway through getting dressed and ready to go outside for errands. A weird tingling sensation happens during that strange not like real sleep interlude. I try to put myself in a safe place and let it pass. It knocks me out longer the more I fight it. I still have the tingling sensation when I become alert enough to get the rest of the way ready and out the door. This doesn't happen later through the rest of the day (the uncontrollable sleep part). I do have swallowing difficulty sometimes. Have to consciously keep my windpipe clear.
This is interesting, Audrey. Has this been happening since you were first diagnosed?
@@davisphinneyfdnI will have to come back to this because it is more involved while I'm thinking about it and I'm trying to get out the door to an appointment. Am in the fog of it again right now. Trying to get going. :)
Hi can I get an y medication please
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