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“The Future of Parkinson’s Disease Treatments,” Jason L. Crowell, M.D.
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- Опубліковано 6 сер 2024
- 2021 Neuroscience Expo
“The Future of Parkinson’s Disease Treatments,” Jason L. Crowell, M.D.
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What a presentation! Bravo 🎉
Thank you for this lesson. It's important for Parkinson's patients to have confidence that we are not forgotten, that there are sustained efforts to deal with the symptoms of this debilitating disease and to perhaps terminate its progression. Maybe there will be a method to restore health. I don't want to be a walking pharmacy !
thank you, excellent, clear, understandable informative video.
Thanks so much. Very encouraging 👏👏💜
This is really fascinating
What about Akidin?
do all PD patients develop lewy bodies even if there is no mutation in SNCA gene?
Excellent vidéo very clear and concise. I am newly diagnosed and all I received was a handout and a prescription. This video gives me hope so that I might not have to resort to plan B
Hi, do you mind if I ask what plan b is? I was diagnosed 4yrs ago at 40. I currently take 8 sinimet in one day. When it wears off I get slow and rigid and stiff..it’s really hard. No tremors yet. I exercise every day. No really cure except dbs..for those in rough shape..❤️
I am a physician, Gastroenterologist, and knew quite a bit about Parkinson’s disease, having cared for a lot of patients from the GI standpoint and from my training, the diagnosis hit me and my wife quite hard. I was diagnosed two and a half years ago. I couldn’t believe it! Over the three prior years before diagnosis, I had noticed that I could not hold a pen properly and even my physician type handwriting had become much worse than normal. I started having some cognitive, perception issues and significant trouble swallowing. After a proper work up, it turned out to be a neuromuscular oropharyngeal cause, and turned out to be from the Parkinson’s. I later developed some tremor, mostly left sided. I have a fantastic wife, two great kids. I want to be around and able to enjoy my family for as long as possible. Since the diagnosis, I have read more, become more involved with an online Parkinson’s community. I am pushing very hard with recommended Kunime medicine at home weekly with a PD therapist who has a master’s degree. With excellent neurological care from Dr. Fabien and kunime herbs medication, I am doing reasonably well and I have no balance issues. I have remained as positive and optimistic as possible. I feel very strongly about the Kunime herbs and want to help in any way possible to improve treatment and a cure for people with Parkinson’s! Many of kunime medications that are helping me now are new. Www.kunimeherbs.com
Me too! Couldn't agree more.
Research "Photo bio modulation" (PBM)
I just received diagnosis as well Elaine.
Just as much of Physical has been my focus/ sharpness etc….
I’m a tennis pro so this is really hard. Have you found any supplements to help with brain function?
I've Parkinson's