I think Parkinson’s disease should be taken more serious more research more effort to prescribe a place for patients to exercise diet a Parkinson’s physality to help and encourage patients to slow down progression with physical therapy.
I’m sorry to be so pessimistic but I don’t think we will find any cure in our lifetimes. We just don’t have brilliant people in science anymore and it’s too complex a problem to solve. Everything is touted as a game changer but none of them pan out.
I empathize with your frustration. The human brain is the most complex machine in the world. But I firmly believe in research and science. There are SO MANY bright mind working on so many diseases...and we need more
I am the peasent of Parknens last seven years Early my arms movement extra body, after this my i feel i can't walk properly and my both feet fold and I can not walk this time i can't walk with out take medicine l take Ronirole, 2mg , senement / senement extra, no Kemprodran, Pk maz Selgin but now I am not walk and do not reunion matter. Please advise me regarding my problem.
Thank you for sharing your story. I would talk to your doctor and ask for a referral to a neurologist, particularly one that specializes in movement disorders.
I had DBS back in 2015, I was DX with PD in 2005. My DBS is a Medtronic device with 2 power packs. When I had my DBS everything got better. Before I was not sleeping at night and was bouncing off of walls. DBS is the greatest in helping control of the curse
I had too brain surgeries at the U of M For a bleeding aneurysm 17hr each surgery back in 2000 October. 24 Years later I am Having tremors. I am 64years young. I am wondering if this is related to my surgeries. Cerebral aneurysm it was bleeding, Dr Thompson surgeon said I was very strong. I am Strong and fighting Parkinsons.
Aside from the mild speech and walking, I haven't had natural BMs since January. I have been turned away by three doctors. I'm presently able to purge myself with two liters of water over several hours followed by a bottle of Magnesium Citrate. It takes a couple of hours for it to work for me, with several trips to the bathroom. I do this every third day.
My so-called PD has been with me over 20 years, mostly without treatment or tests. Deficency of Vitamin B-12 mimics PD symptoms. But not a single doctor tested my B-12 levels. I rarely see a doctor now, due to their lack of hearing me.
I am Parkinson patient I am taking syndopa pluse tablet three times a day and Nearoban tablets and Blood thinner once at night kindly suggest any other information or medicine is suitable for me
I had a very aggressive case of Parkinson's and bad tremors. I had Fus treatment and my Tremors were abolished within 2 hours and I was given my life back. Check out my documentary on RU-vid.. Tremor Documentary 2022. Absolutely amazing.
It's interesting seeing the differences in treatment, especially in DBS. The previous doctor I met was much more keen to do DBS much sooner after diagnosis and they do it asleep now and in cases can do everything in 1 surgery. My current doctor told me she rarely recommends anyone for DBS and not for many year into the diagnosis. So many different perspectives to this but it is known not to be a cookie cutter disease.
I appreciate your feedback. Thank you for sharing your experiences. You're absolutely right in that one diagnosis (e.g. Parkinson's Disease) can present very differently in different people. That's why as physicians, we need to treat the *patient*, not the illness.
