Experiences with

Auditory Stimulation

v=yZsQ1FZtHw0 Most of us know about binaural beats, rife frequencies, rhythmic auditory stimulation, multiple wave oscillation etc and may even find them beneficial.

https://www.sciencedirect.com/science/article/abs/pii/S1094715924011188 A trial of spinal cord stimulation in a VERY small number of patients showed that it reduced painful symptoms. However, I have SEVERAL reservations. The trial doesn't say what medications the patients were taking.

Hi friends, Anyone with speech issues - can you please share your experience with this wretched symptom? I have a range of issues from festinating speech to stuttering and anywhere in between. I have been trying to get an appointment with an SLP practitioner and it has been difficult to find one

Lifestyle Recommendations - Anti-inflammatory diet (leafy greens, oily fish, berries) - Intermittent fasting (16:8) or cyclic ketogenic diet - Moderate regular exercise - Vagal nerve stimulation techniques (breathing, HRV training) - Avoid anticholinergic and P-gp inhibiting drugs unless necessary 6.

had DBS five years ago lately my left arm which worse affected side feeling numb and has electrical feelings. any one has the same? What could it be?

I’ve tried everything exercise, diet, CL, DBS. Cl does not help at all. DBS does not help. I have dystonia on my right side. Constant pain in my shoulder, hip, and feet. This is the end. Don’t tell me to think positive!! I’m begging God to take me now. My poor hubby and kids (adult). What can I expect

I decided a few weeks ago to begin reducing my meds along with increasing the stimulation. My stimulation has now gone up to 2.0 from 1.0. My medication is now just 6×100mg stalevo from 9×100mg. Apart from the dyskinesia and occasional headaches I'm quite symptom free.

https://www.science.org/doi/10.1126/sciadv.ado4927?fbclid=IwY2xjawJVMGZleHRuA2FlbQIxMQABHRBDa9RJWMGOFOYxLDnqxNsFaANf9RTriEX2OOQMySm4AdwkZzAJlkgGmg_aem_C7Z_4PXuqgDEIWF8E8v8jg

As a follow up to my recent post...and to recap, 6 months into Tinnitus that started following performing at a gig with excessively loud stage volume....on Mirtazipine for 4 months (hoping to taper off in August) and 10 CBT sessions in...... I currently take care with noise, wear hearing protection

Hi all. You might remember that I recently posted about voice issues. There was a great response which I’m thankful for. However,I think I’ve realised that there are definitely two things at work: one is the PD of course and your possible solutions were pertinent here. Second though is the DBS which

Read the story : https://www.scientificamerican.com/article/new-form-of-parkinsons-treatment-uses-real-time-deep-brain-stimulation/

The new adaptive system adjusts stimulation levels automatically based on the person’s individual brain signals. https://apple.news/AGaCfygkITMytjSd7gJe2CQ

Hi, I just had DBS and am looking for a P/T that specializes in PD. I am in Northern New Jersey but it seems like all the qualified people are in NYC. TIA.

I'm scheduled for DBS surgery in June (and I'm excited I'm going to be able to get the newly approved adaptive device from Medtronic). But I have a question that my neurologists have not really been able to clarify for me, so I was hoping for some lived experience from any of you (the "hive mind").

I found a message that says I've been here more than 5 years: So I finished the book... kaypeeoh profile image kaypeeoh • 5 years ago • 5 Replies I didn't know what to expect, maybe a primer on running and PD. Lots of aphorisms similar to Just Do It and Git 'er Done. Learned that standing is

Deep brain stimulation halts Parkinson’s disease-related immune dysregulation in the brain and peripheral blood, Brain, Behavior, and Immunity, Volume 123, pp 851-862, https://www.sciencedirect.com/science/article/pii/S0889159124006792

https://neurosciencenews.com/fda-parkinsons-dbs-28438/

There are many of you or your loved ones who have had DBS. Your experiences are scattered around HU, and it becomes very difficult to search and refer. Please if you could share your respective experiences and current status here, it would all be at one page for reference.

I had DBS 1 and half years ago. It's been a disaster. Prior to having it I could be fairly active. I was experiencing an off period where I could hardly move. So, I had the DBS and the result was I can no longer walk, and now I have lost my voice. Has anyone experience of switching the DBS off?

) specifically Vagustim ----- have ordered and awaiting delivery of the Vagustim device which is based on stimulation via both ears of the vagus nerve / dysfunction of the autonomic nervous system.