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. It is a German

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

A recent study indicates that DBS may not only reduce symptoms but could also potentially slow the progression of the disease—good news for individuals with DBS and an important finding for future treatments. Rhonda L. McFleder et al., 2025. Deep brain stimulation halts Parkinson’s disease-related

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?

80 y.o. husband diagnosed with PD a little over one year ago (Nov.27 '23) not started on Sinemat until March 24 '24 which he is still on. Aside from several non-motor symptoms + mild hand tremors, the issue is dizziness which started as mild lightheadedness about 4-5 years ago, gradually

I just want to share my thoughts about DBS. I’m going to be in absolute agony for 2 more weeks. My DBS equipment is implanted, but it can not be turned on for two weeks. My symptoms are now so painful and debilitating. It’s not funny. Awful painful constant dystonia! I started the process nine months

https://www.researchgate.net/publication/317720822_Complementary_and_Alternative_Therapies_for_Restless_Leg_Syndrome_An_Evidence-Based_Systematic_Review Complementary and alternative therapies have been found to be effective in both primary and secondary RLS. The severity of primary RLS symptoms can

After the successful surgery on new years eve. I went for the 'switch on' this week. The process was exciting and much quicker than I had expected. The Dbs nurse connected her medtronics setup software to a device that I held over my inserted DBS implant. She ran a couple of routines where the software

My husband has PD ( 9 years now) hes 63. He has DBS and it was very successful in treating tremor, stiffness, slowness. However he has a new symptom and we are not sure what it is...its just been a few days...He feels a tightening and cramping sensation in his thigh and calf muscle. We wondered if it

On December 13, 2022, The Today Show aired an amazing story about Dr. Tass's Stanford Gloves for the treatment of Parkinsons. The gloves worked to relieve many of the symptoms of PD through stimulating the brain non-invasively with gentle vibrational pulses administered in a special pattern to the wearer's