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.

Has anyone found an implanted spinal cord stimulator helpful for failed back surgery?

If you develop CIPN during chemotherapy, and it becomes permanent, can you subsequently find it has progressed to another site some years after the original diagnosis? I finished 6 cycles of Docetaxel in October 2019. Once the stabbing pains and feeling of being electrocuted had worn off, I was left

for sleeping through the night I take two 25 mg quetiapine and three 36.5/145 rytary. For anxiety I take one .25 mg clonazapam 3x a day. I have been on this regimen for quite a few years now, and it has been very helpful. The quetiapam /rytary helps me fall asleep and get back to sleep if I wake

Has anyone yet forked out £600 to see if the Nurosym Vagus Nerve Stimulation device helps reduce their RLS or depression/anxiety? My RLS is completely controlled but I'd be interested in trying it for my MS fatigue and brain fog. There was a 2023 study on 15 RLS patients and vagus nerve stimulation.

Parkinsons presenting attaining the leg in ability to stand and walk due to pain after a knee replacement. I really did not have a tremor. I went to many physicians trying to figure it out. They found cordcompression my cervical spine had a big operation didn’t help just got infected with Proionobavterium

Guys. I think that the time has come for me to own up to depression. Unsure if this is as a result of PD or the configuration of life’s circumstances over the last year. As some of you know, I had DBS about a year ago which some will point to as being the culprit but I don’t believe that this is the

Advice needed Daughter 18 with endometriosis in second year of college doing A levels then onto university hopefully, however is still struggling daily with pain and is affecting her college attendance. She has been working from home when unable to get into college and always completes her work to the

I’m quite sure that the research that is mentioned in a recent paper (2022), with the title ‘Vagus nerve stimulation and Atrial Fibrillation: revealing the paradox’ will lead to the most promising, non-invasive treatment for AF ever. It’s a must-read for everyone with a heart out of sync. Talk about

In preparation for my DBS procedure next month im going to hospital to have an MRI under general anesthetic this coming Sunday. I've read that the most common drugs used to anesthiatise are not good for people with Parkinsons given they Disrupt dopamine, and can really affect their post procedure recovery

I have been on a carnivore diet for 6 days and already noticed that I don’t have to take medication as often. I did DBS in 01/23 but take C/L extended release every 6 hours. I saw multiple YouTube videos and read 2 books about the diet. A few videos featured Mimi Morgan who completely reversed PD or

Abbott announced it has initiated a pivotal clinical trial, called the TRANSCEND study, to evaluate the use of the company's deep brain stimulation (DBS) system to manage treatment-resistant depression (TRD), a form of major depressive disorder. The US Food and Drug Administration (FDA) granted Abbott

Last falI had been incredibly impressed by the moderator of the DBS Facebook page in his responses, and I thought If I can be as well-spoken as he is 25 years after I’ve had DBS like he is, so I decided to proceed with the surgery. The surgery did not go well. The surgeon nicked an artery in my brain

There was a post to the technical paper in Nature Medicine a few weeks ago about an innovation to traditional DBS. Adaptive DBS involves putting in brain sensors to automatically increase or reduce the amount of stimulation. Medscape had an optimistic review of the technology here: https://www.medscape.com

my name is Jude and I was diagnosed with PD about 16 years ago. 18 months ago I had DBS and the result was amazing. I had diskynesia badly enough for friends to say that I made them feel Seasick! Well, I woke from the anesthetic cured of it. It felt great to be still. The downside was a loss of

My neurologist has recommended for DBS . As per the data ,I am informed that the success rate is 90%.Here also the neurologists are divided in two. Few says that medicine will continue even after DBS while other say no. I would request those who have been operated for DBS to share their actual experience

Chronic adaptive deep brain stimulation versus conventional stimulation in Parkinson’s disease: a blinded randomized feasibility trial. https://www.nature.com/articles/s41591-024-03196-z.epdf

Hello all, I am new here and wanted to share my story. In Feb. 2018, my left foot started to drag and for many years before my left arm would not swing. I probably had this symptom for years and considered it my normal way of walking. It has been 7 years with increasing dosages of levodopa. Throughout

Hi! I’m at the end of the road for CL. Can’t take more and can’t boost it more. And only get 10 minutes of on time. Wait listed for DBS, appointment is months away Exercise 90 minutes per day with walking and stretches. Strict plant based oil free diet. 90 minutes of prayer each day So anyway I’m not

I am a 82 year old male and was diagnosed with Parkinson’s 10 years ago. My neurologist is recommending that I have a DBS surgery to deal with my symptoms. He indicated that overtime medication is less effective and this is my best option. I’m hopeful that some who have had it will share their