Neuralink brain implant brings back the voice of ALS patient with thought-to-speech BCI

[Redaktion]

As patients with amyotrophic lateral sclerosis (ALS) nerve disease lose control of their muscles, they lose control of their vocal cords as well. The Neuralink brain implant has managed to restore the voice of one such patient.

https://www.notebookcheck.net/Neuralink-brain-implant-brings-back-the-voice-of-ALS-patient-with-thought-to-speech-BCI.1406566.0.html

[Kenny Valare]

My wife was diagnosed in August 2023 and at that time she could still walk and do most things just slower and a weakness on her left side. 2 years down the line she was completely wheelchair bound. She lost both arms and speech was also affected and her neurologists kept saying, "There's no medical cure." and asked us if we would like to try out an alternative natural ALS/MND treatment that was formulated to treat ALS of which we accepted because neither the standard treatments like riluzole nor high-dose B12 did very little for my wife. we tried different supplements that didn't work, so this January, We tried the ALS/MND protocol which was the best decision ever! her symptoms has eased over the last 5 months. Her strength returned, and she now speak soundly. my wife feels like a new woman, She's now able to walk again and has not used her wheelchair in 3 months. We got the formula from this website www.Limitless naturalwellness . co m. each person is so very different. I am sending u love and hope x

[Kenny Valare]

My wife (55) was diagnosed Lou Gehrig's disease (ALS) in February 2026. She started displaying symptoms in July 2025. We were referred to an ALS clinic and began all the blood tests, MRI"s, etc. our neurologist stated that this looked more like an autoimmune than ALS but all of the autoimmune treatments were not effective. Referred to another ALS clinic were they confirmed diagnosis of sporadic limb onset ALS. In November 2025, she was using a cane to walk due to foot drop and leg weakness. She had fasciculations in her arms and back, clonus in her left leg, and weakness in her right arm and hand. Currently, she was 100% dependent on me for her care. She had virtually no use of her arms, hands and legs. She struggled with more things that have time to list here, her neurologist asked us if we would like to try out an alternative natural ALS/MND treatment that was formulated to treat ALS of which we accepted because she would not have survived if our primary care physician hadn't given her attentive care and attention, so in July, she tried the ALS/MND protocol—the best decision ever! Her symptoms eased, her muscle strength returned, and she no longer need the feeding tube. She feels like a new woman, and she can walk and exercise again. We got the ALS/MND protocol from ww w. limitlessnaturalwellness .com this is a breakthrough for PALS and their CALS.