Four years since symptoms. Initial BodyScience start date Oct 2024 (10 months ago), Protocol to include: Astrocyte Protocol, Intrathecal Stem Cells and Filgrastim. For an explanation and citations on protocol (   • New Therapies in ALS: Fecal Microbiot...  )

00:00:00 Amy introduces Greg, who was diagnosed with ALS in 2020. They discuss their collaboration and the improvements Greg has made since November 2023. The goal of the video is to present Greg as the new face of ALS, showing that the disease can lead to remission and improvements, rather than the old narrative of decline. Greg shares his progress, explaining that he can now do household chores, cook, and grill without assistance. His voice, which was previously weak and limited, is now clear and understandable, allowing him to communicate effectively in various settings. Additionally, his fine motor coordination has significantly improved, enabling him to perform tasks that were once impossible.

00:05:00 Greg shares his experience of using a special controller to play video games and the improvements he has made in his daily life. He mentions that he was previously unable to walk upstairs without difficulty, but now he can do so without stopping. Greg also discusses his independence in performing chores and taking care of himself. The improvements came about through a strategy that addressed underlying triggers, including the ASITE protocol and ineal stem cells. The video aims to show the progress made by people with motor neuron disease or ALS, reframing the disease's perspective and giving hope for ongoing improvements. Greg's symptoms had been present for four years, and the process took ten months, but improvements were seen throughout.

00:10:00 Amy discusses the importance of mindset, diet, and not giving up for individuals dealing with motor neuron disease or those who have a loved one with it. They emphasize the impact of depression and anxiety on the immune system and how giving up can negatively affect it. Greg shares his personal experience of dealing with chronic infections and the challenges of managing them with a depressed and anxious immune system. He encourages viewers to focus on improving their mindset and making necessary lifestyle changes, such as setting boundaries, practicing meditation, and cleaning up their diet. The speakers emphasize that getting better from this disease requires hard work, dedication, and commitment to making positive changes.

00:15:00 Greg shares his experience with improving his health by making lifestyle changes and educating himself about unhealthy foods and household products. He mentions the importance of avoiding seed oils, checking restaurant ingredients with the Seedo Scout app, and avoiding room deodorizers, perfumes, and candles due to their contribution to poor air quality and inflammation. Greg also emphasizes the need for a medical strategy and personal commitment to making lifestyle adjustments in order to effectively manage his disease, which he believes is treatable and responds to the right combination of treatment and lifestyle changes. He encourages viewers to focus on getting better and envisioning their own improvement, rather than relying on external factors or rhetoric.

00:20:00 Greg shares his experiences with various approaches that have shown improvement in his condition, including cannabis oil, functional mushrooms, and the Stam Stack. He started incorporating CBD, THC, and medical mushrooms into his routine around March of the year, and credits these additions for the support he has received. Greg emphasizes that as a medical clinic, they are not making claims or recommendations but personally, he has seen significant benefits. He also mentions that they focus on strategy, running labs, and figuring out a strategy rather than strict diets or a large number of supplements. Greg concludes by encouraging viewers to stay tuned for future videos and sharing that he was once in the full picture of someone with ALS with symptoms for four years, but now appears very different, marking a new era and face of ALS.

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