Michael getting major improvements in ALS Lou Gehrig's disease at BodyScience life June 2024

History:
End of 2021 Covid infection followed by significant post-covid fatigue and “alarming pulses/electric shocks in brain”

Oct 2022 Rt
Lt Neuropathy in soles of both feet. Started in sole of Rt foot first just behind the toes then began on the left side only at night time. Initial fall. November/December 2022 – Increased falls. Right leg “giving out”. Tingling in both feet worsens, weakness right leg

January/February 2023
Foot drop on right side

May 2023
Brain fog and fatigue worsened substantially. Twitching/fasciculations started in upper/lower limbs

June/July 2023
ALS Diagnosis

January 2024
initial visit to BodyScience

June 2024 video of this interview
June 2024 Improvements:
improvement in volume and tone of voice
self-reported improvements in breathing
able to “stand” with less assistance and move feet
significant decrease in brain fog
increased energy – able to go out multiple times in a single day
Caregiver findings – easier to lift, less assistance required

At BodyScience, we have been working with ALS since 2019. That is when we had our first reversal (we have had three more since). Over the past 4 years, we have been developing and refining our strategy and therapy targets.
During 2021 until 2022, we focused largely on pathogen control including Lyme, Herpes viruses and other infections. In 2023, we combined that pathogen “kill strategy” with a regenerative focus aimed at repairing damaged neurons rather than simply eradicating the infections.
Mid 2023, Amy developed three Glial Cell focused approaches to support Motor Neurons. The Astrocyte Protocol is one of them.
Amy also developed several new stem cell technologies, again, focused on repairing post infection rather than just pathogen eradication.
The Astrocyte Protocol was launched in November 2023 and has shown remarkable, lasting benefits.
This is NOT an FDA approved therapy for ALS, we acknowledge that results vary. This video is for educational purposes only. It is not intended to make any claims or to provide medical advice. It would be our hope that therapies for ALS become more widely available. If you are an academic center interested in working together to make this and other treatments accessible and affordable, please contact us.

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