Experiences with

Amyotrophic lateral sclerosis (ALS)

(ALS).

RELYVRIO (previously known as AMX0035 in the U.S.) is an oral, fixed-dose combination therapy for the treatment of adults with ALS RELYVRIO significantly slowed the loss of physical function in a randomized, placebo-controlled clinical trial in ALS https://www.alzforum.org/therapeutics/relyvrio

https://www.google.com/amp/s/www.hurriyetdailynews.com/amp/turkish-scientist-works-on-cure-of-als-with-celery-180151

https://www.healio.com/news/neurology/20230207/athira-announces-clinical-trials-for-alzheimers-parkinsons-als-treatments-in-2023

Last year, I was diagnosed with ALS. I went to Mayo for a second opinion and it was determined I do not have ALS. The doctor stated I have tremors from anxiety and possible drug prescriptions. I followed up with my doctor upon my return home and we do not feel it is prescription related.

I know it is for ALS but it gives me hope that AI can deliver so fast. https://www.vergegenomics.com/news-blog/verge-genomics-initiates-first-in-human-dosing-in-phase-1-trial-of-novel-therapeutic-for-als

There is a Parkinson's/ALS/Dementia syndrome. Smell loss isn't a part of ALS. Curious to see the results. https://www.michaeljfox.org/smell-loss-brain-health?ps_cid=fb-a1b1R00000AQ7sB

Denali Therapeutics Announces Key Anticipated 2023 Milestones for Its Therapeutic Portfolio for Neurodegeneration and Lysosomal Storage Diseases January 9, 2023 Four programs expected to progress in late-stage clinical studies for MPS II (Hunter syndrome), ALS, and Parkinson’ disease More here :

Hi everyone, we are MASSIVE fans of Chicago Med and in one of the latest episodes a patient has MND/ALS (and I know we're all here for PSP/CBD), now he has a cold/chest infection and he's using a Voice bank/computer to relay his wishes to the hospital doctors.

Recently he believes he has ALS. Panic attacks are ongoing and affect every part of his life . He's been dxd with social anxiety, ADD, OCD. He is so super awesome and doesn't deserve to live his life like this. He has had years of therapy.

Do we really have any drugs that can stop ALS progression?

Paternal uncle: ALS. Brother: Colon Cancer. Me: PCa. If it is environmental then maybe we need to move.

Parkinson's disease is a smouldering campfire - ALS is a raging wildfire. How does glyphosate travel to the brain? Small incremental doses from eating contaminated food are enzymatically transported by the vagus nereve via the gut/brain axis. The result is a smouldering inflammatory process.

Abs lymphs (ALS) were 82K in July. Got 1st Evusheld 8/23. Got Covid 8/31 and started Paxlovid same day. 5 days later, 9/5, felt great then went on a vigorous 31 miles bike ride (probably too soon for such exercise). Then rebound on 9/12 with positive home test.

It is also under development as a medical countermeasure for nuclear and radiological emergencies and as a treatment for neurodegenerative diseases like Parkinson’s and /MND.

Neurological condition, Parkinson, ALS, you name it and I thought it. I come to realize that since I walk so much and eat basic healthy. It could be I'm low on magnesium. I stopped into walgreens and talked to the pharmacist. He recommended Calcium and magnesium.

I think regardless of the countless neurologist who say I don't have als every time I feel the muscles go missing or won't engage I ho into panic Then I get huge depersinalization and derealization that happens and just lose my mind crying. I am a 39 year old male by the way.

This specific time, Ive been dealing with twitching muscles for no apparent reason but of course my anxiety takes over and creates a narrative that I must have ALS.

Furthermore, data from phase II clinical trials have shown TUDCA to be safe and a potential disease-modifier in ALS. ALS is the first neurodegenerative disease being treated with hydrophilic bile acids.

After reading this article, the notion that Parkinson's disease is idiopathic and Alzheimer's disease and ALS/MND have no known cause is ludicrous.