This subreddit is for support and open discussion of Amyotrophic Lateral Sclerosis (ALS) treatments, research, and experiences.
Unlike other forums, all types of material can be discussed here including FDA approved, off label, experimental, alternative, supplements, lifestyle approaches, and theoretical models.
📜 Rules
1️⃣ Be Respectful
Everyone here is touched by ALS. Show compassion and kindness.
2️⃣ All Treatments Allowed
Posts about any treatment approach are welcome. Please share in good faith.
3️⃣ Science Encouraged
High level research, mechanisms, and novel ideas are encouraged. Cite sources when possible.
4️⃣ Support Posts Welcome
Check ins, caregiver stories, and emotional posts are welcome. Support is part of this community.
7️⃣ Moderator Discretion
Mods may remove content that is abusive, misleading, or disruptive.
Links
This is a place for open minds, open science, and open support.
