CHS Survivors: It’s Time to Turn Our Pain Into Data
For too long, Cannabinoid Hyperemesis Syndrome has been dismissed as "just a stomach bug" or "all in your head." We’re changing that. I’ve just launched a new community for CHS survivors, and our first mission is gathering real-world data to help researchers understand this condition.
If you’ve lived through the cycles, the ER visits, and the "hot shower" phase, please take a moment to add your voice to our community survey. Your experience is the evidence we need.
This survey collects data on CHS symptoms and recovery to aid patients and doctors in understanding and treating the condition. Participants can contribute to mapping recovery timelines, proving the effectiveness of treatments, and identifying triggers. The survey emphasizes privacy, ensuring all data is anonymous.
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