I understand its not a full agonist, but didn’t realise it was Mild… can you send me some info or studies on it only being ‘mild’ and not activating opiate receptors? I ask Because ive had some serious nods off high doses that Im certain wouldn’t occur if it was just a ‘Mild’ partial agonist. That being said I completely agree with the sentiment and the thought behind it, and I will definitely er on the side of caution. Thanks for your input and sorry to hear of your losses 🙏