I received an email from the place I got diagnosed saying they would never share diagnosis results voluntarily, and would not give access to those results, without a legal battle. Their stance is that their patient’s rights fall under HIPPA and applicable state privacy laws, making them confidential. They sent out a statement saying they do not support any kind of registry that lacks full informed consent, and that they stand with the neurodivergent community.
Based on the wording the hitlerites in the gov’t are using to describe how they’ll get our data, it might actually be through medication, vaccination status, and disability claims on medical records, but don’t quote me on that (and please fact check me if I’m incorrect, I’m pretty tired rn).
It scares me that no mention of protecting minors’ privacy and safety are being mentioned much. I can’t imagine how scary this must be for younger folks right now. Stay safe out there, and keep your wits about you.
I received an email from the place I got diagnosed saying they would never share diagnosis results voluntarily, and would not give access to those results, without a legal battle. Their stance is that their patient’s rights fall under HIPPA and applicable state privacy laws, making them confidential. They sent out a statement saying they do not support any kind of registry that lacks full informed consent, and that they stand with the neurodivergent community.
Based on the wording the hitlerites in the gov’t are using to describe how they’ll get our data, it might actually be through medication, vaccination status, and disability claims on medical records, but don’t quote me on that (and please fact check me if I’m incorrect, I’m pretty tired rn).
It scares me that no mention of protecting minors’ privacy and safety are being mentioned much. I can’t imagine how scary this must be for younger folks right now. Stay safe out there, and keep your wits about you.