Chronic “Lyme” is always associated with co-infections. A lot of people have very serious systemic infections that go undiagnosed due to not testing positive for the “lyme” bacteria. Many go untreated because medicine doesn’t want to deal with the diseases it’s created. These diseases are ultimately created by drug resistance brought about by over drugging with pharma that destroy the microbiome in numerous ways. Many people do not succumb to the same micro-organisms if their pharma histories are minimal....

Why did I mostly stop writing? Because I was dealing with something I no longer knew how to talk about. Mostly because people really don't like reading about disability. All the able-bodied ableists who want to pretend that somehow disability must be the fault of the person suffering from it. Yeah. Lots of my readers too. The comments became unbearable and remain that way. I mostly keep them turned off. I've written a few new pieces on my own idiosyncratic experience of TD. I thought I'd share with you Robert Whitaker's long and well-researched piece. (continue reading, click through)

I have gone to practitioners but, Ayurveda, at foundation, is about learning to listen to your body and know how to feed it, move it, rest it and take care of it as needed. That is always our job in the end. I never found a practitioner who could deal with my extreme and multiple issues either. I couldn't even leave my house for 5 years as I was bedridden. I started these practices on my own at home in my bed. I am no longer bedridden. I am no longer nonverbal. I still have tardive dyskinesia and I still love Ayurveda with a profound gratefulness as it helped me be in touch with my body. This is good stuff for anyone in life at anytime. ...

Tardive Dyskinesia is brain damage. It is a medically induced (iatrogenic) INJURY caused by 500 different drugs often used in psychiatry, gastroenterology and Parkinsons. People are rarely told of the risk. It's often referred to as a side effect of the drugs. This is offensive. A side effect is not a crippling life long disease... Continue Reading →

I've posted a couple of times about having TD. It is an awful debilitating, crippling and disfiguring disease caused by iatrogenic injury. I just discovered the National Organization for Tardive Dyskinesia so I thought I would share. There is very little accurate or clear information about this disease. I have avoided doctors mostly as I've not encountered anyone that seems like they would do anything other than harm. Neurologists who treat TD are prone to use psych meds and the MDs I saw mostly shamed and dismissed me as crazy. I did have a psychiatrist who was also a friend diagnose me and it's very clear that I have TD. I go from being physically okay to being able to hardly stand up in the same day. I suffer from acute and chronic pain in my face, head, neck and shoulders. I am often totally unable to function as a result of this drug injury. I've written very little about it because this site was about recovering after coming off psych meds and well, I've got my mental health but I am not well. It's likely I will never be well. My only goal now is to learn how to cope better. As readers of this site know I've exhausted all manner of behavioral and lifestyle healing methods. This is not an easy ride. (click through for more)