Joe A.,

If you haven't already looked into Ginkgo Biloba Extract, you might give it some consideration.

https://pubmed.ncbi.nlm.nih.gov/26979525/

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494382/

Art

For anything that is inactive during sleep, I would use castor oil packs.

TD is a symptom, not a "disease", treat the cause, probably some sort of toxin or infection, or probably both. Use MMS (chlorine dioxide) follow the protocols, it might be months before it gets all the infections and toxins out, but keep at it.

Just a quick answer, until I have time for more. I have experienced this with my son. Truehope, Empower Plus vitamins. I ignored it for a while, not believing it could help, but it did. Call them, they have counselling and experience and will do their best to help you both.

I read this on a website for people who have tardive dyskinesia

Resources to Help You Live Better with TD

Living with tardive dyskinesia can be lonely. Ashamed by the jerky movements, some people with TD become reclusive, avoiding social gatherings and being seen in public places. Connecting online with others that live with TD can be a profound experience and an excellent source of friendship and support.

Support groups are very often the best way to collect names of experienced practitioners, effective treatment information, and tips gleaned from lived experience. Here are some organizations to reach out to:

The National Organization for Rare Disorders (NORD) is loaded with helpful information on a host of rare diseases and since 1987 has been helping people pay for life-saving or life-sustaining medication that they couldn't otherwise afford.

The CureSZ Foundation has created a Tardive Dyskinesia Expert Panel. Persons with schizophrenia who are experiencing TD can use the panel to find a clinician and obtain a second opinion about medications and courses of treatment.

TD Support Groups on Facebook

• The Tardive Dyskinesia Group
• The Tardive Dyskinesia Awareness Group