Re: I’m confused

Forgot to add — my physician thought about adding ivermection, but decided against it as it often doesn’t work a second time. So she is saving it in case I need it later.

In addition, while she has treated numerous covid patients successfully, she has one patient using Ivermectin for long term treatment (months) and insurance is pushing back. She said I need to be on medication long term (for six months after my skin clears) to address long term risks of neurological effects and possible hard to treat “cancers”. As anyone with this disease knows, the brain fog is as troubling as the skin symptoms. While my lyme tests were negative, as was a test for aspergillus mold, it is assumed an unknown spirochete bacteria is present.

So you DO need to see a doctor for a long term Antibiotic prescription.

Bacteria can also form stubborn biofilms. So, whether we are empirically addressing a bacteria (fenbendazole helps break down the biofilm), a parasite (which carries bacteria), or even a virus, this approach is a broad one. I first saw my physician monthly, and now quarterly, for follow up. Her expertise has been incredibly helpful and I am one of the very few lucky ones to have my doctor’s support. So I feel obligated to share. She combines both standard and alternative treatments with her patients, and as a practitioner of functional medicine (who she says recognized Morgellons 10 years ago!), her primary concern is effective treatment (vs. long theoretical discussions). I find myself similarly frustrated with people who want o study morgellons forever versus jumping in and devising a treatment, which certainly can evolve. People are suffering, and their disease is progressing. While the approach I am on may not ultimately be the optimal treatment, it is reversing the disease and I am healing. Healing takes time; and time takes time. By sharing, I do hope someone can take this and even improve upon it. Sharing adds to our collective intelligence. God bless. Tweet