I live in a medically rich area in NE . I nearly died from Mold illness . Not ONE MD knew anything about biotoxin illness . so ? There are no local " Medical providers " to consult. I still live with exposure . I am no longer in the new Apt . which nearly killed me. I am however still exposed to mold . Not as sick but still sick. Housing in the N E is almost all moldly .Functional MDS are mold literate . At $500 etc per visit ? This artist is on her own. I mention these issues because your info is great but housing is an issue for EVERY * Moldy * I know . Housing shortage . Rents doubled. Leaving is rarely an immediate option unless you have support. I've healed thru orthomolecular . Hepa filters . I had 30 % lung function for 16 months and not ONE MD knew what was causing it or *what * to do. This is largely a silent pandemic. Unless patients can find mold literate Allopaths , w/i the health care system ? We are on our own. Thanks for your advocacy. !
Sorry this happened to you. 😢I am in the same boat. Bought first home that sellers KNEW but didn't disclose extensive black mold issue. I almost died. That was 2018. I have moved 3 times since, lost two cars and an rv along with most of my belongings, financially and socially devastated and still being exposed!! The housing crisis is making things infinitely worse. I am working on developing a project to address this all, but in survival mode with symptoms most of the time so it's difficult, but we all deserve better!! Mold is the true pandemic and it's killing and ruining lives!! We need safe housing NOW!
My child and I are living in mold. I've contacted the board of health, and they confirm the mold. My landlord won't fix a thing. My question is, are the urine mycotoxin tests accurate? Thank you
They can be. But to make sure they are, it is good to take some glutathione before to help the body excrete the toxins. However, if you are in a moldy house, there is 100% chance these toxins are in your system.
Unfortunately, I can't move, and have been living with mold for several years now. I did have a remediation though. I have MCS, and I am homebound. What are the main things I could do to support my system? I have had some Nervous System work, which helped a lot (somatic experiencing). What if someone can't move because they're too sick, or whatnot. What are some tools?
