Seeking Support and Awareness for Rare Dust Mite Acariasis

Hello everyone,

I am reaching out to this community in hopes of finding support and raising awareness about a rare and debilitating condition I am experiencing, which I believe to be a severe form of dust mite acariasis. My situation is unique and goes beyond typical allergy or dermatological issues. Here is a detailed account of my journey:

Initial Symptoms and Infestation:**

Over a year ago, I began experiencing unusual symptoms that progressively worsened. Despite vigorous daily cleaning, my home became extremely infested with microscopic acariform mites. These mites are not just present in my environment; they are entering my body 24/7, even when I am in public. They have completely taken over my food, making it difficult to eat at home. They also attach themselves to my father, who inadvertently brings them into the house from his daily activities.

 

**Physical and Neurological Symptoms:**

I first noticed a wound on my back that wasn't healing properly and felt movement in that area and throughout my body. My symptoms have since escalated to include:

- Almost complete loss of consciousness due to severe lightheadedness

- Intense headaches and fever

- Neck pain and chest pain

- Vision problems

- A sensation of spider webs blowing on my skin

- Hearing splitting and crunchy noises in my head, coinciding with the movement of the mites

 

I believe these symptoms may be indicative of neurological damage caused by the mites.

 

### Medical Documentation and Challenges

 

Despite multiple visits to emergency rooms at UMMC, St. Dominic, and Merit Health, I have not received the proper testing or diagnosis. My symptoms have often been dismissed as psychological, but I am certain that what I am experiencing is real and not a hallucination.

 

### Seeking Connection and Support

 

I am sharing my story to connect with others who might be experiencing similar issues and to raise awareness about this rare condition. If you or someone you know is dealing with similar symptoms, please reach out. Together, we can support each other and advocate for better recognition and treatment of this condition.

 

Thank you for taking the time to read my story. Your support and any information you can share would be greatly APPRECIATED.