Hi and welcome to the inside scoop on what I have been going through. Diagnosed with Lyme disease in 2018, it took nearly two years to find an infectious disease doctor that would take on my case. Diagnostics and treatment started in 2020. My case was determined to be chronic with a permanent immunocompromised status. This disease is very advanced and continues to plague me with complications, slowing progress. These last 5 years have been especially hard, but I’m still here. Financially this has ruined me and the surge in cost for my insurance and meds have put me in a dire predicament that is no longer sustainable. Any help would be appreciated. Even if it’s just sending me food. ❤️