Lyme Disease CIRS Medical Expenses

My name is Tyna. My story is long. We believe i had a possible tick or insect bite around 2008-2009. It was not diagnosed as lyme until 2015. I have had many difficult years with MANY medical expenses. Recently in 2016-2017, things took a turn for the worse and it entered my neuro system pretty aggressively. I began having trouble with daily functions like walking, cooking, driving, etc. I had two hospitalizations in June 2017 and 2 weeks of daily IV Rocephin treatment in July. I have made some progress THANK God, it is slow going right now though. I still am having massive histamine responses and can only tolerate 7 foods. I also am dealing with massive GI issues and  possible ulcers yet am allergic to many of the medications for these issues. Also my balance and feelings in certain parts of my body have not completely returned yet not to mention massive anxiety from this unsettling 24/7 vertigo feeling for 8 months. Lyme disease is very tricky as some may know, so conventional western medicine does not have a cure for 'chronic' lyme as of right now. I also have to pursue lyme literate drs, alternative healtcare practioners and energy workers to help with different aspects of this illness. NONE of the just mentioned are covered by insurance. As difficult as this is to reach out like this, if you happen to read this and feel like contributing, it is greatly appreciated, as my expenses have been phenomenal this summer from bills to help eradicate or greatly reduce the  lyme bacteria/virus's numbers. I am confident i will prevail through these stormy seas and i thank you so very much for your help on this difficult journey.