After going into ER in 2015 with nerve shooting pains in legs and back skull area, fever, severe headaches, numb arms/hands/feet, after a embedded tick was removed I was turned away with no tick tests because I didnt show a "typical rash" at first. Now almost 2yrs later, I have been suffering with significant symptoms including a POSITIVE Test for anaplasmosis tick disease, diagnosed with 7 liver tumors and 1 complex cyst that developed, loss of hair/appetite/weight loss, overheating in face and rash over legs and neck, pain in stomach, sensation loss in arms and legs, losing memory, emotional instability, dizzy spells, irregular painful menstural, and horrible skin issues just to name a few...I have been seen at my ER numerous times and then sent to Mayo clinic with STILL NO HELP OR TREATMENT for my late stage lymes. I need help from an out of state Lymes doctor that has successfully treated other patients dealing with the same patterns I have went through. I am a divorced single mom of 6 on one income and cannot afford the out of pocket costs that us lymes patients are stuck with because lymes literate docs due to controversy in the medical field and lack of knowledge cannot accept insurances because lymes is still not known to be "chronic" or not and most think a short term antibiotic is a cure all. This is only the case for early stage lymes not late! My hopes is that through this campaign I can fly out of state to get to a doc that knows how to treat my situation safely and fly me there and still be able to pay my bills back home so my kids and I dont lose our home or my lack of income due to time of work.