Lyme disease treatment

Hi, my name is Ashley Campbell and my daughter’s name is Tuesday. She’s 13 years old and has been battling Lyme on and off for 7 years. Some years have been okay and some years have been unbearable. Her Lyme was in remission for a couple of years until Covid hit. Covid is notorious for bringing viruses out of dormancy and she’s been living in hell ever since. She’ll have days she can’t walk or even stand without support. She has tremors, fatigue, vision disturbances, nerve pain, joint pain, muscle pain, headaches, vomiting, fevers, hot flashes, high resting heart rate, heat intolerance and will collapse on bad days if she walks too far. She was recently diagnosed with connective tissue disorder from Lyme dissolving her collagen and then colonizing in the tissue. We have tried every treatment you can imagine and more. Her body either doesn’t respond or rejects it completely and symptoms come back twice as strong. My husband is working 100 plus hours a week and I’m staying home to care for her. Insurance doesn’t cover any of this. We have maxed out credit cards, taken out loans, and are selling everything we can. But this disease is relentless and is completely draining us. There is a treatment facility in Franklin, TN called Biologix Center that has a 92% success rate with Lyme and it may be our only option left in the United States. They have two plans. If she needs to stay for two weeks, it’s $12,500. If she needs to stay for three weeks it’s $18,100. We have been very hesitant to ask for help because that’s not who we are, but we are running out of resources and our daughter really needs help. Anything is appreciated beyond words. Thank you so much.