What are the chances of my Lyme not going away?

Before I ask my question I'll explain what I've been through. Sorry if it's a bit excessive.

Around Mid July of 2015 I began having issues with joint pain in my left knee and ankle along with foot drop and swelling. I wasn't able to walk and it felt like someone was digging razors into my skin when touched. I had a doctor that tried to diagnose me with MS but after my mom pushed for the Western Blot to be done and the result came back with Band 41 for the flagella as present. The doctor then gave me Doxycycline for two weeks and in that time I also started physical therapy after going 6 weeks of not being able to walk or work. After the first week of Antibiotics my sensitivity went down to my mid shin and my doctor claimed it wasn't Lyme otherwise I would have been better already.

I've been through a lot since then, we switched doctors and found a LLMD who also prescribed me Azithromyacin to go along with the Doxy. My left arm began to show the same symptoms as my leg around the time I met with my LLMD and I also met with a neurologist just to be on the safe side. I had to go from Azithromyacin due to the fact that every time I took it, it gave me diarrhea( Sorry TMI.) to Ceftin. The Ceftin made me so nausea's that I was bed ridden and couldn't go to physical therapy which made me feel worse, and I couldn't even attempt to try detoxing. My family doctor prescribed me nausea medicine which helped me take my antibiotics along with begin detoxing the way I should have in the beginning if I knew what was going on.

The symptoms of joint pain moved to my lower back and right leg around Christmas of 2015 and my LLMD suggested that I stop the Ceftin. The symptoms went away and I began feeling better while I continued taking the Doxy. along with a transfer factor and taking various vitamin supplements. about mid January the day before the full Moon and a major snow storm my mom and I went to our local supermarket and I was trying to talk to my mom to let her know we needed more peanut butter. Thing was, I couldn't say the word Peanut butter. I knew what it was in my mind, but I couldn't form the word. As I tried to speak or find a way to let her know what I was talking about my head began to hurt on my forehead and my right temple. The harder I tried to speak, the worse the pain got. After leaving the store with all the things we needed ( I was able to let my mom know you use peanut butter for toast so she knew what I was talking about) I began to stutter and zone out like I was extremely tired. I had a couple of episode before this, around 11:00PM where basically the lights were on but no one was home. My mom contacted my LLMD due to the fact that my head started hurting more and I had slurred speech to go along with a stutter. My parents took me to the Emergency Room on my LLMD's recommendation due to the fact that it could be the sign of a stroke or the Lyme moving to my brain. BY the time we made it to the E.R I couldn't speak.

They ran CT scan for stroke and an MRI on my brain and ran blood. All good, so they gave me I.V Rocephin and within about 30 minutes to an hour later my speech was back to a stutter and I could form words with my lips.They kept me over night and were planning on doing a Spinal tap to double check the diagnoses of Lyme, But since I was doing better they released me as long as I promised to see my family doctor and neurologist as soon as possible. I was able to speak but with a very bad stutter, but I would make fun of myself so there wasn't any worry about me being to blue. After we were home a day later I had an anxiety attack and had a lot of issues with those until I saw my family doctor and was prescribed Clanozapan. Luckily soon after that I saw my LLMD and they prescribed me Minocycline and Cipro (which is know to cause tendon rupture) and after beginning those two antibiotics my speech improved along with my every time I attempted to speak. Of course I began having tendon pain and as per my LLMD's instructions I stopped taking the Cipro.

I am doing a lot better, I no longer have any more anxiety attacks and I only have joint pain when I get cold just as today I am having some pain in my hip for some reason. My family doctor went ahead and cleared me so that I can return to work after months of not working, and I am also looking forward to starting college in the fall semester so I can get my general's done and hopefully become a registered dietitian.

I know that a lot of people are considered in remission or cured after two full moon cycles of no new symptoms or old symptoms resurfacing. Mostly due to the fact that the bacteria reproduces every four weeks if I am not mistaken.

I'm terrified that I am Chronic, and I know many people live with Chronic Lyme. I don't know the exact time I was infected so I can't know for sure. But What are the chances that my Lyme won't go away? Every day I try to be positive, but I can't help but think what if?

Thank you Girlie for responding.

I officially started antibiotics in September, 2015 to present time.

So, you're doing better, but still have a few symptoms?

Are you still taking the minocycline?

Your post was fine...I just wanted clarification..that's all.

Okay, so you're continuing to take minocycline daily.

So, with Vital Plan, you are taking the Cat's Claw and Japanese knotweed?
(Those herbs are good for LD)