6 / 28 / 2020Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â Â ENTRY TWO
It is a little ridiculous the way things work out sometimes in life. Ridiculous as in… uncalled for, extensive, unnecessary, crazy. I have always been in perfect health. There was that one time I had cat-scratch fever when I was a kid but other than that I never had any issues, never broke any bones. We thought my chest pain way back in 2015 was just leftover remnants of grief, because my mom had a similar pain ever since we lost my sisters a few years before. I was told it was anxiety, figured that my stress as work was considered just that, along with eating too much pizza and called it a day. It no longer started to make sense a year and a half later when the pain increased during my most mellow of moments and all I felt like doing was napping. Sure, every college student loves a good nap, but that just wasn’t how I rolled. Naps were for the weak, I could get so much done in the time of a nap. Yet I always felt like I needed one.
Low and behold, we gave up trying to reason with it and just decided to go to the doctor and ask about it again. Oh, and maybe run some tests just in case. All the basic ones. If we need to do more then we’ll figure it out. We didn’t need to. The last test that came back showed that I was positive for a local happenstance called Lyme Disease. I got the call while I was driving on my way to work in Bangor. I kind of freaked out. Called my mom afterwards and cried over the phone a bit shaken up, mostly because I didn’t know what it meant. I use to think that I overreacted because most of the time a little thing like a brief disease from a tick was just a handful of days worth of pills and you’re done. I wasn’t done. In fact, we screwed up. I took those antibiotics and, without realizing it, woke up the rest of the disease inside of me that was dormant for years. I was down for the count. Well, not really, not yet.
A lot of doctors don’t understand Lyme. They just don’t. My pediatrician didn’t. My mom didn’t, not that she was a doctor but a master researcher. We tried so many things for 10 months. Crazy things. Ridiculous things. Almost more ridiculous than the disease itself can be. Almost. Essential oils, salt and vitamin C, cannabis, GI health supplement program. Nothing worked. Nothing made anything better. I got worse actually. In the fall, I went to the ER twice because of extreme stomach pain but no one could tell what was wrong. That was because you can’t really see an over abundance of bad intestine bacteria with ultrasounds or a CT scan. My mother, a master researcher as I must repeat, got me in as one of the first patients of a new Lyme clinic in the town over in December of 2017. This doctor, let me tell you, is my favorite man on earth.
I didn’t go back to college that spring. Finally I was down for the count. Treatment sucks. It really sucks. The way herxing works is that you take your medicine and slowly increase it over time. When you increase it, all your symptoms increase by tenfold for a short while, killing off the Lyme bacteria quicker than your body can process the toxins their death releases. In the end, you feel worse in order to feel better. Herxing isn’t meant to last long. You have your period of misery and you’re suppose to feel better than you did after the herx than before it. Not only that, but I had to change my entire diet due to small intestine bacterial overgrowth from that absolutely ridiculous pyramid scheme health program. I’m still bitter about it. I’ll probably always be. Had to drop so much money on an antibiotic that was literally sent from God Himself. I did get better.Â
I went back to college in the fall of 2018, ready to take everything back on. Keep on keeping on really. I was always cautious of not doing too much otherwise I’ll get knocked down again. But here’s the thing about New England. We have old buildings. Old buildings include this lovely stuff called mold that can make one’s life miserable if your immune system is already compromised. I was feeling great, better than I had for awhile, but the longer I was back at college the worse I started to feel. I had to go home in the spring, finish my schooling and rest. Graduation consisted of so many tears but I’m glad I pushed through. Glad it was over though I was sad.
It was officially time to get to work. Heal from mold exposure, heal from Lyme, and take my life back from this disease that just kept hanging on. Doctor and I hit the ground running this past winter. Once I finished the protocols from mold detox we increased everything else so that I could be free quicker, sooner, and more efficiently. It was rough but in the end it was so worth it. In April, I started taking my physical well being back into my own hands. Exercising consistently for the first time in three years. Bread, sugar, coffee have returned to my diet. As of now I have been free of all Lyme supplements for two months. Aside from my sprained foot... I have been healthy and able to work consistently without struggle.
Now there’s a lot of things I’ve learned in this time. I can’t tell you the amount of times I went up to the altar at church, at camp, at college for healing. Going to a Pentecostal college where they preach healing with the laying on of hands and that all you need is to have faith that God can do it... truly gives you the right environment. I read books. Memorized verses. But in the times where it was really bad, I was confused as to why God didn’t or wouldn’t heal me. I still don’t quite understand why He didn’t heal me during those other times and I could have received my Bachelor’s without problem, where my dad could have saved money instead of going into debt. But God works in mysterious ways and if there is ever a more true statement... I honestly doubt it.
Lean on Him. Lean on Him even if you don’t get it. Lean on Him even if you think you know the better way and everything is crashing around you. There is no other force that is more stable than Him. I vented to Him often. I know we’re suppose to have reverence for God and respect and fear, which I do have all those things, but sometimes there would be a day where I just had it and told God how I really felt. Even when I yelled at Him, He still comforted me. There’s a peace that passes all understanding, literally. And it’s because of this experience with Lyme that I learned new ways to trust Him, to be guided by Him and to listen to Him. To find hope in hopeless, suffocating places. So maybe there were a few reasons why I wasn’t healed on the spot, who knows but God?
The other week I put the box away. The box I found in the school’s “blessing room” of free stuff that I stored my supplements. The l leftovers and the medical papers all went inside and I put it up in my closet. I did it on the anniversary of Bailey’s, my sister’s, death. Right now I think it means a bit more than what I currently understand. Okay God. I’m ready for what’s next.
                                 --Amberthyst










