The seemingly never-ending journey that every chronically ill person has to wade through. 🙅♀️🤷♀️
I've been fighting the Lyme battle for quite some time, which means that at some point I've tried almost every diet under the sun. Gluten-free, fat-free, dairy-free, vegetarian, vegan, paleo, keto, you name it... I've done it. It can take quite a while to find out what works best for you in the realm of food, and there are so many different nutrition theories that are constantly telling you what you should or shouldn't eat. I've learned that diet is different for everyone and that one man's food is another man's poison. For me, I eat organic, and I've completely cut refined sugars from my diet. And that's how I eat so I'm not sick on a constant basis!
I've discovered a weird social quirk through all this "dieting" business though, and that is that a lot of people often feel uncomfortable when you choose not to eat at any social event that involves food. I've often had people make comments about my weight or about how I can't just think I'm better than everyone else because I eat differently. Honestly, I do not think down on people for what they eat, and when I talk about my diet it's because I have a passion for health and wellness, and I'm seriously just trying to stay alive in my Lyme battle! 💪💚❤️😁
Comment down below what you eat to manage your illness, or if you have any funny stories about people jumping to conclusions about your diet! The more we share, the more we can care and understand where others are coming from!
The process of emotional detox that weighs in your stomach and makes your heart physically ache.
So often people who suffer from chronic illness are misperceived to be "negative" or "attention seeking" because of the grief that comes with the trial. The truth is that I generally consider myself to be a happy person, but I've lost SO MUCH in my time of illness. I've lost people I love, and I've lost some of my dreams and aspirations and my ability to achieve them. It's only NATURAL and HEALTHY to grieve. Grief just comes with the territory, and taking time to fully experience and feel those emotions is part of processing and coping with the pain.
The key that we all keep seeking for peace. The key is that we don't give up. In order to let go of the pain, we first have to allow ourselves to feel it. It's okay to take time to grieve and it's okay to not be okay. As we experience this form of pain we can come to a place where we can remember that there is hope and happiness ahead.
When you have a friend who is chronically ill, it's important to hold space for their grief with them. It's important that we don't constantly criticize because it seems like the negativity is frequent. It's important that we love those who are suffering so much that the love can heal the grief and we can be the happy and joyful people that we were meant to be.
Comment below if you experience grief with your illness and some of the things that help you through it!
Welcome to the beginning of Chronically Beautiful's "Chronic Illness Truth" series where we share bluntly honest truths with you about the reality of living with chronic illness! This series will serve two main purposes:
#1: The first purpose is to educate the healthy and help cultivate love, compassion, and understanding to the chronic illness community. The best way to help and serve others is by coming to an awareness of the suffering all around us, and the more knowledge we have, the greater our opportunities we'll have to help.
#2: The second purpose is to build the chronic illness community through sharing things that everyone can relate to so that nobody feels alone or forgotten in their chronic illness journey. Most of these truths that I post will be specific to Lyme disease, but I'm sure that almost anyone with any chronic illness can relate, and that will help us to make connections and form a greater community of support and understanding!
Chronic Truth #1:
It is very common for people to ask me what my illness is when they find out I have a chronic illness, and it's also very common for others to feel uncomfortable about asking. I just want to clarify that it's completely okay for anyone to ask about my illness. It doesn't make me uncomfortable, and I often enjoy the conversation that comes from that question.
One of the funniest things to me is when people mispronounce Lyme disease. Seriously, it's probably one of the easier illnesses to pronounce and yet so many people throw an S at the end of it! Go figure!
Believe it or not, I've actually had people ask me if my illness comes from limes, and it actually comes from a tick or any other biting insect that can carry the bacteria. It can also be passed down to your children, as is my case. My mom has had Lyme from a tick bite since she was nine, and therefore I was born with it.
It never ceases to amaze me how strong anyone with a chronic illness is. I've spent many a morning wondering how on earth I'm still alive after the night before, and yet I'm still here and I'm still kicking! I've seen this phenomenon among many chronically ill people. We truly are WARRIORS who fight long and hard for our lives, and as we do so we often feel worn down and exhausted from fighting the fight. Nevertheless, we value life, and we continue to fight in hopes that we can be healed and then help others on their healing journey.
Comment below if you've ever had someone mispronounce your illness, or if you're completely amazed at how you're still alive! And stay tuned for more of our Chronic Illness Truth series!
Lately, I've found myself pondering the pure and seemingly sparkling crystals that so frequently fall from the sky these days. Snow is a funny thing in that there is no one snowflake that is exactly the same. Each has its own Divine design, and the path that each snowflake takes to reach the ground is unique to that particular snowflake and looks different depending on its time and place.
Similarly, we as human beings walk different roads, come to different bumps and turns, and come equipped with our own unique design that God blesses us with when we came down here. I often wonder why my path in life often seems so different than other's may be... but then again I'm sure that all of us experience that daunting perception at some point in our lives.
With that in mind, I've watched many people suffer from chronic illness and the wide range of differences that come from being sick. This phenomenon is something that would do everyone some good if they took the time to look into the hearts and minds of these people who suffer on many different levels. The fact of the matter is that there are no two chronically ill lifestyles that look the same. We're all simply moving along on our own individual paths, trying to survive the best that we can.
The words "chronically ill" are usually accompanied by a substantial amount of expectations and perceptions from others. There's a certain "type" and "look" that apparently we're all supposed to have, but the reality is that some of us just don't have that "look" but that doesn't make our lives any easier, and it doesn't take our painful circumstances away.
The majority of people view illness by the book. When you're sick you lay in bed with body aches and head congestion while consuming large amounts of ibuprofen or Tylenol to relieve that pain and wait for it to pass. It may take a few days of discomfort, but it passes, and you move on with daily life. Others simply push past the pain and continue their daily lives and are lucky enough when their symptom cease, despite the need to persist in their prior commitments and responsibilities.
Now when you're REALLY sick it's a little different. When you're in unbearable amounts of pain, you rush to the doctor, load up on pain medications, and wait for hard-working health experts to diagnose and treat you. And after countless tests and hours, these loving and caring doctors treat you with medication or surgery, and you go home ready to recover and your pain eventually passes so you can live a normal life.
This is what illness looks like, right? This is how we manage our health and wellness so we can feel vitalized and renewed, right?
A flu virus is one thing, but being chronically ill is an entirely different paradigm that requires a lifestyle change and a realization that maybe being sick isn't what you thought it was in the first place.
Many chronic illness patients do spend a lot of time in the hospital, and many chronic illness patients do treat their symptoms with pain medications, which is definitely not something to downplay and consists of an incredibly difficult road. But my story and many other's stories are different, and that doesn't make any of our pain less valid or less painful.
What most chronic illness patients don't tell you is just HOW MANY doctors they had to go through in order to find one that would finally help. What a lot of us don't talk about is the PTSD that comes from how badly we're treated by people, and the desperation we all have to find answers. And what a lot of us don't tell you is that hope may not be found in a doctors office or in a medication, and that doesn't mean that we're crazy or that all of our symptoms are psychosomatic. It simply means that our path is different, and our answers are different.
I'm never in the hospital.
I've don't take any medications.
I treat my symptoms with natural food, remedies, and protocols.
And I never managed to find one doctor in my area that helped me very much.
And the things I'm doing now are HELPING ME TO HEAL!
My symptoms can range from tremors to being light-headed, to passing out after taking a shower, to skin lesions, panic attacks, extreme fatigue, and severe abdominal pain. But sometimes the pattern is that one day I can feel healthy and strong, and the next day I can hardly function at all.
Sometimes I feel like I'm losing my mind.
Other times I feel free and hopeful.
I pray every day for the feeling of the floor falling out from underneath me to cease, and for the grief that comes from illness to pass. Some days it does. Some days it doesn't. And that's just a normality for me and many others.
Chronic illness is a wide spectrum of struggle and perseverance, and there is no one size fits all. For some of us, it's doctors and hospitals on the daily. For others, it's constant protocols that never seem to end. And for others, it's diet change and learning how to be healthy half of the time and sick the other half of the time. For others, it's all of those things combined and it's often overwhelming and exhausting trying to keep all of the daily health routines straight.
Whatever it is, and no matter your place in your journey... your pain is valid and I urge you to heed not the expectations and perceptions of others who have never walked in your shoes. It would do the world some good if all of us could increase our love and compassion towards those who suffer in any way. The more we're aware of the suffering around us, the more empowered we can be to pull others out of the swamps and dark places that we all can find ourselves in.
Despite the difficulties and the struggles, there are some things that all chronically ill people have in common:
All of us are warriors. All of us have battled sore affliction. And all of us are beautiful, resilient people who are seeking to live life to the fullest and emerge out of the norm of society to bring light and healing to a world that craves those things. As we're sculpted into the warriors that we are, we're transformed on our path and seek to touch the world with our newfound being, just like the snowflake that travels to the ground to ultimately bring beauty into our lives and nourishment to our earth.
I sense extreme pressure that builds up in my chest and makes my nerves tingle from my heart all the way to the tips of my fingers. Pressure that makes me fear the future and gives me a severe distaste for my present. Pressure that brings tears to my eyes when I least expect it and leaves me looking at myself in the mirror wondering who that girl is.
I'm not completely sure where this pressure comes from, but I have a slight notion that it originates from past traumas. Memories of insufferable pain from Lyme disease for long nights. Recollection of people that I love making promises they never intended to keep. Thoughts of being hurt by the harsh words and actions of people who don't even seem to understand how much effect you can have on another's human heart. This odd awareness for past experiences flashes through my mind when I least expect it, and leaves me feeling like something inside me is crawling up my spine. I can't stand it, and for once I'd like to just be me and not have to worry about being crushed again by the insensitive human temperament that so many seem to possess.
I want my heart back, and I want to feel comfortable in my own skin again around other people.
When I'm occupying my own space, I get to experience a sense of acceptance of the girl that screams to be free. In my sanctuary, I have the privilege of being that girl that doesn't eat sugar and experiences a thrill from eating healthy food. I'm that girl that can sense things that others can't and is allowed to be highly sensitive to smells, tastes, sights, and the little beauties that are all around us, and it's not crazy, it's insightful. I'm that girl that sings her favorite song as she's walking down the street and wears maxi-dresses for no special occasion, just because she can. I'm the girl that jumps up and down when she gets excited over seemingly insignificant things, and I'm that girl that obsesses over to-do lists and loves schedules, but also loves feeling free as a bird! I'm the girl that never does anything half baked, and it doesn't matter if everyone else executes everything in their lives with half the effort, because she can be happy living in her full and vitalized life. I'm the girl that lavishes my entire heart in her endeavors and thoughtfully verifies that the beautiful living creatures that she comes in contact with can experience the intense Divine love that she can bestow.
I'm also that girl who can be smiling one minute with gratitude that she's not in pain and crying the next because coping with trauma from illness is SO HARD. I'm that girl that can laugh at the humor in life one second and be on her knees in prayer the next praying for release from severe anxiety and depression. I'm that girl that can be on my feet and doing yoga one day, and in bed with a heating pad hardly being able to move the next, because Lyme disease sometimes breaks you. But when I experience my whole being in a safe place for myself, I don't feel completely insane for the various and rapidly changing ups and downs. When I'm safe, I can accept that I'm just a girl with a chronic illness who is trying to learn how to heal to the best that she can and sometimes she's dissatisfactory and defective at it, other times she thrives, and that's okay!
In the presence of large groups of people, everything changes and I often find my indestructible and merciless brick walls building up around my heart as a protection against the naysayers. I often can feel the lock and key as I stuff my personality in a corner for the meantime. I often feel trapped to be like everyone else, and if a little part of me comes out it could be dangerous in the hands of people who disagree or misinterpret. I often find myself performing the act of the perfectly composed woman who wasn't just in excruciating pain the night before and can be wherever it is I need to be because I'm expected to be there, even if my body cries otherwise. Concealing my thoughts, holding my tongue, not venturing too close... Because if you unexpectedly get too close to someone who bites... you're left suffering on levels that they don't understand simply because they haven't experienced their severe adversity yet. Protecting myself is chaining, exhausting, and lonely. And for that reason, I choose my safe space as often as I can.
Everything changes in the presence of people who misunderstand and misinterpret. And the unfortunate truth is that so many people throw wrath and fear at others simply because they lack the ability to reach their hearts into someone else's. So many lack the ability to be raw and honest with themselves and others about their lives. We all struggle, and if the human struggle was a shared effort where we all sustained each other, there wouldn't be so many who feel the need to live a double life.
I often wonder what it would look like if it were possible to compile all the tears from human suffering into a box, how big that box would have to be. And if people had a chance to witness how large that box was, if it would soften their hearts in a way that made them slightly more sensitive to the people around them and slightly more aware of the hearts that are crying out for help. If we knew how deep other people's waters were, would we take extra time to stop and help them so that they don't drown? And if everyone stopped and helped the people in deep water, maybe all the water as a whole would be lessened to the point where we could all patiently wade through less troubled waters together. Maybe if we all decided to be a little more real, and a little more honest... then maybe those who suffer wouldn't feel the need to live a double life because then they would know that they weren't along and that there were strong hands waiting to lift their aching hearts.
God doesn't expect us to live out our lives in cold hard shells so as to not let other's notice our pains. God desires us to love and lift the hands that hang down. God wishes us to let love penetrate so deep that we can all feel His Divine love through each other. I hate the pressure I feel to live a double life as a chronic illness warrior (and I know I'm not the only one), and I've found that I'm more effective at bringing light into other's lives when I'm simply striving to be my best self. Maybe all of us could come to that realization in a way that could change the world.
It recently occurred to me that I've been fooling myself. I've faithfully proclaimed on social media year after year since I was diagnosed my deep hope that the next year will be easier, or that it will be better than the year before. I've hoped, and prayed, and fought my way into society's view of a "better" and "easier" life, only to find that this "easier" life that I'm seeking for doesn't exist. There's no such thing as "easy" in the vocabulary of a chronic illness fighter, and it turns out that the moment you think that the chronic illness battle has become "better" or "easier," something else painful and heartbreaking will come along that will try your resilience and test your nerves. And then after you've made it through that trauma, your illness will flare again. Due to this eternal pattern that keeps kicking me, I have finally reached the point in my life where I can say that I am no longer hoping, wishing, or praying for an easier year ahead!
Sounds like I've reached the point of intense embitterment, but I wouldn't exactly call it that. In fact, I've finally discovered that this statement that I'm making isn't a negative or chaining statement at all. In fact, admitting to it is probably one of the most freeing experiences I've ever had!
For as long as I can remember, my family's motto has always been "we do hard things." I was taught growing up that working hard and doing things that appeared to be difficult would bless my life and create a stronger person inside me. I was taught that striving to achieve things that were seemingly out of my reach was healthy and something that should be practiced on a regular basis. Back then it never occurred to me that there was something harder out there than Saturday morning chores, striving for a 4.0 GPA, and losing a best friend. Hard things came and went when I was young, but eventually, there will come a time in all of our lives when those hard things won't just leave. There will come a time when those hard things stick around, and you'll find yourself on your knees begging for relief more than once.
I've been in that place for years now, and I think I'm finally beginning to understand and live the truth that adversity and affliction has a divine purpose. Things may not get easier in the moment, but that's okay. Because God promises us better things through our suffering and God sustains us every step of the way. It's through the hard things that I've developed sensitivity to God's precious mentoring that He blesses my life with.
C.S. Lewis says that "God whispers to us in our pleasures, speaks in our conscience, but shouts in our pains: it is His megaphone to rouse a deaf world." I think my world has been roused and it's been a loud and painful awakening, but completely worth it. Many of us have probably experienced that this year, and what a blessing to say that we've learned this lesson firsthand.
I'm not going to begin to pretend like I have life all figured out. In fact, I often find myself in prayer expressing how unsure I am about life. But there is one thing that I do know:
Sometimes life is absolutely awful. Sometimes it's blood, sweat, and tears to make it through the day. And sometimes it seems absolutely unbearable. Other times life is magical, joyous, romantic, and absolutely beautiful to the point where you can't seem to breathe in enough of the moment, and you wonder what you could have possibly done to be blessed with such a perfect moment in life. And other times life is somewhere in between... mundane and boring. And the reality is that in order to live life to the FULLEST, every single one of these experiences is absolutely necessary. Because without the pain we wouldn't appreciate the joy. And without the mundane, we wouldn't appreciate the magic. And the glorious truth is that we have a loving God who sustains us through it all. How loving and merciful He is to enable me to do the hard things, even if they seem to be never-ending.
So this year I'm not praying or hoping for things to be easier. I'm hoping and praying for the strength to endure the hard, the wisdom to appreciate the magic, the patience to remain hopeful through the mundane, and the courage to submit to God's will even if it's more difficult than past years. May we all have the ability to discover those places of balance and vitality in the year to come.
Stay in bed and cry all day, and you're not trying hard enough.
Show improvement and look beautiful, and you're not actually sick.
Share your terrifying reality with others, and you're seeking attention.
Keep to yourself and pretend that everything is okay, and you're not actually sick.
Smile, and you're not in pain.
Cry, and you're in more pain than the people around you can tolerate.
I've found myself spinning this dizzy cycle in my head lately and trying to understand how I'm supposed to act and feel as someone with a chronic illness. I've found myself listening to the discouragement that comes from this vicious cycle from other chronic illness warriors. And I've seen lots of posts on social media expressing the same concerns in attempts to understand what exactly we're supposed to look and feel like as chronically ill people.
Unfortunately this perception that other people can sometimes give is frustrating and causes a lot of guilt and an unnecessary inward struggle. I often put extra pressure on myself because apparently there is a certain "look" that chronically ill people have and if we don't fit that particular "look" then we're not an acceptable sick person. The irony of that is that nobody actually knows what that "look" is. They just believe that it's different from whatever vibe we're giving off.
I believe this pattern can be found in any kind of misunderstood suffering. If you haven't been through it yourself, you don't understand, and while it's okay to not understand, it's also important that we increase our love and compassion towards that level of suffering because generally, the person is already suffering enough without that extra pressure. We don't need to put that pressure on ourselves or others because the reality is that PAIN AND JOY CAN COEXIST, and it's okay!
Your Traumas Don't Define You
"I don't want to be known as the sick girl."
I remember having that thought when I was at my worst. I remember feeling extreme frustration from my desire for people to offer extra love and kindness that I desperately needed at the time, but also to know that there is more to me than Lyme disease. It seemed to me like I couldn't have both and I remember feeling like I was never enough because I was now some disease that controlled my entire life and trashed my hopes and dreams for my future.
Fortunately, that was never the case at all, and I've since learned that it's not your traumas that define you. I have Lyme disease. That doesn't mean I am Lyme disease. Your traumas, afflictions, and adversities in life are there to shape and refine you into the person that God intends for you to be. They exist to soften you and shape you. It's through the furnace of fire that we become flexible and transformed into something beautiful. The piece of coal that never had to undergo heat and pressure was still just a piece of coal in the end. We may come out with a few burns. We may be wounded. But we're not eternally broken or stamped with our eternal label. Nobody comes out of this life with a big stamp on their forehead that states their largest trauma.
It's not our traumas that define us, but how we choose to respond to those trials. And sometimes our response is a day in bed or a day in tears or simply doing the best we can do at the time, and that's okay. And other times that response is laughing through the tears and smiling through the heartache, and I've learned that those days are often some of the best days. Some of those days are the days that we learn important life lessons that change us forever. On those days there is no "look" that I feel the need to have. It's just me in my most raw form, and sometimes that form is exactly what I need to be in the moment.
A friend once told me that it's okay to cry. It's okay to stay in bed for a little while. It's okay to be debilitated for a moment. Just don't freeze. The joyful message is that even in moments of pain and paralysis, we don't have to freeze. We can continue on to the best of our ability with hopeful hearts. Our best efforts are always counted in the sight of the Lord, and when we're given that knowledge, we don't have to submit to all the views of other people. When we press forward the best we know how in our adversities, we can come to a place of self-love where we can be happy with our own state of being, whether that be in tears or in laughter.
How is it possible for joy and pain to coexist?
I've often found in life that opposites can regularly coexist. I've found that I can make a list of things I love about myself, while simultaneously making a list of things I hate about myself. I've found that I can be in pain and still find things to smile about. I've found that even when I feel hopeless, there's still hope in the journey.
How is that possible? How can pain and joy exist at the same time? That phenomenon is made possible through a loving God who keeps His promises, and a Savior who was sent to succor and sustain us when we can't manage to sustain ourselves.
First, God promises us that ALL trials come to an end, even if the end isn't seen in this life.
John testifies in the book of Revelation of the people who "come out of great tribulation and have sanctified themselves... that God will wipe away all tears from their eyes." (Revelation 7:14-17)
He then later testifies of God's people and how "God shall wipe away all tears from their eyes; and there shall be no more death, neither sorrow, nor crying, neither shall there be any more pain." (Revelation 21:5)
And then there is our Savior, who He Himself declared at the end of His sufferings: "It is finished." (John 19:30) There will come a day when every single one of us will be able to declare that "it is finished." Our sufferings do come to an end, not always through death, but through healing and enabling love and power made possible through Christ.
That fact alone is something to rejoice about.
Second, God consecrates all of our afflictions for our good and promises us that our glory in heaven will be returned twice as much as our suffering on earth.
Peter tells us that the trial of our faith is more precious than gold. And "although we may be tried with fire we can be found unto praise, honor, and glory at the appearing of Christ." (1 Peter 1:7)
He then later tells us to "think it not strange concerning the fiery trial which is to try you, as though some strange thing happened to you: But rejoice, inasmuch as ye are partakers of Christ's sufferings; that when his glory shall be revealed, ye may be glad also with exceeding joy." (1 Peter 4:12-13)
God reveals to us in those words that we can REJOICE during our fiery trials. That does not diminish our pain. That doesn't say that we're not actually suffering on such a horrendous level. That doesn't tell us that we're not allowed to feel our pain because that's a sign of weakness, and we lack faith if we feel pain. It declares to us that suffering isn't a strange thing to our Father, and He understands, and He promises hope for a better future. We can be ourselves, and we can find joy in the moment. Not the kind of joy that promises no pain and tear-less eyes, but an inward joy that declares in our hearts that this too will pass.
It's okay to look like you're struggling. It's okay to look happy and beautiful. You should absolutely share your reality with others, and if you feel the need to fake it until you make it then that's okay too! It's okay to smile when you're in pain, and it's okay to cry in front of people even if it makes them uncomfortable! Life is full of ups and downs that we were meant to experience. And as we become accustomed to pain, we are granted the blessing to experience joy, even in the midst of suffering.
Thank goodness for a merciful God and Savior who loves us through it all.
I'm Claire Dalton, I'm 22 years old, and I suffer from endometriosis, anxiety disorder, depression, arthritis, joint pain, muscle pain, chronic fatigue, and a whole host of other symptoms that can be wrapped up in a pretty little package that is referred to as CHRONIC LYME DISEASE. I'm bold, strong-willed, and driven, and when my quality of life was ripped out from underneath me, I desperately needed all of those qualities to keep myself alive. My story is a story of blood, sweat, tears, and a family burdened with Lyme disease who chose not to quit and still chooses to stay and fight every day. Lyme is brutal, but not brutal enough to kill us.
My story begins when I was a teenager my junior year of high school. I was sixteen when my mother became gravely ill and bedridden in a more permanent manner. I don't ever remember my mom being completely healthy. She frequently experienced flares of illness of every kind throughout each winter season, and in the summer it would improve. Come to think of it, this was my pattern as well, but we never gave it a second thought because we were so frequently met with comments like, "it's normal for kids to be sick all the time" or, "all kids are frequently sick during flu season." That was the belief in my culture, my home, and my family, and we didn't realize how wrong that statement was until one day my mom went down and didn't come back up. One day everything simply plummeted... and this time waiting it out didn't make it better.
I went to school like a normal teenager. I looked like a normal teenager. I worked hard and studied hard like a normal teenager. But my home life was far from normal and I was often filled with overwhelm and fear because I never knew whether or not my mother would be alive when I came home from school that day. It almost seemed at times like we were simply waiting for death to pass over our house because death would mean the release of pain for my sweet mother. Our home was often filled with moans, groans, screams, tremors, and seizures due to how much pain she constantly suffered from. I desperately wanted my mom to live, but not like that. Not while death seemed so close on such a constant basis. Hospital runs, medications, being forced out of our house, trial and error of every diet under the sun! It was a living hell in my house, and I prayed so often for the feeling of the floor being ripped out from underneath me to cease.
Medications made things worse. Doctors assumed my mother was psychologically unwell. Friends and neighbors stayed away in fear of "catching it" or simply not knowing what to do. My mother went undiagnosed and misdiagnosed for a seemingly endless period of time. We craved a diagnosis. We craved answers. We craved an ending to the constant suffering.
In the year 2014, we finally received a diagnosis. Chronic Lyme disease. We received a diagnosis only to find that there is no proven cure and no doctors in our state that knew very much about Lyme disease. We searched elsewhere for answers and protocols, and the long and arduous journey of healing for my mom began.
Meanwhile, I worked hard to graduate from high school. I recall major brain fog, severe anxiety, extremely painful menstrual cycles, and a constant state of stress in high school. It never occurred to me that I could be diagnosed with the same disease I listened to my mother scream from night after night, but my first semester as a freshman in college was my trigger, and I went down fast.
I remember existing in a constant state of panic in college. Nothing ever felt right and my heart and nerves often felt tightly clenched as I spent many dark nights experiencing panic attacks all by myself. My heels and feet would hurt and ache every time I walked across campus to the point where I tried buying gel inserts for my shoes that never worked anyway. I couldn't remember hardly any word that came out of my professor's or tutor's mouths, and I had to come home and sleep for three hours just to make it through each day. I suffered from severe excoriation disorder and would claw at my own arms until they bled and would leave massive scarring. I had major joint and muscle pain, and my menstrual cycles were nearly unbearable. My hair kept seeming to fall out in massive amounts, I'd break out in skin lesions, and I was losing weight faster than I could count.
"Your test results came back positive." That's not a sentence any college student wants to hear, but I heard it and my heart sank. Doctors appointments, tests, and 30 vials of blood later, I knew I had Lyme disease. I also knew that if I didn't change my lifestyle and get on treatment soon, I'd end up being the one in screams.
I started my first treatment while I was still going to college. At the time my mom had been on a cancer protocol for about a year that was known for being very beneficial to Lyme patients. So far that protocol had healed her to the point where the screams had stopped and there were some days that she could get out of bed. We decided at the time that the best route was for me to go on the same treatment. This began an entirely new way of living.
I remember throwing everything out in my pantry and changing my entire diet. No more sugar, dairy, meat, gluten, citrus fruit, tomatoes, or spices of any kind for a while. I didn't know how to cook and I submitted to eating bland food for quite a while. I remember sleeping with oxygen tubes to prep for treatment the next day. I recall waking up early, taking all my supplements and my treatment, and hoping that I wouldn't herx too hard so I could make it to all of my classes that day. At the end of every day, my treatment required me to record all of my vitals and rate each symptom from one to ten. I so often marked high numbers on each symptom, my heart rate was always in the hundreds, and I always seemed to be bone cold. My grades dropped dramatically, and everything felt awkward and uncomfortable. I had good days and bad days, but the bad days usually left the good days as recovery days. The problem with Lyme is that it usually gets worse before it gets better. As was the case with me.
I left college before the semester was over. I felt like a failure, but I fell to the floor and cried tears of joy when I finally reached home that day. It felt so good to be home. It felt so good to know that at least now I could be sick in my own house. I looked in the mirror that night and wondered who the girl was that was staring back at me. I pleaded to God for help. I knew I had a long road ahead of me. I just don't think I knew what that entailed.
The herxing was brutal at first. I remember my first major herxheimer reaction was so excruciating that I lost my ability to get up and walk to the bathroom by myself. I recall my head throbbing every time I opened my eyes, and my entire body hurt so bad that I couldn't lay on one side of my body for too long because the weight of my own body was too much. I remember everything spinning, and passing out in front of my bedroom door after I attempted to walk by myself. What I didn't realize then was that overcoming that herx was the first of many baby steps to getting my quality of life back.
After a year of that treatment, I changed my diet again. I gradually reintroduced spices, dairy, gluten, and meat back into my diet, taking care that everything was organic, whole, and clean. I had no desire to eat refined sugar again, and I still don't. I found myself gaining some of my life back as symptoms began to peal off little by little. The severe pain that came with endometriosis was torture every month, but the improvement of symptoms the other times of the month gave me hope for healing. I continued trying different protocols. I tried high dose vitamin C IVs, magnesium injections, large amounts of supplementation, and light exercise as I could. Some things started to clear. Others didn't. Lyme disease always seemed to leave me frustrated and confused because things would come and go and extreme pain left me scarred with memories and fear of if or when it would come back.
The Sauna Detox Protocol is the treatment that CHANGED MY LIFE. After a vigorous two months of sweating it out in a sauna, I began to feel like I had my life back. My skin cleared, I began to gain the weight that I had lost, my hair started growing back, my pain lessened, and the herxheimer reactions decreased. I gained my energy back and my panic attacks eased. My brain fog, fatigue, and cognitive dysfunction lessened, and even my endometrial pain improved! I never believed that I would get my life back, but to a point, I did. I don't have non-stop excruciating pain anymore, and I can't begin to express how thankful I am for the healing that I have been able to experience in the past two years.
Now, I have the unique opportunity to look back and contemplate everything I've been through, and I often take time every day to allow myself to feel the emotional pain that comes from experiencing such large amounts of physical pain. I still struggle with severe anxiety, lower abdominal pain from Endo, and excoriation disorder and I'm still fighting to overcome. I now treat my Lyme with AmpCoil, and I've found that if I don't regularly practice treatment and self-care my symptoms will reappear. What helps me function is consistent 8 hours of sleep every night, drinking half my body weight in oz. of water every day, and only consuming organic and whole foods.
PTSD is a real thing that Lyme patients suffer from, and I often find myself having flashbacks of severe pain flares that leave me paralyzed for a time. With that said, I often find myself holding onto God's love in those moments, and that gives me a reason to keep going and keep striving for a cure. I am not "cured." I do not live an easy and symptom-free life at all times... but there have been so many blessings and miraculous amounts of healing that have taken place in the past couple of years, to which I am incredibly thankful for.
To anyone suffering from a chronic illness... I've learned that even in the darkest nights, there is HOPE FOR HEALING. Some of us in life are called to pass through the darkest nights and the scariest of circumstances, but those experiences are for our refinement and for our good. The road ahead may be full of darkness, but there's always a light. I've now gained the wisdom to know that it takes more than one protocol to find healing. It usually takes many tools in your toolbox to survive the depths of Lyme disease. I've also gained such a love for the concept of suffering and why some are called to pass through such deep adversities. I'm learning every day how to accept my illness and love and appreciate the good moments. I'm learning to love my scars, for they are my battle wounds that tell the story of how I overcame something horrendous. I'm learning how to be patient and flexible with God's timing instead of my own. And I've gained a passion for loving and helping people who suffer through dark misfortune and come out stronger in the end.
Chronic illness warriors are INCREDIBLE people! If you want to learn about resilience, dedication, desperation, hard work, and perseverance, love somebody who is sick. Because when you get sick for the long haul, something inside you begins to bloom that is the only thing that will keep you going during your most desperate nights. And then one day you'll wake up and realize that the bloom inside you grew into a garden of flowers that you didn't know you were growing.
Some days are good. Some days are bad. Some days are bland and some days are more than I feel like I can handle. Progress is not a constant upward motion, but a roller coaster that makes you want to scream at times and laugh at others. It's all about learning how to enjoy the ride. This is Lyme disease. This is invisible illness. This is my Lyme life.
You can find more information on the Sauna Detox Protocol HERE
The holidays are meant to be joyful! Thanksgiving is a time to reflect on blessings throughout the year, and a time to express gratitude to loved ones and to our loving God who blesses us with more than we deserve or comprehend. So if that's true, then why does it simultaneously seem like the holidays are a time of mourning and grief for so many individuals who have suffered a loss of some sort? Why does a heavy heart often creep into our celebrations and merriness?
Suffering is a universal concept. We've all experienced loss in it's many relentless forms:
The loss of a job or an opportunity.
The loss of a loved one through death.
The loss of a loved one through betrayal, or simply the choice they made to leave.
The loss of health and therefore, quality of life.
The loss of hope that there is happiness and joy in the future.
At times the amount of loss in life seems unfair and insufferable.
The holidays are the time when it seem like our losses should return and magically reappear so the holes in our hearts can be filled for that short period of time when we're "supposed to be joyful." I often find myself wishing for the holes in my heart to be filled once more just for the holiday season... but life doesn't work like that. Instead we must find a way to fill those holes with new reasons to rejoice. This year I've found that obtaining a thankful heart might just be a tool in our toolbox to finding joy despite our grieving hearts or pained bodies.
When I was at my darkest place in my illness, I didn't believe that gratitude could change anything, and I often went about my day filled with bitterness and resent for people who were blessed to live their lives pain-free. Being thankful for what I have would do absolutely nothing in relieving my physical pain, so why should I try so hard when I felt I had nothing to be thankful for? Why should I try so hard now when my past pains often burden my heart in a way that seems unbearable in the moment? Gratitude will not take the PTSD from my nerves and mind. Gratitude won't make my heart any less heavy. Gratitude won't take my past or future flares from occurring. So does it matter at all?
The answer is yes! Practicing and expressing an attitude of gratitude and thanksgiving changes you. Allowing thankfulness to envelop your heart and senses can be the difference between having a happy holiday and having a hollow holiday. Will it relieve all of the pain from the injustices of life? Of course not, but it will take the edge off in a way that gives you the power to endure the pain, and endure it well. A thankful heart often reminds us that there's always a reason to keep going, even if your circumstances are less than desirable.
With that said, there will always be times when gratitude will seem unreachable.
I didn't feel thankful during my panic attack today.
I didn't feel thankful during my endometriosis two weeks ago.
I didn't feel thankful when my heart pinched with pain when I was reminded of the loss of someone I love on Thanksgiving Day.
So what? Do we throw the towel in and quit? NO! We recognize that we're not always going to be happy, and allow ourselves to feel our pain. We then get up and trek onward with hope in our hearts for a better future and faith that God will give us the strength to endure. And when we feel like we can't even do that, we plead with our loving God and lean on His strength and gratitude until we can find it in ourselves. God is waiting to help us hold our burdens, we simply have to ask to put it in His hands for a time.
I'm not going to pretend to be the expert on gratitude. I'm not. But I invite you to take time to write five things you're thankful for everyday. IT WILL CHANGE YOUR LIFE. I never knew I had so many things to smile about until I took a little time everyday to be thankful. Even if you can only find gratitude for the chair that you are sitting in, it is more than some people have. So take time to feel and express gratitude. It may not take your pain, but it will transform your pain into something beautiful.
This year I'm thankful that the years past are over and that I don't have to live in that consistent darkness anymore. I'm thankful for the health I do have. I'm thankful for the people I've lost so that God can heal and open my heart to new people that I can love. I'm thankful for life, breath, and hope that my Savior, Jesus Christ, instills in my heart if I allow Him too. There's always something to be thankful for... we simply have to take time to see it.
I found myself reminiscing today. I found myself look back, and then regretting it. I frequently resist moments of nostalgia that creep into my mind merely because the happy memory is usually accompanied by a deep ache that penetrates the strongest of walls around my heart. Happy memories are often escorted by laughter that's been silenced, love that somehow managed to slip through my fingers, and time that's been burned over with more time. It often feels like the road behind me is coated with blood and ash which drives me to never look back and fear the moment I choose to take a step forward.
I suppose this is grief at it's finest. I often grieve the life I had before, or the life that never existed because it was replaced with pain and tears that were accompanied with my diagnosis. I often grieve when I watch young people that are out living their lives without a thought as to how they feel physically, or what they eat, or what they're breathing in. I suppose that ignorance is bliss... but I never got to experience that bliss in my first years of young adulthood, and I the grieve the idea that maybe I've missed something. I grieve the idea that my moments of bliss were replaced with heartache and pain... and that just can't be fair. Becoming so well acquainted with grief at such a young age just can't be fair.
I remember when I was six year old and my pet rabbit died. I cried for one night.
I recall when I was fifteen and my best friend betrayed me. I cried for a week.
I was sixteen when my "first love" broke up with me and I cried for a few weeks.
I was seventeen when I lost the presence of my mother in my life to a disease the robbed her of her quality of life. I cried every time I came home to her screams of pure agony.
I was eighteen when I lost my will to live after I was diagnosed with the same disease I watched my mother suffer from for so long. I cried for years as I fought long and hard for my life. I still cry if I think about those moments for too long.
Perhaps I'm just an "emotional person." Perhaps I don't have what it takes to cope with real life. Perhaps some of those things were silly at the time and weren't worth my tears... but despite everything, I've found that it's possible that our hearts are meant to bleed this hard. Maybe we were meant to be broken so we can be healed and revived twice as strong. Maybe life is fair simply because it's so unfair for everyone. How does one experience pure joy if they are never exposed raw pain?
I've bled and cried, I've kicked and screamed, I've complained and raged, I've faithfully and willfully continued to put one foot in front of the other despite the hardship. And what's come from it all is a sense of comfort despite the strong discomfort that plagues me regularly. I suppose the kind of bliss that comes from ignorance isn't really bliss at all because someday you'll find yourself in the sick bed... and you'll wonder what went wrong... just like I did.
I've come to love my sensitive nature. I've come to appreciate my keen sense of air pollution and unreal food. I've come to smile at the funny looks I get from people who can't comprehend why I eat organic. I often ask myself who in their right mind would want bliss if it is required to be accompanied with ignorance? I've come to realize that joy and bliss are two different things, and wisdom doesn't come with age... it comes with suffering...
I've come to gain a deep love for people who suffer on deep and penetrating levels. I've gained a deep respect for people who suffer in ways that change them forever. Suffering that erases the ignorance and replaces it with a sense of comfort and peace even in the storm of discomfort and pain.
These kinds of people are warriors. These kinds of people are the people that have been sculpted in the midst of adversity. These people have let go and let God transform them into beings of light and vitality. These are the people that have discovered great depth in life. These are the people that have experienced the great ache that leads to resilience and fortitude that I myself have not yet mastered.
Perhaps hearts were meant to bleed this much. Perhaps bodies where meant to break down. Perhaps tears were meant to be shed. Not because we live in a cruel universe... but because God has a Divine Design that can transform blood into healing, breaking in wholeness, and tears of grief into tears of rejoicing. May we all learn that lesson in hopes that we can grow in strength and everlasting joy.
Perhaps we all need to reminisce sometimes... Because the past is at times our greatest teacher and mentor. And in the meantime, I've come to love the sound of my feet walking in the direction that God intends for them to be... because the blood and ash behind me doesn't matter at the sight of beauty and light ahead of me.