Someone you know is sick with Lyme disease. It could be a friend, a family member, a significant other, or just an acquaintance. Whoever it is, you’ve got some questions. Or maybe you don’t, but you want a better idea of what the heck is going on. This entry will hopefully offer some explanation, and can probably be applied to a variety of chronic illnesses. Whether you or a loved one has been diagnosed with Lyme, these 10 things are going to be really useful to know.
1. Lyme disease in an invisible illness.
What does this mean? It means that when someone with Lyme is feeling absolutely horrible, they are likely looking no different on the outside than they do on one of their “really good days.” This disease (usually) doesn’t present itself with super obvious visible symptoms. Normally, you won’t see a Lyme patient with their legs wrapped up in casts or with huge bleeding gashes on their bodies. Our symptoms tend to be more internal. Things like extreme fatigue/weakness, joint and muscle pain, dizziness, nausea, anxiety, and brain fog aren’t necessarily easily detected just by looking at a person. It can be hard to understand how a person can be feeling so horrible when they look “fine.” Oftentimes, they even seem to be acting fine! This brings us to point number 2.
2. Lyme patients quickly become amazing actors.
Let me explain. When you’re sick with a cold or the flu for a couple of days, maybe even a week, you likely spend that whole time in bed or on the couch, maybe complaining about how miserable you feel. Definitely not venturing out in public and likely not even leaving your bedroom. You probably tell your friends and family you’ll see them when you’re feeling better. You feel too horrible for the company. Simple tasks like food preparation and household chores are put on hold. Basically, life is put on hold. Which is acceptable when it only happens for a week at a time, probably once or twice a year. Everyone gets sick, it’s okay, it happens, it sucks, but life goes on.
When you have a chronic illness, you often wake up every day feeling like you have a horrible flu and the worst hangover of your life all rolled into one dreadfully uncomfortable package. As easy as it would be to stay in bed and not talk to anyone or do anything, you know these symptoms aren’t going to just disappear tomorrow or even next week. This means you try to push yourself as much as you can to do normal things. Some days you might not be able to push much more than making yourself dinner. On other days you might venture out to the store or to see a friend. Your friend might tell you how great you look. “You must be feeling better! You’re out and about!” You’re conversing and laughing, and you look like you’re feeling fine!
Unfortunately, a lot of the time, it’s all an act. When you’re chronically sick you learn pretty quickly that wallowing and complaining about symptoms and refusing company leads to a very lonely and isolated life. People quickly get tired of hearing you complain about how horrible you’re feeling, and you quickly get tired of being stuck in bed with no company. So when you can, you get up, you go out, and you put on a show. You smile, and you laugh, and you act like you aren’t feeling any pain or discomfort at all. It is difficult and heartbreaking to live your life “pretending.” It’s also extremely exhausting. And sometimes, in the middle of this act, symptoms get worse, and you find it harder to appear normal. This often leads to point number 3.
3. Symptoms can come slowly at times, but other times quickly and suddenly.
Sometimes, we are feeling okay, and all of a sudden, it seems like the floor has been ripped out from under us. We might need to sit or lie down immediately. We might even pass out. This can be confusing for people that aren’t sick. Just a second ago, we were okay. What happened? At times, symptoms really do come on very quickly. It’s the nature of Lyme. It happens. Other times the person wasn’t feeling well at all, to begin with, but was doing a pretty good job of acting fine (see point number 2). They might have been feeling pretty horrible, but not SO horrible that they couldn’t fake feeling okay. Then, their symptoms got worse, and it seemed like they went from 0-10 in a few minutes. A lot of the time, though, what is likely happening is they are going from a 7-8 out of 10 to a 10 out of 10 in pain/discomfort. They have just learned to hide the 7/10 well. 10/10 is much harder to hide, and quite frankly, when you’re in this much discomfort, acting fine takes a back seat to get yourself, and your body stabilized.
4. Lyme treatment requires a special diet.
When in treatment for Lyme disease, there will likely be a laundry list of foods you need to avoid. If you’ve ever eaten with someone with Lyme, you’ve probably seen this first hand. Most of the time, we need to adhere to a very strict, very healthy diet in order to limit inflammation and toxins in our bodies. We have enough of these to go around already from the Lyme and co-infections! Normally our diets consist of avoiding gluten, dairy, and sugar. Often times we have other sensitivities to add to the mix, like soy, corn, eggs, and nightshades. If it’s annoying for you, take a moment to imagine how much more annoying it would be if you had to stick to this bland diet 24/7. Everyday. And be feeling like complete crap while doing it. Be thankful you’re able to eat what you want and feel fine for the most part.
5. Lyme treatment causes something known as a “herxheimer reaction.”
Or a “herx” for short. Similar to how chemo makes a cancer patient feel worse when someone with Lyme disease takes antibiotics, antimicrobials or anti-parasitics that cause a large amount of die-off, this releases a huge amount of toxins into the body. This basically results in all of our regular symptoms being amplified as it takes some work for our bodies to get rid of these newly circulating toxins. Often times our bodies are so overburdened that they are not efficient at detoxing these toxins well, so it’s a difficult process and definitely not an easy one to endure at all. Unfortunately, it is often necessary to push through this in order to make improvements.
6. Many Lyme patients are not well enough to attend school or work.
This doesn’t make them lazy or unmotivated. When you are so sick that even simple tasks like showering and preparing meals are extremely difficult, school and work are out of the question. This is something I’ve dealt with personally, and even more so in the last year. I have had so many people tell me, “You are so lucky! I wish I could stay home all day and sleep in and not go to work or school!” This literally makes me want to scream. I promise anyone who thinks it would be “fun” to be stuck at home chronically sick, without any obligations, is completely and totally wrong. Maybe if you were feeling nothing more than a little under the weather the first few weeks, it would be nice to relax. Then you’d probably go a little stir-crazy. You’d be tired of boring daytime TV and hearing about everyone’s eventful days out in the real world. You’d want social interaction. You’d want to leave your house! Now pile on top of that the fact that most of the time when someone with Lyme is stuck at home, they aren’t just feeling slightly under the weather. They are feeling like death. Sometimes, the simple task of breathing feels impossible. This is honestly not an exaggeration. This kind of sick doesn’t feel the same as a simple cold or flu. It feels like torture. Please do not minimize our suffering by calling us lucky. Nothing could be further from the truth.
7. There is no “magic bullet” or quick fix for late-stage Lyme disease.
You might be wondering why your loved one with chronic Lyme is STILL sick. I mean, it’s been months, years even! Why isn’t the treatment working? Shouldn’t they be cured by now? The truth is there is no easy answer for those of us who have late-stage Lyme. Things might have been much different for us had we been diagnosed and given proper treatment at the beginning of our illness, but Lyme has now had months or years to run rampant throughout our bodies, and it has no intention of leaving quietly or without a fight. I personally was sick for 8 years before I was diagnosed with late-stage Lyme. I have been in treatment for about 9 months and have only seen minor improvements. But looking at the big picture, 9 months isn’t such a long time when it took my body years to get to this state.
Another thing that comes into play here is no one treatment will work for everyone. Each Lyme case is unique and will respond differently to different treatment options. Often times a Lyme patient will need to try several treatments, even several doctors or practitioners, before they find one that allows them to make considerable gains. This process most definitely tests out patience. It might be testing yours, too. Again, it’s important to remember that however frustrated you are getting with the lack of progress a friend or family member has had, your loved one is likely feeling 100 times more frustrated and even disappointed in themselves for not being better yet. Try to be patient and reassuring, as staying hopeful and persevering when nothing seems to be working is difficult but absolutely necessary.
8. Lyme disease treatment is extremely expensive and likely not covered by insurance.
The problem with Lyme disease is that standard treatment options are geared towards those that catch it within the first few weeks of symptoms. In most of these cases, a few weeks or a few months of antibiotics are all that is needed to regain health. These short-term treatments are usually covered by insurance. When Lyme disease becomes late-stage, however, treatment is much more complicated. A few weeks of antibiotics will not even come close to curing the patient. Furthermore, there will likely also need to be adjunctive treatments added to the patient’s protocol, like vitamins, supplements, and herbal remedies. When it comes to late-stage Lyme we have to pull out all the stops to get better. Sometimes this means traveling to doctors on the other side of the continent, maybe even the world. Or try new cutting-edge treatment options that are pricey and paid for out of pocket. This is a bit of a nightmare for us, as we already have the huge burden of failing health to carry and don’t need the added stress of coming up with enough money to get better. If you want to help your friend, offer to host a bake sale or fundraiser to help raise money for their treatments. It will probably mean more to them than you know.
9. Lyme disease can be extremely isolating.
When you’re chronically sick, you often miss out on a whole lot. Little things like parties and get-togethers. Big things like graduation and vacations. It’s hard. It’s heartbreaking. And it’s difficult not to feel extremely alone at times. If you have someone with Lyme in your life you’ve likely witnessed them canceling plans because they were too sick to attend. This might have been annoying to you, but I can assure you they felt completely horrible about it and wish more than anything they didn’t have to cancel on you. If you have a friend with Lyme, offer to come over and visit them. Or pick up some groceries or Lyme-friendly take-out for them. Even come help them cook a few meals to make the next week easier. Help them advocate for better awareness so it’s not such a struggle living with a disease many know nothing about. Reach out to them. Try to put yourself in their position. Would you find it easier to have friends who tried to help or ignored your situation completely? Maybe you’re waiting to see them until they are feeling better. Unfortunately, it could be a while. Make an effort to make it happen sooner rather than later. It will be appreciated. It will show your friend you are one of the few who doesn’t abandon your loved ones when times get tough. That makes you a great friend and an amazing person. Hold that title proudly!
10. We are just regular people, too; this can happen to anyone. Get informed and be compassionate.
Something I did before I got sick was taking my health for granted. Sure, you hear about people getting cancer, getting scary rare diseases, going through tragedy, etc. But that kind of stuff just always happens to other people. Never to you, right? The truth is Lyme disease (and any chronic illness for that matter) can happen to anyone. No one is immune. Sometimes it’s easier to just put this stuff to the back of your mind and not think about it. That way, you don’t have to deal with it. But what happens if one day you find yourself or someone close to you suffering from chronic illness? Would you not want people to at least try to take the time to get informed, understand to the best of their ability, and do what they can to make it easier on you?
A huge thank you to Shannon for sharing this post with us. This blog was originally posted on Lymeless and Lovely on 1/9/2014, and reposted and edited in collaboration with Shannon. Check out her Youtube channel Radlikemad.
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I loved this. My family have been so unsupportive and ignorant. This is everything I wanted to say but they wont listen. Will be sending then this article. Very well put and nuch politer than i can say itat this point! 😉
I’m so glad it was helpful!
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