Strep Throat Natural Remedies

I'm fairly sure strep throat is something everyone can relate to. We've all had it at one time or another in our lives. And everyone rushes to the doctor for the rapid strep test (and maybe a regular test if the rapid test is negative) and then a bunch of antibiotics. Like most illnesses, the key is how your immune system handles it, and strep throat is no different. For us Lymies, strep throat, or the side effects of it, can linger around for quite some time because our immune systems aren't capable of fighting them off.

The other issue for Lymies is something that most people take for granted: to antibiotic or not to antibiotic, depending on what treatment we're currently on. Sometimes we're already on antibiotics, but strep gets through anyway and we need to add an extra med. But sometimes we're in a rest period, where we need to let our bodies heal from all the antibiotics we've previously taken, and adding a new med during this time isn't really the best option. Of course, sometimes we have to do it anyway, because what's worse than strep throat? Strep throat that's untreated.

Up until now, like most people, I thought antibiotics was my only choice when I came down with strep throat about a month ago. As soon as I saw those tell-tale white spots on my throat, along with the other symptoms, I rushed to the phone to call my doctor.

But on the way to the phone, I spotted my Cowden products, and I took a second to think things over. There was a reason my doctor didn't want me on antibiotics right now. And I had no idea if Cowden would get messed up if I threw a bunch of antibiotics into the mix. So I thought, "I can give it a little while. I'll do some research first." I figured there had to be a way to get rid of strep throat naturally - something I'd never really thought about before.

What I came up with was that there are quite a few natural methods to get rid of strep. I'm not going to list them all because it would take forever, but I'll just tell you what I tried and why.

Essentially, I used Organic Raw Apple Cider Vinegar and Oil of Oregano. My reason for selecting these two was that I'd already read up on their benefits for other reasons (Lyme, candida, general wellness, etc.) and knew they worked for certain maladies. As it is, I've been taking oil of oregano regularly for a while, and when I feel a cold or something coming on, I up my dose and it gets rid of the illness quickly.

So what did I do? I increased my dose of oil of oregano and started taking apple cider vinegar. I had already been taking oil of oregano twice a day, so I went to three times a day. I gargled with some apple cider vinegar mixed into warm water, and I also drank some apple cider vinegar mixed in water twice a day. In addition, I occasionally swabbed some oil of oregano directly on the white spots on my tonsil (yes, it only infected one, and I think starting this regimen quickly kept it from ever getting to the other tonsil) using a Q-tip.

The results? Pretty amazing. The strep still had to run its course. The white spots did linger for a little more than a week, but they got smaller each day. The sore throat was manageable. It never got out of hand. I did spike a fever about four days after starting the treatment, but a fever is a way of your body telling you it's fighting something off. I took that as a good sign that my immune system was working against the strep. I kept up the oil of oregano and apple cider vinegar after the symptoms and spots disappeared, just to be safe.

In the end, I'm pretty confident that I did have strep even though it was never confirmed by a doctor, and that I beat it without antibiotics.

Better than Baseline

Better or worse than baseline is a term many Lymies use to describe how they're feeling. It's difficult for most people to understand that a "good day" for someone with Chronic Lyme is probably worse than most people's bad days, so comparing it to our "baseline" is a better way to describe it. So if I feel "awful" on a regular basis, I call "awful" my "baseline" and then if I feel a little better than "awful" I can say my day is "better than baseline." To a Lymie, "better than baseline" is a nice change.

I'm happy to report that I've had a few "better than baseline" days recently. They still haven't been great, but slightly better than what I'm used to. My pain has been not as bad and I can move around a little easier. My energy level is up a bit, although I'm still horribly fatigued. So when I'm up, I can do more than usual, but I still need to nap as much as normal.

It's only been a few days like this, but the fact that I noticed them is what's important. I'm trying not to overdo it when I do have the extra energy so I don't ruin my chances of having more "better than baseline" days.

I'm currently one month in to the Cowden Protocol, and I would guess that's what I can attribute these positives to. I have a long way to go in the program, so I'll keep taking it day by day. I hope to see continued improvement, even if it's in tiny increments. I'll take any little bit I can get!

For anyone interested in starting Cowden, you can receive 25% off your first order from Nutramedix by using this link and discount code TAF16. The code will only work with the link supplied.

Cowden Protocol

If you're a Lymie like me, you've probably heard plenty about the Cowden Protocol, but for those who don't know, here's a bit of a summary. The Cowden Protocol is an herbal treatment for Lyme disease and many of its co-infections (the lesser-known infections that can also be transmitted, many in less time than it takes to get Lyme, from a tick bite, among other methods of transmission). Cowden takes a systematic approach to treatment, mixing detoxification in with the herbs that fight infection in order to make the treatment more tolerable than other methods, like oral or intravenous antibiotics. The herbs are also rotated through a specific schedule to kill off what is likely to be present as other infections die. It is a 9-month program, with the option to continue until full health is realized once complete.

Although Cowden does not need to be purchased through a medical professional, it is best when followed under the care of a LLMD (Lyme Literate Medical Doctor) for assistance with side effects and other issues. I've been purchasing my products through Nutramedix, although they can be purchased through other websites as well. (See link and discount code at the end of the post.) After trying many other remedies, Cowden has been recommended to me by my LLMD, so I started it almost a month ago.

As I mentioned in a previous post, part of the protocol involves drinking 96 oz. of water a day. Other than the normal benefits of drinking a lot of water, this is done to help detoxify your body as the bacteria die off. One of the biggest complaints of Lymies is the Herx reaction, which is when you feel worse from treatment before getting better. This occurs when the dead bacteria linger in your system. People experience this in different ways because the symptoms of Lyme vary so greatly, but the main theme is that whatever a person's weak spots are, that's where they tend to feel the Herx the worst. By drinking so much water, you flush the dead bacteria from your system before they have a chance to cause problems.

If you do experience any kind of Herx reaction, the program has instructions for taking additional detoxifying herbs to get rid of it. It is even suggested that you slow down the program until the Herx goes away. While 9+ months is a long time to take to complete the program, many Lymies have been suffering with the effects of Chronic Lyme (or whatever doctors want to call it these days) for years upon years, taking forever before they are even diagnosed and then struggling through treatment after treatment with little to no results. A 9-month protocol with minimal Herx reactions is as good or better than many other treatments.

So, my experience so far? Fairly neutral, but I think that's to be expected at less than a month into the program. As I type this, I'm suffering from a mild migraine (yes, there are varying degrees, and after living with them for so long I've learned many coping mechanisms), joint pain, typical fatigue, back pain, and neck pain, to name a few things. I can't ever be sure whether a migraine is a Herx reaction or just my normal symptoms, so I increase my detox herbs just to be safe, but in the end I'll most likely have to take my prescription medication to get rid of it.

But I can report that I'm up to the full dose of Samento and Banderol for the month without having experienced any major setbacks. These are two herbs I've tried before and I've always had major Herxing that caused me to lower the doses for a time before continuing up to the full doses. So that's a positive for the program. I know Samento and Banderol do something to kill off Lyme and co-infections, so if they're working quietly without causing a Herx, I can at least operate at my level of normal while on the program.

I'll check back in a little while to let you know my progress. There are other herbs that will be mixed in eventually, so I'm curious to know whether they'll make a difference.

If you use this link and the discount code TAF16, you'll receive 25% off your first order from Nutramedix.

Water

Everyone knows there are many benefits to drinking a lot of water. I don't need to rehash what we learned in 3rd grade health class here. But I've had to challenge myself to drink 96 oz. of water a day recently, and I've found some interesting things.

Why do I have to do this? Well, I'll be starting the Cowden Protocol next week. (Most Lymies will at least be familiar with the name, but Cowden is a set of herbal supplements that you take in rotation to help eradicate Lyme and co-infections. More on Cowden in another post.) One of the main rules of Cowden is that you MUST drink 96 oz. of water for it to work. I suppose this helps flush out the dying bacteria from your system.

In preparation for Cowden, I figured I better get used to drinking so much water each day. When I was still able to work, I used to drink plenty of water, but I'll admit my consumption has dwindled since I've been so sick. Sometimes just getting out of bed to get a drink isn't worth the effort. Now that I'm forcing myself to do it, here's what I've found:

1. Water bloat is a real thing. Sometimes when I try to drink a lot of water at once, I feel it sloshing around in my stomach. It's uncomfortable for a while until it begins working its way through my system. I don't know if that's a result of digestion/absorption issues from Lyme or if it's normal. I never know if things are normal anymore.
2. There aren't enough hours in a day. 96 oz. of water is a LOT. I drink water with all my meds and supplements and with my meals. I also drink it throughout the day. I limit myself to 2 cups of coffee a day (yeah, I know I shouldn't have any, but it helps my migraines) and I also drink 2 cups of Natural Care Tea as prescribed by my LLMD. Other than that, it's only water. I thought I was drinking a good amount, but once I measured out 96 oz., I was shocked at how far short I was each day. Sometimes I'm trying to chug the last cup right before bed and sometimes I just don't drink it all. Hopefully by the time I start Cowden I'll be more used to drinking that much every day.
3. It makes you pee a lot. I know this seems obvious, but I feel like I'm pregnant again with how often I have to go! 96 oz. in, 96 oz. out. Only unlike when I was pregnant, it's more like Niagara Falls than a babbling brook. When I used to drink more water regularly, I don't recall having to go so much. I don't know if that's another issue with my body's breakdown, or maybe it's my fuzzy Lyme memory. And since I sometimes drink that last bit right before bed, I wake up and have to go. Sleep interruptions are not a good thing, so I need to work on drinking more earlier in the day.
4. It reduces my hot flashes. This has been a shockingly pleasant side effect. I have no idea if it will work for everyone, but it has been a noticeable decrease for me. I've had hot flashes since surgically-induced menopause in July of last year, and I've tried pretty much every OTC remedy out there. I've been hesitant to go on long-term hormone replacement therapy for several reasons, so I've stuck to the OTC stuff and sweated it out. Literally. When I have hot flashes, I can be dripping sweat in an instant. But since I began drinking 96 oz. of water a day (or as close to it as I can get), I've felt a big difference. The number of hot flashes has dropped and those I do get aren't as intense. Major bonus and reason enough to keep drowning myself daily.

Maybe in time I'll see other benefits to all this water. For now, it still feels like I'm forcing myself to drink it every day. But keep at it, and in a week I'll start Cowden, which lasts for 6-9 months. I'll let you know how things are going soon.

Homemade Lip Balm

Since winter has finally arrived in my neck of the woods, I thought it would be a good time to share my recipe for homemade lip balm. My family goes through lip balm like water in every season, but particularly more so when it's cold. If you're anything like we were, you're spending a ton of money on lip balm (anywhere from $1 to$20 per tube!) and possibly putting unnecessary chemicals on your lips, which means they end up in your mouth. I've also got a graveyard—okay, a drawer—full of products I've tried that didn't work as expected.

My solution? Make my own lip balm!

With this recipe, you can make it just the way you like it—and for a fraction of the cost of store-bought products. It might take a few tries until you get it just the way you like it, but in the end you'll have a product that works and you'll save a ton of money.

What you'll need:

• 12 Lip balm containers (I prefer these twist-up tubes, but you can use small pots)
• 1 Tbsp. Coconut oil
• 1 Tbsp. Shea butter
• 1 Tbsp. Beeswax (It comes in different forms, but the pellets melt easiest)
• 20 drops essential oil of your choice (I prefer peppermint)
• 1/8 tsp. Vitamin E
• Glass measuring cup with pour spout (there are other options for pouring, but I've found this to be the easiest)
• Frying pan
• Water

How to make lip balm:

1. Fill the frying pan with some water and bring to a low boil. Turn heat to low-medium. Set the measuring cup in the center of the pan without letting any water get inside.
2. Use approximately equal parts coconut oil, beeswax, and shea butter. More beeswax will create a firmer product. You can experiment with how much or little you prefer. Add all three ingredients to the measuring cup and melt over low-medium heat, stirring to combine.
3. Once melted, add Vitamin E and essential oil and stir to combine. You can use more or less of these as preferred.
4. Pour liquid into lip balm containers. If the container you melted it in doesn't have a pour spout, you can use a dropper. Top off containers once they've sat for a minute. Let sit for a few hours before capping.

If you want to get fancy, you can add labels and give these as gifts. I've been sharing mine with extended family, and so far everyone likes them.

I spent about $50 on supplies, but coconut oil is something I keep around the house anyway since I use it for a ton of things. I've already made approximately 50 tubes of lip balm, and I have barely made a dent in the beeswax, shea butter, vitamin E, and peppermint oil. The tubes at $0.20 each will be my only expense for a while, so while my first few batches seemed to cost $1 each, they really will cost much less in the long run.

Anyone miss me?

Wow, so it's been over 3 years since I've posted anything here. I guess it's time for an update if anyone's still reading this.

My health seems to only be deteriorating no matter what medications I try, and I've tried them all. I've done 2 rounds of IV antibiotics, countless oral antibiotics, natural and homeopathic remedies, OTC remedies ... you name it, I've tried it. I was recently on Samento and BLt for 3 months, and all of my symptoms got worse. My doctor and I couldn't tell if it was a herx reaction or actual worsening of symptoms, so I stopped those medications.

Nothing got better.

I'm now on 2 oral antibiotics: Omnicef and minocycline. This will be another 3-month trial. 3 weeks in, and I haven't seen any improvement yet. In fact, the detox medications my LLMD had me on (Burbur and Pinella) made the migraines worse, so I had to stop taking them. I realize sometimes you have to suffer through the worsening in order to get better, but with my current symptoms it was just too much.

The joint pain is the worst it's ever been. My fingers hurt so badly that some days I can't type. Other joints are also problematic, but my fingers seem to be taking the brunt of it. I have some kind of nerve issue going on in my lower back that causes random pain. It's there right now, and it essentially makes it so no position is comfortable. Then there's the extreme fatigue. On a normal day, I take about a 2-hour nap even if I got a good amount of sleep (I'm currently on Ambien because some immune factor on my blood work was low, and the doc says this immune factor regenerates when you sleep so I clearly wasn't getting solid sleep even if it felt like I was). If I've been active, the fatigue worsens, sometimes even after just a short while on my feet. Then it's a 2-nap kind of day. There's lightheadedness, tinnitus (my left ear is practically screaming at me all the time), swollen lymph nodes, migraines, general aches and pains, stiff joints (no matter what position I'm in, when I get up, my body just doesn't want to move), and random things that come and go at random times. Last night it was a tight muscle in one foot. So strange. I stood up and my foot just wouldn't move properly and I could feel the pull in the muscle.

That list could go on for a while, but you've probably stopped reading already. I'll just leave it at "Lyme sucks." I'm not sure I'll ever know if it's still Lyme, or maybe a co-infection, or perhaps the immune damage is already done to my body and can't be fixed. Whatever it is, it certainly makes life difficult.

I stopped working a while ago. I'll save the disability spiel for another post. For the moment, at least that's one less stress to deal with. Right now, I'm just working on the latest round of antibiotics and waiting for the results of a lumbar x-ray to find out what's causing the issue in my back. None of my current pain meds (I take tramadol and gabapentin daily) are helping it. Heat doesn't make it any better. Nor ice. Massage makes no difference since the pain isn't coming from a muscle. Fingers crossed the x-ray gives a hint of the cause.

Hopefully future posts won't be so negative, but this is just to give a general update on the last 3 years. I've been hoping to be able to post positive news. Maybe one day soon I'll have some.

Herx is a four letter word.

Herx reaction - when existing symptoms are stirred up and make you feel worse before getting better. That's the story of my life for the past 10 days. Everything hurts. I have fevers. I'm exhausted, well more than usual. I'm lightheaded. The blurry spot in my left eye is back. My toes are going numb.

I know I'm supposed to see this as a good sign, but it's still hard to live through it. At least I am pretty sure of what caused it. I'm taking Tindamax in addition to the IV antibiotics and that seems to be what is kicking my ass. Five more days of this medication. Yes, I'm counting.

In case that wasn't enough, I now have to take a mega dose of vitamin D2. It seems that my vitamin D just continued to decline so we had to try another route. What I was taking over the counter was D3. The D2 is taken once a week, and hopefully causes a shorter reaction time than taking a daily dose. I can't say that I'm not having any reaction to it... I've still been getting migraines and lightheadedness, but the reactions do seem to be less than with the OTC version. So, I'm working my way through it and hopefully the reactions will continue to decline while my D level rises. And at the end of the day, the increase in D should contribute to feeling better.

Sitting in the IV suite with others has its advantages because I have now found that many of us have low levels of vitamin D, and one other person also has an allergic reaction to it as well. It's nice to know I'm not alone.

It's been a while

Most days I'm too exhausted to write. Or too nauseous. Or too achy. It was a long road to get this sick, and it will be a long road to recovery.

For now, I'm celebrating a minor victory. My health insurance didn't want to pay for the medication that my doctor wants to treat me with. It took about 3 weeks to get the approval, and then they only approved 20 treatments, instead of the 60 that my doctor wants. Yesterday, the office staff spent an hour on the phone with my insurance company, and got approval for an additional 30 treatments. Still 10 shy of what my doctor wants, but we're getting there!

Otherwise, yesterday was pretty crappy. As if I don't have enough going on, I've come down with a cold and sore throat. Lots of body aches and pains, too. Today is starting off a little better. Hopefully this keeps up.

Day One

Today was interesting. The doctor has me on 2 medications. The first is the same one that I was on last time. The 2nd is supposed to help the first one work better. Although the first one took longer than the usual hour to drip (just to make sure I didn't have a reaction to it since it's been a while), there were no problems. The 2nd medication needs to drip for over an hour to avoid reactions to too much at once. Mine took closer to 2 hours. And I'm glad, because I guess things could have been worse if it had gone faster.

About 10 minutes before it was done, I started to get itchy. I didn't really think too much about it. Lots of things can make me itchy. But one of the nurses insisted I take benadryl before I left. She said I looked a little flushed, which is one of the side effects. I didn't really want the benadryl since it makes me so sleepy. I was worried about driving home. I'm glad I listened to her though.

A few minutes into the car ride, the itching got much worse. I mean, I felt like I didn't have enough fingers to scratch everything! My right wrist was on fire from the itch, and then it moved to my hand. After that, I noticed that my hand felt funny. My palm and thumb started swelling. My fingers got a little swollen, just enough to feel strange when I tried to bend them. This lasted until after I got home.

I guess it was good timing that the benadryl kicked in right after I got home. The swelling didn't progress anymore, and the sleepiness took over. By the time I woke up, my hand was mostly better and the itching was gone. I can only imagine how bad it would have gotten if I hadn't taken the benadryl.

Let's hope that tomorrow is better!

Round 2

It's all in my head... at least the proof is all in my head. After IV antibiotics, 2 different oral antibiotics, and some antimicrobial medications, I'm still not feeling any better. I'm worse, actually. Lightheaded more frequently, body aches, joint pain, numb toes, a blurry spot in my left eye, and the list goes on. The specialist finally ordered a brain SPECT scan, which showed several areas of decreased blood flow to my brain, one area of no blood flow, and one area of abnormal flow. All of this is indicative of inflammation from chronic lyme.

So, today I am going in for insertion of a new PICC and tomorrow I will start round 2 of IV medication. This time will be a combination of different medications which are supposed to better cross the blood-brain barrier. I'm hoping for some better results this time. All I can do is keep fighting.