HoneyColony CBD Oil: A Review

** “I have been given this product as part of a product review through the Chronic Illness Bloggers  network. Although the product was a gift, all opinions in this review remain my own and I was in no way influenced by the company.” **

If you are a first-time visitor, well, HOWDY!! And thanks for stopping by! Here are some other posts you might like check out:

Don’t Read This if you are Grateful for your Illness

The Long Lyme Con Continues…..

How are Lyme Disease and AIDS Alike?

Now, onto the review!

Hi, my people! Well, here we are, post-election in the states and moving quickly towards the holidays.

When I was first diagnosed with Chronic Lyme disease, now almost 4 years ago, I thought I knew what it was all about. You get bit by a tick, you might get sick, and then you are treated and cured quickly. HAHAHA!  Little did I know! So once I began researching this crazy and unpredictable disease, I began realizing that there is no CURE. That in many cases, including mine, Lyme cannot be merely treated with 14-28 days of oral antibiotics. Not even. And I began to understand, especially after being sick 6 – 12 months, that I was going to have to try out some unconventional, non-Western medicine options, to treat this bacterial infection.

I had been hearing and reading about CBD oil long before I decided to try it out. Information was mixed but the one common denominator seemed to be QUALITY of the product. Yet, I had no idea where to even begin. My first foray into the CBD sphere was, and now regrettably, a product I found and purchased from a seller on Craigslist. I know, I know. Believe me, I really was clueless, and in my Lyme social circle, no one had a recommendation for me. But I knew that I wanted to try this option. No Bueno. Honestly, I think there was turpentine in it. I tried to take it a few times, but the taste was just so disgusting, I could barely gag it down.

From that point on, I realized, and the hard way, that I needed to invest in QUALITY. I continued my research and then recently, I was offered an opportunity to try out HoneyColony’s CBD Oil. I have tried this company’s products in the past, and I have not been disappointed. I jumped at the chance to try out their CBD Oil.

Quality CBD Oil!
http://www.honeycolony.com

HoneyColony’s CBD Hemp Oil is a blend of several ingredients, including Teasel root as well Astragalus Root. You can visit this page for a much more detailed list and explanation. I have tried both of these roots before in the past with some positive effects, but not at the same time and not as a part of a CBD Oil mix. When my product arrived, I was really excited to give it a shot!

I know some people may be hesitant to try CBD Oil as there is a lot of misinformation out there, including that it makes you “high.” However, according to HoneyColony, “Cannabidiol (CBD) is extracted from the Cannabis plant and has no euphoric properties whatsoever. This formulation offers all the health benefits of CBD without the feeling of being high.” At no point of my using this product have I ever had a euphoric feeling or a feeling of being “high.”

The first stop I made before adding this product to my daily routine was at HoneyColony’s  13 Commonly Asked Questions about their Superior CBD Oil product ranging from ingredients to usage. Since this quality CBD oil is mixed with coconut oil (no weird ingredients in this product!), this oil has a very smooth taste. There is no aftertaste nor did it bother my throat or stomach. It is silky sweet and easy to administer.  I take just a drop in the morning and then one at night. While I haven’t necessarily seen a huge impact in the morning for myself (and mornings are so, so difficult for me), I have experienced an effect in the evening. While I struggle with getting up, the joint stiffness and fatigue, lately, I have really been having sleep issues. I can go to sleep, but then I tend to wake up 3-6 times a night. It’s been a serious hindrance in the past few months.

Bundles are available!
http://www.honeycolony.com

So I started taking a drop of oil about an hour before bedtime as suggested on the  13 Commonly Asked Questions page. This seems to help me relax enough to get to sleep. Recently, I have also started taking a drop when I wake up during the night. Doing this has been beneficial in helping me get back to sleep and to stay asleep throughout the night!

Look, HoneyColony products are top-quality products! Yes, the price is higher, but again, the QUALITY is worth every penny. I’ve tried enough other inferior CBD oil options to pay twice over what the cost of one of HoneyColony’s CDB bottles cost.  I’ve thrown away more that I care to share. And this bottle that I received about a month ago is still more than half full. I won’t go anywhere else in the future to purchase CBD Oil other than HoneyColony!

Happy Sunday, my friends. Take care – B

P.S. If you are a first-time visitor, well, HOWDY!! And thanks for stopping by! Here are some other posts you might check out:

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The Pandora Lyme Box

*I wrote this back in July 2015. But all is still relevant, if not more so. When there are over 300,000+ new cases of Lyme a year across our nation, why aren’t the CDC and IDSA doing so much more for the population at large? And why aren’t these organizations being held more accountable for their actions or lack of actions. #LYMELIESCOSTLIVES

Hi out there! Today I listened to the Diane Rehm show and if you caught it as well, it was a program about Lyme disease. Honestly, it didn’t shed any light on the disease for me personally and yet again, some of the guests continued to perpetuate some of the Lyme disease myths floating around. Now granted, I am not a scientist, I am not a researcher, and I am not a doctor. But I am one of the many suffering from this disease so I have read as much information as I can get my hands on about Lyme and I will continue to do so. At this point in my game of Lyme, I feel like I know enough to make fairly decent decisions regarding my own care.

Listening to the program and reading comments on Rehm’s FB page really struck a chord with me in that there are so many people out there suffering from the elusive Lyme bacteria, Borrelia burgdorferi (B. burgdorferi). And so many of us are not even close to getting the help we need. The medical community is at odds as to what to call the condition where patients suffer symptoms of Lyme after treatment; it is also at odds with whether the bacteria is actually present after treatment or not. On the show, Dr. John Aucott from Johns Hopkins Bayview Medical Center basically agree that yes, in rare cases, patients still suffer from symptoms after treatment but he would not call it Chronic Lyme. He sidestepped this so many times…well anyway. Instead, he made it clear that if, and only rarely, patients have lingering issues, it is due to an immune response but not due to persistent bacterial infection. He stated this as a fact when in reality, this has not been proven as not true in a human subject.

**The two awesome posters above are from a wonderful website and patient advocavy.Please visit http://www.lymestats.org

But how do we even know or how can we even begin to dismiss the idea that this bacteria, one of the most, if not the most, complex and intelligent bacteria we know of, cannot persist? Just because we do not have the means or the way to find out should not lead then to dismissal. I think back to things in the past that were dismissed and then later, after the technology and testing and imaging came to pass, after the WAY to see something became clear, we changed our minds because we actually had the TOOLS to figure it out? Now I am not necessarily trying to make direct analogies here but think about this: women used to be treated as mentally ill if they suffered certain symptoms after delivering a child. Ever read “The Yellow Wallpaper” by Charlotte Perkins Gillman? But then as years went on and doctors focused and researched, this “condition” turned out to be a physical one and not merely a “mental” condition we now call postpartum depression. The same comparison be said about depression in general. We didn’t know what it was, we know now, we know it can be hereditary….and on and on.

I just cannot then figure out why the medical community, in this country for sure, is so fixated on sticking to standards set by IDSA, the Infectious Disease Society of America, in 2006. Like many of us, I wonder why more money has not been put into finding out so much more about a disease that is now affecting 300,000 plus here in the states? I just cannot wrap my head around it!

SOURCE: http://nocturny.deviantart.com/art/Pandora-s-box-340317104
SOURCE: http://nocturny.deviantart.com/art/Pandora-s-box-340317104

I know I live in a bubble, don’t get me wrong. I have yet to have anyone in my life doubt that I am still suffering from something, no matter what the terminology. Not everyone has that kind of support system. Why don’t more medical and science professionals care about Lyme? Or why are they staying away from researching Lyme? Let’s just say that the radio show today did not answer any questions for me. In fact, it only made me think about more questions I have about Lyme disease! On that note, dearies, I must take leave of you.

Until we meet again, peace -B

Ever-Changing Symptoms

I was really hoping these last few weeks of school would go very smoothly. I’d made it this far, limping metaphorically, but since spring break, I wasn’t doing too horribly. My protocol since March this year has been herbals only, and so the hope is that my body in conjunction with the herbals can combat the Lyme and send it packing. Yes. I completely understand that after taking a multitude of antibiotics for over 30 months including IV abx is hard on the system. Yes. I understand that my gut flora is messed up. Yes. I know it will take awhile to get my system back on track. Yes, yes, yes. Got it.

Knowing now what I know about Lyme disease and the various ways to treat it, would I go back and do the same thing? Most likely. When I was first and finally diagnosed with Lyme disease, I was severely ill. Not only had I had Lyme for who knows how long active in my system, I also had a viral overload. Several viruses that we normally have once and then build an immunity to had reactivated in my system thanks to the bacterial infection. So, yes. I think treating with antibiotics was the best choice starting out. It took almost 9 months to truly see any difference in what I was experiencing. I didn’t herx either for about the first 9 months. I was one sick puppy.

Very rarely do I forget that I am still dealing with Lyme. It won’t let me forget. If it isn’t one thing, like severe fatigue, then it is another, like nausea and migraines. The symptoms seem to come and go with no rhyme or reason although the headaches seem to stay my constant companion. When my LLMD first started treating me in 2013, she said that “we want to progressively get to a point where you have more good days than bad.” Sounded like a great plan to me. And sometimes, that is the case for a few weeks at a time.

Recently though, I have had a string of pretty rough days in a row. As soon as I can, I will post about what is going on. Right now, I am just trying to put my nose to the grindstone and get through it. Consequences of this situation right now are that I cannot work, so I have been out this week. Of course, I am grateful that I have so much support at my work and people who understand, but I feel bad that my students miss out. But if it had to happen, this really is the better time of year since we are getting close to finals and summer break. It’s been an emotional rollercoaster for a couple of weeks, and I am really ready to get better and get back to work.

So for those of you with Lyme disease out there or a chronic illness, do you also experience a fluctuation in symptoms? Are they triggered by anything that you can pinpoint?

Peace -B

Afterfalling.jpg
via optimisticquotes.org

 

 

 

 

Winner, Winner!

These past 3 weeks have been kind of a blur. Week before last, I had severe nausea. No vomiting. But let me tell you, the nausea kicked my butt. I missed a couple of days of work, and it was a huge pain to get into my doctor’s office. I saw her PA and he prescribed me an anti-nausea medication along with Tama -Flu. He told me that most likely I had picked up a bug. And since I am a teacher, this seemed plausible. Except for the fact that my left elbow has been hurting daily, my left knee has been hurting, and there’s the nausea to top it all off.

I took all of my meds as instructed. Then last week, I caught a cold, I guess. Luckily, I already had an appointment with my doctor that I had made months in advance and forgot to cancel. This time I had all of the above plus lower back pain and the incessant cough. After xrays for my back and a check-up, I was diagnosed with Bronchitis which I do get occassionlly.  I was sent home with antibiotics and a day off from work. Before I left the office, my doctor ran a CBC as well as a Lyme test. She does this almost every 3 months to see what if anything is showing up. You can check out more information about Lyme disease testing here.

Winner-2-copy

Honestly, I didn’t think twice about the bloodwork since it is done so regularly and most of the time, not much changes. This time, however, I am a winner of the Lyme contest! I tested 100% CDC positive for Lyme. Again. I have not had this result since I tested almost 3 years ago to the day when I was first diagnosed. Yet, this is not a new infection. In fact, this is the SAME infection as I have had for several years now!

I am sure this is why I have felt yucky these past few weeks with no relief.

My guess is that since I was taken off of the antibiotics in November, the bacteria have now come out to play. Oh, Borrelia burgdorferi, you are definitely a worthy opponent! See, this bacteria is very smart. It can and will leave the bloodstream to hide in tissues, joints, muscles, brain, nerves. Anywhere it can burrow to be out of harm’s way. It can also build cysts around itself for defense.  Anyway, NOW WHAT? My doctor put me on a Z pack. But that is only for 5 days. What am I doing about this for the next 3 weeks until I see her again and my other doctor out of town? As you can see, I’m a little freaked out about it all. I have a call into my doctor to check on this treatment protocol and in the meantime, I am going to see a Rheumatologist who supposedly treats Lyme. We’ll see.

All I know is I have to keep trying whatever I can to get rid of this infection. It has reared its ugly head at a time I thought I could move beyond traditional medicine to treat and boost my immune system. But it has proven me wrong for now. I hope all is well in Bloggerland. Take care and make sure you always assume ticks are out there whever you live!

Peace – B

 

 

Nobody Said it was Going to be Easy

TGIF! Wow. What a week. I really hope yours was better than mine. As I have mentioned in some of my previous posts Turbulence of Lyme SymptomsFire in the Hole, and Derailed, there is a lot of inconsistency in how Lyme will manifest itself each and every day. There are some things, in my case, that stay pretty constant such as daily headaches, joint pain, and fatigue. But then there are those other issues that crop up from time to time, I guess maybe they are flares?, and it is impossible to prepare. What’s the saying, the devil is in the details?

thermometer-temperature-fever-flu-medium

And so last Sunday, I started having severe nausea. It lasted the entire day. I couldn’t eat, sleep or do anything. I just laid in bed, trying not to move around. The moving made the nausea worse. Indeed, it was a day where I just wished I could get out of my body for even like 10 minutes to get some relief. I chalked it up to eating some jalapeno sausage that morning; I knew I shouldn’t have eaten it but it was delish but soooo not worth it.

Unfortunately, no. The illicit sausage was not the problem. On Monday, when I tried to get up to get myself ready for work, I felt really nauseated. Then, the headache joined in. There was no way I could make it to work, let alone teach all day. Monday and Tuesday were more of the same. In the meantime, I was trying desperately to get into my Lyme doctor (LLMD) but there were no appointments available- for the entire week. Whaa? They were very clear that they could NOT fit me in even if I came in when they opened and waited. When I explained again my symptoms, the front desk told me that a nurse would return my call that afternoon. That was Tuesday. By Wednesday evening, no one had called me. Although I was able to get up and go to work on Wednesday, by that afternoon the nausea was back rearing its ugly head. Now, please do not think that I have an entitlement issue. I realize doctors are extremely busy and overbooked. I realize that there are other patients out there who also need to get in for a visit.

On the flip side though, this is my doctor who is treating me for Lyme disease. I can’t just go “anywhere” to get treatment. Other doctors, and almost all here in the South, are not trained on Lyme nor do they actually believe it exists here in Texas. This is the state of the medical options we have for Lyme here and in way too many other places in the US. In fact, Lyme is endemic to Texas. Check out this research done by Texas A & M University “Lyme Endemic to Texas.” Thus, going to another doctor is really more of a waste of time than anything. The ER was an option if I started having other issues, but mostly it was the severe nausea that was the new thing. All of my other symptoms are dealt with in the daily grind; they ebb and flow. But the nausea. God, it was (is) the worst.

It feels like I need to throw up (sorry TMI!) but I can’t. That kind of nausea. No vomiting though. I tried to stay very hydrated. I tried eating Saltines off and on. Yet, about 30 minutes after eating or drinking tea or Sprite, hello tummy monster! Anyway, I emailed my doctor, and I was able to get in yesterday afternoon. Supposedly, I have a virus. I say supposedly because honestly, I think it is more Lyme related than anything else. But I took what I could get which at this point was to get some sort of relief from this symptom. I was prescribed Tamiflu and anti-nausea meds and told to come back next week if it was still going on. Today was better because of the anti-nausea meds, but I’m still having experiencing the nausea.

This is how the Lyme bacteria works. It is a very stealthy and intelligent. According to Lymedisease.org, “Lyme disease is caused by a spirochete—a corkscrew-shaped bacterium called Borrelia burgdorferi. If not treated as soon as infected, then the chances of it reproducing and getting into every system of one’s body is extremely probable. Now granted, not everything can be attributed to Lyme. But for me, most of the time, my symptoms are directly related to Lyme disease.

Again, I hope you all had a much better weekly journey than I did. Take care – B

 

 

 

On the Antibiotic Wagon

I hope everyone is staying cool. Temperatures here have been raging at around 105 degrees and that is the REAL temperature, not the heat index which is even higher. For the love of God, it is hot. Between noon and about 7 p.m., it is way too hot for me to go outside. The heat just completely zaps me.

I had my doctor visit a few weeks ago. Things seem to be pretty status quo in that my numbers are all hovering basically at the same place as in June. Here’s where I stand right now: CD57 – 33, Lyme bands 23 and 41 showing IGG and band 41 IGM, EBV is reactivated; it had been inactive since April, Mycoplasma finally under control, and HHV6 active again. In all honesty, this is for the most part where I was at the beginning of last summer. What I expected was my doc would put me on another course of antibiotics since I have been on amoxicillin for about 5 months now. Instead, on the patient lab VM, she said we were going to take a break from the antibiotics.

http://netdna.tinyhouseblog.com/wp-content/uploads/2014/03/medicineshow.jpg

It freaked me out. I listened to the VM about 3 times. My brain is like, Are you Sure?!? But there are no certainties with Lyme now, are there. I was so sick when I was finally diagnosed and I have not had more than a day or two break from being on antibiotics in 27 months. In in those 27 months, I have made some significant strides. So, yes, it is freaking me out a bit! I know I need a break, my body needs a break, but I feel like I have lost my walking stick. It’s only been 3 days without meds, and I keep analyzing myself, waiting for new symptoms or for the flu-like monster to rear its ugly head. It’s hard not to worry.

Also, right now is about the most stressful time for me at my job, besides at the end of the school year. In a mere 10 days, school is up and running and so am I. I’m struggling between being happy to return to the classroom after a nice summer break and the dread of becoming severely ill. While I know it is not a good thing to worry and stress, it’s there in the back of my mind, the What If? Meditation, and I use that term very lightly as I am just dipping my toe into that arena, is helping some. The breathing combined with focusing has helped me clear my mind some. Like one of the mantras in AA, I’m taking it One Day at a Time. Or one hour at a time. It’s just a challenge for sure.

Anyway, I’m on the wagon, and we’ll see how it goes. My next doctor visit is early October. By then, the weather will still be hot, but the evenings and mornings will be cool, school will be in full swing and hopefully, my immune system will have stepped up and kicked some butt.

For those of you not on antibiotics, or taking a break from them, any suggestions on how I can support my immune system right now? I appreciate any and all recommendations.

Till next time, friends, -B

Mycoplasma, Anyone?

The Challenge!
The Challenge!

So, at my doctor visit a few weeks ago, we decided to retest for co-infections. I was tested in March 2014, along with the test for Lyme disease. At that point no other infections were showing. Now, two years later, and I am still feeling like every day is a real challenge as far as symptoms go. Dr Horowitz, in his book, Why Can’t I Get Better? , examines the possibilities of other infections going on along with the Lyme. A multisystemic illness as well as approach to treatment.

We decided to  check again for the big 3, Bartonella, Babessia, and Ehrlichia.  We also decided that we check for Candida, Mycoplasma, and the MTHFR mutation. I brought these up based on Dr. Horowitz’s book. Now, in September, my doctor wanted to do a through genetic DNA test. This test would give us info on several possible MTHFR mutations, it would reveal how well I process certain medications, and it would help us know what medications, both antibiotics and pain meds, are best for me. But the insurance denied such shenanigans and with my looming deductible of like $1,200 to meet first, well I had to pass on that test, unfortunately. At least for now.

Anyway, back to this most recent visit and blood work. Results are in: none of the Big 3 were positive. No Candida issues. Cool! But, I do have Mycoplasma, reactivated EBV, and an MTHFR mutation that hinders my processing of B vitamins. Ok, ok.

I won’t lie. This information freaks me out a bit. Actually, a lot. I mean I know many people are dealing with co-infections. It’s just damn. Lyme bacteria is complex and intelligent enough on its own. Now, add Mycoplasma pneumoniae to the mix. This is the bacteria that causes walking pneumonia. And then the EBV is active, the virus that causes mononucleosis. I’m basically hosting a crazy party in my body, and I didn’t even get an invite. Excuse Me?!?

Now what? Honestly, I’m not sure yet. My doctor has this extremely annoying system where you go for your visit, then do your blood work, then wait 6-8 weeks for a follow-up appointment wherein we discuss the lab work from   2 months ago. Makes really no sense to me but then again, I’m no doctor. What I am trying to say is, she didn’t change my meds for now and I won’t see her until April. Then, I guess we talk about the co-infections.

However, a dear friend sent me Healing Lyme Disease and Coinfections by Stephen Buhner. He goes into great depth about all of the mycoplasmas of which there are several, and how to treat verbally. Some of what he goes through is the details about how this bacteria works on cells, etc. This part is very detailed and I am pretty lost. From what I have read, this bacteria is also extremely deft and intelligent as well. He states that the coinfections work synergistically. Again, WTF?!?

I’m trying to take this all in stride, research as much as possible, and understand what all of this means. Please wish me luck as I will most definitely need it.

Anyone else dealing with a Mycoplasma infection? And if so, how is it going and what is the protocol for treatment?

Please check out http://lymediseasechallenge.org   Today, March 1st, the Challenge Begins!!

Hope this finds you pain free and Happy. -B

Word Loss

**WARNING – THIS POST IS DEPRESSING. PLEASE DO NOT READ IF YOU ALREADY FEEL DOWN.

These past 2-3 weeks have not been good for me. I am struggling in every single area of my life: work, personal, mentally, physically. I have not been optimistic in awhile. Between attempting to cope with my cognitive issues, which have become many of late, along with the physical challenges of nausea and body pain, my personal relationships are indeed failing. I can see it happening, but I don’t know what to do to make it stop. Any of it.

I do my best at work. I know my attitude is not always optimal, but I am really trying my hardest. Communication is difficult even on a “good” day. And communication, well that’s kinda “my thing.” It’s something I take great pride in and something I have been good at my entire life. But not now. Although an overused analogy, my brain feels like swiss cheese. I can’t remember regular words such as pliers, consistency or ambiguity when I need these words. My short term memory is almost nil at times. I keep asking co-workers and my husband the same things over and over. I feel like I am slowly going insane. Not being able to remember, not being able to recall basic words while speaking, spelling words incorrectly all of the time is so very frustrating and aggravating. This proceeds to heightening my anxiety and my anger. I imagine that to some degree, this is what is is like to have the onset of Alzheimer’s.

And so, my negative persona and my overall hostility rises. I avoid conversations like the plague. I don’t want to talk because, to myself, I seem to make no sense at all. I imagine that others feel the same when I speak. I am alone. I feel so singularly alone in this.

There is no quick fix, and I get it. I have been very patient and open to any and all treatment over these past two years; I have diligently taken my meds. I do my best to keep my diet in check, I try to stay upbeat and optimistic. I am still working full-time. Yet, I still lose.

I still have the dreaded headaches every day. Joint pain. Every single day. I have made some progress with endurance but I still exhaust quickly. While, I think when in the midst of a migraine and nausea, “this is the worst!” really, the slow decay or what seems like decay of my memory and cognition is ultimately the issues that worry me the most.

For if I can’t use words correctly, beautifully, exacting, then who am I? Always one to rely on my wits and sarcasm, without these, I can’t and won’t ever find my way home, back to who I am. I know, I know. One day at a time. Like the Indigo Girls sing, “We’re sculpted from youth, the chipping away makes me weary.”

Right now, I am weary.

Peace. – B

All the Noise, Noise, Noise!

Howdy! Hope we are all having some relief!  Lately, I have developed a sincere noise sensitivity. At first I thought , oh, I can’t really hear well (although I have never had any issues with my hearing). Then, it was, oh, I am just getting old (although I really am barely middle age). And then, I finally realized that I am having some certain noise sensitivities! This is a newer symptom, and it seems to get worse as I progress in my treatment. I have read about people having both noise and light sensitivities with Lyme, but I have always been very sensitive to light  and only just recently am I noticing the noise issues.

Hmm. No bueno! I don’t seem to struggle much when it is a one on one conversation but if the pitch is too high or low, watch out! My poor husband. We get up early for work, about 5:15 a.m. and there are some mornings like today, that I keep telling him to please lower his voice a tad to the point where I can’t even hear him. Then he is like WTH?!?!  It’s a weird feeling when this happens. It is almost like the sound travels in my ears directly to my brain and zaps it. My thoughts start jumbling up and my head starts to hurt. Does anyone else have this experience?

Of course, it is waaaaay worse in a crowd, and by crowd, I mean like more than 4 people. Haha! No, really. In a crowd, there are just so many different noises and pitches and inflections. I try to focus on one, but I just can’t. When this happens, I get really frustrated. Some places/situations I have issues: when one person is talking to me at the speed of lightening, talking on the phone, parties, classes, stores. You name it. Pretty much anywhere there is a cacophony. It for sure makes it even more difficult to socialize…..What is “that”, you ask? 🙂

It’s been happening more and more lately so I am going to discuss it with my doctor on the 22nd. However, I am guessing there is nothing that can be done? I mean besides becoming a hermit which I have down except for this silly working thing. I am making light of all of this but it can be really irritating and depressing. Anyone else dealing with this phenomenon and if so, how do you do it without becoming the Grinch, like me?

GrinchPeace and joy to all of you. Thank you so very much for stopping by and reading.  – B

Sunday Morning Coming Down

“Well, I woke up Sunday morning, with no way to hold my head that didn’t hurt…” – Kris Kristofferson

Up and at ’em, kind of early this morning. I honestly feel like I have a hangover. However, no alcohol was consumed. Scout’s honor! Not one drop! Lyme seems to suck the fun out of everything. Just a disclaimer: before Lyme, I did enjoy having a couple drinks on the weekends. My favs included white wine, and in the summer, some beers. But all of that has come to a complete halt as of, or even before, my official Lyme diagnosis. My body cannot handle alcohol.

On one hand, we can chalk that up to a Plus. On the other, it really does suck that I sincerely cannot have even one drink without feeling like a truck has run me over. Sometimes, like today, I feel like a truck has run me over anyways. Fun. A couple of reasons to stay away from adult beverages as a lymie is one, the sugar. The bacteria feed off of the sugar and LOVE IT! So, let’s work on not giving the bacteria Borrelia burgdorferi or Bb any more ammunition. It already has the upper hand here! And second, many of us are being medicated with antibiotics. Strong stuff too and at high doses. Alcohol can definitely minimize the effectiveness of the meds and again, we don’t want to hinder our ninja fighting machine anymore than what is absolutely necessary. When I do treat myself, and rarely, to a drink, it is something to enjoy. How do you feel after consuming alcohol? Or is there any other foods/drinks that trigger symptoms for you?

Wishing you all a Happy Sunday. -BHL-980[1]