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Deseret Biologicals (DesBio) Series Therapy for C.Difficile (C.Diff) Treatment Review - Homeopathy 

6/1/2016

6 Comments

 
Lady of Lyme: Deseret Biologicals C Difficile Series Therapy
If you have ever had C. Diff then you know what a miserable and exhausting infection it is. In fact, even more so, it can be a fatal infection, especially in those who are immune compromised. I had C. Diff in 2013, it took me 6 months to kick it, and in the end it was an FMT which saved me. After that I thought I was in the clear and took even more precautions with handling mail or anything from the outside. I should note I was NOT on antibiotics when I got C. Diff in 2012, and I also was NOT in a hospital or anywhere that I could have got it. I was housebound and bed bound, so I have no idea still how I got it, but I digress.

Fast forward to the end of 2015 and I came down with C Diff yet AGAIN. This time I got it from my Home Health nurse. She said a few of her patients had been dealing with it, and since she came from the homes of those patients into my home it was quite clear how I picked it up. Again, it just goes to show that all it takes is 1 single spore on my nurse's bag for me to catch it. When you are immune compromised with Lyme Disease you have got to be so overly cautious and careful. Even though we cleaned after my nurse left really well, it just took that 1 spore going unchecked to catch it. This time however I thought I could kick it fast by just going straight to FMT in the first place, but that did not work. I did about 10-15 FMT's and NONE of them stuck. I was taking Florastor and probiotics and did nothing differently than I did in 2013. I still to this day do not know why it did not work. I used the same donor, did it for days on a row, and followed every specific protocol. It is a complete mystery to me, but after 4 months of no success and lots of pain it led me to realize that I needed a new plan of attack.

I happen to be incredible intolerant to both of the antibiotics used for C.Diff, so that was not an option for me. This is when I decided to give the Deseret Biologicals C.Difficile series a try, since I had luck with their other series therapies in the past. I will say I was a bit pessimistic that these homeopathic vials would kick something as insidious and persistent as C.Diff, but I also knew that this stuff worked amazingly in the past, so I had hope.

For 2 months I was on this treatment. Each 'series' or box takes 1 month to complete, and I did 2 boxes (the required amount). Each series has 10 vials, and you take 1 vial under the tongue every 3 days. Each time I took a vial I had no bad side effects, and 1 great surprise, in that it stopped the diarrhea completely. It worked incredibly for calming things down in my gut, so much so that I could hardly wait to take the next dose! Some days I actually had to spread my 3 days out to 4 because it would constipate me so much. It might sound negative, but trust me when you have C.Diff it is a welcome surprise.

When I finished both series I waited a week and then re-tested for C.Diff. I was nervous because my colon still hurt in a funny way, which is very specific to C.Diff, however I did not know if it was just left over damage from the many months of carrying this pathogen, or if the bacteria was still there. I sent my stool in for an advanced culture, which looks for the antigens and if there is so much as 1 spore in the stool it will be found. I am happy to report that my test came back NEGATIVE! This series therapy, completely on its OWN eliminated the C.Diff from my colon. Completely. I actually cried tears of joy, because it was SO gentle, and so easy on my body (especially in comparison to antibiotics), and It really worked. I want to shout it from the rooftops!

For full transparency I did take these probiotics and Florastor as well, but I also take those in my every day life with or without C. Diff. When you have an infection like C. Diff it is even more imperative to re-populate with good bacteria. The probiotics I use are also special, because they are histamine reducing, which means it also helped a lot with general inflammation in my colon during this time. I wrote a whole post about it here if you're interested! Florastor has the ability to neutralize toxins A and B which are released from the C. Diff bacteria as it dies, and are the toxins which cause all the damage and pain in the colon. I think it is crucial to have Florastor on board as you are killing off the infection itself. 

If you have C.Diff and it is not getting kicked with antibiotics then PLEASE ask your doctor for this! It is physician prescribed only, but it is completely homeopathic. It is incredible, I can not possibly say more good things about it. I finished this series back in February of 2016, and it is now June. I have been perfectly fine since then, and everything is going great thankfully!

If you are curious about how the series therapies work in the body, or the science behind it, here is an explanation I wrote up on how it is used for Lyme Disease. The same concept is happening here, just with C. Diff.

If you have any questions, please feel free to ask in the comments below. I hope this can be helpful for someone else who is struggling with C.Diff and at their wits end like I was.

God bless,
Christina

6 Comments

My Experience Using ACT (Advanced Cell Training) for Lyme Disease - An Honest Review! 

2/24/2016

59 Comments

 
Lady of Lyme: And Honest Review of ACT Advanced Cell Training
Since this is the section of my blog where I speak about different Treatments, I wanted to share a long delayed post about my experience with ACT - Advanced Cell Training. Every time I tried to find a review (prior to starting), all I found was a few blogs praising it but they didn't really explain much and they also are close to/with the creators of it. I'm not saying that they were influenced, but that didn't hold much clout in my mind. I wanted a real review that talked about all aspects. So, I am here to share my side of the experience using ACT, which is MUCH different than what you normally hear, and hope to answer as many questions as possible.

In a nutshell, does it do what it promises? Yes, and no. Did it work for me? No.

I did ACT for 3 months, from August 2014-October 2014. The first month is free, in that you pay and if you don't feel like it's doing anything you can get a full refund and stop. That seemed pretty fair to me, and was a big part of the reason why I jumped in. I figured it can't hurt to try! I went into this with a completely open mind. It made big promises and the reviews on the Facebook page were amazing. The method can seem a little "out there" to some, but I genuinely felt like if THAT many people got well then who am I to judge it or look down on it? Why not give it a try and see if I can add myself to the list of success stories? So, I did this with a completely open heart, just wanting to experience what ever would come my way. Maybe I was even a little bit desperate at the time, because I began this in August which is during the early stages of my health downfall, and at a point where I felt very hopeless. ACT was essentially my hope.

I did not tell anyone I was doing this, and afterwards still didn't share that I ever did it. Until now. Why? Reason #1 was that I didn't want or need anyone's opinions to cloud the process. I wanted to do this and give it my all, and getting flack for it or just hearing a, "oh my friend did that, it didn't work" comment would discourage me. I didn't want that. Secondly, I didn't share afterwards either because at one point I thought I might go back to it. I stopped because I got so ill from it (more on that later), and thought I could finish up at a later date. Now that I know that is highly unlikely I'm willing to talk about the ins and outs of this process.

What is Advanced Cell Training and how does it work?
This was my million dollar question too, because no one really explains what the heck it is until you get into the class. I could not find one review that talked about it in depth, but rather it's just a surface explanation.

The ACT website says: Advanced Cell Training (ACT) is a cellular behavior modification program. This simple and non-invasive healing process can be done from home by phone and internet. There are no pills, herbs, supplements, or machines involved. We have all trained ourselves to do things such as ride a bicycle, dance, play a sport or musical instrument. This is accomplished through focus, intent and practice. It’s called muscle memory, though it is really the cells that retain the information. ACT uses the same premise and applies it to the autonomic systems of the body, including, but not limited to the immune, digestive, elimination, endocrine and respiratory systems. We believe it is actually easier to train the body to do that which it is designed to do, rather than what it was never intended to do. While playing piano and golfing is not inherent in our DNA, our immune system is. Restoring proper bodily function at the cellular level can restore homeostasis. That is when the body processes stress, removes toxins, kills pathogen (viruses, bacteria, parasites), stops overreacting to allergens, and nourishes and protects itself; restored health is the likely result.

Soooo, what the heck does that even mean? Once I got into "class" (via a group conference call) on the first day all was explained. Essentially this is how it works: First we are read groups of code words, usually lasting about 3-4 minutes, which aren't even really words but rather snippets of words put together which the brain understands on a deeper level. For example we might be read IMGBORRELIA818 or something of the sort, which to the naked ear makes 0 sense but to the subconscious it does. There are pages and pages of codes that get read to the class, and they are read at lightning speed. I laid down, eyes closed, and just listened. After that is finished we are instructed to listen to an hour of a repetitive melody to "set" the codes in the brain. We got a CD and could download it to any computer or phone, so it was convenient. I laid down, put the music on and rested. (We also had to tap our thalamus for the first 5 minutes of the music). After the hour is up, you have to call a special phone number and get "set" with a few more words, and then listen to the hour of music again. The whole process (class, codes, music, setting, music) takes about 3 hours total. It seems long, but it's a small price to pay for health so I really was not phased. We met once a week like this, and each week we were to report our progress to Gary. We sent an email that had a list of our top 10 biggest concerns and then we rated how they felt on a scale of 1-10 each week. This is how people see progress, because as the weeks go on the numbers should go down from the 10's where it began to 1's and 0's. Also, during each class call Gary speaks to a few of us on the call personally so we all can follow along on each others progress.

Week 1 - Day 1
Going in to class on day 1 I expected to feel nothing. We were warned of the herxes to come, but I thought there is absolutely NO way in God's green earth that words and music could do anything to me. I really didn't. I guess I was a doubter in that respect, but it just seemed like an outrageous idea. I had conversations with my mom laughing at how stupid that would be. Well, guess who felt like an idiot the next day? Me. Because it knocked me on my butt. While listening to the music I had fatigue and exhaustion hit like no other, and the following 24-48 hours were hell. I am not even joking (but I wish I was). Let me just tell you that I have done a lot of treatment during my many years with Lyme, and I understand herxes, and can usually control them to an extent. But oh no, the herx I got from this ACT class was unlike anything I have ever felt. So intense, lots of pain, lots of everything. Once it eased up I remember asking myself what the heck I got myself into.

This continued on for the next 3 weeks, and essentially that's why I decided to continue on past the first "free" month. There was no doubt that it worked on some level because I reacted strongly and intensely, much to my great doubt. I wanted to continue, because even though the herxing was terrible, I was committed to coming out on the other side. In fact, our class of 26 still had all 26 students going into week 5, which tells me that everyone else likely felt the same way. I was also encouraged because some of the participants already were having massive changes in their symptoms for the better. So, I hunkered down and continued on into September.

Around this time in week 5 Gary realized that I was having a really hard time with the codes, and my body was being beaten up badly. This was, by no exaggeration the sickest I had been from a treatment of any kind. I get how insane that sounds, but it's true. I wasn't able to eat hardly anything, my mom was giving me sponge baths regularly because I couldn't physically move to shower, I had to sleep with my mom for her to watch me at night (had some intense episodes happening), and so much more. I was really freaking out about what the heck was happening to my body because it was intense, and sudden and I wasn't getting relief. At this point Gary spoke to me one on one and said that for some students he gives them "side codes" which are a smaller set of codes specifically created for ME to help ease my herxing and get my body to detox properly. I said sure, did the side codes, and that was the first time I had any ounce of relief. It felt like someone took 100lb weight off of my body, and I was so thankful.

This was short lived though, because by the time I did the codes for week 6, the herxes hit again and stronger than ever. At this point Gary veered me away from the course of the class and said that instead of giving me codes for bacteria, viruses, protozoa etc (which is what we have been getting in class until then), that he would give me codes to work on emotional blocks. Typically the emotional portion of the class doesn't come until much later, but he began me on it earlier separately because he felt that the class codes were much too strong for me and the emotional blocks were what were holding me back.

Now, if there was EVER a time for me to scoff at something, it was now. And boy did I scoff. I thought, "are you kidding me, what emotional blocks? oh good, it's obvious this is a bunch of hokey zen craziness and I'm done here." The idea of emotional blocks impeding my healing was laughable so new-agey to me at the time, and then the idea that code words could fix them and help me was even more absurd. I honestly almost quit at that point, and the only reason I didn't is because I was sitting there at week 6 feeling supremely WORSE than when I began. I felt like I couldn't quit or else I would be stuck in that, and I really wanted to come out on the other side. So, I continued.

Guess who again felt like the idiot the next week when the emotional codes made me herx EVEN worst? Yup, you guessed it, ME. At this point I realized that everything I thought I knew, I didn't know. And I was also ashamed that I was so judgmental about something. My attitude really shifted, and I realized whatever the heck this ACT business was, it was very real. That can't be doubted. Weeks continued, and so did the downward spiral. I had a few moments where I was like "oh good, I'm over this now!" But then I would get thrown right back into it. Advanced Cell Training took my body, chewed it up, and spit it out. I would be on the phone calling the ACT offices, trembling like a leaf, in tears, asking for someone to make this stop. And I kept getting told that it would all go away very soon so I need to keep on, and when it broke I would feel like a new person. I believed in this so much, and I tried so hard to keep going. But by week 12, I couldn't do it. I was a shell of the human that I was when this all began. My body was one toxic jumbled mess, and even I couldn't understand how I got there. At the end of October 2014 I stopped. At the time it was just a pause until I got stronger and could finish, but ultimately it was the end for me.

Afterwards..
If you read my main blog, I talk about how I relapsed hard at the end of 2014. Depression, which is something I had NEVER experienced before, reared its ugly head. That, coupled with being the absolute most sick and in pain that I had ever been put me at my low point. In November I missed being a bridesmaid in my best friends wedding, and my soul was crushed. I had so much hope and faith that this program would help me GET to the wedding, not the other way around. Following that I had bouts of severe pancreas and liver issues, leading to several months where I was genuinely unsure how I would make it or climb out of that low point. I never in my life was as sick as I was then.

Now, do I blame ACT fully, or even at all? No, I really don't. Not one bit. And that's because the program did what it said it would. It said it would use words and music to make my body attack and kill pathogens. Did it do that? Yes, I 100% believe it did. But my body wasn't strong enough to handle it. For whatever reason, I was the exception to the rule that ACT works for "everyone." Maybe it would have, had I decided to continue, but I physically couldn't. ACT could be a Godsend for so many, but for me ultimately it was anything but that. I was an optimistic skeptic going in but had that desire to heal and really felt like I could also be a success story along with the others. I don't know why I wasn't, but I can only assume that wasn't in my healing plan, and I'm okay and at peace with it.

This post is not in any way discrediting ACT, because if anything I know it does what it says and I admit it freely. But, it is vitally important for me to put my voice into the mix in case anyone is researching doing Advanced Cell Training and wants to hear both sides. Or maybe, someone is like me and feels like the outsider who doesn't understand what is happening. Have no fear, you are not alone! For some people it just does not mesh well with their bodies.

So that's everything, I think. If I left anything out or anyone has any specific questions please do ask, because I am more than happy to share anything. Or email me, if you would like to ask privately.

All the best,
Christina


Disclaimer: if you leave a comment defending ACT or arguing a side, it will be deleted. That is not the purpose of this space. This post is just my objective story about what happened to me personally. As I stated above, yes there are people who love ACT and get better. You can find such stories all over their official Facebook page. This is just my experience in an honest and detailed format. If it worked for you I'd love to hear that, but no comments which argue will be tolerated. I still urge people to read all sides and form their own opinions, and I support and encourage ACT to anyone who feels like it's right for them. I wish everyone healing and great success in whichever way they choose to pursue it.
59 Comments

Round 1: Vial 4 of Giardia Lamblia Series Therapy

8/8/2014

2 Comments

 

This dose was interesting because not only was it the toughest to date, but I also learned I was taking the medicine completely incorrectly... (Insert face palm here)

So I took dose 4 and within hours I was miserable. I hardly slept that night, the next day was what I would equate torture of my stomach to be, and the following night/day just kept getting worse. By Tuesday (which just so happened to be my birthday) I was in so much pain that I really couldn't move. I was curled up in a ball totally not understanding why my usual go to stuff wasn't cutting the pain. Stomach pain like I can't even explain. So I had my mom contact the head Dr over at Deseret Biologicals to ask if this kind of severe reaction is normal.

Long story short I was taking the medicine improperly. It was my knowledge that I put the vial under my tongue at once and hold it there for a minute and then swallow. This is how my other 2 Series Therapy treatments worked so I just assumed they all worked the same way. This is when I found out I was supposed to take the contents of the vial, put it into a bottle of water, and sip it slowly throughout a 12 hour day. NOT take it all at once. Hence my ridiculous and incredibly painful die off herx I was experiencing. He said to take probiotics to absorb the toxins in the stomach (weird right)? I had never heard of that before but I didn't argue. I took a large dose of about 70 billion probiotics & within minutes I felt like a new person. My stomach cramp lifted, the gnawing ache that was at a 10 on the pain scale melted away, and I was so happy I cried. It turned my weeks of hell around so quickly. Very thankful.

I wish I could say that continued forever but my stomach only tolerated a few of these high doses before it actually created more problems than good. So it was kind of a trade off. Either way I am instructed to take 5-6 days off treatment to recover then go back in with vial 5 this time correctly. So.. I will be posting how that goes in a few days.

Hopefully no one else makes the mistake I did, but if you somehow landed on this page and are reading this because you also did it then stop and break!! I really didn't think I could physically get through the next 45 days (or however many I had left) in the shape I was in, and still am in. I hope to recover and have an easier time with the rest of treatment. I'm sure it won't be a walk in the park but any amount of less awful I will take!

Until next time

Xoxo,

Christina

2 Comments

Round 1: Vial 3 of Giardia Lamblia Series Therapy

8/4/2014

0 Comments

 

Dose 3... What can I say about dose 3 except insert a picture of a skull and cross bones? Oh man, this one was a doozy. In fact I had to wait an extra 2 days to take dose 4 because that's how intense it was. Basically it's kind of like every tummy symptom you can imagine happening at full throttle around the clock. That's the only way I can describe it delicately. This treatment is seriously no joke. If you have had a long standing infection of Giardia then unfortunately getting rid of if is no walk in the park. But it just solidified that this was a major part of what has held me back stomach wise and I'm just thankful to have sometning available to me to treat it other than antibiotics. I'm on to dose 4 now, I'll report on that in a few days!

- Christina

0 Comments

Round 1: Vials 1 & 2 of Giardia Lamblia Series Therapy by Deseret Biologicals 

7/25/2014

2 Comments

 
This treatment is NO JOKE. It is not for the faint of heart. Not to scare anyone off, but you really have to be mentally prepared to go into battle with this beast. I took Vial 1 and that first night really took me by surprise. I just did not image it would be that bad and definitely not that fast. I was struggling all night with cramps, nausea, acid reflux, and being in a ball with my heating pad. I think that night I got about 2 hours of sleep tops. That whole day following went the same way, I couldn't eat more than a bite or two of food max. I went to bed thinking it would be a better night, but much of the same. I had an episode in the morning that got very severe, so it's a bit of a roller coaster as far as when the symptoms came and went. By day 4 i finally got some much needed relief and my appetite came back. Unfortunately that was when I was due to take the second dose (vial 2). I took the dose in the evening and by 3am the symptoms were back full force. I am writing this now on day 5, and my stomach is like in a giant sheet cramp. I also am having really severe hunger pains. They are deep deep rolling cramps that feel like you have not eaten for days. Almost like when you feel so hungry that you will be sick. I get those pretty severe and nothing helps. Even if I can choke down some food that often times does not help either. Hunger pains are a very common symptom of Giardia so I think I can expect to be fighting that off for a good majority of it.

I will be keeping this blog up and updating every single vial as I go through the 60 day treatment. I take one vial every 3 days, and there may be instances where I push it out a 4th day due to symptoms being too severe. I certainly don't want to overdo it. So, this is the place where I will honestly talk about that. I want to stress that this is NOT to be negative. This is to be informative. A lot of people who want information about certain forms of treatment can not find it readily on the Internet. This treatment blog is meant to be very honest so that anyone who is interested in how this feels or what it does will know. I refuse to sugar coat the truth because that would be unfair and untrue. So, you will get the truth here no matter what. People should have the right to know what they are getting into.

Anyway, t
hank you for reading!

xoxo,
Christina
2 Comments

Signing up with Young Living: Difference between Customer & Wholesale Member

7/13/2014

1 Comment

 
If you simply want to sign up with Young Living and skip this post then click HERE. It takes you straight to the sign up page.

I have shared my love of oils in many places online, and by word of mouth. But the biggest question I get is "Where Do I Get The Oils For Myself?" The oils I use are Young Living, and I picked them out of all the other brands because they are Medical Grade, which means they are safe to ingest. A lot of cheaper essential oils you find in drug stores are NOT medical grade, they are perfume grade and can not be taken internally. So there is a huge difference in quality. Young Living is the best of the best, you only need a drop or two of an oil to experience amazing results. Everyone with whom I have shared the oils has been instantly hooked, so I of course want to share with as many people as possible.

If you decide you are curious about the oils and want to try them out for yourself you can go to Young Living's website and create an account to be able to purchase. You will be given the choice of signing up as a Customer or a Wholesale Member. This is confusing to a lot of people so I wanted to share the differences, and the enormous benefit of becoming a Wholesale Member instead of a Customer.

Lady of Lyme: Signing up for Young Living. What is the difference between a customer and wholesale member?
Lady of Lyme: Difference between a customer and wholesale member for Young Living
There really are no hidden tricks or anything of the sort. Signing up as a Wholesale Member means you can buy the oils at 24% off retail cost, which to me was the selling point. The only 'commitment' is that you need to buy $50 in oils a year to keep your status as Wholesale Member. BUT if for any reason you don't do that, it's no problem. Simply call up Young Living and they will re-instate your membership for you. You never have to sell a thing (I haven't sold anything once in my 7 months), and it's basically just an awesome way to get a discount on oils so you can try more of them out and experiment with its many uses.

Now, on to the next question. "When I sign up, which kit should I buy?"
When you sign up as a Wholesale Member you will have the option to buy some of the kits at amazing prices. There are a few to choose from, but the best bang for your buck is the Premium Starter Kit. It comes with 11 oils so you have a little bit of everything which gives your freedom to really experience its benefits. It also comes with a diffuser and some other samples. The graphic below does a great job of explaining this:
Lady of Lyme: Difference Between a Customer and Wholesale Member at Young Living
Although that Graphic is from another site (Confident Mom), I want to note that if you do sign up all of those benefits are still included. I will send you a Quick Reference Guide to get you started, and offer access to private Facebook pages (with a wealth of information), and access to monthly SpreeCast's if you choose. I believe the best way to find the relief these oils can give you is to have a large variety, and the Premium Starter Kit includes all the most popular ones with the most uses.
Signing up as a Wholesale member with Young Living has really been the best decision I have made for my health in a long time. It has benefited not only myself, but also every single member of my family. I want to note that this post isn't intended to sell you guys anything, but to inform. I have seen a lot of people sign up as a Customer and I think it's because they do not fully understand the benefits of being a Wholesale member, or getting a Premium Kit. I thought taking some time to explain would help those of you who are seriously considering this.

If you want to sign up as either a Customer or Wholesale Member, click HERE

And if there are ever any questions about the oils or how I use them then please by all means feel free to shoot me an email, I am always happy to help: cskova01@ladyoflyme.com

xoxo,
Christina
1 Comment

Slacking On Updating...

1/29/2014

0 Comments

 
It's been a while since I have updated the Treatment blog! I finished a few rounds of the Borrelia series, and then I began doing Visual Therapy to restore the brain damage from the Lyme. I have also began a few new supplements that have been very helpful. I will be doing a full update and review on the main blog page within the week :)

xoxo,
Christina
0 Comments

Vials 5-10 - 3rd round of Borrelia Series (Lyme)

6/3/2013

0 Comments

 

I did a terrible job of keeping up with this like I should have! But it was mostly because the symptoms stayed pretty much the same. It was an ebb & flow of exhaustion & energy.

Some days I could do a lot & not really ever hit a wall. Other days just waking up was a task. So the fatigue was the most obvious issue, when it would come I just wanted my space & to rest. But when I felt good I felt REALLY good. Seeing those bright spots were what made me happy because I realized it really can be that good always at some point.

As of now the motion sensitivity is still a big issue. I will update on that if hopefully it progresses.

But overall this round wasn't too gut wrenching. Not great, but I made it through thank goodness.

Xoxo,

Christina

0 Comments

Vials 3-5 : 3rd round of Borrelia Series

5/19/2013

0 Comments

 
I'm halfway done with this round of treatment! YAYE!

Vials 3-5 were much of the same. Nausea, fatigue, migraines & stomach aches. So, basically the usual stuff that comes with treatment! The nausea & fatigue is probably the most frustrating to get things accomplished. I want to eat & do more PT and things out of bed but it's been a bit hard.

All in all I am hanging in there! I can't complain too much because I'm able to still tolerate it & that's what matters. Got to keep it going!

Xoxo,
Christina
0 Comments

Vials 1-2 : 3rd round of Borrelia Series (Lyme)

5/18/2013

3 Comments

 
I'm back on treatment!! What a happy & also scary thing it was to get back on the horse, but now I feel like there really is no stopping me. I have quite the perseverance. I am starting my Third round now. I'll do at LEAST a third & fourth round before making decisions on what is next.

Sooo vial 1 wasn't too awful. I should add that prior to starting treatment I was incredibly sick. Herxing for like a week straight. I then got an IV which as it flushed out toxins herxed me even MORE. I can safely say that way the longest & toughest herx I have had in probably almost a year. It was frightening how much of a grip Lyme got over me again. I was nervous to begin with vial 1 but I knew it was now or never.
With that being said I had my fair share of anxiety & stomach aches with this dose. But it was do-able.

Vial 2 gave me some insane exhaustion. Last night I was so so exhausted I literally felt like I was drugged. Slurring my words, barely made it to take my contacts out & just complete zombie mode. Nothing could snap me out of it but sleep itself. A long 12 hour coma is what I experienced. And no I didn't wake up feeling much too rested! But, my body has to rest & it was practically begging for it.

Vial 3 tomorrow. I'll keep this posted!

Xoxo,
Christina
3 Comments
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