Recovery Updates


Recovery Update – November 2008

Alright… November.

What a roller coaster month. So much happened it seemed two months long. The summary in my November chart is almost a post in itself, but let me break it down here.

OMG… this neuropathy is diving me crazy!

The month started out with an upswing in the tingling and weird muscle sensations I've been having up and down my right side since the beginning. Only this time they were making guest appearances on the left side. This had never happened before and it really started to freak me out. Anything new that effects me physically sends me off the deep end with worry. I keep thinking I have MS or ALS or some other devastating autoimmune acronym.

This combined with the fact that my LLMD told me a few months back that he thought I'd "be off antibiotics by December" really confused me. So much, in fact, that I really sort of lost it. I was ready to drop my LLMD, move to a dark cabin above the tree (and tick) line in the mountains and start the Marshall Protocol or some other equally wacked out treatment.

Luckily I talked myself off the ledge and, with the help of a friend, set up an "emergency" meeting with my LLMD and his physicians assistant.

Hey doc, can I have some of that crack you're smoking too?

In the meeting with my LLMD I laid it out for him; essentially, the recovery picture he'd been painting for me was not matching the reality I was experiencing. He'd told me in August that he thought I was doing pretty well and that I'd be off antibiotics by December (now). I explained to him that not only was I not feeling that significantly better, but some of my symptoms, namely the neuropathy, was worse. What the hell's going on?

Well, it turns out that it was my level of exercise that threw him. When I originally went to see him in May 2008 I told him that I was not doing any exercise. He jotted down something like, "Athlete not exercising" in his notes under the assumption that I was unable to do any. The truth was that I was voluntarily not doing anything because I thought it was detrimental to my over all health picture. I did explain this in the initial meeting, but he must have omitted writing that part down.

In this same meeting he told me that it was okay to workout and that I should do as much as I can manage. I think I went for a run that afternoon.

Several weeks passed and we again discussed my level of exercise. I told him I was back to running 15-20 miles a week with my coaching and biking 30 or so. He jotted this down too and then compared it to his previous notes. To him it seemed as if he had taken me from couch surfing to running/biking 50 miles a week in just a couple of months. Not bad, and I don't blame him for jumping all over this. Unfortunately, it wasn't true. I probably wouldn't have been able to do as much as that upon my first meeting with him, but it's likely that I could have managed half that effort/distance.

So, after a long discussion and clarification session about what he was thinking and what I was experiencing we finally came to a place of mutual understanding. This was a big relief for me and somewhat of a recovery breakthrough. To organize and rally my LLMD, his PA, my wife and myself together in the same room and clearly articulate what was going on and get us all headed in the same direction was very fulfilling. One of the few times that I've felt in control of my life in the last year or so.

To IV or not to IV, that is the question

After all of the hugging and hand-holding was over we discussed what to do next about my treatment. My LLMD seems to think that I'm no longer absorbing the oral antibiotics. We talked about what's involved with a PICC line and  the pros and cons. We also discussed intramuscular (IM) Bacillin shots. Both of these get around the digestive system and get right into the bloodstream resulting in a more effective attack on the spirochetes.

The jury is still out on what to do. I'm seeing my LLMD again in a week and we're going to take up this topic then. Stay tuned.

Dear Mepron. You Suck

I continued back on the Mepron after my short-lived rash issue when initially starting it. I think it's helping. I no longer have the palpitations that I lead me to start taking it and for that I'm glad. Still, there are random days when it makes me feel like crap. I'll take it and then 30-45 mins later suddenly, wham! Brutal stuff.

Happy Thursday the 13th

For some reason on the 13th I felt great. Not 100%, but really pretty good. I felt positive and my brain fog, though still there, wasn't in the way of things. I was hoping that it would continue for a few more days, but it didn't last. Everything slowly returned to "normal" over the next 2 days. Lame, but a sweet reminder of what's (hopefully) down the road for me.

Run Forrest… run!

Speaking of the road… after over a year of non-competition I did my first road race in Central Park. I covered that in a post here. An awesome experience considering there was a time that I thought I'd never wear a race number again.

Chinese medicine and acupuncture

This deserves it's own post, but I started seeing a Chinese medicine practitioner. So many people say that herbs have helped them as much as drugs. I figure it's just another piece of the puzzle.

Thankful for Thanksgiving

I use holidays and other milestone dates to compare back and see what kind of improvements I'm making. We were in Atlanta again for Thanksgiving this year with my wife's family. Thinking back, I was pretty worthless last year. I recall having to take a nap almost every day and being generally lethargic the entire time we were down there. This year I was pretty engaged — took the niece and nephews to the aquarium, played some basketball, cooked a Mexican dinner for 11 people and generally hung out. Not bad.

On the down side, I tried to stick to my diet, but it was all but impossible. Not having a fridge stocked with exactly what I need combined with the fact that I've been urgently trying to keep my weight up and I simply couldn't manage. I stayed away from the obviously bad things like soda, sugary cereals and such, but I couldn't resist my Mother-In-Law's homemade apple pie. I gained 5lbs!

To sum up…

Like I said, a lot of stuff happened. The first part of the month was horrible, but the latter half was pretty good. I try to remind myself of this fact on days when I feel bad. The good days are coming (they are, right?). I just need to wait for them.

My November chart looks pretty similar to October's and the averages at the top correspond to the overall visual. They're down, but not significantly. Interestingly though, it's very different from September's chart and the averages are way down when compared to it. So, in the glacial speed of Lyme treatment, I guess that's significant progress.

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Recovery Update – October 2008

I totally forgot to post an update for October.

I've been really busy with work and family stuff. I've also been trying in general to think less about Lyme and more about getting on with my life. That's not to say that I feel significantly better and don't think (obsess?) about it every day. I just decided to not spend so much time trying to solve what seems to be an unsolvable problem. If I get better, great. If not, so be it. There's really nothing more I can do.

Anyway, back to October… Saw Dr. R on the 15th and we talked about Babesia. I've been having some shortness of breath (like being at altitude), occasional heart palpitations and some pain in my feet. I'd read that these were symptoms of Babs and Dr. R agreed. He put me on Mepron and Zithromycin which seems to be the default combo for this.

I started it, but about 10 days in I developed this itchy, blotchy rash all over my chest, arms, legs, feet; basically anywhere my clothes rubbed my skin. At first I thought maybe my wife had switched up the laundry detergent, but no. I called Dr. R's office they told me to stop all meds until things cleared up. I did and about 4 days later I was fine. They couldn't tell me if it was an allergic reaction or a reaction from the Babs, but I asked around on LymeNet and several people had had simliar experiences with Mepron. By the end of the month I was back on it and have not had any further rash issues, however, I think I'm having absorption issues. More on that next month.

In addition to starting the Mepron/Zith I started to really ramp up the herbal stuff. I've been really interested in better incorporating herbal Lyme treatments as well as immune-support and detox helpers into my regimen. It's all fantastically confusing and I haven't the patients for it, but I've learned quite a bit from reading online and emailing with other sufferers who've worked with them. I think I've mentioned them before, but Grapefruit Seed Extract and Samento seem to be at the heart of treatment for most people going the herbal route. I've been toying with them, but through the latter half of October I really started to take it all seriously.

Over a period of 3 weeks I worked my self up to about 13 drops of GSE and Samento once a day. This is somewhat faster than they recommend, but I'm not very patient. I think I started at 5 drops and then added a drop each evening until I started to really feel bad (herxing?) and then left it there. I was getting ready to start splitting up the dosage and begin to take it in the morning and the evening, but then the Mepron rash hit me and I decided to stop everything.

Sadly, I've yet to get back to it even now in mid November. However, I did go to see a specialist in Chinese medicine last week and expect to be taking more herbs soon. Check back next month for more details.

Sorry for the lame-ass update, but that's about all I can recall. Will do better in November.

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Recovery Update – September 2008

September? What… it's over already?!

The month completely flew by. Mostly because we were away for almost half the month in Vermont and Cape Cod, but also because I've been really busy with work. Or, I should say, not working. On top of all my other troubles I got laid-off from my job right at the end of August.

The lay-off didn't have anything to do with Lyme. I worked for a small technology start-up company and we lost our main investor. We were forced to cut a bunch of people and the entire creative department (me and the girl who worked for me) were let go. They told me it was purely a financial decision and that it had nothing to do with my performance. I'm pretty sure this is true because it was a pretty easy job (at least when compared to some of the big ad agency jobs I've had) and I was able to totally manage the hours and workload.

So the work I've been doing revolves around trying to get my portfolio up to date and taking care of some things I didn't have time to do when I was working full time. I've also been trying to figure out what to do next. I've got some ideas, but advancing them has been tough. Now that we're back from vacation I hope to gain some traction.

Health-wise September was the typical roller coaster (see September symptom chart). Right at the end of August, Dr. R changed my abx again and it sent me into a pretty huge herx. This lasted through the first week and a half of September and, at it's peak, was pretty rough. Most of the issues are neurological — tingling, numbness, brain fog — and emotional — depression, anxiety. I get some stiffness and aches and pains when I over do it with exercise, but it's no worse than when I use to over do it before I got sick. The only difference now is that overdoing it is a lot easier. I've continued to train my running groups without any trouble. This has been a great outlet for me. I really enjoy working with them.

As always, the brain fog is the worst. I can totally manage the other stuff, but not having my brain work properly is really hard. It's like having the worst hangover ever. I simply can't process top brain stuff very well. Things like complex instructions, reading comprehension and mentally juggling to do list items is really tough. Oddly though, I'm able to manage bottom brain things pretty well. Stuff like running and other physical activities. I'm also able to ride my Ducati at a pretty confident level.  This last thing being of great importance to me. It's so awesome to get on and ride. It infuses a little sense of control into an otherwise out of control life.

And that's it… everything is more or less the same. Perhaps a slight improvement in my fatigue, but it's hard to tell. Everything is sooooo slow. Stay tuned.

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Recovery Update – One Year

Today marks the one year point of my illness.

In some ways it’s hard to believe that it’s only been a year, but in others it seems like forever since I became ill. Forever.

I took this at sunrise the morning of

It also marks (roughly) the 6 month point in my Lyme treatment. Technically it’s October first, but close enough. This marker has simply flown by. I can’t believe that 6 months ago I was sitting in Dr. Meed’s office, who I went to see about getting on the Marshall Protocol for Chronic Fatigue Syndrome, only to have him tell me that my symptoms "smelled like Lyme" and suggest that I go the "traditional" abx route.

In a weird way I’m happy to have reached this milestone. Every year my wife and I go to places and do things on a regular schedule — Canadian lake house for 4th of July, Cape Cod for Memorial and Labor Days, etc. These trips have always been filled with lots of activities like boating, swimming or just chasing kids around the beach. Additionally, I often used these trips as little training camps for intensive biking or running sessions. My favorite 50 mile ride is through the hills of Truro in Cape Cod. 4th of July last year I bought a new wetsuit and swam everyday up in Canada to break it in. Miles and miles of activities; vacations revolved around sports and training.

That’s why going a full year is somewhat of a relief. Every little vacation over the past year was a reminder of how my life has changed. I didn’t bring the bike to the Cape once and I only did a few short to mid-distance runs here and there on other trips. The new wetsuit hasn’t been out of the closet since September of last year. Everything was constantly measured against "last year". Last year I rode here as a training ride for race X. Last year I ran there as a training run for race Y. Last year I worked out for 4 hours and didn’t feel half as tired as I do now from just going to the store and back. Last year, last year, last year.

Thankfully now I feel the pressure is off. I’ve lived through going to every place that reminds me of the old "me". I’ve learned to sit my ass on the beach with the family all day instead of training. I’ve learned to drive to and from the store like a normal person instead of running there and back with a backpack to carry my purchases. I’ve learned to… relax and enjoy the downtime of vacation a little more. I still wish it was by choice and not because I’m physically limited (damn, I hate admitting that), but… well, that’s the way it is today.

And I guess that’s the upside of all this. I spend more time with my daughter and my wife; the two most important people in the world to me. Plus, I read books again… or at least books not about nutrition and training. I discovered Tai Chi and have made visits to the Fire Lotus Zen Buddhist temple here in Brooklyn to learn about meditation. I’ve also improved my overall diet by cutting out unneeded sugar, dropping "bad carbs" and eating more vegetables. I have also gained a better understanding of natural treatments, healthy herbs, supplements and the like. All of these are things that I’ve wanted to do for some time, but had just never been able to "find the time" to do. I have a better view on the small things in life, the innate beauty of life and what’s really important.

It was with this idea in mind that I wanted to mark the one year anniversary. I took 10 days off and my wife, daughter and I took a trip up to visit some friends in Huntington, Vermont — one of the most beautiful parts of the state. From there we swung over to Cape Cod to stay at the in-laws. This morning I got up alone at 5:45am and drove to Nauset beach to watch the sun rise. The above picture is from that moment; a powerfully gorgeous transition from night to day. It was warming to witness it on what, to me, is a milestone morning.

I look forward to the coming year. Without over-ladening it with self-significance I feel that I now have a new yard stick with which to measure the changes in my life. Hopefully it will be full of improvements and show an upward trend in my health.

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Recovery Update – August 2008

August sucked. A lot.

I went through two really rough patches. One was brought on by my over doing the exercise. The other by a change in my medication.

I sort of covered the exercise issue in the post with the August symptom chart. Basically, I pushed myself too far. The result wasn’t unexpected. In the back of my mind I knew I was overdoing it, but I wanted to see how much was too much. Now I know.

The drug switch was much worse. It really sent me into a bad place both physically and mentally. Dr. R took me off the Omnicef, Zithromax and Flagyl (I hated Flagyl) and put me on Biaxin (500×2) and Plaquenil (200×2). These two are supposed to be a good combination. I’ve read about several people who did well on these drugs. Plaquenil is a antimalarial drug that reduces inflammation and, when used in combination with a macrolide like Biaxin, has strong anti-Lyme properties. Something about changing the pH levels in key cells elements to annoy the spirochetes.

He also told me to "continue taking the Minocycline", but I thought he told me during our last meeting to go off it. So I started taking it again.

All of my symptoms peaked dramatically almost from day one of this new collection. Really horrible brain fog and tingling — the worst I’ve experienced. I also felt sick to my stomach and really fatigued. For the first time in treatment I had to cut back on the prescribed dosages to stay functioning. I called Dr. R’s office to inquire if I wasn’t perhaps experiencing side effects from the new meds, but his physicians assistant told me that my reaction had the "characteristics of a herx". She told me to go off the Mino all together for the weekend, but I only cut it in half, opting to take it at night so that I could sleep through the worst of it.

After about a week things started to come back to "normal" and I started taking the prescribed dosages of everything. It’s a pretty potent mix, but I do feel some improvement. I’ve been having more good days than before starting the new meds and generally feel pretty okay. Pretty okay’s not too bad, right now.

I’ve been working on doing my stupid anti-candida protocol as well as incorporating the "nutracuticals" that Dr. R wants me to take into my diet, but it’s hard. And it’s a lot of damn pills to swallow every day. Something like 25!
That’s it for now. Next month will be my one year anniversary. Woo hoo!!

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Recovery Update – July 2008

I’ve decided I’m officially fed up with this Lyme bullshit.

What an utter and complete drag.

Now that that’s out of the way, let me get to everything else. As I sit here and think about it I’m realizing that there’s actually so much that I think I’m going to have to break it up over several posts. Let me start with getting some emo stuff off my chest. I’ll follow it up later with treatment specifics and their results as well as my horrible new diet.

So, as I get closer and closer to the one-year point of my illness (September 24th) I find myself often spiraling lower and lower emotionally even while I slowly (ever so very slowly) seem to be getting better. The Groundhog Day effect of waking up to this life gets evermore challenging. Recently, the better days have been coming more frequently, but the bad ones (like today) seem to hit harder.

But like the song goes, “always look on the bright side of life”, right? To do this, I keep mental (and sometimes physical) lists of things that make me feel good and positive about life. This practice isn’t some self-help or Power of Positive Thinking technique that I saw on Dr. Phil (I’ve never actually seen the Dr. Phil show). It’s just something that I’ve sort of done all my life to get through rough patches… of which this is the roughest.

For example, here’s a recent inspiration:

While doing a long run up in Cape Cod last Saturday I watched as a leaf falls from a tree branch overhanging the road ahead of me. Without breaking stride and without any wild grasping I catch the leaf in my hand as I run. A smooth, effortless, graceful action.

Now I know that this in it self isn’t all that remarkable, however, I enjoy looking at these things through a broader lens — a lens of interconnections and associations; couplings between seemingly unrelated things and events. A sort of Zen-ness of everything being everything. Through this lens I see that, perhaps, all of the events in my life have come together to put me in this exact spot at this exact time to catch this leaf. I imagine that Lyme disease has screwed up my life in such a way, affecting the time and space of my existence, to put this leaf in my hand.

But so what, right? What actual value does catching a leaf really have? None, but that’s what I enjoy about it. There is no inherent value in catching the leaf and it changes nothing in the fabric of existence, but the fact that I was there to catch it means volumes to me. It represents some magical connection between… well, everything… and it’s within this thought that I find a little beauty.

These moments are why running and athletics are so incredibly important to me. I experience little bits of beauty every day when I’m out and about, but it’s during running or biking that I feel them most. Because of this, I feel that staying physically active is truly the greatest weapons in my arsenal of treatments against Lyme. While so many people are stuffing headphones in their ears to listen to their special Nike+ workout playlist or tune in the TV at the gym to kill the “boredom”, I use running/biking to unplug from life and plug in to living. Had I not been tuning in I may have miss my leaf entirely. The beauty of the experience drowned out by some techno beat.

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Recovery Update – June 2008

Waaaaaaay late with this.

Almost half a month. Sorry, but with being away for the 4th of July holiday at the beginning of month I didn’t have the ability to wrap everything up for June.

Just as well because there’s not a lot new health-wise. Looking back to last month’s update I suppose I do feel better than I did after going on the new abx, but overall, from a 30,000 foot view I’m not feeling that much better. I think my brain fog waned some as I’ve gotten over the initial herxing, but I’d say it’s still worse than before I started the new scripts.

However, there is good news. I’ve been getting out and exercising quite a bit. My coach has hired me to help coach some of the classes he runs for the top running store in NYC — JackRabbit Sports. While some might say that doing this might be the reason why I don’t feel much improvement, I have to believe that it’s helping and providing what little success I’m feeling. It certainly provides a mental boost. Sometimes I don’t want to stop running or get off the bike because I feel so great when I’m doing it. I loath to go back to feeling tired, tingly and foggy again.

Dr. R gave me some new meds at the end of June that I’ve been on now for a few weeks. They’ve definitely changed the way I feel. Again, not so much better, but just different. I guess I’d describe it as a different herx. Some things are better, some things are worse. Six of one, half dozen of the other. More about that in July’s update when I have a better feeling for it all.

Oh… I wanted to say "thank you" to all the strangers out there who’ve emailed me well wishes and kind thoughts. It’s really great to hear from you. Again, if anyone wants to contact me, you can do so here chronictriathlete (at) gmail.com.

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Update – May 2008

Update_08_2
Another big month. New doctor, new drugs and, perhaps, a new page turned in my saga as I finally feel as if I’m making some progress in my recovery.

I’ve been on the Minocycline and Azithromycin for just over 2 1/2 weeks and they’ve really been kicking my ass. Horrible, almost unbearable, brain fog has been plaguing me since about 3 days in. It’s without a doubt my biggest issue and is far more significant than any muscle or joint aches that I have and more debilitating that the fatigue. It’s also the hardest thing to explain to someone who’s not had it. It’s almost like being brain damaged. Thoughts just don’t line up like the use to. Concentration is sometimes difficult and I sometimes loose my place mid-thought if I’m even slightly distracted. Highly frustrating.

Sleeping as also been a challenge. I have good nights and bad, but it’s recently been getting better. I attribute this to the fact that I’ve been doing regular exercise. Nothing like "training", but I’ve been getting out and running 10 miles a week and putting in about 3 hours of bike time on the road or trainer. Everything is at a slow or slowish pace, but at least I’m able to get out and being active. Though I feel far, far from what I was back before getting sick it really feels fantastic to be doing something.

This is all due to Dr. R giving me the thumbs up to workout. In fact, he told me to "hammer" it if I can. He explained that the fact that I was able to exert myself was indicative that I was not suffering from co-infections. He said that people with B. burgdorferi are, to varying extents, able to be active while those suffering with Babesiosis are generally knocked out for a days after even light exercise. Finally some good news for me.

So that’s all I’ve got for now. I see Dr. R in a couple of weeks for a follow up. I’ll, of course, post the results from that. Stay tuned for other stuff in the mean time.

Update – April 2008

Update_07_2
[I'm thinking about changing my approach to this blog. I think I'm going to start doing monthly wrap ups along with posting my symptoms chart. For me, it's easier to follow my history this way. Maybe it'll be more helpful for others reading as well.]

So where are things? Let’s see… it’s been a crazy. As you can read in my posts over the last few weeks April has been a big month. I went from being committed to going on the Marshall Protocol for my Chronic Fatigue Syndrome to taking a mad amount of antibiotics for chronic Lyme Disease and learning about what an utterly insane issue the disease is.

The redirection has been both physically and emotionally exhausting. When I talked to Dr. Cooke and she told me that my IGeneX tests had come back positive it was hard to hold back the tears. I felt this incredible sense of relief. I finally had a diagnosis to hang my hat on. I was so incredibly thankful to finally know what my major malfunction is.

Still, that said, chronic Lyme is no walk in the park. In some ways I liked having CFS better — well, "liked" isn’t the right word, but I guess I felt a little more hopeful for a cure with that diagnosis. People have been known to cure it and move on with life. With Lyme however, it seems there really isn’t a "cure". Unless you catch it immediately it’s more like something you "manage" for a lifetime. A complete remission of symptoms is possible, but there’s always a possibility of relapse. Such is the nature of the bug that causes it.

I’m currently still on the antibiotics therapy prescribed to me by Dr. Meed, but I have an appointment to see a nationally recognized Lyme doctor next week. He came highly recommended from Lymenet, an online community I’ve been trolling, as a local LLMD (Lyme Literate Medical Doctor). I’d like to give his name here, but I’m not sure that I should. As I’m quickly learning, there’s a tremendous medical and political controversy surrounding the treatment of chronic Lyme. Something that’s entirely too complicated to go into right now, but it’s been described by some as a "witch hunt" against LLMDs who treat it. Some have lost their licenses to practice medicine and even more have stopped treating patients due to the pressures applied by politicians, community officials and the insurance companies.

The trend with patients seems to be to only mention your doctor’s name by his last initial. This way, the theory goes, if I post here that my doctor gave me such-and-such a prescription — a prescription that goes against the guidelines of certain governing bodies — and lawyer from said governing body was to read it, he or she wouldn’t be able to figure out which doctor I’m talking about. Personally, I think this is absurd. I mean, if someone’s bright enough to get through law school there’s a pretty good chance that they can figure out who Dr. R in NYC is, but still… I don’t want to be the guy who’s blog pages are Exhibit A in a case against a doctor who in many cases is the final hope for people.

So, yeah… I’m seeing "Dr. R" (shhhhh!) here in NYC next week. Oddly enough, he started as a psychiatrist. Seemed strange to me that a shrink would treat Lyme, but after thinking about all the neurological symptoms that come with the disease, it makes sense. On his website he says that he also offers family counseling for patients. This makes real sense as I think family members often have a really hard time understanding and coping with the changes that come with a loved one having Lyme. I know my wife could benefit from some understanding.

I saw a video interview with Dr. R on a local Rhode Island news station’s website (sorry, couldn’t get the link out of the Flash) where he said he’s treated over 3,500 cases of Lyme. Impressive. Let’s hope he’s a major help for me.

I Have Lyme Disease

Lyme_positive
So it’s confirmed (pretty much)…I have Lyme. Holy !@#$%&*

I say “pretty much” because I still need to talk to my new doctor, Dr. Steven Meed, about my results. They’re from IGeneX and, as I mentioned previously, he’s running another test via Stony Brook because he’s not a fan of IGeneX. I’d like to get his perspective, but for all intents and purposes I’m considering myself a Lymie.

According to IGeneX’s analysis, I tested fairly positive for Borreliosis. However, I do not meet the positive criteria for the CDC or New York State. Fortunately that doesn’t matter much anyway since most doctors who treat Lyme don’t look to the CDC’s criteria and New York has the most stringent criteria in the country. See the bottom of this post for the exact IGeneX results.

I’m into my second week of Doxycycline and still feeling worse than when I started, but I’m feeling less of a spike in symptoms (herx) after dosing in the evening (200mg). It feels a little more even with just some minor peaks and valleys. I read somewhere that the bugs are only (or mostly) killed off when they migrate or multiply or whatever it is that they do to move around and grow. This only happens once every few weeks and people have reported having cyclical herxing every 4 weeks or so. I’ll be on the look out for that.

I’m still concerned about my viruses. My HHV-6, EBV and Pp titers were pretty high. Dr. Meed said that this is because of the Lyme. It’s beating up my immune system so the viral levels come up. His thinking is that if I treat the Lyme and get my immune system back on track it will take care of the viruses the way it’s supposed to. I hope this is true.

So… what a whammy, right? For the last 6 months… well, 4 months really, I’ve been living, eating, breathing Chronic Fatigue Syndrome. I was ready to turn life on it’s ear and enter the dark and mysterious world of the Marshall Protocol. Now here I am with a real name to my condition and a somewhat more practical approach to treatment. Of course I’m fully aware of the fact that it’s highly unlikely that this is going to go away in the next few weeks. I expect a time line of many months followed by a lifetime of continued vigilance against relapses, but at least there’s an event horizon for getting my life back.

As promised above, for those of your reading and researching, here’s exactly what my IGeneX results say. I was also tested for Erlichiosis, Bartonella, Babesiosis, but the titers were in the :20 and :40 range and clearly negative.

IGENEX IGG RESULTS = Positive
CDC/NYS – RESULTS = Negative

IGG:
18 kDa. -
22 kDa. -
**23-25 kDa. ++
28 kDa. -
30 kDa. -
**31 kDa. IND
**34 kDa. -
**39 kDa. IND
**41 kDa. ++
45 kDa. -
58 kDa. ++
66 kDa. -
73 kDa. -
**83-93 kDa. +

IGM:
18 kDa. -
22 kDa. -
**23-25 kDa. IND
28 kDa. -
30 kDa. -

**31 kDa. ++
**34 kDa. -
**39 kDa. -
**41 kDa. +
45 kDa. -
58 kDa. -
66 kDa. +
73 kDa. -
**83-93 kDa. IND