Keep the Mind Strong and Lyme Symptoms

Posted July 20, 2014.  Controlling my mind was a big part of my recovery.  Even on the worst of days, in the most heinous of pain, I always believed I would recover.  I would hear nothing else and I would admonish any doctor who told me I would always be sick.  Keep the mind strong.  Don’t listen to the naysayers.  Lyme disease is a bacteria/spirochete.  It’s tricky, but like any other bacteria, it can be eradicated from the body. If your LLMD (Lyme Literate Medical Doctor) tells you different, move on to a doc who says it can be eradicated and has seen that in his or her patients.

Lyme disease does not have to be a life sentence.  Simple cell biology.  Keep jumping, keep going.  Two steps forward, one step back. Progress. Conquer.

Keep the Mind Strong and Lyme Symptoms

Keep the Mind Strong and Lyme Symptoms

 

Posted in Lyme Symptoms | Tagged | Comments Off on Keep the Mind Strong and Lyme Symptoms

No Antibiotics and Lyme Symptoms?

Posted July 16, 2014.  I’m up in the San Juan Islands right now, between Canada and the US.  It’s my 6th day of intense hiking, sailing, kayaking, rock climbing, swimming (rope swing into a lake!) and general round the clock fun.  5 years ago, I was bedridden with Lyme disease and couldn’t have even imagined this life I’m living.  My life is better now than it was before I had Lyme disease.   (I know for those of you who are still suffering, that is hard to believe, but it’s true!)

I get a lot of messages from people who either do not want to take antibiotics or think they cannot take antibiotics.  I respect that, but I would say that if at all possible:  Take antibiotics along with herbals or whatever else you are using.  The Lyme disease spirochete is VERY smart and chances are you have a host of co-infections as well, at least I did.  In my opinion, it is not the time to mess around and “try” different things.  When I first went to my LLMD (Lyme Literate Medical Doctor) he had me sign a form saying that I wanted to take antibiotics. I thought, “Why the heck would I not want to take antibiotics? I want to get rid of this crap!!”

I understand there are people for whom antibiotics really aren’t possible.  People can have allergies and simply not be able to tolerate them.  But, if at all possible, after consulting with a very experienced Lyme doctor, I hope you can add antibiotics to your regime.  I know there are very good doctors who use only herbs, but anecdotally I would say it’s good to add some antibiotics as well, to get to the point of 100% eradication.  You will herx from them and it will be rough, no question.

Doctors prescribe antibiotics for acne.  Remember that.

As far as the gut goes.  Probiotics, probiotics, probiotics!  I took mine at midnight every single night without fail. I would wake myself up, if I were lucky enough to be sleeping.  (Sleep was a luxury I didn’t much enjoy when I had Lyme disease and the awful Lyme symptoms.) I took a literal handful of probiotics each night, billions of organisms.  Oh, and did I mention I did it every single night without fail?!  

Consistency is critical.

If you can take antibiotics, I would really encourage you to.  No matter what, be aggressive, BeRentless and be cured!

Notice the hat and white shirt for hiking.  I’m out there enjoying life… but being careful! OK, there is an island calling me now, I’m off!

Antibiotics and Lyme Disease

Antibiotics and Lyme Disease

 

 

Posted in Lyme Symptoms | Tagged , | Comments Off on No Antibiotics and Lyme Symptoms?

FDA to Regulate Testing for Lyme Disease

Posted July 9, 2014.  Ugh.  Some lawmakers are asking the Obama administration for stricter oversight of laboratory  testing, including those labs which test for Lyme disease.  Of course we want reliable, decent labs out there providing services, but the lab that ultimately diagnosed my Lyme disease and co-infections correctly was not FDA approved. The FDA approved lab that I had used initially told me twice that I did not have Lyme disease.

More government oversight of laboratories is not going to help Lyme disease patients.

“FDA regulation of Lyme Disease Tests would be contrary to the public health, stifling innovation and negatively impacting patient access to this valuable category of diagnostic laboratory services, which includes many ‘gold standard’ DNA sequencing assays, newborn screening tests, and tests for rare diseases,” a petition reads.

Read the full story here:  http://www.thesunchronicle.com/news/local_news/lawmakers-urge-federal-oversight-of-lyme-disease-tests/article_c9df8979-5a2d-5c41-b7bd-8a7010911be4.html

Labs and Lyme Disease

Labs and Lyme Disease

Posted in Lyme Symptoms | Tagged , | Comments Off on FDA to Regulate Testing for Lyme Disease

New Treatment Coming and Chronic Lyme Disease

Posted July 8, 2014.  Stay tuned, this looks interesting.  From Northeastern University.

New Treatment for Chronic Lyme Disease Coming

New Treatment for Chronic Lyme Disease Coming

 

3Qs: A new path to curing chronic Lyme

disease

April 10, 2014 by 

Ear­lier this year, the Cen­ters for Dis­ease Con­trol and Pre­ven­tion pro­jected the number of undi­ag­nosed cases of Lyme dis­ease to be 10-​​fold higher than pre­vi­ously believed. Of the newly iden­ti­fied 300,000 people infected each year, between 30,000 and 60,000 fall into the cat­e­gory of having chronic Lyme, where symp­toms per­sist despite zero evi­dence that the pathogen remains in their bodies. With the sup­port of a Lyme Research Alliance grant, Uni­ver­sity Dis­tin­guished Pro­fessor of Biology Kim Lewis in the Col­lege of Sci­ence is exploring alter­na­tive approaches to curing chronic Lyme dis­ease. We asked him to explain his research goals and why now is the per­fect time to find a cure.

University Distinguished Professor of Biology Kim Lewis is an expert in the field of bacterial cell persistence, wherein dormant cells remain elusive to antibiotic onslaught and allow patients to remain symptomatic despite negative test results for decades. Photo by Brooks Canaday.

Why is Lyme a difficult disease to identify and treat?

Lyme is one of those puzzling chronic diseases: while people that are treated by antibiotics shortly after they’re bitten by the tic get cured, about 10 to 20 percent don’t. So, the question is, Why not?

There two schools of thought about that. The more standard among physicians is that the lingering effects—which could last years without resolution—are effects of the immune system having a perpetual response long after the pathogen is gone. These are aches, pain, fatigue—people are really miserable.

The second school of thought is that the pathogen is still there in a dormant form. And that’s where we come in. We are experts in dormant bacteria that are tolerant to antibiotics. We call them persister cells.

What do you hope to accomplish with the new grant?

I think we can contribute two important things apart from asking whether Lyme, like other pathogens, forms persister cells and whether that would explain its chronicity.

First, the treatment regimens for people with chronic Lyme are inadequate because nobody has done the proper clinical microbiology work. We need to find the best possible antibiotic or antibiotic combination for killing the pathogen. It has not yet been done because it’s difficult, it’s time-consuming, and it’s fastidious. On top of that, most clinicians don’t believe that chronic Lyme is caused by the pathogen in the first place, so why bother? But we have extensive experience with existing antibiotics, and we know which ones, in principle, will diminish the persister cell population from our work with other pathogens. So, right away we can give some recommendations to those physicians who will prescribe antibiotics for chronic Lyme. Within half a year, we should have a better regimen.

Second, we will check the experimental compounds we’re working with in the lab on other pathogens, for their effectiveness against Lyme. We’ve published a number of papers linking persisters to clinical manifestations of the disease, so that’s been widely accepted, but with Lyme you don’t even know whether symptoms are caused by an irreversibly wrecked immune system or if it’s the pathogen in its dormant form.

The first compounds we’re going to test against Lyme are pro-drugs, which we’ve already found to be fairly effective against persisters of e. coli and a number of other bacteria.

We only started our Lyme work this summer, so the drug discovery may take some time. But at a minimum, we will give patients a better regiment of existing antibiotics. It’s not just empty promises, where at the end of the road there will be nothing. In drug discovery, you never know whether your drug will fail or not be approved. But by exploring the effectiveness of existing antibiotics, we can promise that patients will do better than they’re doing right now.

Why is now the time address Lyme disease?

It’s a perfect time to attack the problem now because there is an unmet need. There is this growing epidemic of Lyme disease and a growing number of people with chronic Lyme who do not have adequate therapeutic options. On the other hand, we’ve learned a lot from studying other infectious diseases and how to control them.

We had an important breakthrough last year with MRSA, a devastating infection affecting many patients. It’s extremely difficult to get rid of the pathogen, and the main outcome is often amputation of a limb or death. We figured that in those cases patients die or suffer limb loss because the pathogen forms these dormant persister cells that are not killed by regular antibiotics. We were able to identify a compound (called ADEP) that activates protein degradation in those cells and forces them to [self-destruct]. That encourages us that we can similarly treat other infectious diseases including Lyme.

That particular compound (ADEP) doesn’t act against borealis, which causes Lyme—we tested that. But we now know considerably more than we knew even five years ago and our capabilities are considerably better now. That’s why I think this is a great time to attack the problem.

– See more at: http://www.northeastern.edu/news/2014/04/lewis-3qs/#sthash.fsYD9fNS.dpuf

Posted in Lyme Symptoms | Tagged , | Comments Off on New Treatment Coming and Chronic Lyme Disease

Rock Musician and Lyme Disease

Rock Musician and Lyme Symptoms

Rock Musician and Lyme Symptoms

Posted July 8, 2014.  I can relate.  I never had a bulls-eye rash, nor did I ever see a tick.  Good article to share:

By   From the Huffington Post

How a Rock Musician Inspired One Family Dealing With Lyme

Disease

This spring I took my 15-year-old son to hear the band Typhoon and its lead singer, composer and guitarist, Kyle Morton. Typhoon is an indie rock band from Oregon whose 11 musicians combine inspirational lyrics with resonant melodies, weaving together guitars, violins, drums, horns, xylophones and a kitchen sink of other instruments into a big band sound.
My son and I were mesmerized by Typhoon’s performance. Like Morton, my son is a guitarist who composes songs for his own rock band. But there was another reason we attended the concert. Morton and my son have something more in common than a love of guitars and rock music. They share an illness that infects300,000 people in the United States each year — Lyme disease.

Lyme disease is a bacterial infection that is spread through tick bites. According to the CDC, typical symptoms include fever, headache, fatigue and in fewer than 50% of reported cases, a skin rash that sometimes looks like a bull’s-eye. If left untreated, infection can spread to joints, the heart and the nervous system.

Complicating matters, Lyme isn’t the only microbe carried by ticks. Ticks can spread other diseases with such strange sounding names as Bartonellosis,BabesiosisEhrlichiosis and Anaplasmosis. In addition to Lyme, doctors must detect and treat these other “co-infections.”

I first heard about Morton a year ago when Scott Simon interviewed him forNational Public Radio (NPR). In the interview, “Songs for a Lost Childhood,” Morton talks about his childhood battle with Lyme disease. During this time, he endured multiple organ failures and a kidney transplant, the kidney donated by his father.

Some of Morton’s music reflects the mental and physical pain he suffered as he battled for his life. In his song “The Lake,” he writes how he contracted Lyme as a teenager during a Fourth of July visit to his uncle’s lake cabin:

I wandered down into a quiet place
Where the grass grew tall as it met the lake
There was a different bug must have bit my leg
Though I never saw it.

My own son was diagnosed with Lyme disease five years ago. My family had no warning. Like Morton, we’d never seen a tick or a bite mark, let alone one of those characteristics bull’s-eye rashes. One morning my son rolled out of bed limping and complaining of painful, swollen knees. In the days that followed, he suffered from headaches and fever, disorientation and fatigue. Worse, he cried often and was in an emotionally fragile state.

Morton’s experience, poignantly detailed in “The Lake,” sounds eerily like my son’s:

Back at home I cried in my room…
I was sick in bed I could barely move…
as my body turned against itself.

It was painful to watch our son suffer, and my wife and I dedicated ourselves to learning more about treatments for Lyme disease. We were distressed to discover that opinions within the medical community are deeply divided regarding the best approach for treating persistent Lyme disease. Persistent, or chronic, Lyme diseaserefers to the condition of those patients whose symptoms continue after a short-term dose of antibiotics. One group maintains there’s no convincing biological evidence for the existence of chronic Lyme infection, and that long-term antibiotic treatment of “chronic Lyme disease” is unproven and unwarranted. Opposing groups believe current Lyme testing is largely inaccurate and likely to miss patients with chronic and ongoing infection. This group feels that long term antibiotic treatment is needed for those patients with chronic symptoms.

Unfortunately, Lyme patients and their families are caught in the middle. Many parents confront a blizzard of conflicting literature on how to treat their children or where to go for help. Others are forced to travel endless hours or across states to find a doctor adequately trained to help them, or pay thousands of dollars for treatments that are rarely covered fully by insurance.

Another of Morton’s songs, “Common Sentiments,” reflects this frustration:

When am I gonna feel better?…
I’ve been a patient for a long time now…
Oh what am I waiting for?
A spell to be cast or for it to be broken!

2014-07-05-Mymusicianson.jpgIn my own son’s case, we first questioned why our child had been so unfortunate. But we gradually discovered he was one of the lucky ones. Though my son’s infection had probably lasted several months, our doctors caught the disease before it had infected his nervous system. His doctors treated him with a lengthy course of antibiotics, and today he’s leading the normal, healthy life of an active high school teenager.

Still, our experience made us wonder about those parents and their children who aren’t so lucky. Parents who don’t have the resources, time, or ability to pursue the best treatment options for their child, or kids whose Lyme disease wasn’t caught at an early stage.

My heart goes out especially to kids suffering from persistent Lyme disease. Many are too sick to enjoy memorable events, like homecoming dances, recitals or championship games. Others are tethered to their beds, too exhausted to play outside or with friends. Robbed of their youthful energy, they often can’t lead the full lives they’re entitled to.

In his NPR interview, Morton described how his illness affected his life. “I found that getting sick, it obliterated any sense of these kinds of monumental truths… like that I would grow up and that I would be strong and tall.” Or, as he poignantly describes in his song “Hunger and Thirst”:

And it has occurred to me that I have spent my whole life
Starting over…
Cry, pining for the things I could have been,
Could have been.

Like many other anguished parents, I don’t want to see more children having to settle for what could have been. I hope that the global medical community will come together to find a cure for Lyme disease, especially for those children who suffer from persistent symptoms. The guiding principles for bringing medical professionals together from both camps should be humility, openness to new approaches and putting the needs of sick children first.

Despite his heart-rending ordeal, I nonetheless found in Morton’s experience both hope and inspiration for children suffering from Lyme. While Lyme disease closed off some of life’s options to him, it also channeled his talents into a music career. Morton adapted to what life had thrown at him and achieved fulfillment. And while he fights a continuing battle with Lyme, his heartfelt songs are a testament to our ability to confront and endure debilitating illnesses.

Watching my son sing along with Morton at the Typhoon concert was an uplifting and touching experience. My son’s favorite song is “Morton’s Fork.” As Morton sang this song he cried out, “You are alone,” but was met by the band’s response, “We’re all in this together.” It was a moment where, for one night at least, this parent felt optimistic that one day we might still overcome this cruel disease.

2014-07-05-typhooninconcert930ClubWashingtonDCMarch2014.jpg

The author would like to thank National Public Radio, Kyle Morton, Typhoon, and Roll Call Records for their permission to use the interview transcripts and song lyrics contained in this article.

To learn more about the detection, prevention, and treatment of Lyme and its associated diseases, consult your physician or local health department, or visit theCenters for Disease Control and Prevention, the International Lyme and Associated Diseases Society, the National Capital Lyme and Tick-Borne Disease Association, the Lyme Action Network, and the Children’s Lyme Disease Network.

John McCormick and his sons William and Connor are the authors of the newly released book, “Dad, Tell Me A Story,” How to Revive the Tradition of Storytelling with Your Children (Nicasio Press 2013). For more information about family storytelling and their book, visit the authors’ website and blog athttp://DadTellMeAStory.com.

You can also follow the authors on Twitter or join them on Facebook.

Follow John McCormick on Twitter: www.twitter.com/DadTellMeAStory

Posted in Lyme Symptoms | Tagged , , , | Comments Off on Rock Musician and Lyme Disease