11 Lyme Facts I Wish I’d Known Sooner…

When I was a kid, I never quite fit in at school, but the outdoors were my refuge—every day, I came home and found peace and quiet in our woods.  Little did I know, nature was about to stab me in the back worse than anything the other kids might’ve said.

Growing up, tick bites were an inevitable part of spending time outside—unavoidable but only a nuisance.  I was bitten so many times that I can’t possibly remember them all.

Sure, my family had heard about tick-borne illnesses like Lyme disease and Rocky Mountain Spotted Fever, but all of us were healthy and had always been told that Lyme didn’t exist in our area.  Besides, there were blood tests and antibiotics, so we assumed there was nothing to worry about.

But in the fall when I started middle school, my parents and my coaches were alarmed that I suddenly became too exhausted to do a lap around the field.  My knees and hips ached as if I’d aged sixty years.  Dark circles dripped from my glassy eyes.  Strangers commented on how ill I looked and asked if I was okay.    

I went to the doctor, and he tested me for Lyme, mono, and leukemia.  Everything was negative.

“It’s just some virus,” he said.  “You’ll be fine.”  And the doctor sent me on my way with no answer, no advice, and no help.

Twelve years later, I’m still not fine. 

I spent the rest of my childhood and teens fighting miscellaneous physical problems that doctors gave up on understanding.  At eleven, when I first got sick, I couldn’t go to school anymore because my energy was so limited, and I inexplicably developed learning disabilities.

Doctors told me time and time again that my ailments were because I was “just depressed” from homeschooling and too much isolation—no one believed my depression was a result of physical illness.

And worst of all, a few months after the mystery sickness began, I got PANS—an infection-triggered autoimmune condition that attacks the brain.  This left me with severe OCD, wild mood swings, anxiety, ADHD, and more, but I didn’t get diagnosed or treated until I was nineteen.

Yet perhaps most disturbing of all is that it took another two years after discovering I had PANS to get diagnosed with Lyme disease—a decade after that first “mystery illness.”  If we knew PANS was caused by infections, and I’d grown up playing in the woods, why didn’t any doctor more thoroughly investigate Lyme as a trigger?

In 2016, just months after I’d seemingly beaten my PANS symptoms into remission, I had a tick bite during spring break, developed a flu-like illness a couple of weeks later, got heart problems, and descended into a severe PANS relapse.  I tested positive for Lyme, Babesia, and Tick-Borne Relapsing Fever.  Nine months after the bite, I started treatment.

Treatment can be up to thirty pills per day!

May is Lyme Disease Awareness Month…

As one of the largest PANS/PANDAS blogs, I’d do a huge disservice to not encourage all of you to learn more about Lyme disease.  Not everyone with PANS/PANDAS has tick-borne infections, but our community is disproportionately affected, and some of you might not know this.

You can throw all the penicillin in the world at a case of PANDAS, but if that person also has Lyme, they won’t fully recover.

Lyme is the “Great Imitator” because it’s a systemic infection which has over 300 possible symptoms.   Many chronic conditions, including PANS/PANDAS, can be caused or exacerbated by Lyme.  Therefore, I’d like to share a few facts that I wish someone had told me twelve years ago in the hopes of saving someone else years of suffering:

1) The CDC Lyme tests your doctor gives you miss at least 35-50% of cases. 

You can use Igenex Labs for more accurate results, however…

2) Lyme disease is a clinical diagnosis.

Diagnosis isn’t based on tests results alone—it takes into account your history, symptoms, and possible tick exposure.

3) You don’t have to remember getting a tick bite to have Lyme.

Many ticks are so tiny that it’s easy to miss them. Lyme can also be passed from mother to baby, and there’s evidence it can be transmitted sexually, too.  Some studies have found that mosquitos and fleas also carry Lyme.

4) You don’t have to get a rash to have Lyme.

The characteristic bull’s-eye rash shows up less than 50% of the time.  It can also be in less-visible areas of skin, or it may not look like a bull’s eye at all.

5) Lyme is in all fifty states and every continent except Antarctica.

6) Thirty days of doxycycline isn’t a cure for everyone. 

If you catch Lyme quickly, some people get better with this treatment.  However, at least 40% relapse because the Lyme bacteria are excellent at hiding from your immune system and changing form to avoid being killed by antibiotics.  No study has ever proven a month of doxycycline cures chronic infection.

7) The published studies supposedly refuting “Chronic Lyme” are deceiving. 

Scientists claim that longer courses of doxycycline don’t improve symptoms—and they’re probably right.  However, no Lyme specialist that I’ve heard of treats persistent Lyme with only a single antibiotic for months on end like some of those studies.  (And don’t get me started on the conflicts of interest hindering better Lyme research.)

Most Lyme doctors’ clinical experience has led them to treat with herbs and supplements to strengthen the immune system, as well as combinations of antibiotics—often pulsed so that there are weeks both on and off antibiotics to discourage the bacteria from becoming resistant.  The best doctors also realize that every case is unique, so each patient’s treatment plan is unique, too.

8) It’s rarely just Lyme.

Most people with Lyme have other tick borne-infections like Babesia, Bartonella, Ehrlichea, anaplasma, and others because ticks often carry multiple infections.  If you’re diagnosed with Lyme and don’t also treat the co-infections, you won’t get better.

(This is another flaw of some studies—they don’t account for the possibility that their Lyme patients had other tick-borne infections.  Babesia, for example, is a protozoa that can’t be killed by Lyme antibiotics.)

10) Prevention is the best medicine.

I got bitten in 2016 while wearing so-called “Deep Woods Tick-Repellant.”  I walked through tall grass in boots and long pants (which I had sprayed thoroughly) and checked for ticks that night, and I thought all was well.  Apparently you can’t count on tick spray alone to protect you…

  • Wear clothes infused with permethrin when spending time outside.
  • Consider a repellant with DEET, and be sure to spray your shoes.
  • Put all your clothes in a hot dryer for at least thirty minutes after you come inside, because ticks can survive the washing machine.
  • Check your whole body and take a hot shower as soon as you can.
  • Check your pets for ticks, because they can carry them into the house.  Keep in mind that products like Frontline only kill ticks that have attached, and even then, it takes a few hours to work. 
  • Don’t let your dogs sit on furniture or get in bed with you. (I know, I know—I love dogs, too, but I’m now contented to snuggle with them on the floor… After checking for ticks!)

This site here has a lot of great prevention tips.

11) You can get better.

Many doctors believe you’ll never eliminate the infection, but you can get better and go into remission with appropriate treatment.  It might be a very, very long road, but it is possible.  I feel like I’m getting more and more glimpses of hope myself as time goes on.

Despite my difficult journey, my life is not a tragedy. 

It may have taken a decade to get a diagnosis, but thanks to treatment (both for PANS and Lyme), in 2017, I graduated college.  I’m still healing, but if my recovery continues, I plan to go graduate school this fall, too.

I’m so much more than my illnesses, but fighting Lyme and PANS has made me who I am, helped me find my passion, introduced me to wonderful people, and given me a gratitude for being alive that I wouldn’t have otherwise.

I want to use my story to raise awareness.  I want to help others get the care they need so they can recover and move on with their lives, too.  Will you join me?


Lyme Resources:

 

6 thoughts on “11 Lyme Facts I Wish I’d Known Sooner…

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  2. I was diagnosed with Lyme disease 5 years ago and was taking Antibiotics and Nonsteroidal anti-Inflammatory drug which seemed to help. However, I still suffer from some of the symptoms. My symptoms have always been chronic fatigue, joint pain, and even neurological problems in controlling hand and leg movements. I am a 54 year old female. the Antibiotics wasn’t really working and I could not tolerate them for long due to severe side effects, so this year our family doctor started me on Natural Herbal Gardens Lyme disease Herbal mixture, We ordered their Lyme disease herbal treatment after reading alot of positive reviews, i am happy to report with the help of Natural Herbal Garden natural herbs I have been able to reverse my symptoms using herbs, my symptoms totally declined over a 8 weeks use of the Natural Herbal Gardens Lyme disease herbal mixture. My Lyme disease is totally reversed!

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