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by Jennifer Crystal

August 27, 2020

Every few months, Jennifer Crystal devotes a column to answering your questions. Do you have a question for Jennifer? If so, email her at lymewarriorjennifercrystal@gmail.com.

Do you usually feel a tick bite? Does it itch?

Ticks are sneaky little creatures. You don’t feel them bite, because they inject an anesthetic when they do. Less than 50% of Lyme patients recall a tick bite or rash. This is also because ticks tend to bite in hard-to-spot places such as the scalp, the groin, the armpits, the belly button, and behind the ears. The bite site or rash can itch, but doesn’t always. And while a bull’s-eye rash is a tell-tale sign of Lyme disease, not all Lyme rashes, known as erythema migrans or EM, present as such. They can be spotty or blotchy, appearing any time from immediately after a bite to months or years later, in different parts of the body. My own rash was a series of red dots on my forearm. They weren’t raised, and didn’t itch. I didn’t give them much pause; neither did the nurse at the summer camp where I was working. Years later, after I was already bedridden with multiple symptoms, bull’s-eye rashes appeared on both of my elbows.

The bottom line is, if you have any kind of rash, it’s best to get it checked out by a Lyme Literate Medical Doctor (LLMD), but you also should not look to a rash as the only indicator of Lyme disease. Instead you should be on the lookout for flu-like symptoms like fatigue, muscle and joint aches, fever, and headache. It is always better to be safe than sorry with Lyme. See an LLMD, and take antibiotics if you suspect Lyme, even if you end up doing so prophylactically.

When you were bedridden, were you sleeping a lot?

You would think the answer to this question would be yes, and I wish it was. That is to say, I was exhausted, and certainly needed the sleep. I could barely muster the strength to walk to the mailbox, or up a flight of stairs. I was too tired to concentrate on books or TV. It felt like the worst case of the flu I ever had, and all I wanted to do was sleep.

But I couldn’t. This was one of the most frustrating parts of battling Lyme, babesia, and ehrlichia; my body could not get the rest it so desperately needed. Sure, I got physical rest from lying in bed, and occasionally, when I got lucky, I nodded off for a bit. However, most days—and nights—my brain would not shut off. I would lie awake praying for sleep, trying every calming exercise possible: meditating, listening to relaxing music, counting sheep. When I did sleep, I had hallucinogenic nightmares that left me even more tired.

I finally saw a sleep doctor who did both neurofeedback and cognitive behavioral therapy. I was able to sleep better at night—though my crazy dreams never fully went away—and was able to nap in the afternoons. Once I started getting adequate rest, my body was able to heal.

What is the best treatment for migraines?

I talked about dealing with headaches stemming from tick-borne illness in my post “Not All Headaches are Alike: What’s Causing Yours?”. Migraines can result not just from Lyme but from other tick-borne illnesses such as babesia or bartonella. Babesia is a parasite that drains oxygen from the red blood cells. This symptom called, “air hunger” can cause excruciating headaches; I used to get migraines several times a week. Over-the-counter painkillers did nothing for them. Prescription migraine medication helped in the short-term, as did rest. It helped to stay away from screens when I felt a migraine coming on.

But my migraines didn’t really ameliorate or disappear until I adequately treated the infections that were causing them. For me, this meant years of antibiotic treatment for Lyme disease and months of anti-malarial treatment for babesia, but everyone’s protocol is different. Now I only get a migraine once in a blue moon, usually when I’ve pushed myself too hard physically or neurologically. Then I know it’s time to slow down and get some sleep.

Related posts:

Living with Lyme Brain
To Sleep, Perchance to Dream
What is Air Hunger, Anyway?
Not All Headaches Are Alike: What’s Causing Yours?


jennifer crystal_2

Opinions expressed by contributors are their own.

Jennifer Crystal is a writer and educator in Boston. Her memoir about her medical journey is forthcoming. Contact her at lymewarriorjennifercrystal@gmail.com.

 

 

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**Comment**

Great questions.

For #1, we call that “wired, tired.”  It’s when you would give up your left arm to sleep, but you can’t.  Then there are times when you can literally fall asleep standing up. Both are common with tick-borne illness.  Again, Lyme is only the tip of the spear.  Many patients are infected with numerous pathogens – including parasites.  Parasites are known to cause insomnia and some find this to be even worse during full-moons when there is heightened activity.  If your Lyme treatment isn’t addressing insomnia, please copy this off and discuss parasite treatment with your practitioner:  https://madisonarealymesupportgroup.com/2017/10/03/removing-parasites-to-fix-lyme-chronic-illnesses-dr-jay-davidson/  Some really improve on dewormers like Ivermectin and Albenza (One of Klinghardt’s protocol sis within the link).  Warning: you need to be under the direct supervision of an experienced doctor has dewormers have been known to kill the worms borrelia is hiding in, exposing them now to antibiotic treatment which can cause massive die-off and high levels of inflammation.  https://madisonarealymesupportgroup.com/2016/06/03/borrelia-hiding-in-worms-causing-chronic-brain-diseases/  This is particularly dangerous in the brain:  https://madisonarealymesupportgroup.com/2016/08/09/dr-paul-duray-research-fellowship-foundation-some-great-research-being-done-on-lyme-disease/

For #2, I completely agree that the BEST treatment for migraines and headaches caused by tick-borne illness is appropriate treatment.  Get to the root cause of the pain.  This goes for pain anywhere and everywhere within the human body.  Drug levels are also important.  True story: the pharmacist didn’t tell me they ran out of 500mg tablets of Azithromycin and switched my prescription to 250mg – meaning I should have been taking TWO tablets, not one.  Not knowing this, I continued to take one tablet and suffered with the worst shoulder pain known to mankind.  When I finally figured it out and started again with the full dose, guess what?  Yep.  PAIN GONE.  POOF!  This shows the importance of blood levels.  This is also something to keep in mind generally throughout treatment.  It is my opinion that many are not on high enough levels and by switching that up, you can make good progress.  I’ve seen this over and over with patients who don’t seem to be responding.  Dr. Burrascano talks about this important topic here:  https://madisonarealymesupportgroup.com/2018/12/28/the-history-of-lyme-disease-dr-burrascano/ (Video in ILADS link within article)  I highly recommend you watch the entire video, but I highlight it here:  https://madisonarealymesupportgroup.com/2019/02/22/why-mainstream-lyme-msids-research-remains-in-the-dark-ages/  Another nuance he discusses is “cycling” antibiotics – meaning, once you have become symptom-free for 2-3 months, you stop all drugs and wait.  If symptoms return you hit it hard again with antimicrobials until symptom-free status is achieved.  He states that he and many of his patients became symptom-free for good after