Lyme Sucks

I don’t know if I’ve told you this before, but I have Lyme.

Oh, maybe I have and it slipped my mind, that would be typical. I may have written a past post announcing it (minus the trumpet) to “get it off my chest” or just let you know where I’m at. But, these days, it’s really bothering me.  Read on (or skip to the next, likely more exciting blog)!

And while we’re on the subject of blogs, please forgive my lack of being fancy. I chose my blog style years ago because it was the second one that came up (and the first one looked even more amateurish). I am not of the spend time embellishing or make my blog look pretty kind. do admire the enthusiasm of those who can.

Sorry guys, you’re stuck with boring blog-ery today!

And fonts, let’s chat about those shall we? I know I’m making mistakes (and not caring to correct them) so if you have poor eyesight, you might like my style. I am one to use the TITLE fonts for no other reason than they’re right there and easy.

Let’s skip to the real reason for today’s post.


I am back from NYC after a week, my loved one had surgery and is doing very well, thank you; however, I feel like a colony of bugs are crawling on my back. Everyday. I’ve finally unpacked and somehow finished laundry (for three), and each and every task leaves me tired. I need some killer concoction, like someone to develop an anti-lyme, energy infused, super cell power drink.  I know a lot of people who could use that!

Do you?

Well, if you don’t have lyme or know anyone who does, you are bored about three paragraphs ago. I’m sorry. I usually don’t write here but I don’t know what else to do! Four antibiotics haven’t worked. I should say the first one did and for one month I felt marvelous, like I hadn’t since my twenties or teens. I mean I walked two miles every morning before 8:00 a.m. which anyone who knows me is a feat to be awake, let alone dressed and walking! But…then….boom, it was followed by three that failed. Even the same one, two weeks afterwards.


I’ve taken some special bark (yes bark in capsule form) from South America. Noooot worrking. I’ve tried a lot of the recommended herbs and try to cook with them (HA, the key word: cooking) but so far, to no avail.  Next up, IV antibiotics and that is coming once my loved one has recovered from surgery.  We have another month or so for that. I am “Nurse Wendy” for now on duty 24/7. (Private nursing is costly, I’m hired at home for free!) Stress, ah, that is another blog. Isn’t illness stressful?

So I’m researching lyme, what can I do, going on-line to poke around and there it is. Incidentally, in case you’re wondering where I’m at, I am not early stage lyme unfortunately. (If “wish” and “lyme” had to be used in the same sentence, that would be it.) And while no doctor has said the words “Wendy, you have late stage, a.k.a. Chronic Lyme” I fit late stage lyme. If you have it and it affects your joints and memory and gives you Bell’s Palsy, you know what it is.  And it is a beast. The more I read about it, the more hopeless I feel.

Until today. Well, sort of, it was a bittersweet website I landed on. Nothing under the sun prepared me for what I read.

“Most of the long-term effects and conditions are neurological or nervous system related and are not able to be cured at this time.”



I suppose nothing prepares you for reading what you have has no cure. BUT, then I felt a glimmer of hope, a glimmer. While it doesn’t help anyone at this present moment, myself included, with symptoms, a cure, at this second. IT WILL! And maybe when we’ve earned enough money and they’ve developed the technology – because we know insurance won’t cover it – just maybe we can be candidates and reverse some of the damage it has done to our bodies.

Stem cells…hmm….far out. And they’re hopeful! Well this has lightened my gloom a bit and I hope yours. Did I mention my smile is symmetrical again? Oh, the Bell’s Palsy comes and goes. (My mom swears she can hardly notice. I think she is being nice, a mom you know, though it has been behaving lately.)

(Gosh, I’m gonna hate this post on my time-line. I’m one giant whiner today!)

SORRY y’all. (I only went to college in Virginia, but “y’all” can surface at the oddest times, like today. Oh, i know what it is. I’m missing a college roommate reunion in Richmond. Got it. You know it all comes from somewhere!)

Peace out & have a good day. Support your Lymey loved ones. If you have it, I feel ya peeps, I do.

And remember, there IS hope despite my dreary disposition. It may not feel like it, but this stem cell has me excited. It could be decades before it’s available to you and me, and affordable, but I’ll stand in line. Well, when I feel up to it. I might have to ask you for help.

Peace out!   #Limey


2 thoughts on “Lyme Sucks

  1. Oh honey, “I’m sorry..” doesn’t even begin to cut it.

    I’ve noticed a flurry of celebrity lyme disease memoirs on Amazon lately (they’re either out or will be published soon) and it seems like an epidemic. I live in Northern California and we have the dreadful lyme disease around here.

    You’re an amazing, amazing, person, Wendy! If anyone can kick Lyme’s ass, it’s you I wish I was rich because you know I’d be your Patron and get you all the high-tech, costly treatments around.

    Thinking of you, and thanks for filling us in on the latest. Ask for help whenever you need to – I’ll help spread the word.
    I hope your significant otter is feeling much better – she’s so lucky to have you!
    XOXO Dy

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