Welcome to Lyme Thriving…
I have spent most of my life being very busy, doing lots of things, and often avoiding dealing with myself by hiding in the busyness of it all. The Universe began giving me wake up ‘taps’ with recurring flare ups of Lyme disease. I would do things to ‘fix’ my body and then go back to life as before. In January of 2011 the wake up tap was replaced with a Universe-delivered smack to the side of my head, with the instructions to SIT, STAY, and BE.
I was very ill and gladly put myself on the couch and stayed there, however, me being me, I chose to ignore the BE part. Rushing straight to my second line of defense, which looks like intellectualizing everything, I lay on the couch and put my brain to work, working to understand my sickness, my life and my choices.
This was not what the Universe had instructed, and I was dealt another smack to my head, this time so hard it jumbled up my brain, leaving me in a perpetual brain fog and with cognitive challenges that hindered my ability to process thoughts properly, and sometimes made speaking a challenge.
With nothing I could do and little I could think, I was left just BE’ing. And in that space of nothingness, I experienced the richness that is life, the wonder that is my Self, the Oneness that we are, and I learned some lessons.
My experience of life was no longer at the affect of my illness, and I began the journey back toward health and well being, back to the love of Self where nothing is ever wrong and all is well with the world.
As part of a large community of people suffering with chronic Lyme I am committed to making a difference to any and all. To borrow a phrase from Marianne Williamson: “I share (my lessons) with an open heart, I hope you will listen with an open mind.”






I am so moved by this! Where have I been????
I have to drive 3 hours in each direction, out of state, in order to see a dootcr for my undiagnosed Lyme Disease and probable coinfection(s). By the time I see him, I will have had 5 weeks of antibiotics (doxy & flagyl) and then six weeks off of antibiotics. I’ve had 2 negative ELISA tests, despite the fact that the ELISA test isn’t recommended for late Lyme. I had acute arthritis in my ankles and acrodermatitis chronicum atrophicans on my hands/feet that all responded to antibiotics.
You have observed very interesting details! ps decent site.
Thank you!
A few years ago, my sister was tenllig me that her 5-year-old daughter had been very rebellious lately if she asked her to do something, her daughter ignored her, only obeying after my sister got frustrated and started yelling. A couple of weeks after our conversation, my sister found out that her daughter had suffered a serious and permanent hearing loss. She (AND her husband, who is an otorhinolaryngologist) felt very guilty about thinking Ava was just being rebellious.Anyway we live in an area with endemic Lyme disease, and know many people who have been infected, some long-term, in some cases with terrible consequences. Thank goodness Max’s infection was found so early!!
Yes, mid-diagnosis and un-diagnosis of lyme can lead to awful consequences. Best defense against Lyme is simply living healthy and being aware. And we do what we can to continue to raise awareness. Glad to hear Max’s infection was found early.
Hey, I just stopped by to visit your site and thought I’d say I enjoyed myself.
Thank you…please visit again.
Pulling a nymph tick with tweezers is IMPOSSIBLE That is how I got inetefcd.It is impossible not to leave the head in. These are the size of a poppy seed for Goodness sake get hold of a proper Tire Tique or tick puller, otherwise you run a serious risk.I’m not sure about the 36 hours either, the bacteria seems to be present in the tick’s saliva I followed medical advice (so called!) and used ether, tweezers and that’s how I got inetefcd. Please learn by my mistake!
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Dont’ beat yourself up! It was over 10 years ago that you had it, and more often than not tegnaee boys really are just being lazy.One of my friends from work was also recently diagnosed with lyme disease, his was almost missed because he’d just had back surgery so his lethargy was attributed to post-op tiredness. Luckily, he saw the rash and went to his dermatologist who diagnosed it.I can remember as a kid, always seeing Public Service Announcement commercials to check for ticks, but now adays you don’t see them as much. I wonder if people are starting to forget?
There is a lot of controversy around the diagnosis and treatment of lyme disease and it certainly doesn’t get the attention it deserves, although many are doing whatever they can to raise awareness. I remember hearing about it years ago, but it easily got forgotten or became secondary to other headlines. Glad your friend was diagnosed…hope he is doing better now.
If you want to completely reeovcr from chronic lymes, my advice to you is what worked 4 me. Animal fats, such as chicken, pork, beef, goose, duck. Have a diet with loads of fat like, any remaining fat drink it. It will stimulate your NK cells, make your cells more rigid (afterall our cells are 50% saturated fat like breast milk. The palmitic acid has shown to kill Candida and other bacteria like e-coli. Protect yourself from dangerous biotoxins with fats (protects brain, NS & heart). hope 4U
The question is-is our fibro due to hnivag had Lyme, or other tickborne disease, in the past? Or IS the fibro/CFS unrecognized chronic tick disease? The infectious disease doc I saw (who formerly practiced in the northeast, in the heart of tick disease country) suspect my chronic EBV titre is actually indication of tick disease, perhaps undiagnosable Lyme, perhaps something not yet named. I’ve been bitten dozens of times-I can’t see how I can NOT have contracted something that causes my multiple symptoms.
I don’t know the answer to that, perhaps nobody really does. This is why I felt so comfortable following the advice of my LLND to simply detoxify my body, and support my immune system back to a healthy state so that it could deal with whatever wasn’t working in my body. This, along with some internal soul searching brought me back into a state of wellness.
You are amazing, just so you know.. I saw a documentary on Lyme disease and they were saying in New York there are Dr’s who have studied this and they give u a hep lock and strong antibiotic’s for 1 year and your cures.. Another thing is the people who get Alzheimer’s, Parkinson’s and ALS who have died they biopsy there brain and have found 90 percent have had lymes disease.. Interesting one must think.. Get better and stay strong…deb
Also the drug companies don’t want anybody to know because the drugs for all these diseases are big money maker’s..
Such beautiful words, thank you, thank you. How are you doing now? Can you speak more about your story and if you are still in treatment now? I also find that with lyme disease, it has taught me to slooooooow down and appreciate the things in life that we didn’t before.
Thanks again for your blog, can’t wait to read more.
-R
I’m well. Definitely live a more balanced life. I actually take down time. One thing I learned was that I don’t have to be sick to rest. haha! There are some things I do for maintenance, like bio-resonance every 6 weeks. But essentially life is now the new normal. Earlier in the year I had some bumps in the road….felt foggy, inflamed, fatigue….but a couple of weeks of my supps, some detoxing, loads of lemon water and some introspection had me come back into alignment. I do not live like a saint, love to have a good party night, and when I get really excited about a project I pull some really late nights. I am far more aware of the impact so am quicker to put some extra sleep and nutrition back in, and much to my surprise, I sometimes even say no to things so that I don’t have to through the rebalancing. This is also new.
I’m still learning and practicing, still fail sometimes, but definitely building stronger muscles around honoring myself. I’m very much a work in progress. Thanks for reading and your questions.
Regarding bio-resonance therapy, Dr Weil completely discounts it as doing anything. Of course if it is helping you, who cares what Dr Weil says.
I’m not taking anything to treat anymore. I did many, many things to deal with the illness and I have no idea what worked the best. I had a foundation of detox, diet, supps, bio-resonance and chiropractic care, and then added a multitude of other things that just felt good to me. At some point I stopped worrying about what other people said worked or didn’t.
Haven’t taken anything for Lyme in over a year. Just live with more balance in all areas and have a new perspective of life and myself. I’ve been well for a year now.
Take it from me, this woman loves a party night!!! But she’s also super sensible about nutrition and these days, getting enough rest. She’s my best friend and I can’t believe she’s the same person. If you have lyme Listen to everything she says because she is the healthiest I’ve seen her in a long time. Love you JR!
I love your site, it is pretty gutsy to put your story out there, you sound like your really with it. I have traveled that road also, but I don’t have all the answers, we can learn from others wisdom also. I have booked marked and tweeted it.
Hi Jenny,
How wonderful for you that the Universe, God, LOVE, Higher Power, whatever one believes, gifted you the opportunity to BE. You are so on target. Far too many of us spend lots of time “doing” because we are driven, and that’s just not healthy at all. Once we discover the peacefulness and fulfillemnt that always results from choices based an awareness of love and adundance that is within each of us, we shilft into a state of BE-ing and enjoy a life more centered on core values that are healthful for ourselves and orhers. Wishing you the very best of happiness and wellness:) EdC
I discovered I had Lymes this year and have been feeling better with a some new products I have discovered. I am walking better and my energy is coming back. I have to take my products every 12 hrs or I can feel the critters making a come back with in 2 hours if I miss the dosing. I am using only natural products.
So happy to hear you are doing better. Best of luck with your protocols. Keep listening to your body and remember that you are your own most powerful ally. Your thoughts about yourself and life, if loving and expansive, will raise your whole vibration and your body will follow suit, supporting your healing process. The ‘feeling’ you have of ‘critters’ coming back are probably just neurological impulses. Try not to visualize ‘critters’. Perhaps something more positive like your neurological system doing it’s job beautifully and sending impulses to you to remind you of another dose of good stuff for your body.
Much love. xoxo
Hi, what are you taking?
Yeah!! Checked and it’s was very interesting!!!
This is SO true of so many of our journeys. May you continue in Love Light and Healing