Lyme Disease

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Why do we suffer with chronic Lyme? 

And why are conventional medical doctors so resistant to look at the massive emerging evidence with an open mind to find answers rather than look down at those of us who are ailing and have done research if we can't understand what we read, or better yet, what we see with our own eyes.

After viewing this video, I challenge the "There Is No Such Thing As Chronic Lyme" crowd to investigate themselves with their advanced degrees and celestial opinion of their point of view.



Due to the failing health of Dr. MacDonald, there are others who are continuing with his research.  One researched who has suffered from Lyme herself, recently spoke at the annual ILADS conference, Dr. Eva Sapi you can watch at

Advancements are being made on combinig certain  enzymes to further enhance our ability to break down the biofilms and destroy large colonies of spirochetes, but for now, Lumbrokinase (Boluoke)

See my own Biofilm Busting Protocol


 My Crash

When I was first diagnosed with Lyme disease, I felt so relieved!  Months of non-conclusive tests, frustrating evaluations, and the growing sense of was going to be all behind me now!  I had Lyme disease, and I was actually relieved to have all that fear and worry over. 

Little did I know that my nightmare had only just begun.

That was over four years ago.

Life has been a living hell for those years, and there is just barely a flickering light at the end of the tunnel.

My LLD believes that I have been suffering with Lyme, Bartonella and Babesia for most of my life. Yes, it does explain the mystery illnesses, the infected organs that had to be removed without a clear diagnosis.  And yes, it also explains the mysterious loss of hearing, and the excrutiating pain in my abdomen that would come and go...

Does any of this sound familiar?

Now I have significant evidence pointing to a subnormal immune system - will it ever end?

Well, I used to do most of my work on the computer, so it was natural for me to begin my search for answers there.  But after weeks of searching, while my symptoms were going from bad to worse, I finally gave up trying to make sense of the conflicting information on the computer, and started buying books instead. 

That is when I began to really understand the complexity of my disease.

That was the beginning of my education, and the beginning of what has become a "calling" for me.

As a result of this ordeal, I have dedicated my life to helping others, and that is what I hope to do with this website.

You will find all the latest medical and scientific information about chronic Lyme (See the left menu) along with product recommendations and alternative healing protocols. This information is constantly updated. Also be sure to visit my Lyme Blog which povides treatment and diagnosis discoveries and news alerts.

I hope you don't have Lyme disease.   But if you do - remember this - you aren't alone.



PS My protocol changes as I try different things in desperate attempts to reclaim a portion of my previous life.  Read about my own treatment and ongoing recovery here.





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Jenna Smith has chronic Lyme disease

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