News and resources for neurological Lyme disease and co-infections.
He describes taking a blood sample from a nervous dog suspected of having Lyme disease, and as the vial filled with blood the dog shook his head strenuously which knocked the syringe from the doctor’s hand and sent the needle flying directly into Dr. Stuers arm.
My recovery, due primarily to stem cell therapy in India (with a little side credit going toward pre-stem cell antibiotic therapy, as stem cells only have the ability to repair the body but cannot kill bacteria), is still mine to keep.
I think that we can all relate to this! A fellow Lyme-sufferer from a Lyme forum allowed me to reprint this very touching essay. “Hi to all of my friends and family,
But I am now convinced that, at least in my neck of the woods (northeastern Pennsylvania), Lyme is easy to get and hard to treat!
Is the admission of Lyme in Canada coming too late?
You may want a little more background about my health protocols, so I also have a free e-report that I have made available called “Diet Soda Makes You Fatter Than Regular and 10 More Shocking Health Truths.” This is available at my website – www.nutrientbalance.com – and more information is available there as well.
Have you ever felt alone on your Lyme journey? Have you ever felt confused and helpless? That used to be me. Hi everyone, I’m Rachael and Jenna has graciously allowed me to share my story (and a new resource) with you today. I’m 19 and have likely had Lyme for about 11 years. I remember [...]
Every three weeks, I felt my energy increase. A side effect of the infusion is a throbbing headache – my first one last 3 days – as bad as my worst migraine – but with lots of water and Benadryl (doctor’s orders), the headaches became less severe until they are now almost completely gone (I take Excedrin Migraine at the first hint of the throbbing and it dissipates.)
What do I attribute my slow recovery to?
First, I must emphasize as always that I am NOT a medical doctor and can only share my experience – each of us have what I call Lyme disease cocktails, and each of us have unique “operating systems” medically speaking with our infinitely varying immune systems, our inflammation response, age, underlying health condition, genetic coding, and number/virility of disease(s) and diet. So what will work magically for one person will not do a thing for another. I know, this is all very frustrating!
It’s only recently that I’ve found out that this is a protocol, the Cowden protocol, which I have highly altered. I believe that with my fast changes and with using the microbials that my body tells me to, I am chasing the microbes around, until ultimately they have no place left to hide. Now I feel almost normal.
