Hi good people. It's been said that if you have any of these bands in your labs then you have LYME D: 23 31 34 39 83/93; yet my labs didn't: 41KD 41KD; 41KD 58KD. MY labs video:
and even my infection specialist agreed on that; yet she refused to treat me for a possible hidden Lyme D. because the CDC rules that said I should be treated unless I have a positive western blot.
However, I've been told that my body may not present antibodies cause Lyme can leave blog stream go into muscles bones so I won't get a RXN even showing up these tests are over 60 percent inaccurate. They said that should then treat for my symptoms, get a complete health history look at environmental issues; work on food sensitivities; hormone and thyroid imbalances.
And of course I do have all these stuffs since I was diagnosed with Hashimotos. Later on I realized I got candida and last liver and/or gallbladder issues. However, I've read they all can be caused by Lyme in the first instance. So I am kind of in circles.
My symptoms do NOT resemble the typical Lyme D like: Achy, stiff, or swollen joints. Headaches, dizziness, fever. Night sweats and sleep disturbances, Rashes, Cognitive decline etc. However, I DO have:
*tiredness all the time and sleepy
*muscle weakness (possible potassium deficiency)
*borborygm (stomach noises)
*possible gluten sensitivity (yet I tested negative on labs)
*possible candidiasis (yet I tested negative on labs, but in a homemade glass water test I tested positive)
*heartburn that irradiate in my back (h. pylori)
*knees pain (I've read it is caused by candidiasis but also lyme)
MEDICINE & VITS:
*NDT for thyroid (hashimoto, caused for lyme disease accordingly)
*MMS 1000 + DMSO protocol (haven't notice any dramatic changes. I've read it was because candida needs to be treated first).
*easel root (for lyme but without success. I still feel this tiredness all the time)
*Magnesium, pottassium, D3, NAC (for mucin), olive oil (just in case I have fat liver), orange oil, parsley tea with ginger (water retention), and garlic (for h. pylori).
So my question, do you guys think I still have LYME DISEASE yes or not?
ps: I don't have a job nor insurance at the moment to pay for the igenex test, so for now I have to rely on my symptoms.
Thank you for your thoughts.