Is it normal to feel tingling, numbness, and pain in arms, hands, legs, and feet with Lyme? Is that considered neuro lyme or regular lyme? What helps to alleviate it? Also I have very disrupted sleep and always wake up at 3:30 am and can't go back to sleep. Anyone experiences this?
I myself have the numbness and pains, I also do have disruptive sleep patterns, sounds like lyme symptoms to me. Have you seen a lyme doctor?
I have seen three doctors and all tell me straight out I do not have lyme according to the Quest test which only showed one band reactive - IGM 23.
I can't get anyone to believe me or take me seriously and treat me. The scariest feelings though are feelings of confusion and disorientation especially when I am trying to work or in a store with lots of lights. I am allergic to the cephelasporins and doxy so I don't even know how they would begin to treat me. I ordered a kit from Igenix but I wonder if there is anyway to bring the bacteria out of hiding so that more bands can show on the test to get a CDC standard positive so that my doctor can treat. Any suggestions?