a Neuro is not a good person to see to determin lyme from my experience.. Mine think im nuts to even think so even tho pa is very popular for lyme. So i dont really deal with them when it comes to lyme at all because they diagnosed with ms and are sticking to it even tho they ruled out nothing else. You would want to see an LLMD you have to go to a webpage and register and they will send you names and help you find one since they are low profiled.... And the only lab for the testing you should use is Igenex ..... I made a post in the Lyme forum called MS or Lyme, you can probly find it on my profile page and they all told me a bunch of information on that post that helped alot... you should check it out! Good Luck and hope that post heps!
Hey renschwa I am also inbetween lymes and MS i am diagnosed MS from no proof really but have way more symptoms that dont involve ms and involve lyme. Ive had the basic lyme test come back neg. but my doc said that dont mean anything at all because its a very unreliable test and have to do more if you want you can messsge me all of your symtoms you have or ever had and we can compare and there are alot of websites that give u a Lyme checklist compared to an MS checklist
Thank you. I have not yet seen a neurologist. Just seeing an ortho right now b/c this seemed ortho related when it first started.
Who should I see to determine if this is Lymes?
Lyme can mimic MS, so make sure you get it ruled in or out. I've been diagnosed with lyme and many of your symptoms are the same as mine. Have you been tested for anything yet? Have you had any MRI's? I suggest you get a lyme Western blot done. Make sure you get a copy of the results. Even if you are overall NEG, if you have ANY reactive or POS bands it may be significant.
Good luck to you and hope you find some answers soon. There is also a lyme forum here, so if you need any help or have questions please join us :)