Hi Kikikaia
I'm sorry you're here but glad you found us. I'm also in SD area and can recommend my LLMD if you're interested.
I would not pay for any test other than IGeneX lab and their WB. The "New to Lyme?" thread explains the testing issues. - at this point IGeneX is most reliable and usable if you happen to pursue insurance coverage. It's 100% worth the few extra dollars.
Also, I'd try provoking a more reliable immune response by taking olive leaf extract herb for about
4 wks before you do the IGeneX test. With all of the other tx and drugs you've been on trying to get an accurate dx, it's tough to know exactly how your immune system will react but I had good success provoking my immune system and I know others have, too.
You should also look into a bartonella or bart-like infection or BLO (bart-like organism). It's famous for causing stiff neck and lymph node issues in neck/head and headaches. Not to suggest that Lyme can't, but anything neck/head might also be from bart and you can get infected w/ bart from same Lyme tick or from fleas, many other ways.
I can also recommend my Lyme-friendly neurologist in SD. He has many Lyme pts and knows what to look for. He likes to suggest that most neuropathy is caused by inflammation, so anti-inflammatories might help (do NOT use steroid products - they reduce immune response, which can cause even worse problems with the TBDs - Tick Born Diseases).
But as others have shared, you'll need to get to a Lyme specialist in order to get accurate Lyme and coinfection diagnoses. You are exhibiting classic TBD symptoms - Lyme has been found in SoCal. The urgent care and typical MDs are not trained to identify sx or diagnose.
-p
Post Edited (Pirouette) : 8/6/2017 12:47:20 PM (GMT-6)