Need Help with LLMD reference, please

Hello community....I wondered if any one can help send a list of northern LLMD CA doctors to me....a dear friend is getting worse and worse,,,,trying to see doc(s) who don't know or won't recognize Lyme...he tested neg, but feels the many years of symptoms and a known tick bite should be pursued further, as do I. I used the once every 30 days feature online but only found out of area doctors, neuros....he is feeling so badly now closer to where he lives would be super which is a 50/60 mile radius of Auburn CA 95603..i thought I pulled one up in Santa Rosa, but now cannot find the info. I have found one in Auburn, it is not a good contact, not practicing, etc..
He is close to Roseville, Grass valley, Auburn, and would prefer if he has to go long distance, to stay above the bay area..north Marin OK, I found two yesterday in San Rafael area and passed along info to them. Anyone in a serious decline knows that travel is hard, when you are ill, low. Last "detour" he took was a lost year taking prescribed pain meds.....in which time he only got worse!!! weaning OFF them completely he realizes they were masking the illness...needs help and quick..

.I now know myself certain reactions one can get when the word Lyme is mentioned to doctors......see that first hand with my Dad's doctors. No one will enter into conversation regarding it. And we all live in a VERY VERY tick occupied area!....
help is highly appreciated, just write back if you need my gmail to send info to.....I've been trying to help him any way possible, feel that time is critical now. ....his wife has some test results that were out of the norm ranges, but she not sure if they relate to the possibility of Lyme or not. they were not Bb. He's had all kinds of Dr's see him. Classic. Thanks very much for response, in advance.

Hi Stacyposh ----it just occurred to me this might be outside the rules of conduct (always thinking late) and I'd rather not post my mail addy publicly...and so I'd better not go there..apprecite your offer tho....I wish there were published lists online!!...hopefully they will get help locally, my friend and his wife via face to face support groups that meet near Sacramento and in the foothills surrounding. .....he was emotionally shot down yesterday when he phoned some doctors in the bay area and asked out of curiosity the cost of AB therapy, ...I think he guessed at an amount and the ladies on the phone just laughed at him (not kind manners)---felt very very bad for him...their ins might not cover, at all---so is therapy just for those with the right insurance and funding? those are the sorts of things going to support group might shed light on....he is a classic case of getting the run around, for years, medically----declining all the while.

Thanks so much---that occured to me in checking other profiles, ..i saw the addys under some member names, not others. Appreciate the help

Thanks so much, Traveler!! I've talked to you before.....have not been here in a long while...so have questions too, pertaining to me...but those, later....think I will get the HW addy! my friend really needs contact info, and soon.

I have done lots of reading, research, in the past year (even OTHER vector bugs, UGG that surfaced here, I'd never seen)....I have concluded it is very likely my whole family has had Lyme, possibly generationally..backwards on both sides to the 1850s!! it was lot's And lot's of clues, falling into place but especially one's backwards history, and health history and WHAT you were exposed to, WHERE you lived and worked, what HOBBIES and OCCUPATION.......all that makes the puzzle "come together"..... Doctors never truly do this--it is so important the overall picture (perhaps LLMDs do delve, i don't know)

my 90 year old pa, tick exposed when only a toddler in Eastern Oregon, in the mid 1930s..he filled in lot's of family history orally for me.., his own recent (69 to now) health history supplied many clues, too. Sadly his symptoms none of which were ever related to possibility of Lyme--he would forgo antibiotics at his age...system very delicate,..we eat garlic, stay home. Non of us tested, as yet --him, me, my Brother. Just survivin', but with some knowledge, now---knowledge is good. So sad my mom suffered all her life with a cough, likely related to her exposure, leading to underlying immunity issue/allergies. My Pa is still very sharp for his age, mentally----we are somehow, blessed with serious yet not too debilitating health issues. (functioning, chronic)

Tragic loss of kitty cat last summer means no more pets for me now, both flea and tick issues....we had a HUGE number of ticks last year--they were plentiful!!.it was mind boggling...and no more garden for me either...attracts deer--last year the loss of cat made me so sad, I let the well established garden go to the deer, --loss was monetary, too....:-( ...(garden needed a taller fence around, I had no heart to remedy it, went into mourning over the cat) I'd rather buy organic local veggies, and not invite the critters to dinner, I will have to pet other peoples cats....I'm 54, never been without a cat, for very long. We have old growth trees all around us, expensive to fall, so they must stay, I'm not squirrel or bird friendly any longer (they are HERE, but no longer encouraged with feeders, or water sources) I no longer dry clothes on the line....last tick I spotted? on a pillowcase, a nymph..I ALMOST folded it up and imported inside--thot, hmmm, I'd better check that speck...... Ah rural life.....

Def still an unfolding story, Lyme!
again--thanks!
CA Kid