This is topic POLL : How Many LLMD's Have You Seen? in forum Medical Questions at LymeNet Flash.


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Posted by seibertneurolyme (Member # 6416) on :
 
1) How many LLMD's have you seen? Were any specialists?

Hubby -- 2 regular LLMD's and 1 LLMD neurologist

2) Were your LLMD's in-state or out-of-state?

Hubby -- all 3 out-of-state

Thanks,

Bea Seibert
 
Posted by Aniek (Member # 5374) on :
 
One LLMD, a rheumatologist.

Since I'm a disenfranchised DC resident with no state and no vote in Congress, the second question doesn't apply. But my LLMD is 40 minutes away, so basically in state.
 
Posted by Michelle M (Member # 7200) on :
 
I'm very lucky.

Just one great LLMD.

A short drive -- hour and a half away (75 miles), far northern California.

Family practice doctor.

Michelle
 
Posted by Lymetoo (Member # 743) on :
 
quote:
Originally posted by Michelle M:
I'm very lucky.

Just one great LLMD.


ONE for me...in state!
 -
 
Posted by groovy2 (Member # 6304) on :
 
One-- and she is real good
She used to have lyme so
she understands and knows where
you are coming from--

I started getting Better in days--AAhhhh

Saved my life For Sure --Jay--
 
Posted by bettyg (Member # 6147) on :
 
1 "beginner" LLMD 15 miles away...

1 LLMD/holistic MD 9 hrs. roundtrip.
 
Posted by mag (Member # 8920) on :
 
2 Family Medicine doctors
4 Neurologists
1 Infectious disease doctor
1 LLMD in California -- 1 hr away
Took nine months to get a diagnosis with treatment

This could be a great national poll

mag
 
Posted by Mathias (Member # 5298) on :
 
2 LLMD's

1 LLNeuro

1 LL ID

Only been treated by the LLMD's.
 
Posted by Mathias (Member # 5298) on :
 
2 LLMD's - In state

1 LLNeuro - OOS

1 LL ID - In state

Only been treated by the LLMD's.
 
Posted by Bluetick (Member # 8467) on :
 
Just one - 3 hour drive out of state.
 
Posted by maeflower21 (Member # 4379) on :
 
3 LLMDs out of state

Internal medicine, hematologist/oncologist, neurologist and GI specialist all in state
 
Posted by luke339 (Member # 8580) on :
 
3 thus far.

First one i went to lost my blood results before seding them away waited a month to find that one out (obviously did not go back to her).

Second one gave me ceftin for 20 days, said because i did not react to the abx in that amount of time he does not think I have Lyme
although Western Blot IGM showed band
31++
34 IND
39 IND
41 IND

Third LLMD took a look at results (from Igenex) and listened to what I told him of my symptoms. Thought right o way that I had Lyme and thats my major problem right now along with some co-infections (which he is testing me for right now).

Hopefully We will see results soon, cause i am twitching everywhere now, even after i open my mouth my muscles twitch on nmy neck. pretty weird feeling.
 
Posted by pab (Member # 904) on :
 
Jake & Jordan have seen 2:

1st - 1250 miles one way
2nd - 625 miles one way

Both were out-of-state.

My husband and I are also patients of the 2nd LLMD.
 
Posted by iceskater (Member # 8655) on :
 
Woke up 2/26/05 unable to walk.
Several ER visits. Two hospital admissions.
Three neurologists , in two hospital stays thinking I was okay and finding nothing ( two hyperintense signal flares in brain, but I am okay ? [bonk]
My family doctor treating me.
Lyme titers found.
Move in with parents who started to take care of me.
Parents dr tx me with Iv Rocephin.
Wheelchair/walker
Consult with and tx from 2 LLMD , out of state, in conjunction with parents GP.
Lyme literate neuro opthamologist and retinal specialist and glaucoma specialist here in town- macular degeneration and optic neuritis from lyme.
Pain management will be next.
GP doing a good job, despite my severe neuro lyme and all the nasty little co's that we have found so far. [dizzy] Gp going to ILADS conference this past fall, going again this year, attended Eastern shore conference. Consulted Dr B. Family GP now has 8 patients in her practice with lyme ( all this past year). My doctor by virtue of the fact that had so many patients starting to be diagnosed, had to learn very fast and study alot and consulting the big guns.I know I have missed some doctors along the way to post as having treated me and said nothing was wrong. I just want to forget those jerks that knew nothing about Lyme. In summary, a laundry list of learned medicine men who learned nuttin' about little tickies. [cussing]
 
Posted by Andie333 (Member # 7370) on :
 
I've only seen one LLMD since starting treatment in June.

I'm getting steadily better, so I see no need to seek another opinion at this point.

My LLMD is out of state, about 1 and 3/4 hours drive. Not bad.

Andie
 
Posted by HEATHERKISS (Member # 6789) on :
 
On my 3rd.
 
Posted by GiGi (Member # 259) on :
 
I did not see any LLMD. I was treated by a medical doctor who is aware of Lyme Disease. Also addressing all possible underlying conditions of a chronically ill person is what cured me from Lyme Disease and all other problems I had for a number of years.

That taught me to be the only approach to conquer Lyme.

Take care.
 
Posted by lucy (Member # 7802) on :
 
In spite of the Lyme, I feel incredibly lucky to have a great LLMD 15 min. away. Other than my PCP(who I had to bully abx out of),and the neuroligist fool I saw for a second opinion, he's the only LLMD I've seen.
 
Posted by trueblue (Member # 7348) on :
 
1) LLMD neurologist (diagnosed me)
2) LLMD (family practioner, my all time favorite)
3) LLMD psych (evaluation)
4) LLMD rhuemy
5) LLMD internist
6) LLMD ID

Numbers 3 and 5 were in state; not the same state, but the state I lived in at the time.


The first may not deserve the LLMD label. As a matter of fact I tossed her into the Alligator Pit! Anyone see the Alligator Pit lately?
 
Posted by Lymetoo (Member # 743) on :
 
This one??

Alligator Pit
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=3&t=013882#000003
 
Posted by JimBoB (Member # 8454) on :
 
0
 


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