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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » ILLINOIS OR CHICAGOLAND? -LLMD -DR?

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Author Topic: ILLINOIS OR CHICAGOLAND? -LLMD -DR?
ChicagoFog
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I am having trouble finding a LLMD in Illinois.
Can someone help me out? All the contact info I am pulling off the Internet seems outdated as the phone numbers are disconnected. Even an Indiana or doctor in Wisconsin would help...

PM me or email: [email protected]

Thanks!

Posts: 1 | From Chicago | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Lymetoo
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check your PM

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
NP40
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Sent an e-mail
Posts: 1632 | From Northern Wisconsin | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
lynem
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I am also a Chicago person looking for the same information. If anyone can help, I would be grateful. Email is: [email protected]
Posts: 1 | From Dundee, IL | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Jacqi
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I could use this info as well. I live in NW Indiana

--------------------
J

Posts: 91 | From Northwest Indiana | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
bettyg
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pm sent to jacqi....
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Munch
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Hi! Can somone recommend a LLMD in IL? I'm new to this board. I've been going to the Detroit Fibro and Fatigue Clinic for the past year with not much improvement in symptoms.

I was told I was negative for Lyme by FFC. Igenex IgM Western Blot Results: INDeterminate ** bands **23-25, **34, **39 and ++ positive to band 30 and **41.

Igenex IgG Western Blot Results: INDeterminate bands **31, **39, **83-93 and ++ positive to bands **41 and 58.

Thanks for any help! [email protected]

Posts: 192 | From Dwight, IL USA | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
bettyg
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munch, i sent you PM, private message name and my 46 pages newbie links/advise [Smile]
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LisaS
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If you guys dont find one in Illinois, I have an LLMD in Southern WI. If youre interested let me know.

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https://www.facebook.com/profile.php?id=1660435643

Posts: 1078 | From Lake Geneva WI | Registered: Nov 2006  |  IP: Logged | Report this post to a Moderator
char
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Lymetoo and others-

Could you pm me also this info?

I just posted same question, particularly Western Suburbs, (near Dundee).

Thanks a lot,

Char

Posts: 1230 | From US | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
bettyg
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CHAR, sending you pm on your post. [Wink]
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buggedbylyme
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I would like the same info for llmd for a dear

friend in the western suburbs of Chicago . I'm

convinced that he has Lyme. He and his wife will

be visiting next month and I want to have info

all put together for him.

Thanks!

Posts: 70 | From essex fells, nj | Registered: Jul 2006  |  IP: Logged | Report this post to a Moderator
bettyg
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BUGGED, i sent you pm now. [Big Grin]
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Polaris
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Need to find a LLMD in Chicagoland or Indiana. Thanks.
Posts: 31 | From USA | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Polaris
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Hello, anyone there?!
Posts: 31 | From USA | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Munch
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Thanks to everyone for sending me PMs with doctor referrals. I'd like to leave some feedback for others interested in LLMDs in IL.

I saw Dr. Z (Chicago) in March 2007. He states that he is not a LLMD but seems to be the only doctor on the "Good List" for Illinois.

He is a Internal Medicine Doctor. He was very nice and listened to me. I was asked to bring my medical records. He copied a few but didn't look at them.

Dr. Z told me I had "post Lyme autoimmune disorder". My husband and I thought that was a laugh. How could I get a post-dx when I never could get the dx?

Dr Z and I do not agree on my use of pain meds or B-HRT (hormones). I've had to fight and claw to get my treatment pieced together thus far. I have HPA issues.

The very long string of doctors that I've seen since 1981 have diagnosed me with hypothyroidism, fibromyalgia and chronic fatigue. I've got a long history of GERD, endometriosis and a knee replacement.

I also have sarcoidosis and may possibly have polycythemia vera. There's something abnormal about my bone marrow and blood production.

Dr. Z is very much against steriods. I take 5 mg. of hydrocortisone 3-4X per day or a 20 mg. dose in the AM. Without adrenal gland support my thyroid meds don't work.

For the past year, I wasted a ton of money at the Detroit FFC. They did a Igenex WB (my results posted on this thread) but do not know how to read it. I was initially told I had Lyme based on a Quest WB. I was given Doxy. Then I was told to off Abx.

For these reasons, I've decided to persue treatment with Dr. C (MO).

Posts: 192 | From Dwight, IL USA | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
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quote:
Originally posted by Munch:
For these reasons, I've decided to persue treatment with Dr. C (MO).

Excellent choice! [Smile]

Keep us posted on your progress! Where's your test results??

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
   

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