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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in ILL

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Author Topic: LLMD in ILL
bedazzled807
Junior Member
Member # 27251

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Please help I am looking for an LLMD in or close to Joliet, IL I am at my wits end I just tested neg on the ELISA and Western blot but I am positive I know it is LYME I have every single symptom although not at the same time I have seen (in the last year)
neuro, optometrist, ent, rhematologist and the list keeps going I was diagnosed with Fibro at Loyola 2 months ago but I know in my heart that is not what it is since I tested neg my PCP wont treat although I have done a lot of research and it seems there are a lot of people with Lyme and test neg
Posts: 1 | From Illinois | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

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Welcome! [hi] We are happy to have you. I sent you a private message (pm), click on the flashing envelope. [Smile]

Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!

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I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.
Posts: 3897 | From New Hampshire | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
pj1954
LymeNet Contributor
Member # 11722

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private message sent !
Posts: 294 | From sw chicago suburbs | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
pmerv
Frequent Contributor (1K+ posts)
Member # 1504

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Have you tried IllinoisLyme?
http://health.groups.yahoo.com/group/illinoislyme

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Phyllis Mervine
LymeDisease.org
Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001  |  IP: Logged | Report this post to a Moderator
hoot
LymeNet Contributor
Member # 19281

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I was exploring this in the past with my son. Now I think my hubby may have lyme. I know there was a doc in (central?) WI that treats lyme (Dr. H) but I lost the info. I am looking for someone in Illinois or the one in WI that I am speaking of.

Please PM me.
Posts: 236 | From Illinois | Registered: Feb 2009  |  IP: Logged | Report this post to a Moderator
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

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Hi, Hoot! I sent you a pm.

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I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.
Posts: 3897 | From New Hampshire | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

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PM sent

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--Lymetutu--
Opinions, not medical advice!
Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
hoot
LymeNet Contributor
Member # 19281

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Thanks!
Posts: 236 | From Illinois | Registered: Feb 2009  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

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Hi - just wanted you to know I had fibro for 25 years that turned out to be Lyme. And, I had a known tick bite, with the fibro symptoms beginning about 10 weeks later. I am on clindamycin antibiotics, which takes my fibro pain to zero.

We're all different when it comes to meds, but I want to let you know that when you find the med that works for you, the pain can go down.
Posts: 13117 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
pj1954
LymeNet Contributor
Member # 11722

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is 30 mins away close enough ?? did you get my private message ?
Posts: 294 | From sw chicago suburbs | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
hoot
LymeNet Contributor
Member # 19281

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That is perfect if people recommend him/her.

Thanks!
Posts: 236 | From Illinois | Registered: Feb 2009  |  IP: Logged | Report this post to a Moderator
   

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