This is topic looking for a doctor in Chicago, IL in forum Seeking a Doctor at LymeNet Flash.


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https://flash.lymenet.org/ubb/ultimatebb.php/topic/2/8337

Posted by jemison (Member # 18993) on :
 
Hi,

I have been dealing with lymes disease for four years. I had intravaneous rocephin and it knocked it out for a long time. Now my lymes symptoms are relapsing from time to time. My sympotms are fatigue, muscoskeletal pain (most painful and present), joint pain, and 'lyme fog'. It is the most difficult thing in my life and I really need help.

ARE THERE ANY SPECIALISTS IN THE CHICAGO AREA???

My insurance is consolidated health plan.

Please let me know if you have any information...

G
 
Posted by bettyg (Member # 6147) on :
 
welcome george! so sorry to read about all your pain, etc. fyi, we have LYME disease with no s on it ok! correct drs. when they say it too as it's named after LYME, CONN.


CHECK YOUR PROFILE FOR NAMES ILL/S. WISC. folks in illinois have NOT had any luck in your state!


Welcome; i'm so glad you found us!! You've come to the right place for education and support!


Dr. Burrascano's most recent "Diagnostic Hints and 2008 Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @

http://www.betterhealthguy.com/images/stories/PDF/LYMDX8RX2008-October.pdf


Dr. B's Supplement List
http://www.lymepa.org/Nutritional_Supplements.pdf


this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005


please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you!
@ http://tinyurl.com/58eyou

sorry, link takes you to END vs. beginning, so just use UP ARROW and go to the TOP for detailed info! thanks!
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please go to my newbie links, copy the entire thing, and then print this off....FINANCIAL BURDENS compiled by melanie reber
print off pages 74 - 92; outstanding info there. i believe there are a few more general comments there without links!! print that off too as it's newer info from members thru their own personal, tragic experiences.


Betty's POSTING GUIDELINES . many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.

please edit your post by CLICKING PAPER/PENCIL ICON to right of your name. that opens up BOTH subject line and body text.

now please break up your WORDY SENTENCES into one sentence paragraphs. Then hit ENTER KEY ``TWICE`` after each paragraph; we need that space for comprehension.

NOTE: you do NOT have to use "", just show the name of person you are responding to, and then type your comment.

IF you need to use "", PLEASE DELETE "BOLD" CODES so it's regular type text we read vs. the DARK, HARSH/PAINFUL BOLDING. delete the first 4 characters of 2ND LINE of a ""

[QB] just delete these 4 characters, and BOLDING is GONE! my eyes will really appreciate that; it's one very bad side effect of my having lyme for 38.5 years!! xox

then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND

we thank you for helping us; [Wink] otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me.
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People seeking doctors might be able to get help from their state online information and support group. Nearly 3,400 people belong to state groups. Some of the groups are small but more than 20 of them have 50 or more people and seven have over 100.

To find your state group, go to
http://health.groups.yahoo.com/group/statenamelyme

Type your state name and lyme as one word, like this -
http://health.groups.yahoo.com/group/newyorklyme

South Carolina is the only state that needs a hyphen between the statename
and lyme, e.g. http://health.groups.yahoo.com/group/southcarolina-lyme

The groups are moderated and you have to apply. Most don't allow doctor names, but once on the group, you can ask for doctors in a certain area and ask people to email you privately.
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