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» LymeNet Flash » Questions and Discussion » Medical Questions » New doc does think chronic lyme....interesting thoughts

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Author Topic: New doc does think chronic lyme....interesting thoughts
pme
LymeNet Contributor
Member # 31621

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Well...finally one of the docs believed me and is going to start me on doxy.

I went to go see an ND who was the partner of someone who was on the LLMD list. I went over the usual history and she said...neuro lyme. She said it had been undertreated before and that I have had it anywere from 3 to 10 years.

She helped me decide to stay part time until the end of the summer to see how treatment goes. She also said it didn't even matter what the blood tests said, though she wants to run some.

She said the treatment will determine if she is correct.

I thought it was interesting because I thought the cause of the flare was sinus surgery (stress of surgery on a sleep deprived system). She said she thought that all the abx I was on for sinus infections prior to sinus surgery kept the disease at bay and that once I had the surgery, and didn't need the abx for sinus infections it was allowed to grow/flare.

Finally......somebody looked at the big picture and is willing to do something about it.

I feel hopeful.

--------------------
Tick bite in 2006, bullseye rash, treated with 2 rounds of 2 weeks of doxy. (once in 2006, once in 2009)
Dx with chronic Lyme May 2011.
LLMD April 2012, Treating with omnicef/zith
Lots of supplements!

Posts: 640 | From Connecticut | Registered: Apr 2011  |  IP: Logged | Report this post to a Moderator
Deshi
LymeNet Contributor
Member # 30949

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congrats! i hope you make a full recovery
Posts: 105 | From Ca | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
Laura_W
LymeNet Contributor
Member # 31491

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[Big Grin]

[woohoo]

--------------------
10/10 EIA 1.4+, 41 (IGG), 23 (IGM)
Bitten over 20 years ago.
Currently not treating, looking for a Dr who will work with my insurance lol.

More muscular, cognitive, nerve issues than joints. Facial droop and blurred vision.

Posts: 323 | From Michigan | Registered: Apr 2011  |  IP: Logged | Report this post to a Moderator
payne
Frequent Contributor (1K+ posts)
Member # 26248

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you are your own advocate...
Glad to hear you found a believer.
press on -
the road is long and broken,
That leads you back to
Your life again.

--------------------
TULAREMIA/rabbit fever ?

Posts: 1931 | From mid-michigan | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

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Very good job, pme!

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
ukcarry
Frequent Contributor (1K+ posts)
Member # 18147

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Glad to hear that someone is thinking outside the box! Good luck,

Carry

Posts: 1647 | From UK | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
lpkayak
Honored Contributor (10K+ posts)
Member # 5230

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whoopee! a doc with a brain!!! gives us reason to hope

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
philly78
Frequent Contributor (1K+ posts)
Member # 31069

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This is wonderful news! Yay for you.

--------------------
When faced with pain you have two choices....either quit and accept the circumstances, OR make the decision to fight with all the resources you have at your disposal.

Posts: 1000 | From PA | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
lyme in Putnam
Frequent Contributor (1K+ posts)
Member # 11561

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[Smile]

--------------------
He took u to it, He'll you through

Posts: 2837 | From NE. | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
   

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