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» LymeNet Flash » Questions and Discussion » Medical Questions » Frontal lobe dementia?

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Author Topic: Frontal lobe dementia?
hshbmom
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Any documents support lyme as a cause of frontal lobe dementia?
Posts: 1672 | From AL/WV/OH | Registered: Jun 2006  |  IP: Logged | Report this post to a Moderator
joalo
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Up.

--------------------
Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006.

Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
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Try looking up research done by Dr M of NY.
He found the Lyme Bb spirochete in the brains of 7 out of 10 deceased Alzheimer's patients. I think the research was linked to Yale?

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Dear hshbmom,
I found valuable links to neuropsychiatric Lyme info via this website:

http://www.lymesite.com/neuropsychiatric_lyme.htm

Keep asking...
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bcb1200
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Well..I can give you my direct experience. I'm a 35 yo male. I didn't get diagnosed until 5/3. Before that I had a brain MRI. It was "normal" with the exception of a slight suggestion of "bilateral cortical atrophy of the parietal lobe." This is basically a type of dimentia.

I then had a spect scan. It was abnormal...luckily the pattern was not indicative of alzheimers or dimentia. But it does make sense now that I know I have lyme.

--------------------
Bite date ?
2/10 symptoms began
5/10 dx'd, after 3 months numerous test and doctors

IgM Igenex +/CDC +
+ 23/25, 30, 31, 34, 41, 83/93

Currently on:

Currently at around 95% +/- most days.

Posts: 3139 | From Massachusetts | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
bcb1200
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I think brain mri's and especially spects are good for lyme.

Dr. B even references them as typically spects will be abnormal with lyme.

My eeg was normal.

Finding an ll neuro is good. But if you can't, go to a regular neuro and get it anyway. Just take your results to your llmd.

I found out I had lyme they day I had my spect. When I followed up with my neuro, he said the spct was abnormal and he wanted to do a spinal tap to find out why.
I said "no thanks" I know I have lyme as I tested positive and this all makes sense.

I'm on day 22 of treatment and am feeling a bit better. Most of my symtpoms are mild neuro (ear, eye, dizziness, leg twitching)

I'm feeling the best I have in 4 months this week. Hope this is a good sign that I'll make a full recovery.

--------------------
Bite date ?
2/10 symptoms began
5/10 dx'd, after 3 months numerous test and doctors

IgM Igenex +/CDC +
+ 23/25, 30, 31, 34, 41, 83/93

Currently on:

Currently at around 95% +/- most days.

Posts: 3139 | From Massachusetts | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
hshbmom
Frequent Contributor (1K+ posts)
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Thanks to each of you who have responded. I appreciate it!


I plan to give this information to a friend.

Posts: 1672 | From AL/WV/OH | Registered: Jun 2006  |  IP: Logged | Report this post to a Moderator
   

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