This is topic Can Brain fog and dizziness be part of a herx? in forum Medical Questions at LymeNet Flash.


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Posted by Clint31 (Member # 16420) on :
 
For the first time i've had brain fog for about 5 days now. It feels like 'drowsy brain'. It also feels similar to when i was getting off paxil. No matter how much I sleep or if I've just woken up from sleep, I cannot get my brain to wake up. I think this is brain fog.

I have also had some dizziness for the last 5 days... but only when I'm thinking about it.

Can these be parts of a herx, and if so I've definitely been herxing for 5 days.... doesn't make sense.
 
Posted by Alv (Member # 15192) on :
 
How about herxing 1 year in a row...non stop for a day !

It is funny as one bug goes down the others activates...So if you have more than just lyme ...you can herx for very long.

Now that I have 3 bugs and 2- or 3 in remission my herx can be a few days and turns around ....but before with all of them together ...NON STOP brain "FOG" better say BRAIN SWELLING that can not fit the skull.
 
Posted by Clint31 (Member # 16420) on :
 
are you saying having brain fog is better than brain swelling, or you're saying you believe my brain is swelled and that is why i'm having non stop brain fog?
 
Posted by Clint31 (Member # 16420) on :
 
ttt
 
Posted by sixgoofykids (Member # 11141) on :
 
Clint, I think Alv meant brain swelling was a better way to describe her experience. [Smile]

Anything seems to be normal for a herx.

In the beginning, now my situation is different than yours, I was undiagnosed 30 years, sick for 4 years prior to diagnosis, pretty much bedridden at that point .... so in the beginning I often was so dizzy I needed help walking.

Now, with Lyme near remission but still dealing with active babesia, here's an example of what can happen. I asked my daughter a question. She answered, "How are you feeling, Mom?" I answered, "Bad, why?" She said because I had just asked her the very same question two minutes earlier.

I said, "I did?" Even after she reminded me I still didn't remember. She asked if I wanted her to write down her answer this time, LOL.

This is reminiscent of how bad I was, and sometimes it pops up here and there.

I know yours sounds different than this, but this is how the brain symptoms manifest for me. And, yes, it does get better. I'm so happy for you that you have caught it so soon, even though it still will be a tough few months for you.
 
Posted by HaplyCarlessdave (Member # 413) on :
 
Yes, "brain fog" is very often a part of the "herx" reaction. It probably doesn't mean your brain is actually swollen, though it might feel like it is.
The cause of the "fogginess", or lack of mental clarity and a "confused" feeling, is usually neurotoxins released from dying lyme or other spirochete-type bacteria.
BCDave
 
Posted by soonermom (Member # 14494) on :
 
I recently was put on levaquin by my GP for a "sinus infection". I have taken this class of drug before with no problems whatsoever.

Even though it was only 5 days, I was having difficulty forming words and was speaking slowly and my hubby told me I was slurring my words. This may sound crazy, but I almost wondered if I would have a seizure or something.

It just felt like my brain wasn't connecting and working like it should. I called my LLMD and they thought it was a herx and to stop all antibiotics until it passed.

I was terrified to stop (on doxy also, and 5 days of levaquin was over) but when I did, I actually felt normal again. (I am seriously wondering about bartonella now??)

I keep saying that if this stuff wasn't happening to me, I don't think I could believe it all!
 
Posted by sixgoofykids (Member # 11141) on :
 
Sooner, I was diagnosed with bart based on my response to Cipro taken for something else. [Smile]
 
Posted by Clint31 (Member # 16420) on :
 
So wait just a minute here... the brain fog... and all the head symptoms......... which are slowly tapering from my hell week last week and last weekend.

There could be a positive lying behind it? (That I'm getting better)
 
Posted by lymielauren28 (Member # 13742) on :
 
I definately think it was a herx. Sounds like you just killed a lot of bugs, and the result was more toxins than your body could eliminate at one time.

When I'm in a herx my brainfog is unbelievable...I don't even feel like I'm a part of this world.

And yes, I think you're getting better [Smile]

Lauren
 
Posted by Keebler (Member # 12673) on :
 
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Clint,

This makes perfect sense. It's very rough, but quite typical.


Have you had a chance to read some of the books about lyme or some of the articles at ILADS' site?

I think you will be relieved to know that many of the symptoms that are scary to you now are all par for the course with lyme and lyme treatment.

Brain fog is classic. No one gets out of the lyme experience without that.

Although, dizziness can have many causes, most lyme patients experience various degrees and types of vertigo at all points of illness and during treatment. Ginger capsules or ginger tea can help tremendously.


To read - in the articles and books - about all you are going through helps you know that you are not alone but also helps you know that it's all part of the process.


This can get better, but it's no walk in the park - it's a long journey. One stroll at a time - with many time-outs.

Hopefully, your rest sessions will be of a healing nature.

Good luck.

=================


www.thehumansideoflyme.net

see the side menu - you will be going "oooh" and "ah-hah!" and much more will fall into place regarding the understanding of TBD.


The book "Cure Unknown" also will explain a lot about the process and how a family found there way out to the other side.


=================


Topic: TINNITUS: Ringing Between The Ears; Vestibular, Balance, Hearing with compiled links

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=065801


==================

Key word here: SOLUTION


This book, by an ILADS member LLMD, has a lot of good information:


http://tinyurl.com/6lq3pb (through Amazon)

THE LYME DISEASE SOLUTION

- by Kenneth B. Singleton , MD; James A. Duke. Ph.D. (Foreword)

You can read more about it and see customer reviews.


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[ 26. August 2008, 06:14 PM: Message edited by: Keebler ]
 
Posted by Keebler (Member # 12673) on :
 
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Clint,

I just thought of one of the books that helped me so much when I was first diagnosed:

www.amazon.com/s/ref=nb_ss_gw?url=search-alias%3Dstripbooks&field-keywords=Everything+you+needed+to+know+about+lyme&x=0&y=0

Everything You Need to Know About Lyme Disease and Other Tick-Borne Disorders, 2nd Edition by Karen Vanderhoof-Forschner (Paperback - Mar 14, 2003)

--


It saved my life.


-
 
Posted by seekhelp (Member # 15067) on :
 
Keebler, any other books you recommend? I am interested in buying a couple. I know Lyme Disease Solution is also supposed to be good.

I'm not as interested in Cure Unknown if it's more about controversy of Lyme than how to treat. I am well aware of the "controversy" after seeing many, many doctors. [Smile]
 
Posted by Clint31 (Member # 16420) on :
 
quote:
Originally posted by Keebler:
-

Clint,

I just thought of one of the books that helped me so much when I was first diagnosed:

www.amazon.com/s/ref=nb_ss_gw?url=search-alias%3Dstripbooks&field-keywords=Everything+you+needed+to+know+about+lyme&x=0&y=0

Everything You Need to Know About Lyme Disease and Other Tick-Borne Disorders, 2nd Edition by Karen Vanderhoof-Forschner (Paperback - Mar 14, 2003)

--


It saved my life.


-

Thank you Keebler.

That one sounds good...

I am gonna look for it at Barnes and Noble on friday when I go
 
Posted by Lymetoo (Member # 743) on :
 
absolutely yes! Any lyme symptoms on the list can show up during a herx.
 
Posted by Keebler (Member # 12673) on :
 
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Books? someone asked.


These are my three favorites and I'm sure most people get tired of seeing me recommend these. Still, even if one is not "into" alternative treatment, the last two offer much insight about lyme and self-care.

Singleton's is a huge help.

----------------


This book, by an ILADS member LLMD, hold great information about pharmaceutical and complementary treatments:


http://tinyurl.com/6lq3pb (through Amazon)

THE LYME DISEASE SOLUTION (2008)

- by Kenneth B. Singleton , MD; James A. Duke. Ph.D. (Foreword)

You can read more about it here and see customer reviews.


=================================


http://tinyurl.com/5vnsjg

Healing Lyme: Natural Healing And Prevention of Lyme Borreliosis And Its Coinfections - by Stephen Harrod Buhner

www.gaianstudies.org/lyme-updates.htm


==================================


http://tinyurl.com/5drx94

Lyme Disease and Modern Chinese Medicine - by Dr. QingCai Zhang, MD & Yale Zhang

you can access his web site through www.hepapro.com or try www.sinomedresearch.org and use "clinic" and then "clinic" for the passwords or call Hepapro.


-
 
Posted by Keebler (Member # 12673) on :
 
-

www.amazon.com

(through the link here and right on to the book's page: http://tinyurl.com/6xse7l )


The Potbelly Syndrome: How Common Germs Cause Obesity, Diabetes, And Heart Disease (Paperback) - 2005


by Russell Farris (Author), Per Marin (Author)

8 customer reviews and you can look inside the book

about $13.00 -


Editorial Reviews


Potbelly syndrome (PBS) is a metabolic disorder that affects about one-third of the adults in industrialized countries.


Its most important symptoms are abdominal obesity, high blood pressure, and type 2 diabetes. Contrary to popular belief,these conditions are caused by chronic infections, not by bad habits. (poster's note: well, unless one DOES have bad habits.)


PBS is initiated by a small, long-term excess of the stress hormone cortisol.


The extra cortisol stimulates our appetite and slows down our metabolism. It makes fat accumulate in places where it isn't wanted or needed. Most of the fat settles around our waists, but some of it settles in our liver and muscles.


Liver and muscle cells aren't supposed to store fat, and the fat prevents them from working correctly.


As a result, we feel tired and hungry much of the time. As our potbellies grow and our PBS gets worse, our blood pressure, cholesterol, insulin, and blood sugar levels rise.


Most of the excess cortisol is produced in response to mild, chronic infections. Some of the germs that cause PBS also produce sores in our arteries. When these sores are large enough, they can block arteries and cause heart attacks.


"The Potbelly Syndrome" explains how to diagnose and treat some of the germs that cause PBS and heart disease.


If you've done everything you were supposed to do and still gained weight, became diabetic, or had a heart attack,or if you are a medical professional who suspects that there are serious gaps in the current understanding of obesity, diabetes, and heart disease, "The Potbelly Syndrome" will provide you with the answers you need to bring about better health.


About the Author

Russell Farris is a retired artificial-intelligence researcher who spent most of his life solving problems for the U.S.

Navy. After suffering a heart attack in 1998, he began to apply his problem-solving skills to the study of heart disease and related illnesses.

Per Marin, M.D., Ph.,is a distinguished scientist, physician, and clinical teacher from Sweden. He has been writing about obesity since 1985, and many of his eighty-two publications deal with the effects of cortisol on weight and health.


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