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» LymeNet Flash » Questions and Discussion » Medical Questions » Has anyone else been diagnosed hypoglycemic after you found out you had lyme ?

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Author Topic: Has anyone else been diagnosed hypoglycemic after you found out you had lyme ?
lymesc?
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I never had this till I got sick .

My dr. suggested a glucose test (3 hours in the drs office !)

I thought i was going to die!!

My blood sugar level peaked at 95 and then dropped fast to 43 .

I thought the nurse was going to run me over bringing me a soda to make me drink it .

But it seems to be reactive hypo I cant hardly work out or anything ( not that i feel like doing that now anyway) without it taking a nose dive .

If any one has had this problem please let me know .... and let me know if it improved during your treatment for lyme .

Thanks !!!!

Posts: 36 | From south carolina | Registered: Mar 2009  |  IP: Logged | Report this post to a Moderator
venus
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I wasn't diagnosed with it, but i was having crazy fluctuations before I was diagnosed with lyme. My body was not regulating at all. I lost considerable weight. Now I know it was from the lyme. It has gotten better.

Kathy

--------------------
Severe neurological problems. Probably sick for years. Became chronically sick in Aug 2007. Undiagnosed for another 15 months. Started treatment for lyme and bart Sept. 2008. Improving, but very slowly.

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Keebler
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-

Lyme plays havoc with the entire endocrine system. For more about that, authors below get into explaining that and what you can do about it.


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


This book is specific to lyme and other chronic stealth infections.

The author discusses the endocrine connection and effects of STRESS on a person with such infections.

You can read customer reviews and look inside the book at this link to its page at Amazon.

http://tinyurl.com/6xse7l


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


by Russell Farris and Per Marin, MD, PhD


==========


Be sure to scour this for all the self-care, diet and nutritional supplement advice:


http://www.ilads.org/lyme_disease/B_guidelines_12_17_08.pdf

Dr. Burrascano'sTreatment Guidelines (2008)


==========


This book, by an ILADS member LLMD, holds great information about treatments options and support measures:


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.

Web site: www.lymedoctor.com


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


http://tinyurl.com/3fd9mz - - 20 pages


THE REQUIREMENTS OF PROTEIN & AMINO ACID DURING ACUTE & CHRONIC INFECTION . . .


Anura V. Kurpad - Institute of Population Health & Clinical Research, Bangalore, India


129. Indian J Med Res 124, August 2006, pp 129-148. Review Article.


Excerpt: " . . . In general, the amount of EXTRA protein that would appear to be needed is of the order of 20-25 per cent of the recommended intake, for most infections. . . ."


- Full article at link (or google the title if it does not go through).


-

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Leelee
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lymessc, I have hypoglycemia, too. It is an awful feeling.

I have had it for years and years although, like a lot of things, many doctors dismissed my complaints.

Finally, a friend suggested I see a nutritionist. I brought her my blood work. She took one look and said I was hypoglycemic. My fasting glucose level was 49.

She gave me an eating plan and I have followed it diligently for several years. It helps a lot, but even so, I crash for no known reason.

I had my first LLMD visit last week. He made a clinical diagnosis of Lyme and Bartonella. We are awaiting my test results from Igenex and Fry.

He said hypoglycemia can be a symptom of Lyme. That makes sense to me. I guess the bacteria eat up all my food stores.

--------------------
The ultimate measure of a man is not where he stands in moments of comfort and convenience, but where he stands at times of challenge and controversy. Martin Luther King,Jr

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Geneal
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I have it now too. I always had issues with sugar though.

When I was initially diagnosed my blood sugar was high.

Of course I felt like my sugar was low and kept putting sugar in.

Diflucan and florinef can cause low blood sugar too.

When my stomach growls, if I don't eat I feel I am going to keel over.

Small frequent meals help a lot.

Hugs,

Geneal

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kreynolds
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Yes I was diagnosed Hypoglycemic after the diagnosis of LD

--------------------
Diagnosed CDC + 6/2007

Quest: + IGG Bands 18,23,39,41,58,66 and 93.

Quest: + IGM Bands
23,39

Quest: + Bartonella (B.Henselea & B. Quintana),+ Babesia, and + Mycoplasma and Lyme-Induced Addisons Disease

+ Biofilm blood test 12/2010

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lpkayak
Honored Contributor (10K+ posts)
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i was dx before i knew i had lyme...but i might have had it then.

with tx and diet changes it is so under control i'm not sure if ii have it anymore

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

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electrolite
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Yes, I was also diagnosed with hypoglycemia after being diagnosed with Lyme.

I don't know what all it takes to be diagnosed, but I had a glucose level of 60 (non-fasting), so my doctor said I was probably hypoglycemic.

Other times I had a glucose level of 80 or 85 when fasting. Any thoughts?

--------------------
I was diagnosed with Lyme Disease in August 2007, but I now feel it was a misdiagnosis. I was finally properly diagnosed with Chemical Sensitivity in February 2011. My life has changed drastically since then.

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tdtid
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I was actually diagnosed with it before I was diagnosed with Lyme Disease but for five years of being undiagnosed, I was testing positive for all sorts of random things but being told, "something else is still going on".

So whether the hypoglycemia was due to lyme or would have happened anyway, it's hard to say, but yes, I do have both and wonder about the connection.

It's no fun and yes, that 3 hour fasting test where you have to drink the sweet stuff had me shaking and tremoring before the test was even completed. Ugh.

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

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