strong vinegar smell coming out of body

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rosesinjanuary
Veteran Member


Date Joined Oct 2007
Total Posts : 748
   Posted 5/11/2010 5:23 PM (GMT -7)   
i previously asked the question about rancid vinegar body odor.
turns out it can be candidia overgrowth like wine turns to vinegar when yeast dies it gives off vinegar smell. maybe this is good no body wants yeast, let it die.  it wasn't olfactory hallucination i had 2 people sniff test my clothes,  i know gross but necessary. out of curiosity do u think any lyme docs ever get on this board? the reason mi typing is missing caps is i am feeding face with chips cant hit cap button.

Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4151
   Posted 5/11/2010 11:11 PM (GMT -7)   
Doubtful Lyme docs have time to get on this board...

Anyway, I get ammonia fumes coming from my body from time to time, especially if I put vegetable oil on my skin, or certain essential oils on my skin (particularly peppermint or other mint family oils, but many others also do this to me). I'm convinced it is from Lyme...I know Lyme gives off ammonia.

Take care,
-Razzle
Chronic Lyme Disease, Chronic Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, chronic Lymphopenia, etc.; G-Tube; Currently weaning off TPN.
Meds:  Pulmicort, IV Doxycycline, Heparin (to flush PICC line), Claritin, Singulair, Domperidone, Colloidal Silver (topically & nasally), probiotics, Liver support herbs, Ailanthus, digestive enzymes, homeopathy.


Kodak
Regular Member


Date Joined May 2010
Total Posts : 74
   Posted 5/12/2010 12:43 PM (GMT -7)   
I have a silimar odor after I pee. It smells like I've been eating asparagus but I havent.
I thought it was from the herbs I've been using. I also put herb oil on the bottoms of my feet.
If I am this saturated with the herbs I cant see how the spiroketes can live in it.

Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4151
   Posted 5/12/2010 3:43 PM (GMT -7)   
Unless they've adapted to it or are hiding in protective biofilms...
-Razzle
Chronic Lyme Disease, Chronic Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, chronic Lymphopenia, etc.; G-Tube; Currently weaning off TPN.
Meds:  Pulmicort, IV Doxycycline, Heparin (to flush PICC line), Claritin, Singulair, Domperidone, Colloidal Silver (topically & nasally), probiotics, Liver support herbs, Ailanthus, digestive enzymes, homeopathy.


Deejavu
Veteran Member


Date Joined Aug 2005
Total Posts : 3847
   Posted 5/12/2010 5:29 PM (GMT -7)   
Hi Kodak,
 
I used to take a product called Neuro-Antitox which rid my body of ammonia.    If you or anyone else is interested in this product, let me know and I will post where to buy it.
 
Razzle, yes, lyme bacteria most definitely produces an overload of ammonia.
 
Hope this helps,
Denise
It's all about the Immune System mixed with a large dose of Positive Thinking and Detoxing Daily!
 
This song is about my years with chronic lyme since 1995 and being in remission for over 4 years:  http://www.youtube.com/watch?v=ds81S61UvPA
 


rosesinjanuary
Veteran Member


Date Joined Oct 2007
Total Posts : 748
   Posted 5/12/2010 6:14 PM (GMT -7)   
hi guys
it takes a lot to surprise me but honestly the stuff coming out of me is strong I am going to go take another bath, and its been a very bad head day, the back of mi head is just unbearable? I took like 5 tylenol hubby rubbed it I think i'll use the last of mi davidot if i can find it. when I quit lyme doc 3 or so years ago had to order darvicot off line and i am finally using the last, as soon as i can move i will go to a family dr and see if he can help does anyone know if it costs money to have lyme records from lyme dr sent to a regular doctor? thanks
lisa

Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4151
   Posted 5/12/2010 11:38 PM (GMT -7)   
Rosesinjanuary,

It doesn't usually cost anything if one doctor faxes records directly to another doctor, as long as you sign all the required release forms.

I hope your pain goes away quickly.

Good luck,
-Razzle
Chronic Lyme Disease, Chronic Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, chronic Lymphopenia, etc.; G-Tube; Currently weaning off TPN.
Meds:  Pulmicort, IV Doxycycline, Heparin (to flush PICC line), Claritin, Singulair, Domperidone, Colloidal Silver (topically & nasally), probiotics, Liver support herbs, Ailanthus, digestive enzymes, homeopathy.


rosesinjanuary
Veteran Member


Date Joined Oct 2007
Total Posts : 748
   Posted 5/13/2010 11:35 AM (GMT -7)   
Thanks Razzle
the quanity of the paperwork would be so huge I did not know how they'd handle that part/ thanks for being so nice. Mi head is fine but I soaked myself and the bed AGAIN so tired and we live in a town that has one grocery store I can get food 2times as cheap at walmart which is a 30 minute drive, our college boy is home and wow can he eat so lets see need food no energy body filthy bed needs changing again. I am going to buy sheets this is ridiculous well now that I have procrastinated and complained i'll let u go : )

Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4151
   Posted 5/13/2010 3:35 PM (GMT -7)   
It is best to ask about fees, if there are a lot of pages to send to the other doctor.

Take care,
-Razzle
Chronic Lyme Disease, Chronic Bartonella (clinical dx only), Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut issues (dysmotility, non-specific inflammation), UCTD ("Secondary Lupus-Like Syndrome"), Osteoporosis, chronic Lymphopenia, etc.; G-Tube; Currently weaning off TPN.
Meds:  Pulmicort, IV Doxycycline, Heparin (to flush PICC line), Claritin, Singulair, Domperidone, Colloidal Silver (topically & nasally), probiotics, Liver support herbs, Ailanthus, digestive enzymes, homeopathy.


rosesinjanuary
Veteran Member


Date Joined Oct 2007
Total Posts : 748
   Posted 5/13/2010 7:46 PM (GMT -7)   
thanks I will
I always say I am going to go but don't I am afraid of drs i mean I love some of them like mi gynecologist and mi old lyme dr. but I just get depressed making the appt. Im better now, nobody but anpther lymie would understand how it can come and go. : ) my girlfriends sisters co-worker got bit by a tick and 2 days later was puking ( my girlfriend just called me) that seems fast I mean it seems like it takes longer to get sick after bite but they put him immmediately on antibiotic, so things have improved snce a few years ago.

GirlInKS
New Member


Date Joined Dec 2013
Total Posts : 2
   Posted 12/4/2013 1:23 AM (GMT -7)   
If you smell like vinegar, you absolutely need to get the levels of chlorine checked in your blood. This condition is called acidosis or being acidotic. The vinegar smell coming out of your skin is prochloric acid. So find a doctor that can figure out why your body is trying to get rid of the chlorine in this way. If are overweight, have weird allergies and joint pain, you may be a prime candidate for acidosis. Your doctor will need to figure why your body is not getting rid of the chlorine the normal way... hope this helps. I don't have Lyme, but I was acidotic and got put on meds and I no longer smell like vinegar. The whole world smells totally different too because I was only smelling the vinegar in the pores on my nose. Crazy. Good luck. Get help now!

Deejavu
Veteran Member


Date Joined Aug 2005
Total Posts : 3847
   Posted 12/5/2013 6:33 AM (GMT -7)   
Welcome GirlinKS!
 
Are you suffering from lyme?  If so, you have come to the right place.  As far as smells are concerned, from all my research and personal experience, the main culprit is ammonia.  When lyme bacteria die off they leave many toxins, one of them being ammonia. 
 
Below are some good articles written by Dr. Jernigan:
 
Lyme Toxins: The Primary Cause of Your Symptoms:
 
 
And the blog below talks about the alkaline brain, ammonia and diet:
 
High protein foods such as grains and meat contain an amino-acid (the breakdown unit of protein) called L-arginine. L-arginine in foods and as a nutritional supplement should not be taken in cases of hyperammonemia. Research reveals that ammonia (NH3) + arginine + manganese = increased nitric oxide (NO) up to 53% in astrocytes (brain cells), leading to increased brain swelling. “Manganese in excess is neurotoxic and causes a CNS disorder that resembles Parkinson's disease (manganism). Manganese accumulates excessively in astrocytes, which renders these cells more vulnerable to its toxicity.”

When localized brain swelling increases due to ammonia, symptoms, which may be mistakenly called a Herxheimer reaction, increase dramatically as the brain energy metabolism becomes disrupted. The primary symptoms of profound fatigue and increased pain-sensitivity can escalate to critical.
 
 
Denise
Totally healed for over 7 years ~ used Dr. Jernigan's protocol from his book "Beating Lyme Disease"

Our bodies are wise as they can heal themselves, all one has to do is nourish them and detox daily. I come back to help others for others helped me when I was sick. Pay it forward! :-)

http://javuviews.wordpress.com/2013/04/24/how-i-became-better-from-chronic-lyme/
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