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Chronic Vertigo, Inflammation And Fatigue

vertigo inflammation

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6 replies to this topic

#1 houseofdavid

 
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Posted 07 July 2014 - 07:47 PM

Hi all,

 

I am new to this forum and decided to post my current situation with two hopes: that others may have some acquired wisdom they can share, and to also help anyone else out there who may be struggling.

 

I have had chronic vertigo, inability to concentrate (foggy headedness), inflammation in the glands and inner ear, and sore throat for 17 months now. The symptoms ebb and flow, with some days being more tolerable and the flare-ups making me bedridden.

 

The symptoms began during the flu season and began with a flu-like illness that developed into the syndrome. I saw two general practitioners who were puzzled and sent me to an ENT.  The ENT diagnosed the vertigo as the type that occurs when the crystals in the inner ear get shaken up and said he 'didn't care' about the chronic sore throat or swollen glands. He sent me to a physical therapist who disagreed with his diagnosis and said the vertigo was likely due to neuritis, or inflammation of the nerve in the inner ear, which is thought to be caused by a viral infection. This is much more likely, but doesn't explain why I cant shake it, and there is no accepted cure for neuritis.

 

I have been gluten free for several years. (Prior to that, I was a vegetarian and ate massive amounts of wheat gluten daily and so developed Candidiasis (thrush), another saga that involved skeptical or hostile doctors and the necessity to do research and self-diagnosis.)

 

In the last two weeks I've also developed joint pain in the right hand and my vision is sometimes blurry or 'off'.

 

The evidence seems to point towards some kind of autoimmune disorder, such as lupus, rheumatoid arthritis or thyroiditis.

 

I'm now looking into lectins in food and their apparent connection to immune suppression/disorders in some people, but the research is scant.  I'm going to eliminate high-lectin foods (grains, legumes, dairy and nightshades) for a week to see if this impacts the symptoms.

 

Has anyone ever experienced anything similar, or has any substantive information about the lectin connection?

 

Thanks so much and so nice to see this forum!

 

megan


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#2 Pegleg84

 
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Posted 09 July 2014 - 07:55 AM

Oh dear. Vertigo is not an easy thing to deal with. Especially that constant.

I was pretty sure something was up with my inner ear a couple years ago, as my mother also has occassional vertigo. After a battery of tests and the ENT telling me nothing was wrong and maybe see a neurologist... I looked at my diet.

For inner ear problems, they recommend cutting back on salt and dairy. Low sodium (not no sodium) made a difference (I still get a bit dizzy if I have too much salt). Cutting out dairy, particularly casein, made an even bigger difference.

Then came soy. Oh soy. Cutting soy from my diet has made a massive difference in my health. if I get into it, I get brain fog, dizziness/unsteadiness, joint pain, mood swings, etc etc.

 

Now, it sounds like your vertigo is pretty serious, but I would recommend cutting out soy and dairy for a while, completely (including soy lectin). Cutting nightshades might not be a bad idea as well. Try a month. See if it makes a difference, then add them back one at a time (for nightshades, this means each individual veggie at a time) and see if you react.

It might not completely solve your problem, but it might help, particularly with the brain fog, blurry vision and joint pain.

 

Hopefully others will have better advice, but at the point changing your diet is probably the best and safest thing to try.
(also, make sure no gluten is sneaking into your diet)

 

Welcome to the forum, and good luck.


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~ Be a light unto yourself. ~ - The Buddha

- Gluten-free since March 2009 (not officially diagnosed, but most likely Celiac). Symptoms have greatly improved or disappeared since.
- Soy intolerant. Dairy free (likely casein intolerant). Problems with eggs, quinoa, brown rice

- mild gastritis seen on endoscopy Oct 2012. Not sure if healed or not.
- Family members with Celiac: Mother, sister, aunt on mother's side, aunt and uncle on father's side, more being diagnosed every year.


#3 houseofdavid

 
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Posted 09 July 2014 - 10:04 AM

Thanks so much for your response.

 

I had arrived at a very similar conclusion about my diet. I am a blood type O and began following the blood type diet several years ago with huge improvements in my health. But when I stopped and really considered my diet over the last few years, I realized I haven't been keeping to the protocol enough. For example, corn and potato products are hazardous for type O's because they agglutinate, especially in the joints and can cause joint pain. But all of those pesky gluten free products out there are based on corn and potato flours. I had also refused to give up my coffee ( I live in the pacific northwest!) and my red wine, both of which are not good for type O's.

 

I've stopped the coffee, the wine, and the processed gluten free products and am back to basics and strict compliance with the type O diet and I feel better already. (This would also mean I'm not eating any more goat cheese products, half and half in my coffee, or the sodium in the processed foods, so there is consistency with what you advised.)

 

I should say that I do understand that the blood type diet is considered controversial and I am not using this forum to advocate or debate it. I can only say that even my partial compliance with it brought me benefits, and full compliance with it has already brought more.

 

Thanks so much, and all the best,

 

megan


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#4 skullgrl

 
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Posted 09 July 2014 - 10:27 AM

Have you considered the possibility of Gluten Ataxia? See if any of the other symptoms of it sounds like you. I was gluten-free and I still developed G.A. due to trace amounts of gluten.

 

Hope you figure it out and feel better!

 

Edit: Just thought to mention I have swollen lymph nodes too.

Edit Edit: Don't forget that Celiac disease is an auto-immune disease, so if they think it could be auto-immune and you come back negative on the things you mentioned it could be that you are a Celiac.


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Diagnosed with Celiac Disease May 2013.

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#5 SMRI

 
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Posted 20 July 2014 - 02:41 AM

Do you have ringing in your ears or have you noticed any hearing loss--maybe feel like people are mumbling a lot?


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#6 skullgrl

 
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Posted 20 July 2014 - 08:06 AM

Yes, although its not my biggest complaint. I also have an issue where if I'm doing something else and someone starts talking to me and I don't really hear them, I won't hear them at all. Actually, thinking about it now I do have problems with it sounding like people are mumbling a lot! 

 

Your vision problems, I have Visual Snow. Is it anything like that?

 

I suggest you buy Gluten Freedom, by Dr. Alessio Fasano. Apart from it being an amazing book otherwise, it has a helpful section on the neurological issues/nonresponsive Celiac disease. His "Fasano Diet" has really helped me, although I did start it before the book came out based on basic information on here. Your issues with potato and corn could simply be an issue with all/most premade gluten-free food. I know I can only tolerate a couple of certified gluten-free (10ppm, by GFCO) things in a day and even then its things like peanut butter or spices.


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Diagnosed with Celiac Disease May 2013.

Gluten free ever since.


#7 SMRI

 
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Posted 20 July 2014 - 12:29 PM

Get an an appointment with an ENT that deals with Meniere's disease http://www.mayoclini...on/con-20028251 . Your symptoms are very similar and hearing loss and ringing in the ears are an unfortunate side effect of this.


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