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Celiac vs wheat allergy
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Nikster57



Joined: 09 Aug 2005
Posts: 66
Location: Houston, TX

PostPosted: Wed Aug 31, 2005 9:25 pm    Post subject: Celiac vs wheat allergy Reply with quote

Sorry guys, I haven't been on in several days. I think I asked Al for a response on this one and don't remember where it was.

My question is: If my allergist says I have a wheat allergy, do I actually have celiac? Done the gastro guy and came back inconclusive. I just was tested for food allergies, again, and they called me and told me that many of the food allergies they tested me for were very very high. They origianally told me back in 2002 I had a wheat allergy but I didin't know what that meant and until several months ago, was fine but got sick a lot and thought it was just an allergy to who knows what.I'm going Friday for the dreaded "needles in the back" test. Been gluten free since June 12. Thanks in advance.
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Nikki from Texas
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Andi
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PostPosted: Wed Aug 31, 2005 10:41 pm    Post subject: Reply with quote

From what I understand, they are separate. But, you could have both.
From what I've read, the symptoms are different - wheat allergy would be more respiratory symtpoms, hives, etc. and gluten intolerance is digestive and/or neurological. I would be interested to know how many times they cross over - what percentage of people have both!
My mom definitely has wheat allergy with hives, itchy throat, etc. right after she eats wheat, but isn't very inclined to be tested for gluten intolerance at this point, even though she does have a very "sensitive" stomach and nerve damage...too bad I can't experiment on my own family...hehe...I mean that in a nice way! My mom finds that she doesn't get a rash or hives when she eats white bread though...
Andi
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Nikster57



Joined: 09 Aug 2005
Posts: 66
Location: Houston, TX

PostPosted: Thu Sep 01, 2005 2:29 pm    Post subject: Reply with quote

I get the hives and the respiratory from allergies. Can't do antihistamine until after they do the test tomorrow. Can't wait to pop that Zyrtec. HEHEHEHE. I'll find out more tomorrow. Thanks,
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Nikki from Texas
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aklap



Joined: 02 Oct 2004
Posts: 7817
Location: WI, USA

PostPosted: Fri Sep 02, 2005 10:29 pm    Post subject: Reply with quote

Hi Nikki,

Here's one of those posts (I think there is another one....but can't find it LOL! I do have a hard time with loosing stuff here)

Many times Wheat Intolerance (Gluten Intolerance) is considered the same as CD.

Wheat Allergy is often used to describe CD. But in reality they are 2 different things.

Here are some sites that do a pretty good job at explaining the difference

http://www.grandtimes.com/Gluten-Free.html (this has a bunch of other interesting stuff in too).

http://www.foodintol.com/wheat.asp

I hope this helps!
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Al

“We cannot all do great things, but we can do small things with great love.” Mother Teresa


Last edited by aklap on Mon Dec 12, 2005 7:02 pm; edited 2 times in total
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Nikster57



Joined: 09 Aug 2005
Posts: 66
Location: Houston, TX

PostPosted: Sat Sep 03, 2005 3:07 pm    Post subject: Reply with quote

Thanks Al. Must be gluten intolerance becausemy allergist says I am no longer allergic to wheat but I am still allergic to buckwheat. Also, what I thought was true; is. I AM allergic to soy and all legumes for that matter. Thanks for the websites. I kept them as favorites. You are my walking encyclopedia for the internet!!!!!!!!
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Nikki from Texas
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aklap



Joined: 02 Oct 2004
Posts: 7817
Location: WI, USA

PostPosted: Thu Apr 13, 2006 4:17 pm    Post subject: Reply with quote

bump
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Al

“We cannot all do great things, but we can do small things with great love.” Mother Teresa
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aklap



Joined: 02 Oct 2004
Posts: 7817
Location: WI, USA

PostPosted: Mon May 29, 2006 4:06 pm    Post subject: Reply with quote

bump
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Al

“We cannot all do great things, but we can do small things with great love.” Mother Teresa
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sarahceliac



Joined: 18 Jun 2006
Posts: 189
Location: MA

PostPosted: Thu Jun 22, 2006 9:14 pm    Post subject: Reply with quote

When I was told that I had celiacs, the Dr. had checked the gidian count (sp.) My count was a little above a normal persons. I had constant bloating, a lot of nautia, and that was the cause to run the test. I wasn't having other signs. So I wonder if I have CD? When I eat gluten it goes quickly through my system, luckily that is the only thing I experinece with bloating. I follow a GF diet and most times am fine. Gluten will sneak in sometimes and I know immiediately. I was told I have a mild case and that celiacs can come about all of a sudden at some time in your life, something triggers it. Or you can be born with it. When i was diognosed I was under a tremendous....... amount of stress and wonder if that set it off. The nuerological symptoms are deffinetly there, I have MS. I am 2nd guessing if I have CD. Any comments??
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Kathie



Joined: 27 Jan 2006
Posts: 676
Location: Florida

PostPosted: Fri Jun 23, 2006 10:43 am    Post subject: Reply with quote

sarahceliac wrote:
When I was told that I had celiacs, the Dr. had checked the gidian count (sp.) My count was a little above a normal persons. I had constant bloating, a lot of nautia, and that was the cause to run the test. I wasn't having other signs. So I wonder if I have CD? When I eat gluten it goes quickly through my system, luckily that is the only thing I experinece with bloating. I follow a GF diet and most times am fine. Gluten will sneak in sometimes and I know immiediately. I was told I have a mild case and that celiacs can come about all of a sudden at some time in your life, something triggers it. Or you can be born with it. When i was diognosed I was under a tremendous....... amount of stress and wonder if that set it off. The nuerological symptoms are deffinetly there, I have MS. I am 2nd guessing if I have CD. Any comments??


Stress is a great trigger for CD, my trigger was pregnancy, however when I am under a lot of stress even the smallest little crumb can set me off. I also read a book a number of years ago in which the author believed there was a connection between undiagnosed CD and MS. It was "Can A Gluten Free Diet Help? How?" by Lloyd Rosenvold, M.D. ISBN 0-87983-538-9

Personally I don't believe there is such a thing as a mild or severe case of CD, people's reactions may differ from mild to severe but in my opinion the difference in villi damage is determined by how much gluten you digest and how long you go before someone figures out you have CD. I think its wrong for doctors to put a "Mild" label on a disease, it mistakenly gives people the impression that because they only have a mild case they can occasionally cheat and it will be ok. When I was originally diagnosed I had villious atrophy, my villi were flat. This year I had another endoscopy and my villi looked perfectly healthy, however I know for a fact that up until 2 weeks before my test I was unknowingly ingesting gluten on a pretty regular basis, atleast 2-3 times a week. Before the original diagnosis 2 weeks would not have been enough time for the villi to heal. I know because it took close to a year before I could tolerate lactose and all my symptoms went away.
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Noatak



Joined: 13 Nov 2005
Posts: 482
Location: Massachusetts

PostPosted: Fri Jun 23, 2006 12:22 pm    Post subject: Reply with quote

From reading posts on this forum it has convinced me that people with CD know so much more about the disease than doctor's do! We live it every day and learn all the nuances of the disease and get to know things a doctor or person without CD would never be able to fathom.

Mine was sent into high action mode by menopause but I had symptoms all my life....hindsight is 20/20 and that couldn't be more true. I had GI problems all my life, off and on, and I am convinced it was the reason I needed an emergency appendectomy when I was 8 years old. It was so inflammed, it nearly burst.

Sarah...right before the big blow-out a year ago, I was experiencing the worst nausea ever. I've never been pregnant but I could imagine it was like a bad case of morning sickness. Plus I was very bloated so your symptoms sound very much like CD. I would not be surprised in the least if CD was connected with MS.....CD can also involve nerve damage so the two are similar. One thing that I found interesting from having my gene testing done was the fact that if a person has 2 markers (one from each parent), the degree of severity from CD can be worse than a person with one marker. Maybe that explains why some get severe villi damage faster than others do or some do not have villi damage showing on an endo. I do agree with you on the fact that CD is CD and whatever the background, get rid of the gluten! Very Happy
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Fidissimus



Joined: 17 Mar 2006
Posts: 1411
Location: Portland, OR.

PostPosted: Sat Jun 24, 2006 11:37 pm    Post subject: Reply with quote

Kathie wrote:
I also read a book a number of years ago in which the author believed there was a connection between undiagnosed CD and MS. It was "Can A Gluten Free Diet Help? How?" by Lloyd Rosenvold, M.D. ISBN 0-87983-538-9


Thanks Kathie! I had no idea about that - I've got a cousin with MS who's been pretty healthy so far, but isn't GF - however very recently she's started to take a turn for the worse in her health. Maybe this will help her? I will send her this info ASAP!
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Jenn

GF BD: Feb. 2001
Free of wheat, barley, rye, oats, rice, dairy, eggs, almonds, pineapple and brewers yeast.
http://graindamaged.blogspot.com/
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aklap



Joined: 02 Oct 2004
Posts: 7817
Location: WI, USA

PostPosted: Sun Jun 25, 2006 12:22 am    Post subject: Reply with quote

CD has been mis-dx'ed as MS due to the fact that brain lesions caused by CD look similar, plus a host of other things that I have not actively looked into.

You can find more info here: http://brain.hastypastry.net/forums/showthread.php?p=26417#post26417

It's definitely something that should be considered. Heck...what is there to lose?
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Al

“We cannot all do great things, but we can do small things with great love.” Mother Teresa
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Fidissimus



Joined: 17 Mar 2006
Posts: 1411
Location: Portland, OR.

PostPosted: Sun Jun 25, 2006 12:54 am    Post subject: Reply with quote

Thanks Al,
I'll send this info to her as well and maybe she'll see some improvement? I hope so - and will try to keep you all posted of her health if the GF diet works.
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Cheers!
Jenn

GF BD: Feb. 2001
Free of wheat, barley, rye, oats, rice, dairy, eggs, almonds, pineapple and brewers yeast.
http://graindamaged.blogspot.com/
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sarahceliac



Joined: 18 Jun 2006
Posts: 189
Location: MA

PostPosted: Sun Jun 25, 2006 7:52 am    Post subject: Reply with quote

So I wonder if MS makes the gidian (sp.) count high too? I only had the blood test for CD and only the MRI for MS. My meds for MS help and I have known about the MS since 99. Celiacs just became known a year ago. My nuerologist said the two are not linked???? I had asked about that. And he is a very... well known Nuerologist. The ones that suffer from these diseases tend to deffinetley know more than the Dr.s sometimes.
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Sarah
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Deb



Joined: 23 Oct 2004
Posts: 166
Location: Long Island, New York

PostPosted: Thu Nov 23, 2006 6:49 am    Post subject: Reply with quote

Just wanted to add to this theory--I am totally gluten free now for over 5 yrs and I do break out in hives if wheat touches my skin.
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