Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Rash Question


hayley3

Recommended Posts

hayley3 Contributor

I have a rash that I've had on and off, for some time.  It itches like crazy, but then hurts too.  Tiny painful red bumps (some have blisters) but they are not in the specific locations I have seen in the descriptions.  If you've had the rash is it in other places besides the knees and buttocks and elbows?  I did have a rash when I initially became sick, that was below my elbows. (I thought I was allergic to the dish liquid I was using) but the doctor said I had scabies.  It lasted 12 years and now I have this rash that I thought was chiggers for years which comes and goes.  It comes back in the same place every time but is also now growing to other places.  I was wondering if anyone has had a rash on any other parts of their body besides those I listed or if the rash had changed location ever?  The last time I had this rash, I had tried some wheatgrass.   This time I am sick but was eating wheat right before I got the cold/sinus infection that has taken me 10 days to recover from.  I'm still recovering actually, but feel like it's finally easing up.

 

I'm fighting to get an appointment at the Dermatology clinic at the VA.   

 

Cheryl


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Tomislav Newbie

Dermatitis Herpetiformis, DH, is a painful skin rash that manifests as a direct result of untreated or undiagnosed celiac disease. It is commonly known as “celiac disease of the skin" .It can also manifest below your elbows, but more often it manifests at males than females. So basically I cannot be 100% sure about what i should tell you except that you should visit a dermatologist ASAP.

hayley3 Contributor

I really didn't want to push for them to do a biopsy, if I was way off base here.  I know most rashes are very similar, which is why dermatologists most of the time have no clue unless they do a biopsy.  I didn't know the rash was mostly in men.  Interesting.

 

Cheryl

Tomislav Newbie

Rashes might be caused by many things , although I wanted to ask you if u got any other symptoms besides rashes that might indicate Celiac disease?

hayley3 Contributor

Rashes might be caused by many things , although I wanted to ask you if u got any other symptoms besides rashes that might indicate Celiac disease?

Just the stuff in my signature and if I don't eat gluten, I don't ever get sick, even with a low white blood count.  I did get an appt with the dermatologist!  Lucky break there, thanks.

 

Cheryl

GF Lover Rising Star

Hi Haley.

 

Have you had Celiac testing? or are you pursuing a DH diagnosis.  Your a prime candidate for Celiac, rash or not.

 

Colleen

hayley3 Contributor

Hi Haley.

 

Have you had Celiac testing? or are you pursuing a DH diagnosis.  Your a prime candidate for Celiac, rash or not.

 

Colleen

Yes Colleen, I've had testing but I was mostly gluten free for many years.  My gene came back positive (1 in 35 chance Dr said) but endoscopy only showed inflammation, other tests were negative.   I'm hoping the rash will come through for me.  I thought the rash was chiggers for a long time.  Hopefully they are prepared to biopsy it tomorrow and will do it right.   I believe there's a lot of lab mistakes/mishaps and that's why we have so many undx'd people who are ill.  I've been in limbo far too long.

 

Cheryl


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



GF Lover Rising Star

Not surprising you test negative...with being mostly gluten free for so long.  Don't be disappointed if the biopsy is negative.  There can be many different rashes to get with Celiac.  It's the whole autoimmune thing.  Have you ever considered a gluten challenge?  Or is diagnosis at this point not that important to you.

 

Colleen

hayley3 Contributor

I tested negative last December.  I've been eating a  little gluten since last October.  But I have gluten free oats in my pantry, so I really keep nothing in my house, but I ate out once a week and I did indulge in some donuts.  Slowly I ate more and more but this was after the testing.

 

A diagnosis is important to me.  I'm thinking the rash has returned because I've been eating gluten and the reason I've just caught a terrible cold which has lasted two weeks and turned into a sinus infection/bronchitis which is something that hasn't happened in 3 years.  I used to be sick constantly.  And now I remember why I stuck to the diet.  

 

And if the rash is back and it's related to Celiac, surely it would be positive?

 

Cheryl

GF Lover Rising Star

When I say related, I mean all kinds of different rashes can show up but it may not be DH, just some kind of rash.  Since your eating gluten again now IS the time to do testing again.  Make sure the Derm knows the proper protocol for biopsying DH (must be taken from clear skin adjacent to an active sore)  If it does comes back negative, get another set of blood tests done, again, since you have been eating gluten.  2 pieces of bread for 6-10 weeks should be sufficient.  So guage if you need to eat gluten a bit longer or are set to be tested.  

 

I hope all that made sense, I'm still on my first cup of coffee  :D

 

Colleen

hayley3 Contributor

When I say related, I mean all kinds of different rashes can show up but it may not be DH, just some kind of rash.  Since your eating gluten again now IS the time to do testing again.  Make sure the Derm knows the proper protocol for biopsying DH (must be taken from clear skin adjacent to an active sore)  If it does comes back negative, get another set of blood tests done, again, since you have been eating gluten.  2 pieces of bread for 6-10 weeks should be sufficient.  So guage if you need to eat gluten a bit longer or are set to be tested.  

 

I hope all that made sense, I'm still on my first cup of coffee  :D

 

Colleen

Thanks Colleen, I am going to make sure they are testing for DH.  Honestly just looking at the rash and comparing it to google images, I'd say it's positively DH.  Some has blisters, the rash comes back at the same place but then this time I have a new area, the bumps have that dark redness I am seeing in the pictures, and it's on both sides of my body.  The only thing I don't know is, my rash appeared but then the next day I'll see some new places, which is like poison ivy but I definitely don't have poison ivy, esp on my back. (I think...lol)

 

This is my last chance for a diagnosis.  I'm pretty sure I had the rash in 1980 and they missed it then.  And then later they said the rash on my arms is Discoid Lupus, before that they said it was something else.  Having it near my elbows in the beginning and the doctors calling it scabies is what makes me think it was DH then.   :(  So I'm worried they will miss it again.

 

Cheryl

hayley3 Contributor

Well there went my last chance.

They said DH is only on the knees and buttocks.  It can't be on the torso or anywhere else.  She said it looked herpetic on my leg but like bug bites on my torso.  Oh and she was also wanting to give me medicine for shingles but that's rash she thought it was bug bites.  I don't think shingles itches, it's more painful like herpes.  So that's the end for me....She refused to do a DH biopsy.

:(

GF Lover Rising Star

Ok.  Couple of things.  DH can be pretty much anywhere!  Singles can be extremely painful and itchy.  Your Doctor doesn't seem to be very well informed.  I guess you could always continue to eat gluten for the above mentioned lenght of time and get blood tested again.  

 

Sorry for these difficulties you are having.  You can still just eliminate gluten for life and feel better.  

 

Colleen

appletree729 Apprentice

It's only the end if you choose to make it the end :)

 

Go see another dermatologist and request (demand) a biopsy.  Bring in some literature with you that describes DH and the similarities between what you have and DH, the proper way to do the biopsy, etc. and use it if they question the need to biopsy.

 

Be respectful and polite and have a line on hand to say if you start feeling frustrated..  like "listen, I very much respect your opinion and knowledge on these things, but I've been suffering from this condition for many years.  Please, I'd like to respectfully request that you perform a biopsy."  And then stop talking.  It's like sales - the less you say the better.  The minute you "request" the biopsy, just shut up ;) Put the ball in their court.  

 

In my experience, there are not many doctors that will flat out refuse a direct (and reasonable) request like this unless you keep talking and saying things like "I'm use not sure what it is…"  "do you think this looks like DH?" etc because that gives them something else to answer and to refuse to do it in an indirect way "oh..  this is not characteristic of DH, so there is no need for a biopsy"

 

If you say "I'd like to respectfully request that you perform the biopsy now".  They either have to go ahead and (reluctantly?) do it, or they have to say a direct "no" to you, which is uncomfortable. :)

hayley3 Contributor

Thanks Colleen.  At this point I'm not sure what I'm gonna do.  I'm still recovering from this cold.  I'm on the 3rd week now. 

 

I've had fever blisters which is the same virus as shingles.  It does not itch until it starts to heal.  Have you had shingles and found it itchy?  What I have is excruciatingly itchy.  But if I rub those spots, it's painful too. 

 

@appletree...I think the problem was she shut me off the minute I said I would like her to do a biopsy for DH.  I even asked what does it hurt to do a 2nd biopsy, you are doing one already, why not do one to test for DH?  And she said No, and then gave me two different excuses.  First she said a DH biopsy was a special test and secondly they weren't allowed to do a DH biopsy until they did a regular one first.  I did tell them my allergist thought I had celiac disease in hopes they would take his word over mine but nope.  I don't have insurance to go to another Dermatologist.  I only have health insurance as a veteran and I have to go the Louisville, Ky VA Hospital.  Which is really the worst health insurance to have but it's health insurance.

 

That doctor was determined it was shingles; even trying to give me medicine.  I'll eat my hat if the biopsy comes back as shingles.

I've had a few biopsies over the years and half the time they come back with the wrong diagnosis though and when the biopsy is later redone it comes back with a completely different corrected diagnosis. 

 

Cheryl

GF Lover Rising Star

Shingles can be itchy, not itchy, painful, not painful...If can manifest itself differently.  For the cold sores, look at your toothpaste, mouth wash etc. for Sodium Laural Sulfate.  Ditch it if it does and purchase one without.  Switching has helped many with cold sores including my self.  

 

Maybe it will come back as Shingles.  Then you'll have your answer.  If it isn't Shingles, you can mark it off your list and continue from there.

 

Colleen

squirmingitch Veteran

Cheryl,

I am so sorry this is happening to you & you have been frustrated for so long. I'm afraid I'm about to give you worse news --- News that you don't want to hear being that you want an official dx so badly. And I'm sorry I'm so late seeing your post. I usually prowl the dh forum so didn't catch this since it wasn't posted there. 

 

Geez, where to start? The VA, I'll start there. Personally I think the VA health system is crap. Why do I think this? My husband was actively being treated in the VA health system for over 20 years. They don't have a clue. IF you manage to get the extremely rare GOOD doc at a VA, they are hindered by so many stupid protocols that it's insane. The protocols almost seem designed to prevent any health care going on. I understand you don't have any other health insurance coverage so are forced to use the VA (been there, done that too). If you ever manage to get a correct dx using the VA then I'll eat my hat.

 

DH can & does present any where on your body. This elbows, buttocks, knees thing is so antiquated & short sighted!!! There are plenty of respected medical references out there that clearly state that dh can present anywhere. It seems the medical community at large reads no farther than elbows, knees, buttocks & then they slam the mind shut; they fail to read the part that says those are the most common locations. The most common locations does NOT mean the ONLY locations. Is it any wonder that this myth keeps being promulgated? If 90% of the people biopsied for dh are the ones presenting with it on their elbows or buttocks or knees, then the figures will only reflect those presenting with it on their elbows or buttocks or knees; the rest are left out of the equation. In other words, the figures are skewed & do not reflect an accurate sample of the population because the majority of derms refuse to do the biopsy of the patient presents with it on other portions of their body. 

 

A dh biopsy MUST be done correctly & all too often it is not. Generally, the derm does not even know that it is to be taken from clear skin adjacent to an active lesion. For accurate results on a dh biopsy, the patient MUST be eating a gluten containing diet the same as if they were going for the celiac blood panel or the endoscopic biopsy. If the patient has been gluten free then they will have to do a gluten challenge or the biopsy will turn up negative.

60% of celiacs who have dh test negative on the celiac blood work. They also tend to test negative on the endoscopic biopsy. A dx of dh IS a dx of celiac disease & no other tests need be performed.

 

DH can & does come & go at will whether one is eating a gluten-free diet or not. It may take 2 years or more on a strict gluten-free diet before one is free of the rash b/c the antibodies are deposited under our skin & until they go away, we suffer. It can take longer than 2 years or it can take less -- we are all individuals & it does depend on how long we went undiagnosed.

 

DH does not ALWAYS present as blisters. Go to the dh forum & read the sticky posted at the beginning.

 

Most celiacs with dh do not exhibit the extent or extremes of the GI symptoms that our fellow celiacs w/o dh do. We tend to have milder GI symptoms or none at all. The damage to our villi is patchier. 

 

Everything I've read says it's more common in men than women but that does not mean women don't have it. I can tell you there are FAR more females who have dh that post or have posted on this site than males. Perhaps this is just b/c women tend to post on public forums more than men.

squirmingitch Veteran

I forgot to answer one of your questions.

Can dh present in places on your body that it has not presented before? ABSOLUTELY!

 

DH can be aggravated by NSAID's. tylenol seems to be the least aggravating but Advil, Nuprin & all the rest are to be avoided.

 

DH is sensitive to iodine intake & it can cause or worsen a flare. A low iodine diet can help to keep this from happening or ramp down a flare. See thyca.org for a low iodine diet (minus the gluten of course).

hayley3 Contributor

Shingles can be itchy, not itchy, painful, not painful...If can manifest itself differently.  For the cold sores, look at your toothpaste, mouth wash etc. for Sodium Laural Sulfate.  Ditch it if it does and purchase one without.  Switching has helped many with cold sores including my self.  

 

Maybe it will come back as Shingles.  Then you'll have your answer.  If it isn't Shingles, you can mark it off your list and continue from there.

 

Colleen

 

Thanks Colleen....Yes but it would've been much simpler for them to just do a biopsy....while I was there...ugghhhh  And the reason I had a cold sore (it was beneath my nose) was because I had been blowing my nose for two weeks due to the sinus infection.

hayley3 Contributor

Cheryl,

I am so sorry this is happening to you & you have been frustrated for so long. I'm afraid I'm about to give you worse news --- News that you don't want to hear being that you want an official dx so badly. And I'm sorry I'm so late seeing your post. I usually prowl the dh forum so didn't catch this since it wasn't posted there. 

 

Geez, where to start? The VA, I'll start there. Personally I think the VA health system is crap. Why do I think this? My husband was actively being treated in the VA health system for over 20 years. They don't have a clue. IF you manage to get the extremely rare GOOD doc at a VA, they are hindered by so many stupid protocols that it's insane. The protocols almost seem designed to prevent any health care going on. I understand you don't have any other health insurance coverage so are forced to use the VA (been there, done that too). If you ever manage to get a correct dx using the VA then I'll eat my hat.

 

DH can & does present any where on your body. This elbows, buttocks, knees thing is so antiquated & short sighted!!! There are plenty of respected medical references out there that clearly state that dh can present anywhere. It seems the medical community at large reads no farther than elbows, knees, buttocks & then they slam the mind shut; they fail to read the part that says those are the most common locations. The most common locations does NOT mean the ONLY locations. Is it any wonder that this myth keeps being promulgated? If 90% of the people biopsied for dh are the ones presenting with it on their elbows or buttocks or knees, then the figures will only reflect those presenting with it on their elbows or buttocks or knees; the rest are left out of the equation. In other words, the figures are skewed & do not reflect an accurate sample of the population because the majority of derms refuse to do the biopsy of the patient presents with it on other portions of their body. 

 

A dh biopsy MUST be done correctly & all too often it is not. Generally, the derm does not even know that it is to be taken from clear skin adjacent to an active lesion. For accurate results on a dh biopsy, the patient MUST be eating a gluten containing diet the same as if they were going for the celiac blood panel or the endoscopic biopsy. If the patient has been gluten free then they will have to do a gluten challenge or the biopsy will turn up negative.

60% of celiacs who have dh test negative on the celiac blood work. They also tend to test negative on the endoscopic biopsy. A dx of dh IS a dx of celiac disease & no other tests need be performed.

 

DH can & does come & go at will whether one is eating a gluten-free diet or not. It may take 2 years or more on a strict gluten-free diet before one is free of the rash b/c the antibodies are deposited under our skin & until they go away, we suffer. It can take longer than 2 years or it can take less -- we are all individuals & it does depend on how long we went undiagnosed.

 

DH does not ALWAYS present as blisters. Go to the dh forum & read the sticky posted at the beginning.

 

Most celiacs with dh do not exhibit the extent or extremes of the GI symptoms that our fellow celiacs w/o dh do. We tend to have milder GI symptoms or none at all. The damage to our villi is patchier. 

 

Everything I've read says it's more common in men than women but that does not mean women don't have it. I can tell you there are FAR more females who have dh that post or have posted on this site than males. Perhaps this is just b/c women tend to post on public forums more than men.

Yes I know squirmingitch.  I think the VA used to be much better than it is now.   Even the doctors that come in from the University of Louisville, they just seem to have no desire to help figure out what's going on.  They really don't care I think. If I was a doctor, the unusual cases would intrigue me more.

 

One thing I've read about DH is, that it is symmetrical (both sides of the body), so I'm wondering does it mean that if it's on one shoulder it HAS to be on the other shoulder.  For me, it was on the backside of both legs, both sides of my torso, although not in identical proportions, but was also on my right front thigh, arm and breast.  I don't think shingles even goes that far.  And because it was prominent on my left side of the torso, she declared it shingles, when she never bothered to look at the right side.

 

I didn't know that...that even though you had the rash, you must be eating gluten for it to show up as positive.  The minute I got sick, I stopped eating anything gluten or anything that is SIBO aggravating.  Because I have SIBO, I've never been able to tell if gluten bothered me because I get GERD, constipation, sick, etc.,  after eating bread but don't know if it's the SIBO or if it could be the gluten.  My allergist (who is outside the VA) has pushed to have me genetic tested and pushed to get me the celiac tests and endoscopy because he felt I had celiac.  I had that rash on my elbows in 1983 after they removed my gallbladder, which they said was scabies.  So after doing some reading I thought, HEY!  This could be the celiac rash after all.  Because gluten-free now seems to be a fad to those who aren't sick, most doctors think we actually want to have celiac when that is not true. Who in their right mind would want to go gluten free without good reason! 

 

Cheryl

squirmingitch Veteran

You're right that a hallmark of dh is the symmetry and you have the symmetry but it can still appear on one side & not the other on occasion so don't think that b/c it's not ALWAYS symmetrical that means it isn't dh. Also, while it IS uncanny & mind blowing how it can echo on each side, the echo isn't ALWAYS identical in proportion. However, boy oh boy, when it is, it's simply astounding. Also, I found, sometimes it will not appear on the other side until a few days later so there is that too.

hayley3 Contributor

I would've died if mine had been identical on both sides...yikes!

 

For years I thought I had poison ivy too, and just found out those are not poison ivy plants but boxelder saplings around my yard.   And when the rash would show up somewhere else the next day and the day after, I thought I was somehow spreading the poison ivy.  I did discover that very hot tap water was the only way to get any relief from the maddening itch but it works although drastic.

 

Cheryl

squirmingitch Veteran

When I had my first "all over" outbreak, I got these particular groupings on my lower abdomen directly over where each ovary lies. These were so identical in shape & size that it looked as if I was a human inkblot & had been folded in half to make the same markings on each side. Or like I had matching tattoos. it wigged me out something awful! This was before I knew it was dh. With everything else that was going on with my body (all celiac related unbeknownst to me at the time) I was sure I was riddled with cancer. When those showed up it was almost a relief ~~~ I thought my ovaries were rotting to my outer skin & I remember thinking, "at least I now know where the cancer started". Remember, I was also  heavily affected by celiac induced brain fog. :rolleyes:

hayley3 Contributor

I'm sure it was a relief when you figured out it wasn't cancer. 

That's kinda neat yours was an identical, mirrored image, did a doctor get to see that?  Mine sorta looked like braille dots on one side of my torso and poison ivy every where else.  I always have to be different so the docs have no clue.  lol

 

Cheryl

squirmingitch Veteran

No, the docs didn't get to see that, only the discolored skin it left behind which now, by this time, has disappeared.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.