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

First Doctor Visit


Mindy Sue

Recommended Posts

Mindy Sue Newbie

Hello. My 13 year old daughter was diagnosed with Celiac from a blood test 2 weeks ago. We are going to see the pediatric gastro doctor this coming Monday. I am completely new to this and overwhelmed by all the info on the internet. What questions should I ask the doctor and what information should I get? Should she have further tests done? She has started the gluten free diet even though I have read she should wait until she sees the specialist but I was initially told we wouldn't get an appointment for 6 to 8 months. She also is in such pain so we went ahead and started the diet. She has somewhat improved already! Any suggestions are greatly appreciated.

Thanks,

Mindy


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



Celiac.com Sponsor (A8-M):



Skysmom03 Newbie

First of all, blood test alone can't diagnose celiac disease. It could have been an unreliable test. To check for sure, she will have to have an endoscopy done to biopsy her small intestine. DO NOT start the gluten free diet yet. It can make the biopsy inaccurate. Your pediatric gastro will tell you this as well when you go in.

I have two people in my home who have celiac disease. My husband was diagnosed a year and a half ago and my 9 yr old son was diagnosed a month ago. My husband got really sick when they found it. He thought is symptoms were normal.... Until he lost 40 lbs. We checked my son because celiac disease is genetic and sure enough he had it to. My husband has apparently had it for years and my son has had it for about two or three according to the doctor.

It is a life changing event. But nothing to be frightened of ( unless you choose not to follow the diet) . It is all about reading labels. Google is our new best friend! My son Aja's handled it well, he has seen his dad follow the diet for sometime now so he is use to it. We order a lot of things without the bread and we find safe goodies that he can have. He takes a multivitamin everyday. Also beware of Claus, glues, stps, and envelopes as well as soaps and shampoos! If you have any questions feel free to ask. I am no expert but with to Celiacs in the house. I have to be well informed..... I am the minority after all!!! :)

Skysmom03 Newbie

I wouldn't think it would take that long to get an appointment! This can be quite serious after all.

kareng Grand Master

There is no need to worry about stamps and envelopes. That is one of those internet myths that will not die. Most glues are fine, also. A 13yr old should be able to be careful with glue but all Elmers are gluten-free .

StephanieL Enthusiast

First of all, blood test alone can't diagnose celiac disease. It could have been an unreliable test. To check for sure, she will have to have an endoscopy done to biopsy her small intestine.

This isn't exactly true any more. They are looking now at 5 criteria for dx. and a biopsy may not be needed.

That said, I agree with not starting the gluten free diet until you see the GI, it's only a few days just to be sure they don't want to do the endoscopy.

Hang in there!

Celiac Mindwarp Community Regular

StephanieL

Please could you list or link to the 5 diagnostic criteria? My doctors only recognize blood test and biopsy and I need all the help I can get to convince them!

Mindy Sue

Good luck with a diagnosis for your daughter

my3monkees Rookie

The pediatrician diagnosed my daughter without the endoscopy. Technically I think her chart reads "probable Celiac". She improved so drastically when we did a food trial, the doctor was willing to work with that. The ped. GI was 2 hours away and my daughter didn't want to go back to eating the gluten for the challenge. The doctor even told me, what was the point, weather the test was preformed or not, she needed to be gluten free. The test wasn't going to change the outcome. The diet worked stick with it. If at some point in the future, my daughter wants to be tested, she could do the endoscopy then.

I agreed, I wasn't willing to put a child who had been sick and miserable for so long, through more misery, just to get an official test result! JMO


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



Celiac.com Sponsor (A8-M):



StephanieL Enthusiast

StephanieL

Please could you list or link to the 5 diagnostic criteria? My doctors only recognize blood test and biopsy and I need all the help I can get to convince them!

Hi MindySue,

Here is a link to the abstract of the publication (not sure where to find it without paying but I am sure it's available I just did a quick search as the kids are being crazy right now). The last line lists the criteria they are suggesting. Biopsy is listed but if you have the other 4, he (who is THE Celiac Dr. here in the US) says that's good enough!

Open Original Shared Link

Celiac Mindwarp Community Regular

Great, thanks.

GottaSki Mentor

Open Original Shared Link

Great link!

Thanks Stephanie :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • 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
    • DebJ14
×
×
  • 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.