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 Time Visit


meg1970

Recommended Posts

meg1970 Newbie

Hi,

I'm new here, but I've been cruising the forums just taking in what I can. My name is Megan, and I have a daughter that is almost 17 years old, who has been miserable a lot of those 17 years, with pains that just can't be explained. She has also suffered from allergies her entire life, and has never had a clear day. We recently took her in for another round of allergy testing, to see if anything had changed from when she'd been tested when she was 5. We found she is "allergic to life" as she likes to put it.. all grasses, trees, cats, dogs, feathers, some molds, weeds, and a few others I'm probably not remembering off the top of my head right now. However, we mentioned the stomach issues, and wondered about food allergies.. and mentioned the things that seemed to trigger her most. When tested, THOSE all came up negative. After talking with friends & co-workers, they've mentioned the idea that maybe she has a problem with glutens. I was told she would need to see a pediatric gastro- since she is not yet 18. I searched for a couple of weeks, and everytime I thought I'd succeeded in finding one, I'd not like the reviews I'd read on them. I wanted to know I that I'd found a doctor who at least knows about gluten issues and what to look for and how to explain it, etc. Anyway, I finally settled on the only one I could find. We see them next week.

So, the question being, has anyone had experience dealing with Children's National Medical Center out of D.C.? I'm not actually going to the main facility, but one of the sattelite offices in Maryland. It's a good 50 miles from home, but it was closer than going to D.C. for me. I'm not really sure what to expect for the first visit, but I know I have to drive over an hour to get there, and over an hour back, and I'd sure hate to sit there forever waiting, and then only see someone for 15 or 20 minutes. Are there specific things I should be saying or asking? I almost feel like I'm drowning, trying to read the info out there.. all the terms seem so foreign to me.

I look forward to any knowledge that can be passed my way, in a way I can understand it.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I would ask if there is any lab work you could get done first. Might save you a trip.

You might have sent them her previous records and most recent blood work, but I would get a copy & take them with you. Keep them in your purse incase they don't have it.

meg1970 Newbie

I would ask if there is any lab work you could get done first. Might save you a trip.

You might have sent them her previous records and most recent blood work, but I would get a copy & take them with you. Keep them in your purse incase they don't have it.

I didn't even know a doctor would submit to ordering labs prior to meeting with you. I seem to fight any doctor we see to get anything done. I just really hope that the fact we are going to something that is supposed to be pediatric specialized in all these fields, will take the time to be with us and not just brush thru the visit.

mommida Enthusiast

See about tests that can be run. i.e. stool testing for parasites, Celiac panel,

Be prepared the doctor will suggest scoping. Ask all the questions you can think of from there. What are you doing the test for? Ruling in or out possible disorders.

Keep a food journal with food (intake time & amount/ please list all ingredients), symptoms (time), BM (time & consistancy). Some doctors may take this seriously, others won't. I can help you find a possible food intolerance reaction. Some reactions can cause reactions for 12 days.

  • 2 weeks later...
meg1970 Newbie

So yesterday was the initial visit.. we were there for quite awhile. He spent a good deal of time listening to us, asking a lot of questions, did a quick examination of her and discussed what he wanted to do next. He did order labs.. LOTS of labs.. 4 vials of blood, urine, and stool sample. He is also asking her to follow a low lactose diet for the next 2 months as well as once again trying the miralax & prescription prevacid stuff. We see him again the end of March, to see if the changes we make that way, in any way help her or not, as well as if anything shows in the labwork. I can call them for lab results- I don't have to wait the 2 months for that, but he would not be calling just to give me lab results. He said that if she doesn't see any improvement, or the labs do not indicate anything specific, at that point when we see him in March, he may want to order an endoscopy & colonoscopy. My mother in law just informed me this weekend as well, that 3 people in the family have recently been diagnosed with Chrons Disease, so I did mention that to him as well. I took in the bloodwork that she had done this past summer, which was just a general screening, and did not have a lot on it, plus, everthing was in the "normal range" that was on it. I told him we'd experimented with taking her off glutens for a brief period and he got a little upset, wanting to make sure how long it had been she was off of them, and how long since she resumed normal eating. I assured him it was only for a week, and it was about a month ago, so he was fine with that, but wanted to be sure the only thing we changed for now was to go low lactose- no milk, cheese, pizza, ice cream, etc.. however, he encouraged yogurt. Fortunately, we will be able to see him at another office, slightly closer to us than the one we went to yesterday, so the drive won't be near as bad. And better still, how thourough he seems to be, and interested in everything we can tell him, and wanting to know about her diet, bowel habits, and any other issues that may be of concern. (I mentioned that she is always freezing, cold to the touch, and complains of being cold almost all the time, since I wasn't sure if that was a symptom of anything.) At this point, it's just a waiting game.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,203
    • Most Online (within 30 mins)
      7,748

    Sarahmegan
    Newest Member
    Sarahmegan
    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

    • trents
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.