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

Kids, Doctors, Insurance


lonewolf

Recommended Posts

lonewolf Collaborator

I have multiple food allergies and have just figured out that I have to go completely gluten-free, rather than "gluten light" as someone else put it. I have spent a ton of time and money trying to get my health back (pretty successfully) and have made sure my kids have eaten "healthy" food, but not gluten-free. Now I'm concerned about all of them. I want to have them all tested, but what do I say to a doctor without him/her thinking I'm a hypochondriac? And how to make sure the insurance pays for it all? Our insurance only covers doctor visits and tests if the child has a specific problem to be checked out. And there's the problem of non-cooperation with a couple of the kids. I wish I had done this when they were little!

I have 2 boys and 2 girls. My oldest (14 yo girl) is terrified of needles and says that she'll go gluten-free for a week to see if anything happens. She is healthy, but has horrible PMS and debilitating cramps 1-2 days every month. There are a few other minor issues with her and she doesn't tolerate dairy or eggs well. My 12 year old daughter is very fiesty. She won't go gluten free unless she has a test to prove she needs to. She's good about eating my gluten-free food at home, but would cheat anywhere else. She has a chronic stuffy nose and wild mood swings, but no other apparent health problems. My 10 year old son is allergic to milk, is a tiny bit overweight, can't stop bed-wetting and complains about stomach aches a lot. I'm most concerned about him. My youngest is adopted, but has dark circles under his eyes (actually, we all do, except my husband) and really bumpy, rough skin. I wouldn't leave him out of the testing.

Any suggestions on how to get a doctor to order tests? I'm interested in the gene test for myself, since I'm not going back to gluten anyway. Has your insurance paid for all this testing? And, any suggestions on how to convince a strong-willed 12 year old that mom isn't crazy, just trying to take care of her?

Thanks,

Liz


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



Celiac.com Sponsor (A8-M):



taweavmo3 Enthusiast

I really feel for you, that's a tough situation. Have you been dx'd with celiac, or gluten intolerance? I would approach the pediatrician with the fact that there is a family history of this, and the current literature states that all 1st degree relatives need to be tested. Bring some paperwork in if you have to...and if the doc sees how prepared you are, that may help your case. Be pushy if you have to, sometimes you just can't worry about what the doctors are going to think about you. If they treat you in a demeaning way, find another doc. You are only looking out for the best interest of your children, and trying to save them from years of possible health problems. Some docs will not test for celiac unless the patient is knocking on death's door (sometimes not even then!), and nothing is going to change their mind. Find a doc who takes your concerns seriously, and looks at you as a partner in your child's health. I've always liked nurse practitioners myself, I have found them to be more open minded and willing to really listen to me. But, that's just my experience of course.

I wish I had some advice on getting your kids to stick to the gluten-free diet. It's very easy with my 3 year old, since she doesn't know any better. But my 6 year old, who's tests are still pending, will be a tough sell. He has developed a disdain for all things gluten free. I think he'd rather have the tummy aches and terrible rash, than eat gluten-free food! He eats totally gluten-free at home, but buys his lunch at school. It will definately be tougher with him, since he doesn't feel all that sick.

Good luck....wish I could be of more help to you!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,974
    • Most Online (within 30 mins)
      7,748

    LRB
    Newest Member
    LRB
    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)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.