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

Sooo Frustrated!


vanillazeis

Recommended Posts

vanillazeis Rookie

OK, i thought about putting this on a different board, but seeing as the only people that can relate are the "parents of kids or babies with celiac disease" here i am. Our 3 year old (7-23-04) is recently diagnosed with celiac (7-1-07). I asked her GI specialist about my husband and i getting tested, and his "theory" on the whole thing was- you both need a blood test, but if you have gi symptoms the blood test is not good enough, you also need an endoscopy. Well i have no GI symptoms at all, but through trial and error i have found that i can not get my insurance to pay for my blood test unless i have symptoms, so im going to wait a few months, come up with some symptoms, and get my test. My husbands test was covered, and he had it done last monday. He went to his appt. alone (my first mistake, as he knows nothing about celiac, other than not to feed our kiddo stuff i havent approved) and apparantly he told the dr. his symptoms, which include, diahrrea (pretty often), constipation, gas, belly aches, and blood in his stools (which my 3 yr old also has). Well apparantly this Dr. heard blood in the stools and completely ruled out celiac (he still did the blood test because my husband new better than to come home without doing it ;) he told my husband an endoscopy was not needed but a colonoscopy is. That frustrates me, because he sends my husband home with a pamphlet about the importance of screening for cancers when there is a problem, and im sitting here thinking, arent cancers a long term affect of untreated celiac disease!? Why not investigate what the cause may be at the same time as trying to find the problem!! My husband has had symtoms of celiac his whole life, starting from when his mother introduced solid foods, and he became lactose intolerant, she always says he got better, but then eventually formed an intolerance to soy as well. He and his sisters all had potbellies as children, although they were skinny kids. My husband and one of his sisters are also diagnosed with ADHD. His celiac blood panel came back negative today. I'm worried that his sisters and parents might think that if he showed up negative, it must come from my side, and they wont get tested. Am i overreacting? Should i drop it and give this dr. the benefit of the doubt? Should i insist they do the endoscopy when they do the colonoscopy? Should i make him switch dr's, does he sound like he might be one of those dr's that know nothing about celiac disease? Thanks guys!


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



Celiac.com Sponsor (A8-M):



ptkds Community Regular

IMO, you should probably insist that they do the endoscopy during the colonoscopy. About 6 yrs ago, I had a colonoscopy done, and they found pre-cancerous polyps in my colon. So the colonoscopy is a good idea. They won't have to do much to just do the endosccopy done.

He can also try the diet and see how he feels from that.

As for the family, don't bother. I have 2 aunts that most likely have Celiac, but they refuse to even be tested because they don't want to eat a gluten-free diet. One of them is suffering from severe diverticulosis, but she won't bother getting tested. It's frustrating, but it is their life.

ptkds

vanillazeis Rookie
IMO, you should probably insist that they do the endoscopy during the colonoscopy. About 6 yrs ago, I had a colonoscopy done, and they found pre-cancerous polyps in my colon. So the colonoscopy is a good idea. They won't have to do much to just do the endosccopy done.

He can also try the diet and see how he feels from that.

As for the family, don't bother. I have 2 aunts that most likely have Celiac, but they refuse to even be tested because they don't want to eat a gluten-free diet. One of them is suffering from severe diverticulosis, but she won't bother getting tested. It's frustrating, but it is their life.

ptkds

Thanks for your help! My husband is a little stubborn, but i think he might agree to go gluten-free atleast for a few months as a trial. Both of my husbands parents have dirverticulitis, but they are both getting tested, so yay for that! I just dont know whether to put my husbands sisters through getting tested, when it's only their niece that has been diagnosed. opinions?

kbtoyssni Contributor

It is frustrating that the doc insisted it's not celiac, but I'd agree that a endoscopy isn't a bad idea. What's the age you're supposed to start getting those anyway? Since it seems suspicious that your husband has it, I don't see a problem with his sisters getting tested. Maybe they don't have it and they go on with their lives. Maybe they do and you can save them years of misery.

vanillazeis Rookie
It is frustrating that the doc insisted it's not celiac, but I'd agree that a endoscopy isn't a bad idea. What's the age you're supposed to start getting those anyway? Since it seems suspicious that your husband has it, I don't see a problem with his sisters getting tested. Maybe they don't have it and they go on with their lives. Maybe they do and you can save them years of misery.

thanks for the advice! The age to start getting a colonoscopy is 50. I think that's what you meant, i dont think there is an age to get an endoscopy. My husband is only 26, but i do agree that the colonoscopy is not a bad idea. i guess the problem is that i feel a little insuperior to waltz in and demand that my husbands dr (who happens to be the head of this practice) perform an endoscopy as well. I guess at some point im going to have to start being a little more confrontational, im just not that way by nature. I'm getting better now that my little girl has been diagnosed with celiac and started school. I have to be kinda loud to get her taken care of properly :) thanks!

Nikki'smom Apprentice

I agree a colonoscopy is a good idea especailly if there is blood in the stool. My DH had Ulcerative Colitis (colon removed) starting in his early 20's. Now that our DD has been diagnosed with Celiac he wishes he knew about it back then because he thinks he should have tried being gluten-free before he had his colon removed. So personally I say go for the colonoscopy and then see what they find (hopefully nothing serious) and if need be then be pushy on the endoscopy. If you can get them to do both at the same time even better.

As for his sisters keep mentioning it but in the end if they don't want to help them selves then their is nothing you can do.

I know what you mean about feeling like it was a mistake not going with DH to the dr. That is how I used to feel if I didn't go to the gastro with DH. It actually got to the point the gastro would ask me the question about what was really going on not DH! LOL

Good luck!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,037
    • Most Online (within 30 mins)
      7,748

    cbattiato
    Newest Member
    cbattiato
    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

    • Scott Adams
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
    • Beverage
      Exactly which blood tests were done? There are a few different ones and some docs don't do them all. Also, your results and reference ranges for each?
    • Jmartes71
      Thankyou so much for your words.Its a hard battle when a supposed well known hospital whose celiac " specialist " has down played me because my colon looks fine and put it in my medical and so pcp doesn't take seriously. In their eyes we all carry that gene.Im having alot of bad days trying to be positive because of it.
    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
×
×
  • 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.