Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Celiac.com!
    eNewsletter
    Donate

Post Diagnosis Diet Confusion From Md


shellybean

Recommended Posts

shellybean Newbie

Hello everyone-

I have recently been diagnosed with Celiac, and am experiencing some confusion with the instructions my doctor gave me regarding my diet.

I have yet to get my biopsy, as I am low income and have to wait for the county to approve me for this procedure, but my blood test came back positive, and I have been fairly ill for the last five years.

After diagnosis, I asked my doctor to go over the gluten free lifestyle and the best ways to avoid cross contamination, as well as keeping a gluten free kitchen (my partner still eats gluten).

According to my doctor, she said there is no need for me to worry about cross contamination, or eating wherever I like. She said that it is stupid to have "celiac take over my whole life," and that as long as I am not intentionally ingesting gluten that I should heal, since my nutrients "aren't that bad." This is contrary to everything that I have read, or heard about celiac disease up to this point, and I am not apt to believe that I was given the best advice.

If someone could clear up the confusion for me that would be great. I am being really diligent about not eating gluten because I am tired of being sick. And if cross contamination is going to continue to cause me to have bouts of horrible digestive issues like I've been having, I am not understanding the advice my doc gave me.

Thank you so much!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Doctors do not learn any thing about diet in med school. Go to an expert and maybe copy this and give it to your doctor.

Open Original Shared Link

Link to comment
Share on other sites
shadowicewolf Proficient

Uninformed doctor is uninformed.

So not true.... not true at all....

Link to comment
Share on other sites
Adalaide Mentor

Your doctor is an idiot for a variety of reasons.

Telling someone to go gluten free before an endoscopy is, in short, moronic. It can lead to a false negative. Of course, false positive blood work is pretty much unheard of so it isn't the worst thing in the world except that your doctor (based on his level of stupidity) will then cease to take anything you say seriously.

No doctor would dream of telling someone with a nut allergy not to worry about cross contamination. It could literally kill them. I can't fathom why a medical profession, of all the people, would be one to not take a medically necessary diet seriously. The first time you eat out, share the toaster, don't clean the counter well, let your partner taste your dessert off your fork or some such and end up locked in a bathroom for a night you'll see that it does need to be taken seriously. Please, please, see the newbie thread over in the coping section.

Your doctor is grossly misinformed and if you will be relying on someone for continued medical care in the future after an endoscopy I highly recommend seeking someone with a background in celiac in your area if at all possible. At the very least a "go google it" is far less dangerous than what your doctor is doing, at least then the doctor is admitting that they aren't informed and they can't help.

Link to comment
Share on other sites
Takala Enthusiast

Dear God. :blink:

Congratulations on not taking the doctor's advice on this one.

Treat it as if you have a peanut allergy. Altho the mechanism and reaction is slower, and it won't kill you outright, quickly, very small amounts of gluten, ingested daily, continue to stimulate the auto immune response which tells your body to attack itself, which then leads to another series of physical ailments. Why risk this ?

And you will become more sensitive to trace amounts, over time. So maybe the first few years, you won't get hammered by a bit of cross contamination, but later on, you very well might be.

Some doctors will tell patients not to be perfectionists, under the impression that if they give them permission to be less that absolutely perfect, then the pressure lessens on them to cheat. So you may have a doctor with a diabetic patient say maybe a treat once or twice a year won't kill you. But, people will interpret that too liberally sometimes, and think that if they don't "feel" sick, they then can keep on cheating once a week, etc. Like diabetes, gluten- damage may not show up immediately, but it is going on, inside, and it will malnourish you over time, creating not only problems with your gut and digestion, but your skin, liver, gall bladder, stomach acid/reflux, bones, kidneys, bladder, reproductive organs, nerves, brain function, thyroid..... I could go on and on. There is also a neurological variation which attacks the brain and nerves and even can affect your vision, and causes a loss of balance and symptoms similar to MS. The "neuro- people" (& that's me in that category) tend to be more sensitive to trace gluten, just as the DH (skin rash) people are.

The easiest way to avoid cross contamination is to have a gluten free home, if that is not possible, (and don't feel bad if that doesn't work out, the significant others vary in how they handle this, mine is flexible and will eat anything that I bake) then your work spaces and your porous utensils and porous cookware (plastics, rubber, wood, teflon, cast iron) should be clean and dedicated gluten free. This can be as simple as laying down a paper towel automatically every time you start anything on the counter, replacing or duplicating a few essential cookware items, such as the toaster, colander, cutting board, and tupperware, and go from there. Anything you dip a spoon or knife into, then rub on regular bread or whatnot, should not be used by you, you should have your own gluten free mayonnaise jar, butter, etc. Avoid crumbs ! Paper towels and permanent sharpie markers are your friends. I have a wheat- allergic dog who reacts pretty severely compared to how I do (I have never puked on the floor like that :o) so we had to ditch gluten in ALL of our pet and livestock feeds too, so he wouldn't puke and scratch himself crazy - and he's a drooler, so I don't want him licking me with that stuff, either. The dog, and the horse allergic to certain horse type feeds, which sets off his other allergies, have actually taught me more about cross- contamination in real life than I expected. You can have one cat eating cheap food with gluten, drinking out of a stock tank or water bucket, which the dog and horse have access to, causing a LOT of problems in 3 other species !

If you advance to eating out, it will be trial and error until you find places that are safe and know how to really do gluten free for gluten free, but it is do- able. But you will need to be vigilant, because there are a few that are less than stellar.

Link to comment
Share on other sites
shellybean Newbie

Thank you guys so much for making me feel less insane. It's difficult because for the last few years I was treated as though I was imagining being sick (especially odd considering that my ethiopian feed the children belly that would last for weeks would cause me to shoot from a size six to a twelve within a day). It just felt kind of odd for her to be treating me as though my medical condition was not a "real" medical condition with a "real" treatment. You may as well tell someone who has depression to avoid really horribly written pop songs about love. In short, I think my doc is full of it, and I am glad that I am ignoring her advice. Thanks again, and I am hoping to be feeling better soon!

Link to comment
Share on other sites
shellybean Newbie

Doctors do not learn any thing about diet in med school. Go to an expert and maybe copy this and give it to your doctor.

Open Original Shared Link

Also, I stumbled across this the other day. I'm not too far from U of C- they do amazing work there! Thanks again!

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



Cara in Boston Enthusiast

Please get a new doctor if possible. Also know that any future tests, once going gluten free, will no longer be accurate, so a future negative test does not mean you don't have celiac.

Both my son and I have it and we react differently to different amounts. My son is VERY sensitive, so we avoid any possibility of cross contamination. We don't eat out (unless it is a 100% gluten-free facility) and he doesn't eat any food prepared in someone else's kitchen (unless they happen to be gluten free). He reacts to even the smallest amounts and will be sick for weeks.

Our doctor said to be a careful as you need to be to keep your antibodies at a normal level (retest at 3 months, 6 months, one year).

We even avoid gluten-free food if it is packaged in a facility that processes other foods that contain gluten.

Your first degree relatives also need to be tested . . . even if they have no symptoms.

Cara

Link to comment
Share on other sites
megsybeth Enthusiast

I think ultimately what we should all be going for is gluten free all the time. However, I do think that there's something to be said for assessing your own sensitivity because we are all so different. I've only been gluten free for about two months, my son one, so it's all very new for me. But personally I do eat out and eat some products that are "processed in facilities that also process wheat". My home is %100 gluten-free and I plan out all meals, etc., but I would rather see how we do at this level before getting highly restrictive. Honestly, we allow ourselves small exposure to toxins of all kinds every day. It's not a pretty thought, but we're always finding a balance that works for us.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,034
    • Most Online (within 30 mins)
      7,748

    Toslebury
    Newest Member
    Toslebury
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Katiec123
      @RMJ it makes sense as it’s something I’ve experienced more than once. Currently 24 weeks and baby is doing well! Will be seeking more medical advice today 
    • Manaan2
      Thank you! This is great information and perfect timing because we have our first appointment for a second opinion tomorrow.  
    • trents
      Bright blood in the stool would indicate bleeding down at the lower end in the colorectal area as opposed to the small bowel below the stomach where celiac manifests damage to the villous lining. Are these blood stools persistent? It's not unusual for this to happen once in a while to most anyone when a small surface vessel breaks, kind of like a nose bleed. As Scott Adams said, you must continue to consume regular amounts of gluten if the specialist will be doing additional testing for celiac disease, which could include an endoscopy with biopsy of the small bowel lining.
    • Bev in Milw
      Checkouts gluten-free recipes at twww.redstaryeast.com We tried a bread machine years ago and weren’t happy with results. Bread machines have pre-set rise & bake times.  Unfortunately, the program doesn’t adjust to slight differences when measuring, relative humidity or temperature of ingredients & in kitchens.  Lots of efforts for ONE odd- sized loaf that hard to cut into useable slices.  College-aged son found best use for bread machine was as heavy duty mixer that ‘kept dust in the box.’  He would pre-measure ingredients for 2-3 loaves & use machine mix up individual batches.      Since gluten-free bread needs  to rise only once, each recipe of dough went into a loaf pan. Pans sat counter to rise—time dependent of temp in kitchen. Then, baked in oven until he, not machine, decided it was done.     Took ~10 min extra up front to measure & mix additions but adds nothing to rise & bake times.     Loaves are great for slicing (Slice extra before freezing!). One mess to clean up, saves time & energy since you need to bake  as is half as often (If  you plan to bake lots more than bread, opt for KitchenAid/ heavy duty mixer instead.  Cover with dish towel to capture dust!)     Personally, I’m sure I had as a kid since I’ve never been a fan  of bread. .  Have been wrapping corn tortillas around things for 40+ years.  Can still get a dozen 12-pks of tortillas for same or less than price as 1 load of gluten-free bread. PLUS. the tortillas have more nutrients!         
    • CelestialScribe
      Welcome to the forum. You are lucky because in Korean food, many classic meals such as bibimbap without sauce, barbecue meats and some kinds of soups generally do not have gluten. But it is a good idea to confirm with the restaurant workers for safety reasons. Regarding certain locations, I enjoy going to places such as Plant in Seoul and Sprout in Busan. Moreover, using applications like HappyCow or TripAdvisor can assist you to discover additional choices in the regions you plan to visit. One big tip: it is good to know some important Korean sentences, for example 'I cannot eat gluten' (geulluteuneul meogeul su eopseoyo)  or 'Does this have gluten?' (igeoe neun geulluteuni deureo innayo?) because they can be very helpful. If you are considering getting a local guide, I'd suggest this one https://gowithguide.com/korea They were very helpful when I needed to find places with gluten-free food options because they provide tours tailored to your preferences. Good luck with your travels! 🍻
×
×
  • Create New...