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 Our Content
    eNewsletter
    Donate

Options / Opinions ?


Daisys mom

Recommended Posts

Daisys mom Newbie

Ok.. Without making a book here .. My daughter  (now 20 yhad a lot of GI problems.. so after being DX'd with GP  I asked our family Dr to test her for Celiac's  .. He said that her test came back at a 21 (1-3 being normal) this was over a year ago .. 

 

So in addition to the C diet she could not eat Fruit or veggies and meat was a no no .. it was mostly  potatoes and junk food (little bit of chicken).

 

 

Ok so her GP is now gone.. and the Dr we saw that was a specialist for GP said he didnt think she had Celiacs 

(needless to say she got off all food restrictions and eat anything she wanted ie bread etc) 

she has been tested again same results as well as having a genetics test... all say she still has Celiacs..

 

She still doesn't feel well... So she has decided to go back on a gluten-free diet !!  Ok.. here is the newest kink in our

plans.. We are being transferred half way across the country, ( we will be driving about 6 days as we also have a 3 yr old ) We leave in 3 weeks 

 

So as much as I hate to ask this... Do we go ahead and start gluten-free or just cut back ,, I guess my question is 

 

Did yall just get up and go gluten-free OR did you wean your self off ?  Should we start now? Or weight till we get moved?

 

Thoughts ?? 

 

 


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



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

If you can, go gluten-free now. Eating gluten-free while travelling for 6 days will be a hassle but it is probably preferable to feeling sick in the car for 6 days.  Plus you will probably travel in the future so setting the precedent now that eating gluten while on vacation/travelling is fine is probably not a good idea. She needs to be gluten-free, all of the time, for the rest of her life, or she will pay for it with health problems just 10 years down the road in areas like infertility, nerve problems, arthritis, bone loss, etc.

 

Eating gluten-free is a bit of extra planning while travelling.  She will need a cooler so you all can picnic as much as humanly possible. Bring gluten-free bread for sandwiches and make or buy a bunch of gluten-free muffins or loaves for snacks.  Bring a bunch of fruit, veggies, nuts and pepperoni sticks... stuff like that.  Travel with a grill and cook hotdogs or steaks in front of your hotel room in the evening.  It can be done, you'll just have to change the way you usually travel - it's almost more mental work than anything, as you make the changes she needs.

 

Best wishes with the move.

 

ps.  You should probably get the rest of the family checked, and rechecked every 2 years for celiac disease as it has a genetic component.

SMRI Collaborator

Could she not eat the fruits, veges and meat because it made her sick or because the dr said no?  Also, is she 20 years old? I would suggest doing the endoscope and the rest of the bloodwork and maybe other testing if she really can't eat fruits, veges and meat.  There isn't anything left to eat after that so she needs to find something she can eat.  If her marker came back at 21 (assuming the tissue IgA test) she has Celiac and needs to be gluten-free but she also needs to find out why she can't eat anything else.  A 20 year old should easily be able to travel and eat gluten-free by packing gluten-free food, finding gluten-free places to eat along the way, etc.

Georgia-guy Enthusiast

With traveling for 6 days, and you do have 3 weeks to prepare, I would go ahead and start the gluten free diet. As others said, get a cooler, pack gluten free snacks, bread, etc. there are coolers you can plug into the power adapter in the car to provide power like a fridge.

However, I'm sure y'all don't want to eat snacks and sandwiches every day. You will probably have a hankering to eat out. If you are like me, you probably already have an idea what your travel path will be, and a daily goal to teach before stopping for the night. Go ahead and post the cities you will be in at meal times, and people on here that live in those areas can recommend good trustworthy places to eat. (I would start a thread in the "restaurants and dining" forum for that.)

Daisys mom Newbie

Could she not eat the fruits, veges and meat because it made her sick or because the dr said no?  Also, is she 20 years old? I would suggest doing the endoscope and the rest of the bloodwork and maybe other testing if she really can't eat fruits, veges and meat.  There isn't anything left to eat after that so she needs to find something she can eat.  If her marker came back at 21 (assuming the tissue IgA test) she has Celiac and needs to be gluten-free but she also needs to find out why she can't eat anything else.  A 20 year old should easily be able to travel and eat gluten-free by packing gluten-free food, finding gluten-free places to eat along the way, etc.

No the "diet " for  GP (Gastroparesis) is a gluten filled diet.. NO fruits no veggies.. rarely any meat..  breads and pasta are ok. baked potatoes etc.. Basically the stomach does not empty (in her case) or empties slowly.  

 

As for the testing I am not truly sure what kind of test other than blood.. but of the 4 "specialist" we saw 2 scoped her and neither did any bi opsies or looked for Celiacs ,, and a 3rd just ordered a genetics blood test which also came back positive.

 

they now say that her GP has cleared up as there are 2 kinds one that goes away after a while adn one that does not.

Daisys mom Newbie

Thanks for all the ideas and we will be planning the trip over this weekend and I have bee thinking along the lines of finding things that we could do at rest stops etc for breakfast and lunch .. an then a restaurant for dinner.

BethM55 Enthusiast

There are apps to help you find gluten-free friendly places to eat.  Find Me Gluten Free is a popular one.  I've used it when we travel.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,837
    • Most Online (within 30 mins)
      7,748

    RyanOB
    Newest Member
    RyanOB
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Dawn Meyers
      Hi I have celiac disease and the dermatitis herpetiformis rash Also other autommune diseases.  I have had bad side effects to all the vaccines I have had and now my Doctor wants me to have the pneumonia vaccine.  I am concerned because of some of the bad side effects I have had in the past example Hep B after shot couldn't  move arm for several months.  Flu shot and COVID was sick right after shot. Told not to get anymore. My lung is inflamed and have a cough I can't seem to get rid of. Very concerned 😟. 
    • knitty kitty
      @Manaan2,  I'm so happy to hear you're going to try thiamine and magnesium!  Do let us know the results!   You may want to add a B 50 Complex with two meals of the day to help boost absorption.  Thiamine interacts with each of the other B vitamins which are all water soluble.   When supplementing magnesium, make sure to get sufficient calcium.  Calcium and magnesium need to be kept in balance.  If you choose a calcium supplement, take two hours apart from magnesium as they compete for absorption.  Take Calcium with Vitamin D.  Vitamin D helps calm the immune system.   For pain, I use a combination of thiamine, B12 Cobalamine, and Pyridoxine B6.  These three vitamins together have analgesic effects.  My preferred brand is "GSG 12X Takeda ALINAMIN EX Plus Vitamin B1 B6 B12 Health Supplementary from Japan 120 Tablets".  Alinamin is another form of thiamine.  It really is excellent at relieving my back pain from crushed vertebrae without side effects and no grogginess.   Look into the low histamine version of the Autoimmune Protocol Duet (Dr. Sarah Ballentyne, a Celiac herself, developed it.)  It really helps heal the intestines, too.  It's like a vacation for the digestive system.  Add foods back gradually over several weeks after feeling better.   I'm so happy to have pointed the way on your journey!  Let us know how the journey progresses! P. S. Add a Potassium supplement, too.  Potassium is another electrolyte, like magnessium, that we need.
    • Manaan2
      @knitty kitty I can't thank you enough!  My husband and I already started looking into those supplements.  We definitely plan to give it a try.  We've been against the Miralax since it was originally advised by PCP, but because of the level of pain she experienced on a daily basis, we decided to try it.  We've made many attempts to gradually decrease but due to her pain and related symptoms, we've kept her on it while trying all sorts of other dietary adjustments pre and post diagnosis specific to food; so far none of those efforts have made a significant difference.  I will definitely share how she's doing along the way!
    • BIg Nodge
      Hi, I have recently embarked on the gluten-free journey. I have what to me seems like a somewhat confusing set of test results and symptoms. I have been impressed by the accumulated knowledge and thoughtfulness as I browse this forum, so I figured I'd make a post to see if anyone can offer any insight. I know there are many posts like this from new users, so I have tried to do my baseline research first and not ask super obvious questions.  I'm 43, overall very healthy. No history of gluten sensitivity or really any of the classic GI symptoms. About three years ago I started to experience intermittent bouts of fatigue, chills/cold intolerance, and shortness of breath/air hunger (sometimes feels like a hollowness in my chest, hard to describe). The symptoms over time have become fairly significant, though not debilitating, I am able to exercise regularly and am fairly physically active, continue to perform well at work. But for example I have gone from someone who consistently ran hot, was always cranking the a/c, to someone who wears a down vest inside at work in winter and get chills if the a/c even blows on me in summer. I get tired and lose energy even when getting decent amounts of sleep, and have to have my wife take over on long drives that I could previously handle with no problems. More generally when I am experiencing these symptoms they seem to crowd out space in my mind for focusing on my family, my hobbies/activities etc, I sort of withdraw into myself.   I happened to be experiencing these symptoms during an annual physical with my PCP a few years ago, he observed post nasal drip and suggested it was allergies and that I treat it with claritin. At first it seemed to respond to claritin (though not zyrtex), but over time I became unsatisfied with that answer. There didn't seem to be any seasonal rhyme or reason to my symptoms, and I felt like I was on an endless loop of taking claritin, then stopping, not being sure if it was even making a difference. I did eventually get allergy tests and found modest allergies to dust and pollen, which didn't feel like a smoking gun.  I then started seeing a natural medicine doctor who was much more willing to explore my symptoms via testing. The first thing that came back abnormal was elevated thyroid peroxidase antibodies/TPOs, 137 IU/mL vs a reference range of <9. At the same time my thyroid panel showed normal thyroid hormone levels. So it appears my immune system is attacking my thyroid even though it is working fine. I got a thyroid ultrasound at the time, it was clear, but with some abnormalities such that they suggested I get is scanned again in a year. These are certainly risk factors for a thyroid autoimmune disease, though my thyroid seems to be working fine for now.  From here my doctor considered celiac due to the murky thyroid/celiac links, so we did a panel. Results were as follows: TT IGA <1 U/ml, TT IGG <1 U/ml, deamidated gliadin IGA 24.6 U/ml, deamidated gliadin IGG <1 U/ml, IGAs 170 mg/dL. Readings greater than 15 considered high by my lab for the first four, my IGAs are within reference range. So basically just the deamidated IGA popped, but my IGAs are normal. I also notice on the tests that my thyroglobulin was high, 86.7 ng/ml vs a range of 2.8 - 40.9.  My doctor suggested that it certainly wasn't conclusive for celiac, but it was possible, and likely that I have some sort of gluten sensitivity. She suggested going gluten free and seeing how I felt as opposed to doing a biopsy. The best theory I can come up with is perhaps I am a silent celiac or just have a gluten sensitivity that doesn't produce immediate GI symptoms, but is still doing damage and over time has caused leaky gut. So now gluten is getting into my blood, and my immune system is attacking it but also mistakingly attacking my thyroid.  So that's what I did, went gluten free in October. It's been about four months, and I am really not feeling any difference. I still get the same symptoms that come and go. My bowel movements may be a bit more regular, but it was never a major issue before so I would consider that a minor improvement. I know that it can take a while to see improvements, and I am going to remain gluten-free and see how I feel. But I am definitely questioning whether I really understand what is going on, and am open to any thoughts or suggestions from the forum. Sometimes I wish I just went ahead with the biopsy before going gluten-free. While I would certainly be down to start drinking IPAs again ahead of a biopsy, you know, for science, I feel like at this point I would be throwing away four months of work and am better off staying the course and seeing what happens. But I'm really not sure.  I know there is a lot of thyroid knowledge on these boards, along with the celiac expertise, so I'm curious if this resonates with anyone's experience. And I'm interested in what sort of timelines people have experienced in terms of feeling improvements for some of these non-GI symptoms like chills, SOB, brain fog etc. Thanks in advance. 
    • cameo674
      Does it taste like black licorice?  It said it was chewable.  I do not like that flavor.     Since the burn at the back of my throat is there everyday, I usually only take something when it is unbearable and keeping me from ADL especially sleep.  
×
×
  • Create New...