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

Help!- Newly Diagnosed


Babygirl6915

Recommended Posts

Babygirl6915 Explorer

Hello All!

Just wanted to say hi & get a little bit of feed back if I may. I was diagnosed this past Friday (yea! <_< ) as having Celiac's Disease & also a severe allergy to Dust Mites (but that's another topic entirely). For YEARS i have gone to allergist after allergist who told me nothing was wrong with me & long story short, I made my way to an Internalist for a Thyroid panel & he sends my blood off for a complete work up & it comes back no thyroid problem but Celiac's Disease. I have been caught a little off guard by all of this. Does anyone have any helpful insight, tidbits, experiences, or sources for helpful info that you would like to share? I am kinda freaking out so anything @ this point would be super helpful! Thank you!


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



Celiac.com Sponsor (A8-M):



Lisa Mentor
Hello All!

Just wanted to say hi & get a little bit of feed back if I may. I was diagnosed this past Friday (yea! <_< ) as having Celiac's Disease & also a severe allergy to Dust Mites (but that's another topic entirely). For YEARS i have gone to allergist after allergist who told me nothing was wrong with me & long story short, I made my way to an Internalist for a Thyroid panel & he sends my blood off for a complete work up & it comes back no thyroid problem but Celiac's Disease. I have been caught a little off guard by all of this. Does anyone have any helpful insight, tidbits, experiences, or sources for helpful info that you would like to share? I am kinda freaking out so anything @ this point would be super helpful! Thank you!

Welcome to the Club! You have just found yourself the best source for celiac information available.

First, start simple - meats, seafood, potatoes, rice, fresh veggies and fruit, nuts with simple seasonings. Dairy is often hard to digest until the villi heal.

You also need to check your toiletries to include lotions, makeup, lipstick, shampoos...in other words anything can can get into your mouth.

As we all say, the learning curve is steep but it is very doable. The key to success is to learn to read labels, call companies with products in question and diligence.

We have some great folks here who a dedicated to helping those that come behind them. So, please feel comfortable to join in and read as much as you can from these post and ask away.

Babygirl6915 Explorer

Thank you very much Lisa! I am feeling a little better than I was yesterday already. There is some very helpful information on here that makes this all seem not so bad...

pedro Explorer

Hi Welcome.

This is best site for learning searching, and most important to ask questions.

Please don't be afraid of asking, you will receive lots of advice and most important lots of support with the new changes.

Welcome.

happygirl Collaborator

Jessica:

Welcome to the board! This is the best resource out there.

Here are some pieces of advice that I hope will be helpful.

Check out the book in my signature, written by a leading Celiac expert. You can get it at the bookstore or order online. Its GREAT.

Try Tinkyada rice noodles. I've tried a ton of brands, and these are the best! www.tinkyada.com. You can find them in many stores, health food stores, online, etc.

Stay on the board, read, read, read, and ask questions.

I have two pieces of advice that I think are the core of living sucessfully with Celiac Disease (Celiac, not Celiac's...I think we ALL called it that to start with....I even asked how to say it!!!)

1. Learn to successfully read labels. Its the only way to be independent and make informed decisions. Don't rely solely on lists or what someone says...they can be outdated, or ingredients have changed, etc. The combination of your label reading and others opinions, taken together, will be invaluable.

2. Don't eat ANYTHING unless you know a. the ingredients and if they are safe and b. how it was prepared. Having safe ingredients is only part of the equation. Knowing how something was prepared is equally as important. (It is not safe if the ingredients are gluten-free, but you use a knife that just cut a regular wheat sandwich, and then use it on yours).

Let us know what we can do to help......happy to have you on board!

lcbannon Apprentice

It can be a little overwhelming at times but stay right in there and you will find you feel better, and the better you feel the better you can cope with it. Tons of info and support are here and all over the web you can find receipes to help. You do not mention your age, but I know the younger you are sometimes the longer it takes to jump on board with this. I have a 23 yr old DD who feels much better when she eats gluten-free, but she is just not ready to make the commitment it takes-- YET..

Good luck...

Babygirl6915 Explorer

Thanks very much happygirl for the book suggestion, i will definitely read that! And thanks for the Celiac thing... When the doctor told me what i had i had to ask him how to spell it!!! B)

lcbannon- I am 24 years old, work full-time & am getting my Bachelor's Degree @ night. I am very intersted in leading a gluten-free lifestyle but it will be VERY hard at first considering my schedule! Right now i am eating alot of fruit b/c it is easily available & leftover dinner for lunch. Hopefully once i get a better feel for all of this keeping food available wont be so hard.

Again, I cant thank you all enough for the information... Every little bit helps! :)


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



Celiac.com Sponsor (A8-M):



Calikat4 Rookie

I can relate 100% -- I too had to ask my dr to spell celiac AND I was diagnosed in grad school (bye-bye fast food and pizza delivery)! Four years later, though, and it's so much more manageable. Everybody here is right -- this is THE spot for celiac and gluten info. It's been so helpful for me. Here are some tips I picked up along the way...

Shop at health food stores -- Whole Foods, for example has a gluten free bakery section (biscuits, bagels, some awesome treats!) If you don't have a lot of those stores, you can order things online through the glutenfreemall.com or glutino.com

Contact companies -- some places (like Nestle) were so helpful that they sent me gluten-free lists and multiple coupons. There have been times I have stood in a grocery store w/ my cell phone just to make sure I can eat a product.

Cook at home -- meats, fish, fruits, veggies. There are also tons of gluten-free cookbooks and recipes out there.

Eating on the go can be tricky, but remember that some fast food places will do a "protein style" (no bun) burger (like burger king). I also get some meats and cheeses at the deli and just roll them up w/ some mayo. There are also gluten-free crackers (rice crackers) and fruit and nut bars (Lara bars are really good) that you can carry around w/ you.

In the beginning, I had a rule of thumb when it came to deciphering hidden glutens -- if I couldn't pronounce the ingredient, I didn't buy it. But once you get a good base of the things you like to eat, it gets easier.

Don't forget to check your medications -- some contain gluten. There are lists on the internet and sometimes I just contact the manufactuers to make sure.

And it may sound corny, but remember that it's a slow process. It's okay and normal to feel frustrated and depressed, especially in the beginning. It took me a good 6 months to get over the whole "poor me" thing. But remember that it gets a whole LOT better when you stick with it.

Babygirl6915 Explorer
And it may sound corny, but remember that it's a slow process. It's okay and normal to feel frustrated and depressed, especially in the beginning. It took me a good 6 months to get over the whole "poor me" thing. But remember that it gets a whole LOT better when you stick with it.

It funny that you mention that... I didnt really realize it until yesterday but this whole thing has kinda of depressed me. Its more anger though.... Anger that i have gone through years & years of the "different doctor, different opinion" game & in the end it was something this simple. Not simple to fix but all it was is an allergy! And sadness that if i want to feel better that i am going to have to make some HUGE life changes. Hopefully as i start to feel better these feelings will pass. Thanks so much for the helpful reply Calikat4! ;)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,906
    • Most Online (within 30 mins)
      7,748

    wellthatsfun
    Newest Member
    wellthatsfun
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      @Shining My Light, Yes, celiac is spelled differently in Great Britain.  Yes, please do consider us as part of your support circle.   I had a serious Vitamin D deficiency, too.  I learned Vitamin D acts as a hormone when at levels between 78-100 nmol/L.  Mine was in the single digits.  I had been in declining health for years without answers.  I had developed hormone problems and clinical depression among other symptoms.  I corrected my Vitamin D deficiency with high doses to get my level up quickly.  Yes, it's safe.  Here's some studies done on high dose Vitamin D. https://pubmed.ncbi.nlm.nih.gov/34737019/ https://pubmed.ncbi.nlm.nih.gov/39125420/ https://pubmed.ncbi.nlm.nih.gov/35470105/ https://pubmed.ncbi.nlm.nih.gov/30611908/ My Vitamin D deficiency was just the tip of the deficiency iceberg.  I was deficient in the B vitamins, too.  Celiac Malabsorption affects all the vitamins and minerals, not just one.  Here are some articles about how the B vitamins and even Vitamin D help lower anxiety... https://pubmed.ncbi.nlm.nih.gov/33848753/ https://pubmed.ncbi.nlm.nih.gov/35156551/ https://pubmed.ncbi.nlm.nih.gov/35851507/ https://pubmed.ncbi.nlm.nih.gov/35851507/ https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/
    • Shining My Light
      @trents I’m pretty sure what I’m left with when separating celiac to other causes is my 10% being a virus. The one I had about 3 weeks before taking this TTG test. Everything I’ve read says type 1 diabetes, rheumatoid arthritis, hepatitis and some viruses are what could cause the elevation. The other blood tests I had I can compare things against.  I’m going to give your article a thorough read. My support in my circle is very small at the moment.  @knitty kitty I think before EGD I would like to do the DNA test. I’m going to start keeping a better journal also.  I’ve read a crazy amount of these “articles” - these two I’ve not seen. Some articles spell celiac differently. Thank you for sharing! I’m gonna dive into those.   I started seeing the functional medicine doctors from fluctuations in my hormones and major anxiety. Recently I realize it’s mostly health anxiety also so this is more challenging to depict real from imaginary thus all the research and the back and forth. I know anxiety to be a common symptom in perimenopause. I’ve fought it my whole life however. Likely due to lots of different trauma but seeing her was my last ditch effort to try something to avoid SSRIs, HRT, etc. She told me not to blame everything on my hormones when there could be an underlying problem, so she ran some tests to see if anything stood out. The TGG tests stood out.  I do find it very interesting now that I think about it that I don’t desire bread, pasta and pizza. Sometimes yes, but mostly no. I guess I didn’t give that much thought. Also didn’t realize that those foods do contain more gluten than the tortillas and cake/baked goods. About 3 months ago I started ordering meal kits to make dinner easier. I went back over the menus that I picked. I have probably had bread and pasta a hand full of times over the last couple months prior to having that blood test. We used to get pizza every Friday and stopped doing that also. I’m all fairness about 2 months leading up to these blood tests I had less gluten containing foods than I thought.    I’ve been praying for wisdom. Thankful to find some counsel from people who I believe have dove harder into this than most doctors have. Thanks for all the advice. It’s appreciated more than you know. 💕
    • Alibu
      @knitty kitty My whole family has migraines and I started getting them at age 19, so I'm not sure mine are related to gluten, although I do feel like obviously the more inflamed my whole system is, the more likely I am to suffer from more of these things.
    • knitty kitty
      @Alibu, Just wanted to add... Migraines can be caused by thiamine insufficiency.  I used to have them, regularly, but haven't since supplementing with thiamine in the form Benfotiamine or TTFD (tetrahydrofurfuryl disulfide) and Magnesium Threonate.  These forms get into the brain easily and really improve migraines.  I do still get Ophthalmic migraines which are triggered by computer screens.  It's permanent damage from nutritional deficiencies.  An Erythrocyte Transketolace test is a more accurate test for sufficient thiamine. Keep us posted on your progress!
    • Alibu
      @knitty kitty Thank you for those, I will definitely bring them up!  I did send a message to my doctor basically asking what they think so I'll go from there.  He may very well just decide that this was enough to diagnose celiac, but I have no clue what his thoughts are right now.  I also asked for a second opinion on the pathology.
×
×
  • Create New...