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

Im New!


Guest Clo-Jay

Recommended Posts

Guest Clo-Jay

hi! wow im glad im not the only one with celiac because it sure does feel like it sometimes.

im 15 and was told i had celiac disease last october after being quite sick for a while, i was very anemic and had liver problems and then i had to have loads of blood tests and i biopsy on my duodenum and then they told me i had celiac disease :(

its hard. i still dont cope with it very well, i miss a lot of foods.

i want to get a book or something, i want some recepies lol

anyway, not quite sure if im doing the right thing here, or if anyone will even see this but thanks if you did!

love

Chloe


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



Celiac.com Sponsor (A8-M):



SunnyDyRain Enthusiast

Welcome! This website will help you wonderfully! We have lots of "seasoned pros" and then people like me who are finding out the hard way how things are.

This site will give you reciepies and book suggestions! Just keep reading and you will find more than you ever wanted to know about Celiac!

pedro Explorer

Welcome hoem. This is the best place to learn, cry and receive support.

For you first steps try to keep everything simple. Fresh vegetables, fresh meat, fish, and then start adding others foods aslong they are gluten free. One member has a great list of products that you can eat. Her name is NoGluGirl. She can post the list for you.

Here you will find so much help and please ask as many questions as you need. This is the place you can feel relax.

Hope you feel better. I know is overwhelming at first, but it will get easier.

Best regards.

Guest j_mommy

I recommend "Living Gluten Free for Dummies"! It's a good book, easy to read(not boring) and has alot of useful info! I've passed around to my family so they "Get" what celiac disease is!

THere are some awesome recipes here!!!! I've been baking all morning....wasn't in eth mood to eat just bake so I made the "to die for brownies" and choc chip cookies. Taking both to a cookout tonight!

Good Luck!!! Sometimes it gets you down but in the end I'm ok with it b/c I know I feel MUCH better!

DingoGirl Enthusiast

Nope, you're not alone, we're all here to help! :) Welcome.

This site it where I learned virtually EVERYTHING the first few weeks. These are the people who live it! Such a great place. Ask any questions you may have. It really does get easier......and J Mommy's recommendation on the book is a good one.

See ya!

Guest KG in FL
hi! wow im glad im not the only one with celiac because it sure does feel like it sometimes.

im 15 and was told i had celiac disease last october after being quite sick for a while, i was very anemic and had liver problems and then i had to have loads of blood tests and i biopsy on my duodenum and then they told me i had celiac disease :(

its hard. i still dont cope with it very well, i miss a lot of foods.

i want to get a book or something, i want some recepies lol

anyway, not quite sure if im doing the right thing here, or if anyone will even see this but thanks if you did!

love

Chloe

Welcome and you are not alone. I have the celiac in my family but my daughter is 15 and I feel for you at your age in dealing with this. Fifteen is kind of a changing time and you must be sure to keep your willpower with food when out with your friends. I know with my daughter, it's an age where they all want to find friends who are like they are, do the same things, etc. Thier crowd. I hope you have some supportive friends. You will find them if not. It is imperative so that you can stay strong and live your life to the fullest. You can't do everything you want to do if you are weak and sick.

But the good news is... you can do it all- everything you want!! Only one small catch- don't let gluten slip into your food!! On this messege board (you are very smart to find this so soon!) you can find out everything you need to know about what you can and cannot eat. Where the hidden gluten lurks! And how to order at the resturants, which restaurants to go to. How to deal with holidays, birthdays and all that. But really how you are not alone. There are MANY of us out there. Older and younger. Male, female. My son (not celiac) is starting college this fall and if he ends up with celiac (it is hereditary) I already know of students at his college he can hook up with. In a way, it's kind of like our own group or club!

So try and make the best of it although there are and will be some challenges, but do not be afraid to ask for help. You already did here and I know everyone is happy to hear from you and answer anything we can. And most people on this web site know EVERYTHING!!! It's a wealth of knowledge and caring! Any subject you have a question about, I'll bet you can find it here. Or someone will find it for you! And just keep reading this web site so you know you aren't alone, you are not the only one going through this, having to make these changes.

Some products you might have to order on-line, some things not. Fresh stuff is best, but you have probably been told that your whole life!! And now it's time to be healthy!! It's all on this web site. Great information and ideas. Recipes and inspiration when you get a craving you can't control. We've all been there. What you can make or buy to replace all your favorite pasta's and pizza's. Breads and hamburger buns. Crackers and, well, you get the point! So-

Good luck and keep reading and posting!

roo#9 Newbie

Hey Chole,

I am new to this site too. I was diagnosed about 2 years ago and it has not been easy. But I have gotten used to it and we have some good recipes now.


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



Celiac.com Sponsor (A8-M):



jacqui Apprentice
hi! wow im glad im not the only one with celiac because it sure does feel like it sometimes.

im 15 and was told i had celiac disease last october after being quite sick for a while, i was very anemic and had liver problems and then i had to have loads of blood tests and i biopsy on my duodenum and then they told me i had celiac disease :(

its hard. i still dont cope with it very well, i miss a lot of foods.

i want to get a book or something, i want some recepies lol

anyway, not quite sure if im doing the right thing here, or if anyone will even see this but thanks if you did!

love

Chloe

Hi Chloe,

Welcome! celiac disease is not as bad as it seems, really. It will get easier. My family and I had to go gluten free (gluten-free) April 2006. At first I would dream about cheesy buttery garlic bread and wake up licking my lips, but that only happened 2x. I aslo found out just after finally finding an authentic NY pizza place in Sacramento, CA! Talk about poor timing!!! That bumbed me out...

I would say the best way to deal/cope with the celaic diagnosis is to:

1. Let your friends, family, teachers ... know about celiac disease. So many people do not know what it is all about and actuially so much is coming out that it confuses me at times. Sheesh even most of our (forum guys and girls) doc's do not know much about celiac disease!!

2. Do not be shy or embarrassed about needing to ask for the manager or to talk to the chef when you go out to eat. Most food places are aware of celiac disease or are willing to accomadate you.

3. If anyone says it is no big deal, just respond hopefully it won't cause cancer, other autoimmune diseases...since you now eat gluten free. Or something back.

4. Don't get discouraged when even a loved one doesn't quite get it. And trust me there will be someone you thought you could count on or lean on and they will not understand or will make small of your diagnosis. My Mom was not on board at first and of course said it must be my Dad's side and vice versa, but now she is like an Advocate for Celiacs. Any ear she can get will hear all about celiac disease, which gets the person researching it on line.

She also was embarrased when I went out to eat with her, but when she came to visit I finally figured out to call the restaurant first and speak to the Chef (preferrably) or Manager on Duty and plan a meal with them. When we would get to the restaurant they knew what I needed and usually what I wanted to order...

5. There are all kinds of recipes on this sight to check out and there are a couple of cookbooks that have been suggested. The one we bought is, "The Gluten Free Gourmet Cooks Comfort Foods".

Hope this helps!

Jacqui

Guest Clo-Jay

thanks everyone for the welcome :)

there is sooooo much that i find every day that i cant eat, gluten is everywhere lol

love

Chloe

little d Enthusiast

Welcome Clo-Jay

It was not to hard for me at first but it got really hard for me later when all my test came back negative and I just wanted to prove the doctor wrong and started eating regular food again I only hurt myself in the process, but I am trying now to get back on track with eating what I need to. Don't get too discouraged like me and do more harm to yourself, tell your parents when you are in need of more food that you can eat, it just maybe good for them as well. When i make dinner my husband does not know sometime when it is Gluten free, last week I made some like hamburger helper from Mrs Leepers that was a chicken dinner and my family loved it. So not everything taste like cardboard, or dirt, it is not too scary. Hope that this helps a little

Donna

loco-ladi Contributor

I am recently gluten-free myself and have found that for me the best way to deal with my "before" food cravings is to search do the legwork, fingerwork whatever it takes to find the replacement....

Yes I have had chocolate chip cookies, brownies, pizza and am currently on the lookout for crackers, my dintymore beef stew just isn't the same without my crackers, so I got the "DM", and on the lookout for crackers and I WILL find them!

Oh yeah, and sugar cookies are being made right after breakfast tomorrow anyone coming over! lol!

grey Explorer

Hi Chloe!

There are a lot of new people on the boards and I can't believe how welcoming everyone has been, answering questions (again and again, I imagine) and being supportive. I'm ok with most of the kinds of food, but I'm still dealing with 1) that I can't just go to a restaurant on the spur of the moment, or get a snack in a coffeeshop anymore and 2) that gluten is in some soaps, cleaning products, and cosmetics! You're definately not alone.

Remember, all that gluten-free chocolate and Haagen-Daz ice cream! (I can't eat choc., but I'm a HD junkie)

grey

little d Enthusiast
Hi Chloe!

There are a lot of new people on the boards and I can't believe how welcoming everyone has been, answering questions (again and again, I imagine) and being supportive. I'm ok with most of the kinds of food, but I'm still dealing with 1) that I can't just go to a restaurant on the spur of the moment, or get a snack in a coffeeshop anymore and 2) that gluten is in some soaps, cleaning products, and cosmetics! You're definately not alone.

Remember, all that gluten-free chocolate and Haagen-Daz ice cream! (I can't eat choc., but I'm a HD junkie)

grey

This is why I love everybody here they are so welcoming, so warm, we can fight like brothers and sisters, one big happy family. Im addicted I don't want to leave because it is like everybody knows what you are going through. It is great.

Ok I know enough of the mushy stuff

Donna

yes I have an addicting personality I'll blame on the Gluten :lol::lol: It is good at time and really bad the other times here it is good, because I am learning so much. :rolleyes::rolleyes:

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,861
    • Most Online (within 30 mins)
      7,748

    Priscilla Buxton
    Newest Member
    Priscilla Buxton
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.