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

Whine Alert - What Is Going On?


sahm-i-am

Recommended Posts

sahm-i-am Apprentice

I am going to apologize upfront. I normally don't complain. Even though I'm an only child, I normally suck it up and do it. But this gluten free diet SUCKS! Sorry - really am. I know I'm working on little sleep and feeling terrible, but I really need to vent. You guys are here and willing to read. I will spare my family.

I have been celiac disease for 3 months. Never had symptoms before, they found out through a series of tests in which they originally diagnosed me with lymphoma. So, now that I have been gluten free I have had the worse case of bloating, gas, heartburn, insomnia. WHat is that about?! One positive thing is that I managed to gain 15 lbs. and the doctor wants to see some more, but hopefully that will slow down. I don't want to feel this way and I would rather go back to eating gluten. I felt better then, even though I know I am doing damage to my intestines. I won't eat gluten, don't worry - I'm a mom, but really? Is this normal? Will this pass? Do I need to have allergy testing done to see if I'm allergic to something? Any advice will be read and cherished.

Thank you for listening to my whine. You may now go get your life back!

Wendi


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



Celiac.com Sponsor (A8-M):



GlutenFreeManna Rising Star

What are you eating? Give us a run down of your typical meals and snacks and maybe we can make suggestions of what to cut.

Also, I know you're not going to want to hear this, but, have you tried cutting out dairy as well? Many people are temporarily lactose intolerant when they first go gluten free. The good news is if you cut it out for a while, you may be able to add some back in later. After 5 or 6 months dairy free I was able to have yogurt (which has very little lactose) and hard cheeses. I'm 7 months gluten free now and I still can't do cow's milk or ice cream, but there are tons of substitutes that satisfy just as much. If it's not dairy, soy is a another big one that people have problems with.

curiousgirl Contributor

I am going to apologize upfront. I normally don't complain. Even though I'm an only child, I normally suck it up and do it. But this gluten free diet SUCKS! Sorry - really am. I know I'm working on little sleep and feeling terrible, but I really need to vent. You guys are here and willing to read. I will spare my family.

I have been celiac disease for 3 months. Never had symptoms before, they found out through a series of tests in which they originally diagnosed me with lymphoma. So, now that I have been gluten free I have had the worse case of bloating, gas, heartburn, insomnia. WHat is that about?! One positive thing is that I managed to gain 15 lbs. and the doctor wants to see some more, but hopefully that will slow down. I don't want to feel this way and I would rather go back to eating gluten. I felt better then, even though I know I am doing damage to my intestines. I won't eat gluten, don't worry - I'm a mom, but really? Is this normal? Will this pass? Do I need to have allergy testing done to see if I'm allergic to something? Any advice will be read and cherished.

Thank you for listening to my whine. You may now go get your life back!

Wendi

Hi Wendi! I'm new to this life-style, too. Diagnosed mid-May and I can see it's going to be a bumpy ride. Hopefully not a long and bumpy ride, though, as I'm scurrying to find anything I can on this disease and gluten-free eating. I thought it was going to be easy just cutting out food with gluten...just eating "clean" as they say. But, for me, there have been other allergies popping up...things that I would never have imagined I'd be allergic to.

It's difficult for me to be diligent since I want to slip back into denial when something becomes confusing (like understanding food labels, and all the scientific names they use and wondering if there's gluten within those scientifically named ingredients). But, I keep reminding myself to EAT CLEAN...fresh food...no canned, no frozen, no bottled.

I've been getting lotsa information from this site and am so thankful it exists!

sahm-i-am Apprentice

What are you eating? Give us a run down of your typical meals and snacks and maybe we can make suggestions of what to cut.

Also, I know you're not going to want to hear this, but, have you tried cutting out dairy as well? Many people are temporarily lactose intolerant when they first go gluten free. The good news is if you cut it out for a while, you may be able to add some back in later. After 5 or 6 months dairy free I was able to have yogurt (which has very little lactose) and hard cheeses. I'm 7 months gluten free now and I still can't do cow's milk or ice cream, but there are tons of substitutes that satisfy just as much. If it's not dairy, soy is a another big one that people have problems with.

GFManna - Yes, I'm in total denial about the dairy - I probably need to cut it out to see if that helps. Is there a test they can do for that to see if a person is? My mom and I have just started baking gluten-free and getting used to this lifestyle change. I hate to throw another monkey in the works! But, I need to put on my big girl pants and deal with it. Thank you for the encouragement.

Wendi

GlutenFreeManna Rising Star

GFManna - Yes, I'm in total denial about the dairy - I probably need to cut it out to see if that helps. Is there a test they can do for that to see if a person is? My mom and I have just started baking gluten-free and getting used to this lifestyle change. I hate to throw another monkey in the works! But, I need to put on my big girl pants and deal with it. Thank you for the encouragement.

Wendi

Were you diagnosed with a biopsy of the small intestines? If your biopsy results showed any villi damage at all that is an indication that you will be lactose intolerant. The villi in you intestines produce lcatase, which you body needs to break down lactose. If you have damaged villi then you won't be able to produce enough lactase to break it down, hence the bloating, gas, and cramping. When you eat cheese or drink milk you are giving your body food it can't digest. Over time your intestines may heal and you may be able to add it back in.

Also since you mentioned you have been baking gluten free more be very careful about what gluten free grains you use and how much gluten free baked good you consume. Recent studies have been posted on these boards showing that many gluten free grains are cross contaminated. There are people on this board that cannot eat anything made with gluten free flours because they are hype-sensitive to CC. So you might want to keep a food diary and log what you eat and how you feel each day. Some reactions can be delayed for up to 72 hours after you eat so it's hard to track down what is making you feel bad if you don't have it all written down.

Lastly, I hope your Lymphoma tests all show up negative, but I'm sure your oncologist has already told you that type of cancer is one that untreated celiacs can develop. All the more reason for you to eat mainly a whole foods diet--as many fresh fruits and veggies and hormone/antibiotic free meats as possible. Try to stay away from sugary stuff and processed stuff, even though there is a lot of processed stuff that is gluten free, that doesn't mean it's good for you to eat it everyday.

sahm-i-am Apprentice

You are both right - I need to eat clean and fresh. The intestinal biopsy showed a very small amount of villi damage at the very top of my small intestines but most of the intestines looked great. He said it is very rare to diagnose someone Marsh stage 1 but that is what I am. It is interesting because you would think that if I had so little damage done why was I so malabsorbed? He still thinks something else is going on since my intestinal wall and lymph nodes are still enlarged. Lymphoma has been ruled out, but they are keeping a close eye on it. They had a hard time with my biopsies from the lymph nodes in my abdomen.

So, today I started taking dairy out of my diet - not easy, but hey, if we can do the gluten-free diet this should be easy, right? I think I'll turn into a bunny for a while and eat salads and fruits. Lord help me if I develop some reaction to fructose and other such issue that I've read about! :blink:

Thank you ladies - you have been a source of comfort. Today is a new day and my pity party is over! And I slept good last night - that always help!!!

Take care,

Wendi

vbecton Explorer

Wendi, glad you are feeling better! I am 3 months into this diet as well. I was in big denial about dairy, but I let that go (tears streaming down my face). I'm a clean eater (aside from the mysterious cupcakes that landed in my belly), mostly all organics, yada yada yada, but I'm still experiencing major bloat, gas and other fun intestinal things. When I was on gluten my symtoms weren't anything compared to what I've got going on now. I've cut out gluten, diary, soy, corn, processed foods, and nightshades. Not sure what else I could cut out, but I sure hope this gas gets better soon or my hubby will probably want to move out :)

I'm starting to sound like a drag, but I guess I'm saying I understand. This gets very frustrating. I feel like a guinea pig. I look forward to the day when I can eat foods covered in baked cheese...ummmm


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



Celiac.com Sponsor (A8-M):



sahm-i-am Apprentice

Wendi, glad you are feeling better! I am 3 months into this diet as well. I was in big denial about dairy, but I let that go (tears streaming down my face). I'm a clean eater (aside from the mysterious cupcakes that landed in my belly), mostly all organics, yada yada yada, but I'm still experiencing major bloat, gas and other fun intestinal things. When I was on gluten my symtoms weren't anything compared to what I've got going on now. I've cut out gluten, diary, soy, corn, processed foods, and nightshades. Not sure what else I could cut out, but I sure hope this gas gets better soon or my hubby will probably want to move out :)

I'm starting to sound like a drag, but I guess I'm saying I understand. This gets very frustrating. I feel like a guinea pig. I look forward to the day when I can eat foods covered in baked cheese...ummmm

I hear ya, Vbecton! I look at people in a new light now - those free to choose whatever they want to eat. I feel like a scientist analyzing everything that goes into my mouth and recording results. Like this afternoon - I was feeling good. Had a bunch (small bunch) of red seedless grapes and WHAM! gas, bloating, totally wiped out! What is that? :o

If I'm gonna blow up eating healthy I may as well blow up eating a Krispie Kreme donut! Just kidding, but seriously, sometimes I wonder.

Good to know we are not alone!

Wendi

vbecton Explorer

Had a bunch (small bunch) of red seedless grapes and WHAM! gas, bloating, totally wiped out! What is that? :o

ME TOO! It seems to happen everyday between 10-11am no matter what I eat. I even cut out eggs 3 days ago thinking that was my new culprit. UHHHH. But, no, the gas loves me so much it just keeps showing up. Everyday. Like a stalker. I have no idea what causes this, but I'm trying to figure it out :blink:

T.H. Community Regular

I hate to say it but...that sounds an awful lot like fructose malabsorption. :( It's a condition that, they think, might occur in folks with gut issues, like celiacs, IBS, etc... There's some information about it here, and what foods set it off:

Open Original Shared Link

But, some other possibilities? (just throwing out anything that comes to mind, here)

How well did you wash the grapes? They could have been looked over by someone with gluten on their hands and been contaminated.

You could have a problem with sulfites (some info. on that here: Open Original Shared Link ) this article mentioned that fresh grapes can have a fungicide with sulfites sprayed on them.

speaking of - you could be having a problem with the pesticides used on the grapes. Were they organic or conventionally grown?

And...that's all that comes to mind. So sorry this is happening to you - hard enough to lose the gluten, and when other stuff goes crazy, it honestly feels so darn frustrating, yes? Hope this resolves for you soon!

I hear ya, Vbecton! I look at people in a new light now - those free to choose whatever they want to eat. I feel like a scientist analyzing everything that goes into my mouth and recording results. Like this afternoon - I was feeling good. Had a bunch (small bunch) of red seedless grapes and WHAM! gas, bloating, totally wiped out! What is that? :o

If I'm gonna blow up eating healthy I may as well blow up eating a Krispie Kreme donut! Just kidding, but seriously, sometimes I wonder.

Good to know we are not alone!

Wendi

vbecton Explorer

I hate to say it but...that sounds an awful lot like fructose malabsorption. :( It's a condition that, they think, might occur in folks with gut issues, like celiacs, IBS, etc... There's some information about it here, and what foods set it off:

Sign me up for the looney bin now :blink: . I just read this sight and it was very informative about fructose malabsorption. Strange thing is one of the main needs for digesting fructose are amino acids...of which I am low in. DANG IT!

I'm going to try the 72 hour elimination of fructose just to see if my symptoms resolve any. Is this simply a diet and response thing, or is this something my GI doctor could test me for?

But, if mine happens to be a fructose problem and not a problem with all the other things I've cut out, then I'm having a food reintroduction party ;)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    Sonya Haskin
    Newest Member
    Sonya Haskin
    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

    • 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    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • 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.