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

Dont Feel Better - Could It Really Be Dairy?


i-miss-cookie-dough

Recommended Posts

i-miss-cookie-dough Contributor

sorry if i keep posting

the same "dont feel good" posts.

but just looking for hope.

been 6 weeks gluten free

and still feel

totally nauseas

and tired.

pretty much

all.

the.

time.

just feel like i should

be gettting

SOME relief from the no-gluten...

ya know?

i eat dairy at least 2x a day...

do you really think cutting that out

could REALLY help my symptoms?

anyone know of any decent

dairy free milk or yogurt...

i just want to feel normal again.

hard to remember what that feels like...

: (


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



Celiac.com Sponsor (A8-M):



confusedks Enthusiast

It could definitely be dairy/casein. I would eliminate it for a couple months and see what happens. It is really common that Celiac patients can't break down dairy while their villi are healing.

The good news is that there are some really good dairy free products (just make SURE they are gluten free).

Kassandra

jerseyangel Proficient

Hi--

Yes--dairy can definately keep you from beginning to heal. The tips of the villi are responsible for secreting the enzyme that we need to digest dairy products. As you are gluten-free, and you heal, the tips will (hopefully) grow back and you will most likely be able to tolerate the dairy again.

I suggest cutting dairy completely for at least 3 months--then try it again to see if there's any reaction.

Other foods like soy and corn can cause ongoing symptoms, too--but I'd start with the dairy and see how you do.

1965kid Apprentice

I have been on this new found gluten-free diet for 5 weeks now.

Guess what?

Every time I consume Dairy I get that bloated, rumbly in the tumbly, Big D, awful feeling.

So, I am quite sure that my Celiac, which I am sure I have had since I was about 7 years old, GAVE me a Lactose intolerance.

Will it get better?

From what Ive been told here and read elsewhere, maybe.

But for now, Milk is the DEBIL! :D

I KNEW the other day when I ate ice cream. I was Sooo tore up!

No more milk for me.

I still eat Whey with no problems however.

It's really not a big thing for me, because I never ate much ice cream, or chocolate, and I never did like ceral. Im an eggs and bacon/sausage kind of guy!

As for feeling normal again.

If normal is what other people eat. Id say we ain't gonna be normal anymore.

But we can be the best we can be!

Eat to live, not live to eat!

frec Contributor

At least try going lactose free, which is easier than going entirely dairy free (no whey or casein as well). I react more obviously to dairy than I do to gluten. There are lots of good dairy replacement products--well, let's be honest, I've never found any decent cheese since I am completely dairy free, and there is casein in most soy cheeses--but there are lots of choices for ice cream, yogurt, chocolate, and drinks. Trader Joe's has a good assortment of dairy free drinks and usually have the best prices. I like their store brand soy milk, and I love Almond Breeze milk. Lots of people like rice milk, and there is some new hemp milk now too. There is good soy ice cream and sorbet almost everywhere--Whole Foods has an especially good assortment. They even have different flavors now--when I was first diagnosed all I could find was vanilla. You can also find dairy free chocolate, especially dark chocolate.

Try again in 6 months or a year and perhaps your intestines will recover. One factor in recovery is how old you are. Good luck.

BRUMI1968 Collaborator

I would go with rice milk, almond milk or hemp milk. Avoid the soy. So many folks are intolerant of it, that it's best to stay away. There is a rice yoghurt I've seen at health food stores as well...have not tried it - don't like yoghurt really.

Make sure you get pacific brand rice milk or almond milk for gluten-free. Or there are others no doubt, but not Rice Dream - that has gluten. The hemp milk is nice because it has good omega oils.

Anyway, I'd definitely cut it out - I can't have dairy at all or I get totally constipated - to the degree of one pat of butter getting me had for days on end. I finally just gave up with it.

I have been making "cheese" from various nuts, lemon juice, garlic, etc., and it is pretty good. So that's always an option when you get to feeling better and want to experiment in the kitchen.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,188
    • Most Online (within 30 mins)
      7,748

    Leeila
    Newest Member
    Leeila
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...