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

Need Help With Breakfast!


Nat1

Recommended Posts

pondy Contributor

I desparately need some ideas. Being gluten free, dairy and egg free, what can I have for breakfast that is high in protein? gluten-free cereals just don't cut it...I've been eating a great protein bar but just realized I shouldn't eat it because it has oats.

What do you eat for breakfast? Please help!

Thanks!

Udi's bread - toasted - with natural peanut butter & honey works for me! I get some protein, it fills me up & stays with me a long while. Happy eating!


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



Celiac.com Sponsor (A8-M):



Nor-TX Enthusiast

Is the dairy free because of lactose-intolerance?

I ask because some lactose-intolerant people do well with Greek Yogurt...I think some of the bacterias in yogurt make it easier to digest.

As for my breakfasts, I usually do either gluten free cereal or string cheese and fruit. Occasionally spoonfuls of peanut butter if I need a protein boost.

I have total dairy intolerance -lactose and casein. It's pretty funny because cheese is my favorite food even though I can't and don't eat it.

seashele2 Newbie

I have total dairy intolerance -lactose and casein. It's pretty funny because cheese is my favorite food even though I can't and don't eat it.

A doctor gave an interesting talk including the subject of gluten and dairy similarities at our GIG meeting last weekend. Many celiacs, maybe even most, are dairy intolerant. Lactose intolerance is totally different as it is a sensitivity to milk sugar, not protein. The incompletely digested dairy protein chain shares peptides with the incompletely digested gluten grain proteins. The increased intestinal permeability of someone with celiac or gluten intolerance allows the dairy peptides to cross into the bloodstream, the same as the gluten grain peptides do, and the body reacts to them as invaders.

I want to do research and see if that is also why since my celiac diagnosis, I am unable to eat other foods as well. In fact, the list of things I can't tolerate grows yearly.

Nor-TX Enthusiast

A doctor gave an interesting talk including the subject of gluten and dairy similarities at our GIG meeting last weekend. Many celiacs, maybe even most, are dairy intolerant. Lactose intolerance is totally different as it is a sensitivity to milk sugar, not protein. The incompletely digested dairy protein chain shares peptides with the incompletely digested gluten grain proteins. The increased intestinal permeability of someone with celiac or gluten intolerance allows the dairy peptides to cross into the bloodstream, the same as the gluten grain peptides do, and the body reacts to them as invaders.

I want to do research and see if that is also why since my celiac diagnosis, I am unable to eat other foods as well. In fact, the list of things I can't tolerate grows yearly.

Me too. Now I am finding that peanut butter makes my lips tingle. Spoke to the doctor and his answer was, "Well then don't eat it." :)

I find I definitely cannot do eggs, onions, garlic, spicy foods and I am suspecting something strange is going on with soy but I haven't done a food log on it yet. Still overwhelmed with all the rest. I am getting ready for thyroid surgery and total knee replacement. My doctor suggested that I take my own food to the hospital....

Looking for answers Contributor

I'm right there with you - also throw in the fact that I prefer whole foods vs processed, and I found myself lost for what to eat in the morning. Most mornings, I'm not in the mood for meat so that further complicates matters. But here are some of my standard breakfasts:

Raw tahini butter or peanut butter (about two tablespoons) mixed well with applesauce (about two times the amount of applesauce to nut butter of choice (by the way, I'm allergic to nuts, so if you could eat them, almond butter would be a good choice here). Then I add a dash of cinnamon and vanilla, and mix it up really well. I then pour this over blueberries and top the whole thing off with different seeds: chia, hemp, flax, you name it, if I have it, it goes on top. I sometimes even add dried coconut and cocoa powder. You

Nor-TX Enthusiast

I'm right there with you - also throw in the fact that I prefer whole foods vs processed, and I found myself lost for what to eat in the morning. Most mornings, I'm not in the mood for meat so that further complicates matters. But here are some of my standard breakfasts:

Raw tahini butter or peanut butter (about two tablespoons) mixed well with applesauce (about two times the amount of applesauce to nut butter of choice (by the way, I'm allergic to nuts, so if you could eat them, almond butter would be a good choice here). Then I add a dash of cinnamon and vanilla, and mix it up really well. I then pour this over blueberries and top the whole thing off with different seeds: chia, hemp, flax, you name it, if I have it, it goes on top. I sometimes even add dried coconut and cocoa powder. You

seashele2 Newbie

Me too. Now I am finding that peanut butter makes my lips tingle. Spoke to the doctor and his answer was, "Well then don't eat it." :)

I find I definitely cannot do eggs, onions, garlic, spicy foods and I am suspecting something strange is going on with soy but I haven't done a food log on it yet. Still overwhelmed with all the rest. I am getting ready for thyroid surgery and total knee replacement. My doctor suggested that I take my own food to the hospital....

In addition to my celiac, I can not tolerate dairy, soy, MSG, corn, and sulfites. I am continuously ill, but hadn't placed the sulfites until my daughter's pediatric gastro mentioned, after learning I was allergic to sulfa drugs, that with all the other things we avoid, it must be difficult to eat low-sulfite too. None of my doctors had suggested that connection. We eat a lot of eggs in our house and season anything not sweet with onion and garlic and all of those things are apparently naturally high in sulfites so have to be deleted. I am trying to wean myself off of those but am still getting more than I should and I feel it when I do eat them.

The last time I was in the hospital was in 2007, and yes, I took most of my own food. I took a plastic "Rubbermaid" bin filled with stuff to at least snack on when they couldn't figure out what to bring me. I took cereal, crackers, cookies, peanut butter, etc. I was happy I had that with me and at that time, the only thing I wasn't eating was gluten. One day I ordered a fruit and cheese plate and it arrived with crackers on the plate. I called dietary and asked what part of gluten-free they didn't understand. They told me to just not eat the crackers - and added - Duh! I demanded a supervisor and a dietitian came to my room and I reamed her for the staff not understanding cross-contamination and how dangerous that was, in a hospital especially. They brought me a new fruit and cheese plate with no cracker crumbs on the plate, but I figure they probably did something else to it since I complained. I hope over the past 4 years, things would be better in hospitals on that front with gluten-free becoming more "mainstream" but if I have to go back in the hospital for anything planned in advance, I will take my own food again since my list has increased.


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



Celiac.com Sponsor (A8-M):



Nor-TX Enthusiast

In addition to my celiac, I can not tolerate dairy, soy, MSG, corn, and sulfites. I am continuously ill, but hadn't placed the sulfites until my daughter's pediatric gastro mentioned, after learning I was allergic to sulfa drugs, that with all the other things we avoid, it must be difficult to eat low-sulfite too. None of my doctors had suggested that connection. We eat a lot of eggs in our house and season anything not sweet with onion and garlic and all of those things are apparently naturally high in sulfites so have to be deleted. I am trying to wean myself off of those but am still getting more than I should and I feel it when I do eat them.

The last time I was in the hospital was in 2007, and yes, I took most of my own food. I took a plastic "Rubbermaid" bin filled with stuff to at least snack on when they couldn't figure out what to bring me. I took cereal, crackers, cookies, peanut butter, etc. I was happy I had that with me and at that time, the only thing I wasn't eating was gluten. One day I ordered a fruit and cheese plate and it arrived with crackers on the plate. I called dietary and asked what part of gluten-free they didn't understand. They told me to just not eat the crackers - and added - Duh! I demanded a supervisor and a dietitian came to my room and I reamed her for the staff not understanding cross-contamination and how dangerous that was, in a hospital especially. They brought me a new fruit and cheese plate with no cracker crumbs on the plate, but I figure they probably did something else to it since I complained. I hope over the past 4 years, things would be better in hospitals on that front with gluten-free becoming more "mainstream" but if I have to go back in the hospital for anything planned in advance, I will take my own food again since my list has increased.

I understand. I'm not sure what I will bring, but I would hate to have a gluten episode when I can't walk to the bathroom!

Emma-Lee Rookie

Open Original Shared Link

Try this site! I would try a smoothie with lactose free yogurt. You could even add protein powder for a complete meal!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    2. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Alarming

    4. - Maggieinsc commented on Scott Adams's article in Winter 2026 Issue
      5

      Celiac Disease and Longevity: Can Treatment and Healing Improve Long-Term Survival?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,318
    • Most Online (within 30 mins)
      7,748

    direne
    Newest Member
    direne
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
    • xxnonamexx
      Thanks for the info. I have been taking the ones you recommended but when I saw this I was curious if it was something else to add to the journey Thank  
    • Jane07
      I used to be able to get the Rivera yougut i havent been able to get it lately. I like getting it did say it did say gluten free. I just looking for a good yogurt that gluten free that i can add some fruit and nuts to any suggestion would be helpful  thanks
×
×
  • 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.