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

SimplyCeliac

Recommended Posts

SimplyCeliac Newbie

Hi everyone,

A few years back my doctor told me that he believed I might have Celiac disease and to start trying to remove gluten from my life. A month ago he confirmed that I have Celiacs. He also told me to remove processed sugar from diiet because it doesn't help with the disease

So now I am trying to figure out this new lifestyle and I have all sorts of questions that I  need help with.

Food wise:

It is very hard to find gluten-free foods that don't have sugar in them. How do you tell the difference between good sugar and bad sugars? I understand the difference between natural and not, but some products seem to be all-natural, but have a high sugar count. Does that make sense?

I pretty much eat on bananas all day because they are the easiest thing to grab and go with my busy lifestyle. Does anyone have any tips on things that stay well and can be eaten quickly [like in a minute or less]?

Depression:

I have been suffereing depression for a few years now as well. Has anyone experienced their depression improving after removing the gluten completely or does it get worse? I finally had mine under control and now I feel depressed everyday. Does it get better?

Fatigue/Forgettfulness/ Lack of caring:

I am constantly tired and just not there anymore. I forget things like not other; I also have frequent blackouts where I don't remember what exactly I was doing. I also have lost interest in a lot of things.  I don't know whether this is the disease or something else.

Beauty Products:

I know they say to avoid gluten in beauty products. Does anyone have any brands they can recommend? From supermarket brands to salon products, I would like to get a grasp on what i can use. Lip Balm in particular because I"m a chapstick addict.

Cross-contamination:

How worried should I be about this?

I suppose those are the questions I can think of right now. Besides that, does it get better?


 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Welcome to the club!

 

There is no Celiac reason to eliminate sugar.  Not sure what the doc was going for there.  Maybe he just didn't want you eating a bunch of gluten-free junk?   :unsure:

 

On beauty products - the ones that might get in your mouth are the most important to be gluten-free.  For example, I don't worry about mascara but I do worry about my face lotion as I am always getting it in my mouth.  Those little egg lip balms are gluten-free.  Have fun "flavors". Eos?  

 

 

This is them Open Original Shared Link

Georgia-guy Enthusiast

Welcome to the club, and happy early birthday! (Sorry, I cheated and looked at your profile)

As for your questions:

-Sugar, I have no clue how to tell the good from bad aside from maybe if you look at the ingredients and see if it says "cane sugar" (but don't quote me on that one)

-Quick foods, there are several snack bars (I know nature valley has an almond crunch I think it is) that are gluten free. Just check the labels! Kroger has the shelf tags for most of their gluten free products that say "gluten free" on them.

-Depression and lack if caring I'm gonna combine cuz they go hand in hand. I have noticed my overall outlook on life has improved. Most of my lack of caring/interest in things was mainly because I always felt like sh**, so as I've been off gluten and feeling better, I have more interest in things.

-Beauty products....I'm naturally sexy so I don't wear any.

beth01 Enthusiast

Since Karen and Georgia guy commented on some of the other issues, I am going to comment on the depression.

 

The way I have looked at my new diagnosis is kind of like going through the 5 stages of grief.

 

1. Denial and Isolation - how can I not be able to have gluten?  I was eating it every day, that can't be my problem.  The lab results tell me I can't, but I want a damn Choco Taco ( I really need to figure out a way to make them gluten-free).  Then the isolation - I can't go out with my friends anymore, they are all going to think I am a freak.  I might as well just stay home.

 

2. Anger - You are mad at everyone, mad at the doctors for taking so long to diagnose you, mad at your spouse because they just don't understand - they can eat all that yummy goodness and you can't, mad that no one truly understands what you go through on a day to day basis, how much pain and anxiety you have had.

 

3. Bargaining - I think the doctors are wrong, maybe I should go get a second opinion.  Maybe if I eat a nice big old bowl of shredded wheat, I won't get sick - they're wrong.  Maybe if I eat a little it won't harm me.

 

4.Depression ( the fatigue and not caring is a part of this, the forgetfulness is more brain fog) - This is really unfair.  One minute you are up, the next you are down.  You are fighting with friends, fighting with spouses, again no one understands.

 

5. Acceptance - You finally realize this is a good thing.  I now know what my problem is, I can fix it.  It takes time, but it does get better.  Once you get your diet under control, it gets even easier.  I am not nearly depressed as I was three months ago, but glutenings really have a bad effect on my moods. 

 

The brain fog lessens, but it is one of the things for me that is taking a long time.  I started to feel worlds better within a week of my diagnosis. My migraines have gone completely and I was having them four times a week ( I should say I haven't had one in three months, don't know if they are gone forever).  I still have pain and nerve damage, but those might never go away.  For the first time in my whole life I know what it's like to be regular ( or as regular as my body will let me).  I am not nearly as emotional as I was three months ago, but it's still hard.  Most on here will say that the first year is the worst. You are going to find that people in your life are either going to be very understanding or they aren't going to be at all.  At least with my experience so far there doesn't seem to be an in between.  This forum is a wonderful source of information full of a lot of people that understand just what we are going through.

 

Good luck with your new endeavor and welcome to the club!

NatureChick Rookie

 

Sugar:

Though sugar of any sort doesn't help anyone, I'd probably just do low sugar for now rather than try to eliminate all of it and go gluten free at the same time. Though trying gluten-free foods is one way of lessening the ways in which you feel deprived early on, long-term, you'll probably end up cooking more foods for yourself from scratch so the amount of sugar in your diet will go down anyway.

Beauty Products:

I tried eye shadows and foundation from a brand called 100% Pure. I'm not a huge fan of how the foundation applies, and the color selection for the shadows is limited but they are good enough for how infrequently I wear makeup. But I do like that all of their ingredients are less toxic than those that you find in mainstream products. 

Cross Contamination: Take it seriously. The first few months will likely include lots of accidents so don't bee too surprised when they do. Most people spend at least the first 3-4 months getting glutened on a regular basis until they figure out some hidden sources or realize that what they hoped would be safe actually isn't.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.