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

A Little Input Please


beth01

Recommended Posts

beth01 Enthusiast

I was diagnosed three weeks ago and have been as gluten free as I can right now ( mistakes have been made by the newbie).  I was wondering ( and I know this sounds like a rather stupid impatient question), when will I start to feel better?  I am still waking up every day nauseous, and am still relying pretty heavily on the dicyclomine for the cramping and am still using my heating pad every day for the pain.  I have had two glutenings in the last three weeks, have been keeping a food diary, and am trying to stay away from any processed foods.  I started vitamins right away, cleaned my house from top to bottom ( no gluten here), cut out dairy, just fresh fruits, veggies, and whole meats.  I have eaten Chex, kind of my go to food right now, seems it the only thing that doesn't make me feel like crap. The insomnia is getting worse, the constipation is back with a vengeance, and along with it all is the frustration.  I know it takes time and possibly years for your body to heal from this especially after being sick for over 20 years, but I haven't worked in months and the money is running out and I am not sure how long before I start to feel better so I can go out and get a job without having to call in sick or have to take a nap. lol

After re-reading this I sound like a whiner and am asking questions that you might not be able to answer since everyone is different, but thought maybe a little feedback might be helpful and maybe a little advise as to things I can change.  Thanks for taking the time to read my pity party and thank in advance for any advice given :)

 


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

Hang in there! If you can avoid the glutenings, you should feel relief soon. It took me about six weeks to see improvement. Everyone heals differently though. Some take a bit longer and others less.

Good job on cleaning gluten out of your house. Do not eat out until you are feeling better. Every glutening sets off your system and can take 1 to 3 weeks to recover. Be diligent. Keep snacks with you to avoid eating at restaurants. Simple foods to encourage healing.

You will get better!

GFinDC Veteran

I'd dump the Chex cereal for now.  Some people report reactions to it.  Instead eat eggs, meat or cooked veggies for breakfast.  The simpler your diet is (fewer foods) the better for healing.

 

Some starting the gluten-free diet tips for the first 6 months:

Get tested before starting the gluten-free diet.
Get your vitamin/mineral levels tested also.
Don't eat in restaurants
Eat only whole foods not processed foods.
Eat only food you cook yourself, think simple foods, not gourmet meals.
Take probiotics.
Take gluten-free vitamins.
Take digestive enzymes.
Avoid dairy if it causes symptoms.
Avoid sugars and starchy foods. They can cause bloating.
Avoid alcohol.
Watch out for cross contamination.

Telith Newbie

Just a question, before you knew Gluten was the culprit, what made you feel better?  When I get glutened, I buy ginger ale, and let it go flat while I drink an energy drink.  I don't know if it's the caffeine or the increase of my metabolism or just the brain to body connection of "something is wrong, we need to step up our game" placebo effect but it just makes me feel better. Even the smell of Blue Amp just makes me feel better.  It's horrible for me, no doctor will ever recommend it, but dammit I feel better and I feel better enough that I'm able to focus on what I can actually do to make my symptoms go away for real.  Which is important.

 

You may want to look at what you're cooking with, I know it's a pain in the ass to replace everything, but you don't have to do it all at once, just enough to be able to make sure you're not accidentally getting old contamination making this worse.

 

I started physically feeling better after two weeks, but I had no appetite, was afraid of food, and my digestive symptoms have always taken a back seat to migraines, fatigue, brain fog, and depression, which all lasted much longer.

 

I personally would suggest rice porridge (It's pretty much just over cooked rice as soupy or thick as you want it) with whatever you feel like adding.  I use broth when I'm truly feeling horrid and then slowly add veggies, cheese, and protein like fish or chicken as I feel better/ actually feel hungry instead of knowing I need to put fuel into my body.

 

Everyone is different, we all have our own tricks. Unfortunately it takes a while to figure out which tricks work for you.  That's been the hardest part for me.

nvsmom Community Regular

Are you eating Chex with milk?  About 50% of celiacs are lactose intolerant at diagnosis because our villi which make the lactase that digests the milk sugars (lactose),and if our villi is damaged, it just can't make enough lactase to handle milk. Fortunately most celiacs regain the ability to handle milk after about 6 months gluten-free.

 

I would advise dumping milk for a few months and see if that helps.  Hopefully you'll start feeling better soon.  Most people start seeing some improvements in the first month, but we usually advise that a good 6 months gluten-free are needed to get a better picture of how the gluten-free diet is helping you.

 

Best wishes.

Fenrir Community Regular

I'm about 10 days in of being gluten-free. I don't think I've been glitened yet but I have seen some marginal improvements.

 

My bloating, gas, joint pain and headaches are improved. Overall GI function is better. However, no improvement yet in the upper right quadrant pain.

 

I'm guessing it could take a while for everyting to fix itself.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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.