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

New Things To Try...


luvrdeo

Recommended Posts

luvrdeo Apprentice

I am frustrated, and need to vent.  Let's start with that!  Here's why...in a short version - colitis is still giving me fits, so my gastro told me I'll be on pills for life.  This is unacceptable to me.  SO...I sought out a naturopath doctor, who put me on all kinds of new things...Metagenics UltraInfam shake stuff, a Theramedix digestive enzyme, and something else that I left at home dealing with Omega's.  Anyway, I've been on them all for almost a month now, and things have gotten worse with my constant D.  I'm not digesting anything.  To top it all off, I've gained some weight this year due to all the crap pills my gastro doctor had me on...and after a month of hard-core working out, my pants are STILL all too tight.  Anyone have any good advice for me?  I feel like I'm getting nowhere with all of this...why does it have to be so hard?  Ok, done feeling sorry for myself :)


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



Celiac.com Sponsor (A8-M):



dilettantesteph Collaborator

That Natropath may have suggested something that contains gluten contamination.  I suggest a whole foods diet.  Good luck.

user001 Contributor

Well I have to say, I have tried to lose weight before being diagnosed and it was DARN NEAR IMPOSSIBLE! I have lost 60lbs for no reason over my life and gained 40 back for no reason. I have been having some digestion issues but have gotten the D under control pretty effectively. I take kyolic brand kyodophulis and I drink a protein shake that has some amino acids in it because it seems to be pretty gentle on my stomach. Eating in the morning still causes me pain but no D or C thankfully. Occasionally if i over do it like on my birthday, I will have a bout of D. I have been looking into enzymes for myself and It seems like some people don't necessarily need them and they seem to cause problems like D if you don't. My opinion is to contact all of the producers of those products to grill them about processing and shared equipment and see if you are possibly having some cross contamination issues. Discontinue the enzymes, take acidophulis or kyodophulis instead, keep the shake and omegas if they are ok to take and see if things improve in a week. Eat a whole foods diet and make sure to cook your vegetables a little bit because they can be hard for you to digest.

luvrdeo Apprentice

When it comes to food...I've tried it all.  Doesn't seem to matter what I do or don't eat, I have constant D - the colitis is out of control.  All my veggies are either steamed or roasted, keeping them soft.  My meals consist of a shake/smoothie in the morning with fruit and some coconut or almond milk, lunch is turkey or chicken with veggies and maybe some sweet potato and a few almonds for crunch factor, and dinner is a salad with turkey or chicken and more veggies.  It can't get any cleaner.  Obviously none of what the naturopath gave me is working...even though they all state they are gluten-free products.  I've tried the acidophulis and got no results, maybe I'll try the kyoduophulis instead.  I was hoping to find a natural way to calm down the inflammation internally...

user001 Contributor

The inflammx is supposed to be good. I would keep it, try adding the kyo and removing the enzymes for a week.

 

edit to add- Have you ever used ginger? It helps with my arthritis and it is supposed to help with inflammation in general. I take about a 1 inch piece of fresh ginger put it in a blender with a cup of water and puree the whole thing. I simmer it on the stove for a few minutes, add tiny bit of honey or sugar and strain it over ice. I like to add a squeeze of lemon too because lemon is supposed to be alkaline which is good.

SMRI Collaborator

Many medications are plant based and basically the same thing as the "natural" stuff you get from your homeopath.  Just because they are "natural" doesn't mean they are better so you may be having the same issues on those pills because they contain the same ingredients or some of the same ingredients in the medicine from the GI doctor.  Not knowing your history, have you been tested for allergies?  I know my daughter can not eat beef or chicken so maybe that is what is causing your problems and not the medications?  She is young and should have no issues losing weight and could not lose a pound, even with a good diet and lots of exercise (she is a college athlete).  She stopped eating beef and chicken and has lost 10 lbs and is back to her ideal weight.  She still has some issues with D and is being tested for Celiacs though.  I'm pretty confident she has it since I now do and I have the genetic pairs and she has way more symptoms than I do.

luvrdeo Apprentice

The inflammx is supposed to be good. I would keep it, try adding the kyo and removing the enzymes for a week.

 

edit to add- Have you ever used ginger? It helps with my arthritis and it is supposed to help with inflammation in general. I take about a 1 inch piece of fresh ginger put it in a blender with a cup of water and puree the whole thing. I simmer it on the stove for a few minutes, add tiny bit of honey or sugar and strain it over ice. I like to add a squeeze of lemon too because lemon is supposed to be alkaline which is good.

He told me to only be on the inflammx for a month...not sure why??  I haven't tried ginger, but know all about how it can help.  I wasn't ever sure how to include it into my day, so thank you SO much for the suggestion!  I will start on that right away.


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



Celiac.com Sponsor (A8-M):



luvrdeo Apprentice

Many medications are plant based and basically the same thing as the "natural" stuff you get from your homeopath.  Just because they are "natural" doesn't mean they are better so you may be having the same issues on those pills because they contain the same ingredients or some of the same ingredients in the medicine from the GI doctor.  Not knowing your history, have you been tested for allergies?  I know my daughter can not eat beef or chicken so maybe that is what is causing your problems and not the medications?  She is young and should have no issues losing weight and could not lose a pound, even with a good diet and lots of exercise (she is a college athlete).  She stopped eating beef and chicken and has lost 10 lbs and is back to her ideal weight.  She still has some issues with D and is being tested for Celiacs though.  I'm pretty confident she has it since I now do and I have the genetic pairs and she has way more symptoms than I do.

I haven't been tested for allergies, it was something the naturopath and I discussed.  I too am young, athletic, healthy, and have these 10 lbs that will not go away...so, I guess I better get tested for more foods than just the gluten!  This is so helpful, I've often wondered if one of the "healthy" foods I'm eating might be what the real issue is.  What does your daughter eat for protein now?  I'm not a big pork fan, so I'd be stuck with just turkey I suppose!  :)  I hope you get some answers with her, it sure has been a frustrating journey for me getting diagnosed.

user001 Contributor

He told me to only be on the inflammx for a month...not sure why??  I haven't tried ginger, but know all about how it can help.  I wasn't ever sure how to include it into my day, so thank you SO much for the suggestion!  I will start on that right away.

The ginger drink I told you how to make it actually pretty delicious if you like ginger! Even before knowing I had celiac disease or knowing it was helpful I used to make pitchers of it for bbq's in the summer.

SMRI Collaborator

I haven't been tested for allergies, it was something the naturopath and I discussed.  I too am young, athletic, healthy, and have these 10 lbs that will not go away...so, I guess I better get tested for more foods than just the gluten!  This is so helpful, I've often wondered if one of the "healthy" foods I'm eating might be what the real issue is.  What does your daughter eat for protein now?  I'm not a big pork fan, so I'd be stuck with just turkey I suppose!  :)  I hope you get some answers with her, it sure has been a frustrating journey for me getting diagnosed.

She eats a lot of peanut butter, yogurt and cheese :D.  Unfortunately that doesn't help you.  Beans are good sources of protein.  She certainly has an interesting medical history and for the most part is healthy but still has some lingering issues, mostly D and migraines now so I'm thinking that Celiacs might be the last piece to the puzzle.  I'm actually really surprised she has not been tested already with everything else she has going on.

luvrdeo Apprentice

She eats a lot of peanut butter, yogurt and cheese :D.  Unfortunately that doesn't help you.  Beans are good sources of protein.  She certainly has an interesting medical history and for the most part is healthy but still has some lingering issues, mostly D and migraines now so I'm thinking that Celiacs might be the last piece to the puzzle.  I'm actually really surprised she has not been tested already with everything else she has going on.

It took me 20 years to get them to test for celiac...so, I get that one!  I used to have major issues with headaches as well, and they have gone away 100%.  The D though...that's the battle!  I love yogurt and cheese...could totally live on that!!!  :D

cyclinglady Grand Master

If I consumed coconut or almond milk, I would have D every single day (that includes all milk products too). Perhaps you have an intolerance to either of them. Something to consider.......

Celiac Ninja Enthusiast

The ginger drink suggested above is a must :D Reeds ginger soda is a quickie for nausea, diarrhea, vomiting, motion sickness....yadda yadda. Probiotics like greek yogurt, which you might like, is great for gut relief. I get the Wallaby Organic low fat Greek Yogurt that's certified gluten-free.

 

We have similar gut swelling issues, mines after being glutened. Are you possibly being glutened? Cross contamination? Even spices can have gluten in them, stuff with white vinegar is iffy as well. Maybe check everything thoroughly.

ezgoindude Explorer

Sup guys,

 

I don't have much advice, as I'm a newbie in this realm of chronic inflammatory diseases, but I have one question for luvrdeo...

 

How did you doctor discover you had lymphocytic colitis?  Would you mind saying what tests provided evidence of it?

 

I ask because one thing that stood out for my new GI is my biopsy showed mild eosinophil count in a few patchy areas.  Visually I had a perfect colon.  Its frustrating since my eosinophil blood count is normal,  no pathological evidence was seen of intestinal damage but my fecal calprotection came back showing mild inflammation,  which they say could be anything, including celiac or NCGI.....

 

its crazy as I can't seem to gain any weight, stuck at 140lbs... =(

Gemini Experienced

If I consumed coconut or almond milk, I would have D every single day (that includes all milk products too). Perhaps you have an intolerance to either of them. Something to consider.......

This is what I was thinking too. Too much milky stuff does me in.......

user001 Contributor

The ginger drink suggested above is a must :D Reeds ginger soda is a quickie for nausea, diarrhea, vomiting, motion sickness....yadda yadda. Probiotics like greek yogurt, which you might like, is great for gut relief. I get the Wallaby Organic low fat Greek Yogurt that's certified gluten-free.

 

We have similar gut swelling issues, mines after being glutened. Are you possibly being glutened? Cross contamination? Even spices can have gluten in them, stuff with white vinegar is iffy as well. Maybe check everything thoroughly.

Reeds is amazing!!! I am so glad that I discovered ginger and that I like the taste. Its seriously helps more than NSAID's with the pain from arthritis.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Hmart replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    2. - trents replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      10

      Help I’m cross contaminating myself,

    4. - DebJ14 replied to Jhona's topic in Introduce Yourself / Share Stuff
      30

      Does anyone here also have Afib

    5. - Hmart posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,924
    • Most Online (within 30 mins)
      7,748

    Mckshane
    Newest Member
    Mckshane
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
      I have a lot to learn!  Thank you
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
    • Hmart
      The symptoms that led to my diagnosis were stomach pain, diarrhea, nausea, body/nerve tingling and burning and chills. It went away after about four days but led me to a gastro who did an upper endo and found I had marsh 3b. I did the blood test for celiac and it came back negative.  I have gone gluten free. In week 1 I had a flare-up that was similar to my original symptoms. I got more careful/serious. Now at the end of week 2 I had another flare-up. These symptoms seem to get more intense. My questions:  1. How do I know if I have celiac and not something else? 2. Are these symptoms what others experience from gluten?  When I have a flare-up it’s completely debilitating. Can’t sleep, can’t eat, can’t move. Body just shakes. I have lost 10 pounds since going gluten free in the last two weeks.
×
×
  • 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.