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

Ulceratice Colitis Or Not?


francelajoie

Recommended Posts

francelajoie Explorer

I've been having loose bowel movements accompanied by blood and mucus. Most of the time it's only blood and mucus...no stools. I go to the bathroom, and as soon as I get out of there, I feel like i have to go again. I don't know what is wrong with me. I haven't been glutened or anything cause i've had this over 2 months now. I don't feel sick at all. I just have gas and very rare bloating.

Anyone ever hear of Dr. Dahlman's protocol? I've actually ordered everything to do the first months treatment. (Not cheap...cost me 200$). I really hope it starts working. If not, I guess I'll have to go see a doctor again. <_<


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



Celiac.com Sponsor (A8-M):



LKelly8 Rookie

Wow, that sounds like ulcerative colitis to me. My sister has UC, after years of on-and-off prednisone treatment she's finally in remission with a drug called 6-MP.

Open Original Shared Link

I went to Dr. Dahlman's website and read a few pages. To be blunt I think he's a quack :wacko:. Sorry!

Open Original Shared Link

Celiac is the only autoimmune disease that can be cured/treated through diet. I have rheumatoid arthritis and for years I got caught up in the diet-cure scams. A waste of money and worst of all a waste of precious, precious time. If you have UC get it treated by a board certified gastroenterologist now, before the disease progresses to a point of no return. (ie: surgery - or worse)

:unsure: I apologize if I offended. I feel very strongly because of my own experiences. YMMV.

francelajoie Explorer

I actually decided to call my family doctor and get referred to a gastroentorologist at the Celiac center in Boston. Hopefully they'll find something...not too serious I hope. I'm scared they'll make me do the gluten challenge cause I wasn't really diagnosed with Celiac (no colonoscopy)...just gluten intolorence by blood test.

I'll let you know when I find out.

Nancym Enthusiast

Dr. Fine says NSAIDS are terrible for colitis, are you taking any?

justjane Rookie
Dr. Fine says NSAIDS are terrible for colitis, are you taking any?

Sorry to take over your post but I have a question! Nancy, can you tell me what NSAIDS are? I have mild active colitis and chronic active colitis and this would help me sort it out and feel better. I was diagnosed with colitis and basically left in the dark because they were testing for Celiac all that time, which came out negative both in the blood tests and the biopsy. I have done much better on a gluten-free diet, however, so wondering if I still might have it or gluten intolerance. I was 16 when I was tested....

Thanks,

justjane

francelajoie Explorer
Sorry to take over your post but I have a question! Nancy, can you tell me what NSAIDS are? I have mild active colitis and chronic active colitis and this would help me sort it out and feel better. I was diagnosed with colitis and basically left in the dark because they were testing for Celiac all that time, which came out negative both in the blood tests and the biopsy. I have done much better on a gluten-free diet, however, so wondering if I still might have it or gluten intolerance. I was 16 when I was tested....

Thanks,

justjane

Same here...what are NSAIDS?

I am only taking the following supplements which are Dr.Dahlman's protocol:

Lactoviden, Bifoviden, Metagest, Intesol, Azeo-Pangen, and Ultrainflamx. I had to stop taking all this cause I have been waking up in the middle of the night with pain in what I think is the higher part of my large intestine or just to the right of my stomach. Not sure what it is. Thats why i decided to go to my doctor.

penguin Community Regular

NSAIDS are things like asprin, motrin, advil, pepto-bismol, excedrin, and other antinflammatories.

If you look on the bottle, there's usually a warning about ulcers and abdominal bleeding


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



Celiac.com Sponsor (A8-M):



jesscarmel Enthusiast
I actually decided to call my family doctor and get referred to a gastroentorologist at the Celiac center in Boston. Hopefully they'll find something...not too serious I hope. I'm scared they'll make me do the gluten challenge cause I wasn't really diagnosed with Celiac (no colonoscopy)...just gluten intolorence by blood test.

I'll let you know when I find out.

Hi

I go to the celiac center in boston. who are you seeing? i think you will like it there!

good luck and i hope you feel better!

Jess

Nancym Enthusiast

They always warn about ulcers but it can also affect the upper GI tract, like the small intestine. Yeah thing like Advil, Aleve, aspirin, ibuprofen. I guess Tylenol isn't an NSAID, but it has its own set of problems (liver damage).

IrishKelly Contributor

I was told by a regular gastro Dr. i might have UC...but then i went to a holistic Dr. and he went over a list of symptons (such as pale floating stools, bloody stools, leg cramps, headaches, etc...) and low and behold i'm glutent intolerant. Once i eliminated the gluten (even though all blood tests were negative) i'm sooo much better. He said the colitis would get even better/completely go away over the course of six months...as long as i stay gluten free.

lindalee Enthusiast

Just got an email that a specialist from Mayo is going to be in new mexico speaking of UC and crones if any one is interested I'll look it up.

Nancym Enthusiast

Dr. Fine got into the gluten sensitivity by way of researching UC and microscopic colitis. He said that basically microscopic colitis looks very similar like villious atrophy only in the large instestines. He thinks there is a big connection between gluten and colitis.

mle-ii Explorer
Dr. Fine got into the gluten sensitivity by way of researching UC and microscopic colitis. He said that basically microscopic colitis looks very similar like villious atrophy only in the large instestines. He thinks there is a big connection between gluten and colitis.

Having both Microscopic Colitis (Lymphocytic) and gluten sensitivity (and the gene for celiac) I agree 100% with Dr Fine's connection.

francelajoie Explorer
Hi

I go to the celiac center in boston. who are you seeing? i think you will like it there!

good luck and i hope you feel better!

Jess

Hi Jess,

I got an appointment with Dr. Cheney. I've hear really good things about her. She must be really good, I can only see her in February. I hope it all works out good. My appointment is Valentine's day. I think we're gonna stay in Boston and have a nice dinner.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,890
    • Most Online (within 30 mins)
      7,748

    glutenhater11
    Newest Member
    glutenhater11
    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

    • Ceekay
      I'm sure it's chemically perfect. Most of them taste lousy!        
    • Rejoicephd
      Hi @JulieRe.  I just found your post.  It seems that I am also experiencing thrush, and my doctor believes that I have fungal overgrowth in my gut, which is most likely candida.  I'm seeing my GI doctor next week, so I'm hoping she can diagnose and confirm this and then give me an antifungal treatment.  In the meantime, I have been working with a functional medicine doctor, doing a candida cleanse and taking vitamins. It's already helping to make me feel better (with some ups and downs, of course), so I do think the yeast is definitely a problem for me on top of my celiac disease and I'm hoping my GI doctor can look into this a bit further.  So, how about you?  Did the candida come back, or is it still gone following your fluconazole treatment?  Also, was it awful to take fluconazole?  I understand that taking an antifungal can cause a reaction that sometimes makes people feel sick while they're taking it.  I hope you're doing better still !
    • Scott Adams
      I'm so sorry you're going through this—the "gluten challenge" is notoriously brutal, and it's awful to deliberately make yourself sick when you've already found the answer. For the joint pain, many people find that over-the-counter anti-inflammatories like ibuprofen can help take the edge off, and using heating pads or warm baths can provide some direct relief for the aches. For the digestive misery, stick to simple, easy-to-digest foods (like plain rice, bananas, and bone broth) and drink plenty of water and electrolytes to stay hydrated. It feels like the longest month ever, but you are doing the right thing to get a clear diagnosis, which can be crucial for your long-term health and getting the proper care. Hang in there; you can get through this! This article, and the comments below it, may be helpful:    
    • Scott Adams
      Daura Damm (a sponsor here) uses AN-PEP enzymes and filtering in their brewing process to reduce/remove gluten, and it actually tests below 10ppm (I've see a document where they claim 5ppm). 
    • trents
      This topic has come up before on this forum and has been researched. No GMO wheat, barley and rye are commercially available in the USA. Any modifications are from hybridization, not laboratory genetic modification. Better toleration of wheat, barley and rye products in other countries is thought to be due to use of heirloom varieties of these cereal grains as opposed to the hybrids used in the USA which contain much larger amounts of gluten.
×
×
  • 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.