Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Encouragement


FruitEnthusiast

Recommended Posts

FruitEnthusiast Enthusiast

I’ve been gluten free and recovering from gluten intolerance for almost two years now. I was so sensitive to many other foods too, I’ve been one of the many on here who have had to adhere to an extremely limited diet all this time. Gluten and dairy have been out permanently from the start. I currently eat no grains at all, no nightshades.

 

My diet is stable and unchanging at this point. It’s limited to vegetables, fruit, almonds, sunflower seeds, chicken and fish. No condiments other than olive oil, lemon juice, sea salt, black pepper, evaporated cane juice crystals (very sparingly). I only eat whole foods I prepare at home, or canned/frozen fruit/veg. I haven’t eaten out or at anyone else’s house in 2 years.

 

I still find that my body is so sensitive to changes. Each time I have tried anything new I pay for 2-3 months afterward - each time the SIBO problem flares back up again. Since I also deal with a slow transit digestive issue it complicates everything. 

 

The last new food I tried was almond butter. The brand I liked changed to a pre-mixed type instead of the oil at the top type. I ate two jars of it over a month and I’m still recovering from that after for over two months. It had to have been hydrogenated which made it not only a processed food but a bad one, major oops on that one.

 

It made my SIBO start up again. I can’t tolerate the antibiotics for SIBO, or peppermint caps. The Motil Pro caps my ND just put me on that were mostly ginger made me really sick (nausea, headache) for the last two days. Better today. No more SIBO related supplements for me. My food has to be my medicine - lots of alkaline vegetables - it’s not anything to jump up for joy about, but as long as I stick to what works I don’t regret it.

 

I’m dying to use apple cider vinegar in my salad dressing! I’m afraid to - I already had a problem with mold - anything fermented or cultured - before the gluten problem. I think I’d be ok with more seasoning - garlic, paprika, cayenne, herbs. I want to buy a blend as long as it doesn’t have any grain binders in it. I’ve been told to avoid onion as it can be irritating I guess.

 

There are positive changes. I’m don’t feel sick nearly as often. The brain fog is soooo much better. I can think clearly again after all this time… in some ways that makes me more impatient to get better.

 

I’m hoping to hear from anyone who can relate to this and offer encouragement that I will be able to expand my diet at some point and move beyond this to a somewhat normal life again.


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



Celiac.com Sponsor (A8-M):



BlessedMommy Rising Star

It's hard, very hard, when you have multiple issues going on at the same time. In addition to gluten intolerance, I can't tolerate dairy either and use very little sweeteners or sugar, due to a weak immune system.

 

It sounds like you've done a really great job of stepping up to the challenge though and making the best of it! That must be incredibly difficult. 

1desperateladysaved Proficient

We share many sensitivities.  I shudder to think of trying apple cider vinegar or anything fermented!  We  began our gluten free trek about the same time.  I have had many ups and downs too.  I successfully (I think) added more foods back in after using IgG to help my gut heal and digestive enzymes to help break down my food.  I still avoid spices of nearly every kind, peppermint, and have had some memorable battles with cross contamination.  My mind is clear and I have some energy.  Still I am accessing damage and dealing with the symptoms that are left.

 

D

IrishHeart Veteran

SIBO is treated with antibiotics, probiotics, or a combination of both.

Do you take a broad spectrum probiotic?

IrishHeart Veteran

We share many sensitivities.  I shudder to think of trying apple cider vinegar or anything fermented!  We  began our gluten free trek about the same time.  I have had many ups and downs too.  I successfully (I think) added more foods back in after using IgG to help my gut heal and digestive enzymes to help break down my food.  I still avoid spices of nearly every kind, peppermint, and have had some memorable battles with cross contamination.  My mind is clear and I have some energy.  Still I am accessing damage and dealing with the symptoms that are left.

 

D

 

 

What does "using IgG to help heal my gut" mean? 

IrishHeart Veteran

FE, I am pretty sure we discussed all this with you recently on this thread here:

 

 

https://www.celiac.com/forums/topic/106681-need-a-dr-referral-in-long-beach-ca-area/#entry908507

 

You may need a doctor's help at this point. If you are still feeling poorly, something is amiss.

 

Just offering my honest, humble opinion here.

FruitEnthusiast Enthusiast

SIBO is treated with antibiotics, probiotics, or a combination of both.

Do you take a broad spectrum probiotic?

 

I tried Metronidazole, but I couldn't take the side effects, bad headaches, and I'm allergic to the other one the Dr recommended, Eurythromycin, so that was a bummer.

 

Yes, I've taken two refrigerated probiotics from a health food store daily for over a year. But, what do you mean, broad spectrum? Mine have Saccharomyces Boulardii + MOS, and the other one has 3 types of Bifidobacterium and 7 types of Lactobacillus in it. Does that sound like the right kind? There are tons of types in the case at the store. I'm taking what my Naturopathic Dr recommended, but she's been wrong before, so I don't know.

 

I haven't actually been tested for SIBO, but my digestive symptoms and BM results fit the description when I go visit the ole' bathroom. Sorry if that's TMI. I'm beyond embarrassment at this point.


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



Celiac.com Sponsor (A8-M):



FruitEnthusiast Enthusiast

FE, I am pretty sure we discussed all this with you recently on this thread here:

 

 

https://www.celiac.com/forums/topic/106681-need-a-dr-referral-in-long-beach-ca-area/#entry908507

 

You may need a doctor's help at this point. If you are still feeling poorly, something is amiss.

 

Just offering my honest, humble opinion here.

 

Not really, I had asked for Dr referrals before. I have a GI and an ND already who have tried their best. Gotta Ski said the Doctors at UCLA were best with newly diagnosed people. I find more helpful info here than at the Dr, anyway so that's why I'm asking for input.

IrishHeart Veteran

 

 

I haven't actually been tested for SIBO, but my digestive symptoms and BM results fit the description when I go visit the ole' bathroom. Sorry if that's TMI. I'm beyond embarrassment at this point.

 

If you have not been tested for SIBO, I would not assume that is what you have, hon.

GottaSki Mentor

Not really, I had asked for Dr referrals before. I have a GI and an ND already who have tried their best. Gotta Ski said the Doctors at UCLA were best with newly diagnosed people. I find more helpful info here than at the Dr, anyway so that's why I'm asking for input.

 

Actually, what I said is Dr. Harmon is an excellent celiac doctor and still may be the best choice if you want to establish care with a gastro that has celiac knowledge.

 

I stand by that -- if you are not improving, you need an excellent team of doctors -- a Primary that will think outside the box - or at least consider all possibilities, along with the best Gastro and Allergist you can find - again -- in my opinion.

 

"You are in a bit of a pickle....I would hate for Dr. Harmon to be a wasted effort as he does specialize in Celiac Disease and you are well beyond wanting celiac testing as you already live completely gluten-free...perhaps there is a gastro that has more experience with SIBO...or maybe you should ask your primary to order a SIBO test for you?

 

I still think Dr. Harmon is an excellent choice if you want to establish care with a gastro that has extensive celiac knowledge."   pulled from FE's doctor request thread

FruitEnthusiast Enthusiast

I’ve been gluten free and recovering from gluten intolerance for almost two years now.

I’m hoping to hear from anyone who can relate to this and offer encouragement that I will be able to expand my diet at some point and move beyond this to a somewhat normal life again.

 

Thanks so much Irish Heart and Gotta Ski for your input on SIBO. I will look into that further. I hadn't really intended that to be the subject of this post but I really appreciate you catching that. The Doctor's I've seen haven't been too helpful so far, but I can look further to see if I can find anyone with more experience with gluten/Celiac. Looks like UCLA is the best place to start. I have an appointment there already. I'll try to have more of an open mind about what they have to offer.

 

I'm still interested in hearing from anyone who can offer understanding and encouragement because I start to feel sad sometimes going through this so long and I really wanted to hear someone tell me that they've gone through it and come out on the other side. I believe I will get through it, but it helps to have company along the way and to hear from anyone who's beyond where I am now.

GottaSki Mentor

Ah...gotcha ;)

 

In my opinion, this place never disappoints to support those that need a little encouragement.

 

Good luck to you....I do hope you are feeling better very soon. :)

FruitEnthusiast Enthusiast

It's hard, very hard, when you have multiple issues going on at the same time. In addition to gluten intolerance, I can't tolerate dairy either and use very little sweeteners or sugar, due to a weak immune system.

 

It sounds like you've done a really great job of stepping up to the challenge though and making the best of it! That must be incredibly difficult. 

 

Thank you for your kind, understanding, and supportive response, it's what I needed to hear most of all :)

NoGlutenCooties Contributor

I had an overgrowth of bad bacteria years ago - no one mentioned "SIBO" but it was determined via a stool test.  The normal number for the bad bacteria was under 200 and I was at over 12,000.  I had absolutely no interest in antibiotics as they do not discriminate and just kill everybody and I blame them for the problem in the first place.  The chiropractor I was seeing at the time suggested Colosan.  It is a magnesium-oxide powder that breaks down in the intestine.  When it breaks down it releases magnesium and oxygen.  The magnesium helps bowel function (a little too much if you take more than the recommended dose) and the oxygen kills the bad bacteria while it feeds the good bacteria.  This works because the bad bacteria are anaerobic and die when exposed to oxygen, but the good bacteria actually thrive on oxygen.  It took 6 months for my bad bacteria number to come down from 12,000 to about 1,000 and another few months to get back down under 200.

 

I don't remember what the stool test was or what the numbers mean - this was over 20 years ago.  But the Colosan really works and it's gentle - as long as you ease into it and don't take too much.  I was only taking about 1 teaspoon per day, once a day.

FruitEnthusiast Enthusiast

Thank you, yes what I have is an overgrowth of bad bacteria, I think I wont try to give it a name. I cured it once already through diet using alkaline foods, green smoothies, staying away from sugar, I don't even drink juice anymore. It does take time, lots of time.

 

I was doing really well, then I gave my ex husband another chance which threw off my diet all over again as he wanted to make my food more interesting. He's back out of the picture for six months now after being back together a year. He was going to take care of me but instead it was a year of extreme stress and just backslide in general. It added a year and a half to my recovery time! Now I live alone again and I can focus on me. I'm back to the alkaline foods and I am having progress, just slow.

 

Each time I try to speed up the healing time with a supplement I have a bad reaction that makes me feel worse. I am very sensitive and have slow digestion to begin with. The Colosan sounds interesting, I'm really glad to know about it.  I know I can tolerate magnesium, I take it every day already. I do have a problem with anything that tries to move too fast through me as my body can't cope and it causes severe internal distress. It's amazing how many health professionals you can see and still not get all the info.

 

I still haven't had a stool test. My naturopath insisted that the basic stool test most people get wouldn't be conclusive enough, even though I asked for it several times. She insisted I get one that costs $400 (which I can't afford) to pinpoint exactly the type of bacteria in order to treat it. My GI seems really good but he didn't suggest a stool test, he just wrote a prescription for antibiotics. I don't like to take them either, then when I did the side effects were too awful to tolerate.

 

I think I know what the problem is and I know what to do for it, and I just have to be patient. I got myself well once already doing what I'm doing now. I'm reluctant to try new doctors because they generally just get in there and try new things to speed up my healing which just make me feel worse. Most recently it was the ginger caps. I'm still recovering from that days after stopping them.

 

You said it took six months plus for you to get your bacteria imbalance under control, which helps me tremendously. It takes time to heal, just like I keep saying. It helps me to keep going and not be alarmed by the slow process. It is what it is. I find rest, lots of sleep, and keeping stress to a minimum help as much as anything. Those things help me feel well enough to take my walks which keep my spirits up as well. Thanks so much.

ashleigh2 Newbie

Hey there! I am so sorry to hear about your continuing frustrations and problems with food. It can be very challenging and I wish I could wave a magic wand and make this all disappear for you, but I unfortunately cannot. 

 

While reading your original post, I felt that you were victimizing yourself-you don't want to do that! Many other people out there suffer exactly the same way you do-you are not alone in this, I promise you that. Empower yourself by focusing on what is working, not letting the negativity in, and know.. this too shall pass. 

 

It sounds like you have an extremely restricted diet. Are the foods you are avoiding being avoided because you have been tested for allergies or because you felt they were not good for your body? Adding foods and eliminating foods with the help of a professional can actually be more detrimental to your health. If you take away a food for too long, you can actually create an intolerance to it, making it harder to add back in later. If you take away certain foods because you believe it to be a trigger, when in fact it is something else, well then that's no good either. I highly recommend working with a trained professional in gluten awareness, an allergist, herbalist, naturopathic doctor, or someone who truly understands what your needs are. 

 

Don't limit yourself to avoid going out to eat, not visiting friends, ect..that can actually increase the anxiety and depression around food, and only hinder your healing even more! You don't want that and we don't want that for you! Happy people heal faster. Bring your own foods, carry snacks, eat before you go out, and educate your friends about your dietary choices so you can have more fun living a fulfilling life!

 

Lastly, don't let others feel sorry for you. You need to gain the right perspective. Enjoy the time with your friends and family without putting all this pressure around food. Make it about the company, not about what's being served. Remember why you are doing all of this-to improve your health. 

 

You will heal, you will get better, you will get through this. You may not be able to do it alone, and thats ok!! reach out to professionals and get the help you truly deserve! 

IrishHeart Veteran

. If you take away a food for too long, you can actually create an intolerance to it, making it harder to add back in later. If you take away certain foods because you believe it to be a trigger, when in fact it is something else, well then that's no good either. I highly recommend working with a trained professional in gluten awareness, an allergist, herbalist, naturopathic doctor, or someone who truly understands what your needs are.

With all due respect, this is simply untrue. That is not how food intolerances work at all.

 

If I do not eat lobster or watermelon for months on end, I do not "suddenly trigger an intolerance". Intolerances occur when someone is actively eating the food protein.

 

In fact, on an elimination diet, the only way to know for sure you have a food intolerance of any kind, is by taking a food protein out for 3-6 months which  may diminish the reactions to that food and then, you can add it back in to see if you have less of a reaction. Every health care professional I know  agrees this is how it works. 

 

Who exactly is a "trained professional in gluten awareness"? I am thinking that some of us with celiac who have walked this path for awhile may qualify for that "title".

:)

FruitEnthusiast Enthusiast

While reading your original post, I felt that you were victimizing yourself-you don't want to do that! Many other people out there suffer exactly the same way you do-you are not alone in this, I promise you that. Empower yourself by focusing on what is working, not letting the negativity in, and know.. this too shall pass. 

 

Don't limit yourself to avoid going out to eat, not visiting friends, ect..that can actually increase the anxiety and depression around food, and only hinder your healing even more! You don't want that and we don't want that for you! Happy people heal faster. Bring your own foods, carry snacks, eat before you go out, and educate your friends about your dietary choices so you can have more fun living a fulfilling life!

 

Lastly, don't let others feel sorry for you. You need to gain the right perspective. Enjoy the time with your friends and family without putting all this pressure around food. Make it about the company, not about what's being served. Remember why you are doing all of this-to improve your health. 

 

You may not be able to do it alone, and thats ok!! reach out to professionals and get the help you truly deserve!

 

Wow your description of me sounds like someone else. I am one of the most positive people I know. I keep expecting to be well each time I have a good day because I'm such an optimist. I've had to learn to wait and see if the good lasts or I'm let down.

 

This is one place we can be real about what we are going through. I am so sick and exhausted that I have been unable to work in a year. I'm not choosing to stay home, some of us are sick enough from this that we don't yet have the choices you seem to have. I don't have the energy to even shop for my own food lately. So telling me to "get out and have fun" is not exacty... well, helpful. I can see I haven't been as forunate as you have in finding the right healthcare professionals so I'm still working on that. I'm very happy for you that things seem to be going so well for you and I am going to find encouragement in that for my future. I'm sure you meant well, but it came across to me, uh... a bit insulting. I think it's important to remember to be sensitive with those of us who are still very ill. Thanks just the same. Take care.

GottaSki Mentor

Wow your description of me sounds like someone else. I am one of the most positive people I know. I keep expecting to be well each time I have a good day because I'm such an optimist. I've had to learn to wait and see if the good lasts or I'm let down.

 

This is one place we can be real about what we are going through. I am so sick and exhausted that I have been unable to work in a year. I'm not choosing to stay home, some of us are sick enough from this that we don't yet have the choices you seem to have. I don't have the energy to even shop for my own food lately. So telling me to "get out and have fun" is not exacty... well, helpful. I can see I haven't been as forunate as you have in finding the right healthcare professionals so I'm still working on that. I'm very happy for you that things seem to be going so well for you and I am going to find encouragement in that for my future. I'm sure you meant well, but it came across to me, uh... a bit insulting. I think it's important to remember to be sensitive with those of us who are still very ill. Thanks just the same. Take care.

 

I agree completely with this statement.

 

For those of us that do not heal right away -- no one has the right to suggest we are not trying hard enough. 

 

Sorry, I had enough of that prior to diagnosis - I will never let someone suggest that to me again.  Glad you did not.

 

Hang in there FE!

FruitEnthusiast Enthusiast

Thanks for your support GS!!!

ashleigh2 Newbie

With all due respect, this is simply untrue. That is not how food intolerances work at all.

 

If I do not eat lobster or watermelon for months on end, I do not "suddenly trigger an intolerance". Intolerances occur when someone is actively eating the food protein.

 

In fact, on an elimination diet, the only way to know for sure you have a food intolerance of any kind, is by taking a food protein out for 3-6 months which  may diminish the reactions to that food and then, you can add it back in to see if you have less of a reaction. Every health care professional I know  agrees this is how it works. 

 

Who exactly is a "trained professional in gluten awareness"? I am thinking that some of us with celiac who have walked this path for awhile may qualify for that "title".

:)

 

 

Well it's a good thing I didn't mention anything about lobster or watermelon then huh?? You are correct, food intolerances happen when a person eats the trigger food but it can happen if you do not consume that food for a period of time. Everyone's body is different and I'm not saying it will happen to everyone who doesn't eat a certain food for a certain amount of time, its called bioindividuality.  With all due respect you are entitled to your opinions but this is in fact a truth. This is my field of study and I make a living helping others go gluten free, many who have celiac. I am a trained professional in gluten awareness, that's who! Just because I wasn't diagnosed with Celiac does not mean I haven't walked a very hard and difficult path on my journey towards becoming gluten-free. I've been gluten-free for over 3 years and think I have gained enough experience and helped enough people to be able to be called a gluten free expert :) plus I went to school for this :)

ashleigh2 Newbie

Wow your description of me sounds like someone else. I am one of the most positive people I know. I keep expecting to be well each time I have a good day because I'm such an optimist. I've had to learn to wait and see if the good lasts or I'm let down.

 

This is one place we can be real about what we are going through. I am so sick and exhausted that I have been unable to work in a year. I'm not choosing to stay home, some of us are sick enough from this that we don't yet have the choices you seem to have. I don't have the energy to even shop for my own food lately. So telling me to "get out and have fun" is not exacty... well, helpful. I can see I haven't been as forunate as you have in finding the right healthcare professionals so I'm still working on that. I'm very happy for you that things seem to be going so well for you and I am going to find encouragement in that for my future. I'm sure you meant well, but it came across to me, uh... a bit insulting. I think it's important to remember to be sensitive with those of us who are still very ill. Thanks just the same. Take care.

I didn't mean to be insulting. I'm sorry it came across that way. My "tough love" style isn't for everyone

kareng Grand Master

Well it's a good thing I didn't mention anything about lobster or watermelon then huh?? You are correct, food intolerances happen when a person eats the trigger food but it can happen if you do not consume that food for a period of time. Everyone's body is different and I'm not saying it will happen to everyone who doesn't eat a certain food for a certain amount of time, its called bioindividuality. With all due respect you are entitled to your opinions but this is in fact a truth. This is my field of study and I make a living helping others go gluten free, many who have celiac. I am a trained professional in gluten awareness, that's who! Just because I wasn't diagnosed with Celiac does not mean I haven't walked a very hard and difficult path on my journey towards becoming gluten-free. I've been gluten-free for over 3 years and think I have gained enough experience and helped enough people to be able to be called a gluten free expert :) plus I went to school for this :)

Please provide some real scientific basis for this statement of fact - "it can happen if you do not consume that food for a period of time."

Also, please explain how a a person is a "trained professional in gluten awareness,". Is that a med school field?

IrishHeart Veteran

Well it's a good thing I didn't mention anything about lobster or watermelon then huh?? You are correct, food intolerances happen when a person eats the trigger food but it can happen if you do not consume that food for a period of time. Everyone's body is different and I'm not saying it will happen to everyone who doesn't eat a certain food for a certain amount of time, its called bioindividuality.  With all due respect you are entitled to your opinions but this is in fact a truth. This is my field of study and I make a living helping others go gluten free, many who have celiac. I am a trained professional in gluten awareness, that's who! Just because I wasn't diagnosed with Celiac does not mean I haven't walked a very hard and difficult path on my journey towards becoming gluten-free. I've been gluten-free for over 3 years and think I have gained enough experience and helped enough people to be able to be called a gluten free expert :) plus I went to school for this :)

 

Well, I started out with the words "with all due respect" but you've come back with a few posts that are already abrasive.

I suggest two things: When you come into an established community of forum members, you start out on the right foot.

(1) You don't tell people they are "victimizing themselves" and (2) you don't state things as facts without evidence.

That's not how we roll on here. This is just IMHO, of course.

 

To use your same argument: I've been gluten free for over 3 years and I've helped enough people to be called a gluten expert, too. Yet, but I don't start out "helping" with a new group of people by telling them what I think about them and I certainly don't give wrong info. (at least I try very hard not to)

 

What "school" did you attend that makes you any more qualified? As far as I know, there are no accredited schools offering degrees in "gluten" or celiac.

 

GottaSki Mentor

I didn't mean to be insulting. I'm sorry it came across that way. My "tough love" style isn't for everyone

 

You are a brand new member here.  I find nothing "light" or "loving" about your comments.  "Tough Love" has to come from someone that has established respect with the intended recipient.  You have not established this here.

 

While you may think you understand what it is like to have Celiac Disease because you removed gluten and feel better....I can tell you from personal experience that problems associated with this disease do not always have a simple solution.  

 

If you are here to further your understanding of a very complicated disease - great, there are many of us that have researched Celiac Disease along with its various associated diseases, disorders and complications for many years.  

 

Feel free to read, learn and ask questions, but if you choose to respond in the same condescending manner or refuse to provide sources for unsupported claims that we have seen in your introductory posts, you will not be welcome here.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,878
    • Most Online (within 30 mins)
      7,748

    Donna petrie
    Newest Member
    Donna petrie
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      71.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for sharing, Karen. Certainly a needed reminder what we already knew (and I've posted many times on this forum) but sometimes forget, namely, autoimmune disorders tend to cluster. Where one is found, you can look for others to show up eventually. The thing that is unusual in your son's case is the onset of several of them at such a young age. My sister in law, who is in her early 60's has Crohn's and struggles with constipation so I don't think that is unusual with Crohn's. If nothing else, it's the outcome of not eating much because of the pain. Now that you know what is going on with your son and the Crohn's, we hope he is beginning to improve.
    • Nathan.
      Hi there. My son is turning 16 this month. He had an endoscopy and biopsy to confirm celiac. He went gluten-free and his pain never got any better. I think it got worse. Months went by. The pain started around 7th grade. He missed a lot of school in 8th grade, and a whole lot in 9th grade. He couldn't go to school in 10th grade. All along the gastroenterologist prescribed Hyoscyamine, didn't help at all. Cyproheptadine, no less pain. Peppermint oil, ginger, Miralax, Senna. Doc said he was constipated, but I couldn't get him to have Miralax daily. Eventually he went on Linzess and no senna or Miralax. Sorry this is long, there will be a point.  We gave his school not just a doctors not, but everything, and U of M makes a lot of notes. They still turned us in for Truancy.  I didn't get him enrolled in online school fast enough.  The school would not recommend an online school and i didn't know which one to choose.  Doc thought it was nerve pain and mental. He recommended the u of m my pain program.  Nathan did so good, 3 days a week supposed to be for 4 weeks.  Never missed, always on time.   After two weeks, they discharged him. Said it was not  benefitting him.  Pain went on. I had been asking if there were any other test they could do. Ultrasound, colonoscopy. Doc said we can do it, but I don't think we'll find anything.  Finally he had a colonoscopy and another endoscopy.  Guess what, they did find something. They found a ton of tiny ulcers everywhere, from the esophagus to his rectum. They think Crohn's. I understand they didn't check for that because he was more constipated, not much diarrhea. He is getting an MRI with contrast on Sunday. Also they want him to do a cal-protectin (give a poop sample). Then an appointment on the 16th to talk about treatment. Then the probation officer on the 17th. In the meantime he is taking Budesonide extended release.  $276.00 for 30 pills, and that's with insurance. Also he was diagnosed with hyperthyroidism, Graves disease a few months ago. If it is for sure Crohn's,  it will be three autoimmune diseases. If someone is gluten-free for a month or more, and the pain is no better, don't stop looking. I was beside myself. Did they think he was exaggerating, lying? I was considering taking him to a holistic doctor, who would probably recommend Peppermint oil and ginger.  He's such a good kid. Kind of an introvert. He was on the 9th grade soccer team. He would try to go to practice and kept having to stop, the pain was that bad. Every time he ate, it didn't matter what, gluten-free chicken tenders, mac and cheese, pizza, ice cream, all gluten-free, he would eat a normal amount but stop and say, I can't eat anymore, my stomach hurts.  If anyone reads all this, thank you. I had a gut feeling, no pun intended, that he had an additional problem. They found celiac and stopped looking. If you don't feel better, keep on your doctor to check further, keep looking.   Take care, Karen  
    • Scott Adams
      Most likely cross-contamination I believe.
    • cristiana
      I think it takes different people different amounts of time, but in my own case I had pain,  bloating and loose stools for some time, exacerbated by a lactose intolerance, which eventually went.  I would say the really bad diarrhea got better quite quickly, but the bloating pain carried on for a few months, until I was told to give up lactose for a few weeks.  That helped enormously and once I realised milk and yoghurt was the cause, after a short break I went back to lactose very gradually and felt a lot better.  Now I can tolerate it well. From Coeliac UK "The enzyme lactase is found in the brush border of the small intestine. This is why people with coeliac disease can be deficient in lactase at diagnosis. Once established on a gluten free diet, the gut is able to heal and lactose digestion returns to normal. Lactose intolerance is therefore usually temporary." So if this helps your daughter, this doesn't mean you have to give up lactose forever, especially as dairy is such a good source of calcium for growing kids.   Bear in mind you should be able to reintroduce it. As for fatigue, this can be due to vitamin and mineral deficiencies,such as iron, vitamin D and B12.  Were these levels tested?  If not, I would suggest you get them done.  If your daughter is deficient in these, it is vital you address the deficiencies, and get the tests redone in a few months, particularly the iron, because too much can be dangerous.
    • knitty kitty
      Hello,   The medication in these inhalers can cause a thiamine deficiency if used by someone already low in thiamine.  We don't absorb sufficient amounts of vitamins and minerals due to the inflammation and damage done to our villi in Celiac Disease.  Even a long term strict gluten free diet may not provide sufficient amounts of vitamins and minerals.  There are eight B vitamins that all work together.  Thiamine deficiency often shows up first because our bodies use so much of it and it can't be stored very long. Thiamine deficiency symptoms can appear in as little as three days.  Without thiamine, the other B vitamins may not be able to function properly.   Thiamine is needed to clear lactic acid accumulation caused by the inhalers: Shoshin beriberi provoked by the inhalation of salbutamol https://pubmed.ncbi.nlm.nih.gov/12951730/    Significant Lactic Acidosis from Albuterol https://pmc.ncbi.nlm.nih.gov/articles/PMC5965110/ Albuterol-Induced Type B Lactic Acidosis: Not an Uncommon Finding https://pmc.ncbi.nlm.nih.gov/articles/PMC7263006/ Lessons of the month 1: Salbutamol induced lactic acidosis: clinically recognised but often forgotten https://pmc.ncbi.nlm.nih.gov/articles/PMC6964186/ An Overview of Type B Lactic Acidosis Due to Thiamine (B1) Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC10731935/   Thiamine has antifungal and antibacterial properties.  Thiamine helps keep Candida in check.  Thiamine helps keep SIBO in check.  Thiamine helps with black mold, Aspergillis infection.  Riboflavin helps fight Candida infection in the mouth. Riboflavin Targets the Cellular Metabolic and Ribosomal Pathways of Candida albicans In Vitro and Exhibits Efficacy against Oropharyngeal Candidiasis https://pubmed.ncbi.nlm.nih.gov/36625571/   Thiamine deficiency can make ones voice hoarse and can cause localized edema.  Niacin deficiency can make ones voice hoarse.  (Niacin deficiency and Thiamine deficiency can each cause irritability, agitation, and lability.) Hoarseness in pellagra https://pubmed.ncbi.nlm.nih.gov/21507655/ Hidden Hunger: A Pellagra Case Report https://pmc.ncbi.nlm.nih.gov/articles/PMC8152714/   Anesthesia can cause B12 deficiency.  B12 deficiency can show up as mouth sores and geographic tongue, diarrhea, and dementia. Vitamin deficiency, a neglected risk factor for post-anesthesia complications: a systematic review https://pmc.ncbi.nlm.nih.gov/articles/PMC11823251/ Neurologic degeneration associated with nitrous oxide anesthesia in patients with vitamin B12 deficiency https://pubmed.ncbi.nlm.nih.gov/8250714/ Subacute combined degeneration of the spinal cord following nitrous oxide anesthesia: A systematic review of cases https://pubmed.ncbi.nlm.nih.gov/30144777/ The Effect of Vitamin B12 Infusion on Prevention of Nitrous Oxide-induced Homocysteine Increase: A Double-blind Randomized Controlled Trial https://pmc.ncbi.nlm.nih.gov/articles/PMC4052402/     Eating a diet that is heavy in carbohydrates can precipitate a thiamine deficiency.  As the amount of carbohydrates consumed increases, additional thiamine is needed, otherwise the carbs will be stored as fat.   Thiamine deficiency disorders: a clinical perspective https://pmc.ncbi.nlm.nih.gov/articles/PMC8451766/   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/   The deficiency symptoms of some of the B vitamins cause gastrointestinal symptoms that resemble the same symptoms as when being glutened.   Thiamine deficiency can present as vomiting, diarrhea and abdominal pain (Gastrointestinal Beriberi).  Niacin deficiency can present as diarrhea (Pellagra = diarrhea, dermatitis, dementia, then death ).  B12 deficiency can present as diarrhea or dementia.  Not everything is caused by hidden gluten.  Gluten free processed foods are not required to be enriched with vitamins lost in processing like gluten containing foods are. Blood tests are not accurate measurements of vitamin levels, but do talk to your doctor and nutritionist about supplementing with the eight B vitamins, Vitamin C, the four fat soluble vitamins and minerals like magnesium.  Your physician can give you a shot of B12 before anesthesia administration.   By the way, Celiac Disease genes have been traced back to having originated in Neanderthals.  I'm not a singing teacher on the net.  I earned a degree in Microbiology after studying nutrition because I wanted to know what vitamins are doing inside the body.  I've experienced nutritional deficiencies myself. Hope this helps!  Keep us posted on your progress!
×
×
  • Create New...