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

Self-diagnosis


welshy

Recommended Posts

welshy Newbie

I'm pretty sure i'm intolerant to gluten and dairy as a couple of years ago i went gluten and mostly dairy free for a year and all my IBS (constipation and bloating pre-dominant) symptoms cleared up and i had regular menstrual cycles for the first time in 5 years! Since then i haven't been able to stick to this diet as i go in and out of believing that i have these intolerances as i've never been formally tested as my doctor won't. However, ultimately i'm certain that i'm gluten and dairy intolerant (and potentially soy intolerant) but i found the diet so limiting and lost almost a stone in weight. Whilst the weight loss was nice i'd didn't feel that it was naturally me. Plus, i hate being awkward when i'm eating out or over a friend's house and feel guilty about subjecting my husband to my dietary limitations. Consequently a week hasn't gone by when i don't suffer with IBS like sypmtoms, depression, anxiety and fatigue. Yet i can't seem to return to this diet because i'm afraid of it being so limiting and losing weight again. Plus i can't seem to muster up the will power. Can anyone else relate to this? Am i being ridiculous? I suppose ultimately my health is the most important thing and my husband and i want to start a family this year so i'm desperate to get my symptoms under control before then. I'm glad i've found this forum and hope that someone can offer advice and reassurance. Thanks


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



Celiac.com Sponsor (A8-M):



par18 Apprentice

Note quite sure what it is you are looking for in terms of support. If in fact you do have undiagnosed Celiac/gluten intolerance then the only way your symptoms will subside is that you start and "stay" gluten free from now on. That said if it is mainly a question of willpower and the only way you feel you would be compliant (and your husband supportive) is with a doctor's diagnosis then I guess you should continue to eat gluten and maybe you will be able to obtain one. The one thing I would not advise is to repeatedly start and stop eating gluten while you are trying to get diagnosed. This will only confuse anyone trying to determine what is wrong. If the only way you get relief is when you eliminate gluten (and dairy) from your diet then what does that tell you? Concerning yourself with the social implications of the diet at this point should be the least of your worries. As far as the husband aspect is concerned has he indicated that he would not support you if you had to adopt this diet. The most important thing should be to figure out what is wrong and then address those other issues later. I can appreciate how inconvenient this lifestyle is as I have been doing it for almost 3 years now. I do however appreciate the fact that my "IBS" symptoms are gone and have not returned since going gluten free. That alone for me makes this lifestyle "worth it". Thousands if not millions of people do this every day so you will not be alone. So far you have already succeeded in finding this website and asking for help. Also this website is open worldwide 24/7 so there is a good chance someone is always online to answer questions or offer advice. As far as losing or gaining weight I was only able to gain weight "after" going gluten free and having my gut heal to the point I was absorbing again. Hope this helps and good luck.

Tom

welshy Newbie

Thanks for your reply Tom. Not really sure what i'm looking for either! I suppose i was just introducing myself and explaining my struggles with what i'm certain is a gluten and dairy intolerance. I think i've finally got to the point where i don't feel a doctor's diagnosis is necessary. My husband is supportive and agrees that the diet is the way forward so i guess the only think i need to do is accept that is going to have to be a way of life for me and get on with it. This is the hardest part for me i think. I desperately want to feel well again and energised so i have to remind myself of this in order to stick to the diet. As ridiculous as it sounds, the real thing i struggle with in terms of the diet is what to eat for a packed lunch in work! Breakfast and dinner aren't a problem because they're always gluten and dairy free, it's just what to take into work for lunch?

missy'smom Collaborator

For some inspiration, check out this site and her list of links.

Open Original Shared Link

This is how I pack a lunch for my son everyday(6 days a week) and how I pack food for myself in various situations. The recipes and foods on these sites are not all gluten-free but you can take away the concept and adapt some recipies to gluten-free. I spend only 10 min. tops in the morning preparing it. OK, rice takes longer than 10 min. but it can cook unattended. I keep a stash of homemade convenience foods, like meatballs, in individual portions in the freezer and warm up or deep fry in the am., add some rice or pasta freshly cooked in the am and fruit and fresh or frozen veg. and we're go to go.

cinnamonroll Newbie

Also, if you still want a diagnosis but don't want to go back on gluten, since it seems like you are feeling better, something I read about on these forums is enterolab (Open Original Shared Link), they can do a stool test, which they say is more sensitive than a blood test, and you can be off gluten for up to a year I believe and still get accurate results. I want to get this, even though I am pretty sure, the scientist in me needs proof to back it up. I'm just waiting to get a job that pays more because I"m pretty sure my insurance won't cover it.

glutenfreemeg Newbie

Hi Welshy,

I registered today just so I could reply to your post, because I feel like I'm in the same boat and wanted someone to commiserate with! I'm sort of self-diagnosed as well, I've been gluten-free for 5 weeks now and I feel so much better. But since I don't have an actual diagnosis from my Dr, once in awhile I question my decision to eat gluten free and I think I'm just being obsessive about it. I really do feel better, but there's been a handful of days in these last 5 weeks where I have a bit of my symptoms back, and sometimes I don't know if I accidently ingested gluten, or if my symptoms are related to something else. I haven't been cheating, but sometimes I feel kind of silly being so strict about this diet when I don't really know for sure that gluten is my problem. (Okay, I'm pretty darn sure that gluten is my problem, I just would feel more confident if a scientific test told me that.)

This whole gluten free journey has been a bit of a mental journey for me as well. I'm just trying to make the decision to stick with this for long run. Sometimes I think I should eat a huge pile of whole wheat bread to test myself, but in my head I already know that would knock me out on the couch with a bloated stomach and painful gas cramps, so why do it.

So, while I don't have any great ideas for you, just wanted to let you know that I don't think you're ridiculous! I feel the same way and I question myself all the time. But really, in the end it's all about the results, and since my results have been mostly good, I'm sticking with this for now. Feel free to share any other frustrations! I totally understand!

Megan

Glutina Rookie

Hi! My story is similar...I am posting a thread about it in fact right after this...but just a quick recap: I am basically a self-disgnosis as well, with the encouragement of my doctor (explains in my thread) because my blood test came back negative...but between the time that I had an ultrasoudn and the follow up appointment, I went gluten free and feel so much better! I understand the whole thought process of "wow...this is a lot of work for a self-diagnosis"...but really, you are the only one who TRULY knows what feels right and helps your symptoms. Trust your body!

-Glutina:)


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



Celiac.com Sponsor (A8-M):



wowzer Community Regular

Hi, It sounds to me like you know you are celiac. I had a negative blood test, but still went gluten free because I had so many symptoms. My symptoms leaned more toward DH. When I look back before going gluten free, I was avoiding a lot of it anyway. Probably why my test was negative. For me over the years I had many unexplained very itchy rashes diagnosed as many different things. All I know is that I don't want to itch like that again, so it is gluten free for me. Even my family doctor saw improvement in me after a few weeks, so he said stay on the diet. Now I try to avoid gluten, but somehow it seems to find me. Hersheys/Cadbury candy being the latest. Grrrrr. To me seeing the positive results are well worth the hassles. Good Luck

welshy Newbie

Hi Megan,

Many thanks for your reply- it's so good to know that there's someone else in the same boat. At the mo i'm working up to a completely gluten free diet - not quite there yet as i'm eating oats. I suspect that as soon as i've cut them out i'll feel much better. I'm also barely eating dairy- just have milk in my tea/coffee. I keep going back and for because i don't trust my own self-diagnosis even though i know it's right. I've actually tested my diagnosis and eaten a sandwich and the cramps, bloating, exhaustion and constipation as a result so aren't worth it. This has definitely confirmed to me that gluten free is the way to go (i still get cramps and bloating from oats but nowhere near as bad). So i definitely share what a mental journey it is with you! I too would feel more confident with a doctor's diagnosis but I don't think i'll get an accurate one, even if i could persuade him to give me the test - which is a massive task in itself. Therefore, i have resolved to be strong-minded and just go completely gluten-free- you're so right, the results do speak for themselves we just need to be confident with that. The mind - body battle is a tough one!

Thanks Megan, it's great to know i'm not alone.

Sarah

welshy Newbie

Dear all,

Thank you so much for your replies. They were really encouraging and i feel more able to continue on my gluten free journey. Thanks again :)

glutenfreemeg Newbie

No Problem! :) You could always try gluten-free oats, I love my oatmeal so I bought a bag of those.

Nancym Enthusiast

Here's how I look at it.

There's the trade-off of your long-term health versus your habits and convenience. Eventually you could be looking at diabetes, lymphoma, colon cancer, liver failure, memory and brain issues and many autoimmune diseases. Basically an unhappy, severely compromised physical state for the rest of your life. Thinking long term, you might be on a colostomy bag, needing to use a walker, having to test your blood sugars all day long, be on the waiting list for an organ donation, in and out of hospitals and doctor offices, in dreadful physical pain from autoimmune arthritis and having to suppress your immune system with drugs (to the point you could die from a common cold) not to forget being constantly tormented by the symptoms of IBS. These are all some of the awful things that strike gluten intolerant people.

Maybe if you think on that awhile you'll find the strength to change your eating habits permanently. If not, go hang out in a nursing home for awhile and you can probably find a lot of people there suffering the end results of a poor diet. So many people don't know why they're ill and they suffer in ignorance, but you know why you suffer. You could change your destiny.

When I look at gluten food I say to my "poison". It works.

Phyllis28 Apprentice

I pack my lunch for work 5 days a week. For me, leftovers are the key to eating lunch. I make extra when I cook and package them into single portion meals. I reheat them in the microwave at work.

Also, I use a large softsided lunchbox or softsided can cooler for lunch. I put in BlueIce Mats to keep everything cold. That way I have everything at my desk and don't have to use the shared refrigerator.

I choose to stay gluten free to feel well and maintain my longterm health. I don't like being sick and gluten makes me sick.

welshy Newbie
Here's how I look at it.

There's the trade-off of your long-term health versus your habits and convenience. Eventually you could be looking at diabetes, lymphoma, colon cancer, liver failure, memory and brain issues and many autoimmune diseases. Basically an unhappy, severely compromised physical state for the rest of your life. Thinking long term, you might be on a colostomy bag, needing to use a walker, having to test your blood sugars all day long, be on the waiting list for an organ donation, in and out of hospitals and doctor offices, in dreadful physical pain from autoimmune arthritis and having to suppress your immune system with drugs (to the point you could die from a common cold) not to forget being constantly tormented by the symptoms of IBS. These are all some of the awful things that strike gluten intolerant people.

Maybe if you think on that awhile you'll find the strength to change your eating habits permanently. If not, go hang out in a nursing home for awhile and you can probably find a lot of people there suffering the end results of a poor diet. So many people don't know why they're ill and they suffer in ignorance, but you know why you suffer. You could change your destiny.

When I look at gluten food I say to my "poison". It works.

That's actually a really helpful way of looking at it. I'm so going to tell myself that it's poison everytime i eat gluten. To be honest, over the last few weeks whilst eating some gluten (but not wheat) i'm just been feeling sicker and sicker and getting more and more exhausted. So am now thoroughly fed up with this state and can't wait to see results from going gluten free (which i know will work because in the past when i was gluten free for a year i've never felt so well!). Can't wait :)

MJK Newbie
I'm pretty sure i'm intolerant to gluten and dairy as a couple of years ago i went gluten and mostly dairy free for a year and all my IBS (constipation and bloating pre-dominant) symptoms cleared up and i had regular menstrual cycles for the first time in 5 years! Since then i haven't been able to stick to this diet as i go in and out of believing that i have these intolerances as i've never been formally tested as my doctor won't. However, ultimately i'm certain that i'm gluten and dairy intolerant (and potentially soy intolerant) but i found the diet so limiting and lost almost a stone in weight. Whilst the weight loss was nice i'd didn't feel that it was naturally me. Plus, i hate being awkward when i'm eating out or over a friend's house and feel guilty about subjecting my husband to my dietary limitations. Consequently a week hasn't gone by when i don't suffer with IBS like sypmtoms, depression, anxiety and fatigue. Yet i can't seem to return to this diet because i'm afraid of it being so limiting and losing weight again. Plus i can't seem to muster up the will power. Can anyone else relate to this? Am i being ridiculous? I suppose ultimately my health is the most important thing and my husband and i want to start a family this year so i'm desperate to get my symptoms under control before then. I'm glad i've found this forum and hope that someone can offer advice and reassurance. Thanks

Hi

I found out by accident really that i was gluten intolerant. I went on a low carb diet to lose weight and realized in about a week that my sugar was not going low...I had no bloating and my years of awful gas was gone..... my migranes gone and many more things. I went back on bread and all the other stuff and wham right back to what i was. I went to the doctor and asked for tests and he said he does not believe in testing that i know I need to be off them and that is end of story. I too went off the diet cause i thought why do it with out a diagnosis when the extra money could go to my kids. I have one boy with chronic constipation and one boy with severe eczema...so now i want them tested and again...does not believe in it. I am now on a gluten free diet for 6 weeks...i feel great...I will not come off it again.

Mk

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. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.