Get email alerts Get Celiac.com E-mail Alerts  




Celiac.com Sponsor:
Celiac.com Sponsor:




Ads by Google:






   Get email alerts  Subscribe to FREE Celiac.com email alerts

Day 1 No Gluten
0

63 posts in this topic

As far as the rice bread is concerned..... I have found that if you put the rice bread in the Microwave for a minute or so, it will soften up nicely... you might want to try that next time.... Have a nice day.... Nancy :)

0

Share this post


Link to post
Share on other sites


Ads by Google:

I'd been having rice bread for years. and found i liked the EnerG brand best.

But it's not even CLOSE to how great breadmaker bread can be. Over thxgvg my sister showed me how easy it is and how great gluten-free bread CAN be.

I'm getting a breadmaker very soon. Heck maybe today - the loaf i brought w/ me on the plane back from sis's is almost gone !

0

Share this post


Link to post
Share on other sites

I'm just a hiar over 4 days gluten-free, I am in the middle of having a cold spell, I know a few people here talked about the Raynuads(sp) it makes my bones ache and shiver, my teeth clench, I get nervous and so cold, I shiver, trembel and feel weak, it doesn't last more than an hour usually and I use sweaters and blankets, and heat to stay warm (in south Florida) It comes with a horrible nassau afterwards a poisones feeling...but not this time! The sick feeling was always the worst for me the one thing I'd do anything to be rid of! I would always be so sick right now!!! I'm not at all sick, a bit weak but not at all sick! This is some good news for me...

0

Share this post


Link to post
Share on other sites

I've been following your posts and it brought back a lot of memories

of starting the gluten free diet. I, too, had a lot of chills, not feeling well,

laying in a fetal position for hours at a time. My poor husband thought

I was dying, he couldn't do enough for me. Finally with his support,

cooking, and shopping I slowly started to improve. We learned the diet

together, he started a notebook and has an uncanny way of

remembering foods that made me sick. It took 9 months for all the

symptoms to go away completely except for the insomnia which I still

have. You really will get better, I had no damage to my villi, but I

had been sick for years. Keep up the good work.

0

Share this post


Link to post
Share on other sites

Like you, McDougal, I am really new to this. I was only diagnosed last week through blood test and biopsy.

I'm finding it a challenge and also interesting to begin learning what foods affect me now. I've been (or tried to be) gluten-free for 6 days. Now that I haven't been filling myself with things that made me feel so sick all the time, I'm finding it easier to work out just what foods I am sensitive to. Thatt's an art in itself.

It seems that I am sensitive to wheat, oats, corn, barley and rice. I'm also discovering things each day which I am a bit suspicious of. Potato caused me pain today, so it has been put on my ' if in doubt, leave it out' list. B) Cabbage, brussel sprouts are definately out too. I am wondering about eggs too.

I see a dietician in a couple of weeks, but I am learning sooooo much here, with all the wonderful insite you great people have.

What do you do when you crave things you know are bad for you? I really feel like a lamington....a square of sponge cake covered with chocolate icing (which I can't eat because of migraines) and rolled in desicated (shredded) coconut. If I knew I could have it, I probably wouldn't want it! Annoying isn't it. :angry:

Anyway, hnag in there McDougal. You're an inspiration. If you can do it, so can I.

Maggie :)

0

Share this post


Link to post
Share on other sites




;) morning maggie--learn as much as you can in here, unless you have found a very good dietician, he/she probably cant help you :( --so many dieticians do not have the first idea how a celiac should eat---my sister is a dietician and she has helped doctors to figure out when a patient is celiac, but she is a rarity ;) --she has trained all the personel in her cafeteria to understand celiacs, everyone of her employees could fix a plate for a celiac- :) ---my mom was in the hospital in midland and my sis, dad, and i went down to their cafeteria for lunch--judy asked what they had on the menu that was gluten free and the dietician had no idea what she was talking about <_< --judy gave her a good talking too :angry: --a 250 bed hospital and the dietician had no idea and the cross contamination issue there was ridiculous, especially being a hospital--like i said, my sister is the exception :P --most hospital food is bad, my sister's cafeteria has locals from town who come there and eat everyday ;) --the food inspector eats there on a regular basis, now how good is that :lol:---i hope you have a good experience with your dietician, just be prepared--deb
0

Share this post


Link to post
Share on other sites

5days gluten-free. Maggie I know what you mean, it is worlds easier for me to see what foods don't agree with me now. It used to be everthing made me ill so I coudn't differentate any (except dairy which made me sick right away and more noticably). I won't eat anything unless I'm 100% sure it is gluten-free right now, I have no desire to, I don't even want my cherished beer, forget it, it's poison, good tasting poison. Good luck Maggie and feel free to email me if you want to compare notes. Doing good here, feeling better and better. I am still very tired and been sleeping like crazy the last 5 days. Had a scare last night when I chugged a bunch of gatorade and didn't feel to well after, checked though and no gluten-free, just some acidity I guess. I have had this big toe pain for 15 years since I dropped a large object on it, the pain has gotten steadily worse over 15 years, there are very few shoes I can wear, nothing other than sandles for more than a few hours. The pain has subsided considerably, the best it's been in memory, very strange, I didn't see that fix coming. Sometimes I feel right now like every problem I ever had has been explained by this celiac. I've always had terrible problems healing, had terrible gum disease as a youngster that woudn't go away, my broken leg confused the doctors with it's slow healing, I get about 4 colds a year, stomache problems as a kid, ect...Still foggy as heck, that was when I first really knew I was sick about 5-6 years ago I started waking in a fog every day, feeling like I was hungover and it never went away, That foggy feeling go away eventually? The sickness was always the worst for me though that is what weared me down more than anything, sapped my will to live and that has improved leaps and bounds. Life is good.

0

Share this post


Link to post
Share on other sites

Another thing I blame the disease on is my broken leg, I broke it after a crash on a bicycle going about 10 miles an hour and slipped in mud, a minor crash, very minor. My foot got caught in the rat trap pedal and I twisted around, Femur broke 100% horizontaly and had several large splits running the whole length, also there were spiral fractures all through the knee, tibia and fibia. Doctors had no explanation for me other than to shrug, say it happens. I did have alot of pain in the leg before and likely had stress fractures in my leg (my own diagnosis) but again it seems the stress fractures can be blamed on celiac. I've been blood tested several times over the years and a couple times was prescribed iron but was never described as anemic(sp) as far as I know. Rambling again, sorry but it helps me :D

0

Share this post


Link to post
Share on other sites
Still foggy as heck, that was when I first really knew I was sick about 5-6 years ago I started waking in a fog every day, feeling like I was hungover and it never went away, That foggy feeling go away eventually?

You know how you read things and suddenly a light bulb flashes and you go, "Aha! now I know what he means!" :D I've been reading about brain fog and thinking, I didn't experience this, but I lived with a constant headache for years and years that would often peek into migraines. When you said "hangover" and since I'm sitting here right now with a very mild one (shame on me) I realized this is exactly the kind of mild headache I used to just live with! So, to answer your question, YES! if you have the same thing as I did/do, this does go away. It's marvelous! The world is a brighter, clearer place, and not just because I don't feel like I have to wear sunglasses ever second I'm outside (rain or shine...people thought I was weird, but natural light always made may headaches worse.) It took a while for mine to go away, I really noticed it about 2 weeks after going gluten-free. Now, whenever I get glutened, I get a migraine then this stupid headache "fog" for 36 hours more.

I have my fingers crossed you'll feel the same way soon. Congrats on your five days, btw!

0

Share this post


Link to post
Share on other sites

Freya, that is exactly what I mean, my migranes only started a month or 2 ago, gone since gluten-free. I like your answer, Thanks.

0

Share this post


Link to post
Share on other sites

It is llike a light has come on! This forum is really incredible. :) There are so many things that we can share about, instead of all the years when we felt we were the only 'weird' person, who felt sick most of the time.

I've had the pains in the abdomen all my life, and never had any idea. Recently, over the past couple of years, my doctor has mentioned IBS. Well, hey, that is part of celiac disease.

I have brain fog all the time too. <_< I'm pleased to know that it will clear somewhat being gluten-free. Also gum disease, muscular and bone pains and anxity/depression.

I'm convinced we have a 'broken thermostat'!!! It's gotta be. LOL I perspire profusely, then get chilled. Then, the pain comes. It's not my hormones, they've been checked, so I reckon that's another celiac disease thing too. :rolleyes:

I thank God for the knowlege you people have gained by the great sharing here, and life experiences which we can share and compare.

It sure gives me a sense of relief having you guys around. Maggie :wub:

0

Share this post


Link to post
Share on other sites
Another thing I blame the disease on  . . .. . . .. ..

hehehehe i remember the realizations like this.

It can be a pretty long list.

I think the times i had a bone chipped when the docs expected to see a break were also somehow related to celiac disease, tho i haven't heard much about bonechips.

0

Share this post


Link to post
Share on other sites

Maggie, yep that broken thermostat and then the pain after, my neck and back are the worst, and in the long run the anxiety and depression have probobly been the worst for me, I feel alot less of both right now and have progressivly so the last few days, still have the hot/cold bone pain and tiredness but I have hope in time from all I'm reading it will get better. I was diagnosed with anxiety and had a horibble 6 month run on xanax about 2 years ago, I don't remember a thing from that time and I just got more anxcious. Over the last year I did alot of things to simplify my life to relieve anxiety so it became more managable but it has made me so weak and it feels very connected to my celiac right now, I feel the anxiety fading away right now. Dealing with a few day to day issues today that cause me stress I notice a big difference, I feel emotionally so much stronger and ready to deal with problems. The illness in my belly and weakness in my body would make me feel near collapse during stressful moments, the kind of stressful moments we all must encounter each day. I had a few of those daily stressful moments today and yesterday and I dealt with it, it was so much easier. The realization it wasn't all in my weak mind is soooo nice. I'm not the wuss I thought I'd become after all.

0

Share this post


Link to post
Share on other sites
Maggie, yep that broken thermostat and then the pain after, my neck and back are the worst, and in the long run the anxiety and depression have probobly been the worst for me, I feel alot less of both right now and have progressivly so the last few days, still have the hot/cold bone pain and tiredness but I have hope in time from all I'm reading it will get better......

    Dealing with a few day to day issues today that cause me stress I notice a big difference, I feel emotionally so much stronger and ready to deal with problems.  The illness in my belly and weakness in my body would make me feel near collapse during stressful moments, the kind of stressful moments we all must encounter each day.  I had a few of those daily stressful moments today and yesterday and I dealt with it, it was so much easier.  The realization it wasn't all in my weak mind is soooo nice.  I'm not the wuss I thought I'd become after all.

Yes McDougal,

My pain is worst in the neck and down the back as well. I get it in other places but these are the worst ones.

My doctor said that it is fibromyalgia, which it may be. I think that fibro probably goes hand in hand with celiac disease anyway.

With fibro, there are 'points' which I think are nerve ends or something...sorry, my brain is on holidays...

I have found that when you feel sick, and in pain, then the depression/anxiety gets a lot worse. I'm looking forward to getting off my meds for that, and it will happen!

Isn't it a great thing that we are all improving daily. :)

And....no, it isn't all in our heads! Hooray!!!

:D Maggie

0

Share this post


Link to post
Share on other sites

NEVER EVER LET ANYONE MAKE YOU FEEL IT IS ALL IN YOUR HEAD--i wish them one week in our shoes and then dare them to say, "it's all in your head"--they would all see us in a different light then :lol: deb

0

Share this post


Link to post
Share on other sites

Last night I was feeing real good and got it into my head I could eat a chunk of cheese, it was gluten-free but It didn't sit good then and now today I'm feeling pretty crappy, more like day 1 than day 6. That's it for dairy for me for a while. I guess it just didn't scare me as much knowing there was no gluten in it.

0

Share this post


Link to post
Share on other sites

Hi to everybody,

wow, i also thought, that's me. And the most exciting thing is, i already made a connection with all my symptoms and celiac, except of the parfumes and stuff. I had that, too. I just didn't make the connection. I also have problems with cigarette smoke. When i was a little girl, it was so bad, that i got my step-dad to quit smoking. I whined all the time, it was really terrible. At the end my desperation was so bad, i thought i suffocate every moment. So i took his cigarette and threw it into his drink. That was the last cigarette i remembered him smoking. :rolleyes: Today he's glad i made him stop...lol.

Well, my husband also stopped smoking because of me. But i didn't need to make a big thing out of him smoking. I just mentioned it and then he tried to quit and didn't touch a cigarette til today. Now he sees how good i feel every day.

And the problem with the parfumes is still very bad. As little girl my mom and my grandmother went on these coffee clatch bus tours and they took me with them. And all the elder women had all these heavy parfumes. Yak, i couldn't even breeth and got terrible belly pain. But well...

What i actually wanted to say is, that i went glutenfree in july this year and about two weeks after going glutenfree i had terrible bone pain everywhere in my body. Then after a few days it was gone again and i never had it again. Then again a few weeks after THAT i broke one of my toes. Then after a few weeks it was back to normal since i had that gluten accident with Amstel light and now my toe is sore again. So don't desperate, with your bones getting better it might take a while and you also might have some bad days, when you already thought, you feel better. But don't desperate, you will get better.

But there's two other things i wanted to ask you guys. I read the things you wrote about fibro and i was wondering. Sometimes (it is very rare now after going gluten-free though) i still have that pain, that shots down from my right hip into my leg and i can't even stand on that leg anymore. It also happens, when i didn't do sport for a while or when i glutened myself accidentaly. I always suggested it's a nerve thing. Could that be a sign of fibro? I'm kind of stiff in my shoulders and back sometimes, too.

And the second thing is, that i have incredible cravings for raw meat sometimes. Especially when i have another one of my fatigue attacks. My husband was already being angry with me, because he is afraid i get food poisoning. Well, but i'm a german and in germany there are some good meals with raw meat and we actually never had that big of a problem with food poisoning from raw meat (you guys are really paranoid). Well, i can't help myself, as soon as he is not in the kitchen, i sometimes shovel that stuff raw into me. I already thought i'm a vampire or so :P . Could that be, because my body feels it needs iron? Has anybody else also had a problem like that?

Nice to see, you're feeling better McDougall!

Nice greetings, Stef

0

Share this post


Link to post
Share on other sites

A couple people asked about the Actonel I take for osteoporosis. I do have side effects from it but they are subsiding quite a bit as time goes on (on it it 4+ months now). My side effects are vivid dreams (weird one, not mentioned in the insert at all), headaches, and arthritis-like pain mostly in my hands; but the latter 2 are easily dealt with with Advil (which is gluten-free!) No nausea.

There are several drug treatments for osteoporosis--a search will uncover them for anyone interested.

Osteoporosis is found in celiacs due to malabsorption--calcium, vitamin D, phosphorous, and magnesium. Supplementing these (and other nutrients too, depending) is often a good idea, but be careful as it's possible to take too much of the fat soluble vitamins.

When I was a gluten eater I had these symptoms: extreme fatigue, steattorhea, headaches, moderately bad foot pain, numbness/tingling in hands and feet and occasional anemia. It was a B12 deficiency my doctor discovered that I researched that finally got me the celiac disease test. Before that, it was "all in my head."

I still get very definite "brain fog" from foods other than gluten so I'm working on being extra careful to avoid my problem foods. It's not fun (especially the social aspects of this) but everyone has something to deal with. I'm just grateful there is a solution! :D

0

Share this post


Link to post
Share on other sites

Hey ya'll

Stef-

I most definitely have multiple chemical sensitivities. Like you, one major trigger is cigarettes/smoke. Also perfume..and air fresheners...they are a killer! (especially those kind that burn or plug in to the wall and are very strong). I'm also sensitive to fragrant soaps and detergents. And those beautiful shops in the malls that are full of candles?...count me out, I can hardly walk in them! (I actually try not to). :blink:

I've always been this way. I get hives, dermatitis, migraines, and my nose runs (kind of strange) if I'm exposed to any of these things.

I would have never dreamed this could be related to my life full of digestive problems if I hadn't been diagnosed and started coming to this site!

Thanks everyone for sharing!

-Julie :)

0

Share this post


Link to post
Share on other sites

I was a silly girl this morning too. :o Yes, I know you're all shoked. I have been feeling pretty good (not great, but improving) up till now, so guess what I did???? :rolleyes:

I decided to have JUST ONE Arnott's Gingernut biscuit B) and guess that happened? Yep, I got crook straight away. Stupid me! It taught me a lesson though. I knew it was full of gluten, and did it anyway.

I made myself a baked egg custard for lunch, (trying to be a bit more careful). That made me sick too. So I guess I either have problems with eggs or milk, or both. I'm beginning to think I do have a lactose intolerance. Even when I have a cup of tea (well, I'm Aussie, we drink a fair bit of tea), I'm getting discomfort and bloating right away.

Stef, smoke, perfume, fly spray, paint...anything like that makes me really sick with migraines.

Also, I was thinking that the pain you discribes from your hip, down your leg may be sciatica. If it is, then it's not connected to coeliac.

It is caused by damage to a nerve called the sciatic nerve, which runs from the lower spine (backbone), down the back of the leg, and under the foot. It is really annoying and can be very painful.

I hurt my back in a truck (semi) accident years ago, and I still get a twinge sometimes.

YankeeDB, I have horrible dreams too. I'll read a few posts here and it seems common. I take 1000mg sodium valproate to help me fall into a deeper sleep pattern, and therefore not be in the dreaming level of sleep.

I take Ginko Biloba complex for my brain. It really helps with the fogginess. ;) and I have double strength apple cider vinegar. it helps digestion and helps build up the circulation. I think it's good for a few other things too, but I can't think of what right now. <_<

I hope this helps someone. Maggie :)

0

Share this post


Link to post
Share on other sites

Thanks again for all the help...it looks like I did glutten myself, I had a small bag of planters honey roasted peanuts late Sunday night, I meant to find out what xanthan gum was but never did until I just now backtracked the things I ate. I guess this xanthan gum has gluten. The bone pain was really bad yesterday, better today, I like to hear about others who say it has gone away after a few weeks:-) I know I will still have some aches and pains as I have beat on my body some, but this is ridiculous sometimes. Hope you guys have a good day.

0

Share this post


Link to post
Share on other sites

Better double check on that McDougall..... I have heard many celiacs use xanthan (sp?) gum for baking, etc. I am pretty sure it is gluten free..... I, of course, have never used it since baking is definitely NOT one of my strong points!!! LOL!

Perhaps there are only certain brands celiacs can use?

Anyone else?

Have a great day!

Karen

0

Share this post


Link to post
Share on other sites

I've seen some brands of Honey Roasted style nuts which had a bad ingred, tho i can't recall which ingred, or which brands.

The xanthan gum isn't the problem tho.

The Sep30-04 edition of the safe-list pdf i use has this for Planter's.

Planters Nuts (roasted & salted only; no "flavors" except Honey Roasted)

According to this, their Honey Roasted are fine. Hmmmmmmm.

And i can't coax an ingred list out of the Planter's site.

Grrrr wanted to see if it had a ModFdStarch or HVP or one of those common problem ingred.

0

Share this post


Link to post
Share on other sites

It was "xanthan" I found to be with gluten, not "xanthan gum" maybe there is a difference? It still could have been the cheese, or just a normal setback I'm sure. My bowels are still fine. My appetite is gone completely and I have always been the type to be hungry at all times.

0

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!


Register a new account

Sign in

Already have an account? Sign in here.


Sign In Now
0

  • Forum Statistics

    • Total Topics
      104,365
    • Total Posts
      920,553
  • Topics

  • Posts

    • Just a quick one to say I got a diagnosis of celiac disease today. I know in the past it's been helpful for me to know the outcome for other folk, so thought I would update. The moral of this story is even with a VERY borderline blood test it's worth persisting. thanks for all the help Sue 
    • Well, I am stressed to the max. I just spent 3 days in the hospital with D and stomach pain, dizziness, chest pain, generally unwell. Then another trip to the ER on top of that. My protein was low and my RBC and hemoglobin dropped below normal in 3 days. Not terribly low, but below normal. I also had metabolic acidosis which still confuses me. I usually eat every 2-3 hours despite it causing pain to keep my energy up and was unable to eat that frequently in the hospital. I usually carry protein with me and had been taking liquid iron which I stopped a few weeks ago because my new endo is not a fan of iron supplements. As soon as I got home from the hospital I started with my protein drinks and blackstrap molasses for iron.  I now have bilateral mild pleural effusions and a nodule on my left lung, which hopefully is nothing, but was not there on a CT back in March. In addition, my left adrenal gland, which also appeared normal in March, is calcified and the report indicates this is most likely due to a previous bleed or infection. My colon appears tortuous (whatever that means) and we are waiting on colon/endo biopsies. I have been gluten-free since March except for cc so expect the biopsies to again be negative.  My primary care is useless. I am in the process of getting a new one I will see on the 7th but need the current one to fill out FMLA paperwork because I both physically and mentally need time to recover. I will have to go off of payroll for 2 weeks but I think I need to. I called the primary's office today to discuss the hospital tests which she does NOT have yet and to ask if we should/could start a low dose of prednisone because my body is attacking itself. My thyroid on ultrasound is also abnormal though my bloodwork thus far is normal. But it hurts on that side. The only reason the ultrasound was ordered is because I asked for it in the first place. The only reason I have started seeing an endocrinologist is because I found one myself. Anyway...I broke down in tears on the phone eith her today and she told me I was having a "manic episode". I have no history of mania. I only recently started taking xanax to help me cope with the stress of being sick. I was not sick until I did this stupid gluten challenge over the winter. My mother was in town and spoke with the doctor on the phone as well who was trying to get my mom to take me to a psych hospital. She also threatened to send the police to check on me. My mother assured her I was in no danger and we hung up the phone in complete shock. Admittedly, I was in tears when I called her and probably sounded like a fucking mess. But I believe I referenced the dropping iron, protein, fluid near lungs, enlarged thyroid and attacked adrenal gland then literally said "my body is attacking itself and I need help" to which she said, "I think you are manic". Lovely. If I was a mess before that phone call it was 10x worse when we hung up.  Anyway, this is the first night it has been extremely difficult to sleep. I admit my thoughts about my odd symptoms keep me up often recently. I mean, who the hell bleeds from or gets an infected adrenal gland?! I am sure it was another time I begged my primary for help. On a side not, the NP at the ER told me the primary should be putting these pieces together and communicating with my other doctors better. He then stated that he used to go to the same practice but left because the practice got too big and like a business. So I got some validation from that chat.  A melatonin or a .25 xanax usually does the trick for me to sleep but I am so disturbed about my interaction today, stressed at my health, stressed that my ex has our son so much because I am always sick (bless him for coming through), stressed that I have to go back to this awful doctor because I will need the FMLA paperwork before I see the new doc on the 7th.  8 months ago, I took a multivitamin when I remembered it and that was it.  End rant. Maybe now that it is off my chest I can finally sleep. 
    • Hi DKH0614, I use aspirin, Pepto Bismol, and peppermint tea or Altoids peppermints.  Pepto Bismol has a soothing effect on the gut.  Pepto Bismol also has aspirin in it.  Peppermint is helpful for relaxing smooth muscle tissue and getting gas out of the stomach. As per KarenG, you may be reacting to dairy.  Dairy has a sugar called lactose in it that some people with celiac have a hard time digesting.  You could try avoiding dairy for a few weeks to see if that helps.  Or try taking lactaid type pills when you eat dairy. It doesn't take very much gluten to cause an immune system reaction.  So it is important to avoid even traces of gluten if possible.  The stuff is hard to avoid sometimes if people around you don't understand how much a small amount of it can affect your body. Let us know if we can help with any  more questions, or if you have concerns we haven't addressed. And welcome to the forum! Also, if you subscribe to the thread (notify me of replies) you'll get an email when people respond to your thread.    
    • After a year and half, if you are eating gluten-free, you shouldn't be having pain from Celiac.  Perhaps you need to find out what is really causing your issues?  Dairy/ lactose is an obvious first place to look.
    • Hi! I am 15 and have been diagnosed with celiac disease for about a year and a half now and I am woundering what do some of y'all use to relive some of the abdominal pains that come along with celiac/gluten allergies?  ( Ibuprofen,  Tylenol, etc.) 
  • Upcoming Events

  • Blog Entries

  • Recent Status Updates

  • Who's Online (See full list)

  • Member Statistics

    • Total Members
      61,439
    • Most Online
      1,763

    Newest Member
    DKH0614
    Joined