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On The Subject Of Memory Problems
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This is a question to those, who HAD memory issues, brain fog, ect. and have since Solved zed problems with a gluten free lifestyle, or... w.e it was that solved zed memory issues for you =D

Keep in mind, I'm looking to see if there is any..Stories of triumph not..depressing tales of ongoing struggles.

not that my heart doesn't go out to those people, it does, I just need to know if anyone's licked this xD

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When I get glutened my short-term memory is terrible. Very ADD-like. I can look at a phone number, turn away and not remember any part of it. I think of something I need downstairs and when I get down the stairs I have no idea why I'm there.

This is almost completely eliminated when off gluten.

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This is a question to those, who HAD memory issues, brain fog, ect. and have since Solved zed problems with a gluten free lifestyle, or... w.e it was that solved zed memory issues for you =D

Keep in mind, I'm looking to see if there is any..Stories of triumph not..depressing tales of ongoing struggles.

not that my heart doesn't go out to those people, it does, I just need to know if anyone's licked this xD

Saw the part of the title about " read the other posts". I'm just dying to say, " but I forgot what they said!". :lol:

Thank you. I feel better now.

I was having a very hard time thinking, remembering, concentrating and finding the words I wanted. It has resolved gluten-free. I think a good portion of it for me, was the fact that I was very anemic. Oxygen wasn't getting to my brain. When I was able to absorb iron, etc, & the anemia resolved partway, I could think better.

I started " exercising" my brain. I played word games & other computer games. I started posting on the Psilly thread. I could write my thoughts and use various words when I wrote. Then I started talking to myself. That forced me to practice speaking. ( really, I'm talking to my dog if anyone notices).

I still forget the word I want. But, who doesn't occasionally? I have to remind myself that it's normal sometimes. Hope that was a hopeful story!

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My brain "on gluten" was nothing like my brain "off gluten". I was like a "stoner" :rolleyes: before I was DXed. An anxious

vaseline-brained stoner. Gluten not only acts as a nuero-toxin, but malasorption creates multiple vitamin and mineral deficiencies and neurotransmitter disruption and so, once the body is RID of it and you ABSORB nutrients once more, you should

stabilize. (says here in the directions.....)

You want a happy story!....ok!

I am almost back to "normal"-- before "gluten head" appeared. I am just over 7 months gluten free and YES!! the brain fog and short term memory issues (and almost all the other brain issues I developed ) have resolved in time :)

I had this strange feeling like I was sleep- walking in my own life for over 2 years. I did things, but later wondered how I did them or looked back on things as if they were "unreal". I became sad, quiet, inarticulate, confused, easily frustrated... and felt "dark". I am normally a very happy, vivacious, chatty and super-organized person. I kept saying to my husband, I feel "surreal" and he would reassure me I was all right. (good thing he never doubted me--I am sure it sounded like I was a total whackjob :blink: ).

I would walk into the kitchen to make dinner and have to THINK about what the hell I was doing in there. It made me frustrated and I would actually burst into tears because I couldn't handle more than one pot on a burner on the stove. Forget doing the bills!!--that simple task took all of my concentration and I made mistakes all the time in the checkbook. If someone were giving me NEW information, I had to write it all down. And ask them to repeat it again.....it was so embarrassing, frustrating and frightening. I had vivid, scary dreams. My brain was working overtime all day/all night. I am the trivial pursuit queen in the family, so imagine my concern when I couldn't recall even simple things--like what I had done the day before!!!

I had trouble reading because I couldn't concentrate or retain what I had just read. This is my passion; I used to read 3 books at a time! I had trouble articulating and had to search for words (I was an English Prof. who spoke in front of large lecture halls without notes EVER ...and then, this happened to me. It made no sense! ) What the hell was going on??

Most of 2008-2010 is "smashed together"... :blink:

Often, I would have to hold on to my husband's sleeve when I went out in public because I felt "overwhelmed and scared" and I could not walk straight. (I have never been shy or afraid of anything in my whole life!)

I ruminated on topics over an over and did not know why.

It was nuts!

I made myself watch/read things that were humorous or made me THINK--so I would stay upbeat and sharp.It was not easy.

I tried to meditate--hahahaha! no way...

and worst of all....I had to stop driving for fear I could not react quickly enough. That really did me in.

When I started researching what was wrong with me, it was very difficult as I had to read things over and over again. I repeated myself while talking and in my writing....I KNEW I was doing it, yet couldn't seem to stop it.

I had MANY scary neurological issues I won't depress you with---but I will say this---THEY ARE NEARLY ALL GONE NOW!!! :) :) :)

I still have a hard time with all that "weirdness" as it seems like it's "compacted" time I lost somehow. That was the scariest sensation I ever dealt with in my life and I do not wish to ever experience it again. It's like being on LSD. Really.

I KNOW when I am accidentally glutened because the first thing that I notice is....I feel strange and "cloudy" in my head ....and I wonder oh no, who slipped me the drugs?? :unsure:

Hang in there!!! It GETS BETTER!!! :)

I just learned yesterday from follow up lab work that my B-12 and

folate and iron deficiency anemias are resolved --

Hooray-for ABSORBING ONCE MORE!!Welcome back, little villi :)

and with it, my brain function is returning....whew! (obviously...look how chatty I am again.. :lol: )

The rest of my symptoms...recovery is ongoing, but getting my BRAIN back is AWESOME!!! B)

Best wishes!

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My memory had gotten to the point where I could not read a book. I would forget what I read as soon as I read it and get lost in the words if the sentence was too long. I couldn't look at an adresses or phone number and remember it for ten seconds even if I focused very hard. I didn't remember dates or even what day it was. There is about a 2 year window of my life in which I remmember very few things. I often burned things when I cooked because I would start a pan on the stove or put something in the oven, walk away and completely forget that I was cooking. Twice I left a pot of water boiling and it boiled dry so the pan was ruined. It's a miracle I never burned the house down. I frequently lost my keys and other things, I locked my keys in my car (once with it running) about 4 times in the course of one year and locked myself out of my home 3 times. It wasn't safe for me to drive (dr took away my license due to seizures) for about a year of the worst part of my illness otherwise I probably would have kept doing that. :o

Now my memory has improved to the point where I can read again. I still can't sit and read a book for a long time though. After abotu 15 minutes of sustained reading my mind is very tired. It's like I can feel my memory trying to rebuild itself. I keep practicing though and hope to get back to where I was one day. I was a straight-A student throughout high school and college who loved to read (considered majoring in English); losing that ability really hit me hard.

My husband has noticed a huge improvement in my memory too. I would forget things I saw very quickly--for example there was a new grocery store being built along the route to church. Every single Sunday for many weeks I commented to my husband, "Oh look they're building a new HT." He would then gently say to me, "Yes dear you pointed that out to me last week, don't you remember?" I didn't remember even seeing that grocery store, let alone pointing it out every week. He told me I often repeated stories to him as well. I don't do those types of things anymore. I remember when I see something new and don't mention it again. I know when I have told him something and don't need to re-hash the same story. With the exception of a few slips now and then I feel like my memory is almost back to what it should be for a 30-something.

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For me it was getting on the right amount of thyroid.

I had awful brain fog this spring, couldn't remember things, couldn't even do simple addition. (Like 12+8=20) I remember driving home from a concert and although I knew the route perfectly well, I suddenly had no idea how far I'd gone, or which of the 3 highways I was on along the way home. I couldn't remember which exits I had taken. Getting out the door for work was a nightmare. In the course of two weeks I forgot lunch, cell phone, wallet, laptop charger, and coffee in various interesting and challenging combinations. Not to mention my constantly lost car keys. About the only thing I didn't forget was my head and only because it's firmly attached.

Adding just a little more T3 hormone totally cleared out the fog in a matter of days.

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I had memory issues where I'd be driving and forget where I was or where I was supposed to be going, couldn't find words, etc...

I think the one thing that bothers me the most is that it was like my brain wasn't making memories. I've had this for over 20 years, and I just remember tiny pieces of it. I barely remember any of my children's infancy (although, ahem, that might have something to do with the lack of sleep, LOL). I was always fuzzy headed and had a hard time focusing and thinking. Depression too, actually.

All gone now, if I'm very, very good on my diet. Most of it turned out to be gluten, but some of the fuzzy headed thing turned out to be food allergies, too. I get no hives, I just feel like I have the flu and I want to crash, and have trouble thinking.

I cannot remember how long it took to resolve...which isn't surprising, eh? :D I think it was a couple months for it all to really disappear...once I'd figured everything out.

But it's one of the reasons that I can stay on the diet, really. I feel like I've suddenly regained myself, like I wasn't existing for all those years, really. And I don't want to lose that every again, you know?

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True story (not one word of exaggeration):

Before going gluten-free, I was known as the queen of lists. I made lists of things I needed to remember and carried these lists and consulted them all the time. If something wasn't written down on one of my lists, then it got forgotten.

After going completely gluten-free, my memory improved so much that now, one of my many nick-names is 'elephant brain.' Honestly. I've got a super-sharp memory. Unless I get glutened, in which case it feels like my brain is filled with cotton, and I can't remember my own phone number. It takes a good 3-4 days for the brain fog to lift after a glutening. Then I go right back to elephant brain.

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True story (not one word of exaggeration):

Before going gluten-free, I was known as the queen of lists. I made lists of things I needed to remember and carried these lists and consulted them all the time. If something wasn't written down on one of my lists, then it got forgotten.

After going completely gluten-free, my memory improved so much that now, one of my many nick-names is 'elephant brain.' Honestly. I've got a super-sharp memory. Unless I get glutened, in which case it feels like my brain is filled with cotton, and I can't remember my own phone number. It takes a good 3-4 days for the brain fog to lift after a glutening. Then I go right back to elephant brain.

I hear you about lists. I had lists all over the place and even a master list for my lists. My wife gave me a notepad one Christmas with a drawing of Santa on it and the quote on it was: "I made a list, checked it twice and forgot it!"

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I was another list maker. My husband has teased me about it for 20 years. Now I find I don't need them anymore. However, I will say that dairy and sugar also act like gluten for me. I get foggy and forgetful when I have any of my "toxic three" as I like to call them.

Does anyone know where the memory portion of the brain is? :huh:

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Does anyone know where the memory portion of the brain is? :huh:

Hippocampus, mostly. Amygdala and striatum may also be involved but it's less clear.

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Wow. I am still in the process of figuring out whether I have celiac, but I totally relate to the memory loss or brain fog. I am only 27, but recently my memory has been so bad that I was starting to think I may be getting alzhiemers. I make lists for each day, can't remember things even when it's important info that at the time I KNOW I will need to remember it later. I didnt know bad memory was part of celiac. Now I have one more of the symptoms to add to the list.

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:blink: Wow...can definatly relate to all of the above! was so bad...I was stuttering! couldn't recognise streets in the town I've lived in all my life!...forget what I was saying or what was said as it was spoken! yikes!...but Most of its better...still finding OTHER culprets though...you guys know the deal!(for you newbies...beware Dairy,soy,nightshades...not everyone mind you...but alot of us have problems with those..for others its corn..sugar..frutose.) LOL! but it is getting better! I agree you have to get passed the malnoutrishon part though! I'm still severely calcium defeicent and vitemen D as well...causing joint and mucsle spasms muscle ticks,bone pain.but things are allways getting better!(the problem with malabsorption is you can take truck loads of vitemens but only absorb alittle...I think my gluten/dairy/soy free vitemen D's are making me ITCH!...just can't win!LOL!) :lol: But I don't lose my keys HALF as much...and I can compleate my sentences...LOL!THE FOG IS LIFTING! Hang in there NEWBIES!IT DOES GET BETTER! :blink::unsure::rolleyes::lol::D
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:blink: Wow...can definatly relate to all of the above! was so bad...I was stuttering! couldn't recognise streets in the town I've lived in all my life!...forget what I was saying or what was said as it was spoken! yikes!...but Most of its better...still finding OTHER culprets though...you guys know the deal!(for you newbies...beware Dairy,soy,nightshades...not everyone mind you...but alot of us have problems with those..for others its corn..sugar..frutose.) LOL! but it is getting better! I agree you have to get passed the malnoutrishon part though! I'm still severely calcium defeicent and vitemen D as well...causing joint and mucsle spasms muscle ticks,bone pain.but things are allways getting better!(the problem with malabsorption is you can take truck loads of vitemens but only absorb alittle...I think my gluten/dairy/soy free vitemen D's are making me ITCH!...just can't win!LOL!) :lol: But I don't lose my keys HALF as much...and I can compleate my sentences...LOL!THE FOG IS LIFTING! Hang in there NEWBIES!IT DOES GET BETTER! :blink::unsure::rolleyes::lol::D

Oh noez lol not the sugar and dairy :'o I have these vicious addict like cravings for those, I was worried it was candidia for the longest time but then I told myself to stop being silly and admit I was just refusing to give them up...still haven't perhaps I should o.o but then.. I'm left with so little xD

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Oh noez lol not the sugar and dairy :'o I have these vicious addict like cravings for those, I was worried it was candidia for the longest time but then I told myself to stop being silly and admit I was just refusing to give them up...still haven't perhaps I should o.o but then.. I'm left with so little xD

:lol: You have alot...you just have to explore new ways of getting it!...check out our FOOD thread...lots of healthy ideas there..lots of ALTERNITIVES! LOL! :lol: You can still have sweets just less refined! your body will get used to it after a while...the cravings will die down! Also...you may not have problems with alot of these things...but it is just a sugestion of what OTHERS have problems with! might not affect you..but it does give you an Idea if glutenfree doesn't seem to be enough!start by checking out the threads on NIGHTSHADES..our most commonfood sensitivity next to gluten!

Try eliminating one at a time...see what happens how you feel! :unsure: Or like I did...pay attention to how you feel after you ate it...like potatoes...or Tomatoes(marinara,tomatoesauce)...Peppers,eggplant(makes me vomit now...didn't use to!)I'd get a horrible stomacheache and bloating...so now Idon't eat it and feelbetter! I substitute sweet potatoes( in stirfry, frenchfrys..ect.)and it worksfine...I actually like them better,sweeter less dry!Now that I'm more healed I seem to bedoing better with salsa and raw tomatoes...still havn't worked the nerve up to try marinara...I had extreamly paifull experience last time! :blink: But you get the Idea!Checkout the "other" food sensitivities thread...good place to start! Don't worry...besides Gluten...alot of sensetivities change as we heal...some don't...but Everyone is different...different symptoms...different sensetivities!Just Hang in there and get better!LOL! :P One day at a time! :lol:

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Oh! Reading this thread just made something 'click' for me! My Mother was diagnosed with Alzheimer's Disease, BUT I believe that she may have had either Celiac Disease or gluten intolerance. The words BRAIN FOG just now hit me hard --I feel bad thinking that she may have had better brain power if only we had known to get her gluten free! (Mom passed away in 2005.)

Makes one really wonder about the 'relationship' between different diseases and illnesses, doesn't it?

I know that I had brain fog pretty bad before going gluten free. It really worried me sometimes -how bad my brain power was. I just added B12 to my vitamin/supplement regimen a couple of days ago, and already I am noticing better brain function -clearer thinking.

Not saying that I have brain fog 'licked', but I believe that I have some improvement.

BTW -I am gluten free since January 1, 2012.

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I was so bad off memory wise that I often could not remember the name of things like "fork", "plate", "knife" & forget (ha-ha) about me remembering just about anything at all! What's for dinner? I don't remember. Did I check the mail today? What day is this? What day is this? What day is this? all in the space of a half hour. My mom's side of the family had Alzheimers including mom. Uncle died of it at 61! I thought OMG! I've got it & got it way early. I'm going to die of it early just like Uncle Bob. I couldn't remember diddly squat.

Fast forward to 6mos. gluten-free & I'm baaaack! I still forget some things but I haven't forgotten the name of a fork in a long time now. I no longer worry about coming off as an idiot half wit when talking to people now. I used to have a fabulous vocabulary & it's coming back. It's so great to be able to call words into my mind again & use them!!!!!! YES!

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I'm really glad to see that lots of people are improving the celiac brain situation =D

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I was so bad off memory wise that I often could not remember the name of things like "fork", "plate", "knife" & forget (ha-ha) about me remembering just about anything at all! What's for dinner? I don't remember. Did I check the mail today? What day is this? What day is this? What day is this? all in the space of a half hour. I couldn't remember diddly squat.

Fast forward to 6mos. gluten-free & I'm baaaack! I still forget some things but I haven't forgotten the name of a fork in a long time now. I no longer worry about coming off as an idiot half wit when talking to people now.

OMG...That is SOOOO true....My hubby just couldn't understand why I couldn't remember what I did earlier in the day...he was convinced I didn't do ANYTHING while he was at work! The truth was ...I just couldn't remember! Heck I couldn't remember what I had for breakfast...I couldn't remember if I HAD breakfast! I'd go all day without eating...then realize I hadn't EATEN by 5:00pm, when I was getting dinner ready! and that was years before everything got REAL obvious! right before I was DX! I so relate to the not remembering what a fork was....Ummmmm...you know ...That THINGY!...With the sharp points! :blink:

Or I'd stop and have a food related question for the boys while making dinner...and it would sound like this..."Ddddddd...ddddd....ddddo....ddddd...ddd...dddd...DO yyyyyu.....dddddoo....yyyyyu......wwwwwwant?DDDDDDo yyyyyu....wwwwwant? uuuuuummmmm....IIIII forggggot!"My God! I thought I was having a stroke!(It didn't help at the time I was light sensetive, my extremities kept going numb, and I was having chest pains and had had a migraine for 2 months straight!)...REALLY SAD AND PATHETIC....then my arm or cheek would start twitching or I would feel like passing out!(turned out to be celiacs/and caesin...the dairy was causing migraines, muscle seisures and hot flashes...go figure!)

I am SOOOO glad THAT is in the past! THINGS are SOOOO much better now! Still have a little trouble remembering how to spell words, and I have ALOT of trouble still with GLUTEN ATAXIA...my hands,calves and forearms especially! but MAN....things are SO much better by a long shot! you totally brought back some memories there! :blink::D

One time I was walking and compleatly lost the feeling in my toes on my right foot and 2 toes on my left...gone ..it was like they compleatly disapeared...not tingly(that happens alot too), but disapeared like they wern't there! Trust me when I say THAT is rather unnerving! :blink::rolleyes::lol:

But a Glutenfree/caesinfree/nightshade/soy free diet ( well mostly soy free...still rooting out the soy, it rears its ugly head in unlikely places...LOL!)...has made a WORLD of difference! and it will get even better when I can beat this malabsorbtion issue I'm sure!Still have along way to go....its only been since sept. 2011. My Doc says it takes a while especially since I have at least 40 years worth of undiagnosed Celiacs damage to heal(I can trace it back to age 6... when I had stomache issues/ fainting spells and severe migraines!....6 yr.olds shouldn't have chronic migraines or fainting spells! with all the bloodwork and catscans, they NEVER thought to test for FOOD allergies!) :( ....But that is a story very often told among us Celiacs! ;) ...Better LATE than NEVER! :rolleyes::D

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OMG...That is SOOOO true....My hubby just couldn't understand why I couldn't remember what I did earlier in the day...he was convinced I didn't do ANYTHING while he was at work! The truth was ...I just couldn't remember! Heck I couldn't remember what I had for breakfast...I couldn't remember if I HAD breakfast! I'd go all day without eating...then realize I hadn't EATEN by 5:00pm, when I was getting dinner ready! and that was years before everything got REAL obvious! right before I was DX! I so relate to the not remembering what a fork was....Ummmmm...you know ...That THINGY!...With the sharp points! :blink:

Or I'd stop and have a food related question for the boys while making dinner...and it would sound like this..."Ddddddd...ddddd....ddddo....ddddd...ddd...dddd...DO yyyyyu.....dddddoo....yyyyyu......wwwwwwant?DDDDDDo yyyyyu....wwwwwant? uuuuuummmmm....IIIII forggggot!"My God! I thought I was having a stroke!(It didn't help at the time I was light sensetive, my extremities kept going numb, and I was having chest pains and had had a migraine for 2 months straight!)...REALLY SAD AND PATHETIC....then my arm or cheek would start twitching or I would feel like passing out!(turned out to be celiacs/and caesin...the dairy was causing migraines, muscle seisures and hot flashes...go figure!)

I am SOOOO glad THAT is in the past! THINGS are SOOOO much better now! Still have a little trouble remembering how to spell words, and I have ALOT of trouble still with GLUTEN ATAXIA...my hands,calves and forearms especially! but MAN....things are SO much better by a long shot! you totally brought back some memories there! :blink::D

One time I was walking and compleatly lost the feeling in my toes on my right foot and 2 toes on my left...gone ..it was like they compleatly disapeared...not tingly(that happens alot too), but disapeared like they wern't there! Trust me when I say THAT is rather unnerving! :blink::rolleyes::lol:

But a Glutenfree/caesinfree/nightshade/soy free diet ( well mostly soy free...still rooting out the soy, it rears its ugly head in unlikely places...LOL!)...has made a WORLD of difference! and it will get even better when I can beat this malabsorbtion issue I'm sure!Still have along way to go....its only been since sept. 2011. My Doc says it takes a while especially since I have at least 40 years worth of undiagnosed Celiacs damage to heal(I can trace it back to age 6... when I had stomache issues/ fainting spells and severe migraines!....6 yr.olds shouldn't have chronic migraines or fainting spells! with all the bloodwork and catscans, they NEVER thought to test for FOOD allergies!) :( ....But that is a story very often told among us Celiacs! ;) ...Better LATE than NEVER! :rolleyes::D

If you don't mind me asking, how did you come to suspect Nightshades? I've seen that a few times but never considered it a whole lot, one other thing, I am quitting dairy in general and sugar if I can avoid it totally, but it is some intense withdrawal I feel like an addict the way I want milk or something lol did you get anything like that? pretty sure one day off it and my back pain is already gone =/

I've been making eggs for breakfast for like, the last 2 years and the last week I don't know what it is but I've constantly left the burner on! going to destroy my damn cookware lol it's weird, I dunno how I can go fine for 2 years and then just start forgetting something so obvious, it's not like I'm rushing for something after it's made o.O

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Hmmm, I had no idea that gluten could make such BAD memory problems...sigh, yet another sign that my dad is also a celiac yet he won't get tested.

I haven't been gluten-free long enough to get better. 2.5 months before starting it again for my biopsies (well, I probably had CC then anyways) wasn't enough to lift my brain fog.

Day 2 of my REAL gluten-free time now. Not long enough :-p

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Hmmm, I had no idea that gluten could make such BAD memory problems...sigh, yet another sign that my dad is also a celiac yet he won't get tested.

I haven't been gluten-free long enough to get better. 2.5 months before starting it again for my biopsies (well, I probably had CC then anyways) wasn't enough to lift my brain fog.

Day 2 of my REAL gluten-free time now. Not long enough :-p

Just wait!smile.gif

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I had a hard time......Wait! What were we talking about? :blink:

As I got better physically, I tried to work my brain. I would talk to myself my dog to work on words. I did different puzzles on the computer. I think it helps. There are memory games, too. Or just try to memorize a list of something - state capitols, presidents, countries and capitols, dog breeds, etc.

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I was losing my memory and ability to think. It got to the point where I couldn't read things I needed to read for work. This was still going on 10 months of eating gluten free. Then I started taking methyl-cobalamin (B12), folate, and some other B vitamins (along with the vitamin D I was already taking) and then the brain fog slowly started to lift. It's still not all the way back yet, but I'm completely functional now. I don't know if it was just time (> 10 months on a gluten free diet) or whether I was deficient in B-12 and folate.

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If you don't mind me asking, how did you come to suspect Nightshades? I've seen that a few times but never considered it a whole lot, one other thing, I am quitting dairy in general and sugar if I can avoid it totally, but it is some intense withdrawal I feel like an addict the way I want milk or something lol did you get anything like that? pretty sure one day off it and my back pain is already gone =/

I've been making eggs for breakfast for like, the last 2 years and the last week I don't know what it is but I've constantly left the burner on! going to destroy my damn cookware lol it's weird, I dunno how I can go fine for 2 years and then just start forgetting something so obvious, it's not like I'm rushing for something after it's made o.O

Its just that it got to a point that EVERYTIME I ate Marinara..Stuffed peppers...potatoes..or eggplant , I'd Get a reaction like I did when I was gluttened! :blink: Horrilbe stomache pain..instant bloating and nausia...usreally ending in me throwing up 5 minutes to 1/2 an hour later!It wasn't allways like that...but started gradualy mostly with tomatoe products at first...but when I became really sensetive right before DX and definatly after...it became more obvious! though I first thought I was being GLUTENED somehow! Then I read about night shades...even posted a thread asking about it!Thats when I REALLY understood the conection!I USED to eat this stuff ALL the time...but my Celiacs hit that saturation point....and now I'm sensitive to ALL kinds of things I wasn't before! Don't get me wrong...there were signs...Sometimes these things would make me sick...sometimes not...but I never put 2&2 together and allways thought it was SOMETHING ELSE! :ph34r::rolleyes: NowI know better!thanks to my fellow Celiacs! :lol::lol::lol:

And yeah...I've set a few fires in my new stove..(using the broiler)...I had 6 inch flames 3 different occasoins setting my tortillas on fire...I like making my own chips using mission yellow corn tortillas/olive oil/hemylaian sea salt...then eating them with Hummas(good way to get your beans/protien!)...but I've forgotten them while waiting and reading the forum...and yes They made a lovely flame as I pulled them out and extinguished them in the sink!LOL! I've left my keys in the freezer...sometimes can't remember the name of things (alot)...but its getting better,It just takes time! :P I don't know how many times I boiled my tea water away and burned the pot! LOL...finally we got a teapot that whistles when it boils...yeah its loud and annoying...but I don't burn the pot! If only they made one for frying pans!LOL! :rolleyes::blink::D

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    • Below is copied & pasted from this thread:   My celiac doctor is Dr. Syed Jafri, in Webster, TX (just south of Houston -- basically the Clear Lake City area), saved my LIFE.  I would recommend him to the whole, entire world.  I was desperately ill, and am still struggling, and he's a wonderful, sweet man who listens and is very proactive in helping you solve whatever problems you're having.  I wish all doctors were like him.  I have to fight and struggle with too many doctors to just listen to me and what I live with, day in and day out.  He's not like that.  Good luck to you.     There are recommendations on this thread too:  
    • I never worried about cross contamination because i was originally told i was just intolerant. after going gluten free i felt so much better up until this last march. dairy and fructose have been giving me problems but both lactose and fructose test came back negative.  this is what my gi doctor emailed me today 
    • Any place you know of to find more info? Seems like I am still in so much pain/bloat, I am not even sure if I would pick the right 5 foods!
    • Don't freak out worrying about other maladies yet. You would be absolutely amazed at the things that can/will resolve on the gluten free diet. Some take longer than others -- neurological seem to take the longest for most people but really, I guarantee, there will be things you had no idea or expectation of resolving will. There were tons for me and then there were things I sort of "woke up one day" & said, "hey, that's gone and that & that & that". Other, larger things had taken my attention so I hadn't paid attention to the smaller things until...... On the other hand, not everything is related to celiac but I bet you wouldn't find a handful of celiacs who didn't say something very similar to what I said above. Yes, thyroid problems are common with celiac but I'll also tell you there are/have been people on here who were hypothyroid before dx but after being gluten-free for a while they actually went back to normal thyroid numbers. My husband is one (yes, we both are celiac - it happens). He was on synthroid for 20 years or more. Guess what? He's not on it anymore. We've had his thyroid panel done several times since about a year gluten-free & he is no longer hypothyroid. 
    • Yes please, that'd be awesome Having a fun time trying to reply on my phone due to broken screen but will be back on tomorrow after results of doctor appointment to get to the bottom of why they've given me seemingly wrong advice re: next steps. Yup I'll admit to pity, anger, frustration and outright fear, been through the mill of emotions in this first week that's for sure. One thing before I go for that; back when I was self-diagnosing I wanted a full thyroid panel (T3, T4 etc.) and also ESR & CRP checks for vasculitis and similar maladies. Now it seems from my reading they can often follow celiac so my worry level of those has gone up a notch, more blood tests ahoy it seems? Main reason for worrying about those is the nearly constant tight / tender head I have at the moment. Top and sides of scalp. Could be the stress tensing the shoulders and occipital muscles at back of head but after the celiac diagnosis being missed I'm fearful of anything else being missed. Did anyone else have this tight head feeling at the start? Feels like the skin is being pulled inwards, sometimes goes down for a few minutes here and there and gets worse when sitting I think. I see the term "brain fog" a lot but luckily don't seem to have too much of that at present, this is more a physical sensation.
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