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

Day 1 No Gluten


McDougall

Recommended Posts

Guest NancyNet

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 :)


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



Celiac.com Sponsor (A8-M):



  • Replies 62
  • Created
  • Last Reply
tom Contributor

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 !

McDougall Apprentice

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...

judy05 Apprentice

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.

Maggie1956 Rookie

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 :)

darlindeb25 Collaborator
;) 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
McDougall Apprentice

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.


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



Celiac.com Sponsor (A8-M):



McDougall Apprentice

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

FreyaUSA Contributor
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!

McDougall Apprentice

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.

Maggie1956 Rookie

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:

tom Contributor
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.

McDougall Apprentice

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.

Maggie1956 Rookie
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

darlindeb25 Collaborator

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

Guest imsohungry

Well stated Deb!!! ;)B)

-Julie

McDougall Apprentice

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.

stef-the-kicking-cuty Enthusiast

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

YankeeDB Contributor

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

Guest imsohungry

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 :)

Maggie1956 Rookie

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 :)

McDougall Apprentice

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.

Canadian Karen Community Regular

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

tom Contributor

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.

McDougall Apprentice

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.

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. - knitty kitty replied to badastronaut's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Still unsure.....

    2. - badastronaut replied to badastronaut's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Still unsure.....

    3. - knitty kitty replied to badastronaut's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Still unsure.....

    4. - badastronaut replied to badastronaut's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Still unsure.....

    5. - knitty kitty replied to badastronaut's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      11

      Still unsure.....


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      129,739
    • Most Online (within 30 mins)
      7,748

    gexewib
    Newest Member
    gexewib
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.2k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      If you're more comfortable starting slow, that's fine, but do increase your dose to 500 mg per day as quickly as possible.  The World Health Organization recommends 500 mg thiamine HCl per day when deficiency is suspected.  Dr. Lonsdale had researched high dose thiamine for decades, and he has used higher doses, 1 to 3 grams in some cases.   Like I explained above, it's at that 500 mg level or higher that passive diffusion happens and thiamine can get into cells.  Inside the cells, thiamine turns the mitochondria back on.  Mitochondria produce energy the cells use to function.  I had been taking a multivitamin containing thiamine HCl regularly and still had become deficient.  Malabsorption of celiac disease really affects vitamin absorption.  I bought a bottle of thiamine HCl.  I was skeptical, too. I thought it couldn't be that easy.  I took 500 mg all at once.  I had improvement within minutes.  I couldn't believe the sensation of energy spreading to all parts of my body.  My brain felt like it was lifted out of a sub-sub-basement by an elevator and lights were coming on, floor by floor, of a skyscraper.  It was mental improvement, mental clarity.  Thiamine is needed for nerves to transmit electrical impulses, so the more nerves transmitting electrical impulses, the more my brain started working better.  The better my brain started working, the better I felt physically.  My muscles had more energy.  I wanted to get up and do stuff.   P.S. Questions are welcome.  "there's no poverty like ignorance, no wealth like knowledge". Keep learning!
    • badastronaut
      Thanks! I think I'll start slow. See what happens. Should I notice the thiamine working almost straight away if I'm really deficient? What kinda of difference did you notice? More mental? Of also physical in the sense of more energy?    Sorry for all the questions! 
    • knitty kitty
      Absolutely no danger of overdosing on the stuff.  Thiamine is nontoxic, and safe.  I had gotten to 1000 mg of Thiamine HCl a day at one point.   Do continue taking the multivitamin with the other B vitamins.  You may want to add a magnesium supplement because magnesium and thiamine make enzymes together.  I like Magnesium l-Threonate (Neuro-Mag by life extension).  You may want to add a B Complex in addition to the multivitamin (take them at different times).  All the B vitamins are water soluble.   With Thiamine HCl, there's a "magic moment" about 500 mg, where sufficient thiamine can get into the cells by passive diffusion, and the difference is amazing.  In thiamine insufficiency, the thiamine transporters (special gates into the cell) shut down.  Thiamine cannot get into the cells until there's a higher concentration outside of the cell.  Once that happens, the  thiamine can get through and go to work inside the cells.   If you're brave, start with 300 mg at one meal and 200 mg at the next meal.  Increase as you feel comfortable.  You may want to stay at one amount for a few days before increasing again.  Just keep adding another 100 mg as long as you keep feeling improvement.  If you feel uncomfortable, skip the next dose.  Thiamine HCL is water soluble and excess is easily excreted.  Don't take thiamine close to bedtime because you may feel too energized to sleep.   Thiamine HCl may feel like riding in the back of a pick up truck on a gravel road.  Benfotiamine feels like you're in a chauffeur driven Rolls Royce.  TTFD feels like you're driving a Lamborghini.  You'll get there no matter what kind of thiamine is taking you there.  Just keep taking it.  The health improvements can be very subtle, but you'll notice in the long run.   I started with 500 mg of Thiamine HCl, to see what would happen and had amazing improvement within an hour.  I took 300 mg with each of two meals and 100 mg with snacks.  I eventually added in Benfotiamine (250 mg  a couple of times a day) and reduced the thiamine HCl.  Later I added in TTFD (50 mg) several times a day.  Just experiment and see what feels right for you. Everyone is different and has a different level of deficiency.   I kept having additional improvement with each type of thiamine.  I've taken thiamine for almost fifteen years now.  I still take all three kinds on maintenance doses.  You have to experiment and see which ones work best for you in which combination.   I'm right here if you need anything.   You'll be fine.
    • badastronaut
      Thanks so much for your replies! no danger of overdosing on the stuff? or having the other B levels going out of whack? I do take a multivitamin with all te other B vitamins at the RDA level. I have bought the HCL version of Thiamine. How long do you need to use the Thiamine? a short periode on high levels and then back to a maintenance dosage?
    • knitty kitty
      Kudos for trying thiamine! On the ingredients label it should say if it's thiamine hydrochloride (thiamine HCl) or thiamine mononitrate or something else.   Thiamine mononitrate is shelf stable and not easily utilized in the body.   Yes, go ahead and try a whole 100 mg tablet.   Take with a meal.  Don't take close to bedtime.  Tomorrow take a 100 mg tablet with two meals. The next day take two 100mg tablets at one meal and 100 mg at second meal.  Keep increasing in this manner as long as you notice improvement.   When I first started with thiamine hydrochloride, I felt like the lights in my head were being turned on floor by floor like in a tall skyscraper.  It's just the brain working properly with sufficient thiamine.  I worked up to 1000 mg a day.  Lots if tablets.  Benfotiamine and TTFD are stronger and are utilized easier, so not as many milligrams ate needed.   I'm happy to answer any further questions!  
×
×
  • Create New...