Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.


  • Celiac.com Sponsor (A1):
    Celiac.com Sponsor (A1-M):
  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

1 Month Gluten Free - Still Some Hiccups


IveGotEffinCeliac

Recommended Posts

IveGotEffinCeliac Apprentice

So I've been strictly gluten free for a bit over a month now and a few things seem to be really improving. Along with this forum, that gives me hope. However, the two symptoms that were/are most concerning for me haven't changed at all.

1. The mental "brain fog" isn't getting any better, and my short term memory...... Forget about it, it doesn't exist. Period. I'm absolutely unwilling to accept that this is how I'm going to function mentally from now on. That's not going to happen. Does anyone else feel this way?

2. The muscle fatigue is like nothing I could have imagined prior to a year ago. I can't squat down to play with my nieces without feeling like my legs are going to give out on me as I try and stand up. This one breaks my heart. I don't even recognize my body in the mirror anymore.

I guess my question at this point is, who all does their own vitamin injections, and specifically what are ya'll taking besides a really good (gluten-free) multi, and a healthy daily dose of Omega 3's?

I'm going to start doing B injections, just wondering what everyone else takes/injects. I'm very comfortable doing self injections both intramuscular and subcutaneous. I've got the fish oil, and multi down pat, now I need to know what else I need to be researching.

Just as an aside, celiac.com is amazing and I'm so grateful to have found this forum.


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



Celiac.com Sponsor (A8-M):



anabananakins Explorer
1. The mental "brain fog" isn't getting any better, and my short term memory...... Forget about it, it doesn't exist. Period. I'm absolutely unwilling to accept that this is how I'm going to function mentally from now on. That's not going to happen. Does anyone else feel this way?

My doctor put my on nystatin for candida/yeast overgrowth and that has really helped with the brain fog, which had lasted even after I went gluten free. Might be something to consider?

2. The muscle fatigue is like nothing I could have imagined prior to a year ago. I can't squat down to play with my nieces without feeling like my legs are going to give out on me as I try and stand up. This one breaks my heart. I don't even recognize my body in the mirror anymore.

My endocrinologist was nagging me to lose more weight (I have insulin resistance) and when I complained that I was physically exhausted all the time he tested my vitamin D and it was insanely low (2, should be 50 with 70 optimal). I hadn't heard of the symptoms of vitamin D deficiency before but they include muscle fatigue. I live in a very sunny place and I never dreamed I could be Vit D deficient, I was more concerned about avoiding skin cancer. I don't drive so I'm outdoors walking to the bus stop etc, so getting more incidental sunlight than a lot of people would. So I would urge you to get that tested. Low vitamin D is associated with some awful things.

Hope this helps - all the best to you.

Takala Enthusiast

Only a month isn't that long.

You could still have cross contamination issues that you are not aware of yet. Be sure you are not accidentally getting gluten from old cooking pans, toasters, colanders, cosmetics or pet foods or somebody else's crumbs. Depending on the amount of damage you have it is going to take awhile to get healed up and be able to use nutrients. You might also have a food intolerance to something else, such as soy or dairy or another food group, and you will find yourself doing better once you get settled with what sort of food agrees with your body and gives you energy.

I found that once my hormones started dropping off after menopause, in my mid fifties now, my short term memory got worse, so I have to develop tricks to work around this, and just accept that the really good, effortless memory I used to have is gone and I now have the regular model. :huh: This means I don't hesitate to write notes about stuff instead of winging it from visual images.

I take a multivitamin, B complex, and a calcium/D supplement, and I eat a lot of blueberries.

This also means that if I want to continue to write things that don't sound like gibberish I have to discipline myself more. I was eating more gluten free carbohydrates early in the day, but that just doesn't work for me, and I seem to think better on proteins and fats. This means I went back to something closer to a specific carbohydrate/Atkins style first meal. I also have to exercise.

IveGotEffinCeliac Apprentice

Only a month isn't that long.

You could still have cross contamination issues that you are not aware of yet. Be sure you are not accidentally getting gluten from old cooking pans, toasters, colanders, cosmetics or pet foods or somebody else's crumbs. Depending on the amount of damage you have it is going to take awhile to get healed up and be able to use nutrients. You might also have a food intolerance to something else, such as soy or dairy or another food group, and you will find yourself doing better once you get settled with what sort of food agrees with your body and gives you energy.

I found that once my hormones started dropping off after menopause, in my mid fifties now, my short term memory got worse, so I have to develop tricks to work around this, and just accept that the really good, effortless memory I used to have is gone and I now have the regular model. :huh: This means I don't hesitate to write notes about stuff instead of winging it from visual images.

I take a multivitamin, B complex, and a calcium/D supplement, and I eat a lot of blueberries.

This also means that if I want to continue to write things that don't sound like gibberish I have to discipline myself more. I was eating more gluten free carbohydrates early in the day, but that just doesn't work for me, and I seem to think better on proteins and fats. This means I went back to something closer to a specific carbohydrate/Atkins style first meal. I also have to exercise.

Thank you very much. Although I'm not willing to accept my memory loss, because I know that it can be reversed, I'll definitely consider cross contamination as a possibility. Thank you so much for the input, and helping me make sure my writing also doesn't sound like gibberish.

tarnalberry Community Regular

How is your sleep? Do you feel tired during the day, regardless of how many hours you spend "in bed" or "asleep"? You might consider a sleep study. What you describe is similar to how I would describe my fibromyalgia, which was significantly contributed to by restless leg (which was contributed to by anemia, but not due to celiac disease).

IveGotEffinCeliac Apprentice

How is your sleep? Do you feel tired during the day, regardless of how many hours you spend "in bed" or "asleep"? You might consider a sleep study. What you describe is similar to how I would describe my fibromyalgia, which was significantly contributed to by restless leg (which was contributed to by anemia, but not due to celiac disease).

I will definitely look into this. Let me ask you this, isn't anemia one of the many different manifestations of celiac due to the inability to absorb iron? I've always had trouble falling asleep. Honestly, I wouldn't imagine it was at all related to my celiac. I've had sleep issues for close to 20 years, and just figured it was a part of life for me. Ambian, lunesta, anti depressants, benedryl, soma's... You name it, I've tried to use it to help me sleep. Definitely ask the doc about a sleep study.

sandsurfgirl Collaborator

I hate to tell you this but it can take awhile to heal and your body can get all wonky for awhile.

Don't hate me, but I wasn't fully well for 6 months. I did get better all the time, but feeling really good and having symptom free days took awhile. At 1 month I was still very very sick and not functioning too well.


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



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

I will definitely look into this. Let me ask you this, isn't anemia one of the many different manifestations of celiac due to the inability to absorb iron?

It certainly can be, but - for me - it developed years after going gluten and dairy free.

Good luck figuring out the sleep issues. A chronic lack of sleep is murder on the body, throwing MANY systems out of whack and creating problems that you might not ordinarily assign to sleep.

IveGotEffinCeliac Apprentice

I hate to tell you this but it can take awhile to heal and your body can get all wonky for awhile.

Don't hate me, but I wasn't fully well for 6 months. I did get better all the time, but feeling really good and having symptom free days took awhile. At 1 month I was still very very sick and not functioning too well.

I'm definitely not hating. There's just this sense of urgency to get myself back to my pre celiac days. My wife is expecting our first child in 8 weeks, and I don't want to be sick anymore when my son is born.

The cross contamination is a real concern of mine. I eat free where I work, (I manage a department at a casino) but there's no definitive way to prove or disprove cross contamination. I eat exactly the same thing at work each and every day. I have plain old cottage cheese with sliced canned peaches. I have plain scrambled eggs with some basic salsa mixed in. I have chopped fresh fruit.. Usually its watermelon and pinapple.

I don't see bringing food to work as a viable financial option. So hopefully I'm not beign cc'd when I eat there.

I totally get it about one month not being long enough for me to feel better. I'll keep pluggin away and hopefully my body really is reparing itself.

IveGotEffinCeliac Apprentice

It certainly can be, but - for me - it developed years after going gluten and dairy free.

Good luck figuring out the sleep issues. A chronic lack of sleep is murder on the body, throwing MANY systems out of whack and creating problems that you might not ordinarily assign to sleep.

Thank you. I've just accepted that sleep will always be a struggle. I can live with that, much easier than I can live with the way my body looks today compared to 2 years ago.

Chakra2 Contributor

I'll chime in with another "it takes awhile" comment. My GI symptoms improved immediately going gluten free, but the other symptoms (brain fog, the blues, fatigue, joint pain) took much longer to clear up. It was 5-6 months before I felt remotely okay for more than one or two days at a time. The things that helped me, I think, were time to heal; eliminating dairy, soy and nightshades (nightshades especially made a difference pain-wise); weeding out more and more contamination culprits (including avoiding all restaurant food for awhile); changing personal care products to all gluten-free shampoo, etc; making the whole house gluten-free (dog food, no gluten at home for husband).

Also, after keeping a food diary to help track down my other intolerances I did notice that eggs make me feel totally exhausted. I eat them once a week or so anyway just for some variety but I now know to expect major sleepiness 1-2 hours later. So between the cottage cheese, eggs, and salsa (nightshades) you could be eating something there that doesn't agree with your body right now. So you might want to explore other food intolerances before you work on the supplement angle. Getting rid of foods that are slowing down your healing will help the supplements work better, in my opinion.

I did try to get my b levels up from the beginning with probiotics (I still take a double dose most days) and fermented foods like Rejuvelac. (google it for a recipe -- and then follow the directions but use quinoa instead of rye or any other gluten grain). So you could try that before you jump to injections.

One caution for the future -- look out for gluten in baby stuff! Switching to gluten-free baby shampoo, lotion, and diaper cream really helped me and my son. I like the California Baby products because they're so clear about their allergen labeling.

I hope you find some relief here before your baby comes. I have never felt as stressed as I did trying to care for my child while I was still sick. Not fun. Good luck!

IveGotEffinCeliac Apprentice

I'll chime in with another "it takes awhile" comment. My GI symptoms improved immediately going gluten free, but the other symptoms (brain fog, the blues, fatigue, joint pain) took much longer to clear up. It was 5-6 months before I felt remotely okay for more than one or two days at a time. The things that helped me, I think, were time to heal; eliminating dairy, soy and nightshades (nightshades especially made a difference pain-wise); weeding out more and more contamination culprits (including avoiding all restaurant food for awhile); changing personal care products to all gluten-free shampoo, etc; making the whole house gluten-free (dog food, no gluten at home for husband).

Also, after keeping a food diary to help track down my other intolerances I did notice that eggs make me feel totally exhausted. I eat them once a week or so anyway just for some variety but I now know to expect major sleepiness 1-2 hours later. So between the cottage cheese, eggs, and salsa (nightshades) you could be eating something there that doesn't agree with your body right now. So you might want to explore other food intolerances before you work on the supplement angle. Getting rid of foods that are slowing down your healing will help the supplements work better, in my opinion.

I did try to get my b levels up from the beginning with probiotics (I still take a double dose most days) and fermented foods like Rejuvelac. (google it for a recipe -- and then follow the directions but use quinoa instead of rye or any other gluten grain). So you could try that before you jump to injections.

One caution for the future -- look out for gluten in baby stuff! Switching to gluten-free baby shampoo, lotion, and diaper cream really helped me and my son. I like the California Baby products because they're so clear about their allergen labeling.

I hope you find some relief here before your baby comes. I have never felt as stressed as I did trying to care for my child while I was still sick. Not fun. Good luck!

Wow, thank you for taking the time with that great reply. I studied up on nightshades, and it's sort of like dairy for me. If I have to give up on my salsa, and tomatoes.... Well, I just wouldn't ever give those up. Eliminating gluten is an amazingly difficult pill to swallow. For me personally, I have to draw the line somewhere. Thank you for the heads up on baby stuff containing gluten. We'll be aware of this and proceed with caution. And thank you. I hope I feel better before he's born too!

fatlazyceliac Newbie

I've only been gluten-free for two months, but went and got blood levels tested anyway. I'm low in Vit. D and borderline low on B12, so just started taking both. We'll see how they help!

IveGotEffinCeliac Apprentice

I've only been gluten-free for two months, but went and got blood levels tested anyway. I'm low in Vit. D and borderline low on B12, so just started taking both. We'll see how they help!

I'll definitely follow your progress! Hope the B and D make a huge difference for you.

IveGotEffinCeliac Apprentice

and thank you!

Looking for answers Contributor

While you're getting all your other vitamin/mineral levels checked out, have them test you for iron deficiency. I can hardly remember my name when my iron levels are low. Also, when my thyroid acts up, my memory loss does too.

IveGotEffinCeliac Apprentice

While you're getting all your other vitamin/mineral levels checked out, have them test you for iron deficiency. I can hardly remember my name when my iron levels are low. Also, when my thyroid acts up, my memory loss does too.

Thank you. I may have to look into another GI. The nurse or secretary at this office is very unhelpful. I got all my levels tested, and she won't tell me anything other than "your results look pretty normal." I'm going to physically drive up there and get a copy of my labs, then I'll have a starting point.

ravenwoodglass Mentor

Thank you. I may have to look into another GI. The nurse or secretary at this office is very unhelpful. I got all my levels tested, and she won't tell me anything other than "your results look pretty normal." I'm going to physically drive up there and get a copy of my labs, then I'll have a starting point.

If your happy with your GI before you switch tell the doctor why your considering changing doctors. Doctors need to know when their staff is rude and unhelpful.

IveGotEffinCeliac Apprentice

If your happy with your GI before you switch tell the doctor why your considering changing doctors. Doctors need to know when their staff is rude and unhelpful.

Thank you! I'll do just that.

michellern Rookie

I hate to tell you this but it can take awhile to heal and your body can get all wonky for awhile.

Don't hate me, but I wasn't fully well for 6 months. I did get better all the time, but feeling really good and having symptom free days took awhile. At 1 month I was still very very sick and not functioning too well.

I have been gluten-free for 1 month now. The nausea is better, but I still do not have an appetite. I am also on a 2 week lactose free trial. Doctor thinks maybe lactose intolerent. I am still not functioning well at all. I am still not able to return to work! I am trying to be patient! :(

jackay Enthusiast

My doctor put my on nystatin for candida/yeast overgrowth and that has really helped with the brain fog, which had lasted even after I went gluten free. Might be something to consider?

Nine months later I still have brain fog and short term memory issues. I've been trying to rid myself of candida for quite some time with natural supplements. I definitely need to see my doctor soon about trying Nystatin.

Can anyone help me out with what a normal dosage is. Is generic Nystatin effective? Is there a chance the generic would contain gluten?

IveGotEffinCeliac Apprentice

I have been gluten-free for 1 month now. The nausea is better, but I still do not have an appetite. I am also on a 2 week lactose free trial. Doctor thinks maybe lactose intolerent. I am still not functioning well at all. I am still not able to return to work! I am trying to be patient! :(

Is losing your appetite a common side effect of Celiac? I just want to eat and eat and eat and eat. Only thing is, I am losing weight rather than gaining.

IveGotEffinCeliac Apprentice

Nine months later I still have brain fog and short term memory issues. I've been trying to rid myself of candida for quite some time with natural supplements. I definitely need to see my doctor soon about trying Nystatin.

Can anyone help me out with what a normal dosage is. Is generic Nystatin effective? Is there a chance the generic would contain gluten?

I feel so relieved to hear that other people experience the same brain fog. I'm really sorry that yours isn't much better. 9 months? Are your villi repopulating?

jackay Enthusiast

I feel so relieved to hear that other people experience the same brain fog. I'm really sorry that yours isn't much better. 9 months? Are your villi repopulating?

I have no idea since I never had an endoscopy nor do I plan on having one. I am hoping it is a candida issue since I am still battling that.

IveGotEffinCeliac Apprentice

I have no idea since I never had an endoscopy nor do I plan on having one. I am hoping it is a candida issue since I am still battling that.

When will you find out?

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Wheatwacked replied to Heatherisle's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      34

      Blood results

    2. - Known1 replied to xxnonamexx's topic in Gluten-Free Foods, Products, Shopping & Medications
      6

      FDA looking for input on Celiac Gluten sensitivity labeling PLEASE READ and submit your suggestions

    3. - Wheatwacked replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      31

      results from 13 day gluten challenge - does this mean I can't have celiac?

    4. - Wheatwacked replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      31

      results from 13 day gluten challenge - does this mean I can't have celiac?

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,411
    • Most Online (within 30 mins)
      7,748

    EBeloved
    Newest Member
    EBeloved
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • Wheatwacked
    • Wheatwacked
      Celiac Disease causes more vitamin D deficiency than the general population because of limited UV sunlight in the winter and the little available from food is not absorbed well in the damaged small intestine.  Taking 10,000 IU a day (250 mcg) a day broke my depression. Taking it for eleven years.  Doctor recently said to not stop.  My 25(OH)D is around 200 nmol/L (80 ng/ml) but it took about six years to get there.  Increasing vitamin D also increases absorption of Calcium. A good start is 100-gram (3.5-ounce) serving of salmon,  vitamin D from 7.5 to 25 mcg (300 to 1,000 IU) but it is going to take additional vitamin D supplement to be effective.  More importantly salmon has an omega-6 to omega-3 ratio 1:10 anti-inflammatory compared to the 15:1 infammatory ratio of the typical Western diet. Vitamin D and Depression: Where is all the Sunshine?
    • Known1
      Thank you for sharing your thoughts.  I respectfully disagree.  You cherry picked a small section from the page.  I will do the same below: The agency is seeking information on adverse reactions due to “ingredients of interest” (i.e., non-wheat gluten containing grains (GCGs) which are rye and barley, and oats due to cross-contact with GCGs) and on labeling issues or concerns with identifying these “ingredients of interest” on packaged food products in the U.S. “People with celiac disease or gluten sensitives have had to tiptoe around food, and are often forced to guess about their food options,” said FDA Commissioner Marty Makary, M.D., M.P.H. “We encourage all stakeholders to share their experiences and data to help us develop policies that will better protect Americans and support healthy food choices.” --- end quote Anyone with celiac disease is clearly a stakeholder.  The FDA is encouraging us to share our experiences along with any data to help develop future "policies that will better protect Americans and support healthy food choices".  I see this as our chance to speak up or forever hold our peace.  Like those that do not participate in elections, they are not allowed to complain.  The way I see it, if we do not participate in this request for public comment/feedback, then we should also not complain when we get ill from something labeled gluten-free. Have a blessed day ahead, Known1
    • Wheatwacked
      Here is a link to the spreadsheet I kept to track my nutrition intakes.  Maybe it will give you ideas. It is not https so browsers may flag a security warning. There is nothing to send or receive. http://doodlesnotes.net/index3.html I tracked everything I ate, used the National Nutrition Database https://www.foodrisk.org/resources/display/41 to add up my daily intake and supplemented appropriately.  It tracks about 30 nutrients at once.
    • Wheatwacked
      Hello @catnapt, That's so true.  Every person with Celiac Disease has different symptoms.  There are over 200 that it mimics.  Too many still believe that it is only a childhood disease you outgrow.  Or it's psychosomatic or simply a fad.  Idiots.  It's easy to get angry at all of them.   You just have to pick at the answers until you find the ones that work for you.  I too suffer from not being able to take the drugs that work for "everyone else".  SSRIs make me twitch ane feel like toothpicks are holding my eye open, ARBs cripple me.  Statins cause me intestinal Psuedo Obstruction.  Espresso puts me to sleep.  I counted 19 different symptoms that improved from GFD and dealing with my nutritional defecits.  I couldn't breath through my mouth until I started GFD at 64 years old.   My son was born with celiac disease, biopsy diagnosed at weaning.   So why are we the one-percenters.  Why, after being silent for so long, does it suddenly flare? There is the possibility that you have both Celiac Disease and Non Celiac Gluten Sensitivity.  NCGS was not established as a diagnosis until 1980.  NCGS is diagnost by first elimating Celiac Disease as the cause, and showing improvement on GFD.  Nothing says you can't have symptoms from both.  Wheatbelly: Total Nutrition by Dr. Davis was helpful to me. We come to the forum to share what we've learned in dealing with our own symptoms.  Maybe this will help someone. Speaking of which if you don't mind; what is your 25(OH)D vitamin D blood level?  You mentioned a mysterious Calcium issue. Vitamin D, Calcium and Iodine are closely interactive. It is not uncommon for postmenopausal women to have insufficient intake of Iodine.   (RDA): Average daily level of intake sufficient to meet the nutrient requirements of nearly all (97%–98%) healthy individuals; often used to plan nutritionally adequate diets for individuals You are a one-percenter.  You may need higher intake of some essential nutrient supplements to speed up repairing the damages.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.