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

Still Lethargic All The Time


Ashy555

Recommended Posts

Ashy555 Newbie

I was diagnosed with Coeliac Disease officially in October last year. I have always gotten really tired but thought it would ease up shortly after going on a Gluten free diet.

 

My initial blood test showed my ferratin levels were only a 3 and my haemaglobin had dropped quite considerably. My gastro sent me off for an iron infusion which sent it up to 900. Since it has been dropping extremely quick but i am assuming that is quite normal as it got so high. My bloods are still normal(since end of dec) except i noticed my platelets have been dropping a fair amount each month. Im due for another blood test this month.

 

Basically i am really struggling to cope. I STILL get night sweats and i wake up every morning feeling awful and sometimes achy. I start to feel a little better as i get myself moving BUT once 10am hits at work, its like i hit a brick wall. I find it really hard to get up in the morning and organise my breakfast and lunch(which is quite necessary as you probably know) I finish work at 5, get home at 6:30 and im in bed by 7.30 - 8.30 at the latest then sleep straight through to 6:30. If i had time i would be napping all afternoon. It is starting to effect my ability to work and my social life. I cannot do anything after work unless i really push myself. I saw my GP in Jan and he said its fairly normal and to keep all my multivitamins up(even though my levels are fine)

 

Is it still considered normal to be this tired almost 5 months of being on a gluten free diet? I just dont understand what is causing it. :(


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi Ashy,

 

Welcome to the forum! :)

 

There are several long threads on night sweats on the forum.  You might find them interesting to read.  Try searching the forum for night sweats and looking for hits with lots of posts.  I think they can be a reaction to inflammation in the body, possibly in the gut.  Inflammation could be from continued autoimmune reactions that haven't tapered off yet for some reason.  It may be that your immune system is going to put up a good fight for a while longer before it relaxes.  It could also be that there is a gluten sneaking into your diet somehow.  Taking a good long look at everything you eat each day is a good start toward finding hidden gluten.  If it isn't something obvious then the next step is to start eliminating things that "might" have gluten even though they don't indicate it on the label.  Vitamin pills, medicines, teas, drinks and anything that you consume need to be verified or better yet eliminated for a couple weeks to see if it makes a difference..

 

Another possible cause of fatigue is hypo-thyroid.  Hashimoto's thyroiditis can cause inflammation in the thyroid gland (throat) and that might cause fatigue and night sweats.

 

A whole foods diet is a great way to troubleshoot food problems.

 

1desperateladysaved Proficient

Did you check for more food intolerances?

Did you try pancreatic enzymes and probiotics?

Do you read every label?

Do you make your food from scratch?

 

I know it is all hard when you're tired.  Please keep up.  My head cleared around the 6 month.  It could have been time, or it could have been new suppliments, or rotational diet plan.  It seemed to me about the 6 month my body really started changing fast.

 

I hope you will have a clear mind soon.  You are moving, even if it doesn't feel like it and even if it is slow and bumpy.

Ashy555 Newbie

Hi Ashy,

 

Welcome to the forum! :)

 

There are several long threads on night sweats on the forum.  You might find them interesting to read.  Try searching the forum for night sweats and looking for hits with lots of posts.  I think they can be a reaction to inflammation in the body, possibly in the gut.  Inflammation could be from continued autoimmune reactions that haven't tapered off yet for some reason.  It may be that your immune system is going to put up a good fight for a while longer before it relaxes.  It could also be that there is a gluten sneaking into your diet somehow.  Taking a good long look at everything you eat each day is a good start toward finding hidden gluten.  If it isn't something obvious then the next step is to start eliminating things that "might" have gluten even though they don't indicate it on the label.  Vitamin pills, medicines, teas, drinks and anything that you consume need to be verified or better yet eliminated for a couple weeks to see if it makes a difference..

 

Another possible cause of fatigue is hypo-thyroid.  Hashimoto's thyroiditis can cause inflammation in the thyroid gland (throat) and that might cause fatigue and night sweats.

 

A whole foods diet is a great way to troubleshoot food problems.

 

 

Thanks for the welcome :) Its nice to know i can come somewhere that people will understand. Not even my Gp seems the understand. He tells me i will get the ocasional bloating and thats about it. When i try and tell him my symptoms he doesnt even seem to acknowledge them.. night sweats... aching joint.. depression.. and in the past month it seems to have calmed down but i used to get real odd experiences. My vision would go a little funny and it felt like i was dizzy or something. I would even get it when lying in bed, so im assuming it was all part of it. He made sure he tested my thyroid and it all came back normal.

 

I have had one particular poisoning(gluten) and that was just a few days after christmas. Most horrific night i have experienced so far. I guess the more i go without gluten, the more sensitive i get so at the moment im very careful with my labels and my parents have decided to go gluten free as well except for the occasional toast in the morning here and there. I went through the pantry with my mum and got rid of every sauce we had containing gluten and replaced them with gluten-free options. Pretty much everything i eat is prepared at home or bought from the supermarker labelled gluten free. I very rarely have take away or go out for dinner anymore :(

 

I was meaning to post in this forum many months ago as obviously when first being diagnosed it is so hard. I actually ended up losing my job in September last year while i was in the process of being diagnosed due to not working effectively. I was just never switched on, i couldnt concentrate at all... I was already feeling pretty depressed and unhappy but this just made me spiral more. I would get angry at minor things including my mum for getting the wrong type of mushrooms who of anyone has been the most supportive and amazing person i knew it was wrong and it broke my heart. I didnt know where this anger came from. I ended up finding a new job 2 months later but it was SO hard adjusting to a completely new lifestyle. The stress caused me to break down multiple times usually at midnight when everyone was asleep. I think i scared the hell out of my parents. It ended up landing me in emergency due to heart palpitations.. which i figured was just stress. A new job plus getting up to prepare my foods every day and travelling an hour to get to and from work and it just made things worse, but i am so glad i now know i am on the road to recovery and hopefully i wont even know myself soon. Like so many people tell me. Turns out this new job was a blessing but i just cant handle all the fatigue. I think i just really need to pull up my socks and try be a bit more positive. I tell you what though.. coeliac disease certainly aint a walk in the park as i am experiencing... like some people seem to think. So glad to know i can come to a place where im not the only one.

GFinDC Veteran

Yep, celiac can be quite a challenge Ashy.  It takes time to get used to eating "right" and learning things to avoid.  But it does happen and it gets easier when you after are used to it.  Kind of like  a walk in the park on a sunny day in spring! :D  we had a long thread about anger issues and celiac a while back.  Quite a few people reported they had unexplained anger or emotional reactions they didn't expect.  Uncharacteristic emotional reactions that is.  Celiac can affect the brain, obviously as it can cause gluten ataxia.  So it's no surprise that it can affect people's emotional estate to me anyhow.  Heck, I had unexpected anger issues for a while myself.

 

That's great that your mom is helping you with the gluten-free diet.  Sounds like she is going gluten-free also, at least at home right?  That should simplify things some.  I don't know if you have pets, but they are another possible source of cc.  But there are gluten-free pet foods available too.  That's the issue with them, their food and how they like to spread it around and share it.

 

It's easy for us to be aware of gluten in foods but people who don't live with celiac tend not to think of gluten at all.  So it can help to be patient with the gluten eaters of the world as they just don't know any better.  Sometimes we have to be very patient. :)

funkflex Rookie

Hi, I too was diagnosed in October, I'm still not where I want to be energy- and stomachwise. So you're not the only one struggling with this. But I really can't say what's normal and what's not. Maybe you should push for further assessment just to be on the safe side.

EricaM15 Rookie

To me it sounds like you're struggling with secondary intolerances. Many people with Celiac are intolerant to other foods that are traditionally considered gluten free. I personally struggled with this--after being on a gluten-free diet for only a month, my symptoms returned. You may be intolerant of all grains the way I am. A small amount of any grains will keep me up at night, make me tired, anxious/depressed, bloated, etc. I'd recommend looking into an elimination diet to narrow down which foods are causing the problem. Cross-contamination may also be an issue.


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



Celiac.com Sponsor (A8-M):



  • 3 weeks later...
Ashy555 Newbie

Ok so i started by seeing my GP and having some more tests done. I have looked at the results myself but have not seen my GP as yet... everything seems to look ok except for my Thyroid.. It seems to have dropped from an average of 1.8 down to 0.7 normal range being 0.5 - 5.0 within a few months. Do you think this could have anything to do with my energy levels? My family and i have decided to start strict paleo again starting next week. Ive been home by myself for the past two weeks and have been worse than ever. I have had absolutely no energy to get up.. i havent been making my breakfast or my lunch(i work at a hospital so they are very stricts with what they advertise as gluten-free which is good) so i have been buying it(its usually a curry or salad) and for breakfast ive been eating a piece of gluten free bread. All the fresh food in my fridge is starting to go off and i feel awful as my dear mum made sure it was stocked so i could eat well but i havent had any energy to make any salads or veges.. or cook any meats or buy anything. Then for dinner i usually have a few crackers, piece of fruit or gluten-free bread so i can go straight to bed. The house is starting to become a complete mess and im not coping by myself. Yesterday I managed to fry up a steak which i could only eat half of. Im hoping when im on this no grain diet i can get some of my energy back.

My doctor has also suggested that i cut my hours back and try and exercise more. Im currently booked in for pt training at 7am every Monday which for the past month i have had to keep cancelling, but i dont think i can cut back on my work as they really need me full time.

cavernio Enthusiast

Did you get tested for any other vitamin problems than iron? B vitamins, all of them, are essential for energy. Lack of B6 can cause night sweats specifically. B12 is another common one that they probably tested for though.

 

If you collapse at work you're no help to them either. I don't see how excersising will give you more energy at this point, it will just make things harder for you. Mild things like short walks and stretches are very helpful for a sedentary job, but I can't think of a single person who sits still for long in a hospital.

 

I would like to think the hospital's gluten free food is safe, but you never know. I'd be worried about curried anything, as I have a hard time finding any sort of mixed spice that claims it's gluten free. The hospital might be going only by ingredients on labels.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.