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

Please Help! Some Questions And My Symptoms


glasgowfranko1981

Recommended Posts

glasgowfranko1981 Contributor

Hello all,

I have a few questions relating to the possibility of my having Celiacs . . .

Just some info before asking my questions:

1. I am a 31 year old male, physically fit, enjoy exercise, varied diet. No history of any allergies.

2. In a high stress media job with a hectic schedule, and a history of stress, anxiety and occasional bouts of depression since my teens.

3. In early January this year I had a bizarre rash appear on my face, unexplained. Disappeared in a few days and didn't think much of it. Quite strange.

4. In May this year I fell ill with a "mystery" illness/virus for a number of weeks on and off (more cold like than anything, but had me incapacitated for a few weeks with severe fatigue, muscle pain and "brain fog" afterwards as well). Things improved for a while, but the symptoms seemed to get getting worse again and again intermittently, the main symptoms being muscle pain in my legs (especially at night, waking me up), clicking joints (new for me at 31), brain fog and severe fatigue (so much so I couldn't even make a cup of tea, or hold a book).

5. Some bowel irregularity, bloatedness/flatulence etc intermittently as well, however, I have always suffered from bowel irregularity due to a blocked intestine (as a child). Overall, the main symptoms with this as a whole is the severe fatigue, brain fog and muscle pain (mostly in my legs).

6. Various blood tests have showed no signs of anything irregular so far, both with doctor and hospital - so, the discussion of something called "celiacs" came up with my GP. The doc suggested cutting out gluten as a test. I done this, and the symptoms seem to have dispersed, until lately when I think I may have accidentally eaten silent gluten in some processed foods.

My questions:

1. Can celiac's main symptom ONLY be the muscle pain (in legs), fatigue and brain fog?

2. Does cutting out gluten improve health for NON Celiacs?

3. How long after gluten has been ingested do typical symptoms come on?

4. How long following gluten being cut should things go back to normal?

5. I have a feeling blood tests will NOT show this up, what other tests are there?

6. Could this list of symptoms be ANYTHING else similar and NOT celiacs?

7. Even on a gluten free diet can stress make this worse?

Special note: My Mum died an unexplained death in 1994 when I was 12 after years of an unexplained illness with all the classic symptoms of Celiacs, which is also currently being investigated by a private investigator as 'undiagnosed Celiacs'.

Any info, suggestions or comments are greatly appreciated.

Thanks in advance!


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Hi glasgowfranko, and welcome:

Celiac disease can strike someone who has been perfectly healthy in the past, just as any disease. For some its main symptoms are fatigue, lethargy, brain fog, joint pain. More common are bloating, flatulence, stomach cramping, diarrhea and/or constipation. Some have neurological symptoms, some have skin rashes. So you fit the pattern on a number of counts. Usually the onset is triggered by physical disease or injury or severe emotional distress. In women it is often triggered by childbirth.

So your doctor suggested the elimination of gluten and you have felt better, until a likely episode of glutening, possibly due to cross-contamination or some unidentified ingredient.

Gluten free has been a fad diet among celebrities and athletes, the latter claiming it enhances performance, the former (supposedly??) doing it for weight loss or to follow the trend. There is no scientific evidence I know of that eating gluten free benefits anyone who does not have a gluten intolerance. In fact, athletes for years have been doing pasta carbo-loading before events :o

Time from gluten ingestion to symptoms varies for everyone, so is not a reliable indicator -- from hours to a day or two.

Time for healing after eliminating gluten is also variable. Depends on individual healing time and degree of damage.

If you have been eating gluten free blood tests will not diagnose celiac disease because they measure the number of gluten antibodies in the bloodstream. Without gluten the antibodies go away and you have to do what is called a "challenge" where you reingest gluten for (let's not get into how long because there is great disagreement on this) a time before the testing.

Many doctors will tell you these are symptoms of IBS (irritable bowel syndrome or, as we call it, I Be Stumped); some may postulate Crohn's disease or various other GI disorders.

The one method of diagnosis which has been used since testing first became common is the upper endoscopy where they take samples of the small intestine and examine them under a microscope looking for damage to the GI tract. Again, in the absence of gluten this can start healing and the testing can be negative. So, in my book doctors should (like in the days of the old wild west) shoot first, ask questions later :D or, in other words, test first, trial the diet later. Because after being gluten free you then have to go back to gluten for testing, and this is often a very painful experience because the body is so happy to be rid of gluten it punishes you when you bring it back :ph34r:

And yes, if you feel stressed, stress can make everything worse, even a pimple on the face before the prom :blink::lol:

If this has not answered your questions feel free to come back with more. :)

SMDBill Apprentice

Hello all,

I have a few questions relating to the possibility of my having Celiacs . . .

Just some info before asking my questions:

1. I am a 31 year old male, physically fit, enjoy exercise, varied diet. No history of any allergies.

2. In a high stress media job with a hectic schedule, and a history of stress, anxiety and occasional bouts of depression since my teens.

3. In early January this year I had a bizarre rash appear on my face, unexplained. Disappeared in a few days and didn't think much of it. Quite strange.

4. In May this year I fell ill with a "mystery" illness/virus for a number of weeks on and off (more cold like than anything, but had me incapacitated for a few weeks with severe fatigue, muscle pain and "brain fog" afterwards as well). Things improved for a while, but the symptoms seemed to get getting worse again and again intermittently, the main symptoms being muscle pain in my legs (especially at night, waking me up), clicking joints (new for me at 31), brain fog and severe fatigue (so much so I couldn't even make a cup of tea, or hold a book).

5. Some bowel irregularity, bloatedness/flatulence etc intermittently as well, however, I have always suffered from bowel irregularity due to a blocked intestine (as a child). Overall, the main symptoms with this as a whole is the severe fatigue, brain fog and muscle pain (mostly in my legs).

6. Various blood tests have showed no signs of anything irregular so far, both with doctor and hospital - so, the discussion of something called "celiacs" came up with my GP. The doc suggested cutting out gluten as a test. I done this, and the symptoms seem to have dispersed, until lately when I think I may have accidentally eaten silent gluten in some processed foods.

My questions:

1. Can celiac's main symptom ONLY be the muscle pain (in legs), fatigue and brain fog?

2. Does cutting out gluten improve health for NON Celiacs?

3. How long after gluten has been ingested do typical symptoms come on?

4. How long following gluten being cut should things go back to normal?

5. I have a feeling blood tests will NOT show this up, what other tests are there?

6. Could this list of symptoms be ANYTHING else similar and NOT celiacs?

7. Even on a gluten free diet can stress make this worse?

Special note: My Mum died an unexplained death in 1994 when I was 12 after years of an unexplained illness with all the classic symptoms of Celiacs, which is also currently being investigated by a private investigator as 'undiagnosed Celiacs'.

Any info, suggestions or comments are greatly appreciated.

Thanks in advance!

I'll just answer based on my situation and my current experience with celiacs. I've been gluten free 6 weeks now and glutened once, just 3 days ago.

1. Some people have no symptoms they can feel at all so I would imagine you could have none, one or any combination of symptoms if you have celiac. I have read many people's accounts and they widely vary. Most common is diarrhea or constipation, brain fog, tingling in arms and hands, and intestinal pain/discomfort. Personally, I had oily stools, skin irritations, constant sinus drainage and throat clearing, muscle weakness and tingling...all in addition to those more common symptoms. I also suffered daily headaches, occasionally resulting in migraines with nausea, vomiting and diarrhea.

2. Gluten free has become a fad, but wheat and other grains are enriched with a lot of goodies. Cutting them out for no health benefit other than fear or following what others do is senseless and expensive, plus may require supplements to replace what other foods were already providing.

3. I was glutened on last Sunday and by Sunday night i could feel a change. The pain started Monday morning and is still not gone, but very much improved.

4. Removing gluten never returns things to normal. Symptoms improve or disappear, but the slightest ingestion of gluten will reverse weeks, months or years of work in the gut. It's a constant battle and there is no end.

5. Other tests will require biopsies. THe most conclusive evidence will be through elimination of gluten in your diet. Tests may come back negative, but your body will not lie to you if you avoid gluten. I felt better in just 2 days of going gluten-free...life changing improvement in 2 days. Others take weeks or months, but mine was almost miraculous when I got my energy back, skin improved, intestines stopped hurting completely, etc. These last 3 days were a quick reminder of how far I had come and now I wish for that great feeling to come back. It's taken longer to be gluten-free, get glutened and get back to feeling normal than it did to cut out gluten and feel great.

6. I won't even venture a guess as to what your symptoms could be. I'm not a medical professional and my own experience is insufficient to accurately guess.

7. Stress makes most anything worse so i'll go out on a limb and offer that it's probably likely stress can make celiac even worse.

Best of luck. If you aren't gluten-free yet, get tested. If the tests are negative and you still believe you may be celiac, go gluten-free on your own and wait for your body to give you results. If you dont' see any results from a truly/completely gluten-free diet, then I'd say the tests were probably right.

glasgowfranko1981 Contributor

Mushroom and SMDBill, thank you so much. You have both answered my questions - a relief in some of your answers to hear that, and in some more questions BUT this is good in both instances and I will get back to my doctor. It's nice to know I'm not alone in a lot of ways. I shall keep you posted. And anyone else, would love to hear your stories/thoughts as well! Thanks SO much!

GFinDC Veteran

My questions:

1. Can celiac's main symptom ONLY be the muscle pain (in legs), fatigue and brain fog?

2. Does cutting out gluten improve health for NON Celiacs?

3. How long after gluten has been ingested do typical symptoms come on?

4. How long following gluten being cut should things go back to normal?

5. I have a feeling blood tests will NOT show this up, what other tests are there?

6. Could this list of symptoms be ANYTHING else similar and NOT celiacs?

7. Even on a gluten free diet can stress make this worse?

1. Can celiac's main symptom ONLY be the muscle pain (in legs), fatigue and brain fog?

Yes, becasue celiac can cause a very wide range of symptoms, or no apparent symptoms at all, as in silent celiac.

2. Does cutting out gluten improve health for NON Celiacs?

This is true in some cases. Recent research identified non-celiac wheat sensitivity as as a separate condition.

3. How long after gluten has been ingested do typical symptoms come on?

This varies widely, mine have occured at 30 minutes in the past..

4. How long following gluten being cut should things go back to normal?

Some positive changes often occur within 2 weeks. But it may take much longer than that also. Since our bodies and the damage are not identical, the responses vary widely. Improvement may start quickly or slowly, and recovery can take months or years.

5. I have a feeling blood tests will NOT show this up, what other tests are there?

The celiac testing includes antibody blood tests. Also an endosopy is often done to take biopsy samples for microscopic review. Additionally Enterolabs does stool testing for antibodies, but it is not accepted as dignostic by mainstream doctors.

6. Could this list of symptoms be ANYTHING else similar

and NOT celiacs?

You may have low thyroid hormone, which is also associated with celiac disease. That can cause severe fatigue (Hashimoto's thyroiditis). Low vitamin/mineral levels can also cause fatigue. Celiac can cause malabsorption which leads to low vitamain and mineral levels. Diabetes can also cause fatigue.

7. Even on a gluten free diet can stress make this worse?

Stress can make fatigue worse, by burning energy that would be available otherwise.

dreacakes Rookie

Hi!

We have some similar symptoms... So I hope I can help!

Firstly, I highly suggest reading LOTS about gluten sensitivity and Celiac. Tests for Celiac are notoriously inaccurate, so you may have it anyway, and gluten sensitivity can be severe, and just as important to treat. I didn't have any major GI symptoms either. I was nauseous frequently, but just thought I had a sensitive stomach.

This video is a great primer, and the website is a good source of info too:

Open Original Shared Link

A lot of the symptoms you mentioned are often caused by inflammation and nutrient deficiencies (like the muscle spasms, which can be caused by a magnesium deficiency.)

I cut wheat gluten out of my diet and actually got *worse* for awhile... some people go through withdrawal. After that, I didn't recover, I actually kept getting worse in some ways. Not until I cut out all gluten (all grains have gluten in them) and went on a healing diet (this one: Open Original Shared Link) did I get better. Now I'm almost totally healed. It's important to know what you're doing, and get the support of a naturopathic doc, or someone trained in healing these issues with holistic, diet and lifestyle focused techniques.

Stress is *terrible* for gut issues. More info here: Open Original Shared Link

And gluten reactions can take up to 36 hours to surface. I usually feel gassy at first, then the next day I am really tired and foggy like I have the flu, and am more apt to have muscle spasms and back pain. But everyone's different.

It depends on how severe your condition is as to how long it will take for you to heal. It's taken me one and a half years of a proper gluten free healing diet to feel better. And I keep getting better all the time.

I hope that helped! Best of luck to you.

AandGsmomma Apprentice

Fatigue and brain fog are some of my worst symptoms. My stomache pain and heartburn went away in days after going gluten free. If I get glutened I can feel it within the hour and it can last several days.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Gluten is a generic term for a protein and carbohydrate combo molcule in grains. So all grains do have gluten, but only the gluten proteins in wheat, rye, barley and sometimes oats are a problem for celiacs. Not all gluten is bad.

dreacakes Rookie

GFinDC-

It is the conventional wisdom that only the gluten in wheat barley rye and oats are problematic. However, a lot of researchers and health practitioners are now finding that all grains trigger reactions in those who have Celiac and are gluten sensitive.

For me, and many other people, we didn't begin to heal until we cut out all the grains.

Here are some articles that go into greater detail:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

GottaSki Mentor

all grains trigger reactions in those who have Celiac and are gluten sensitive

The problem with this statement is that it is misleading.

IMO a better phasing would be:

all grains can trigger reactions in some who have Celiac Disease or Non-Celiac Gluten Intolerance

There are many that heal by the removal of the gluten proteins found in wheat, barley and rye ONLY.

Are there celiacs that need to remove more foods in order to heal - YOU BET - I'm one of them. But the problematic foods are not limited to grains. Dairy, Legumes, Eggs, Nuts, Seeds, Nightshades, Fruits and other sugars can all be problematic to the damaged digestive system. Once the digestive system is healed it is possible to ingest these items without causing further damage, while ingesting the gluten of wheat, barley and rye will trigger the immune response and cause damage, thus can never be consumed again.

Lady Eowyn Apprentice

Just wanted to say great answers!

Would like to add that stress sure aggravates my celiac - seems to make me worse.

Also (please note IMHO) gluten is not a good thing for humans and I think a lot of people have varying levels of problems (tolerance) with it. I would recommend gluten free or at least very gluten light to anyone with any kind of long term health issue. I wouldn't give it to animals either.

My hubby kindly gave up gluten to help me :rolleyes: and he no longer snores :D also his psoriatic arthritis that he's had for over 20 years has improved enormously.

Hope these comments aren't inflammatory in any way - just my view.

GFinDC Veteran

GFinDC-

It is the conventional wisdom that only the gluten in wheat barley rye and oats are problematic. However, a lot of researchers and health practitioners are now finding that all grains trigger reactions in those who have Celiac and are gluten sensitive.

For me, and many other people, we didn't begin to heal until we cut out all the grains.

Here are some articles that go into greater detail:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Hi Drea,

This link is for one of the studies mentioned in your links. It does say there is some increase in nitric oxide in some celiac patients (6 of 10 that were studied), but not nearly as much as for gluten. Four of 10 had almost no change in NO (nitric oxide). They are using NO as a possible marker of inflammation. I agree that corn can affect some celiacs, but not that all grains affect all celiacs. This study shows that 4 of 10 were not affected by corn. Oats are already known to affect 10% or so of celiacs.

So yes, we can have reactions to other things besides wheat, rye and barley. I react to oats myself and other non-grain foods also. Personally I am on a pretty low carb, low grain diet. But that is just part of also avoiding other foods such as nightshades, grapes etc that affect me.

I think the paleo diet is fine for people to follow, and don't see any problem with it. The issue is not all gluten in all grains IMHO, and this study you linked shows that. Please note also that the corn used for the test did test as having some wheat gluten in it. So that may have influenced the production of NO in the corn challenge.

Open Original Shared Link

The manufacturer claimed that their corn product was free from wheat or other cereals. We tested the product at the Swedish National Food Administration (Livsmedelsverket) and it was found to be contaminated with 82 μg/g (ppm), which is less than the usual allowed amount in a gluten free diet (<200 ppm) according to the Codex Alimentarius Standard for gluten free foods, and far less than what has been found to be a safe amount of gluten contamination when correlated with histology in oral challenge studies.Open Original Shared Link It cannot be excluded that the small amounts of gluten present in the corn preparation induced an inflammatory reaction as the mucosal patch technique is very sensitive.

nvsmom Community Regular

1. Can celiac's main symptom ONLY be the muscle pain (in legs), fatigue and brain fog?

It can, but it's a bit less common as far as I can tell. GI symptoms seem to occur the most but those with GI symptoms often have those symptoms. I have fairly serious joint pain and muscle pain myself but I suspect it's related to hashimotos or possibly a yet undiagnosed case of lupus or UCTD.

2. Does cutting out gluten improve health for NON Celiacs?

For some. I have some friends who react quite strongly to gluten but it doesn't seem to last as long as it would for me.

3. How long after gluten has been ingested do typical symptoms come on?

About 15-30 minutes for me. I can feel it for a week or two.

4. How long following gluten being cut should things go back to normal?

Stomach aches started to resolve within days. The bloating and migraines took another few weeks and then the hair growth became noticeable a bit later. I still have a few health issues that haven't improved 4 month in... I'm hoping they will.

5. I have a feeling blood tests will NOT show this up, what other tests are there?

Biopsy and a good result from the gluten-free diet are the only other tests I know.

6. Could this list of symptoms be ANYTHING else similar and NOT celiacs?

Could be almost anything autoimmune related, so many symptoms overlap. Hashimotos could cause many of the problems you mentioned. Lupus, RA, UCTD or MCTD popped into my mind when I read about your pain.

7. Even on a gluten free diet can stress make this worse?

I personally don't know. I've never really noticed. It would make sense though.

I hope you continue to feel better on the gluten-free diet. Best wishes.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,858
    • Most Online (within 30 mins)
      7,748

    Janet1234
    Newest Member
    Janet1234
    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.