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

First Post: Diagnosed Via Low Bone Density - Prognosis?


rukh

Recommended Posts

rukh Newbie

Hi, I'm new here.  I have trouble being concise, but I'll try.  Right now, I could stomp my foot and break a toe. The latest one broke when I dropped a single "D" battery on it for waist height.  The one before that was missing a step going up stairs.  And I've broken other bones too.  The toes are to the point where I just ignore it until it heals in 5-6 weeks.  The worst one put me out of commission for long enough to lose 25 lb of muscle mass from atrophy. It was actually the bone density that lead to my diagnosis of celiac disease, despite many other symptoms being present (caring, but unskilled doctors).

 

My [first, most pressing] question:

 

Those of you that had scans showing low bone density, how much did your bone density improve over time?  Do you still have to be more careful than other people?  Will I ever be able to mountain bike again without fear that a simple dab with break my ankle?  

 

Nobody seems to be able to tell me what the likelihood is that I'll be able to go back to doing active sports without fear.  NIH searches tend to indicate an incomplete bone density recovery is likely, but that doesn't give me a practical answer to the question of what is likely to happen going forward.  I'm in my 30's, so none of the bone density meds are recommended and it doesn't seem like there are any other known causes/solutions.


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



Celiac.com Sponsor (A8-M):



NoGlutenCooties Contributor

Welcome to the forum!

 

I too was diagnosed with osteopenia and I've only been gluten-free for 3 months so what I'm about to tell you is from doctors, folks on this forum, and my own research - not proven by personal experience.  I'm 42 and have been told that once I get all of the gluten out of my system my body will definitely be able to rebuild my bones and that I should be able to get back to normal bone density before I hit menopause.  Menopause makes building bone much more difficult, so I'm working against the clock.  But if they are confident that I can do it and you're only in your 30s then I would suspect you can do it too.

 

Have you had your Vitamin D levels tested?  Low D as well as other vitamins and minerals are common in Celiacs and you should have a full blood panel run to see where you're lacking.  Start taking a good multi-vitamin and perhaps some extra singlar vitamins depending on the outcome of the tests.  Once you've been gluten-free for a few months, start exercising to help your body rebuild bone.  Given that you are so prone to breaks, I would not suggest jumping into lifting heavy weights - start out slowly.  Even walking briskly on a regular basis can help build bone.  After about 6 months of gluten-free get another bone density test and see if your doctor thinks you could safely begin doing weight-baring exercises.

 

From everything I've read, there is hope.  Depending on how long you've been Celiac, how long it takes your body to get rid of the lingering antibodies, how healthy you are in general, how deficient you are in various vitamins and minerals, etc. etc. will all have an effect on how long it will take for you to get back to normal.  Be patient.  It could take a couple of years.  But it's doable IMHO.

 

Good luck!

 

 

(Edit - forgot to mention... probiotics and digestive enzymes help to speed up the healing process and get your gut back to normal so that you can start absorbing nutrients again)

NoGlutenCooties Contributor

One other thing I forgot to mention... be sure that you are 100% gluten-free.  No cross-contamination.  No cheating.  With Celiac it is all or nothing.

cyclinglady Grand Master

I suffered a vertebrae fracture three months after my diagnosis in March, 2013. I am 52 so building bone is going to be tough. I take calcium, vit. D, and magnesium, plus I am on hormones. From my research, the bone drugs do a good job, but they build on bad bone --no cleaning of the bone that your body normally does.

Next, I walked and walked. Lifted weights once my back healed. Bought a new comfort bike and am riding again. My road bike is still in the garage, but I am running again. So there is hope!

rukh Newbie

Thanks for the replies!  

 

My family doctor put me on D in response to my low bone density (actually significantly higher than normal in my hips, low in my spine, extremely low in my extremities).  She never did any of the tests I later found are the first steps when someone my age has low bone density (hormones, gluten sensitivity, etc).  

 

I worry about cross contamination.  No risk of "cheating" here, the punishment is too severe!   I've simply gone without eating when there was no gluten free option, so I know nothing will tempt me.  I get GERD pain to the point of being non-functional if a restaurant poisons me.  My wife's favorite place is also a bakery, and I quickly found out the reason things like fried eggs were making me sick is because there is flour in the air in the room next to the one they cook breakfast in.  If no GERD means sufficient lack of gluten, I've only been poisoned about 4-5 times in the last 3 months.  Is that sufficient reduction in contact with gluten?  Why is it that people say bone density will not rebuild if there is ANY gluten?

kareng Grand Master

Thanks for the replies!  

 

My family doctor put me on D in response to my low bone density (actually significantly higher than normal in my hips, low in my spine, extremely low in my extremities).  She never did any of the tests I later found are the first steps when someone my age has low bone density (hormones, gluten sensitivity, etc).  

 

I worry about cross contamination.  No risk of "cheating" here, the punishment is too severe!   I've simply gone without eating when there was no gluten free option, so I know nothing will tempt me.  I get GERD pain to the point of being non-functional if a restaurant poisons me.  My wife's favorite place is also a bakery, and I quickly found out the reason things like fried eggs were making me sick is because there is flour in the air in the room next to the one they cook breakfast in.  If no GERD means sufficient lack of gluten, I've only been poisoned about 4-5 times in the last 3 months.  Is that sufficient reduction in contact with gluten?  Why is it that people say bone density will not rebuild if there is ANY gluten?

 

If you have Celiac disease, then even a small, tiny amount of gluten, keeps the antibodies going.  The antibodies continue to attack the small intestine and effect absorption of nutrients/vitamins.  

 

For people who just stop eating gluten to see  if it might help with a certain problem -I don't think it is known whether the small amounts from a bakery or a shared colander or a hamburger taken off the bun will hurt your progress or not.  Partially because you don't know if you have Celiac or any other issue.

 

The thing is, osteoporosis & low vitamin levels are very real symptoms of Celiac Disease.  I think its horrible that your doctor wouldn't test you for Celiac before telling you to go gluten free.

 

 

Open Original Shared Link

 

Open Original Shared Link

cyclinglady Grand Master

Thanks for the replies!  

 

My family doctor put me on D in response to my low bone density (actually significantly higher than normal in my hips, low in my spine, extremely low in my extremities).  She never did any of the tests I later found are the first steps when someone my age has low bone density (hormones, gluten sensitivity, etc).  

 

I worry about cross contamination.  No risk of "cheating" here, the punishment is too severe!   I've simply gone without eating when there was no gluten free option, so I know nothing will tempt me.  I get GERD pain to the point of being non-functional if a restaurant poisons me.  My wife's favorite place is also a bakery, and I quickly found out the reason things like fried eggs were making me sick is because there is flour in the air in the room next to the one they cook breakfast in.  If no GERD means sufficient lack of gluten, I've only been poisoned about 4-5 times in the last 3 months.  Is that sufficient reduction in contact with gluten?  Why is it that people say bone density will not rebuild if there is ANY gluten?

My husband found that many restaurants use oil that contain barley. Ask for a clean frying pan (no grille) and butter.

That said, Karen is right, you should get tested. I am officially diagnosed, but my husband is not. He refuses to get tested now that he has been gluten free for 13 years. He would tell you that I have had so much more support from family, friends and medical staff.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Or....did you get tested? I took it to mean that you only had a bone scan and he told you to eat gluten free. But reading back....maybe you did get Celiac tests, too? If that is the case, you can't have a tiny mount of gluten if you can at all avoid it. If that means no restauraunt, then that is what you must do.

GFinDC Veteran

HI RukH,

 

One study showed some remaining intestinal changes (abnormal) after people were on the gluten-free diet for 18 months.  It is not a quick process to recover from celiac intestinal damage.   The antibodies taper off slowly, and may remain active for weeks to months depending on the person.  And the immune system is very sensitive and makes new antibodies whenever it detects a tiny bit if gluten.  Your body thinks of gluten as germs now, and it isn't going to willing let germs invade and conquer your cells.  It's going to fight back.  So keeping as close to 100% gluten-free as possible should be the goal for all celiacs.

 

The villi damage in the small intestine causes difficulty absorbing nutrients (malabsorption).  That causes a whole host of problems in the body as it affects the entire body, not just the gut.

 

I fell about 3 feet and broke my left elbow in 5 places some years ago.  I haven't had any more breaks though and never had a bone density scan.  Recovery for your bone health is likely to take up to 2 years IMHO.  You are dealing with malabsorption and healing at the same time.  There are some vitamins that are supposed to be more easily absorbed.  And some are meant to dissolve under the tongue (sub-lingual).  It might be worth looking into them.

 

The lack of vitamins and minerals can impede healing and recovery.  But your gut may not absorb them right until it heals.  Kind of a catch 22.  So getting it healed is important.  A very simple diet with few processed foods can help at the beginning.  Lots of meat, nuts and veggies is a good diet.  Your body needs protein to build cells.

 

Some starting the gluten-free diet tips for the first 6 months:

Get tested before starting the gluten-free diet.
Get your vitamin/mineral levels tested also.
Don't eat in restaurants
Eat only whole foods not processed foods.
Eat only food you cook yourself, think simple foods, not gourmet meals.
Take probiotics.
Take gluten-free vitamins.
Take digestive enzymes.
Avoid dairy if it causes symptoms.
Avoid sugars and starchy foods.
Avoid alcohol.
Watch out for cross contamination.

Helpful threads:

FAQ Celiac com
https://www.celiac.com/gluten-free/forum-7/announcement-3-frequently-asked-questions-about-celiac-disease/

Newbie Info 101
https://www.celiac.com/forums/topic/91878-newbie-info-101/

blmoreschi Apprentice

Osteoporosis is also what led to my 11 year old daughter's Celiac diagnosis last April. After 6 months gluten-free, her TtG was down to 6 (previously 99) and we presume that her gut is healing well. I have, belatedly, decided to put her on probiotics, too, based on all my reading. Her bone density did not show any improvement in 6 months. Because she is pre-pubertal and about to go through a huge growth phase, we are having to be more proactive about increasing her bone density and are treating her with IV bisphosphonates (such as Fosamax or Boniva). This was not a decision we made easily, and one we are still somewhat uncomfortable with. So - to all of you others out there - please don't rag on me about that. I'm just trying to share my experience with this new poster.

 

I have done TONS of reading on this subject (or as much as I can find anyway) and there is very little pediatric experience with bone density recovery after a Celiac Diagnosis. However, from what I can tell you should be able to expect some normalization in yours in the 2 year gluten-free range. There is a lot more information about adult patients. But, we also found some articles (published in Turkey and Italy) that indicate that 20% of Celiac's don't get the bone density recovery just from going gluten-free. They think there is a secondary autoimmune reaction going on, or possibly inflammation. They did find, however, that those patients responded to bisphosphonate therapy.

 

Good luck to you, and I would suggest all the exercise you can get even though you are worried about fracturing. Our motto is "strong muscles protect weak bones" and we try to avoid contact sports but let our daughter do most everything else she wants to do. Fortunately, she is a dedicated ballerina and that is the best exercise in the world for her to build strong muscles and bones. Maybe you could try yoga?

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. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      5

      Awaiting dermatitis herpetiformis confirmation following biopsy

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

      how much gluten do I need to eat before blood tests?

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

      how much gluten do I need to eat before blood tests?

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

      how much gluten do I need to eat before blood tests?

    5. - catnapt posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

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

    • Total Members
      133,257
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
    • trents
      Welcome, @catnapt! The most recent guidelines are the daily consumption of a minimum of 10g of gluten (about the amount found in 4-6 slices of wheat bread) for a minimum of two weeks. But if possible stretching that out even more would enhance the chances of getting valid test results. These guidelines are for those who have been eating gluten free for a significant amount of time. It's called the "gluten challenge".  Yes, you can develop celiac disease at any stage of life. There is a genetic component but also a stress trigger that is needed to activate the celiac genes. About 30-40% of the general population possesses the genetic potential to develop celiac disease but only about 1% of the general population actually develop celiac disease. For most with the potential, the triggering stress event doesn't happen. It can be many things but often it is a viral infection. Having said that, it is also the case that many, many people who eventually are diagnosed with celiac disease probably experienced the actual onset years before. Many celiacs are of the "silent" type, meaning that symptoms are largely missing or very minor and get overlooked until damage to the small bowel lining becomes advanced or they develop iron deficiency anemia or some other medical problem associated with celiac disease. Many, many are never diagnosed or are diagnosed later in life because they did not experience classic symptoms. And many physicians are only looking for classic symptoms. We now know that there are over 200 symptoms/medical problems associated with celiac disease but many docs are only looking for things like boating, gas, diarrhea. I certainly understand your concerns about not wanting to damage your body by taking on a gluten challenge. Your other option is to totally commit to gluten free eating and see if your symptoms improve. It can take two years or more for complete healing of the small bowel lining once going gluten free but usually people experience significant improvement well before then. If their is significant improvement in your symptoms when going seriously gluten free, then you likely have your answer. You would either have celiac disease or NCGS (Non Celiac Gluten Sensitivity).
    • catnapt
      after several years of issues with a para-gland issue, my endo has decided it's a good idea for me to be tested for celiac disease. I am 70 yrs old and stunned to learn that you can get celiac this late in life. I have just gradually stopped eating most foods that contain gluten over the past several years- they just make me feel ill- although I attributed it to other things like bread spiking blood sugar- or to the things I ate *with* the bread or crackers etc   I went to a party in Nov and ate a LOT of a vegan roast made with vital wheat gluten- as well as stuffing, rolls and pie crust... and OMG I was so sick! the pain, the bloating, the gas, the nausea... I didn't think it would ever end (but it did) and I was ready to go the ER but it finally subsided.   I mentioned this to my endo and now she wants me to be tested for celiac after 2 weeks of being on gluten foods. She has kind of flip flopped on how much gluten I should eat, telling me that if the symptoms are severe I can stop. I am eating 2-3 thin slices of bread per day (or english muffins) and wow- it does make me feel awful. But not as bad as when I ate that massive amnt of vital wheat gluten. so I will continue on if I have to... but what bothers me is - if it IS celiac, it seems stupid for lack of a better word, to intentionally cause more damage to my body... but I am also worried, on the other hand, that this is not a long enough challenge to make the blood work results valid.   can you give me any insight into this please?   thank you
×
×
  • 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.