Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

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




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


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

christianmom247

Recommended Posts

christianmom247 Explorer

Hi all,

 

I was diagnosed with celiac and have been completely gluten free for 2 years.  At that time I had a dexa scan and was diagnosed with osteopenia.  I've been eating healthy foods and plenty of calcium for the past 2 years, but my repeat dexa scan just showed my numbers falling into osteoporosis in my spine.  (Went from -2.3 two years ago to -2.8 now.)  I'm 55, went through menopause at the average age, and am otherwise in pretty good physical shape.  My doctor put me on bisphosphonates, took away my running and other high-impact or bending/twisting activities.  I'm now taking in even more calcium (and trying to juggle it with my iron pill), walking and beginning strength training.  

 

From your experience, there a realistic chance of my spine healing to some extent?  My score went downhill even though I've been gluten free (and repeat blood tests have confirmed I'm not getting into any unintentional gluten).   Maybe it just takes that much time for my gut to heal so I can start absorbing calcium again--or is it too  late?  I could tell you all how hard it is to deal with this on top of the problems and isolation of celiac, but you're all walking the same road and understand.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

yes! :) to expecting improvement.

 

My numbers improved a bit in 2 years, which my doc and I celebrated, although they still indicate slight osteopenia. I hope they improve even further.

 

I take 1500 mg cal/ 1000 mg/mag/1000 ius D. He has had me on this dosage for nearly a year now.

 

Besides calcum-rich dairy products, I eat a lot of green leafies for cal boost and I drink coconut milk. 

 

i can't eat soybeans, but these are the best foods you can eat for calcium,

  • Spinach
  • Kale
  • Okra
  • Collards
  • Soybeans
  • White beans

 

I started weight training and weight bearing exercises like walking and yoga since my constant joint and muscle pain has subsided since diagnosis--and I believe this has contributed to the better numbers on the Dexa scan.

 

I know I am not the only that can give you a positive report and I hope those gals will chime in soon. 

 

Do not think it can't be reversed. Just  keep at it! 

All the best, Irish

Link to comment
Share on other sites
cyclinglady Grand Master

I had a dexa scan last July after fracturing two vertebrae (T7 and T9) doing nothing and just after four months of getting my celiac disease diagnosis. It showed 1 point just above osteoporosis (officially osteopenia) but my doctor suspects osteoporosis in my upper back. I did some reasearch and asked for hormonal therapy (bio-identical) since I was within 1 year of menopause. The request was granted and I started talking more calcium (1500 mg/day)/mag and Vit.D.

I had to give up my bike and running for a year. No problem since I was trying to heal fractures. Instead i walked, taught water aerobics and lamely lifted a few hand weights. It took almost a year for my back to completely heal (no pain or numbness from shifting during normal activities). Started running and riding my road bike close to a year later. Carried a heavy day backpack through Europe this past month and felt no back pain, so I think my bones are improving. I even went roller skating for 4 hours two days ago! I confess that I barely skated backwards because I was afraid of a kid falling and forcing me to fall. You should see those day camp kids skate with their little "walkers" as it is hysterical!

I do not get another bone scan for another year, so I do not know if I am really building bone, but it think I am.

I looked into drugs, but wanted to try hormones first (low cancer risk in my family). I wanted to make sure I was building good bone on top of cleared off bone. You might want to research how the bone drugs work and the side effects of more fractures. If time, hormones and weight-bearing exercise do not cut it, then I will re-consider drugs.

Keep at it! It is possible to build bone, it just takes time. Let's face it, it takes lots of time just to heal from celiac disease!

Link to comment
Share on other sites
Gemini Experienced

I am in the same boat and I think whether you improve or not has many different variables.  I am 55 and post menopausal by 10 years. I am also petite and on a fat day weigh 112 pounds, which may be part of the problem.  I am not as good as some about taking supplements. I do take them everyday but I don't think it is enough. It is hard because I also take thyroid hormone, which can interfere with calcium like iron does if taken too closely together. I try to get some calcium from my diet so only take about 800 mg in supplement form, per day.  But do I run around counting mgs of calcium ingested frm everything?  No, I don't because I work full time, manage celiac and all the cooking that it entails, work out twice a week weight training for the bones and try to fit in some fun and family visits in between. It can be very stressful.

 

I have osteoporosis in my spine and osteopenia in my hip. After 3 years of weight training (lifting heavier weights for someone my size), no improvement but I did stop the progression.  It was the same as 3 years prior and my doctor was happy with that.  I was pissed.  I worked my ass off and no improvement expect I stopped it from getting worse?

 

Here is what I learned......you have to weigh at least 126 pounds as a female to make bone on your own, doing none of the above.  I will never weigh 126 pounds.  I also take thyroid hormone and my doctor kept insisting I was taking too much because of my numbers on the blood work.  I do not go by numbers on my blood work unless I become symptomatic.  I tried cutting it down but didn't get far because I started having symptoms of low thyroid again.  On my dose she thought was too much, I did not have any symptoms of taking too much. Balancing all this is a huge pain in the ass.  I am keeping it where it is because being symptomatic for low thyroid does not work.  You cannot function.

 

I am not sure at this point if someone my size can build bone again and get to normal density.  I am not worried about it too much as I read an article from Dr. Christian Northrup on Osteoporosis and she pointed out that the weight of a bird is fine for their delicate bone structure...they do not go around breaking bones because they have teeny tiny bones.  I also may never have gained much bone density because I am pretty sure I have had Celiac for decades...since childhood.  You can't lose what you never had. What I do know is that I have much stronger muscles, which help to keep a person steady and prevent falls later in life when I am really old.  That is important because

falls are what break bones, not the fact that you have osteo.  I plan on weight training until I croak. I do not take biophosphonates and that is a story for another day.

 

Maybe it will happen eventually that my bones improve in the other direction but I am not obsessing about it any more. I do what I can and keep moving and exercising.  Will tweak my supplements some also.  The good news is I have never broken a bone and I have had some serious spills where I should have broken some and didn't. That works for me!

Link to comment
Share on other sites
IrishHeart Veteran

.  The good news is I have never broken a bone and I have had some serious spills where I should have broken some and didn't. That works for me!

 

You know me, Lucy Ricardo and I am stunned that I have not broken anything either. I tore up ligaments in my ankle two years ago (Doc said it would have been better if I had just broken it so he could have set it) and I have tripped over my own shoes often enough and fallen on my arms, hands. Just bruised. whew! Aside from 3 broken ribs once (don't ask--stupid freak accident involving ice and a pole fence) :huh: and a broken toe (did that just sitting on a sofa--geesh)  I've been fortunate, too.

 

I hope I didn't just jinx myself....

Link to comment
Share on other sites
Gemini Experienced

You know me, Lucy Ricardo and I am stunned that I have not broken anything either. I tore up ligaments in my ankle two years ago (Doc said it would have been better if I had just broken it so he could have set it) and I have tripped over my own shoes often enough and fallen on my arms, hands. Just bruised. whew! Aside from 3 broken ribs once (don't ask--stupid freak accident involving ice and a pole fence) :huh: and a broken toe (did that just sitting on a sofa--geesh)  I've been fortunate, too.

 

I hope I didn't just jinx myself....

Could you clarify that statement, Irishheart?  You were pole dancing on some ice...... :)

Link to comment
Share on other sites
cyclinglady Grand Master

What? Must be over 126 pounds to build bone? Yikes, I will never hit that weight!

I did get two fractures in my back just laying myself down on the ground on my tummy before passing out (too much fried gluten-free chicken and post gallbladder surgery, I guess). Ended up in the hospital because I complained that my back hurt and I could not get off the floor. Docs just worried about my heart. My heart is in great shape. Everyone just overlooked my back until my follow-up visit with my GP. Even then he just mentioned the T9 vertebrae. Did not find out about the second fracture until I requested my hospital records. (Request all medical records, folks!!!!)

My thyroid stabilized after going gluten-free for six months while at the same time finally reaching menopause. My thyroid was whacked out for about two years (swinging wildly from hyper to hypo within days) and I attributed it to the final years of perimenopause though it could have been celiac disease related. I would rather run hypo than hyper any day, but luckily, hypos are not horrible for me. I try to keep up on testing to monitor hypers so that it won't interfere with bone building. I do not want to run hyper ever again.

But osteo will weaken bones and doing simple chores around the house can cause fractures. My best biking buddy's mom, who in her 80's, suffered from over 18 fractures in one year alone. Her vertebrae just kept crumbling. Hummm...she was Swedish, bet she had celiac disease..........

Now, where are my calcium supplements? Time to take a dose.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Could you clarify that statement, Irishheart?  You were pole dancing on some ice...... :)

 

 

:lol: pole fence...it was pole fencing, wise guy! lol  It was buried in snow and running low on the ground.about 1 foot high...guy put it there so kids would not ride their bikes on his lawn.....slipped on the ice, went down thinking" Oh I'm all right, it's a big pile of fluffy snow going to cushion my fall... nope...pole broke 3 ribs....ugh

Link to comment
Share on other sites
Gemini Experienced

What? Must be over 126 pounds to build bone? Yikes, I will never hit that weight!

I did get two fractures in my back just laying myself down on the ground on my tummy before passing out (too much fried gluten-free chicken and post gallbladder surgery, I guess). Ended up in the hospital because I complained that my back hurt and I could not get off the floor. Docs just worried about my heart. My heart is in great shape. Everyone just overlooked my back until my follow-up visit with my GP. Even then he just mentioned the T9 vertebrae. Did not find out about the second fracture until I requested my hospital records. (Request all medical records, folks!!!!)

My thyroid stabilized after going gluten-free for six months while at the same time finally reaching menopause. My thyroid was whacked out for about two years (swinging wildly from hyper to hypo within days) and I attributed it to the final years of perimenopause though it could have been celiac disease related. I would rather run hypo than hyper any day, but luckily, hypos are not horrible for me. I try to keep up on testing to monitor hypers so that it won't interfere with bone building. I do not want to run hyper ever again.

But osteo will weaken bones and doing simple chores around the house can cause fractures. My best biking buddy's mom, who in her 80's, suffered from over 18 fractures in one year alone. Her vertebrae just kept crumbling. Hummm...she was Swedish, bet she had celiac disease..........

Now, where are my calcium supplements? Time to take a dose.

One of the things I learned from the article I read is that the DEXA scan tells you bone density but does not tell anything about the quality of your bone. Small, petite people may show lower density but the bone structure may be strong. Osteoporosis can be over played, in some cases. My own doctor agreed with this and she has patients that have horrible DEXA scores and have never broken bones. My bone density will not be the same as someone who is physically larger than me. But that doesn't mean my bones are less strong. Doctors fail to mention this to some and pressure them to take meds that do not do what they claim. My doc did not want me to go on biophosphonates because of long bone fractures that can occur with them. They can actually weaken bone.

I had an x-ray done at the chiropractors last year when I injured my hip to see what the cause could be. It showed the whole lower portion of my spine. He looked at me and said my spine looked great.......vertebrae looked solid and the discs were well spaced and no sign of any degenerative disease. He also remarked that my bone density did not look bad at all...he questioned the DEXA scan results. I asked another doctor I have if bone density could be judged well from a plain x-Ray and he said yes. If you are at the point where they are telling you that you have osteoporosis, that will be visible on an x-ray. DEXA scans are a one size fits all test method and it just doesn't work like that. I think if I continue doing weight training for the rest of my life, having the muscles I have now and the benefits to bone should help a lot. There aren't a ton of options for building more bone if you don't weigh a lot and I just am not going to obsess about it. I don't do meds and hormone therapy did nothing. I am too far on the other side of menopause to use that safely.

Link to comment
Share on other sites
Gemini Experienced

:lol: pole fence...it was pole fencing, wise guy! lol  It was buried in snow and running low on the ground.about 1 foot high...guy put it there so kids would not ride their bikes on his lawn.....slipped on the ice, went down thinking" Oh I'm all right, it's a big pile of fluffy snow going to cushion my fall... nope...pole broke 3 ribs....ugh

Oh, man.......that's gotta hurt!!!!!!!!!!!!!

Link to comment
Share on other sites
IrishHeart Veteran

I agree with Gem on this issue. My DEXA may have shown some osteopenia, but despite some disc degeneration from OA (cervical spine area) my spine 

(according to a  spine specialist at Albany Med and anyone else who has seen my MRIs)

 I have the spine of a 22 year old.  If only  I FELT like a 22 year old...

Link to comment
Share on other sites

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - BluegrassCeliac replied to lasthope2024's topic in Food Intolerance & Leaky Gut
      7

      This forum might be the last hope I have in my life. Please I beg you

    2. - Scott Adams replied to Nacina's topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    3. - Nacina posted a topic in Related Issues & Disorders
      1

      14 year old with Celiac & EOE still suffering...

    4. - trents replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.

    5. - Fluka66 replied to Fluka66's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      5

      Waiting for urgent referral.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      121,067
    • Most Online (within 30 mins)
      7,748

    myneckmybackmyceliac
    Newest Member
    myneckmybackmyceliac
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • BluegrassCeliac
      Hi,   Not saying Thiamine (B1) couldn't be an issue as well, but Mg was definitely the cause of my problems. It's the only thing that worked. I supplemented with B vitamins, but that didn't change anything, in fact they made me sick. Mg stopped all my muscle pain (HCTZ) within a few months and fixed all the intestinal problems HCTZ caused as well. Mom has an allergy to some sulfa drugs (IgG Celiac too), but I don't think I've ever taken them. Mg boosted my energy as well. It solved a lot of problems. I take 1000mg MgO a day with no problems. I boost absorption with Vitamin D. Some people can't take MgO,  like mom, she takes Mg Glycinate. It's one of those things that someone has try and find the right form for themselves. Everyone's different. Mg deficiency can cause anxiety and is a treatment for it. A pharmacist gave me a list of drugs years ago that cause Mg deficiency: PPIs, H2 bockers, HCTZ, some beta blockers (metoprolol which I've taken -- horrible side effects), some anti-anxiety meds too were on it. I posted because I saw he was an IgG celiac. He's the first one I've seen in 20 years, other than my family. We're rare. All the celiacs I've met are IgA. Finding healthcare is a nightmare. Just trying to help. B  
    • Scott Adams
      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
×
×
  • Create New...