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

Soft Bones


lovetapioca

Recommended Posts

lovetapioca Rookie

I broke my ankle square dancing last month. Broke both the tibia and fibula right above the ankle. Just great. All I did was walk backwards, lose my balance and there goes the ankle. Very embarrassing. Lost balance due to a recent MS attack. Surgeon operated and told my sister I had soft bones. He had trouble getting the screws to stay in. I see him on Thursday and am interested to see what he says about the relation between my soft bones and celiac.

I spent tonight doing some research. Rather depressing since it is as plain as the nose on my face now that I should have a problem. I have unknowingly battled Celiac for about 9 years. I was just diagnosed 2 years ago and immediately started getting my life back but I am extremely sensitive to all traces of gluten. I have been on HRT since the mid-1980s and then due to a breast cancer scare went off of the estrogen cold turkey last August. I am pretty well thru menopause, having the privilege of going thru it twice, once at age 30 after having my uterus & ovaries removed and then again when my body remembered I was approaching 50. Celiac, menopause, stopping estrogen, low thyroid all adds up to high risk of soft bones. I'll find out later which disease I have.

I was walking about 4 miles almost every day. I square dance. I have MS, which I have had since as a child but was not diagnosed until 22 years ago. The MS attack I just had was brought on my stress of an ex-husband......court problems again. First time in 22 years I have had an attack.

I take extra calcium supplements, eat lots of greek yogurt, am almost a health food nut with being so good on my celiac. I'm very healthy if it wasn't for my MS which is more of a hindrance than anything unless this inactivity does a job on me. But, not if I can help it.

Why am I writing this long post? Because anyone out there reading a post on soft bones either, have already had this, or am worried they may have it or develop it. I would love any information anyone has learned that would be beneficial when I approach my doctor in my treatment. We Celiacs have special needs that can easily be overlooked. That is why we have forums such as this. Any info on recovery, diet, things to beware of, etc etc, I would really appreciate. Also any past topics i have missed.

Thank you.


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



Celiac.com Sponsor (A8-M):



Gemini Experienced

I broke my ankle square dancing last month. Broke both the tibia and fibula right above the ankle. Just great. All I did was walk backwards, lose my balance and there goes the ankle. Very embarrassing. Lost balance due to a recent MS attack. Surgeon operated and told my sister I had soft bones. He had trouble getting the screws to stay in. I see him on Thursday and am interested to see what he says about the relation between my soft bones and celiac.

I spent tonight doing some research. Rather depressing since it is as plain as the nose on my face now that I should have a problem. I have unknowingly battled Celiac for about 9 years. I was just diagnosed 2 years ago and immediately started getting my life back but I am extremely sensitive to all traces of gluten. I have been on HRT since the mid-1980s and then due to a breast cancer scare went off of the estrogen cold turkey last August. I am pretty well thru menopause, having the privilege of going thru it twice, once at age 30 after having my uterus & ovaries removed and then again when my body remembered I was approaching 50. Celiac, menopause, stopping estrogen, low thyroid all adds up to high risk of soft bones. I'll find out later which disease I have.

I was walking about 4 miles almost every day. I square dance. I have MS, which I have had since as a child but was not diagnosed until 22 years ago. The MS attack I just had was brought on my stress of an ex-husband......court problems again. First time in 22 years I have had an attack.

I take extra calcium supplements, eat lots of greek yogurt, am almost a health food nut with being so good on my celiac. I'm very healthy if it wasn't for my MS which is more of a hindrance than anything unless this inactivity does a job on me. But, not if I can help it.

Why am I writing this long post? Because anyone out there reading a post on soft bones either, have already had this, or am worried they may have it or develop it. I would love any information anyone has learned that would be beneficial when I approach my doctor in my treatment. We Celiacs have special needs that can easily be overlooked. That is why we have forums such as this. Any info on recovery, diet, things to beware of, etc etc, I would really appreciate. Also any past topics i have missed.

Thank you.

I also have osteoporosis/osteopenia from years of undiagnosed Celiac and my preferred course of treatment has been to do weight training and core exercises, with the help of a personal trainer. The bone meds they like to push on people do not build bone from the inside of the bone....just stops the break down of old bone and deposits new bone on the outside. It can also cause stomach problems, which we do not need, and be a problem especially for Celiacs if absorption is not optimal.

I don't know if you would be able to do this after healing of your ankle but weight training and core exercises might really benefit you from the MS standpoint also. It would make your muscles stronger and that aids balance. I am also post menopausal by 8 years and I stopped BRHT a while back because it wasn't really helping with the hot flashes all that much. Estrogen is important to bone generation but it is not impossible to build bone without it....just a little harder and it takes longer. I am sorry you have a broken ankle and hope you have a speedy recovery but please consider weight training if possible for you. It puts you in a good mental state also.

A woman has to weigh a minimum of 126 pounds to just build bone on your own. If you weigh less than that, you HAVE to exercise or you will continue to lose bone. For a man, the weight is 150 pounds. I will never reach 126 pounds so I have no option but to go to the gym. Not a bad treatment as I always feel so good after a work-out.

BTW...I also have Hashi's thyroid disease so we are very similar. It's an uphill battle but I don't like to lose!

Lori2 Contributor

I have osteoporosis, too. Please be sure to post anything your doctor suggests that might be helpful.

lovetapioca Rookie

Thank you so much for your post. Yes, I will definitely try the weight training and have thought of getting a personal trainer. I had gotten into a great habit of having a 5 lb weight by my couch and would use it while I'm watch TV. However, this is also where I do my ebay and all my computer work. I got out of the habit and it went the wayside. But it is still there and I will put it on my coffee table and start again. It feels good, but just that stupid getting out of the habit. Just a human tendency, I guess. But when I was faithful with the weight, I could tell a difference in time.

If anyone reads this is not familiar with MS, muscle is easy to lose but very difficult to build. Plus it is very depressing because, at least with a lot of us, the muscles just hang and "swing & sway". Just terrible. I've done everything thru the years I could do, but I can tense and the muscle will buff up and instantly when I relax they hang again. Plus last year I was blessed with angel wings. For you young ones, that is the hangy underarms under old ladies like me. This is why I bought the 5 lb weight for my arm.

I started my walking about 4 miles a day as fast as I can, last fall. My chiropractor told me I needed to and he was so right. I should have started it years ago, but it takes time and I didn't have pain. Well, I got butt pain and hence the chiropractor and the advice. Now, I really think the butt pain is from the soft bones. It really helps reading what others go thru and their personal descriptions.

Hopefully, it won't take 4 months to heal my ankle before i can walk. But whatever it takes, then I'll do it. I have been exercising with just leg lifts right now, etc but will need more soon. When healed I will continue the 4 miles a day except on the days I square dance. 1.5 hrs of square dancing is equivalent to 3-5 miles of walking. Plus I'll start with the weight training. No, actually, I will ask the doctor and maybe with a personal trainer I can start that immediately!

THANK YOU! I never thought of that until I typed it! YAY! I think you just saved me! You can't believe what a shot in the arm this has just given me!!! I see the doctor in a few hours....without sleep it appears....and this will be on the main order of business right after they take me out of the torture chair...I have a huge fear that they are going to have to reset my ankle....Been crying a lot today in stark fear. The pain is right up there with childbirth.

I hope I can sleep now. Right before bed, I heard water running, wheeled out to the garage and water was running all over my garage from the AC. I live in a duplex and it was running under the walls and I don't have their phone number...plus it was midnight and I couldn't try to make it in my wheelchair over there. So, that was enough to wake me up big time along with the worries about the ankle pain in the torture chamber.

I will post tomorrow how the doctor visit went. If I don't post, then that will probably mean they put me on some meds for pain.

lovetapioca Rookie

Yes, I will absolutely post what my doctor tells me, anything that might help anyone. Please check my posts again and give me some tips. I am new to this and never worried about bone problems. i didn't realize Celiac was a risk factor. Now the education begins.......

Gemini Experienced

Yes, I will absolutely post what my doctor tells me, anything that might help anyone. Please check my posts again and give me some tips. I am new to this and never worried about bone problems. i didn't realize Celiac was a risk factor. Now the education begins.......

Man, I love your attitude! People.....we have another fighter here! :P Older women have such confidence.

Your MS and bone problems can be made a lot better with weight training and exercise. It won't be easy and it wasn't for me because I had muscle wasting from years of undiagnosed Celiac. I was always the wimpy kid with no strength....NOT ANY MORE! ;)

Please use a good trainer as they teach you proper form when exercising. I think you will be pleasantly surprised that the longer you maintain a strict gluten-free diet, the better you will feel with less pain. I have no idea if my exercise will restore my bones completely but with added muscle strength, you will have far less chance of losing your balance and falling....and then breaking something. It's a win, win situation.

Keep us informed of your progress but look into a personal trainer...honestly, it's the best money I ever spent. I feel pretty good right now and I actually have some muscle that shows. First time for me and I'm almost 53. You absolutely can do it.

Stay away from the meds though, for now. They will likely pressure you but don't give in. Meds are always a last resort.

Good luck and keep using that 5 pound weight! :D Hope your ankle pain goes away soon but ask them for pain meds. You shouldn't have to suffer like that with so many good pain meds out there.

lovetapioca Rookie

I went to the doctor and YAY! I did not have to have my foot reset or shaped or whatever the painful thing is when they bend it how it is supposed to go. Instead, it was doing well. Looked great....well except for the long hair under the cast (Yuk). I have a brace on my foot to be treated like a cast. Now I can ice it better and that felt so good. I cannot bear weight with it for quite some time. The doctor kept to himself on that and I see him again in 4 weeks. Probably a wait and see. I will have to have my leg elevated above my heart for maybe another 4 months, if I understood correctly. Found out I had another break I didn't know about so it was a triple something break. He said even with my bones the way there were it was just because I landed on the floor in just the wrong way.

I asked about the personal trainer and weight training exercises and he said not at the moment. That would be later on. Only if I really wanted a physical therapist then he would OK that but he wanted me to take it really easy right now even though it is hard for me to build muscle. He said I could do some leg lifts or something which I have been doing from the couch & wheelchair, etc. That was enough for now. I guess the fracture was a pretty bad one so I better do as he says. But the ankle is healing good and I had quite a bit of movement and he was happy with that. We'll see how it goes with the brace because this holds my foot much more secure. Soooo heavy. But may build up more muscle. At least I can ice it and wash off my leg, etc.

I asked about an endocrinologist, or who should I go to so I can get started on overcoming this soft bone condition. He advised to go to my primary care physician and have her choose from there. Sounds wise. Also, my neurologist will be given copies of all of the reports, etc. So, even though it doesn't sound like much, I'm happy because it is the assembling of my own little team ready to go into motion. They just don't know it yet. It made sense about waiting about the personal trainer. Since he wasn't really encouraging even the physical therapist, I feel he was just wanting me to take it easy, like maybe he saw I can tend to overdue at times.

It was very nice to talk to a doctor and mention the Celiac and by his reaction it was a very normal question and he thoroughly understood where I was coming from. It is sad but we all know there are some doctors that can make you want to clam up and not say anything, the roll the eye thing. I was happy say there was none of that. Also, when I mentioned the stopping of the estrogen because of the breast cancer scare, he was listening very closely. So, I feel in good hands. It turns out that even though the bone was soft, the special screws he used held well. That was good.

Now, my next move is to call and make an appt with my primary care physican, see how she reacts , where she sends me, and what tests she orders. I will then go the orthopedic surgeon in 4 weeks, then the following week I'll be down in another town about 300 miles away to my neurologist for an MRI for my MS. When I talk with him it will be interesting how the Celiac / MS / soft bones all connect. Especially it will be interesting how they connect with the different doctors viewpoint. I should include the 4th doctor here, since I also see a chiropractor. He is the one that more or less "made" me get out and start my walking program. But that will be a subject of another post. I'll also continue some arm chair & couch exercises and see what I can do. I do ballet conditioning exercises and I might get out the DVD and see what it is like to do while sitting down. Never thought of it. I can probably adapt it easily.

Thank you all for your help & encouragement in my posts.


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



Celiac.com Sponsor (A8-M):



larry mac Enthusiast

I was sick for two years before I finally found a good GI. About six months later I broke a metatarsal accidentally kicking the kitchen table leg (another story). As my personal physician and I were looking at the x-rays of my foot, she say's "Look at your poor, pitiful bones"!

I love my doctor dearly, but really, is that funny or what?

I had one followup visit with my GI about six months after that, and when I mentioned the broken foot incident he immediately scheduled a bone density scan, which indicated I had osteopenia. That was about five years ago.

That's my story.

best regards, lm

  • 3 weeks later...
lovetapioca Rookie

I got the results from my doctor and my bone density is fine. She said that she didn't know what the surgeon was talking about then. I said that the surgeon told me my bones were soft. He felt them. He couldn't use the regular screws but had to use the screws for soft bones. My regular doctor just said that my tests turned out just fine. I told her about Celiac.com and that even though I didn't know much, I had heard there were times that the bone density test was fine yet the person had soft bones and that there was a biopsy or some other test that was needed. My doctor was not aware of any biopsy for a test for soft bones. I requested to see an endocrinologist since that is what was mentioned in our forum. She said there was none in town but if I wanted to find one in another town she could refer me. So, I went to my insurance and found a doctor about 300 miles away and will give that name to my doctor. My doctor said it usually takes 3-6 months to even get in and see one.

I have soft bones and a broken ankle from just falling. I am MS and bad balance. I think I need to see a specialist. I just want to have some treatment before my bones become weak. Has anyone had similar problems?

Lori2 Contributor

Check out this article on the Cleveland Clinic site:

Bone density vs bone quality: What

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.