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

Frightened


Karagirl

Recommended Posts

Karagirl Newbie

Hello, thank you for reading this.

Friday night I slipped on ice on the top of stairs on my deck, and landed hard, sideways-bouncing down 4 steps. I am only 35 years old...and the moment I stopped hitting my backside on those steps I knew I was in trouble. An E.R. visit revealed I had fractured my pelvis. I hit those steps hard, so hard my skin indented and is still indented around a massive swollen butt. I am not a large person. 5'7" and 130 pounds. 6 months ago I was found to be vitamin d deficient. That combined with the history of celiac (diagnosed in 2004) I mentioned/ asked my endocrinologist if I needed a test for osteoporosis (I have also had a hysterectomy at the age of 29) and she just looked at me and said it wasn't necessary.

Now, I am thinking, that I should have pushed much harder.

I just started seeing an orthopedic doctor last wednesday, due to needing help strengthening my left side after suffering a lacunar infarct in Nov. of 2004. This fracture on my right side is leaving me a bit disabled.

Celiac is a serious, life threatening, possibly disabilitating disease. Are there any doctors out there that truly understand this disease and all its ramifications?

I am only 35, and I am strong---but my body is really taking a beating. I don't know what to do anymore as far as being wise about being as healthy as I can be. I am gluten free, but went so long misdiagnosed, that I am afraid it has shortened my life.


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



Celiac.com Sponsor (A8-M):



Dennis wayne Newbie
Hello, thank you for reading this.

Friday night I slipped on ice on the top of stairs on my deck, and landed hard, sideways-bouncing down 4 steps. I am only 35 years old...and the moment I stopped hitting my backside on those steps I knew I was in trouble. An E.R. visit revealed I had fractured my pelvis. I hit those steps hard, so hard my skin indented and is still indented around a massive swollen butt. I am not a large person. 5'7" and 130 pounds. 6 months ago I was found to be vitamin d deficient. That combined with the history of celiac (diagnosed in 2004) I mentioned/ asked my endocrinologist if I needed a test for osteoporosis (I have also had a hysterectomy at the age of 29) and she just looked at me and said it wasn't necessary.

Now, I am thinking, that I should have pushed much harder.

I just started seeing an orthopedic doctor last wednesday, due to needing help strengthening my left side after suffering a lacunar infarct in Nov. of 2004. This fracture on my right side is leaving me a bit disabled.

Celiac is a serious, life threatening, possibly disabilitating disease. Are there any doctors out there that truly understand this disease and all its ramifications?

I am only 35, and I am strong---but my body is really taking a beating. I don't know what to do anymore as far as being wise about being as healthy as I can be. I am gluten free, but went so long misdiagnosed, that I am afraid it has shortened my life.

i am frightened too. malnutrition for so long. three broken ribs in the last year with very little pressure at the time the incidents. i haven't been healing as well as i thought i would very little weight put on. i still have a lot of nerve ataxia even when i'm not contaminated. i don't have any stamina to speak of yet. psychologically it is wearing me down. i'm still blaming myself for all my shortcomings. the light at the end of the tunnel doesn't seem to be getting any brighter. but someone wrote that it gets harder before it gets easier i didn't understand it then but i think i do now. i know the body will repair itself eventually, i just hope that being undiagnosed for sooo long hasn't left me with irreparable damage. keep your chin up it's all can do good luck :D

kbtoyssni Contributor

I feel that I'm the one who has to do all the research on the ramifications of the disease so I can make sure I'm getting the right treatment. Most people your age wouldn't need a test for osteoporosis, but for a celiac I'd recommend it. You're young enough that you may be able to reverse some of the symptoms.

dbmamaz Explorer

I dont have anything really to add, but I just want to say that its so much easier to be scared and down and even feel hopeless when you are sick or injured. You will feel better when this is behind you. Do get pushier w your doctor, bring a freind if it helps, or find a new doctor you feel more comfortable with. You cant look back you and only move forward and do your best to take care of yourself.

babysteps Contributor

although time consuming, sometimes taking a more direct role in your own healthcare is often helpful from the sense of control alone, much less from the (hopefully) more targeted care that should result.

Some drs are open to being educated - if so, gathering a few studies could help. Another approach is to network via local celiac group and/or friends - just tell everyone you talk to that you're celiac & looking for an informed dr. If you have any friends who are nurses (or other healthcare professionals) they often have great insights, too.

Also, for some tests, you can get them yourself w/o Dr referral - IF you have the $ or time to hassle insurance directly for coverage - in our town last week a for-profit company offered 4 "wellness" tests for I believe $120 total, one was a bone density test (via ultrasound? at the ankle). They did this at a local church. [company was Lifeline Screening, the appointment # was 877 547 1583]

Hope you feel better soon and heal quickly!

itchygirl Newbie

I had a spinal compression fracture (at 40) from osteo before being diagnosed.

Ursa Major Collaborator

Kara, that sounds like a pretty bad fall, and you might have broken your pelvis even if you didn't have celiac disease.

I broke my ankle six years ago by just going over on it when stepping on the edge of a driveway. But I had a bone density scan done two years ago, and my bones are strong and healthy. So, I can't blame my fractured ankle on celiac disease. My problem is very weak ankles and wrists.

If you have a scan and it shows osteopenia or even osteoporosis, DON'T let the doctor talk you into taking those drugs that are supposed to make your bones denser. They are big trouble. Not only are they very hard on the liver (needing monitoring), but they stop your bones from renewing themselves. Which makes them look denser on scans, but older bone cells are more brittle. And the worst thing is, that those drugs have been shown to sometimes cause necrosis of the jawbone! Which is VERY frightening for the people who get it and disfiguring, too.

At your age you could arrest osteoporosis by taking vitamin D, magnesium and calcium and avoiding gluten. In fact, it may even completely reverse. But as I said, you don't necessarily have a problem with osteo yet.

Dennis, are you still consuming dairy and soy? Those could cause some of your ongoing problems. Also, have you been tested for deficiencies? You should have that done as soon as possible, so you know where you stand nutritionally, and know where to supplement.

How long have you been gluten-free?


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



Celiac.com Sponsor (A8-M):



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. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,956
    • Most Online (within 30 mins)
      7,748

    Crismedin
    Newest Member
    Crismedin
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.