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 Our Content
    eNewsletter
    Donate

Gold Crowns, Macular Degeneration, No Vitamin D


SandyStPeteFL

Recommended Posts

SandyStPeteFL Rookie

I was diagnosed in Nov of 2008 with the endoscopy and the blood work. In the past six months I have been having bleeding gums with my gold crowns are on my teeth. The dentist has done x-rays and such and can see no problems except that I am having bleeding and irritated gums. But only where the gold crowns are.

Also, upon my last visit to the eye doctor, I have been diagnosed with the beginnings of dry macular degeneration.

Also, upon my last visit to my GP my blood work shows my Vitamin D level is at 15. Should be between 30 and 100. So now I am on 50,000 units of Vitamin D once a week for three months. She also threw out the word Fybromyalgia.

Does anyone else out there have these issues as well? Just curious or am I just the lucky one??


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



Celiac.com Sponsor (A8-M):



gfb1 Rookie
I was diagnosed in Nov of 2008 with the endoscopy and the blood work. In the past six months I have been having bleeding gums with my gold crowns are on my teeth. The dentist has done x-rays and such and can see no problems except that I am having bleeding and irritated gums. But only where the gold crowns are.

Also, upon my last visit to the eye doctor, I have been diagnosed with the beginnings of dry macular degeneration.

Also, upon my last visit to my GP my blood work shows my Vitamin D level is at 15. Should be between 30 and 100. So now I am on 50,000 units of Vitamin D once a week for three months. She also threw out the word Fybromyalgia.

Does anyone else out there have these issues as well? Just curious or am I just the lucky one??

sjogren's disease can be found in celiac patients; there are reports of an increased frequency of sjogrens among celiacs -- but, i can't remember the exact number:

here is some info:

Open Original Shared Link

mostly, but not exclusively, occurs in women and often mistaken for fibromyalgia... my wife was diagnosed with this 2 yrs after the celiac diagnosis. she has the ductal plug (in the lower tear ducts) to keep what tears she produces in the eye (like plugging a drain...), and uses artificial tears frequently throughout the day.

bleeding from gums CAN be due to overly dry mouth, irritated by crown; it is also a classic symptom of other nutritional deficiencies as well, but, i would hope that your doc would have seen those....

SandyStPeteFL Rookie
sjogren's disease can be found in celiac patients; there are reports of an increased frequency of sjogrens among celiacs -- but, i can't remember the exact number:

here is some info:

Open Original Shared Link

mostly, but not exclusively, occurs in women and often mistaken for fibromyalgia... my wife was diagnosed with this 2 yrs after the celiac diagnosis. she has the ductal plug (in the lower tear ducts) to keep what tears she produces in the eye (like plugging a drain...), and uses artificial tears frequently throughout the day.

bleeding from gums CAN be due to overly dry mouth, irritated by crown; it is also a classic symptom of other nutritional deficiencies as well, but, i would hope that your doc would have seen those....

Thanks for that information. My doctor had also mentioned that a couple of months back but I had forgotten about it until you wrote that. I have had dry eyes like crazy for about 6 months as well as dry mouth. I drink about 6, 17 ounce bottles of water a day, plus coffee and ice tea and juices. I go back to see her in another month and a half and I will ask her to re-visit that issue.

Agaom. tjamls fpr tje omfp/

gfb1 Rookie
[snip]

Agaom. tjamls fpr tje omfp/

another symptom is the inability to feel the little bumps on the letters 'F' and 'J' on your leba;ird///

:)

(btw -- don't wait on the artificial tears... just eyedrops and they help significantly. also water is notorious for being unable to make dry-mouth feel better... try a little salt or baking soda in water and rinse periodically. my wife found that sipping gatorade made her feel better -- but, avoid purple so your tongue doesn't change color...)

mushroom Proficient

I had the bleeding irritated gums adjacent to crowns--long ago, pre-gluten-free. I argued a long time with my periodontist about metal allergy; he finally recommended replacing them with ceramic crowns and, miracle of miracles, gums cleared up.

Huge numbers of celiacs have low vitamin D and also osteopenia/osteoporosis.

gfb1 Rookie
[snip]

Huge numbers of celiacs have low vitamin D and also osteopenia/osteoporosis.

it certainly appears that the population at-large (esp those in the north -- with less sun) have greater insufficiencies (if not deficiencies) of VitD than previously thought. although, i don't know of any evidence that celiacs are unique in this regard.

as far as osteoporosis; the prevalence of celiac disease among osteoporotic patients is increased to 1.5-3.0% (as opposed to 1%) and is well accepted. the converse (that celiacs have more osteoporosis than the population at large) has not been appropriately tested.

mushroom Proficient
it certainly appears that the population at-large (esp those in the north -- with less sun) have greater insufficiencies (if not deficiencies) of VitD than previously thought.

Don't forget those in the south too :lol:


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



Celiac.com Sponsor (A8-M):



SandyStPeteFL Rookie
another symptom is the inability to feel the little bumps on the letters 'F' and 'J' on your leba;ird///

:)

Took me a minute on that one.....thanks, I needed a laugh....

SandyStPeteFL Rookie

My doc gave me a bone density test about four years ago (because of my age) and after I was diagnosed last year, she gave me another one....everything appeared to be okay at the time. Then the blood work on the vit D came back low. She told me to sit in the sun at least 15 minutes a day if I can and take the 50,000 units of vit D once a week. Then I will get tested again in two months. I know I do have more color in my face now...not quite so pale.

I go back to the dentist in June for another cleaning.....I will mention the allergy to metals then. He has already suggested removing the gold crowns and replacing with porcelain. Might try just one side of my mouth first. I have three gold in the back on the right and two in the back on the left.

I have an appointment with my doc on Monday upcoming so I will remind her about the Sjogrens and the new issues I have now.

Thanks to all of you for your help and information.....

Jestgar Rising Star
(btw -- don't wait on the artificial tears... just eyedrops and they help significantly.

I use Open Original Shared Link. comes in different formulations (which get thicker). I find I can use the 'moderate' a couple times a day, as opposed to using cheaper stuff every couple hours.

SandyStPeteFL Rookie
I use Open Original Shared Link. comes in different formulations (which get thicker). I find I can use the 'moderate' a couple times a day, as opposed to using cheaper stuff every couple hours.

Thanks, I appreciate the information on the eyedrops. I will check into it.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,008
    • Most Online (within 30 mins)
      7,748

    Wigglywoo27
    Newest Member
    Wigglywoo27
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • DebJ14
      Our son was put on Minocycline for his acne.  It did not solve the acne problem.  He developed drug induced lupus and pericarditis from it and missed an entire year of high school.  He literally went from playing football to bedridden in a couple of weeks.  His PCP tested him for genetic antibiotic resistance and he cannot take any drug in the Tetracycline family.  His gut microbiome was totally destroyed.  In fact he had a stool test done and had no good bacteria, whatsoever.   What did fix his (and his brother's acne) years after the Minocycline debacle was when I was diagnosed with Celiac disease and the kids were tested.  They were both put on a Gluten Free/ Caesin Free diet and within a week both kids were totally free of acne.  The family has now been on the diet 18 years and no acne, except for a teenage grandson who will not adhere.  The big clue that he is eating gluten is that his face breaks out!
    • wellthatsfun
      i am australian. we do have plenty of substitutes, but most are very expensive compared to the originals. i believe i'll just stick to home cooked meals and not have many treats at all. it's sad but it's just so much easier. also, ive heard far too many horror stories of people ordering gluten free food from restaurants and cafés, explicitly telling servers and kitchen staff that cross contamination is a strict no go, and they still get very sick. until i find a reasonably priced fully gluten free kitchen somewhere, i am not eating out for my safety and sanity.
    • wellthatsfun
      thank you all for the kind words and support. it truly means a lot. i know i will adapt, it really just is a grieving process right now though. looking forward to feeling healthier!
    • The Logician
      To Trent’s, yes, from what i’ve read it is not uncommon for digestive systems to become less tolerant to gluten over time. Many types of sensitivity or allergies arise in older people who never had a problem. I don’t see why you are focusing on anything but the fact that after years of my sensitivity to gluten, for whatever reason , it has disappeared after a bout of antibiotics. What i’ve read is antibiotics can make gluten sensitivity worse. In any event, in my case, if I can still eat all the wheat products I want with no reaction after a month or more since my hospital stay this is something that should be investigated. Time will tell.
    • The Logician
      I had a UTI, blood cultures are standard to insure that the infection does not get in the bloodstream which can lead to sepsis and death. In my case there was bacteria in my blood which necessitated 48 hours of antibiotic IV
×
×
  • Create New...