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

Tanning Beds To Increase Vit D?


meme2kids

Recommended Posts

meme2kids Rookie

Does anyone use or been told to use indoor tanning to help increase Vit D?


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



Celiac.com Sponsor (A8-M):



cassP Contributor

Does anyone use or been told to use indoor tanning to help increase Vit D?

OMG- i JUST googled this today- because i recently found out im Vit D deficient... and when i went for a run today there was no sun.

plus i still have a membership at the tanning bed (for vanity reasons)

anyways- from what ive read- the type of UV rays from the sun that DO help the body make vit D are almost nonexsistent at the tanning beds. the tanning beds use different UV rays. at least thats how i understand it.

so... i ordered a premium D3 supplement this week, and will try to get more sun... im a little surprised that i was so low- as i do eat a ton of eggs and fish.

SaraKat Contributor

I used to be a tanning bed person in my teens and 20's and I had a skin cancer removed last year on my shoulder. I would not advise tanning bed use at all. I would try the supplement as the other poster mentioned.

ravenwoodglass Mentor

Please go with the supplements instead. Much safer than tanning and won't have your skin looking like leather by the time your 45.

shopgirl Contributor

I agree with the others. There's nothing about a tanning bed that isn't a bad idea.

Emilushka Contributor

Tanning beds increase the risk of skin cancer up to 10 times or more (depending on how often they are used). The problems they can cause you down the line with deadly cancer, skin problems, and so on greatly outweigh any minor possible vitamin D benefits. We have gluten-free vitamin D supplements. If you have kidney problems and require fully activated vitamin D because your body is unable to process the supplements, we have fully activated vitamin D available by prescription. There are safe ways to get the vitamin - don't risk a deadly cancer!

Ada-B Newbie

I have really severe vitamin D deficiency problems and osteomalacia (adult rickets), I cannot absorb vitamin D supplements (even the 'activated' vitamin D ones on prescription) and still I wouldn't risk a tanning bed! I have to have intra-muscular injections every 3 months but at least I know they won't give me deadly skin cancer.

Oh, and my doctor recommends that everyone should go outside and expose head and hands for at least 20 minutes a day, in moderate climates, a few minutes a day in hotter climates and only in the far North should you need to take any supplements at all, and then only in Winter. Oily fish contains natural vitamin D if you'd prefer to go that route.


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



Celiac.com Sponsor (A8-M):



-AprilSun Newbie

Hello,

I came across this website through a google alert for vitamin D.

In regards to your doctor advising you to use a sunbed this recommendation is becoming more common because unfortunately not all vitamin D is created equal. Supplements or vitamin D that is ingested does not bind to cells as effectively as vitamin D gained through UV exposure. There have been numerous studies that have shown that UV exposure is an independent risk factor in the prevention of things such as cancer and bone disease. One very important piece of research was published in January 2011 that demonstrated that as women got more UV exposure, their risk of developing breast cancer was significantly reduced. This study followed 67,000 French women over a 20 year period, link here:

Joint Effects of Dietary Vitamin D and Sun Exposure on Breast Cancer Risk: Results from the French E3N Cohort — Cancer Epidemiol Biomarkers Prev Open Original Shared Link

The body has over 200 genes with vitamin D receptors and while it is called a vitamin it is actually a hormone. Vitamin D deficiency is associated with increased risk of multiple sclerosis. Scotland is a country with the highest rates of MS in the world. If you live in this region and if your surname begins with Mc or Mac then you have a 40% higher risk of developing MS over your lifetime. A landmark study began in January 2011 to examine the relationship between UV exposure and MS 2000 residents from the Orkney Islands, which has the highest levels of multiple sclerosis in the world. The link between UV exposure and MS has been known for around 25 years and this has been confirmed again this week when the results of an Australian study were published, link here:

Sun exposure and vitamin D linked to MS risk | Reuters Open Original Shared Link

I could write an essay but I will stop at that for now. There is plenty of research to support moderate and controlled UV exposure in order to maintain good health. So don't throw the baby out with the bath water because the ailments that you could end up suffering from as a result of complete sun avoidance can far outweigh the perceived risk of skin cancer.

Anyway, the point that I came in here to make originally relates to the use of sunbeds. IF you are going to use a sunbed but if you do want to do it in as responsible a manner as possible then just follow a few simple rules:

- Start out on the smallest time possible, even if it is only 3 minutes.

- Build your time up slowly, so increase the length of time you spend in the tanning bed one minute at a time.

- Do not go more often than once every two days.

- If you are still red more than 24 hours later then you need to reduce your tanning time, you want to avoid burning your skin.

So you need to get your skin used to the UV exposure gradually, that's why you start out small and increase your time slowly. You also want to give your skin enough time to replenish between sessions so you don't end up looking like a leather handbag that's why you shouldn't go more often that once every two days. The most important thing is to avoid sunburn, which is associated with increased risk of developing skin cancer. So if you are still red more than 24 hours later then you need to reduce your time.

If you do decide to use a tanning bed then what you may find is that you will start out on 3 minutes and do that 3 times per week for one month. After that your skin might be used to the UV exposure and so you will increase your time to 4 minutes for another 2 weeks. From there you might quickly graduate up to 6 minutes where you will stay for another month or two. Then you might decide to increase your time to 8 minutes or you might feel that 6 minutes is perfectly adequate for your needs.

Kind regards,

@AprilSun

*edit: removed the bit link shortener for the link to the E3N French cohort study and replaced with the full URL

Igg postive Rookie

The doctor can give your capsules of high dose vitimin D. He can monitor your level to make sure you are getting the right dosage.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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.