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

Denied Insurance Coverage For Dietician


CeliacChild

Recommended Posts

CeliacChild Newbie

My insurance has denied coverage for a visit to the dietician after my daughter was diagnosed with Celiac Sprue. Has anyone been able to get their insurance to cover this? If so can you share the letter with me? I need help writing a letter to the board to request they review the denial.

Thanks


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



Celiac.com Sponsor (A8-M):



*lee-lee* Enthusiast

my insurance company denied me too. it was $200 out of pocket for an hour consult - no thanks. my GI actually said it wouldn't really be worth it to go anyhow.

i can't help with a letter but maybe the doctor that diagnosed your daughter can? you can also find tons of great info on this board...

Gemini Experienced
My insurance has denied coverage for a visit to the dietician after my daughter was diagnosed with Celiac Sprue. Has anyone been able to get their insurance to cover this? If so can you share the letter with me? I need help writing a letter to the board to request they review the denial.

Thanks

I have no idea what your financial situation is but if you really feel the need to see a dietician, it's money well spent. Having said that, I think if you went out and bought a couple of good books on Celiac Disease, you would learn far more than just sitting there, listening to a dietician who may or may not know anything about celiac disease. Nutritionists and dieticians are not always up to date on every medical condition that requires a dietary change. I never saw one but bought the books and found I didn't need to see one.

There are some excellent ones that focus on kids, specifically by Dana Korn, that would be very helpful to you! Good luck.

sbj Rookie

And if you don't feel like spending money on books just try your library! I found a ton of books at my main branch and even at the smaller local branches.

I found the dietician to be quite helpful but I would speak to him/her BEFORE your appointment to make sure they are prepared. I found mine to be helpful but there is no way that I would have spent $200 out of pocket. It wasn't worth $200.

It's a pity that your insco denied coverage. I can think of two things: (1) ask them if someone with diabetes would be covered to see a dietician. (2) Let them know that other insurers routinely provide this coverage. I am with Kaiser Permanente - they not only provide this coverage but this is considered preventive medicine and is cost-effective for the insurer.

The below link has some interesting coverage about insurance and denial.

Open Original Shared Link

Coverage for dietitian visits: In the U.S., insurance coverage for dietitian visits is mandated by law. Currently the law allows coverage for only a few types of dietitian visits, including coverage for transplant patients and people with type 1 diabetes. Celiac disease is not covered, so any time a newly diagnosed celiac wants to learn about the gluten-free diet from a dietitian, that individual will need to pay out of pocket. ... There is a place for you to turn if you have questions or concerns about insurance issues. The Patient Advocacy Foundation, located in Virginia, helps people with chronic and life-threatening health conditions to sort out their insurance issues. They are a non-profit agency, and they can be found on the web at
www.patientadvocate.org or at the following toll-free number: 800-532-5274.

neesee Apprentice

Try your local health department for help. That's who helped me the most. They hooked me up with the GIG and sent me a lot if information about the diet. Of course that was before the internet! :D

I really didn't learn a darn thing from the dietician anyhow. I was covered 21 years ago, but I wouldn't be now. I was in the hospital though.

neesee

mommida Enthusiast

Almost five years ago, we had an appointment with the dietician.

She called and cancelled the appointment. Her advice was by Dana Korn's book Celiac Kids and come to this website.

The book is helpful and I've learned everything we needed to know from this site. You can't get better advice on a subject than direct contact with people that live gluten free 24/7.

Gemini Experienced
And if you don't feel like spending money on books just try your library! I found a ton of books at my main branch and even at the smaller local branches.

The only drawback to using the library is they don't let you keep the books very long and most newbies will absolutely be using the books for reference for at least 6 months. They are invaluable to own, at least in the beginning. These books do not cost much, I think I spent about $30.00 on 2 of them total and that's not a budget buster. Amazon has good prices on many Celiac related books.

The other important thing to do is buy or borrow a copy of Dr. Peter Green's book, "Celiac Disease: The Hidden Epidemic." It has good information on how to manage this disease the correct way and dispels the false information that is prevalent on the internet. It's important to get it right in the beginning so adapting will be easier. It really isn't as hard as it seems. It's just overwhelming at first but that will change with knowledge. You have to do a little studying in the beginning but it's worth the effort. I can imagine how difficult it must have been years ago but there is so much information out there and good books on the subject, you really can do this on your own, once diagnosed.


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



Celiac.com Sponsor (A8-M):



Dyan Rookie

I haven't tried going through my insurance, but I met with the one at the celiac disease conference in May. And all I can say is, I'm glad I didn't have to pay for that meeting. She just told me to let my daughter eat nachos and and to buy greek style yogurt. I would suggest eating well but still add a multivitamin.

cmom Contributor

My 2 dietician appointments were totally useless. She told me that I could eat Rice Krispies and when I asked her about the fact that it contained barley malt (and this was after being newly diagnosed), she said she really didn't know. I have found out much more helpful info on the forums and through my own research. Doctors haven't been much help either when it comes to the diet. :angry:

debmidge Rising Star
My insurance has denied coverage for a visit to the dietician after my daughter was diagnosed with Celiac Sprue. Has anyone been able to get their insurance to cover this? If so can you share the letter with me? I need help writing a letter to the board to request they review the denial.

Thanks

We did the same thing - went thru the trouble of writing letter to insurance company and got "permisson" to see dietician. The visit was a waste of time. This forum and celiac.com and the celiac organizations provided much more information than the dietician did. Had I known I

would not have wasted the time and effort.

Vamonos Rookie
My insurance has denied coverage for a visit to the dietician after my daughter was diagnosed with Celiac Sprue. Has anyone been able to get their insurance to cover this? If so can you share the letter with me? I need help writing a letter to the board to request they review the denial.

Thanks

Your insurance company will have an appeal process. Call the customer service number to find out how you file an appeal. Upon review by the medical director, (who is a physician and not a claims adjuster) will know that the only treatment for Celiac is dietary modification-- your request for a nutrition consult should be approved. My own consult was initially denied, but was sent to medical review before I even knew it was denied and the medical director approved it immediately.

In the mean time, call the dietician and let her know you are appealing the denial. Do not pay the bill. Another way to insure that we, as Celiacs, get the coverage for medical care is to get the health care practitioners in your corner. If they are denied payment for their services they will become more proactive in making sure they are reimbursed by insurance for their time.

I hear what some of the other posters are saying in regard to the dietician not having much if any pertinent info regarding Celiac disease. By the time I got to see the person my doc referred me to I had already accumulated a file from great sites like this one. Another great source for information is your local library and it is FREE. The resource person will be happy to help you track down books on celiac and will obtain what ever you need from outside libraries if yours doesn't have what you are looking for.

You can do this. Your letter can be brief. The idea is to get it to the doctor's attention at the insurance company.

  • 2 weeks later...
Hummingbird4 Explorer

Mine was initially denied, and then I called them (Cigna) to explain that my doctor ordered me to see the dietician. It's not as if I went on my own for weight loss tips. They said, "Oh, okay, no problem. We'll pay it." I asked them if they needed a copy of the order from the doc and they said they didn't.

It was paid. (And like others have mentioned, the visit was completely useless and a waste of time. I found out MUCH more from this site than any dietician could have told me in an hour. Besides, her specialty was diabetes. She hardly knew anything about Celiac!)

  • 4 weeks later...
curiousgeorge Rookie

Being in canada, dietician at the hospital was covered. I knew at least as much as she did just from reading on the net.

The ONLY useful thing she said was not to eat oatmeal for a year until the tummy heals which I suspect is really good advice. Other than that, she was nice but not particularly useful. I did however enjoy seeing the plastic veggies she had in serving size portions in her office. I realized I was eating way more servings of veggies than I realized.

mamabear Explorer

You might check the benefits for your particular plan. All plans are not equal. I also would advocate you push your insuror even if no dietician benefits exist. Our ONLY medicine is food, but I have yet to find a dietician who knows 10% of what you can find here!

kbtoyssni Contributor

If you do see a dietitian, I would recommend asking a few questions about his/her knowledge of celiac before making an appointment. There are some good ones out there, but most don't have a clue about what you can and cannot eat.

debmidge Rising Star
If you do see a dietitian, I would recommend asking a few questions about his/her knowledge of celiac before making an appointment. There are some good ones out there, but most don't have a clue about what you can and cannot eat.

You're correct....but we did that. I had a conversation with her (dietitian/nutritionist) on the phone and she assured me she was knowledgeable because her sibling has celiac disease. Once we met with her,

however, it was clear to me that she only knew basics: don't eat gluten and read labels. The only GIG info she had was photocopied sheets of what not to eat and a photocopy of a magazine article. I feel at the least she should have had the CSA's Product handbook in her office, several books on celiac for example Bette Hagman books, etc. But she had none of this. She must never really talk or spend time with her celiac sibling....

luvthelake21 Rookie

My DD was also denied coverage on dietitian services. Did not think at the time to see if would be covered to worried about her health than to call insurance company. When we met with her she did not help at all, told DD it would be ok to eat wheat b-day cake once a year and to take a small piece of the communion wafer at church :angry: I knew more about Celiac than she did. I had only studied for two weeks before meeting with her.

Country Girl Newbie

Our dietician visit was covered completely by United Health Care, and it was very valuable. I believe someone already told you to call and ask for a medical review by a physician. I would also call a rep at the company and let them know you will be filing an appeal through your state's Insurance commisioner and the office of the inspector general (both can be done online through your states website). This phrase usually gets me what I want.

cat3883 Explorer

In my area the health food stores will have speakers. Usually they are dieticians and nutritionists. They are free or a very small fee. And my GI's office called me last week about a dietician they are having at his office after hours. The fee is $10. I am now meeting with a nutritionist that I met at one of the health food stores. She also has Celiac. She is teaching me many things. Check with the stores in your area. Good luck.

ek327 Newbie

A knowledgeable dietician should not only be able to help you with what you can and can't eat, but what you should eat--to help with the history of malabsorption, and to find sources of micronutrients found in wheat, but not in rice, potato, tapioca starches/flours. There is much more to eating right for a person with celiac than to "not eat gluten".

fran641 Contributor

My local hospital dietitian does not charge for visits to her. I would check with your local hospital about seeing their dietitian and if they charge.

She is a great lady but all the information she gave me was off the internet. If I did not have access or didn't use a computer the info she gave me would have been enough to get started. But I do need a book (or a few) to be able to look at often.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,546
    • Most Online (within 30 mins)
      7,748

    KimberlyAnne76
    Newest Member
    KimberlyAnne76
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.