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

Personal Labs Testing? Any Experience?


HumanDecency

Recommended Posts

HumanDecency Contributor

Anyone have experience with something like this? Is it legit or a scam? Open Original Shared Link

 

595 bucks is a bit much to drop on an unscientific test. Thoughts within the group?

 

Thanks,

Jesse 

 

 


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



Celiac.com Sponsor (A8-M):



IrishHeart Veteran

Looks like they use LabCorp, the same company that runs the blood work done by my doctor. (so, that part is probably legit)

 

Looks like they are not allowed in certain states (check the website)

 

Not sure what tests you are going to have run and why you may not want to go through a doc to order them (and that is none of my business :D )

but your insurance would cover them if you did it that way.

 

If you do not have insurance or you have not been helped by a doctor, maybe it is a good idea, but I would check to see if any complaints have been lodged about this company before sending them my credit card info.

 

You may still need a doc after you get the results.

HumanDecency Contributor

I plan on using my doctor if he will order them and doing it myself if he will not. My specialist has told me point blank that I do not need to order such tests and that I should stop being silly. I thought that was irresponsible and I found a new specialist. I just can't see him until August. I have a disease which impacts absorption and causes potential malnutrition. I need to figure out if I am deficient in any vitamins and where I stand on other issues. The food allergy test would also be a plus (if that works). I have heard good and bad things. 

cyclinglady Grand Master

Jesse,

 

I can't speak for the lab, but I understand your frustration.  My GI just said to take 2 iron pills and two calcium pills a day.  Told me that typically his patients don't benefit from a dietitian (that's okay for me because my husband's been gluten-free for 12 years, but others?).  

 

Followed up with my PCP after being in the hospital (focus was on a heart attack which I didn't have and nuclear stress test proved it).  Armed with the "Up-To-Date Management blog by Jebbie (pediatrician with celiac disease) in June 2013 in hand, I started the visit with "f/u from hospital but look at this article I found on Celiac.com.  Doc said that he uses the website where this information came from (so legit article).  I asked about screenings for deficiencies.  Told me to go back to my GI or take a multi-vitamin.  Then reviewed the hospital one X-ray -- "humm....broken vertebrae, I guess I should order a bone scan."  The worst yet:  "Some DC patients have bloody diarrhea, but yours isn't so bad you could probably eat a little."

 

Okay.  He's probably limited on procedures (HMO) and he sees a ton of patients who might not have celiac disease and doesn't have time to research everything, but really? (My old PDP/GP of over twenty years retired in December, and geez, he'd give you a PAP to save you time....)

 

Back to the blood test, I took them almost years ago ordered by a MD (Environmental Medicine) who thought outside the "box", lived in the University Medical Library, and a grad of MIT but now retired too.  

He said although they are not 100% accurate, it is at least, a place to start.  Did skin testing too.

 

I found my major food and inhalant allergies (pollen, mold, eggs, casein, whey, almonds, mushrooms and garlic.  Other were less, but I rotated them.  Can eat some tree nuts (walnuts), but not almonds....weird.

 

I still have those allergies, but I'm three months into the celiac disease diet.  It would be a miracle if I could get those foods back, but I'm hoping.  In the meantime, as long as I avoid those foods and the gluten, I'm feeling much better.  Just trying to get through the deficiencies (e.g. iron anemia, whacked thyroid).  Bone scan in August (I'm going on vacation) and then I'll know if I should be safely back on a bike again).  For now, it's swimming and walking!  

 

Go for the testing yourself, unless you can find a savy doc!

HumanDecency Contributor

I finally found a new doc who has agreed to do vitamin deficiency testing and a food allergy panel. I hope this at least helps a little bit because it has been a miserable last few months. I have been gluten-free for 3 months now. The first week was great but now the symptoms just keep cycling through. The most troubling aspect has been my pulse and heartbeat this week. I had to go do the stress test just like you, CyclingLady and it came back clean *thank goodness* but I still get tender and my pulse shoots up to 100 while I am lying in bed at night. I think this is what is waking me up. I generally wake up around 1 to 3 every night and have a rough time falling back asleep. This makes me tired all the next day and just seems like an endless cycle.

 

I don't do well with uncertainty. Thankfully I have this community and maybe a new doc now. I would be lost without help. Just being gluten free does not cut it.

 

Thanks!

Jesse

frieze Community Regular

I finally found a new doc who has agreed to do vitamin deficiency testing and a food allergy panel. I hope this at least helps a little bit because it has been a miserable last few months. I have been gluten-free for 3 months now. The first week was great but now the symptoms just keep cycling through. The most troubling aspect has been my pulse and heartbeat this week. I had to go do the stress test just like you, CyclingLady and it came back clean *thank goodness* but I still get tender and my pulse shoots up to 100 while I am lying in bed at night. I think this is what is waking me up. I generally wake up around 1 to 3 every night and have a rough time falling back asleep. This makes me tired all the next day and just seems like an endless cycle.

 

I don't do well with uncertainty. Thankfully I have this community and maybe a new doc now. I would be lost without help. Just being gluten free does not cut it.

 

Thanks!

Jesse

that early awake ; could be blood sugar related.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Florence Lillian replied to lmemsm's topic in Gluten-Free Recipes & Cooking Tips
      13

      gluten free cookie recipes

    2. - Russ H replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

    3. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      15

      Severe severe mouth pain

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,914
    • Most Online (within 30 mins)
      7,748

    Momxiety
    Newest Member
    Momxiety
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • xxnonamexx
      very interesting thanks for the info  
    • Florence Lillian
      More cookie recipes ...thanks so much for the heads-up Scott.  One can never have too many.  Cheers, Florence.
    • Russ H
      Hi Charlie, You sound like you have been having a rough time of it. Coeliac disease can cause a multitude of skin, mouth and throat problems. Mouth ulcers and enamel defects are well known but other oral conditions are also more common in people with coeliac disease: burning tongue, inflamed and swollen tongue, difficulty swallowing, redness and crusting in the mouth corners, and dry mouth to name but some. The link below is for paediatric dentistry but it applies to adults too.  Have you had follow up for you coeliac disease to check that your anti-tTG2 antibodies levels have come down? Are you certain that you not being exposed to significant amounts of gluten? Are you taking a PPI for your Barrett's oesophagus? Signs of changes to the tongue can be caused by nutritional deficiencies, particularly iron, B12 and B9 (folate) deficiency. I would make sure to take a good quality multivitamin every day and make sure to take it with vitamin C containing food - orange juice, broccoli, cabbage etc.  Sebaceous hyperplasia is common in older men and I can't find a link to coeliac disease.   Russ.   Oral Manifestations in Pediatric Patients with Coeliac Disease – A Review Article
    • cristiana
      Hi @Charlie1946 You are very welcome.   I agree wholeheartedly with @knitty kitty:  "I wish doctors would check for nutritional deficiencies and gastrointestinal issues before prescribing antidepressants." I had a type of tingling/sometimes pain in my cheek about 2 years after my diagnosis.  I noticed it after standing in cold wind, affecting  me after the event - for example, the evening after standing outside, I would feel either tingling or stabbing pain in my cheek.   I found using a neck roll seemed to help, reducing caffeine, making sure I was well-hydrated, taking B12 and C vitamins and magnesium.  Then when the lockdowns came and I was using a facemask I realised that this pain was almost entirely eliminated by keeping the wind off my face.  I think looking back I was suffering from a type of nerve pain/damage.  At the time read that coeliacs can suffer from nerve damage caused by nutritional deficiencies and inflammation, and there was hope that as bodywide healing took place, following the adoption of a strict gluten free diet and addressing nutritional deficiencies, recovery was possible.   During this time, I used to spend a lot of time outdoors with my then young children, who would be playing in the park, and I'd be sheltering my face with an upturned coat collar, trying to stay our of the cold wind!  It was during this time a number of people with a condition called Trigeminal Neuralgia came up to me and introduced themselves, which looking back was nothing short of miraculous as I live in a pretty sparsely populated rural community and it is quite a rare condition.   I met a number of non-coeliacs who had suffered with this issue  and all bar one found relief in taking medication like amitriptyline which are type of tricyclic anti-depressant.   They were not depressed, here their doctors had prescribed the drugs as pain killers to address nerve pain, hence I mention here.  Nerve pain caused by shingles is often treated with this type of medication in the UK too, so it is definitely worth bearing in mind if standard pain killers like aspirin aren't working. PS  How to make a neck roll with a towel: https://www.painreliefwellness.com.au/2017/10/18/cervical-neck-roll/#:~:text=1.,Very simple. 
    • Scott Adams
      We just added a ton of new recipes here: https://www.celiac.com/celiac-disease/gluten-free-recipes/gluten-free-dessert-recipes-pastries-cakes-cookies-etc/gluten-free-cookie-recipes/
×
×
  • 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.