• Ads by Google:
     




    Get email alerts Subscribe to Celiac.com's FREE weekly eNewsletter

    Ads by Google:



       Get email alertsSubscribe to Celiac.com's FREE weekly eNewsletter

  • Announcements

    • admin

      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to Celiac.com's FREE weekly eNewsletter   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes

I Keep Turning Blue
0

Rate this topic

19 posts in this topic

Recommended Posts

Has anyone experienced their entire body (hands/arms, torso, legs/feet) turning blue/gray randomly, I have talked to my dr already but he seems stumped, and doesn't want to do tests until its worse. It started this past summer it happened like 2 or 3 times and it always happened when I had been laying on a flat wooden surface, and it didn't happen again until about 2 months ago. In the past 2 months or so it has happened at least 4 times but now it seem random when it happens, like I was sitting in class on thursday and it started with my hands and then pretty soon I had a blue/gray hue. When it happens, (anytime of day/night) I'm not usually cold, but my extremities start to ache and sometime my hands will tingle, and they get really hard to use like I'm wearing gloves even after the color returns, basically I turn a gray/blue color and my veins become prominent. I also have other symptoms, I have too much energy to sleep, I get about 2 hours of sleep a night, for as energetic as I am I feel really weak, I have had really bad heartburn and indigestion the past couple of weeks, and I have this weird feeling in my throat, kind of dry and like I have food stuck or something.

Any ideas that I can take to my Dr. would be much appreciated.

Thanks

AP

celiac - March 2009

dishydrotic excema - May 2011

Share this post


Link to post
Share on other sites
Ads by Google:
Ads by Google:


is it Reynaud's Syndrome, where your extremities react to cold and turn blue? are you in a cold or warm environment, or does it happen in both?

blue skin can mean lack of blood circulation, which is one reason why it connects to the cold. your blood goes back to the body core to keep your organs going. have you had your heart or circulation checked? i think i would make sure that was ok, if it was me.

sounds kinda distressing!

Share this post


Link to post
Share on other sites

you said you don't turn cold, so I'm guessing a different sort of circulatory problem is also a possibility along with raynaud's. I would highly recommend going to a new doctor who won't say "wait until you're sicker for us to look into this". Your doc... well, doesn't sound like he wants his job; why let him keep it?

Share this post


Link to post
Share on other sites

Getting food stuck in your throat is a symptom of Eosinophilic Esophagitus. There is a known connection to Celiac and EoE.

Share this post


Link to post
Share on other sites

I turn blue sometimes when the air around me changes temp, not just me.My face can turn purple after getting out of the shower. If it's correlated with sleep and energy it might be something you're eating. It might be time for the annoying food diary.

Share this post


Link to post
Share on other sites
Ads by Google:


Thanks for the ideas guys

Madagascar- the temperature doesn't seem to effect me turning blue, but I have noticed that the less sleep I get the more frequently it happens, also I asked my dr if it could be raynauds but he doubts it. I have not had my heart or circulation checked recently, I had an ekg about 5 years ago and it was fine, I was told I had a heart murmer last year, but the dr said I was dehydrated and it went away within a couple days.

I talked to my dr today because my heartburn was to the point where it hurt to eat anything and my mom is concerned that I am only getting about 2 hours of sleep a night. He prescribed omeprazole for my heartburn and told me to go to student health about my sleep problems (as I am attending school 9 hours from home).

I have been looking into other autoimmune diseases and found that I fit the symptoms of Graves disease pretty well, (insomnia, hyperactive, heartburn, increased d, increased hunger and thirst, feeling of something in my throat...) How would I go about getting this tested as my dr. doesn't want to test me for anything until my symptoms increase.

Thanks, AP

Share this post


Link to post
Share on other sites

Could you be getting some CC somewhere? When you say you turn blue is it in lacy patches? Do a search on pics of Livedo Reticularis to see if the presentation might be the same. I have had livedo for many years and it is an indication of gluten CC for me now that I am gluten free. The same applies for trouble sleeping. It can be hard to eat safely when we are in a situation like being fed by a school caf or rooming with gluten eaters off campus.

You may also have another intolerance. The most common ones are dairy and soy. I get horrible heartburn from soy. For me a single dose of Pepto Bismal liquid relieves the pain.

Share this post


Link to post
Share on other sites


Ads by Google:


Thanks for the ideas guys

Madagascar- the temperature doesn't seem to effect me turning blue, but I have noticed that the less sleep I get the more frequently it happens, also I asked my dr if it could be raynauds but he doubts it. I have not had my heart or circulation checked recently, I had an ekg about 5 years ago and it was fine, I was told I had a heart murmer last year, but the dr said I was dehydrated and it went away within a couple days.

I talked to my dr today because my heartburn was to the point where it hurt to eat anything and my mom is concerned that I am only getting about 2 hours of sleep a night. He prescribed omeprazole for my heartburn and told me to go to student health about my sleep problems (as I am attending school 9 hours from home).

I have been looking into other autoimmune diseases and found that I fit the symptoms of Graves disease pretty well, (insomnia, hyperactive, heartburn, increased d, increased hunger and thirst, feeling of something in my throat...) How would I go about getting this tested as my dr. doesn't want to test me for anything until my symptoms increase.

Thanks, AP

I have GERD so i understand fully the heartburn thing. When mine would get bad enough that i couldn't eat, i would drink a lot of water. Also, if it is an issue at night, perhaps look into getting an incline pillow, it keeps your head upward while keeping acid down at night. I would get GERD attacks (acid reflux/heartburn) so bad that i would wake up at night and feel like i couldn't breath. Not fun!

Share this post


Link to post
Share on other sites

Thanks again guys,

ravenwoodglass - it kind of looks like that but not quite as red, mine is more of a blue gray hue. I am really particular about what I eat and I make all of my own food and don't really eat with non-gluten free people, so I don't think I'm getting CC if I am I have no idea how. I do know that I have other sensitivities/intolerances and I am pretty good about staying away from them. Does your livedo get worse when you've had less sleep?

I went to student health and the RNP wants me to try amitriptyline for a week to see if it will help me sleep, and if it doesn't she wants to test my thyroid. she didn't even seem interested/concerned that I have been turning blue. she also said that she doesn't think my main symptoms (blueness, heartburn, and not being able to sleep) are not connected.

thanks again, AP

Share this post


Link to post
Share on other sites


Ads by Google:


Thanks again guys,

ravenwoodglass - it kind of looks like that but not quite as red, mine is more of a blue gray hue. I am really particular about what I eat and I make all of my own food and don't really eat with non-gluten free people, so I don't think I'm getting CC if I am I have no idea how. I do know that I have other sensitivities/intolerances and I am pretty good about staying away from them. Does your livedo get worse when you've had less sleep?

I went to student health and the RNP wants me to try amitriptyline for a week to see if it will help me sleep, and if it doesn't she wants to test my thyroid. she didn't even seem interested/concerned that I have been turning blue. she also said that she doesn't think my main symptoms (blueness, heartburn, and not being able to sleep) are not connected.

thanks again, AP

Please. PLEASE. Get new healthcare providers. Yours are blowing off something that could be very serious.Write a journal of symptoms, take that to your new providers. You want to have it written so you don't forget anything, and so you can include the circumstances under which this happens to you.

  • Upvote 1

Share this post


Link to post
Share on other sites

beachbirdie- thanks for the reply. I have been trying to get a new doctor recently but I am from a small town where there aren't any doctors taking patients I also have an HMO which only covers certain doctors :( but I did manage to get into see a different doctor at student health services. It was kind of a fluke though. I went back because I've started having nightmares and I have been extremely jumpy. the new dr did a full neurological exam and listened to my heart and lungs. she didn't find anything and she was stumped. She said the same thing my other dr said that she would do more research to try and figure it out. she told me that she wanted to test my thyroid, and do a cbc and a complete metabolic work up. she told me to come back in 2 weeks. but she doesn't want to test me until she has a better idea of what she is looking for. mean while she told me to up my omeprozole for heartburn and that it was my choice to continue the amitryptaline or not, as she has no idea if it is causing my nightmares.

Thanks guys

AP

Share this post


Link to post
Share on other sites

That sounds very serious to me. I'm not a doctor so I don't know all the possibilities, but Raynaud's is the only thing I've personally heard of that could describe what you're experiencing. And while I can undestand why any doctor would not think you have that specific condition, since itself it is fairly rare, it's downright stupid to not test for the rare things when he/she is stumped by the usual things. Wikipedia seems to mainly have Reynaud's as a symptom of a list of other diseases, rather than a disease in and of itself. If I were you I'd definitely read up about those diseases and see if you fit the criteria for any of them. Apparently some drugs can cause it? Why are you on amitryptaline and not more modern antidepressants?

Share this post


Link to post
Share on other sites

Thanks for the ideas Cavernio - I have looked into Reynauds syndrome and it doesn't really fit my symptoms because it doesn't seem to be related to stress or cold, mainly it is sleep or triggered by my position. I started having the symptom before I started taking any medications so I don't think its that. I am taking amitryptaline as a sleep aid instead of a antidepressant. My HMO doesn't cover anything prescribed by anyone other my general practitioner so they tried to keep it cheap. They are going to try and get some blood work but I have to work it out with my insurance first

Thanks

AP

Share this post


Link to post
Share on other sites


Ads by Google:


i agree - it sounds like this could be something serious. i don't know how turning blue could be anything other than circulation-related, somehow. Have you done the symptom-checker on Webmd? It's pretty good. It came up with a few possibilities for you, solely on the skin discoloration symptom. the one i wondered about is Thrombocytopenia, bleeding under the skin. That can be caused by drug side effects.

You might look there and see what you think.

Share this post


Link to post
Share on other sites

I finally got my test results back, the dr told me that they were all normal and then just kind of brushed me off.

here are my results, some of them are on the edge of normal. I am curious about the thyroid results because my symptoms seem to be similar to thyroid problems.

glucose 83 <74-106>

Calcium 9.2 <8.4-10.2>

Total Bilirubin 0.3 <0.2-1.3>

AST/SGOT 22 <15-46>

ALT/SGPT 22 <13-69>

Total Protein 6.8 <6.3-8.2>

CRP Inflammatory <0.5 <0.0-1.0>

Albumin 4.2 <3.5-5.0>

Albumin/Globulin RA 1.6 <1.0-2.0>

Alkaline Phosphatas 61 <38-126>

TSH 2.48 <0.47-4.68>

Free Thyroxine 0.78 <0.78-2.19>

WBC 5.1 <4.8-10.8>

RBC 4.46 <4.20-10.8>

Hemoglobin 13.5 <12.0-16.0>

Hematocrit 40 <37-47>

MCV 90.6 <81.0-99.0>

MCH 30.4 <27.0-31.0>

MCHC 33.5 <30.0-37.0>

RDW 12.6 <11.5-14.5>

Platelet count 241 <130-400>

NEUT % Auto 58.4 <37.0-80.0>

Lymph % Auto 32.5 <10.0-50.0>

Mono % Auto 6.7 <0.0-12.0>

EOS % Auto 2.0 <0.0-7.0>

BASO % Auto 0.40 <0.0-2.50>

Neut # Auto 3.00 <2.00-6.90>

Lymp # Auto 1.70 <0.60-3.40>

Mono # Auto 0.30 <0.0-0.90>

Eos # Auto 0.10 <0.0-0.20>

Baso # Auto 0.0 <0.0-0.20>

Erythrocyte sed rate 3 <0-20>

Sodium 142 <137-145>

Potassium 3.8 <3.5-5.1>

Chloride 107 <98-107>

Carbon Dioxide 26 <26-30>

Anion Gap 13 <10-20>

Blood Urea Nitrogen 8 <7-20>

Serum Creatinine 0.7 <0.6-1.3>

Bun/Creatinine rati 11.4 <7.1-23.5>

Thanks Guys

Share this post


Link to post
Share on other sites

thanks frieze

That is what it looks like when i turn blue, although mine is very temporary it goes away about a minute or two after I get up and move, and when I turn blue it is pretty much my whole body, although recently it seems to be affecting single places at a time, like the other day my knees turned purple/blue when I was sitting at my desk but the rest of me was fine. it lasted about 3 minutes and then went away, there was no pain, numbness, or tingling.

AP

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

0

  • Forum Statistics

    • Total Topics
      108,140
    • Total Posts
      939,876
  • Member Statistics

    • Total Members
      66,128
    • Most Online
      3,093

    Newest Member
    DAVOH
    Joined
  • Popular Now

  • Topics

  • Posts

    • Positive biopsy and blood work?  It sure sounds like your doctor made the right diagnosis.   Let me tell you my story.  Diagnosed after going for a routine colonoscopy because I am over 50.  GI saw my chart and noted that I was anemic.  I have a genetic anemia and I was iron deficient as well.  I lived like that my entire life.  But my wise GI ordered a celiac blood panel and it was considered mildly positive.  So, he ordered an endoscopy to my colonoscopy.   I had been dairy free since I was young.  Was told that I had an allergy.  I had not any GI issues with gluten.   I was an avid baker.  I had nut issues and also mushroom, garlic/onion, and egg intolerances.  I had some pretty severe allergies to medications (anaphylactic) and some seasonal allergies along cats and horses.   I was shocked.  My husband had been gluten free for 12 years prior to my diagnosis.  There is no way both of us would have gluten issues.  But...the tests did not lie.  My iron deficiency anemia resolved within months of my going gluten free.  Two months into the diagnosis, I fractured my back doing NOTHING!  I have osteoporosis as a results of having celiac disease.   Grief is completely understandable.  Denial is a part of grieving.  But the proof will be in follow-up blood tests and how you feel.   So, now I can eat nuts (not almonds), eggs (two a day every single)  and dairy.  Yes, ice cream!  I have yet to get back garlic and mushrooms, but I can live with that.   I have Hashimoto’s too.  .  Once you have one autoimmune disorder, you can develop more.  The gluten-free diet may help, not only your celiac disease, but your UC issues as well.   Try the diet.  I think you will be pleasantly surprised!  
    • Hi Sofie! Listen to KarenG.   We both had iron deficiency anemia when we were diagnosed.  Plus, I have Thalassemia which is a genetic anemia on top of the iron deficiency anemia.   Dumping iron into your system is not the solution.  You need to be seriously gluten free.  You are probably unknowingly damaging other parts of your body....like your bones.  Two months after my diagnosis, I fractured my back doing NOTHING!  Think you are just not getting enough oxygen to your brain?  Think again!  It is probably related to celiac disease.  Celiac disease is systemic.  It is not just about villi damage.   But why am I telling a college student this?   You should be researching your autoimmune illness and ensuring that you do not develop Cancer (rare) or another autoimmune disorder like lupus, diabetes, thyroiditis, MS, Crohn’s, or one of the almost 100 other Autoimmune disorders (common).    Get your antibodies down.  Your mild anemia is the least of your problems.  Raising  your ferritin level may help a little, but healing from celiac disease will help you a lot more!    
    • Let my start by giving a brief summary of what I’ve been diagnosed with. Just over the past year I’ve been diagnosed with Celiac, EOE, lactose intolerance, soy allergy, tree nut allergy. Most recently diagnosed with Ulcerative Colitis. The Colitis came 8 months after having found out I had celiac. I have never had problems with gluten in my life. Dairy was something I had to eliminate because of the excrutiating stomach pains I would get from it. But I can have gluten any day and not have a problem.  I was diagnosed with a biopsy and followed by bloodwork. But who’s to say that dairy wasn’t the cause? I just feel like the GI was very quick to jump on the diagnoses without fully understanding my medical history, prescriptions I’ve took in the past ie long term antibiotic use, accutance, and 7 years of constant NSAID use.
    • I think she wants you to be strictly gluten free and heal.  Not give you things to patch up the damage you are causing by not getting your antibodies down and healing.   I am sure  she expected that you would take your diagnosis seriously and eat gluten-free.  4 months after your diagnosis, your antibodies would have gone down better.  But you weren't eating gluten free.  Eat gluten free. Take your supplements.  Read about the correct way to get your iron up - B12, vitamin C, don't take with calcium foods, etc  
    • Hello! I'm hoping to get some advice from y'all about iron IV infusions. First, some background: I was diagnosed with celiac disease at the beginning of June this year (2017).  I had labs done in March and my serum ferritin was 5 ng/mL. Hgb was 11.1, which isn't all that low, but is still flagged as below the normal range. I took 325 mg ferrous gluconate supplements daily for two months, and when my ferritin was rechecked, it was down to 4. The doctor ordered a celiac antibody panel and all of the levels were high. Confirmed with endoscopy at the end of May. A month later, I left for a 2-month study abroad program in France (aka the land of bread and pastries). After returning to the US at the beginning of August, I finally went gluten-free.  At the beginning of September, I returned to my University. Almost immediately, I realized I was really tired and was having a hard time making it through the day without a nap. I finally had a follow-up GI appointment around September 20th with the PA of the doctor who performed my endoscopy (not the same doctor from March). During the appointment, I asked her what we would do if my labs showed an iron-defiency. She told me that we would either do oral supplements or IV infusions, depending on whether or not she thought I'd absorb the supplements. When the lab results came in on the online patient portal, she made no comment on any of the iron-related results, just sent me a message that my antibody levels were still quite high, that I needed to keep up a strict gluten-free diet, and that we would recheck everything in six months. My ferritin was down to 3, Hgb was 10.3, iron saturation 6%, etc.  I was concerned about those results, so I called the PA's nurse and left a voicemail asking what the plan was for getting those levels up and got a portal message back from the PA saying that my hemoglobin was slightly low and will get better over time as I cut out all the gluten in my diet, but that I can start taking supplements if I want to speed up the process. I know that the Hgb still isn't that low, but it seems like the ferritin level is more serious. I went back for an appointment with the doctor who first found the iron-deficiency back in the spring and she seemed a lot more concerned. When I brought up IV iron therapy, she seemed to think it was a good idea. However, she's a primary care physician through my school's clinic, so she can't give me infusions. She called the PA with the intention of finding out whether or not she would change her mind about infusions, and had no luck. Interestingly, the PA's nurse informed her that they don't expect me to be able to absorb the supplements right away, and would consider IV infusions after I've been gluten-free for another six months.  I've done a bit of research on the IV infusions and it seems like I fit the criteria. Based on my antibody levels, I'm clearly not able to absorb iron any better than back in the spring, when the oral supplements did nothing for me. I understand that once my intestines heal more, I'll start being able to absorb iron better and should be able to boost my levels with oral supplements. However, I feel like I need a solution that will help me much sooner. I have a very demanding course load this semester and I'm constantly exhausted. I fall asleep doing homework at least twice a week. My grades are suffering, my mental health is suffering, and my relationships are being tested. I still don't have an explanation for why the PA doesn't think IV infusions are appropriate and I don't understand it. I really don't know what to do next because I'm afraid if I try to talk to the PA again, she'll get annoyed. I know that was super long, so for anyone still reading, thank you for bearing with me!! Now for the questions: 1. Do you think iron IV infusions in the near future would be a reasonable treatment for me? 2. Do you have any advice on how to make them happen? And if you have any other advice that's relevant to my situation, I'd love to hear it!   Thanks so much, Sofie
  • Upcoming Events