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

Heat Sensetivity


SheenaM

Recommended Posts

SheenaM Apprentice

I have an abominable sensetivity to heat that makes it nearly impossible to do things in the summer. I'm writing this with one eye closed right now because of a migraine I've had since Monday when I was at a local theme park. I did everything I could to keep cool and hydrated, but apparently failed, resulting in this migraine that I've had since then. My question for you folks is, does anyone else get this sort of symptom, and were you able to do anything for it? I'm still very anemic after 6 months on the gluten free diet and I'm wondering if that is related? 


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

It seems like I read that thyroid issues can cause heat sensitivity.

cyclinglady Grand Master

Hyperthyroid can cause you to feel hot all the time even in winter.  Being actually sensitive to heat, like it causes severe fatigue, sounds like my MIL who had multiple sclerosis.  There might be other illnesses, but that is one to check out.  But migraines (only had two in my life), might cause you to be heat sensitive.  

I was anemic, but I was fatigued all the time. It had nothing to do with the weather.   It took me just a few months to build up iron stores  using a supplement and consuming iron-rich foods.    Are you iron or B-12 deficient (both are common in celiac disease)?

Make sure you are getting follow-testing for celiac disease:

Open Original Shared Link

 

SheenaM Apprentice

They didn't test blood levels of anything besides the antibodies when they did blood tests. I only know I'm anemic because of the fatigue and the purple fingernail beds. I'm definitely not hyperthyroid as I have more trouble losing weight than gaining.

cyclinglady Grand Master

When was your last lab test to check your anemia (CBC is a good starting point).   Those should  be re-checked after six months, along with follow-up celiac testing that I mentioned previously.  Lab results can let you know where you stand. 

 

Maverita Rookie

I am not saying it is not the heat, but ozone could be a contributing factor.  Where I live, hot sunny days often come with high ground ozone levels.  High ground ozone can cause migraines.  I am pretty much guaranteed a migraine when ozone levels get too high, and it can take a couple of days to get rid of it.  

Bree J Apprentice

I can sort of relate, when I'm not properly nourished (I'm very sensitive to that-- have to have the correct amount of protein and veggies/fruit with any sugar or dairy just to feel good), heat bothers me a LOT. Makes my anxiety bad too (i hate being hot). I've been gluten free for 4 years (when my intolerance showed up) and ever since then go crazy when I'm too hot. Weird that someone else feels this way.

I've never ever thought about checking if I'm anemic. My sores/cuts do take forever to heal..


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



Celiac.com Sponsor (A8-M):



SheenaM Apprentice
On 6/11/2018 at 3:00 PM, Bree J said:

I can sort of relate, when I'm not properly nourished (I'm very sensitive to that-- have to have the correct amount of protein and veggies/fruit with any sugar or dairy just to feel good), heat bothers me a LOT. Makes my anxiety bad too (i hate being hot). I've been gluten free for 4 years (when my intolerance showed up) and ever since then go crazy when I'm too hot. Weird that someone else feels this way.

I've never ever thought about checking if I'm anemic. My sores/cuts do take forever to heal..

Yes exactly this. And if I'm out in the heat I get way more exhausted than I should. Like my body just can't process it correctly.

 

On 6/10/2018 at 8:06 PM, cyclinglady said:

When was your last lab test to check your anemia (CBC is a good starting point).   Those should  be re-checked after six months, along with follow-up celiac testing that I mentioned previously.  Lab results can let you know where you stand. 

 

They never tested anything other than the antibodies that cause the intestinal damage, and that was in January. 

cyclinglady Grand Master

@SheenaM  What?  How were you diagnosed with anemia?  It is a standard blood test given to most when they see their doctors.  Maybe you did not get copies of the lab results.  You should ask for them.  It is your right!  

Anemia is very serious.  You could have a heart attack.  You might need a blood transfusion.  Please follow-up with your doctor.  You also need to know what type of anemia you have so your doctor can treat you accordingly.   Ask also for a complete thyroid panel as autoimmune thyroiditis is commonly associated with celiac disease.  Were you able to get an endoscopy?  You can have other autoimmune disorders that can destroy your small intestinal intestine.  Those should be ruled out.  Get your antibodies for celiac disease re-checked.  They will help determine if your are adhering to the gluten free diet or are at least improving.  It can take time for antibodies to come down, but they should be on a downward trend.  

RMJ Mentor
On 6/10/2018 at 3:19 PM, SheenaM said:

 I only know I'm anemic because of the fatigue and the purple fingernail beds. I'm definitely not hyperthyroid as I have more trouble losing weight than gaining.

Purple fingernail beds and fatigue can have other causes besides anemia.  You may want to get checked out by a doctor to see if you truly have anemia or if something else is going on.

hookedongolf Newbie

I am being tested for Celiac tomorrow, and feel that I have sjogenes but has not been proven as of yet.  I have had heat problems for years and have many of symptoms of sjogenes, thus putting myself on a gluten and dairy free diet while I wait months for Doctors to figure it out. I was tested last week for daily intolerance and I passed, yea, can now put weight back on.  As of the heat sensitivity, I have had it for as long as I can remember.  I gave up tennis and took up golf and drink Gatorade for 18 holes which I understand is good for the auto-immune. 

cyclinglady Grand Master
42 minutes ago, hookedongolf said:

I am being tested for Celiac tomorrow, and feel that I have sjogenes but has not been proven as of yet.  I have had heat problems for years and have many of symptoms of sjogenes, thus putting myself on a gluten and dairy free diet while I wait months for Doctors to figure it out. I was tested last week for daily intolerance and I passed, yea, can now put weight back on.  As of the heat sensitivity, I have had it for as long as I can remember.  I gave up tennis and took up golf and drink Gatorade for 18 holes which I understand is good for the auto-immune. 

I am not sure I understood.  Are you already gluten free?  All celiac testing requires you to be on a gluten diet or the tests will be invalid. 

SheenaM Apprentice
On 6/13/2018 at 8:13 AM, cyclinglady said:

@SheenaM  What?  How were you diagnosed with anemia?  It is a standard blood test given to most when they see their doctors.  Maybe you did not get copies of the lab results.  You should ask for them.  It is your right!  

So I went back and looked and they did do a blood panel and my RBC count is within normal limits. Also, I didn't test positive for both celiac antibodies just the Tissue Transglutaminase Ab, IgA. I lost health insurance due to a job change but I'm getting it back again at the beginning of July so I'll be able to do my follow up then. I guess I need to tell them that I also have the heat sensetivity and ask about thyroid stuff? Also should I ask my gastro about this or my family doc? 

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
  • 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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.