Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Excessive sweating


Ann Eka

Recommended Posts

Ann Eka Newbie

Since I was diagnosed with celiac disease in 2006 and have followed a gluten free diet.  I have noticed since that time I sweat excessively in the summer months and it is been getting worse, certainly not better. Anyone else find this normal?


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



Celiac.com Sponsor (A8-M):



Scott Adams Grand Master

Most members here have reported sweating as a symptom if they get gluten in their diets, do you think your diet is 100% gluten-free?

Also, over that period summer temperatures have been steadily increasing, and the last 2 summer have been the hottest recorded summers on Earth, so you may be sweating more because it's hotter.

Ann Eka Newbie

I am very conscientious about eating a gluten-free diet and seldom if at all get anything with wheat or gluten

Wheatwacked Veteran

Another possible symptom of low Vitamin D is excessive sweating. Certain gastrointestinal problems may make it difficult for your body to absorb fat soluble vitamins.  Signs you are lacking Vitamin D

Ann Eka Newbie

Thank you for responding to my question.  This excessive sweating has been going on for many years, more than 10, and my vitamin D levels are wnl as of March 2023.  These past two summers have been even hotter of course but wondering  if there was any other reason for this this unbearable sweating.  I do not have night sweats, and I am on low-dose hormone therapy.  I appreciate your insights.

knitty kitty Grand Master

@Ann Eka,

I sweated profusely when I was deficient in Thiamine Vitamin B 1.  Thiamine helps regulate the part of the brain that is in control of the autonomic nervous system (things you don't have to think about like blood pressure regulation, digestion, body temperature regulation, etc.).  

One can have a subclinical insufficiency which in times of stress can precipitate a deficiency.  Deficiency symptoms can appear in as little as 72 hours.  One can have a subclinical insufficiency/borderline deficiency for years.  A twenty percent increase in dietary thiamine results in an 80% increase in brain function, thus causing the symptoms to wax and wane mysteriously.

Stressors that require more Thiamine include illness, physical exercise, and hot weather.  Yes, being physically active in hot weather can increase Thiamine demands.  

Read more about it here...

Dysautonomia, A Heuristic Approach to a Revised Model for Etiology of Disease

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2644268/

And...

The effects of endurance training and thiamine supplementation on anti-fatigue during exercise

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241913/

 

The Gluten Free diet can be low in vitamins and minerals.  Wheat (and other gluten based foods) are required by law to have vitamins added to them because milling and processing removes or destroys the vitamins.  Gluten Free counterparts are not required to be enriched with vitamins like gluten based foods.  Eating a diet that includes lots of carbohydrates demands more Thiamine.  The more carbohydrates eaten, the more thiamine is required.  

Hope this helps!

Wheatwacked Veteran
(edited)
On 7/19/2023 at 10:22 AM, Ann Eka said:

vitamin D levels are wnl as of March 2023

Within normal limits for vitamin D, ie. greater than 29 ng/ml only means you are not at risk for Rickets or osteomalacea.  Our bodies need more for the mental health and immune systems to function and for the health of our other bones and teeth and colon cancer.

     " Struggling with excessive sweat? Maybe you’re missing out on these vitamins One of the earliest symptoms of vitamin D deficiency is excessive sweating, especially a sweaty head. Lack of vitamin D will also cause fatigue, bone pain, muscle cramps, and depression."

Edited by Wheatwacked

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



Celiac.com Sponsor (A8-M):



Raquel2021 Collaborator
On 7/18/2023 at 8:29 PM, Ann Eka said:

Since I was diagnosed with celiac disease in 2006 and have followed a gluten free diet.  I have noticed since that time I sweat excessively in the summer months and it is been getting worse, certainly not better. Anyone else find this normal?

Have you had your thyroid checked? Including antibodies? This could also be the cause. 

silverbirchu2 Rookie
On 7/19/2023 at 1:29 AM, Ann Eka said:

Since I was diagnosed with celiac disease in 2006 and have followed a gluten free diet.  I have noticed since that time I sweat excessively in the summer months and it is been getting worse, certainly not better. Anyone else find this normal?

Hi I've had this sweating only my face neck and back I understand how you feel  I've been having this in winter .with me it seems to be my blood pressure  see the doctor ask for your blood pressure to ve checked I'm OK now I have avoid stress  ask at your g.p. surgery for a blood pressure  check. This sounds just like I've been suffering with its do embarrassing when it happens in public  take care 🙂 

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

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,181
    • Most Online (within 30 mins)
      7,748

    Ruby B
    Newest Member
    Ruby B
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
    • Heatherisle
      Daughter has started gluten free diet this week as per gastroenterologists suggestion. However says she feels more tired and like she’s been hit by a train. I suggested it could be the change to gluten free or just stress from the endoscopy last week catching up with her. Just wondering if feeling more tired is a normal reaction at this stage. I suppose it’s possible some gluten might have been present without realising. Have tried to reassure her it’s not going to resolve symptoms overnight
    • DAR girl
      Looking for help sourcing gluten-free products that do not contain potato or corn derived ingredients. I have other autoimmune conditions (Psoriatic Arthritis and Sjogrens) so I’m looking for prepared foods as I have fatigue and cannot devote a lot of time to baking my own treats. 
×
×
  • Create New...