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

DH exacerbated by sweat?


Jane87

Recommended Posts

Jane87 Explorer

DH exacerbated by sweat? Any relation/connection there in your experienced opinions? If I flare up on my (as yet unidagnosed) lower back, it's hugely aggravated by exercise as I sweat on my lower back when I run so it makes it even itchier (100 times itchier)!! My youngest said it looks like "bubble wrap" on my lower back. Anyone else have experiences of DH (or other bumpy, red, itchy rashes) being irritated by sweat?

 

(For anyone that's not read my previous posts I'm due to attend a provisional Drs appointment tomorrow regarding long standing itchy bilateral rashes & I have a family history of Coeliac, Crohn's, Lupus etc.)


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



Celiac.com Sponsor (A8-M):



Victoria1234 Experienced

Oh wow, I can't even imagine dh in a sweaty place! I used to scratch mine till bloody sometimes.  I super hope you get diagnosed quickly and are on your way to healing very soon.

Jane87 Explorer
1 minute ago, Victoria1234 said:

Oh wow, I can't even imagine dh in a sweaty place! I used to scratch mine till bloody sometimes.  I super hope you get diagnosed quickly and are on your way to healing very soon.

Thanks Victoria. I never scratch my elbows  (just run my fingers around the outside as I feel v.uneasy about scratching the bumps, like sickened, so it stops me scratching and my elbows are the least itchy). However when it's on my lower back or both calves I scratch like crazy!!! 

Could it be the iodine in sweat? I'm wondering now as I've been told on here that iodine foods can aggravate DH when injested. 

ejk Rookie

Hi there. I am not formally diagnosed with DH yet (that will happen in Jan or Feb), but my dermo and I are pretty sure that's what I have. I didn't want to be diagnosed in 2017 because I wasn't sure what was going to be happening with healthcare. I didn't want it as a preexisting condition.

Anyway, I exercise almost every day - hiking or cycling - and my sweat does seem to exacerbate the itch and bring new bumps up. Especially around my waistband area. I have been gluten free now for about two months, and the bumps and itching are less, but still there. I've started coating the area (and my behind) with Vaseline before I exercise, and that seems to help.

 

Victoria1234 Experienced
42 minutes ago, Jane87 said:

Thanks Victoria. I never scratch my elbows  (just run my fingers around the outside as I feel v.uneasy about scratching the bumps, like sickened, so it stops me scratching and my elbows are the least itchy). However when it's on my lower back or both calves I scratch like crazy!!! 

Could it be the iodine in sweat? I'm wondering now as I've been told on here that iodine foods can aggravate DH when injested. 

You got me. Without googling I didn't know there was iodine in sweat. I figured it would be like salt in a cut for me, ouch! Or how sweat when it dries just makes you itchier. I have to wear a back brace and when it's hot out I get a rash that itches underneath, even with a tee in between. But nothing as itchy as dh.

Awol cast iron stomach Experienced

Is anything rubbing it clothing a seam etc? If you can alleviate that it may help some too. Although the location sounds most inconvenient.

My biggest issue was rubbing. The sweat seemed to help the clothing bond to me more excebaying the rub. I would have more form fitting workout gear I could wear without underwear. my bum would flare, waistband, and my elbows. The sweat in the bum area with the rub of the band seam on underwear made it worse. I switched to form fitting wicking type material with the seam running more on the sides to alleviate as much as possible. Rinse in shower asap. 

Also a call center phone job my elbows would constantly get rubbed by clothing on my elbow from constant rubbing of my blouse sleeves typing. I made sure I could roll them up.

if you can eliminate the adhesion sweat material rub it may help.

 

good luck

squirmingitch Veteran

Yes! Sweat, heat & humidity drove me crazy with aggravating the dh! DH likes to attack pressure points too. Like AWOL said, waistbands & such. I had to get boy shorts type underwear that were seamless ( I like all cotton). they still had a little seam on one side that ran for about 2". That 2" killed me so I figured out that if I wore them inside out, then the seam did not affect me. Forget a bra!!!!!!! NOPE, no way!!!!! Even now, when I wear jeans, the button part at the front makes dh flare, also where they wrinkle at the torso to leg area when you sit down --- I still get flares there. My dh liked to hit scars too. Old scars, new scars. 


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



Celiac.com Sponsor (A8-M):



Barbie Wickham Explorer
On 12/15/2017 at 5:28 PM, squirmingitch said:

Yes! Sweat, heat & humidity drove me crazy with aggravating the dh! DH likes to attack pressure points too. Like AWOL said, waistbands & such. I had to get boy shorts type underwear that were seamless ( I like all cotton). they still had a little seam on one side that ran for about 2". That 2" killed me so I figured out that if I wore them inside out, then the seam did not affect me. Forget a bra!!!!!!! NOPE, no way!!!!! Even now, when I wear jeans, the button part at the front makes dh flare, also where they wrinkle at the torso to leg area when you sit down --- I still get flares there. My dh liked to hit scars too. Old scars, new scars. 

 

On 12/15/2017 at 5:28 PM, squirmingitch said:

Yes! Sweat, heat & humidity drove me crazy with aggravating the dh! DH likes to attack pressure points too. Like AWOL said, waistbands & such. I had to get boy shorts type underwear that were seamless ( I like all cotton). they still had a little seam on one side that ran for about 2". That 2" killed me so I figured out that if I wore them inside out, then the seam did not affect me. Forget a bra!!!!!!! NOPE, no way!!!!! Even now, when I wear jeans, the button part at the front makes dh flare, also where they wrinkle at the torso to leg area when you sit down --- I still get flares there. My dh liked to hit scars too. Old scars, new scars. 

Reading back to all DH topics posted here, many references to how the DH rash appears and changes or “morphs” over time. I was affected on my hands, elbows, inside forearms/wrists, tops of thighs and the absolute worst, my bottom. I’m posting a few pics of my year and a half of this unknown Rash from He**...  maybe it will help someone else recognize the symptoms of DH... the pressure points, the symmetry of the rash outbreaks and the ever changing rash to full blown and very painful blood blisters. Any activity (even getting dressed) let alone sweating was just cruel.  I’m happy to say my primary care Dr finally correctly dx’ed me, ran the Gluten panel blood tests and confirmed the DH, Celiac Disease that was ruining my life and am now almost Rash free from a  gluten free diet and I chose to take 25 mg a day of Dapsone. 

 

 

Barbie Wickham Explorer
On 12/15/2017 at 11:19 PM, Barbie Wickham said:

 

Reading back to all DH topics posted here, many references to how the DH rash appears and changes or “morphs” over time. I was affected on my hands, elbows, inside forearms/wrists, tops of thighs and the absolute worst, my bottom. I’m posting a few pics of my year and a half of this unknown Rash from He**...  maybe it will help someone else recognize the symptoms of DH... the pressure points, the symmetry of the rash outbreaks and the ever changing rash to full blown and very painful blood blisters. Any activity (even getting dressed) let alone sweating was just cruel.  I’m happy to say my primary care Dr finally correctly dx’ed me, ran the Gluten panel blood tests and confirmed the DH, Celiac Disease that was ruining my life and am now almost Rash free from a  gluten free diet and I chose to take 25 mg a day of Dapsone. 

 

On 12/15/2017 at 5:28 PM, squirmingitch said:

Yes! Sweat, heat & humidity drove me crazy with aggravating the dh! DH likes to attack pressure points too. Like AWOL said, waistbands & such. I had to get boy shorts type underwear that were seamless ( I like all cotton). they still had a little seam on one side that ran for about 2". That 2" killed me so I figured out that if I wore them inside out, then the seam did not affect me. Forget a bra!!!!!!! NOPE, no way!!!!! Even now, when I wear jeans, the button part at the front makes dh flare, also where they wrinkle at the torso to leg area when you sit down --- I still get flares there. My dh liked to hit scars too. Old scars, new scars. 

 

 

I’ve tried to add a few more pics but am limited to 1.95 mgb - I will try again later to add a few more of my hands and bottom 

Barbie Wickham Explorer

 

On 12/12/2017 at 4:35 PM, Awol cast iron stomach said:

Is anything rubbing it clothing a seam etc? If you can alleviate that it may help some too. Although the location sounds most inconvenient.

My biggest issue was rubbing. The sweat seemed to help the clothing bond to me more excebaying the rub. I would have more form fitting workout gear I could wear without underwear. my bum would flare, waistband, and my elbows. The sweat in the bum area with the rub of the band seam on underwear made it worse. I switched to form fitting wicking type material with the seam running more on the sides to alleviate as much as possible. Rinse in shower asap. 

Also a call center phone job my elbows would constantly get rubbed by clothing on my elbow from constant rubbing of my blouse sleeves typing. I made sure I could roll them up.

if you can eliminate the adhesion sweat material rub it may help.

 

good luck

Such a horrid rash, I ended up wearing my hubbys soft cotton boxers, also turned inside and waistband rolled over to prevent the raw rubbing. And yes, no way was a bra in my wardrobe! Good ol seamless cotton tanks, not the bra strap type, was the best I could handle! 

 

Barbie Wickham Explorer

Image censored by Google for being "too shocking".

 

Barbie Wickham Explorer

A picture is worth a thousand words!

 

 

 

Barbie Wickham Explorer
On 12/12/2017 at 12:53 PM, Jane87 said:

DH exacerbated by sweat? Any relation/connection there in your experienced opinions? If I flare up on my (as yet unidagnosed) lower back, it's hugely aggravated by exercise as I sweat on my lower back when I run so it makes it even itchier (100 times itchier)!! My youngest said it looks like "bubble wrap" on my lower back. Anyone else have experiences of DH (or other bumpy, red, itchy rashes) being irritated by sweat?

 

(For anyone that's not read my previous posts I'm due to attend a provisional Drs appointment tomorrow regarding long standing itchy bilateral rashes & I have a family history of Coeliac, Crohn's, Lupus etc.)

Jane, oh I feel for you... I can’t imagine even trying to exercise at the height of my unyet dx’ed DH.... just getting dressed was a dreaded experience for me. The symmetry and bilateral rash and blisters were big clues to my Hero of our family  Dr. (not the dozens of specialists I saw!), along with rash on the pressure points of my body... hands, elbows, tops of thighs and the ultimate worst area, my bottom. I posted some pics prior to this, in reply to squirming itch and cast iron stomachs posts... I’m going to try to add a few more pics here, (site only allows a small upload for each reply). I hope your provisional Dr appt went well and your questions were answered. I’m 2 months into a gluten-free diet and a 25mg daily dose of Dapsone . Every time I try to stop the Dapsone I suffer a new breakout, so I’ll continue until my immune system gets stronger. I had my Thyroid gland surgically removed almost 40 yrs ago due to Hyper-Thyroidism and a very large goiter.  I then quickly went to Hypo-Thyroidism, (Graves Disease) and have since taken Synthroid daily.  I’ve read Thyroid problems are quite common amongst Celiacs and/or Celiac DH patients.  Best wishes to you of a correct diagnosis and  good health to you (and all of you reading this post) in the upcoming New Year! 

Barbie Wickham Explorer
On 12/12/2017 at 1:04 PM, Jane87 said:

Thanks Victoria. I never scratch my elbows  (just run my fingers around the outside as I feel v.uneasy about scratching the bumps, like sickened, so it stops me scratching and my elbows are the least itchy). However when it's on my lower back or both calves I scratch like crazy!!! 

Could it be the iodine in sweat? I'm wondering now as I've been told on here that iodine foods can aggravate DH when injested. 

Victoria- In reference to my previous replies to Jane, Squirming Itch & Cast Iron Tummy, I’m trying to upload a few more pics of my ever changing (& daily worsening of my DH rash). Site only allows small uploads...  I think the iodine is not just bad for the Celiac Disease but your Thyroid Gland as well, it’s not intended as medical advice, just a read observation from this wonderful forum. Best of all to you, wishing you all a healthier and therefore a Happier New Year in 2018! 

Barbie Wickham Explorer
On 12/12/2017 at 1:42 PM, ejk said:

Hi there. I am not formally diagnosed with DH yet (that will happen in Jan or Feb), but my dermo and I are pretty sure that's what I have. I didn't want to be diagnosed in 2017 because I wasn't sure what was going to be happening with healthcare. I didn't want it as a preexisting condition.

Anyway, I exercise almost every day - hiking or cycling - and my sweat does seem to exacerbate the itch and bring new bumps up. Especially around my waistband area. I have been gluten free now for about two months, and the bumps and itching are less, but still there. I've started coating the area (and my behind) with Vaseline before I exercise, and that seems to help.

 

You might want to give a try to Aquaphor,  (the jelly type, just like Vaseline) instead of the Vaseline. I had several Drs tell me it is much better for your skin than petroleum based Vaseline. I found it protected the rash and blisters really well, but I also felt like my skin was able to “breathe” easier than with the Vaseline... Best of luck to you with your upcoming diagnosis! 

Jane87 Explorer
8 hours ago, Barbie Wickham said:

Jane, oh I feel for you... I can’t imagine even trying to exercise at the height of my unyet dx’ed DH.... just getting dressed was a dreaded experience for me. The symmetry and bilateral rash and blisters were big clues to my Hero of our family  Dr. (not the dozens of specialists I saw!), along with rash on the pressure points of my body... hands, elbows, tops of thighs and the ultimate worst area, my bottom. I posted some pics prior to this, in reply to squirming itch and cast iron stomachs posts... I’m going to try to add a few more pics here, (site only allows a small upload for each reply). I hope your provisional Dr appt went well and your questions were answered. I’m 2 months into a gluten-free diet and a 25mg daily dose of Dapsone . Every time I try to stop the Dapsone I suffer a new breakout, so I’ll continue until my immune system gets stronger. I had my Thyroid gland surgically removed almost 40 yrs ago due to Hyper-Thyroidism and a very large goiter.  I then quickly went to Hypo-Thyroidism, (Graves Disease) and have since taken Synthroid daily.  I’ve read Thyroid problems are quite common amongst Celiacs and/or Celiac DH patients.  Best wishes to you of a correct diagnosis and  good health to you (and all of you reading this post) in the upcoming New Year! 

Hi Barbie thanks for sharing your pictures and story! I'm glad gluten-free and dapsone have finally gotten you relief. How many years did you suffer with this?

I've just finished a flare up of this as yet undiagnosed rash so I've the Dr booked me in for bloods tests in the NewYear although Awol and others on this forum have told me that Coeliac blood tests are not always "positive" for DH. I'll upload my latest elbows pics etc below. 

PhotoGrid_1513447590111.webp

PhotoGrid_1513447665189.webp

Jane87 Explorer

PhotoGrid_1513447691457.webp

PhotoGrid_1513447721239.webp

Jane87 Explorer

PhotoGrid_1513447927388.webp

PhotoGrid_1513447777778.webp

Barbie Wickham Explorer

Those elbows look very familiar! I had that rash for a little over a year and a half, and with each break out, the blisters would change, worsen in appearance and the itch got insanely itchier.  The only topical product I found that helped a bit, was GoldBond lotion or liquid spray with Lidocaine.... Drs had me then just use Aquaphor (the Vaseline jelly type ointment) So, yes, I’ve read too that blood tests can have false negatives & positives.  However, my Dr ordered a complete blood work up and then added a special Gluten panel order... I gave  about 6 vials of blood for all tests. I was having so many vitamin deficiencies and off the charts inflammation levels throughout the year & 1/2... it all made such sense when we looked at all my symptoms & also the positive bloodwork. He told me I lit up not like a Christmas tree, but like the entire tree lot. It also made sense why all biopsies and cultures kept coming back as “unknown uticaria”       The specialists were taking samples incorrectly. What should have been a somewhat easy diagnosis turned into just a nightmare. All the misdiagnosis (scabies 3 Times, spider bites, excema, herpes and 3 Drs flat out just said I don’t know, try another Dr.) and the heavy medications prescribed (methatetrix, Otesla, shots of cortisone followed by 6 months of oral steroids, the anti fungals and the parasite pesticides!) I was a mess! All unnecessary and many were very harmful to my overall health. Since I’ve not had many stomach problems,  my Dr. & I decided to just go with the gluten-free diet and Dapsone and see how I responded. Incredibly within 2-3 weeks the Rash was gone from everywhere except for my very worst area, my bottom. I may have some intestinal testing done next year to be sure there’s no damage there. So between the  positive blood test and diet changes are working so well, I’m convinced I do indeed have DH. It’s also genetic and I have 2 first cousins with Celiac Disease. I’ve also learned from people here and the great information site provides, you must still be eating gluten for tests to be accurate. I can’t imagine eating the poisonous Gluten to further confirm DH, so I chose just to go with Diet and Dapsone. I hope you get proper results next month and on to a rash and itch free life!  Below is the picture my Dr found on his own time, on his “weekend” research... he was so excited he phoned me and had me come in first thing that following Monday morning. That picture looked exactly like me! I am his first case of DH in over his 30+ years of practice. 

Image censored by Google for being "too shocking".

Barbie Wickham Explorer
57 minutes ago, Jane87 said:

PhotoGrid_1513447927388.webp

PhotoGrid_1513447777778.webp

Jane your fingers look exactly as mine did! So very painful, I remember feeling like I had broken a glass and shards were stuck in my fingers and hands.... 

Jane87 Explorer
On 12/16/2017 at 11:15 AM, Barbie Wickham said:

Those elbows look very familiar! I had that rash for a little over a year and a half, and with each break out, the blisters would change, worsen in appearance and the itch got insanely itchier.  The only topical product I found that helped a bit, was GoldBond lotion or liquid spray with Lidocaine.... Drs had me then just use Aquaphor (the Vaseline jelly type ointment) So, yes, I’ve read too that blood tests can have false negatives & positives.  However, my Dr ordered a complete blood work up and then added a special Gluten panel order... I gave  about 6 vials of blood for all tests. I was having so many vitamin deficiencies and off the charts inflammation levels throughout the year & 1/2... it all made such sense when we looked at all my symptoms & also the positive bloodwork. He told me I lit up not like a Christmas tree, but like the entire tree lot. It also made sense why all biopsies and cultures kept coming back as “unknown uticaria”       The specialists were taking samples incorrectly. What should have been a somewhat easy diagnosis turned into just a nightmare. All the misdiagnosis (scabies 3 Times, spider bites, excema, herpes and 3 Drs flat out just said I don’t know, try another Dr.) and the heavy medications prescribed (methatetrix, Otesla, shots of cortisone followed by 6 months of oral steroids, the anti fungals and the parasite pesticides!) I was a mess! All unnecessary and many were very harmful to my overall health. Since I’ve not had many stomach problems,  my Dr. & I decided to just go with the gluten-free diet and Dapsone and see how I responded. Incredibly within 2-3 weeks the Rash was gone from everywhere except for my very worst area, my bottom. I may have some intestinal testing done next year to be sure there’s no damage there. So between the  positive blood test and diet changes are working so well, I’m convinced I do indeed have DH. It’s also genetic and I have 2 first cousins with Celiac Disease. I’ve also learned from people here and the great information site provides, you must still be eating gluten for tests to be accurate. I can’t imagine eating the poisonous Gluten to further confirm DH, so I chose just to go with Diet and Dapsone. I hope you get proper results next month and on to a rash and itch free life!  Below is the picture my Dr found on his own time, on his “weekend” research... he was so excited he phoned me and had me come in first thing that following Monday morning. That picture looked exactly like me! I am his first case of DH in over his 30+ years of practice. Image censored by Google for being "too shocking".

Thank goodness you got a Dr in the end that recognised what was happening! I will have to see what my bloods show in January, I really hope they show coeliac, not because I want it but because I feel that's what this is! 

A fair few people yourself included Barbie have said my elbows remind them of theirs! The only thing I'm wondering is, mine never go bloody/open like yours and some other DH members on this forum. I can't stand the thought of scratching my elbows when they flare so I scratch around the bumps. With my back I can't help but scratch as the itch is wild and as it's a flat surface I feel less sickened by the thought of scratching my back and legs. 

Barbie Wickham Explorer

Jane, my rash didn’t go to the bloody,  pressure filled blisters until about a year in. They would get filled with so much fluid they would pop on their own, especially my bottom area and elbows. I hope for you you get a proper dx quickly as I found with each passing week my rash worsened and basically took on a life of its own! Of course, I was poisoning myself daily with Gluten, building up more and more deposits,  which just lead to more breakouts. And each breakout got steadily worse, leading to the bleeding and deep scabs that lasted for weeks. I wish you a speedy dx and a quick recovery next month. Do keep us posted on your progress. Happy Holidays. 

Barbie Wickham Explorer

My fingers went from little bumps to huge fluid filled itchy blisters that would pop, refill, pop again and then would finally scab over. Almost like a burn blister. Just an incredibly painful experience. I so hope you get a proper dx and you’ll be amazed how quickly you will begin to heal & feel better! 

A18DEDF3-5F75-4E7C-BF26-1F86DE78ABA1.webp

ejk Rookie
12 hours ago, Barbie Wickham said:

You might want to give a try to Aquaphor,  (the jelly type, just like Vaseline) instead of the Vaseline. I had several Drs tell me it is much better for your skin than petroleum based Vaseline. I found it protected the rash and blisters really well, but I also felt like my skin was able to “breathe” easier than with the Vaseline... Best of luck to you with your upcoming diagnosis! 

Thank you for the information. I will give Aquaphor a try!

 

squirmingitch Veteran

This is an entire thread with photos of dh.

This is a thread devoted entirely to things people have found helped alleviate their pain, itch, sting, burn of dh.

 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,059
    • Most Online (within 30 mins)
      7,748

    Lynda Huber Davis
    Newest Member
    Lynda Huber Davis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.1k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Kathleen, I am not sure I agree with you that your son is asymptomatic with regard to his celiac disease. The horrible stomach pains you describe in your first post could be celiac symptoms as easily as they could be H. Pylori or viral infection symptoms. Yes, the social impact of having celiac disease is perhaps the most difficult dimension of the disorder to deal with. It requires thinking ahead and providing safe substitutes for snacks and party foods so that your son doesn't feel left out and singled out or different. Some of those feeling are unavoidable but they can be minimized. Dining at eateries is a huge challenge to celiacs as even when you order gluten free menu items they are often heavily cross contaminated back in the kitchen from being cooked together with wheat things or handled with the same utensils. You need to be bold in asking a lot of questions and requesting that your son's food be cooked in separate pots and pans. It's awkward at first but you get used to it. Speaking of CC (Cross Contamination), how careful you have to be with this will depend on the sensitivity level to gluten your son will demonstrate. This can be a challenge to get a handle on for those celiacs who are of the "silent" type. By "silent" is meant they are largely asymptomatic. It is common for sensitivity levels to increase over time when gluten is withdrawn from the diet as whatever tolerance we may have had to gluten when we were being exposed to it constantly may disappear. Whether or not that proves to be the case, it would be important for you to have his antibody levels checked at regular intervals (say every six months to a year) to check for compliance with the gluten free diet. And I would not worry about him touching wheat food products. It is highly unlikely that any significant exposure will occur transdermally. That would only be an issue for the most extremely sensitive subset of celiacs. Of course, you wouldn't want him getting wheat flour on his hands and then putting fingers in his mouth.  At school, you will need to pack his lunches and also have conversations with the school dietary staff to ensure his safety.  I know this all seems overwhelming right now but you are not the only parents who are having to go through this kind of thing. Celiac disease is not uncommon and thankfully there is much more public awareness about it than there was a generation ago. It can be done. It's the kind of thing that requires parents to be willing to find that extra gear of assertiveness in order to keep their child safe and to guard his/her psyche as much as possible. Count your blessings. It could be worse. He doesn't have cancer. This might be helpful in getting off to a good start with eating gluten free. Some of it may be overkill depending on how sensitive to minute levels of gluten your son is:  
    • trents
      Staci, take note of the forms of magnesium and zinc I recommended. With some of the vitamins and minerals, the formulation can be very important in how well they are absorbed. Many of the vitamin and mineral products on supermarket shelves are in a form that maximizes shelf life rather than bioavailability which, in your case, would seem to be a critical issue. And with magnesium, if you use the typical over the counter form (magnesium oxide) you may find it has a definite laxative effect (think, "milk of magnesia") simply because it isn't well absorbed and draws water into the colon. Spend some extra money and get quality vitamin and mineral products and research the issue of bioavailability. There are forum members who are knowledgeable in this area who may have recommendations. Do you have Costco stores where you live? Is Amazon available to you?
    • Kathleen JJ
      And yes, of course it's better to know and we will adjust.  It's just, he's 7 and in our house we can control what he gets. But he plays soccer 3 times a week and in the changing room the boys share candies. I can and will tell him not to accept them any more, but "mistakes" will be made.   I'm really burdened by the potential social impact for him. He so loves to go to a restaurant as a family - I'll guess that's finished. Going to birthday parties at another kids house? I am reading about Coeliacs and apparently the fact that something as much as TOUCHED something with wheat is enough, even if he doesn't feel the symptoms - how can we control that bar from keeping him locked up?    And the worst worry of all: how do you tell a little boy to do all of this to not have symptoms that he does not have. If he'd been having horrible diarrhea or feeling really tired, we could tell him 'see, you feel so much better now, that kind of food was just not good for your body', but now, what will our argument be? For clarity: of course we will put him on the diet, I am not saying I don't believe in the necessity of that, it is just that it will be quite a stretch to 'sell' it to him 😞
    • StaciField
      I’m 41. You have helped me achieve the goals of finding a way of getting nutrients into my body so I will see how it works for me. Thank you so much.
    • Kathleen JJ
      Thank you for your reaction. The reference values are both "<10", although I found a medical paper from Netherlands (I'm Belgian) who use the same values and there the see a positive daignosis as twice more then 200 and a positive biopsie. I didn't see how to change this in my original message, sorry...
×
×
  • Create New...