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Helpful Advice From My Doctor.


Dandelion

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Dandelion Contributor

I used to get really terrible migraine-like headaches daily prior to going gluten free. Now maybe once a month I'll get one. All the pain meds I popped to get rid of them gave me a bunch of ulcers so now I can't take anything but tylenol. So, my gastro. doc told me to drink gatorade to get rid of them and it works! He said a good portion of headaches are due to dehydration and gatorade is the best way to fix that. Thought I'd pass it along. :)


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melmak5 Contributor

Dandelion - that is an excellent point!

I cannot drink gatorade or any other sports drink, but I found that adding celtic or gray sea salt to my water has helped me a lot. It is hard to stay hydrated, but I found once I worked up to 64oz+ of water a day, I really notice it when I skimp.

The author of "Healing Digestive Illness" cites a connection between chronic dehydration and depression. I am not sure I buy it, but its amazing how important water is!

GFhopeful Rookie

thansk for posting - i'll keep the gatorage or dehydration issue in mind. i have been having crazy headaches both before and after going gluten-free. i have been "un-diagnosed" with Celiac and Meniere's (inner ear problem that causes dizzy bouts) and doctor's now are saying that maybe all my symptoms have been coming from migraines and migraine variants. I ended up in the hospital last spring and dehydration was one of the main findings. so maybe, for whatever reason, i am getting dehydrated really quickly and it is escalating these migraines. i am willing to try anything for sure. i am staying gluten free as the doctor said that maybe i was gluten sensitive and gluten can trigger migraines. also, dairy free. like is said, i will try anything to get back to feeling decent again. hope this works for you too.

i havenoticed that since the weather is cooler, i am feeling better too. maybe it is really hard to stay hydrated during hot days for those who are having issues with dehydration. i drank water like crazy and sea salt mixed with sugar and water. who knows?

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    • Samanthaeileen1
      thank you RMJ! That is very helpful advice. Good to know we aren’t crazy if we don’t do the endoscopy. We are going to try the gluten free and see how symptoms and levels improve.    thank you Wheatwacked (love the username lol) that is also reassuring. Thankfully she has an amazing and experienced pediatrician. And yesss I forgot to mention the poop! She has the weirdest poop issues.    How long did it take y'all to start seeing improvement in symptoms? 
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      So her tissue transglutaminase antibody is almost 4x the upper end of the normal range - likely a real result. The other things you can do besides an endoscopy would be: 1.  Genetic testing.  Unfortunately a large proportion of the population has genes permissive for celiac disease, but only a small proportion of those with the genes have it. With family history it is likely she has the genes. 2.  Try a gluten free diet and see if the symptoms go away AND the antibody levels return to normal. (This is what I would do). Endoscopies aren’t always accurate in patients as young as your daughter. Unfortunately, without an endoscopy, some doctor later in her life may question whether she really has celiac disease or not, and you’ll need to be a fierce mama bear to defend the diagnosis! Be sure you have a good written record of her current pediatrician’s diagnosis. Doing a gluten challenge for an endoscopy later in life could cause a very uncomfortable level of symptoms.   Having yourself, your husband and your son tested would be a great idea.  
    • Samanthaeileen1
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