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Start D Therapy Tonight...and


chgomom

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chgomom Enthusiast

Anyone ever had the 50,000 units per week D therapy? Can you offer any experiences...good and bad...or nothing to worry about?

Also...my hair is coming out like crazy....and I have been craving potatoes.....someone said B5, B6 deficiency...when they checked October 12th...she said they were fine....could that change between then and now?

I'm also deficient in Zinc....and A big time so I have started that therapy.

Let me know what your experiences are.....


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chgomom Enthusiast

I'm nervous about taking the 50,000 units....

Nancym Enthusiast

Are you under an MD's care for this?

chgomom Enthusiast

Yes, that how I got the blood tests done.

I have sever deficiency in A and Zinc...D as well and I have osteoporosis, penia and celiac.

I am supposed to start 50,000 units of D once a week for 12 weeks.....tonight....

mouse Enthusiast

under doctor's orders, i took 50,000 units twice weekly for about 6 to 8 weeks. i can't remember the exact time frame. i did not have any problem at all with it.

sorry for the small letters, but fractured my arm and am typing with one finger.

chgomom Enthusiast

Ok..well thats good to know....

Anyone start feeling any better after starting the D therapy?

lindalee Enthusiast

How long have you been gluten free? I had extreme cravings for potatoes all my life until just after going gluten free and I stopped all nightshades. Sorry, I don't know about the D therapy.

Armetta, So sorry about the arm. I've been away. Gotta catch up.


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Nancym Enthusiast

Its great they're using Vit. D for treating bone issues! I've heard though you should take calcium and magnesium at the same time though. The vitamindcouncil.com has a lot of info.

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chgomom Enthusiast

Yeah well my doc said my age with the osteoporosis, she said I have some time and she'd like to see me go the "natural" route before thinking about "meds" Which I am totally on baord with so...I'm just a nervous nelly when I see anything with 50,000 units...yah know....

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      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
      here are the lab ranges.  Normal ranges for tissue transglutaminase are: <15.0 Antibody not detected > or = 15.0 Antibody detected normal for endomysial antibody is < 1.5. So she is barely positive but still positive. 
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