I just saw this show on the PBS channel about Lyme Disease. This lady that has a lyme support group was talking to the host of the program. All her symptoms sounded the same as Celiac, plus her children now have Lyme...
She has been on intravenous antibiotics because she does not absorb the antibiotic pills, but is now off the intravenous & feeling worse again... Only she is getting progressively worse, whereas the people that have celiac and go on the diet get better.

I do know that when I had constant bladder infections and lived on antibiotics that I felt somewhat better, although I was eating wheat.

I wonder how many of these people that have lyme, really got lyme because their immune systems were already weak from celiac, & not only do they have lyme but really the worst thing is the undiagnosed celiac. Be interesting to take 100 lyme people & get the Enterolab gene test...

what do you guys think?