Hi ravenwoodglass,
I did just join the forum on the 15th, and have posted a couple of message/questions, with no returns. I might not be doing something right, but I would love to hear back with some help and input for our son.
Reading your post and your past experiences it sounds as if you might be someone to ask about the neuological aspects of the disease and it's effects. My thought are to be able to get some printed documentation on the ongoing pain from the nerve damage that is done from being gluten, and it does sound like you have had to live through this terrible pain (I am very sorry to hear that you had years of this) reading one of your post in particular about your leg pains and the suffering you endured.
I did call the university of Maryland and spoke to the nurse in the research department, and said the connection with the neuopathy was common and I am waiting to hear back and see about them sending some information that I can sink my teeth into and physically hand it to our son who is in constant foot pain after four attempts with surgery and is on heavy duty pain medicine that still does not seem to "take care" of it.
To mention some behavioral mood swings alone would be enough to say that he is not willing to do some of the investigation on his part with the possible connection to having celiac and wanting this to be his of his life and life syle change. After being gluten free for four years myself I know just how bad I can feel if getting a hold of anything close to gluten. So if I could get some more information to give to him and to try and see if this approach would leave an impression on him to atleast check it out it would be wonderful, because as a mom it is too painful to keep watching him go through all this pain and not getting any relief.
Thanks for listening and I do hope to hear back from you and for your help,
Sandpiper