Guest guest Posted October 19, 2005 Report Share Posted October 19, 2005 Thanks for the support and the advice. I will bring up the possibilty of a conference call next time we see both docs. I think that will be next month. Thanks, Val > > I'd just like to add to Becki's excellent thoughts, that Dr. Passo is > very good at ferreting out the diagnosis. Seeing your son will give him > more info as well. I know that it is exhausting thinking of the > difference between what each specialty is telling you. Perhaps they could > do a conference call together and discuss? That might be an idea. > At any rate, I'm glad that you are seeing Dr. Passo. > and Rob 16 Spondy > > On Wed, 19 Oct 2005 14:00:24 EDT Arthurnator@w... writes: > In a message dated 10/19/05 12:11:59 PM Central Daylight Time, > darksun1889@y... writes: > > > > On the other hand though, the GI clinic has 100's of patients with > > Eosinophilic and is the leading researchers of Eosinophilic > > Gastroeneteris and they said they do not see this as a symptoms of > > Eos Disorder. There is only a half a dozen or so patients suffering > > from these symptoms out of 100's so they believe these half a dozen > > patients are suffering from another autoimmune disorder causing > > arthritic symptoms as well as Eosinophilic. > > > > Hi, > I just looked some of this up and it led me to Cincinnati Childrens > website > for Eos disorders. > From what I understand is eosinophilic is a fancy name for white blood > cells > and in these disorders there are too many wbc in certain areas that > cause > chronic inflimation. > There was a small section on rheumatoligy stating that it can cause > eosinophilic synovitis(swelling)eosinophilic myalgas(pain near a joint > but no > swelling).In another section they mentioned Celiac disease which causes > arthritis but > goes away be eliminating gluten. > Looks like Passo is on to something and if Marissa was to see him and he > found obvious swelling then a joint aspiration sent to the lab just might > show a > high number of wbc. > Even if they can't put the whole puzzle together yet, it looks like they > are > willing to try and treat the mystery symptoms. > I hope the Celebrex works. > Hugs > Becki and 7 systemic > > > Quote Link to comment Share on other sites More sharing options...
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