Guest guest Posted February 22, 2006 Report Posted February 22, 2006 My insurance denied my physical therapy, I got one visit, and now it's on to appeals, only thing I tried to contact my doctor and turns out she is out of the country, the nurse is out to, and she may be going away for a year...I just got referred to her!!!!, Anne --On Wednesday, February 22, 2006 5:59 AM +0000 dindushnyc wrote: > Hi again, > Thank you to everyone who answered! > Thank you for making me feel so welcome - yes, my doctor did do > the Q-tip test and my pain does seem to be confined to the vestibule. > She says my vaginismus diagnosis was just secondary to the normal > human reaction to tense up when confronted with severe pain. In > medical terms: duh. > Thank you for the physician referral. Unfortunately not on my > insurance plan, and affording things is a little difficult in current > medical school debt situation, but I'll find a way to pay for it if > there's no one in my plan who is as good. > A word on coffee: I have no idea how it relates to vulvar pain > (strangely not covered in our gynecology course...) but it was > discussed extensively in our gastrointestinal pathophysiology class. > Two important things: it lowers the pressure at the lower esophageal > sphincter, thereby facilitating acid reflux. If you have acid reflux, > stop the coffee. Even decaf. It's not just the caffeine, it's the > coffee. Second, and more relevant: it's just a nightmare for those of > us with IBS - stimulates the gut like crazy. It's terrible stuff. > And I live on it. I'm hardly one to tell anyone to stop drinking > coffee, but it's definitely not helping us. I'm at least trying to > switch to more benign forms of caffeine.... > Back to celiac: really don't have any desire to step on toes or > irritate anyone or claim to know more (I know that people who have a > disease tend to know a heck of a lot about it). But I do stand by > what I said earlier. Celiac disease affects the small intestines. > You eat gluten. That's where it goes. It doesn't affect the nerves > without affecting the small intestines first. Unless you're injecting > gluten instead of eating it. Not only does it affect the small > intestines, but it affects the proximal (first part) of the small > intestines first - because that's where the highest concentration of > gluten goes. That's one way to distinguish celiac from tropical > sprue - tropical sprue affects the whole length of the small > intestines, which includes the terminal ileum, which is where vitamin > B12 gets absorbed, so you end up with a pernicious anemia. What I'm > trying to say is, small intestine symptoms and anti-gliadin antibodies > are the definition of celiac disease. All of us clearly already have > enough on our plates, I don't think we need to find new diagnoses for > ourselves unless we have small intestinal disease symptoms or anti- > gliadin antibodies. I think those of you with negative anti-bodies > can just put your minds at ease. > Arline, I've been reading the literature on nerve proliferation very > closely and I agree that there are some fascinating hypotheses there. > It does seem to explain my life very well. I just think we need to > make a distinction between nerve proliferation and an inflammatory > response. Two completely different entities.... > Okay, another long email by me and I don't think anyone wants to hear > it. I'll try and stay out of medical discussions. I'm personally > trying to read less because it's honestly driving me crazy. I want to > focus on one treatment at a time. My doctor gave me lidocaine and I'm > excited to finally put those ridiculous dilators to good use. If > anyone has any advice on lidocaine use, I'd love to hear it. > Thanks again girls, > D > > > > > > > > **IF REPLYING TO THIS POST, PLEASE REMOVE ORIGINAL POST, THANKS** > > Our HOME page is http://groups.yahoo.com/group/VulvarDisorders > to search our archives, files, articles, etc. > > *** Quote
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