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And Japongus I don't post enough on here to know who is being sarcastic and who isn't. Carry on..

Dude, I love STS9, and I agree the direction they have gone with Alana is so good. They are coming here next month (Buffalo) and if I'm feeling up to it I'm going to go.. I also enjoy the dead, floyd. I like a little bit of everything. I know a lot of people say that, but I actually mean it...

"and was staggered by just how loud it was inside. Like... obviously these shows are loud, but I took one of my earplugs out for about five seconds to talk to a guy and I was beyond incredulous at the volume of the music. And that was just between bands!" ...It's crazy what we realize once our...

"its all a yuppie weekend turd fest to justify their weekday puritan ways." Sureee. Who are you to judge other people? And to throw everyone into a generic category? You realize there are many different types of music festivals right? ..Based on your response, you probably don't though..

Steve what kind of festivals do you go to? Did you end up going? I have been an avid festival goer for about 5-6 years. I love it. The music. The art. The people. The freedom. Anyways, I ended up with rare condition, Palatal myoclonus, and tinnitus is one of the aspects of it. It sucks, not...

Hello Tolga you're not alone. I have been suffering with this for 2 years. The disorder itself is bad enough, but the lack of answers/information on it, make it even more unbearable. I suffer every day of my life. I cannot work because of this condition. It has effected all aspects of my life...

Hey Poodlechick. I have seen 4 neurologists and 5 ENTs now (and tmj docs/chiros ETC ETC). Yes I have tried keppra-did nothing... And I could probably write a book on some of my horrible experiences with doctors/medicine but that's for another time... Some have legitimately tried to help, but it...

"If your diagnosis is right and you do in fact have PM then I don't see why doctors don't do the botox since that's a very effective treatment for PM." I missed this earlier. Just want to clarify, as I am someone suffering with this condition... Botox only helps a very small part of this...

Hey PoodleChick. A few things.. I was diagnosed with PM 2 years ago now, and this condition has completely rocked my life. My palate is very visiblly moving, and I think if you truly had PM you could clearly see it moving...Look up youtube videos on it. There is a very clear movement...