Good point on the nose. I wouldn't be surprised if a hibernating bear suddenly crawled out the front of that thing.
You brought it upon yourself. You can't discuss posting in the boobie thread in your signature and not expect us to turn that around on you. The least you can do is be an inverse agonist, not a complete antagonist.
Is that all it takes? Damn. And here I thought showing up on the front lawn at 2 a.m. every morning showed my love and devotion. I'm going to continue to not send pms to either Shegirl or DC001 until they show us their tits. That oughtta work.
Dcc001 is getting way too much attention for not posting her boobs, so really she is right there is nothing in it for her. If she holds out she gets a whole thread derailed into talking about her tits, if she posts them she'll get 20 reps.
Everyone knows that Snow's "Informer" is the sure fire way to panty dropping, bitches can't resist getting their boom-boom licked down.
*screeching record* 'Tha FUCK you just say?! GEE WHEEZ BABY PLEASE LET ME TAKE YOU TO AN ISLAND OF THA SEA-COOL BREEZE YOU DON'T FEEL LIKE DRIV-IN WELL BABY HAND ME THA KEYS AND I WILL TAKE YOU TO A PLACE AND SET YOUR MIND AT EASE
Wait a second. You're telling me they have turntables in the bayou? I call bullshit. I bet it's set on a lazy susan, that has a belt attached to it powered by a 3 legged cat and the "needle" is an opossum claw.
NSFW In considering the bioavailability and volume of distribution of a compound, its pKa is generally not a critical factor. As only the unionized fraction of a drug will be absorbed across the intestinal membrane, as well as diffuse across the blood-brain barrier, a drug whose pKa enables it to be unionized in the slightly alkaline pH of the intestine will be more readily absorbed. However, as long as a drug is less than 99% ionized, absorption will generally take place, notwithstanding other factors. Similarly, when the question of diffusion into the central nervous system is concerned, as long as a drug is less than 99% ionized, diffusion into the central nervous system will take place. This is readily seen in nearly all psychotomimetic drugs, such as cocaine, which are largely ionized, yet must cross into the central nervous system in order to exert their effect, and for which no known membrane transporter exists. Even for quaternary ammonium compounds, which always exist in the ionized state, absorption across the intestinal lumen is non-zero. The lipo/hydrophilicity is, however, a more important factor. A drug must be lipophilic enough to be absorbed into the gastrointestinal epithelial cells, yet not so lipophilic that it cannot exist in the aqueous form in blood. Those compounds which are too lipophilic to dissolve in blood, i.e. a long hydrocarbon chain such as mineral oil, can, however, be absorbed through the lacteal system with other fats, enter the lymphatic system, and gain systemic distribution. Yeah, but if she posts them, we get another pair of boobs to look at.