It’s the same with movies. If people wonder why Hollywood doesn’t make more diverse films starring black actors, it’s because the foreign market is all-important now, especially China and that’s all Hollywood cares about. What happened with Star Wars and it’s diverse cast is the latest example because while it became…
ZebraZulu
zebrazulu
It really is.
I don’t think a week goes by where I don’t have cause to use the line, “well then, this would be more, wouldn’t it?”
He was also downright iconic in A League of Their Own. “Get these wild animals away from me!”
My complete ignorance of who Jessica Lowndes is really saved me this time.
It is strange. To the question, Who would you rather hang out with, Sean Penn or a convicted serial killer? IT SHOULD BE AN EASY ANSWER BUT IT ISN’T.
He is the douchiest douche to ever douche.
And the reason it does not show up on blood tests? Because its a spirochete. And spirochetes can burrow themselves out of the bloodstream and into tissue. But this is somehow some heresy voodoo crap to the medical world at large. I’m still trying to figure out why.
There is a long history of doctors dismissing women’s pain, and not treating people of color with the same standard of care as paler patients. I am sure that women of color do have trouble getting chronic pain treated and getting diagnosed if they get Lyme disease or suffer it’s after-effects. I am not at all sure…
That’s interesting. I am depressed, and I always just assumed any weird pains were part and parcel of that. But I have a friend who’s been diagnosed with fibro, and she’s one of the happiest peeps I know. Like, this girl is NOT depressed. Except when her pain gets her down. Do you see this often? Fibro diagnosed folks…
Medicine and the human body are weird. If something works for you, then it works for you and I’m glad you figured out something that made you better. My problem lies in insurance costs that come from unnecessary testing. Thyroid function, Lyme disease, celiac. All of these cost money to the system. And few people…
Right. And 90% of people who think they’re allergic to gluten aren’t. Just make sure you don’t dismiss the 10% who are suffering from real symptoms because of all the delusionals. Something to keep in mind as your studies progress
I think in fairness to people, they can be aware that they are experiencing pain or discomfort that the medical community is unable to diagnose. I actually spent much of my mid-t0-late 20s convinced I had a thyroid problem because I had every classic symptom you could have...but every test or every type came back…
Lyme isn’t a joke, and whether or not “chronic Lyme” is real, all Lyme, and especially late Lyme, need significantly more attention and improved testing, diagnosis and treatment standards. My sister’s life has been destroyed by late Lyme — 10 years before it was diagnosed (she kept taking tests that would be positive,…
What’s the difference between Lyme’s Disease and Chronic Lyme?
You don’t need to be an M.D. to see that Yolanda almost certainly does not have lyme. If I had to hazard a guess, I’d say it’s depression (which can absolutely manifest as physical symptoms) being exacerbated by menopause. It also seems like she’s being taken advantage of by a lot of people selling snake oil cures.
And you would have stuck around for 12 years, otherwise?
At least he didn’t call it his “Tiny Dancer.”
No lie, if they break up my heart will break FOR REALZ. I don’t know these people, and they might be truly horrible, but I don’t know how to live in a world where Posh and Becks are not together.