He is now "out of the closet".
SLE is NOT a girlie 'disease'.
[youtube]lAKOIYsSp8M[/youtube]
REID THIS:
http://hiphop.popcrunch.com/trick-daddy-lupus-diagnosis/
that's an order. The homie is of my home town. We have just two things in common:
We live in Miami, Florida. And we are both going to die.
And neither of us, I bet I can speak for him, is afraid of The Wolf: "lupus".
We deal with life. We could be quadraplegics or any of a thousand other illness-victims.
But, we the people with SLE, are not "victims". WE DEAL WITH IT, and we spread the word:
there is some hope. I think I have a partial "cure" of great value, at least, to myself.
I must get the word out. DIAZEPAM: generic version of Valium, costs less than 25 dollars per month.
I discovered diazepam therapy by myself, by trial and no error. LATER, in researching, I find that one team
of highly paid Univerisity of Michigan researchers are conducting a multi-year study of diazepam-family drugs,
in hope of finding a variant of diazepam, for SLE, a variant, perhaps, that causes no untoward side effects
such as sleepiness or addiction (neither of these "get" me).
I can go for a week without a tablet.
Then the real, nasty effects of lupus and SLE tend to return in full force: the rash, the fevers, the stress-fatigue and mysteriously lamed joints, here, or there, hip, or knee, one or the other, or both. I gimp then.
More later. Save lives. Tell your lupus friends, mostly women, to CHALLENGE their doctors, who throw them Prednisone and cytotoxins (to save the kidney from self rejection), and when the "bitches" bitch too much "I HURT ALL OVER, HELP";
do you know what "they" do then? Put the woman on a lifetime course of Vicodin or hydrocodone (morphine-like, super addictive) happy pills.
Only a fool follows the first doctor.
Ask ten, twenty...get fifty opinions, as YOU, yourself, research on the 'net, whatever ails you.