Do not let your loved ones die of "lupus"

Reid Welch

1 MW
Joined
Nov 18, 2006
Messages
2,031
Location
Miami, Florida
An informational thread. Not controversial, but meant to save, possibly, some lives.

MOST ALL of you know someone with "lupus", or its more dangerous, fulminant form: "SLE"

It is not a "woman's disease."

In this form I will add SLE information.

In subsequent forms you are going to meet men who died with SLE, of SLE.
And also, we will meet some women, dying very young, for SLE in women is much, much more vicious.
 
[youtube]9ez3-Dfcal8[/youtube]
Ray Walston. Fine, happy, long lived actor.
Sorry that the copyright owners do not allow clips of his signature show to air on YT

[youtube]JGyu3_Mr7fk[/youtube]
Beautiful diction, what a man's man!
From an unsold, never-aired pilot for TV

Note: every fine actor is as instantly identifiable as your mother's own face.
Walston appeared for so many years, in so many varied roles, that you, anywhere in the world,
must say, "Gee, I know him from someplace". Indeed, you do! HE is YOU.

He worked his life well, and achieved longevity, by intelligent conservation, to the fine old age of 85;
but...it was SLE that ended his life-walk, not old age.



_________________________
 
What a perfect speaker. She could be an MD for all I don't know.
Yes, she speaks of the late MJ, but by the finish, perhaps you won't
feel so sorry that he went so weird. You will understand more, much more:
[youtube]m7je7cWCH3A[/youtube]
Read her "more info" at the video's site?



Me? I'll talk about my lifetime of what must be SLE symptoms.
I'll do that in another posting form. I'm doing fine. No problems at present, really.
 
He is now "out of the closet".
SLE is NOT a girlie 'disease'.

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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.
 
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