Justus
Proud Member
- Joined
- Jul 25, 2011
- Messages
- 100
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No, I am not the girl on YT, and no I am not spreading lies. My sources on confirming Michael's lupus? This diagnosis was brought before the courts a few years ago, and I PERSONALLY know other close friends of his (whose names I shall not reveal out of respect for privacy) who can confirm he had it and he talked with occassionally of his struggles with it. But he did not speak about it in public and to only a very FEW people, on very FEW occasions. Whether or not the "leaked" autopsy report is real or fake, I don't know. I personally would not trust it, because people can leak things they want the public to think and keep under lock and key what is the truth. I can't see his actual report being leaked so easily, you know? As for Dr. Murray, well who knows? I am not going to ultimately condemn him (because its not my place) nor support his actions. With the propofol, and any other meds he MAY or MAY NOT have been taking that week, I cannot confirm. Nor can anyone else. Like I said, it could go either way. I personally do not agree with the choice of taking propofol, nor with the doctor administering it. I DO agree, that it was a bad idea.
I did not say people had a death sentence at 40-50 years old; I merely stated that it is COMMON for patients to die of cardiac arrest (which is NOT the same as heart attack)around this age. But each case is as unique as each person. Pretty much all forms of lupus have the characteristic malar rash (the butterfly rash) at various times, and it comes and goes. Not just discoid lupus, which does not affect the whole body the way systemic lupus does. Lupus is a connective tissue disease, and most often forms of arthritis are found with it, as well as problems with many other systems, i.e. the back, kidneys, etc. and ultimately, the heart.
Lupus "mimics" AIDS in that it is an autoimmune disorder, attacks the whole body, you have to be extremely careful about germs and sicknesses, the body gets all kinds of sores, and so much more. It is not the same, however, as it is not only acquired differently but have characteristics, as well. Also, with lupus, as with vitiligo, patients are highly photosensitive (sensitive to sun). It "mimics" cancer, when it comes to body sores, various treatments (i.e. chemo is a treatment many use in lupus), and much more. Skin ulcers and oral ulcers are often found, as well. There can be alopecia (hair loss). But again, its not the same. It just mimics various symptoms of cancer, AIDS, and some other diseases out there. I am not going to go into detail about lupus here. It would be far too exhaustive, and anyone who really wants to know can research it for themselves and come to their own conclusions.
I have been studying this disease in-depth for some time, not because of Michael, but because of the work I have been doing with the medical field and I must tell you, it is an awful, painful disease that not enough people are aware of. There is no cure. It can go into remission but thats all the relief a patient can get. Meds help some. Steroidal meds are the most common treatment, like methotrexate, as well as its generics, Plaquenil, and many, many other types of meds and painkillers. And high stress, etc. can make it flare up again. Patients who have it often don't talk about it, because there's too much stigma attached to it, and they feel very self-concious.
It doesn't matter to me what you all think of the information I have to offer. You can think I'm full of BS and crap for all I care. I am just SO tired of the negativity, you have NO idea. Or you can think that maybe, just maybe, I might be onto something here and look more into it for yourslves. I can only say, research the disease for yourself, and be informed on what it is exactly. Use your own heads when it comes to this AND when it comes to the investigation, and draw your own conclusions. Do NOT trust the media, do NOT always trust what the coroners might say, or what Dr. Murray might say, or even what the family members might say. I am NOT saying they are lying, but IF they are, they certainly have enough reason to. It's certainly not justified, but it happens. I don't think I am going to say much more about this issue.
I did not say people had a death sentence at 40-50 years old; I merely stated that it is COMMON for patients to die of cardiac arrest (which is NOT the same as heart attack)around this age. But each case is as unique as each person. Pretty much all forms of lupus have the characteristic malar rash (the butterfly rash) at various times, and it comes and goes. Not just discoid lupus, which does not affect the whole body the way systemic lupus does. Lupus is a connective tissue disease, and most often forms of arthritis are found with it, as well as problems with many other systems, i.e. the back, kidneys, etc. and ultimately, the heart.
Lupus "mimics" AIDS in that it is an autoimmune disorder, attacks the whole body, you have to be extremely careful about germs and sicknesses, the body gets all kinds of sores, and so much more. It is not the same, however, as it is not only acquired differently but have characteristics, as well. Also, with lupus, as with vitiligo, patients are highly photosensitive (sensitive to sun). It "mimics" cancer, when it comes to body sores, various treatments (i.e. chemo is a treatment many use in lupus), and much more. Skin ulcers and oral ulcers are often found, as well. There can be alopecia (hair loss). But again, its not the same. It just mimics various symptoms of cancer, AIDS, and some other diseases out there. I am not going to go into detail about lupus here. It would be far too exhaustive, and anyone who really wants to know can research it for themselves and come to their own conclusions.
I have been studying this disease in-depth for some time, not because of Michael, but because of the work I have been doing with the medical field and I must tell you, it is an awful, painful disease that not enough people are aware of. There is no cure. It can go into remission but thats all the relief a patient can get. Meds help some. Steroidal meds are the most common treatment, like methotrexate, as well as its generics, Plaquenil, and many, many other types of meds and painkillers. And high stress, etc. can make it flare up again. Patients who have it often don't talk about it, because there's too much stigma attached to it, and they feel very self-concious.
It doesn't matter to me what you all think of the information I have to offer. You can think I'm full of BS and crap for all I care. I am just SO tired of the negativity, you have NO idea. Or you can think that maybe, just maybe, I might be onto something here and look more into it for yourslves. I can only say, research the disease for yourself, and be informed on what it is exactly. Use your own heads when it comes to this AND when it comes to the investigation, and draw your own conclusions. Do NOT trust the media, do NOT always trust what the coroners might say, or what Dr. Murray might say, or even what the family members might say. I am NOT saying they are lying, but IF they are, they certainly have enough reason to. It's certainly not justified, but it happens. I don't think I am going to say much more about this issue.
