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she has had 6 more surgreys since now they are going to remove the sternum what i need to know is does lupus affect the mrsa any info i would be very thankful.View Thread
Isn't it odd that animals, generally speaking, remain disease free most of their lives? Generally, animals do not seem to suffer the plethora of diseases humans do.
So why is it that humans, who are organic beings like animals, so innundated with dis-eases? Could it be diet? Possibly, and to a great extent yes.
I have come to the conclusion that humans experience physical disease, generally speaking, because humanity suffers from serious mental/emotional distortions of the Original Thought of our Creator.
This Original Thought is that all beings, all situations, are ONE with Creator. Basically, to show Universal Love for Self, and others, is of primary importance for humans.
I understand people are coming here looking for physical solutions to what people consider an only physical problem. Well I have come to give a new consideration for everyone.
If anything, this new consideration that meeting ALL situations with the Original Thought (Love), will greatly lessen the distortions of mind and body.
Thank you for your time and I pray this condition known as SLE will become greatly lessened for all of you!!
In Love!View Thread
Thanks for reading my post.View Thread
I was diagnosed with sle in 1978; kideney damage in1991; had cytoxan treatments; been on prednisone since 1991 (small dose, 2 1/2 mg./day); and had cancer, successfully treated, last summer. My sle finally went into remission after my disease stayed active for 19 years and 10 months. (November 2010). I was 52 and had been retired for 2 years. I don't have all the answers by any stretch of imagination and I'm always open to listening and learning from other people. We never stop learning, ever.
But I'm someone who was diagnosed back when the survival rate wasn't what it is now, which is real good; I continued to work and was offered early retirement after 32 years of employment. I had some rough days, but I'm here. Luckily I worked for the govt. and was not discriminated against.
I'm here if anyone wants to talk - or teach me something new. I haven't kept up on things since remission.View Thread
There is a lot of information online and it is difficult to decipher it all, especially in my case with so many other things involved. My doctors don't have much, if any, knowledge of alternative treatments so your input would be appreciated!!!
LupylisaView Thread
My urine protein is up to 4300 mg which is the highest it has been in 12 years! It really scares me since I have already had a major bout with lupus nephritis. Back then I was very naive, but now I am very well educated on the subject whcih I am not sure is a blessing or a curse! I guess sometimes ignorance is bliss!I
My bloodwork three weeks ago showed signs of a flare low C3, albumin and high serum creatinine.
My latest bloodwork which was done last Tuesday shows an increase in C3 back into normal range which is good. But my urine protein has increased to 4300 mgs. from 2300 mg three weeks ago.
I have dealing with a low grade fever 99.6-100.0 for the past 25 days plus I have a bad case of bronchitis which is making me short of breath. I just don't feel very well and the though of going through lupus nephritis again scares the crap out of me! I could use some support and prayers!
LupylisaView Thread
About 3 years ago my MD ran some blood tests to figure out what is going on with my body. Two of these tests ANA and dsDNA both came back positive. But, when I visited the Rheumatologist , all tests came back negative. Could someone please explain this to me? I am so confused and frustrated!View Thread
I have several other medical problems such as COPD, urinary retention diverticulosis and just diagnosed with lymphedema. Now I'm not so sure that Lupus is the correct diagnosis. I have tried to read as much as I can on the topic which has done little more than confuse me on the subject. So many diseases out there that the symptoms are similar to Lupus. Can someone please direct me to to quality resources to help me educate myself on the topic. I dont want to be taking unecessary medications that i may not need. I dont want to stop taking meds if Im going to go back to feeling the way I was years ago. Im now taking Prednisone, hydroxycloroquine and methotrexate for the lupus. Also i have seen there may be a reaction between Metoprolol and the hydroxycloroquine and need more info on that.View Thread
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My blood pressure is high and I seem to be allergic or sensitive to most BP meds ( Losartan, irbesaertan, lisinopril and now Tekturna) My question is: Do you know of any other meds that could lower my BP and help protect my kidneys?
LupylisaView Thread
and a thyroid med . I also have 10 other meds that I quit taking for a multitude of different issues . fybromyalgia , Ib, acid reflux, arthitis Antihistamine , muscle relaxers ect. ect. I am hoping for a staight forward answer and hope this Doctor is able to help me . Is this typical to have to go to so many Docs and specialist ? I feel i f I took all the meds perscribed to be I would have liver failureView Thread
My mental Lupus fog has made things frustrating as of late and only those who have experience it can even relate. I'm tired of all the letdowns in my life and feel particularly bad this week.
Does anyone else get sick of all those phony inspirational phrases? "Turn that frown upside down," "Your happiness is dependent on you not what's happening outside." It gets a little old sometimes, especially when it takes everything just to drag our sore butts out of bed.
If I could give this illness to someone with one of those canned answers when I'm feeling down I would. Then they can experience what we go through everyday. Just saying..
Lisatru62View Thread
Sorry I haven't been around. I am not feeling that great and just got labs back with not good so news. C3 is low and serum creatinine is high as is the protein in my urine and my BP.
LupylisaView Thread
I thought all discoid rashes came with some seeping. It is NOT infected, it seeps and comes from all the layers of skin up. Here's some pics on my blog at http://jujuslupus.blogspot.com/ .
I'm on stronger than usual steroid cream now and its healing nicely. I have to be rid of it before feb 22nd when I'm scheduled for anterior cervical fusion.
Does anyone else get these?
And these circling antibodies at the rash area? I understand a little about it and was also wondering if THIS is the reason why no labs have been able to titer or direct ANA result my blood. They say unable to obtain results due to immune complex interference.
Thanks, HUGS, JulieView Thread
Thanks
annView Thread
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