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Reply | Forward Message #32 of 33 |
Re: [menwithlupus] Hello

We-ell... as far as where some of your symptoms are concerned, I only had multi-jointed arthritis syndrome prior to my diagnoses of SLE with Nephritis over 4 & a half years ago.  I believe that it's high time you sought a 2nd opinion elsewhere so you'll find the right answers to what you've been suffering from for so long.

I had to experiment to a wide variety of anti-inflammatory medicines in the past, just to help alleviate the immobilizing pain I was undergoing for about 2 years... and I guess, those self-medications that I did only worsened my condition and further battered my weakening kidneys by shrinking both to almost half their sizes.

I went through 2 kidney biopsies; numerous bone and joint x-rays; IV-based chemotherapies; closely-supervised blood and urinalyses since I was correctly diagnosed by internists at UCLA-Olive View Medical Center (Sylmar, CA), including visits to their Physical Therapy Clinic so I could regain my mobility and independence from crutches and my cane.  I lost weight and was anemic as well, so I had to slowly try other diets just to rebuild what I lost and try my best in keeping unwanted weight off.  But then, that's another matter you'll soon be hard-pressed, keeping!  :)

Right now, I'm on a wide variety of drug combinations that help suppress the disease and also counter the varied side effects given by such as well!  There are times when I get really tired of taking them and skip my doses but that move only gave this condition the extra boost to further assail my already severe case.

My advice is to go get a 2nd and 3rd opinion from different specialists so that you can then put to rest what is ailing you.  You're lucky to have met an uncle who had this disease!  I don't know anyone from both sides of my family to have had this disease so I am lead to believe that I was the first.

It is indeed enlightening, once you find out what's up and then you will try your best to stay clear from anything that may only cause more complications to your fragile body.  Good luck and I hope you'll find your answers soon.

Yours,

~Robert


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Thu Dec 20, 2007 8:19 pm

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Message #32 of 33 |
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I'm Alan, age 57 and have had Lupus since 1974, with involvement of the kidneys and possibly lupus cerebritus (-5 for spelling). I've undergone biopsies, bone...
lupusman_2001
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Jul 19, 2005
2:19 am

weeks in the hospital and the coma....were those at a later age or earlier? what happens during a minor flare? your in remission with just 5mg of pred a day? ...
Mike Whitmore
nsemikew
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Jul 19, 2005
3:53 pm

Hi! My name's Robert and I was diagnosed with SLE with kidney involvement 3 years ago, although the poly-articular (multi-jointed) arthritis attacks have been...
flash_sphere
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Aug 11, 2006
4:27 pm

I have not been diagnosed with lupus by a doctor yet. I never even thought about it till recently i met some biological family(my mom was adopted at a young...
Dale
soarhawk2003
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Dec 20, 2007
7:09 am

We-ell... as far as where some of your symptoms are concerned, I only had multi-jointed arthritis syndrome prior to my diagnoses of SLE with Nephritis over 4 &...
Bob Cabrera
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Dec 21, 2007
9:57 am

Dale, Welcome, sorry the doctor's have not come up with a diagnosis yet. My trek with Lupus started with a rash and kept progressing. Now for the most part...
James Thompson
tigerjlt
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Dec 23, 2007
4:48 am
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