Definitive diagnosis symptoms and conditions

Hi there... I have just found this site and I'm very grateful to everyone who has taken the time to sit down and tell us their story mine is very similar. BELIEAVE me I feel like I am pushing my family away and I'm losing my relationship with the one person who used to make me feel like I was the most beautiful woman in the world.
I'm a 40 yr female have or maybe had a great job that I loved... On April 12 I noticed a small red rash on my lower right leg no big deal went to the Dr. gave me some cream and sent me home well I went to work and by the afternoon things just seem to get bad my legs began to swell and little blisters started to pop up so I went to the E.R. they had no Idea what was wrong with me got me an appointment to see a skin DR. so I went home but the pain from the swelling was so bad I could not walk any longer went back to the E.R. they gave me some pain meds and called in some other DR. things had gone from bad to worse my feet had gotten to big I could not put on shoes and I had bruised completely across the bottoms of my feet they put me on 30mg of PRED. and it seem to be under control sent me home after 3 day in the hospital things were good for about a day or so I thought I would go back to work well that was not a very good idea.... My sister had to come and take me back to the ER where they did 2 biopsies and still have no idea what is wrong with me. so now they put me on 60mg of PRED the rash has gone, lots of scaring on my feet because of the blisters once they broke and dried out but I can live with that....
It's the side effects that they don’t tell you about,
MOON FACE I can't look at myself cause really that’s not me anymore,
WEIGHT GAIN I have always been thick but I can't handle the extra 30lbs I've gained,
MOOD SWINGS are unbearable,
PAINFUL JOINTS, CAMEL HUMP, BLOODY NOSE, BRUSING, SORE TEETH/GUMS, DRY EYES, FAITIGE, and worsted of all
I don’t have a support systems in my life so I'm fighting this by myself everyday, I have 3 kids that I have tried to explain all this to but they don't get it and well my boyfriend he tells me he understands that its the meds pushing him away but if I can't figure away to control this I will lose every thing including my job. I cant even get the energy together half the time to make it up and down the stairs which also comes with the pain of just trying to lift each leg up to climb the stairs, I also have the camel hump which I find very painful, The acne and the hair growth that I have to get wax off once a month cause I feel like a man I feel like a loser and as of the last couple of days I just want to give up I am now down to 20mg per day but I find that I am feeling so sick I cant think straight I hope and pray for each and every person out there that has to take this MED that you get better and I do hope that my symptoms wont come back. Thanks for being here and I’m glad I found this site. I know now that I’m not losing my mind completely. Elizabeth.

my husband took levaquin for pneumonia..it seemed to help that problem..however, after completing the course of treatment he began to feel "uneasy" stomach wise and a week or two later began having unrelenting diarrhea...we are still struggling to find a definitive diagnosis..he is hospitalized at this time...has anyone else had this kind of reaction and if so, what have they done....thanks for responding..milli

I was treated with prednisone for interstitial nephritis in Dec '03. Started at 60 mg for 2 days, then 40mg for 4 weeks. Doctor tapered drug too soon and too fast. Experienced painful swelling of joints of hands, elbows, shoulders, knees and ankles. Plus large, red, hot and very painful rashes and welts on neck, torso, arms, legs, particularly uncomfortable at pressure points like waistband and bra straps/bands (sides of stomach and breasts felt as if on fire). Was put back on prednisone in Feb '04 at 20mg daily and symptoms (which now I realize were side effects) subsided. Currently tapering again starting at 15mg for 3 wks and now on 2nd wk of 3 wks at 10mg...rashes/welts and aches have returned, but not as severe. I will be seeing my doctor in 2 wks for further tapering instructions (kidneys are fine and fully recovered). I had concerns about my "symptoms" being lupus since I got a positive ANA result, albeit a weak one, and my problems stemmed from the initial renal insufficiency. A dermatologist recommended I see and allergist because of the rashes. Although I'm not ruling out lupus or allergies just yet, after reading all the side effects on this website, I would have to think these aches, pains, rashes and swellings are prednisone related and I hope and pray they will go away once I'm off the prednisone. I will persue a more definitive diagnosis if the side effects continue and/or worsen after going off prednisone, but if anyone can offer a timeline as to how long the side effect took to wear off after being on prednisone for about 5-6 months (including tapering period), I would appreciate an e-mail.