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Lupus Symptoms Information
Lupus symptoms Information
Could someone explain there lupus symptoms?
could someone with lupus please explain what symptoms started first and how they have progressed. thanks
Arthritis/lupus symptoms?
I have had a stomach condition for over a year now and my doctor said i might have arthritis as i have swelling of the fingers and toes, and when its cold they are in a lot of pain expeciailly my fingers. The swelling is annoying me and as its colder thats annoying me too. Ive experienced this for about 6 months but its worsened as its colder now. I have recently been really really weak, so much that I have NO energy at the end of the day and i can barely shower & dress at night. I had an arthritis blood test though and it showed completely normal. I don't believe this is in my head because I have all these symptoms. What else could these symptoms mean? Lupus? and is there a test for lupus?arthritis is in my family and one of my parents has chronic fatigue
Can someone thoroughly explain lupus symptoms?
My doctor said I could have an autoimmune disease. I think most of the symptoms are in my head. They said this because they couldn't find out what's causing my chest pain and shortness of breath. maybe 3 days later, I started getting severe back pains, and minor pains in my arms and legs. I also don't understand what they mean by fatigue. I'm tired some times but most of the time I'm up joking and laughing. My back pains are fine in the morning but starts to occur as it gets closer to night. I really need help because it's driving me crazy doing research and just thinking about it. Plus I won't know my lab results until 2 weeks from now
How can I treat lupus symptoms without any dangerous medicines?
I got lupus over the summer so now I have to go to school with lupus. I've been waking up in the morning felling pain in my heels when i put pressure on them. I also fell nauseous when I eat more than I want to. I also cannot stretch my arm out all the way without my elbow hurting, I can only stretch it about half way. I got tapered off of prednisone about two weeks ago so I am no longer taking prednisone and now I take 200 mg of plaquenil daily and that medicine isn't supposed to take effect until about a month doctor said plaquenil takes a very long time to take effect My doctor also said it may be a different kind of lupus because i only have four symptoms which are joint pain muscle pain appetite loss and fevers. I forgot to mention i was a 12 year old male since lupus is more common in females. My family including my extended family and ancestors also have no evidence of lupus. I also try to exercise in PE at school every day but become short of breath a lot faster than when i didnt have lupus doctor also said it mightve been because i was inactive with absolutely NO exercise for a month. And also if you know about something that could open my appetite please tell me about it. I have had absolutely NO medical problems in my entire lifetime other than a couple of colds flus and this lupus. So if you know of any herbs or herbal teas that could help me please tell me thank you very much and i forgot to mention i got a cat 6 month before the symptoms started showing up
Can surgery cause lupus symptoms to syddenly appear?
In December I had a surgery to drain the periardial effusion around my heart. I wasn't really in any pain and I had enery. After surgery I started to hurt everywhere and my eyes became super dry and I started seeing floaters and my ANA went to 1 160 and I am tired all the time but I dont sleep....what is going on? I dont think I definitely have lupus but I do believe surgery aggravated something. I also had a UTI shortly after which I never had in my life.I am on naproxen, colchicine, iron, and protonix.
Why does sunlight make lupus symptoms worse?
I know you shouldn't be out in the sun much if you have lupus and that it makes it worse. I'm just wondering why how it makes it worse but I don't feel like looking it up myself. Please don't pretend I'm smart when it comes to medical terms dumb it down for me if you can.
Lot's of lupus symptoms, but not sure if I should freak out yet....?
I started going to the doctor at the beginning of the school year when my headaches that I've had for years started getting really bad and I had a week of the world spinning in my head along with ringing in my ears. I though it was M ni re's or just an ear infection since I have a history of it. My doctor told me my ear was fine and said I might just have migraines. Took lot's of migraine medicine, including Imitriex. Nothing worked and I switched doctors, my new doctor sent me to a neurologist after nothing worked. My neurologist made me get an MRI, CAT scan, Xrays, EEG, EMG idk the names I had blood drawn five different times, I even had a pregnancy test why idk . My EMG or w e showed that I had a pinched nerve in my back and neck, I took medication and had work outs, but my back still hurts yea, I forgot to mention I have a bad back . My ANA tests came back abnormal, my doctor wanted a lupus profile though he said that he didn't think I had it.My insurance canceled on my before I could get the profile thing done. I did some research on Lupus and then I realized, oh my, I have most of those symptoms.....so I'm not sure if I should freak out or not...Symptoms X Painful or swollen joints and muscle pain. X Unexplained feverX Red rashes, most commonly on the faceX Chest pain upon deep breathingX Unusual loss of hairX Pale or purple fingers or toes from cold or stress Raynaud's phenomenon X Swelling edema in legs or around eyesX Swollen glandsX Extreme fatigueX AnemiaX Low white somethingX HeadachesX DizzinessX ConfusionX mini depressions.So you tell me, I want to know if I should spend nearly a thousand dollars in medical bills...or more if I really do have it...oh, and i get these weird times when the room gets really bright and funny and it gets really hot and i feel really tired and i start sweating and i want to throw up. i just feel really bad, i have to sit down for five minutes, and even afterwards i still feel bad.
Lupus Symptom?
I have 2 blisters on my lips and ulcers on my tongue. Is this a symptom of lupus?
Lupus symptoms can anyone help please?
hi all. i have joint pain in my fingers and ankles, blisters in the back of my throat, feel sick, heavy flu like symptoms, pain near my right kidney and abdomen, feel vague, slight rash on my face which ive had for years which comes and goes. headaches and FATIGUE. i have lupus in my family could i have it? can anyone give me any advice please?
Lupus symptoms?
Over the years everytime I try to WEBMD my symptoms it always points to Lupus. Why is every symptom attached to that specific disease and is it likely I can have it?
About lupus? symptoms? can be fatal? related fibromyalgia?
son has fibromyalgia. i've heard the symptoms are similar to lupus?
Help with possible Lupus symptoms...please?
I have the following symptoms and my primary care physician suspects early onset of lupus. Here is some of what I experience episodes lasting about a week of fatigue, weakness, dizziness, fever low grade during the day, spiking at night to almost 104 hives, aches, fatigue, anemia, muscles twitches through out my whole body, facial redness with warmth, chills, night sweats. My lab tests came back all crazy...most of the numbers were off. A very high Sed rate and CRP. Any help or advice?
What can I do for this Lupus symptom?
My daughter is 13 and has Lupus. She is experiencing bad arthritis in her knees for the past 2 weeks. Her doctor gave her a med. called naproxen but its not doing much for her. I also bought bengay to rub in the area but its not helping much either. She is missing alot of school because of this. Can anyone give me some advice on what to do . Maybe you know of this disease or you have it . Ive also used hot compress' on her knees but that only gave temporary relief. Thanks to those willing to give their helpful advice.
Hypermobility and Lupus...symptoms?
Is there any distinct symptoms that are related to Lupus if you have hypermobility? I have HMS and maybe Lupus, I know there's more to my illness than just HMS .
Other Resources About Lupus Symptoms
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