how long does lupus rash last

If one gets a rash from ARS it will last from 1-2 weeks and it is not a puss field rash nor do you get any type of fluid from it. If you haven't tested for HIV and other STDs from your unprotected sex you should. You can test now and get a conclusive test result.

t been diagnosed with lupus but my butterfly rash has been very persistent the last 6 months or so. no swelling but I was diagnosed with fibromyalgia so pain is a constant part of my life as well as chronic fatigue.

If the doc says you do then there are many types of meds you can take so you can live a long and normal life.With lupus there is a lot of the wait and see thing and if you can do that then half the battle is over with. If the rhuemo doc says you have it watch your kidneys and the sun, get used to appling sun tan lotion every morning it will be your best friend. I can tell you a lupus burn feels worse then a normal sun burn and takes alot longer to get over it.

I was wondering how long secondary syphilis rash/lesions last? How long do they stay on the skin or in the mouth? Like if it were a secondary syphilis lesion on the roof of mouth. How long would they stay?

Hi and welcome to our little MS community, After reading your original post, I would be concerned with any neurologist who is willing to ignore Clinical signs and MRI evidence of dymelination, simply because you don't have 2+ Obands. It would be in your best interest to get a second opinion, preferably with a neurologist who specialises in MS.

it would be my first outbreak if it is indeed herpes. so how long does a normal outbreak last for? how long does it normally take for the red dots to turn into sores? or maybe i don't have herpes? i'm praying i don't have herpes and think some of my symptoms might be psychosematic. but if not herpes, what else could little read dots with white heads be on the underside of my penis be? pls help!

People with Lupus will get a "butterfly rash" across their nose and cheeks. They can also have a positive RA factor because Lupus does joint damage. Wonka is correct that it is difficult to diagnose in the beginning of the disease and you do have to meet 4 out of 11. Your levels (blood levels) will flucuate (becoming normal then abnormal when the disease is active). An ANA is a standard test for Lupus but will also come up positive for other diseases.

I dont have lupus, but a friend of mine found out she does and she is 20. She is going to call me this week to talk. I have read about it and it looks very similiar to hashimotos except the rash and skin issues. Is there anything else different besides the rash? Is it usually treated the same way hashi's is treated or graves? (or could go either way). I am just trying to learn more about this to help her where i can.

is it on the bridge of your nose and both cheeks?? Have you been tested for lupus? If the rash does look like that, it is the hallmark sign of lupus. And I'm so sorry about the no insurance...that must make it really tough. If you are having episodes where you are constantly falling, could you just go to the ER? maybe, if they see you falling down and your other symptoms, they would admit you for testing?

That happens less freaquently now as does the rash. However the headaches are super persistent. Last week I was hospitalized because the headache was so bad and I developed numbness,burning,tingling in the right side. I have been tested for everything under the sun. Creatinine is with one normal limits but steadily rising, urea nitrogen is steadily rising and now outside normal limits and I have developed blood in the urine.

sign which actually did point to Lupus. I cannot remember what he called it and want to look it up. Does anyone know what sign he is referring too??? He then asked if I ever got ulcers in my mouth and I said, actually YES - I had. Like 3 times since January I had non painful ulcers in my mouth and I didnt even know I had them until I ate, then I could feel them on my gums which is what brought me to the mirror to find them.

Hi I just went through the same experience! I've been dx with Lupus now for 6 yrs, but it never went full blown. My ANA has always been low. Now I moved to another state and right away got me a new rheumy, and in the meantime Ive been looking also for a dx of MS, because I started having the tell tail sx ON, vertigo, tingling numbness etc. Plus my sis had been dx with the same sx.

I was wondering how long someone can have Leukemia and go undiagnosed before it is very obvious what is wrong? I am 28 and have had some really crazy symptoms since the birth of my daughter in 2004. It has been a never ending battle of frustration. 3 months after my daughter was born I started having problems with my legs feeling weak and giving out from under me, I lost 20 lbs in 2 weeks, and started to have blurriness in left eye.

Said yes, I do have blood and protein in urine, but not bad, but could be Lupus related. Had rash for 7 months before Plaquenil kicked in, still have muscle pain and weakness but feeling not bad . Doctor says suggests Lupus but won't commit, but also says stay on Plaquenil. Does everyone come away from these appointments feeling like a hypochondriac or is it just me. I have been feeling more like myself lately so maybe I am cured, what do you think?

How long does lupus rash last

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