Thank you! I def hope we all have great days to come......
In this situation I have realized the psoriasis symptoms and sle lupus are very similar... which has become frustrating and stressful and being stressed can only make things worst. Well I just...
I hope you do feel better soon. How long will you be on the prednisone and the other meds; that is a really high does at southerndiva mentioned. But rest assured it will get better... just one thing:...
Has anyone had anything like this happen or heard of anything like this? Please briefly reply :-/ I know its a lot to read but its the only way to explain...
Has anyone had anything like this? please reply briefly :-(...
Thank you for you support I highly appreciate it. I was actually offered to take prednisone but I declined because of the side effects; its pretty scary for me. I know I shouldn't worry so much but...
joints are severely swollen mainly my hands, arms wrists, all joint pain everywhere really. On plaquenil it had been good since i was on in consistent in 2008 from june to november and then stopped...
so back in September of 06 I began getting hives every night around 7pm. It was unbearable because this was happening every night and would go away in the am. So i decided to go to a dermatologist. I...
I'm glad this post was brought up... I don't really know if I should mention it to my doctor which I will be seeing tomorrow. My short term memory is horrible. I don't know how many times I've done...
Hey Lilli, hope you are doing well. I was wondering if you went to nyu hospital for joint disease? I recently started attending in September and they have been the absolute most helpful and...
Great for you! We should always focus and something aside from what we go through with this horrible disease! Staying positive, surrounded by good people and having a great times with loved ones...
Wow! I was wondering myself if it was just me! I'm actually on my cycle now and felt horrible! for the past week... the symptoms go back to normal once its over. I'm so glad I am not alone once...
Please stay positive and keep strong... we all have had hurdles that we all felt the same way... think about yourself and what makes you happy, i know it sounds cliche but its very true. I myself had...
oh wow, thank you for that I'll definitely be asking my doctor about that thank you for the new information. Its really good and important information....
Yes anna24! sometimes my eyes do feel like a burning sort of... i do have dry eyes as well, i've been told that recently, and i wear contact lenses so its worst! @weleetka there had been times were...
Hey everyone... These last two weeks i've been horribly stiff in the mornings and throughout the day. I'm not sure if it might be the change in weather in NYC or all the rain we've gotten; who knows!...
definitely left! always worst and noticeably visible....
Hello everyone, SO yesterday i went to visit my ophthalmologist and i got some not so comforting news... I have vasculitis... He explained what it was but it wasn't so clear to me, it was just...
@kuma you've definitely are in the right place to vent and ask questions... we can all relate to each other in some way... It is very hard for many people who haven't been exposed to what lupus is to...
I completely understand what you mean... If it wasn't for my own research, I wouldn't have probably found out about my condition until it became much worse... My dermatologist actually ordered...
Have you tried public health insurance?...
Thank you so much for your input, I really appreciate it. I see you have a lot of years with the condition and makes me feel at ease that I get the opinion from people that have actually used the...
Hey Everyone... I am new to the site, but I've read some things on here before and always enjoy reading everyone's experiences; which many times have been my own and have been very helpful to me. So...