Hello, a while back I saw some news about a clinical trial designed to investigate Lupus. I would like to know more information about this, ...

Hi I get the butterfly effect on my face but I also have a scab on my face thar itches and hurts and eats in to my face coursing scars ev...

Hi all

My mum was diagnosed with small cell lung cancer and just finished her 4 cycles of chemo. Today we had a consultation to speak about r...

Hi all

I would really appreciate some advice please. I am not expecting a diagnosis just an indication of whether I am being paranoid or not!

...

Hi I hope it's Ok to post this ... Call out to everyone who may be able to make it ... For anyone living in West Midlands UK. Do you fancy m...

Does anyone else here sufffer with HS along side Lupus? I've tried load of different antibiotics, none have been successful. I'm waiting to...

Has anyone had their eyelashes fall out? This is the 2nd episode, the first one was in September - 6 months ago.

Hi, I'm Tiff, and I'm new here. Literally I joined two minutes ago.

I am a 19 year old female who has been diagnosed with Fibromyalgia. When ...

Hi, I m a 44 year old female that has been suffering with lupus 'type' symptoms including a facial rash that flares as symptoms flare, for a...

Hello. My question is: Has anyone tried Serrapeptase and have you used it as a supplement to Zentiva/Plaquenil( Hydroxychloroquine) and Pred...

I have had three sets of bloods for ANA as doctor wouldn't work on just one set and each time this is what they have read

ANA 1: 1600

DNA b...

Good evening, everyone.

I've written a few posts over the last few years whilst undergoing diagnosis and treatment for CNS Lupus. I've had lu...

Hi everyone!

New here! I have been struggling for years and for years I've been told Rheumatoid arthritis, fibromyalgia etc etc etc. Recently...

I'm back on the Plaquenil / Quinoric, Zentiva roundabout. After taking Plaquenil successfully for 23 years, I am faced with the pressure of ...

I had my first appointment at Guys Lupus clinic a couple of weeks ago and I was very disappointed, I guess I was expecting something differe...

Hi all I'm nearly 100% sure I have SLE. I have come to this conclusion by obtaining my medical notes for the last 10 years as my doctors see...

Hi my names lisa, I was diagnosed with SLE in December, my moods highly affected, don't really know anyone else with this illness and wou...

Hi i broke my ankle in may now healed they say but now have constant burning in leg it never goes away i also in same leg get swelling for n...

Research taking place at Uni of Southampton looking at how people use online communities such as Health unlocked to manage their condition.

R...

My younger sister have just been disgnosed with Systemic Lupus Erythromatosus. She complians of tiredness, swollen feet and pains on her che...

I have Lupus and for about 8 months I have been getting debilitating muscle cramps in my legs mostly at night. My Dr says it is not because...

Hi

I was diagnosed with SLE a year ago, pneumonia, pleural effusion, chest infections, coughing etc. My GP has now sent me to a sleep clinic ...

Hi, can someone please interpret my results please.

I tried to cut and paste my results, but it wont let me at the moment. I have typed word...

Since starting prednisolone and hydroxy chloroquine I have already seen an improvement in my energy levels and my muscle and joint aches and...

Merry Christmas! Hope everyone has had a symptom light christmas!

Has anyone else started with onset of O.A early.i am only 39😞

On Monday I was told by a doctor at the hospital that she had talked to several of her fellow colleagues and that they believe I have SLE an...

Hi all. New to this and only just been told I have SLE as I was rushed into hospital last night with severe chest pains/diaphragm spasms. Is...

Hi everyone! I hope you're all doing well and coping with the number of lupus symptoms that cold weather brings. Well, it's cold in Edinburg...

I apologise for this long post thank you for taking the time to read it.

I am at a loss because I've always been led to believe that SLE is i...