I have just been diagnosed and I am scared
My name is Lynette and I am a 19 year old Chinese American female that has just been diagnosed with Systemic Lupus. In my case my Lupus effects my kidneys and blood. I am currently on predisone and I just wanted to express that i am new and that i never knew that something like this could happen to me. Does anyone have any helpful advice? Thanks bunches :)
Help! Support group in Brighton, East Sussex, UK
I have returned to the UK after being diagnosed Lupus in New York at 40. I was made redundant on top of my illness. I am finding it hard to find a support group in Brighton, East Sussex, UK. If any one know's of one, please can you contact me. It would be nice to meet people rather then emails.
I wish you well.