living with Lupus
I am new to this, not only to this site but to chat forums as well. I was diagnosed with Lupus about three years ago and am currently experiencing a flare. I was trying to explain to my family and friends what it feels like and i realised that i don't know anyone else with this illness to try and compare my symptoms to. I know symptoms can be mixed and varied but i began to wonder if anyone else has some similar symptoms to mine. Hence here i am...
Welcome to WHL! We are glad to have you with us. One of the best things about this place is finding people that understand exactly how we are feeling and what we are going through. We are here for you
welcome to the forum! we understand what you've gone through and are going through. Reach out to us anytime. It IS hard to explain to someone what lupus is like. Lupus has so many different dimensions to it making it hard to come up with a short and concise explanation. I tell people it is like a pinball. You never know where the ball is going to go next. At least that's true in my case. With lupus you learn to take life one day at a time and in some cases, one moment at a time. My husband puts it this way: "your lupus is like the Montana weather; it changes every 5 minutes:. He's right. Again, welcome to our forum and visit often!
Hi I'm Alicia and I'm new to lupus as well. I was diagnosed a month ago and
I know absolute nothing only what I read. Tell me about your symptoms?
Maybe we can compare. I would like to help were I can
Hello and Welcome to our family where we certainly understand what you are dealing with, many of us have probably dealt with the same issues as you. You have come to the right place to find understanding, information and support!
I am glad that you are here!
Peace and Blessings
Hi sammy and welcome :). Hope you find what your looking for