To All,
Thank you for your advice and for all the help and support. I wanted to first say that. It has been most helpful to ask my question and get the replies and thoughts of all of you.
LolaLola plaqs was the reason I believe that I had been able to do so much so far. It was good for the fatigue, I don't mean I didn't have any but it helped some. It would be nice if people could get the meds they need, I mean no one asked any of us if we could afford the diseases before we got them so why do they think that making the good meds that help so costly you can't afford them.
lazylegs, you are right it does help and I thank you for reminding me of that. I will try to listen to my body and do what I can to help it.
Cath, I don't know at this point if it would be enough for the med, but I have tried charities and had no reply from any of them but i know they are flooded with people asking for help. I know that my job and life would be easier with the meds.
Douglas, thank you for your support it means a lot to me, as I have not had much in the 15 years of having lupus. I have worked since I was 14 years old and really don't know what to do but work. I love to work that is my problem. If this disease wants to hurt me the most that is the one thing that would make life to hard to handle. I am not a person to be supported by a government as long as I can get out of bed. I don't blame anyone for having government help but I guess I am saying work is my life it always has been.
I have thought about it and if I don't do it I feel later I will be sorry for not taking the chance I have worked 9 years to do. I will be taking the job and hope that my boss will work with me and the lupus to both of our advantages. I will let you all know how it works out.
Thanks so much again for your time,
Tammy