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Current Topic: making the best with LUPAS

my body feels so tired,ache,you name it; sometimes its very hard for me. the morpine sometimes works. you see ive had lupas since 1996 i was told it was cancer then fibromiaga then that i was crazy(that what i felt was all in my head) then i was sent to san antonio,tx to see a RA doctor all this time my pain doctor kept given me support and telling me we would find what was wrong with me so he took it into his hands to do iab work and other tests because of my doctor i found out i had lupas by then i had new symptoms so even after all these i be the frist to say its so hard and for me its getting worse i cant work anymore and no help but i cant give up its not in me besides my wonderful doctor my husband give me support NOT even my family and thats sad because when i feel sick i have to pertend im fine becuse my kids get scared and think im gonna die.so i stay positive no matter how im feeling.today has been very hard i have my daugther typing for me im glad there is a sight for peole with LUPAS stay strong!

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