ok i'll try and cut a long story short (apologies if it is long winded)
For 18 months i have had terrible chronic fatigue as well as muscle and joint pain, memory loss and constant infections (water infections, throat, eye cysts etc) and other things.
GP keeps saying i'm depressed because i had PND 5 years ago and then a few months ago i burst in to tears in his room out of sheer frustration and exhaustion.
DP was in the surgery with DS last week and seen a leaflet on the condition Lupus. I've never heared of it before but when he read it, he immeadiatly thought (in his words) Oh My God this is what She (me) has got! he brought home the leaflet, and reading it as well as some online research i think its a possibility that i could have it? i've also reaserched M.E and CFS and they're all simular symtoms. I've already asked GP about CFS etc but he just says NO.
I really dont think i can face the GP again for him to tell me "no its not that blah blah blah"
I feel so isolated, its ruining my life. even the smallest of every tasks leaves me physically drained. i still have plenty of motivation but when i put it into practise eg taking the DC swimming etc i pay for it doubly the next day.
its a small surgery in a large area where its difficult to get an appointment and then you're made to feel unless your dying then they havent got the time to listen to you. I'm wondering if by going private i'll be taken more seriously and actually get answers? the only thing he did was send me for blood tests to see if i was aneamic.
Sorry for it being long and also for any spell errors :-(