Re: Cushings?
my symptoms started 3 years ago, i was healthy, worked two jobs, enjoyed nights out.. then one day i had a massive pain in my head.. my eye site broke up as if i was looking through glass, i lost my speach (for about 30 seconds) i couldnt stand i thought i was dying!! phoned nhs nurses and mum was told to monitor me if it. Happened again to go to hospital, i had a weird feeling in my face tounge and head that lasted all night. i felt fine again.. this happened another twice each about a month appart. i however had like stabbing shooting pains in my head at least every two days. i then went on to having a massive pain in my head once again and ended up visiting the hospital emergency room 13 days in a row, i had high fever and pains... emergency mri was done which came back fine... was given alot of meds which made me hillusinate and have out of body experiences...
my symptoms now are
Sickness, bloated ness, celiac, coated tongue, candida/thrush recurring in left eAr, mucus from anus, blurred vision, anxiety (really bad), mood irritability, always craving sugar and feel really week if I go with out food too long, gas/wind, constantly burping, fatigue Which doctors are saying is fibromyalgia and me, I sleep all the time, feels like millions of ants are running around inside me (strange I know), shortness of breath, migraines, heartburn, acid reflux, hives, itching, acne, I have loads of boils, dizziness, pains in joints, pains in my teeth, aches everyday, "brain shakes" as if my brain just moves on my head, numbness in hands expecially down the side of my arm and my little finger, numbness in face and tounge, my tounge shakes, pus spots all in my hair.i have pins and needles all the time.. I have terrible flushes in my face I go purple, my hands are cold to touch. I shake a lot. I feel like I'm going insane. I see a cbt therapist to try help me go out. I just feel like I'm going to die.. I also get little water blisters all over my hands
I've been tested for cancer as I wee out alot of blood and pus but it was okay. I get urine infections all the time... I see a celiac doctor who has diagnosed celiac without biopsy via blood tests and my iga slowly going down on a gluten free diet.. She has now sent me for rast blood tests and food allergy tests... I also see a endocrinologist as of last week as the thyroid specialist wouldn't help at all.. I now pay private and have been told I have to do a 24 hour urine test for cortisol and he wants me to start taking some sort of thyroid Meds.. However I've been put on levothyroxine 3 times and it always makes me really bad, but he says there is no other thyroid tablets?! I'm seeing an immunologist on Tuesday to see if he can help xx
Sorry for rambling on.. Hope to talk soon xx