At long last

Sorry i haven't posted for a while, I have been too obsessed with Big Brother to do anything. I did however go to the hospital on August 16th. I had to go all the way to the freeman hospital. When i got there, the queue was out the department door. We queued for about 20 mins. Eventually i got called in to get weighed. So i did, and measured. I was 5ft 5 and very heavy lol... Then blood pressure, i cried when the thingy thingy'd it was so tight it hurt... blood pressue was 146/102 which is quite high apparently. I was then taken to some corridor that seemed MILES away from anywhere else in the hospital. Sat there, crying, coz i was so tired. I read a poster about hip replacement, 4 times, so i know what to expect if i ever need one. Then the doctor came out and my heart sank. I'd waited 10 years to find out what was wrong with me but now the day was actually here, I wasn't sure I wanted to know. I sat in the office with my mum by my side. Told the doctor about all my problems. She got me onto the bed and started to press on my thingy points. I knew that if I felt pain in 11 of the 18 places then she was going to diagnose me with Fibromyalgia. I think I felt pain in all 18 places. I made my way back to my chair and she told me that I did indeed have Fibromyalgia. Mum asked about M.E./Chronic Fatigue Syndrome and she said that it's the same condition in her eyes. It's not in mine but there you have it. So i THINK i have M.E also but i'm not 100% sure. She explained that the NHS doesn't have the resources to help and that in America the condition much more understood. She said that gentle excercise will help so I should get in touch with a gym, there are NHS gyms or something where I would get a discount. Physiotherapy may help but I would have to go private and there are only a couple of drugs approved in the UK. One of which i was prescribed, Amitripylene 10mg. I have to take 1 tablet in the evening, it is to help me sleep, so i can deal with my illness better when i'm awake. She took bloods, well she didn't take them, the phlibottomest took them. To check for Sjorens Disease. She said the results would be sent to me in a letter but I haven't recieved the letter yet and I have to go to GP to have blood pressure done again. She also recommended i get transfered to the Queen Elizabeth hospital in Gateshead where there a doctor who has been researching fibromyalgia and knows more about it than she does. However I have forgotten the doctor's name.