Firstly, I am a 23 year old female who already has longstanding diagnoses of Chronic Fatigue Syndrome (CFS), Endometriosis and Raynaud's. I've learned to live with these and know what to expect from them.
About 8 months ago I began experiencing severe vertigo, nausea, and sleep apnea, for about 1-2 weeks and put it down to an ear infection. About 2 months later it happened again, and then 2 months later, again. I returned to my Doctor who said I didn't have an ear infection and it must be a build up of catarrh, except that shouldn't recur so it was a mystery and we should hope it didn't happen again. Anyway they kept shrugging it off. I thought that was it, but now 2 months later, it has happened again. Only this time I have many more symptoms too. These include: dizziness, complete loss of appetite, difficulty with coordination, burning, numbness and tingling sensations in my limbs, slurred speech, confusion, difficulty swallowing, eye pain and blurring, sleep apnea, difficulty walking straight and general clumsiness. To be honest, I look like a drunk person when I walk. I can control it to some extent but I feel like I am dragging my body along and it is an incredibly slow process, my mind is telling my body to move but my body isn't able to keep up. It's like I am walking on jelly.
I have had CFS for 8 years now and I know this isn't the cause, my CFS symptoms had actually improved shortly before I started experiencing these problems. The sleep apnea is proving the worst at the moment and my Doctors are at a loss to explain why this is, as I am not overweight or a smoker. Therefore they put it down to anxiety, despite the fact it happens when I am at my most relaxed! I have had all sorts of blood tests and all have come back negative. I'm currently awaiting urine results but I'm not holding my breath. Everytime I go to the Doctor's they dismiss my problems as anxiety/depression and I'm getting sick of it, I don't have anxiety atall, though this whole situation is causing me to become depressed. This is what happened with CFS and it took me 6 years to obtain a diagnosis. I don't intend to go through that again!! please if anyone has any advice I would appreciate it, as my family are also dismissive and consider me a hypochondriac.
If you have been through anything similar I would greatly appreciate some feedback.