ME/CFS
Last saturday until wednesday I was in a general hospital ward after I lost complete movement and most sensation down my left side. I had a brain CT scan, neck x ray, brain MRI scan and many blood tests done, everything was fine according to them, except in my first blood test I had a slight infection they said, but didn't say anything else.
As nothing came back on any of the scans and as the doctors all saw my notes and were told about my MH they put it down to that and I saw 4 psychs while on the ward, all at the same time, who I talked to for about an hour, they say they were about 80% sure it was stress related.
I'm not convinced it was stress related and having thought about symptoms I have had over the last few years and having spoken to a few people, I am worried it could be ME/CFS. I have always put things like exhaustion and poor concentration down to my MH, but even when I do get a good sleep I am still exhausted, I have read about ME/CFS on the NHS website and I do have an awful lot of the symptoms. Now let me say I am in no way self diagnosing here, I am just looking at the possibility and will go to my GP in the new year (next available appointment with her is 2nd january)
However, I was wondering if people who do have ME/CFS how did you get diagnosed? Did people fob you off because of your mental health?
I'm just so worried that my GP will say it is all stress and MH related especially as that is what the doctors are saying, but I'm not convinced.
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