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Welcome to Phoenix Rising!
Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of and finding treatments for complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia (FM), long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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Blog entries by Jeckylberry
According to the occupational therapist I am a candidate for a wheelchair grant. According to the psychobabblers I should not be humoured in my 'false illness belief' and therefore must deny my body the 'reward' of wheels.
In 2013 when I first started getting my pseudo-symptoms, I stopped...
Gather round people, I'll tell you a tale of a great mystery... Of a certain magic potion that causes dire ills to a victim even before they have swallowed it!
I'll backtrack a little to last month.
Last month I found me a new doc. I was looking for a new GP as my current one is overloaded and...
Have there been any improvements?
Not really. I mean when I can walk, I walk. I just can't always do it. I don't really see how physio can improve this drastically. I still do the exercises though. The psychologist is nice to talk to but I don't see any improvement on that level. What am I...
I came to Phoenix Rising because I typed the following search into Google:
abnormal eeg and "functional neurological disorder"
I found the link entitled "You think ME is bad - try having a psychogenic movement disorder"
Intrigued I clicked and read the first and following entries to a thread...