Hi,
I am trying to keep this as short as possible, something we should all try as fellow me/cfs sufferers.

Is anyone else there dealing with a severe not just physiological but psychological stress intolerance?
Basically any kind of task can bring me into a feeling of fight or flight, it is definitely different from anxiety, it is more of an extreme stress situation like being in a hurry, I am not anxious though. I get racing thoughts, can not concentrate and easy tasks like making the dishes, talking to a dear friend of mine, just reading a book or merely a train of thought can jumpstart this "reaction", it seems that over the last years I became more and more "reactive". (neurological kindling?)
Obviously there are hundreds of possibilities or reasons why this could be happening, I stopped looking for answers when it comes to trying to pin it down as it will not get me anywhere.
Is anyone out there who has dealt with something like I am describing and it actually got better just by itself over time or did you do something that helped tremendously?
Thank you,
PS: For me everything started getting worse when I stopped a SSRI cold turkey 4 years ago. I slowly became home- and 80% bedbound and diagnosed with severe POTS, HEDS, MCAD and ME.
I am trying to keep this as short as possible, something we should all try as fellow me/cfs sufferers.
Is anyone else there dealing with a severe not just physiological but psychological stress intolerance?
Basically any kind of task can bring me into a feeling of fight or flight, it is definitely different from anxiety, it is more of an extreme stress situation like being in a hurry, I am not anxious though. I get racing thoughts, can not concentrate and easy tasks like making the dishes, talking to a dear friend of mine, just reading a book or merely a train of thought can jumpstart this "reaction", it seems that over the last years I became more and more "reactive". (neurological kindling?)
Obviously there are hundreds of possibilities or reasons why this could be happening, I stopped looking for answers when it comes to trying to pin it down as it will not get me anywhere.
Is anyone out there who has dealt with something like I am describing and it actually got better just by itself over time or did you do something that helped tremendously?
Thank you,
PS: For me everything started getting worse when I stopped a SSRI cold turkey 4 years ago. I slowly became home- and 80% bedbound and diagnosed with severe POTS, HEDS, MCAD and ME.