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PETER DOW

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  1. Hi Tina thanks for the welcome. I have been checked out by my GP on several occasions regarding my symptoms. None of the tests I've had have shown up anything to date. That's why I am thinking that the symptoms I am experiencing are due to long-term effects of SAH. It was helpful to read your reply and others on the site. Sounds very much like none of us escape unscathed. Take care. Pete.
  2. Hi my name's Pete, I'm 57. I had a ruptured aneurysm in May 2007 that was treated within 24 hours with coil embolisation. I was very fortunate in not suffering a stroke, as I believe many people do, following a brain haemorrhage. However, I do get tired very easily and don't have anything like the stamina I had before my haemorrhage. Also find it very difficult to deal with stress and become very irritable when I'm tired. Some of my friends have suggested that I might have ME, but I think my symptoms are down to long-term effects of SAH. Anyone else experiencing similar symptoms?
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