05-09-2014 08:20 AM
05-09-2014 08:20 AM
Yes, the extreme stress and burn-out that accompanies the role of fulltime carers is, like mental illness, invisible to others. Not like a broken leg, using a walking stick, being in a wheelchair. What people can't 'see' (or experience) they don't understand.
So often, carers are the ones who discover their loved ones in their own homes after an attempt to take their lives. Ambulances are called, then the police, then the loved one is rushed to hospital and the carer is left alone in the house to clean up the mess. They send counsellors to counsel witnesses at the scene of serious accidents these day. Why doesn't this happen in cases such as this?
08-09-2014 07:44 AM
08-09-2014 07:44 AM
Yes,I've been through that.Got it from withdrawal from withdrawal..It was a withdrawal symptom that flared up regularly.I know several people who have had the symptom as their longest ongoing symptom.You can look in the mirror and not see yourself.Its a weird illusion.
When did you first experience dr/dp? Some people call it derealisation/depersonalisation.
08-09-2014 07:34 PM
08-09-2014 07:34 PM
I experienced it for the first time many years ago when my son kept trying to take his life. It was a shocking time. I experienced it for quite a while before deciding to see a doctor. Got no help whatsoever.
08-09-2014 07:37 PM
08-09-2014 07:37 PM
Mine got so bad that I started to discover I was doing things like driving on the wrong side of the road and driving through red lights. It's a very scary state to be in.
08-09-2014 07:44 PM
08-09-2014 07:44 PM
09-09-2014 12:56 AM
09-09-2014 12:56 AM
11-09-2014 07:01 AM
11-09-2014 07:01 AM
13-09-2014 10:09 PM
13-09-2014 10:09 PM
13-09-2014 10:12 PM
13-09-2014 10:12 PM
14-09-2014 09:18 AM
14-09-2014 09:18 AM
Cazzie this really resonates with me - I am 71 and I often get the same symptoms - most markedly when I am with the son with Schizophrenia for whom I am Carer - if he is angry, tetchy, stressed the effect on me is to be unable to summon up information I know - a name, date etc - I assumed it was age-related and a sign I was losing it in general. I really believe that it is stress-transference more than memory-fail.
I accept that memory diminishes with age but if I have the same lapse when I am on my own and un-stressed I consciously do not panic and tell myself that if I don't make it worse by agonizing over it, the memory will come and it invariably does.
I have been a member of ARAFMI for years and it is common for members to say that their loved ones can "hold themselves together" in a medical/psychologist interview and even say that they are fine and doing well - when the carer is very aware that this is not so - anything to avoid going to hospital or maybe "losing face". ?
As for other people judging how "well" or "ok" our MI loved one really is - I would love them to just take over the caring task for a month at least - the saying "walk a mile in my shoes" comes to mind
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