....and how are you feeling today?
What effect did it have on you when you were told that you have O.S.A.? Was it one of releif or did you panic and are you still shy wearing your mask in front of your family. I dont think that the mental side of this condition has been discussed much on the forum and I would like to know how people have been coping with issues.
For myself it was one of fascination. probably not one of the usual symptoms of being told your ill. Ive always had a fascination of dreams and sleep and to become a subject of it was quite thrilling at first. Mentally I beleive that I have conquered this condition and now class myself as cured. I have been through most of the psychological issues of osa and learnt to control them except one! Earlier this year I had to rush down to England to my fathers bedside in Boston hospital, where I got to spend 2 hours with him before he died. My father had Lung cancer and when I arrived at the hospital he was on pure oxygen with a fullface mask and struggling to breath, to say I was devasted 2 hours later was an understatement. I had lost my friend and my father.
So now 10 months on, everytime I don my mask, I see my father lying there dying with his mask on stuggling to breath. (Still hurts 10 months on)
I would think that I am not the first person to have psychological issues with osa. I beleive that one day it will fade and when I put my mask on, I will see my father smiling back at me, giving me cause to smile instead of the pain I get at the moment.
I beleive I am one of the lucky ones in the uk because when I visit my clinic we have a chance to talk about issues such as these and the staff are always there willing to listen and to give advise. My issue is a problem for my osa but not with my health as I beleive it to be a healing process.
I think that there are issues out there that are not addressed with osa and like mine some will be painfull and some will be uncontrolable (mask removal) but I urge anyone going through problems like these and ones that are not mentioned is to talk, to find a way to open up and tell someone because it does help you in the long run.
I have named my problem as "Psychoapnea" and beleive that it is a real condition and it should be discussed more openly on the forum, all it needs is you to take that first step like me. It wont be met with ridicule or laughter just a sympathectic ear and hopefully sound advise and if being open for you is too much at the moment then please feel free to PM me and if I can, I will gladly help in anyway I can. Dont suffer in silence, like me.
Graham
What effect did it have on you when you were told that you have O.S.A.? Was it one of releif or did you panic and are you still shy wearing your mask in front of your family. I dont think that the mental side of this condition has been discussed much on the forum and I would like to know how people have been coping with issues.
For myself it was one of fascination. probably not one of the usual symptoms of being told your ill. Ive always had a fascination of dreams and sleep and to become a subject of it was quite thrilling at first. Mentally I beleive that I have conquered this condition and now class myself as cured. I have been through most of the psychological issues of osa and learnt to control them except one! Earlier this year I had to rush down to England to my fathers bedside in Boston hospital, where I got to spend 2 hours with him before he died. My father had Lung cancer and when I arrived at the hospital he was on pure oxygen with a fullface mask and struggling to breath, to say I was devasted 2 hours later was an understatement. I had lost my friend and my father.
So now 10 months on, everytime I don my mask, I see my father lying there dying with his mask on stuggling to breath. (Still hurts 10 months on)
I would think that I am not the first person to have psychological issues with osa. I beleive that one day it will fade and when I put my mask on, I will see my father smiling back at me, giving me cause to smile instead of the pain I get at the moment.
I beleive I am one of the lucky ones in the uk because when I visit my clinic we have a chance to talk about issues such as these and the staff are always there willing to listen and to give advise. My issue is a problem for my osa but not with my health as I beleive it to be a healing process.
I think that there are issues out there that are not addressed with osa and like mine some will be painfull and some will be uncontrolable (mask removal) but I urge anyone going through problems like these and ones that are not mentioned is to talk, to find a way to open up and tell someone because it does help you in the long run.
I have named my problem as "Psychoapnea" and beleive that it is a real condition and it should be discussed more openly on the forum, all it needs is you to take that first step like me. It wont be met with ridicule or laughter just a sympathectic ear and hopefully sound advise and if being open for you is too much at the moment then please feel free to PM me and if I can, I will gladly help in anyway I can. Dont suffer in silence, like me.
Graham
I beleive that its these kind of stories that give you hope, I never got a eurika moment it just gradualy got better. I know for me it will get easier as in the past few years I have lost so many people, my son, my grandson, father in-law, Mother in-law, brother and sister in-law and now my dad. I was quite thankfull of the nightmares that I missed but yet again I will overcome my grief and the passing of someone close but enough of me.....
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