Post by Bookwormprincess on Jun 13, 2011 21:35:10 GMT
Dear friends,
I am currently helping to design and publish an in-house leaflet for the East Kent Early Intervention in Psychosis Service (EIP) about Postpartum Psychosis. EIP is only 5 years old in my area and 3 ½ years ago I was the first postpartum case they had come across. There have since been 4 other Mums. I would really have benefited from reading something specific about my illness rather than floundering around in the dark for what seemed like ages, even after a diagnosis.
So I was wondering if you could put your thinking caps on and pass on any pearls of wisdom about what you would like to see in a leaflet about PP.
Those of you who have had PP will have insight into the illness and can provide information that you feel would have helped you or helped friends and family understand what you were going through or what you wished you’d have known beforehand (that would be a long list probably!). Those of you who didn’t have PP can imagine what it is you would like to know had you never heard of the illness and were sitting in an antenatal clinic browsing literature, i.e. things to look out for etc.
Every expectant mother needs to be informed about PP, even those who have had another form of PNI with an earlier child because it can happen to anyone whatever their history.
One of the team suggested I include a small excerpt of my story and a photo of myself and the boys but as much as I want to make it personable and something Mums can relate to I am not sure I am brave enough for that . What do you think?
Thanks x
I am currently helping to design and publish an in-house leaflet for the East Kent Early Intervention in Psychosis Service (EIP) about Postpartum Psychosis. EIP is only 5 years old in my area and 3 ½ years ago I was the first postpartum case they had come across. There have since been 4 other Mums. I would really have benefited from reading something specific about my illness rather than floundering around in the dark for what seemed like ages, even after a diagnosis.
So I was wondering if you could put your thinking caps on and pass on any pearls of wisdom about what you would like to see in a leaflet about PP.
Those of you who have had PP will have insight into the illness and can provide information that you feel would have helped you or helped friends and family understand what you were going through or what you wished you’d have known beforehand (that would be a long list probably!). Those of you who didn’t have PP can imagine what it is you would like to know had you never heard of the illness and were sitting in an antenatal clinic browsing literature, i.e. things to look out for etc.
Every expectant mother needs to be informed about PP, even those who have had another form of PNI with an earlier child because it can happen to anyone whatever their history.
One of the team suggested I include a small excerpt of my story and a photo of myself and the boys but as much as I want to make it personable and something Mums can relate to I am not sure I am brave enough for that . What do you think?
Thanks x