I just want some support
Posted: Fri Sep 02, 2011 1:45 am
I am 29 years old and I am amarried with two kids 5and 2. I have OBPI in my right arm. My mom had trouble pushing me out and they were supposed to break my clavical but the pulled to hard and the rest is history I suppose.
I know very little about my condition I just found out what it was called ten years ago. When I was a child we really did not discuss it. I think it was painful for my parents so they never pushed the matter, and I guess I wanted to ignore it so I never asked any questions. Im startng to ask questions now because my son is at the age now where the kids around him are starting to notice and ask questions and I noticed him coming to my defense when certain children are not as sensitive. I don't want him growing up thinking that he has to defend me when kids are being mean.
My approach to dealing with it as a child was trying to be positive. When people would ask me about it I would always say it could be worse I could have lost my arm or could not have been here at all, and then everyone would think I had such a great attitude about my dissability. The truth is sometimes I want to scream and curse, the pain and the sacrifices, and always having to find a trick to doing everyday chores gets to you. Now my child having to feel like he must defend my honor is sometimes too much for me to handle. I guess I just want to vent with people who understand what this feels like. I also want more information on my condition.
For years doctors were misdiagnosing my condition. They called it cerebral palsy, then I even had a doctor put in my file muscular dystrophy(?). Funny enough a OBGYN doctor told me what it was called. When I looked it up I was amazed has to how dead on the symptoms were. I had surgery when I was three to correct what they call "the waiters arm" you know when it is twited to the side but other than that I don't know what else was done or could be done. The only person I could ask was my mom and she passed away and my Dad really doesn't know. I just want to be apart of something that can answer my questions and give me a voice to what no one else seems to understand.
Thanks in advance for anyone that replies to me. I have been reading some other posts and it really feels good to know I'm not alone.
I know very little about my condition I just found out what it was called ten years ago. When I was a child we really did not discuss it. I think it was painful for my parents so they never pushed the matter, and I guess I wanted to ignore it so I never asked any questions. Im startng to ask questions now because my son is at the age now where the kids around him are starting to notice and ask questions and I noticed him coming to my defense when certain children are not as sensitive. I don't want him growing up thinking that he has to defend me when kids are being mean.
My approach to dealing with it as a child was trying to be positive. When people would ask me about it I would always say it could be worse I could have lost my arm or could not have been here at all, and then everyone would think I had such a great attitude about my dissability. The truth is sometimes I want to scream and curse, the pain and the sacrifices, and always having to find a trick to doing everyday chores gets to you. Now my child having to feel like he must defend my honor is sometimes too much for me to handle. I guess I just want to vent with people who understand what this feels like. I also want more information on my condition.
For years doctors were misdiagnosing my condition. They called it cerebral palsy, then I even had a doctor put in my file muscular dystrophy(?). Funny enough a OBGYN doctor told me what it was called. When I looked it up I was amazed has to how dead on the symptoms were. I had surgery when I was three to correct what they call "the waiters arm" you know when it is twited to the side but other than that I don't know what else was done or could be done. The only person I could ask was my mom and she passed away and my Dad really doesn't know. I just want to be apart of something that can answer my questions and give me a voice to what no one else seems to understand.
Thanks in advance for anyone that replies to me. I have been reading some other posts and it really feels good to know I'm not alone.