
Supported Employment: The End of an Era
7 months ago


 to visit my parents on July 3rd and will be there for 7 weeks so I have been trying to get stuff ready for that trip. It is really hard to pack for Alaska you never know if it is going to be in the 90's or 50's. And what would you know, Ella has outgrown most of her clothes, at least her pants. It's been a little sad getting ready for this trip, it will be our last long summer in Alaska as we are all moving to Washington next year. I always thought I would be moving back to Alaska, I absolutely love it there. It's funny how things change. My mom has for as long as I can remember had the "everything happens for a reason" attitude, it used to drive me so crazy. As I get older though, especially since Ella has been born I guess I can see what she has meant. Every event in my life has prepared me for where I am. It is so weird, when I first had my quad-screen at 16 weeks pregnant and it came back with a 1 in 201 chance of Down syndrome, I was crying on the phone to my mom. She said " I hate to say this, but if I could ever imagine anyone with a special needs child it would be you." and she said " I always knew you would do something with children." It's interesting because I could totally in vision myself adopting or fostering a child with special needs, but was completely devastated when I had Ella. I guess because it wasn't on my own terms. Anyhow, back to the everything happens for a reason..... I think that moving to Spokane, which is basically because it is better for Ella, will be better than had we moved to Alaska for all of us. My parents are very excited to be moving and starting over again, and Spokane just seems to fit into all of our life styles better. It is so strange though to sit back and think about what you had just a year ago thought your life path was and to see what it is now, but hey "everything happens for a reason" right???? Here is a pic of Ella's favorite thing to do with her dress, EAT IT!!!!
 to visit my parents on July 3rd and will be there for 7 weeks so I have been trying to get stuff ready for that trip. It is really hard to pack for Alaska you never know if it is going to be in the 90's or 50's. And what would you know, Ella has outgrown most of her clothes, at least her pants. It's been a little sad getting ready for this trip, it will be our last long summer in Alaska as we are all moving to Washington next year. I always thought I would be moving back to Alaska, I absolutely love it there. It's funny how things change. My mom has for as long as I can remember had the "everything happens for a reason" attitude, it used to drive me so crazy. As I get older though, especially since Ella has been born I guess I can see what she has meant. Every event in my life has prepared me for where I am. It is so weird, when I first had my quad-screen at 16 weeks pregnant and it came back with a 1 in 201 chance of Down syndrome, I was crying on the phone to my mom. She said " I hate to say this, but if I could ever imagine anyone with a special needs child it would be you." and she said " I always knew you would do something with children." It's interesting because I could totally in vision myself adopting or fostering a child with special needs, but was completely devastated when I had Ella. I guess because it wasn't on my own terms. Anyhow, back to the everything happens for a reason..... I think that moving to Spokane, which is basically because it is better for Ella, will be better than had we moved to Alaska for all of us. My parents are very excited to be moving and starting over again, and Spokane just seems to fit into all of our life styles better. It is so strange though to sit back and think about what you had just a year ago thought your life path was and to see what it is now, but hey "everything happens for a reason" right???? Here is a pic of Ella's favorite thing to do with her dress, EAT IT!!!!





 I was not aware until recently that not all insurance companies paid for the triple or quad screen, apparently it was just covered for those who had a greater risk of at risk babies, due to maternal age etc. My insurance had paid for it with both of my pregnancies, thought I didn't have it with my first pregnancy. Anyhow now all insurance companies have to cover the cost of this test. The current statistic is that around 92% of couples who have a prenatal diagnosis of Down syndrome abort their baby. It makes me sick. After my quadscreen I was told that my baby had a 1 in 201 chance of having Down syndrome. That is a half of a percent. At my age, 25 at the time, my normal chances were 1 in 1200. After a level 2 ultrasound showed no markers for Down syndrome the doctor assured us that our baby was "normal." We could have opted for an amnio but the doctor told us there was a 1 in 200 chance of a miscarriage, which of course we didn't want to chance. I was angry after Ella was born that the doctors had been wrong, and wished that I had known that she had Down syndrome. But I now know that it was definitely best for me that I didn't know. I like to think of myself as a planner, like I HAD to know with both of my kids if they were a boy or a girl so I could prepare for them. So, here is what would have happened if I had known Ella had DS, I would have been on the Internet seeking information non-stop. I would have found all of the medical problems that she could have, and how incredibly delayed she could be. I would have been a wreck. Maybe I would have been better when she was actually born, but I doubt it. I also firmly believe that had I known Ella would have been born way more premature than she was since they told me she was premature because of my stress as it was.
 I was not aware until recently that not all insurance companies paid for the triple or quad screen, apparently it was just covered for those who had a greater risk of at risk babies, due to maternal age etc. My insurance had paid for it with both of my pregnancies, thought I didn't have it with my first pregnancy. Anyhow now all insurance companies have to cover the cost of this test. The current statistic is that around 92% of couples who have a prenatal diagnosis of Down syndrome abort their baby. It makes me sick. After my quadscreen I was told that my baby had a 1 in 201 chance of having Down syndrome. That is a half of a percent. At my age, 25 at the time, my normal chances were 1 in 1200. After a level 2 ultrasound showed no markers for Down syndrome the doctor assured us that our baby was "normal." We could have opted for an amnio but the doctor told us there was a 1 in 200 chance of a miscarriage, which of course we didn't want to chance. I was angry after Ella was born that the doctors had been wrong, and wished that I had known that she had Down syndrome. But I now know that it was definitely best for me that I didn't know. I like to think of myself as a planner, like I HAD to know with both of my kids if they were a boy or a girl so I could prepare for them. So, here is what would have happened if I had known Ella had DS, I would have been on the Internet seeking information non-stop. I would have found all of the medical problems that she could have, and how incredibly delayed she could be. I would have been a wreck. Maybe I would have been better when she was actually born, but I doubt it. I also firmly believe that had I known Ella would have been born way more premature than she was since they told me she was premature because of my stress as it was.

















 
 
 
