October is Down Syndrome Awareness Month and it is also Right To Life Month.
Jim and Alex came home from Mass today and Jim told me that
the priest spoke about Right To Life month.
He spoke about a little girl born with Trisomy 18 and how she has beaten
the odds. She is now 4 years old. Most babies with that do not live very long
and most parents are advised to terminate a pregnancy if it is found out in
utero. I am sure the doctors would say
something like “Why would you put yourself and your family through that only to
have the baby die shortly after birth, it would be best to take care of this
now”.
I have heard story after story of families that have learned
their unborn baby has Down syndrome and be told “It couldn’t be any worse news”
or “this baby will be a burden to you and your family” or “they will never
learn how to ride a bike or walk” or “you won’t ever go on vacation again”. When Alex walked in the door this morning
after Mass, the thought ran through my mind—“how could anyone look at him and
think that he should not have been born?”
Because that is the reality of it------this child that I
carried for nine months, gave birth to, nursed, feed, clothed and cared for the
last 16 years--- some other mom may not have wanted. I was never given a choice because I didn’t
know before he was born, but I wouldn’t have done anything differently. I still would have had him, loved him and
fought for him even if I knew before he was born. Sure—I would have been scared, just like I
was when he was born, but I still would have loved him.
When I look at Alex, I don’t even see Down syndrome. It is not who he is. It is just a part of him. So, when Jim and Alex told me that they were
talking about Down syndrome in church today, it kind of took me aback…I had to
think a second and realize that it was about him.
Alex's Justin Bieber look |
Laurie, I'm so glad that you're sharing your story and I will follow each and every writing. You are such an amazing woman and a wonderful mother. I'm sure your stories will inspire and encourage others.
ReplyDeleteThank you so much Karen! I just want parents to know that the future isn't so scary.
DeleteI've come over from Ben's Blessings. I look forward to reading about your family. I'm glad to see another blog about adults with Down Syndrome!
ReplyDeleteHi Cindy! Thank you!
DeleteStopping in from facebook to say hello. I also have a teen w/Ds. Reagan is almost 18 y.o. and the light and delight in my life.
ReplyDeleteNice to "meet" you!
Hi Amy nice to meet you and Reagan too!
Delete