Hello my name is Crystal and I am the mother to two healthy baby boys, 8 year old Naziir and 8 month old Ahmiir born on July 12, 2016. Both of my pregnancies were very normal both boys were delivered by C-section. I was healthy and active before my kids were born. While pregnant with Ahmiir, all of my scans were normal no problem with the baby was detected so it was a total surprise to all of us, including the doctor, when this little guy came out missing his left hand.
Hello! My name is Taylor, and I’m Jay’s mother. In November 2015 I found out I was pregnant. We were excited and anxious like most first time parents are. We found out (early) that we were having a little boy! We had a pretty uneventful pregnancy up until our anatomy scan. At our anatomy scan we were told they found an extra membrane near our baby boys head and referred us to a specialist. We met with the specialist who told us he had Amniotic Band Syndrome.
When I was born, my left hand had no fingers, just nubs. My name is Kelsey. I am almost sixteen years old. After I was born the doctors did not really know what was exactly wrong with my hand. I was admitted to a children’s hospital as soon as a day old. I had a total of two surgeries. My first surgery was at the age two, they took bones out of my toes to put into my hand. I had to learn how to walk on my feet afterwards.
Hi, I’m 34 and have ABS involving just my toes. I grew up never knowing the cause, my parents were never told. They said it was because I stuck my feet through the amniotic bag and my toes were lost. As I got older I knew that wasn’t true and with the internet available I did my own research and finally know the cause is Amniotic Band Syndrome. I always hated my feet and do envy people who walk about in sandals.
Now I am less self-conscious but still won’t walk barefoot in public.
We had a 20-week ultrasound done and they found a two vessel cord and we were sent to a specialist to make sure that there was nothing more abnormal that they weren’t seeing. When we saw the specialist they noticed that our little girl’s fingers were not separating and they could not see all the toes on her left foot and no toes on the right. We were told that we just needed to wait until she was born to really determine what was going on as the ultrasounds couldn’t really tell us everything.
My son, Oliver was due on 6/11/15. Our pregnancy got complicated around 18 weeks, when the amniotic banding was first detected in an ultrasound. From then on, my husband and I were warned to be prepared for our son to be born with a missing limb and the fact that my amniotic sac had been “weakened” so my water could break at any time starting at 18 weeks.
We went to weekly or biweekly ultrasounds and they tried to monitor where the banding was,
My pregnancy was like any other pregnancy until my 20-week anatomy scan. We found out that our baby boy had Amniotic Band Syndrome and would have only half a portion of his right arm and a full left arm. I, like many others, had no idea what amniotic band syndrome was and had never met anybody else with it.
I was initially sad, fearing the torment and all the things he would not be able to do. Of course, everyone who is not going through it has encouraging words,
After trying to conceive for over 6 years, my husband and I found out in October 2015 we were finally expecting. This was the happiest day of our lives thankfully our prayers had finally been answered. We followed every doctors appointment with extreme excitement hearing our blessings heart beat and seeing them in many ultrasounds but all of that changed on Feb 6th, 2016.
We went eagerly to our 20-week anatomy scan hoping to find out if we would be having a beautiful baby girl or handsome baby boy.
This is my baby Kyren, he was born without his left hand. When I went in for my 20 week ultrasound I was told there was something wrong with him. I went to several different doctors and had multiple tests and ultrasounds done, after all those I was told his left arm didn’t develop all the way and he would be born without his hand. I was so worried and scared.
Once he was born, the moment I laid my eyes on him I saw no imperfections whatsoever he is perfect.
He was born without feet and missing some digits on his hands. Elijah is growing up in a baby house with other younger children with a variety of special needs. If Elijah were born in a loving family he would thrive and grow up to live a full life, never seeing what makes him special as a disability or a limitation. His caretakers at the orphanage take good care of his needs but nothing compared to what he could receive in a family.