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I am the person who started this thread anonymously 6 months ago. I have 3 sons, one who is 10 with ADHD. My now five year old had a diagnosis from a mental health agency since age 2 of ADHD, possible mood disorder, and developmental/language delay. For almost 3 years we worked with speech, early intervention, occupational therapy, neurological pediatricians, a TSS (therapeutic staff support), a behavioral specialist, and more. I was giving up hope and that's why I posted the thread. You know the saying, "if I knew back then what I know now", well it means a lot to me. The only change in my pregnancy was the Lovenox... I am not necessarily saying this caused his problems, but I do believe that it did influence them. We have so many days of ups and downs, our son is special and very difficult. My youngest son was/is showing my 5 year olds previous and current behaviors, so I was really frustrated when posting the thread. After posting the thread, I decided to take him to a different mental health agency. Now after only 6 months we have a new diagnosis' they are PDD/NOS (Pervasive Developmental Disorder Not Otherwise Specified), ADHD, mood disorder, and ODD (oppositional defiant disorder). All opening up a new category of medications available to him. We have mood stabilizers and the difference is like night and day, we still have a few rough days, but most now are "manageable" compared to what we were going through. I think the main thing I am trying to get at is try to do as much research on medications you take, and be prepared for things to be turned upside down at any given time. Always be prepared for anything. Now that we went through the things with my 5 year old, my 3 year olds "common" behaviors are easily remedied since we have "been there and done that". Mom's/ parents are the only people that truly know their children. Most times, we spend the most time with them, more than doctors or specialists that only spend a few hours with them, the important thing to do is find a doctor/specialist that is really going to listen to you. You are your child's advocate and if things are not good for him, then something needs to be done. My son was always sad and mad and on the emotions rollercoaster and never had control over his actions/ body. Now, he is able to tell why he feels things the way he does and seems happier. He is able to control himself now, which gives him satisfaction and the ability to succeed at new things introduced to him. Good luck with your 3 year old, and I hope this has helped.
I was told with my second son that I had a protein S defiency, so my Ob/GYN put me on lovenox. My son has autism, he shows signs after his first birthday. My first son I took nothing and he is healthy. My third son I took nothing, after and he is completely healthy. I wish the same think that I didn't take it. Maybe our lives would be different. I know in my heart it isn't genetic. I found out later that all women have some protein S defiency when pregnant and I didn't need to take it. My heart is sicken and sad and I think drug companies want to make our kids sick, so that can profit off it.
I took Lovenox with both pregnancies but for the whole pregancy with my six year old. It's getting harder and harder to want to get out of bed in the morning because I hate waiting for the episodes to start.
I too was on Lovenox for 32 weeks during my pregnancy and 6 weeks post pardum. My daughter is 21 months old, and is showing signs of PDD-Autism. I was told that I have protien s deficiency while i was pregnant and the clotting factors in my blood were too high. I honestly think baby asprin would have done the job, by I took the advice of my OBGYN and stuck with the injections. I feel awful that this could have been prevented if thats the case. My daughter does not play with other children, didn't walk until she was 16 months old, DOES NOT talk. she doesn't eat with a spoon, she doesn't play normally with toys. She would rather play by herself that with ANYONE else. She is a only child and we are wanting to try to have another, but I am scared to death that this could happen again. I love my child, and want nothing but the best for her, I am not sitting here crying because she could be autistic. I want to find out for sure and start working with her, so that she can lead as much of a normal life as she can. I am also glad to know that I am not alone in the thought that the Lovenox is the culprit.
My son, 3rd child is 3 1/2 and has severe speech delay and probably on the road to ADD or ADHD. My eldest daughter who is 8 and didn't take Lovenox with is a great student . Our experiences seem really too similar and scary! I hope you get this post. My heart dropped when I found these posts. Please let me know if you have found out anything.

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