I have to say…this is hard for me to write. I am the type to focus on the “how to get
better” and not on the “how did we get here?”
But it is part of Marley’s story, albeit, the hardest part. Was it in my imagination? Was she really the sweet connected baby I
remembered her to be? Did the vaccines
take a toll on my baby? So just today, I finally pulled out the baby videos along
side her vaccination schedule and all the doctor’s notes, sat down with a box
of tissues and pressed play. I needed to
know.
The beginning was wonderful.
She was so cute and responsive.
She made great eye contact. By 10
months old, she was starting to use words like bye bye. Then at 12mos, you can see a bit of a
regression after her 12 month chicken pox and polio vaccines. But she bounced back. She is still looking at me when I call
her. At 14 months old, I watched her
play peek-a-boo with the cat through the window and laugh. I watched her have a pillow fight with daddy
laughing when he called her name. She
was mouthing every toy, but she was still talking. When she started walking at 16 months old,
she was saying mama, dada, papa, bye bye, kitty and a few other words. She was late to walk because her left side
was affected by her brain bleed. But she
did it. She was determined. I looked down at the doctor’s notes at age 15
months. She got a clean bill of
health. She was cognitively behind one
month, but was catching up to her adjusted age.
(She was a preemie.)
Then it happened. At
18 months old, she got an MMR and a DTaP.
That is 3 live viruses and 3 dead ones.
Apparently, her immune system couldn’t take it. It rocked her world. The home videos start to turn ugly. We take her to the beach. She cannot pull herself out of the
water. We try for about 30 minutes but
she just screams and thrashes and heads back to the water.
I keep watching. It seems the
only things that can soothe her are music and Sesame Street on TV. She dances, but no longer dances FOR me. She dances because she is rocking to the
music. She no longer looks at me when I
call her name. The tantrums turn
scary. They go on for an hour or longer
sometimes. We even video taped one. It made me shake all over to hear those
screams again.
Then there is the comment that will stay with me forever. Marley’s nana told me, “I used to come and stay at your house and
listen to Marley babble in her crib for at least 30 minutes in the
morning. Just playing. Just using her voice. Then it stopped. I didn’t hear her anymore”. That was like a knife to my heart. The very true realization that there was nothing. No noise.
Just screams. My baby stopped talking.
She stopped babbling. She stopped
responding to me. She stopped looking at
me. She was gone. It was like someone came and took her voice
away one night as she slept. That was
the day the house went quiet.
Our life was pretty ugly for a while. We endured out-of-body like tantrums. Earth shattering screams. Anything and nothing would set her off. She would hurt herself and others during
these episodes. We took her in for an
EEG to check for seizures. It came back
clean but they said that doesn’t mean she is not having them. It just means they did not catch her in the
midst of one. But the worst is when my
rock of a husband finally caved. He
cried. He NEVER cries. He was so afraid of Marley hurting herself. Then is when we started looking for
help. REAL help. Not medication to drug her up. (Believe me, we were offered the open-ended
Rx of Prozac for my 2 year old.) No….we
needed REAL help. We needed to heal our
baby. That is when our autism road to
recovery began.
Chris was surfing the web and he turned to me and said, “I think I found something.” We watched a video of Dr. Bernie Rimland
talking. He is the founder of DAN! Defeat Autism Now! It looked interesting and it was our best
lead since we walked out the pediatric neurologist’s office just shaking our
heads at the doctor’s condescending mannerisms and offering of Prozac to our 2
year old baby girl. We watched Dr. Rimland some
more. This looked interesting. He was saying that our kids are
SICK. That there are many approaches
like diet and supplements that can help.
Chris said “There is a conference in Boston coming up next month.” I remember saying “I don’t think we can
afford for me to go.” And then my life
partner said to me…”I don’t think we can afford for you NOT to go.” And boy was he right. That is why I married this man. When push comes to shove, he stands up for
what is right…no matter the cost.
I did go to that conference in Boston in 2005. I met other moms with similar stories and
learned their successes. I listened
intently to the most cutting edge science coming out of Massachusetts General
Hospital in Boston. And finally, I cried
because I didn’t realize that her 10 loose bowel movements a day WAS NOT
NORMAL. I cried because I had just
watched my daughter slip away. And I
cried because I was finally getting come answers. My daughter would start to get better. I just knew it.
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