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A Mother's Start to Biomedical Treatment

Mar 07

by Tracy Weinstock on 7 March 2012 in , , , , with 3 Comments

My name is Tracy, and my son Aidan and I became part of the Generation Rescue Grant Program in January 2012.  Aidan is our poem, our puzzle, our heart, and none of us can take our eyes off him until autism gives back what it has taken from him. On the surface, we are a mom, a dad, and three amazing boys age 14, 5 (Aidan), and 3. Like many parents, we are trying frantically to keep some semblance of normalcy for our children while the economy and autism shred everything but love and hope.  

We want to share our story with you, and that is terrifying for me, because I don’t know how the story ends yet.   So, instead of starting our story at the beginning where everything was sad and scary and we  were lost, I’ll start with simply how we got to today because today is clear and we have our destination in sight.  

Autism is a long twisty path with lots of dark places and just enough bright spots that we have the courage to keep traveling.  When we get lost, we choose a path and stick to it and hope that it leads us to where we belong.  

Three years ago my house was much too quiet, and I hoped and prayed just to hear Aidan’s voice.  It took months of therapy, but he finally gained a few words and his voice was musical.  I began hoping he would learn to put words together.  When he began putting  2-3 words together , I began hoping  he would learn to tell me what he wanted.  Finally, one day he could.

Two years ago, I began hoping he would learn to ask questions, use real sentences, tell us he loved us.  It happened.


Last year, I began hoping someday he would be able to tell me about his day.  The first time he did, I had to pull the car off the road to hug him. 

 

Two months ago, we joined the Generation Rescue program and  I started hoping that if  we could just figure out how to clear the fog that seems to cloud him, he would learn to carry on a meaningful conversation. 

 

Today my little boy told me he loved me,  what he did at school,  what he wanted to do on the weekend,  asked me about my day, won an argument with his brother, asked me questions while I made dinner, looked deep into my eyes and laughed.  

 

And, for once, I knew I could hope for anything.

 

Can I say he is recovered?  Not by a long shot.  But I know he will be.  He is fighting his way back  and we only just started down this biomedical path.  Every word, every milestone, every glance until now has been fought for so hard and so long.  There have been countless setbacks.   

 

I wonder where we would be today if we had found this path years ago, had known we could try to heal his damage instead of only trying to overcome it.  Watching him swing through the effects of the diet change and supplements has been scary.   There have been days that he is completely lost, running and pacing, talking to himself and I am terrified I am losing him even more. 

 

Trying to heal Aidan feels like being in the ocean, trying to keep his head above water.  No matter how hard I  hang on to him, sometimes a wave crashes over him and I have to just hang on tighter and help him surface.  I'm terrified he won't come back up.  The beautiful thing is that each time he surfaces now he seems clearer, more relaxed, more connected.  I like to think that one day soon we are going to ride a wave safely to the shore.


I am so grateful to be able to share this journey with you, and hopefully reach out a hand to someone who might feel lost.  

About the Author:
Tracy Weinstock, Mommy to 5 year-old Aidan who is currently participating in our Rescue Family Grant Program.

 

If you are interested in trying biomedical treatment learn more about our grant program here.

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Comments

  • What a blessing these things are to us who wondered if they would ever be.... Yes, Amy, that is so true. Your comments about your son's wonderful life gave me one more reason to hope for anything! Playing with friends, success at school..living the dream

    Posted by Tracy Weinstock, 13/03/2012 4:35pm (1 year ago)

  • Tracy, I'm so happy to hear of all the wonderful improvements. I look forward to reading more from you, go Aidan!

    Posted by Marissa Bagshaw, 12/03/2012 6:58am (1 year ago)

  • That brought tears to my eyes... yes, with prayer, hope and love you will continue to be led in the right direction, and then your son's own strength will pick up where yours feels it is fading. My son was so much the same way and now he is on the A honor roll in a very challenging private school (mainstream), plays football with friends on Sundays (though he's more gifted in areas other than sports) and is funny, well spoken and loves to read.
    He just completed six level one swimming lessons and I was the only mom there who choked back tears during each one, thinking how I remember, not so long ago, that if he'd just say 'I love you' I would be the happiest mom on earth. And here he was in swim class, following instructions and almost 'normal' - as they say. At this point (age 11) he still stims and stammers a little from dyspraxia but otherwise it's not easy to pick him out of a crowd as different. And the ways he is different, well, some drive me nuts but I can ask him to tone it down and he does... others are the traits that most say make him charming.
    With his supplements and our mostly organic (as much as we can afford) diet. we're keeping his body on track.
    I just want you to look forward to the many, hundreds of tears you'll cry in the future for the yet-unknown new things your son will try and do successfully, just as telling you about his day. What a blessing these things are to us who wondered if they would ever be.

    Posted by Amy Wilkins, 09/03/2012 1:49pm (1 year ago)

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