These past few months have been a whirl wind of emotions, changes, gains and losses and its been so hard to be as consistant about my blog posting as I normally was. So to my readers :) I apologies for leaving you in the dark lately. It was not done intentionally but rather because there arent enough hours in my day :).
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- More words to his vocabulary ( May I have, Can I have, DoYou want, Can He go ect)
- Plays pretend with his toys daily
- Can tell someone when he needs to go 'pee'
- Better progress with remembering activities from the day before
- Can tell me what my name is(Identify his mothers name)
- Is no longer constipated on a daily basis :)
- Sat still with out crying while his dad cut his hair!!!!
- Received his MB12 injection from his dad while he was awake w/out problems!
- And just this evening, he sat next to me and told me ever so non chalant " I like your nails Mommy" and went back to watching Scooby Doo!!
All I can say is, since March of this year when we originally started Our new Journey of Hope, my son has made HUGE amounts of progress, and I can say with out a shadow of doubt that its all because of the biomedical treatments he is receiving. I can't speak highly enough about his DAN doctor, Dr.Schneider. She is the first doctor that listened and actually agreed with me, that my son was sick and needed help, and she was going to do whatever she could to help him feel better. Dr. Schneider and her staff are fabulous and I would recommend them to anyone in AZ.
Being on this Journey of biomedical treatment is not always so easy. I knew that I would have to listen to harsh critisizm about my sons treatments but I never truely thought it would be as harsh as it has been sometimes. Its sad because people just don't think before they speak sometimes. Having a child with autism, can be an overwhelmingly emotional thing sometimes, and when you have friends or family who say unexpected, uneducated remarks to you, it hurts deeply.
Sometimes, I really have to control myself to not get upset with the nay sayers of my sons progress and treatments. Its hard to hear from friends or family that what you think or what your doing, is not valid. Or worse yet they will say things like "How can I be so sure that it was the vaccines that did this?" Or better yet " Where's the scientific proof?"
To be honest, I'm tired of accepting what our society, or rather I should say our Government... is doing for our kids, which is NOTHING!!!
I won't go down quietly or with out a fight anymore... I will continue to be voice my opinion on what happened to my child LOUDLY... I won't be quieted, I will fight for my childrens rights, especially for children with autism.... I will fight to my last breath for my children and I will continue to say .......
I won't go down quietly or with out a fight anymore... I will continue to be voice my opinion on what happened to my child LOUDLY... I won't be quieted, I will fight for my childrens rights, especially for children with autism.... I will fight to my last breath for my children and I will continue to say .......
HOW MUCH LONGER, will we have to wait!!!!!
And to anyone out there who poses this question to me again " Where is the scientific proof?"
This will be your answer ......
I HAVE ALL THE SCIENTIFIC PROOF I NEED... AND HIS NAME IS MATTHIAS :-)
Much Love,
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