Biomedical Interventions...

People have assumed that I am against anything Biomedical. That is simply not true... I am against doing these procedures to someone who does not have the voice or the ability to say no. I am against using children as guineau pigs for DAN! Doctors and other medical quacks.
Now, if you as a parent, an adult so to speak, wants to shove a suppository up your butt, feel free. If you want to smear smelly cream on your body, go for it. If you want to put a hood over your head for HBOT, be my guest. If you want to sit in front of a person and be berated with ABA, have at it. If you want to hook yourself up to an IVIG, more power to ya.
I am just against the fact that these innocent children are being subjected to these regimens on the fact that parent's think they will be cured or recovered. Use whatever phrase you want....I do not care.

Our children do all the things regular children do. All but the oldest and youngest have good friends, ride bikes, play at the playground, have sleepovers, ya know...things kids are supposed to do growing up.
Many children spend alot of time at our home. Parent's have no problem in doing so. They know their children are well-cared for and treated well in our home.
Our children are well-respected at school and known as the O'Donnell children. Not the autistic O'Donnell children.

I have been questioned on the fact that we used Occupational Therapies, Physical Therapies and Speech for our children.
That is true...we use OT because they could not use a spoon or grasp a pencil. They needed the deep brushing to calm them down. They needed deep pressure through massage to make them calm. They loved the swinging on the big swing, it seemed to make them come together in their minds. They do not require this anymore. They are now able to calm down with few prompts to take a deep breath.....it works wonders for them.
The PT was for Caitlin and Erin only. They never crawled and had some issues with walking.
Speech for all but one of our children. Although Deirdre spoke very early, she was hard to understand. The others did not get words until later in their little lives. Kiernan is still non-verbal...his speech teacher is using the AudioVox with him....he loves it.
We were blessed with amazing therapists who seemed to really love our children. We have had the same speech therapist for 12 years. We had the same OT for 8 years. She went through all of our children.
These are interventions, yes, but they do not tout to cure autism. They are used to help our children succeed in areas they were not successful in. IT WORKS FOR OUR FAMILY.

I do not see the fascination with our family from a select few. If you visited our house, it really is quite boring. Right now, at this moment, little Patrick is waiting for me to get off of our computer. Kiernan is watching his Wiggles video. Meaghan is singing One Tin Soldier. Caitlin is in her room. Erin is watching Country Music Television with her father. Deirdre is in her room listening to The Beatles-her newest obsession. Later, we are going to a birthday party. Meaghan is going to a sleep-over and Erin is going with the Scouts to gaze at the stars this evening.
This is what works for our family. NORMALCY.....

And on a final note for the evening...our youngest, Kiernan, who has been trying to master a spoon for a long time, finally succeeded. He now can hold a spoon and eat like a big boy. This is a major hurdle for this child. We are so proud of him...I cannot wait to tell his teacher on Monday. She has been working so hard with him on this.