I guessed she was on the ASD with your button. They have tested Rees over and over for ASD, but he doesn't fit any of the profiles- PDD, Autism, Aspy. They have finally agreed he isn't ASD, but has sensory issues coupled with severe anxiety and OCD (Obsessive Compulsive just like my DH). The end result is a different label, but some similar characteristics. So we just ignore the labels and do the treatments, therapies, meds, etc that are needed to help out. He's in a fantastic public school system. He is in a regular classroom (he's bright but has LD). He gets pulled out for 2 segments a day for 1:1 (math and reading). Then he is co-taught in the classroom for the other half of math/reading. He gets a special ed Para pro twice a day as well. He also does PT, OT, and Speech twice each weekly. He is very sociable, lots of friends, does great with groups and following directions. Has problems with transitions, loud noises or sudden changes. He's just Rees!
With your DH being gone all the time, I can't imagine how tough it is on you.I am so blessed to have an amazing DH who can be home.
Sometimes I don't want to throw it out there bc I am worried people will judge her or put her in a box that she does not need to be in.
I really don't think Maddy has ASD...I think she is OCD with Sensory Integration Disorder. They said they don't diagnosis OCD till the age of 7 so for now she gets put in PDD NOS. I can't complain though. It has open doors for certain therapies and I am very thankful for that!
It is amazing to see the world through the eyes of a child with special needs. It truly has changed my life and I could not ask for it to be any other way! She was a baby we were not planning to have, she was concieved on an IUD, She was born 8 weeks early and now she deals with all of this. She makes everyday special and I LOVE it!
It is however very hard to not have my husband here. I was so thankful he was here for their surgeries 2 weeks ago. I have done most of their surgeries alone and it was so nice to have someone in that waiting room with me. I was very thankful!
I think it is awesome that you are not sheltering him. There are some parents of kids with special needs that are too worried to take them out and experience all that life has to offer! I think it is great!
This conversation comes at a funny time. This woman I have known for about 5 years now is a friend of mine on facebook. She just sent me a "flair" basically making fun of the "short bus". Huuuummmm, that "short bus" is what Maddy rides to school. It hurt so bad, especially coming from an adult! There are so many things I wanted to say to her but I took the higher road and ignored it. I worry about Maddy and the world she has to grow up in. Sometimes you have to wonder about people! Oh and the best is she goes to my church! GOTTA LOVE IT!
I am so blessed to have an amazing DH who can be home.
? You will have many new friends including myself, I will leave my Cat 12 in a heartbeart 


