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I am a special needs mom to two boys with Autism. I enjoy using new products and sharing my thoughts. I love all sorts of new technology. I have previously done this type of work and shared my experience and did a lot of book reviews. I'm excited to restart this endeavor.
July 2nd, 2004, we closed on our house! NINETEEN years. On the one hand, it seems so long ago. On the other, it seems like just yesterday. The process of building this house was challenging in that we were dealing with Caleb's OCD tendencies, and we didn't really know what we were dealing with. He got so fascinated with garages at that point that if we didn't say "Goodbye" to the garages, it resulted in a full-on meltdown. One day we were going to church, but because we turned in the opposite direction of where we would go to the house, he had a meltdown because, in his mind, we were going to the house. We returned home instead of going to church. It still took us five years to get an accurate diagnosis for Caleb.
I know it's been a while since I've posted, once again. It seems that my blog is always the thing that always gets pushed to the back burner. No matter how much I want to keep it at the forefront, it never happens. I'm just usually too tired at the end of the day to do anything with it. Also, I'm trying to launch my Rodan+Fields business, so that's been taking a lot of my time. [ 531 more words ] http://twospecialneedschildren.com/2017/07/22/update-2/
The last year with Caleb has been very difficult. There haven't been a lot of smiles. There's been a lot of tears, yelling, and screaming. But, last night, I saw more smiles on his face than I have seen in a long time, and it was all thanks to Night to Shine and the Tim Tebow Foundation! I have wanted Caleb to be able to participate in this program since I have heard about it, but as with anything, Tony and I just never know how he is going to do. [ 266 more words ] http://twospecialneedschildren.com/2017/02/12/night-to-shine-2017/
The last year with Caleb has been very difficult. There haven't been a lot of smiles. There's been a lot of tears, yelling, and screaming. But, last night, I saw more smiles on his face than I have seen in a long time, and it was all thanks to Night to Shine and the Tim Tebow Foundation! I have wanted Caleb to be able to participate in this program since I have heard about it, but as with anything, Tony and I just never know how he is going to do. [ 266 more words ] http://twospecialneedschildren.com/2017/02/12/night-to-shine-2017/