What is SPD? How is it treated? What does it 'look' like? How does it 'feel'? Can it be cured?
These are all questions that run through a parent's mind when their child is first diagnosed with SPD and begin their treatment journey. Hopefully, this page can provide valuable information you'll need and the resources you'll need to connect to.
We'll also include information for those of you who have children you know are struggling but aren't quite sure whether it's SPD or something else. Believe me, alot of us have been there. This page is extremely important to Chynna so she's going to make it her main focus here. If you have a question you want answered or want info up here, please feel free to contact us either through the site or directly to Chynna at lilywolf (at) telus (dot) net. She'd be more than happy to help you get to where you need for the information you're looking for.
Chynna isn't a 'professional' expert (yet!) but she has been there and wants to help in any way she can.
