APX GIVES BACK - PWCF CHECK CEREMONY PART 2

Trust the process

So, today has been mentally taxing on me. From finishing up my Summer classes and final tests, to losing a dear, fellow PWS Mom friend, and then taking Cade to his first swim practice for the Special Olympics. I've shared extreme highs and extreme lows today, but as I unwind tonight I feel compelled to share this with whoever decides to read it. Some of you may know this about me, but most probably do not. I have always felt a strong attraction to working with those with special needs. It just always felt right and from a young age I remember looking up local jobs and volunteer opportunities..always searching for something to fulfill that desire. I was actually enrolled in college for Family and Consumer Science and was planning to go into Special Education. I had taken the Parapro assessment and actively looking for Para jobs. Then I became pregnant for Cade and life had other plans. Given my role now to Cade, isn't it ironic? OK, so here is an e-mail I dug up from my in...

Tired and Thankful

I am the parent of an amazing boy. He is 9. He is smart, funny, and happy. I am the parent of a child with Prader-Willi Syndrome... PWS is a complex developmental disability that results from a defect on the 15 th chromosome. Because of an abnormality in the area of the brain called the hypothalamus, these individuals face challenges in learning, behavior and controlling their appetite. The message of fullness never reaches their brain and they are always hungry. The intensity of their food drive can vary but all require support and understanding if/when they are exposed to food or they attempt to seek food. Food security must be considered and provided in all environments and at all times. While I am first Mom to Cade, just as importantly I am his advocate in every aspect of his life for his rare disorder. I am tired. Remaining humble and thankful for all of Cade's progress is so very hard in the midst of advocating. Some days I feel as I...

Ortho and Hippo!

Well, today we had out Orthopaedist appointment to get a baseline treatment for Cade's scoliosis. I was dreading today...so many thoughts. Will I like the doctor? Will they talk about bracing, casting..? I totally did not know what to think. Fortunately, I liked the doctor (For once). He did an x-ray and says Cade has about a 21 degree curve. He says he believes Cade is too little for bracing and that we will keep an eye on him for now. I am fine with that. I do not want to just buy time and chance things getting worse, but I also hope we can stop the progression of the curve with extra PT and core strengthening. It would be so nice for the curve to just not progress and maybe even lessen! The doctor believes we are doing a very good thing by starting Hippotherapy. Today was our second time, and Cade adores the horses. He was so excited to get on! He is so little on that big ol' horse, but he rides so well. Here are a few pics from his first time on the horse.

Our So-Called Life.

Search This Blog