Author Archives: littleperson123

Dwarfism Awareness Post # 6 – Saul Wilson Syndrome is caused by a genetic mutation. SWS is a dominant gene and is not something I inherited from either of my parents. That is something that we only recently learned once … Continue reading →

Dwarfism Awareness Post #5: I love this quote because it explains exactly why I am who I am. No matter what I go through in life I always try to stay positive and keep a smile on my face. I … Continue reading →

Dwarfism Awareness Fact #3 I was diagnosed with Saul Wilson Syndrome around the age 4 or 5. When I was diagnosed it wasn’t called Saul Wilson Syndrome it was referred to as the more medical terminology, Osteodysplastic Microcephalic Dysplasia. Back … Continue reading →

October 2nd dwarfism awareness post: Wow it’s been 6 years today that I had my right hip surgery. This was the first surgery that I had gone in a week prior expecting to have surgery and woke up only to … Continue reading →

October is National Dwarfism Awareness month. All month long I will be posting facts about dwarfism or stories about my life. I also share posts on Facebook and if anyone is interested in following me on Facebook my Blog Page … Continue reading →

Seven years ago this month I started writing this blog. On September 18, 2012 this blog became official. That was the year that I offered up my DNA to Dr. Andrew Jackson, from Scotland, the only doctor to ever come … Continue reading →

When I was a teenager and realized my gift for writing, I hoped one day I would write a book and share my story. That thought was always in the back of my mind but I honestly never thought that … Continue reading →

I have been thinking about this post for a while now and wasn’t quite sure if I wanted to write it or how to even express what I am about to say. But thinking it over for a while here … Continue reading →