Hello people, glad you're all here, reading this thing that is not a chapter. Don't worry, I am working on a chapter for all of my stories, but I found something that I felt I should post about in hopes of spreading the word. What could that thing be? Treacher Collins Syndrome.
This syndrome affects the development of tissue and bones in the face. Some of symptoms of this syndrome is underdeveloped facial bones, a very small jaw and chin, and sometimes even a cleft palate. These are just a few of the symptoms, but I won't go into anymore detail than this.
The reason I brought this up is because recently on gofundme, a site I occasionally use, and came across Abigail Lynn, a 6 month year old baby born with this syndrome, and it was not detected in the amniocentesis or the ultrasound. When she was born the adoptive mother left the crying, and wasn't heard from again. Now the mother can't go back to work fulltime, and needs help, and is hoping to raise 20,000$ to care for the baby.
I'm posting this in hopes of helping this mother and her child. I don't know if it will actually work, but if you get the chance, go to and donate to help this little girl, or anything on there you want to donate to. You can donate on , in case you weren't exactly sure where to donate.
Well, that's it for this little note. I hope you all can understand why I posted this.
Anyway, bye.
