Most people have never heard of Turner Syndrome (TS).
I certainly had not.
But a few years ago, Blogging Friend and DT buddy, Lori Kobular, began sharing about her loving vigilance in caring for her Turner Syndrome (TS) daughter.
I was deeply moved, not only by the quiet manner in which Lori is always helping others and advocating for them, but also by her family and their devotion to one another.
Hi. My name is Donna. Lori and I have become united in a desire to bring an awareness about TS, and vital information to others, by creating this blog and organizing a blog hop with many of our creatively supportive friends.Our blog is not clinical - it's meant to bring information in an easy-to-use, easy-to-read format.
The TS Awareness blog hop is intended to educate people about TS and how it affects girls and their families. Turner Syndrome affects one girl in every 2000-2500. For a quick pictorial look, please see the "about" tab at the top of this blog. There are also buttons in the side bar linking to the TS Foundation and other organizations.
To me, it is nothing short of miraculous that anyone can live missing their 2nd girly X chromosome. Truly magical in a stardust sense!
To me, it is nothing short of miraculous that anyone can live missing their 2nd girly X chromosome. Truly magical in a stardust sense!
A note to Blog Hop designers:
Please read the "DT Guidelines" tab at the top of the blog.
We cannot thank you enough for your kindness in helping spread the word.
AND LEARNING!
Lori and I would love hearing from you. Please leave a comment about your questions or thoughts. We will do everything possible to get back to you. Lori's email address is
Thank you!
