What is Quill?
Quill.org engages students in the writing process through web-based learning activities that teach valuable grammar, vocabulary, and writing skills. It is very similar to NoRedInk and Edmodo's Snapshot feature because you can each activity addresses, measures, and provides feedback on how students met or did not meet specific Common Core State Standards.
Why Quill?
Quill is a non-profit organization, which has designed over 150 activities for elementary, middle, high school, and college students. Each activity takes approximately 10 - 15 minutes and is the perfect tool for warm-up exercises in 1:1 classroom environments or whole class activities. The best part is that students receive instant feedback, which is extremely helpful!
A teacher dashboard provides specific data used to pinpoint areas of strength and weakness. Want to see it in action? Check out the demo teacher dashboard to see it in action!
Need Help Getting Started?
Quill provides numerous tools for teachers to effectively set-up and use Quill in the classroom. Check out the Teacher Resources section filled with how-to-videos, instruction manuals, and tips.
There is even a Getting Started handout for students, which is perfect because there is very little that you have to do as a teacher!
November is Click's for a Cause Month!
For the past three years, November has been "Clicks for a Cause" month. Every time that you visit my blog during the month of November, I will contribute a penny towards the medical fund of a child in need. Here are past beneficiaries of this project.
For the past three years, November has been "Clicks for a Cause" month. Every time that you visit my blog during the month of November, I will contribute a penny towards the medical fund of a child in need. Here are past beneficiaries of this project.
Addison Mae Jacobs was born on January 13, 2015, 4 weeks premature. She was born at only 6 lbs 5 oz and 17.5 inches long. On October 27, 2015, she was diagnosed with Shwachman-Diamond Syndrome (SDS), a devastating disease impacting only one in a million children. SDS is a rare autosomal recessive disorder characterized by exocrine pancreatic insufficiency, bone marrow dysfunction, leukemia predisposition, and skeletal abnormalities.
Addison is currently being seen by nine different medical specialists and her family is coordinating her care between Penn State Hershey Medical Center and Children's Hospital of Philadelphia. There are many expensive surgeries, tests, and medical costs in her future. Due to the costly nature of her care, travel expenditures and having to take significant amounts of time off work, her family has setup a GoFundMe account for Addison, as well as a support page to show updates and her progress.
How Can I Help?
I will be donating a penny for every visit to this blog during the month of November. Are you willing to help too?
- Visit this blog, pray, or spread the word about Addison!
- Become a Coffee Partner and spare $5 to contribute to Addison’s GoFundMe page. Use the #clicks4acause in your message to the family!
- Become a Dinner Partner and spare $25 to contribute to Addison’s GoFundMe page. Use the #clicks4acause in your message to the family!
- Become a Courageous giver and make a flat donation or match my donation at the end of the month to Addison’s GoFundMe page. Use the #clicks4acause in your message to the family!