Welcome to the Tuesday T21 blog hop!
We are so glad that you have stopped by for a visit! We encourage you to look through some of the great posts shared by our readers and then take the time to read those that interest you. If you are adding to our list, thank you for sharing your Down Syndrome-related posts with us. It’s so much fun to read your hints, tips, and happenings. We hope you have fun exploring all the great posts everyone has shared with us.
Please note that only posts related to this topic are allowed to keep the content relevant to interested readers.
Here’s how it works… Each week the Hop will open on Tuesday mornings (open early this week) every week and run until Thursday evenings when it will close. Once closed the hop can no longer be added to for that week (you will have to wait to add till the following week). You are STRONGLY encouraged to visit the posts of others and connect, comment and share any content you feel is fitting. Do follow along here so you can be made aware when the blog hop goes live.
Each week the most popular post will earn a featured spot for the following week. All of the author’s social media platforms will be linked up and a title image featured on the blog hop for all to see.
Okay, so with the technicalities out of the way…let’s get hopping!
FEATURED POST THIS WEEK:
HOW I HELP MY DAUGHTER TO SPEAK MORE CLEARLY,
PART 1: READING
If you are feature, please be sure to grab your button showing you were “featured” on the blog hop, share it on your blog sidebar.
Be sure to check out Sheila and her blog An Extra Blessing.com Shiela also has the most amazing handmade goods in her Etsy shop here and follow her on instgram @an.extra.blessing
Now for this week’s hop:
I love all the story and first hand accounts from this week’s link ups. I really have had so many of the feelings expressed in the stories and can relate. But I have to say my vote goes for Cedar’s Story, The Day a Stranger . . .
I still get this knot in my stomach when people mention Dianna and Down syndrome. I just see her as Dianna and not a child who needs to have a diagnosis. But I need to take these moments and share that in some way with those who don’t have our experience. Thank you for sharing your experience!
Awe, Shiela, thank you. You are always an encourager!