I created Everyday CVI to share the ways our family embeds CVI strategies into our everyday life, so most of what I write will focus on tangible items and how we have used them specifically. However, I have found my free time tied up lately as I have been taking care of some other “everyday CVI” work that all CVI parents need to address on an ongoing basis. I’ve been in the trenches of CVI advocacy.
It recently dawned on me that the practical ways in which I have been advocating for my daughter to receive appropriate vision services is very much a part of our “everyday” with CVI…so why not write some of it down to share with others? As always, I cannot promise that anything I share here will be relevant or helpful to any reader’s specific situation, but at the very least I hope that sharing our story’s recent progress will serve to inspire other parents to NEVER STOP SEEKING THE APPROPRIATE RESOURCES AND/OR ACCOMMODATIONS YOUR CHILD WITH CORTICAL VISUAL IMPAIRMENT NEEDS.
Let’s start at the beginning, shall we? I’ll do my best to summarize our CVI advocacy journey thus far with a few practical suggestions thrown in the mix.