01 May Apraxia Awareness Month 2025 – Connect with Local Businesses
One great way to connect with your community is by reaching out to local businesses! Think of your favorite coffee shop or your child’s karate class. Oftentimes these businesses have come to know you and your Apraxia Star and would love a way to support you just as you support them! This week we are challenging you to connect with one local business in your community.
Cause Partner: Consider asking any of these businesses to be a Cause Partner with Apraxia Kids! They can donate a portion of sales for a month or even for a specific product. Imagine having a blue for apraxia slushie at your favorite movie theater! You can learn more about our current Cause Partners here.
Dine to Donate: Many restaurant chains love having a dine to donate day for your cause! This is a great way to support your Walk for Apraxia and send it to other walk families so that you can meet up while supporting Apraxia Kids!
Round-Up: Ask your favorite bakery or favorite small business to round up for Apraxia Kids! Or shop with one of our round-up partners. Did you know that you can support Apraxia Kids through round-up donations at Walmart, Paypal and eBay? We even have a brand new round-up partner called lasting change where you can round up every credit card purchase you make! Learn more about our round-up partners here.
Sponsorship: One great benefit to being a Walk for Apraxia or National Conference sponsor is that the business can get their name out there! By being a $250 or more donor for the Walk for Apraxia they will get their name on the back of your Walk’s t-shirt. What a great way for them to show their support! It is easy to ask and okay if they say no.
Raise Awareness: The easiest way to get a business involved is by asking them to hang up your Walk for Apraxia flyer or by sharing information about Apraxia Kids and CAS. Just by having the word “apraxia” hanging on the wall, you never know who you might start a conversation with. It might even help a family consider asking about CAS with their pediatrician or speech language pathologist.
One great way to connect with your community is by reaching out to local businesses! Think of your favorite coffee shop or your child’s karate class. Oftentimes these businesses have come to know you and your Apraxia Star and would love a way to support you just as you support them! This week we are challenging you to connect with one local business in your community.
Cause Partner: Consider asking any of these businesses to be a Cause Partner with Apraxia Kids! They can donate a portion of sales for a month or even for a specific product. Imagine having a blue for apraxia slushie at your favorite movie theater! You can learn more about our current Cause Partners here.
Dine to Donate: Many restaurant chains love having a dine to donate day for your cause! This is a great way to support your Walk for Apraxia and send it to other walk families so that you can meet up while supporting Apraxia Kids!
Round-Up: Ask your favorite bakery or favorite small business to round up for Apraxia Kids! Or shop with one of our round-up partners. Did you know that you can support Apraxia Kids through round-up donations at Walmart, Paypal and eBay? We even have a brand new round-up partner called lasting change where you can round up every credit card purchase you make! Learn more about our round-up partners here.
Sponsorship: One great benefit to being a Walk for Apraxia or National Conference sponsor is that the business can get their name out there! By being a $250 or more donor for the Walk for Apraxia they will get their name on the back of your Walk’s t-shirt. What a great way for them to show their support! It is easy to ask and okay if they say no.
Raise Awareness: The easiest way to get a business involved is by asking them to hang up your Walk for Apraxia flyer or by sharing information about Apraxia Kids and CAS. Just by having the word “apraxia” hanging on the wall, you never know who you might start a conversation with. It might even help a family consider asking about CAS with their pediatrician or speech language pathologist.
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