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WDSD 2022 - Recap

WDSD 2022 was such a huge success! The internet finally flooded with positivity and joy. There were many things posted all over the internet so I grabbed a few pics and added them here. I am still trying to catch up on it all. What an incredible day to be a part of and witness. So many of you celebrated the individuals with Down Syndrome so so well. It was LOUD and PROUD!  Thank you so much to every single person that supported the WDSD mission of educating and advocating for inclusion across all platforms. It really is incredible to see what we can all do together and to witness the power of your voices and stories.    Here are...

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YQG WDSD 2021!!

  World Down Syndrome Day - A day to celebrate the contributions made by those with Down syndrome that are in our lives, and communities. WDSD is on March 21st or - 3.21 - to signify the 3rd copy of the 21st chromosome that people with Down syndrome have. Many of you celebrated in your homes this year by wearing your CHF socks (or any mismatched socks), took pics and shared on your social media. Some of you made donations to charities that are near and dear to your heart. I know CHF received many donations on 3.21 and we are so very grateful. We are always so humbled by community support. I shared as many photos via our IG...

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Inclusion - Contribution - Belonging

Think about a time where you felt you truly belonged. Think about your role in that space. Did you feel safe? Accepted? Respected? Were you able to contribute? Were you celebrated for exactly who you are in that moment and not the potential of what you might one day be. But just for you, Just as you are?  Inclusion has been a buzz word for at least a decade. But sometimes we don’t know how to do it properly. It’s not enough to allow someone who is different into a space and call it good. It’s also not about allowing someone into a space and trying to make them “be more like the group.” It’s about seeing everyone as equal...

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February “Off To College” Playgroup

A quiet, cozy, wintery night for our February Playgroup!  It was one of our smaller groups last night but still full of life and laughter. I literally LIVE for this night. We all get to relax, catch up, talk Down syndrome, and PLAY! It's music to my ears when the kids give their parents a hard time about leaving. YAY!!! We must be doing something right!  Love this twining look guys!!!  Hazel was giggling so much playing with Matthew. SWOON! These two were making me melt into a puddle... I love getting this opportunity to visit and see what families are up to. I don't take for granted that everyone is VERY busy, yet still chooses to spend time with...

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Supporting Families

Part of why we started CHF was to be able to support families who may sometimes feel isolated, or who may experience financial hardship due to medical issues that can not be handled locally in Windsor. Some families find themselves on endless drives on the highway going back and forth from Windsor to London, and sometimes Windsor to Toronto. These times can feel desperate, lonely, and scary. These times force people into living a life with no consistency, no routine. It can even force them to take time off work and keep them away from their other family members.   We know, we've been there. When I was pregnant with Hazel, we left the house at 4am with some complications. We...

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