Please Support My Cause
And Thank You For Reading…
My cause is not me. My cause is the Smith-Magenis Syndrome Research Foundation. The work of the Foundation is very near and dear to me, as my eldest son Damian has SMS. This website wouldn’t be the same without Damian being a big part of it. What started simple – me going to museums and writing about them has evolved into a much larger journey. A journey to everything of interest in Connecticut, yes, but also my personal journey being a father to a unique special needs son. That story is woven throughout all the other stories on CTMQ.
Many readers seem to enjoy what I do here. I do it all for fun and have never asked for anything in return. (Compliments are nice though, I’ll admit.)
However, I have made the decision to monetize CTMQ with advertisements (please go read that) – in an effort to raise money for the SMSRF. In the meantime, I humbly suggest that you – yes, YOU – consider donating to the cause. It would mean so much to me and the other families who are touched by SMS in their lives.
Any amount would be appreciated. If you’ve enjoyed anything on this site over the last seven years, or hope to spend more time over the next seven, please donate here.
Thank you. Below is a video from my friend and SMSRF co-founder Missy Longman. We’d love it if you watch.